US20110156003A1 - Systems and Methods for Nanowire Growth - Google Patents

Systems and Methods for Nanowire Growth Download PDF

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US20110156003A1
US20110156003A1 US12/827,098 US82709810A US2011156003A1 US 20110156003 A1 US20110156003 A1 US 20110156003A1 US 82709810 A US82709810 A US 82709810A US 2011156003 A1 US2011156003 A1 US 2011156003A1
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nanowires
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Nanosys Inc
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    • C30B11/00Single-crystal growth by normal freezing or freezing under temperature gradient, e.g. Bridgman-Stockbarger method
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Definitions

  • the present invention relates to nanowires, and more particularly, to improved methods for nanowire growth.
  • Nanostructures, and in particular, nanowires have the potential to facilitate a whole new generation of electronic devices.
  • a major impediment to the emergence of this new generation of electronic devices based on nanostructures is the ability to effectively grow nanowires and other nanostructures that have consistent characteristics.
  • Current approaches to growing nanowires do not facilitate mass production and typically do not yield consistent nanowire performance characteristics.
  • the present invention provides methods for producing vertically aligned epitaxial nanowires (e.g., silicon nanowires) with uniform characteristics such as low taper, comprising providing a substrate material having one or more nucleating particles deposited thereon in a reaction chamber, introducing an etchant gas into the reaction chamber at a first temperature which gas aids in cleaning the surface of the substrate material (and the nucleating particles), contacting the nucleating particles with at least a first precursor gas to initiate nanowire growth, and heating the substrate material to a second temperature, whereby nanowires are grown at the site of the nucleating particles.
  • the substrate material utilized in the processes of the present invention preferably is crystallographic, but may be amorphous.
  • the substrate material comprises crystallographic silicon, either polycrystalline or single crystalline.
  • the substrate may be amorphous SiO 2 , Si 3 N 4 , or alumina.
  • the precursor gas comprises SiH 4 , but may also comprise other precursor gases such as Si 2 H 6 .
  • the first temperature at which the etchant gas is introduced to clean the substrate surface is higher than the second temperature at which nanowire growth occurs in the presence of the precursor gas.
  • the first temperature may be at least about 100° C. higher than the second temperature, e.g., about 200° C. higher than the second temperature, and may occur at a temperature of about 800° C., for example.
  • the first temperature at which the etchant gas is introduced to clean the substrate surface may be about the same as the second temperature at which nanowire growth occurs in the presence of the precursor gas.
  • the first and second temperatures may be about 600° C.
  • the nucleating particles used in the practice of the present invention will suitably be a metal catalyst and will comprise a metal that reacts with the first precursor gas to form a eutectic from which Si may precipitate.
  • Suitable metal catalysts comprise Au, Al, Pt, Fe, Ti, Ga, Ni, Sn or In and in certain such embodiments, may be a Au colloid or Au film.
  • High quality single crystalline silicon nanowires may then be grown by metal-catalyzed chemical vapor deposition (CVD), for example, which is based on a vapor-liquid solid (VLS) growth process.
  • CVD chemical vapor deposition
  • the precursor gas e.g., SiH 4
  • Si diffuses in the catalyst
  • the Si atoms precipitate out at the catalyst-substrate interface to form a silicon nanowire of diameter similar to that of the catalyst nucleating particle.
  • the wires growing on the substrate material can preferably grow epitaxially from the substrate.
  • Nanowires produced according to the processes of the present invention grow out of the plane of the substrate material in an axially aligned vertical orientation, and are capable of transporting electrical charge. It has been found that the methods of the present invention provide nanowires having very low taper along their length, for example, have a taper rate of less than about 2 nm/micron, e.g., less than about 1.5 nm/micron, e.g., less than about 1.0 nm/micron, e.g., less than about 0.5 nm/micron, e.g., less than about 0.3 nm/micron along their length.
  • the first precursor gas utilized in the processes of the present invention will suitably comprise SiH 4 (or Si 2 H 6 ) and may further comprise one or more dopant gases such as B 2 H 6 , POCl 3 or PH 3 .
  • the precursor gas used in the processes of the present invention may suitably be introduced via plasma enhanced sputter deposition. Sputter deposition can be accomplished via any method known to the ordinarily skilled artisan, for example, diode, radio frequency and direct current deposition.
  • in-situ doping such as axial dopant modulation
  • CMOS complementary metal oxide semiconductor
  • the VLS growth method lends itself well to axial modulation of dopant to allow, e.g., for the doping of only certain portions of the wires (and not the entire length of the wire), e.g., at its ends, with a dopant species such as boron or phosphorus.
  • a dopant species such as boron or phosphorus.
  • diborane has been shown to increase and phosphine decrease the decomposition rate of silane.
  • Diborane can thus induce substantial uncatalysed Si deposited on the nanowire sidewalls during growth of the wires which can result in a significant increase in the taper rate along the wires during growth and dopant incorporation.
  • an etchant gas such as hydrogen chloride may also be introduced into the reaction chamber during growth of the nanowires and/or during dopant incorporation.
  • the HCl will produce a relatively low etch rate of the wires at the growth temperature of the wires (e.g., about 600° C. for vertically oriented epitaxial wires), and lead to a passivation layer of Cl on the wires which inhibits the sidewall growth of Si thereby providing good control of wire uniformity (e.g., wires with low taper), and further sterically hindering sidewall incorporation of dopant allowing for axially modulated electronic doping of the vertically aligned epitaxial wires.
  • the partial pressure of HCl during the preclean step is higher (e.g., about 1.0 Torr) than the partial pressure of HCl introduced into the reaction chamber during the nanowire growth process (e.g., about 0.15 Torr) to minimize over-etching of the wires during growth.
  • the teachings of the present invention further allow the synthesis of nanowires with different materials longitudinally along the length of the nanowire, such as would be the case with alternating or periodic segments of different materials or multi-segmented nanowires where at least two of the segments comprise different materials.
  • An example of this would be where adjacent segments have different chemical compositions, such as Si, Ge and/or SiGe.
  • HCl during the nanowire growth process of these different segments will produce a very low etch rate and lead to a passivation layer of Cl which inhibits the sidewall decomposition of SiH 4 or GeH 4 , providing improved control of the Si/Ge and Si x Ge (1-x) axial modulation of vertically aligned heterostructure nanowires with very low taper.
  • various other nanowire structures using different semiconductor materials e.g., such as PbSe
  • PbSe can also be grown using different precursor gases for those other materials.
  • FIG. 1A is a diagram of a single crystal semiconductor nanowire.
  • FIG. 1B is a diagram of a nanowire doped according to a core-shell structure.
  • FIG. 2 is a flowchart of a method for preparing nanowires using an HCl preclean according to an embodiment of the invention.
  • FIG. 3 is a flowchart of a method for preparing nanowires using a combination of an HCl preclean step and introduction of HCl during the nanowire growth process, according to an embodiment of the invention.
  • FIGS. 4A and 4B are TEMs showing a base ( 4 A) and corresponding tip ( 4 B) of a 21 micron long nanowire having a taper rate of about 0.2 nm/micron grown using a combination of an HCl preclean step and introduction of HCl during the nanowire growth process according to the methods of the present invention.
  • nanowires are frequently referred to, the techniques described herein may also be applicable to other nanostructures, such as nanorods, nanotubes, nanotetrapods, nanoribbons and/or combinations thereof. It should further be appreciated that the manufacturing techniques described herein could be used to create any semiconductor device type, and other electronic component types. Further, the techniques would be suitable for application in electrical systems, optical systems, consumer electronics, industrial electronics, wireless systems, space applications, or any other application.
  • an “aspect ratio” is the length of a first axis of a nanostructure divided by the average of the lengths of the second and third axes of the nanostructure, where the second and third axes are the two axes whose lengths are most nearly equal to each other.
  • the aspect ratio for a perfect rod would be the length of its long axis divided by the diameter of a cross-section perpendicular to (normal to) the long axis.
  • heterostructure when used with reference to nanostructures refers to nanostructures characterized by at least two different and/or distinguishable material types. Typically, one region of the nanostructure comprises a first material type, while a second region of the nanostructure comprises a second material type.
  • the nanostructure comprises a core of a first material and at least one shell of a second (or third etc.) material, where the different material types are distributed radially about the long axis of a nanowire, a long axis of an arm of a branched nanocrystal, or the center of a nanocrystal, for example.
  • a shell need not completely cover the adjacent materials to be considered a shell or for the nanostructure to be considered a heterostructure.
  • a nanocrystal characterized by a core of one material covered with small islands of a second material is a heterostructure.
  • the different material types are distributed at different locations within the nanostructure.
  • material types can be distributed along the major (long) axis of a nanowire or along a long axis or arm of a branched nanocrystal.
  • Different regions within a heterostructure can comprise entirely different materials, or the different regions can comprise a same base material.
  • a “nanostructure” is a structure having at least one region or characteristic dimension with a dimension of less than about 500 nm, e.g., less than about 200 nm, less than about 100 nm, less than about 50 nm, or even less than about 20 nm. Typically, the region or characteristic dimension will be along the smallest axis of the structure. Examples of such structures include nanowires, nanorods, nanotubes, branched nanocrystals, nanotetrapods, tripods, bipods, nanocrystals, nanodots, quantum dots, nanoparticles, branched tetrapods (e.g., inorganic dendrimers), and the like.
  • Nanostructures can be substantially homogeneous in material properties, or in certain embodiments can be heterogeneous (e.g., heterostructures). Nanostructures can be, for example, substantially crystalline, substantially monocrystalline, polycrystalline, amorphous, or a combination thereof. In one aspect, each of the three dimensions of the nanostructure has a dimension of less than about 500 nm, for example, less than about 200 nm, less than about 100 nm, less than about 50 nm, or even less than about 20 nm.
  • nanowire generally refers to any elongated conductive or semiconductive material (or other material described herein) that includes at least one cross sectional dimension that is less than 500 nm, and preferably, less than 100 nm, and has an aspect ratio (length:width) of greater than 10, preferably greater than 50, and more preferably, greater than 100.
  • the nanowires of this invention can be substantially homogeneous in material properties, or in certain embodiments can be heterogeneous (e.g. nanowire heterostructures).
  • the nanowires can be fabricated from essentially any convenient material or materials, and can be, e.g., substantially crystalline, substantially monocrystalline, polycrystalline, or amorphous.
  • Nanowires can have a variable diameter or can have a substantially uniform diameter, that is, a diameter that shows a variance less than about 20% (e.g., less than about 10%, less than about 5%, or less than about 1%) over the region of greatest variability and over a linear dimension of at least 5 nm (e.g., at least 10 nm, at least 20 nm, or at least 50 nm).
  • Nanowires according to this invention can expressly exclude carbon nanotubes, and, in certain embodiments, exclude “whiskers” or “nanowhiskers”, particularly whiskers having a diameter greater than 100 nm, or greater than about 200 nm.
  • nanowires examples include semiconductor nanowires as described in Published International Patent Application Nos. WO 02/17362, WO 02/48701, and WO 01/03208, carbon nanotubes, and other elongated conductive or semiconductive structures of like dimensions, which are incorporated herein by reference.
  • nanorod generally refers to any elongated conductive or semiconductive material (or other material described herein) similar to a nanowire, but having an aspect ratio (length:width) less than that of a nanowire.
  • two or more nanorods can be coupled together along their longitudinal axis so that the coupled nanorods span all the way between electrodes.
  • two or more nanorods can be substantially aligned along their longitudinal axis, but not coupled together, such that a small gap exists between the ends of the two or more nanorods.
  • electrons can flow from one nanorod to another by hopping from one nanorod to another to traverse the small gap.
  • the two or more nanorods can be substantially aligned, such that they form a path by which electrons can travel between electrodes.
  • a wide range of types of materials for nanowires, nanorods, nanotubes and nanoribbons can be used, including semiconductor material selected from, e.g., Si, Ge, Sn, Se, Te, B, C (including diamond), P, B—C, B—P(BP 6 ), B—Si, Si—C, Si—Ge, Si—Sn and Ge—Sn, SiC, BN/BP/BAs, AlN/AlP/AlAs/AlSb, GaN/GaP/GaAs/GaSb, InN/InP/InAs/InSb, ZnO/ZnS/ZnSe/ZnTe, CdS/CdSe/CdTe, HgS/HgSe/HgTe, BeS/BeSe/BeTe/MgS/MgSe, GeS, GeSe, GeTe, SnS, SnSe, SnTe, PbO, PbS,
  • the nanowires can also be formed from other materials such as metals such as gold, nickel, palladium, iradium, cobalt, chromium, aluminum, titanium, tin and the like, metal alloys, polymers, conductive polymers, ceramics, and/or combinations thereof.
  • metals such as gold, nickel, palladium, iradium, cobalt, chromium, aluminum, titanium, tin and the like
  • metal alloys polymers, conductive polymers, ceramics, and/or combinations thereof.
  • Other now known or later developed conducting or semiconductor materials can be employed.
  • the semiconductor may comprise a dopant from a group consisting of: a p-type dopant from Group III of the periodic table; an n-type dopant from Group V of the periodic table; a p-type dopant selected from a group consisting of: B, Al and In; an n-type dopant selected from a group consisting of: P, As and Sb; a p-type dopant from Group II of the periodic table; a p-type dopant selected from a group consisting of: Mg, Zn, Cd and Hg; a p-type dopant from Group IV of the periodic table; a p-type dopant selected from a group consisting of: C and Si.; or an n-type dopant selected from a group consisting of: Si, Ge, Sn, S, Se and Te.
  • Other now known or later developed dopant materials can be employed.
  • the nanowires or nanoribbons can include carbon nanotubes, or nanotubes formed of conductive or semiconductive organic polymer materials, (e.g., pentacene, and transition metal oxides).
  • conductive or semiconductive organic polymer materials e.g., pentacene, and transition metal oxides.
  • Nanowire e.g., nanowire-like structures having a hollow tube formed axially therethrough.
  • Nanotubes can be formed in combinations/thin films of nanotubes as is described herein for nanowires, alone or in combination with nanowires, to provide the properties and advantages described herein.
  • the term “taper rate” refers to the diameter of an elongated nanostructure (such as a nanowire) as measured from its bottom end portion less the diameter of the nanostructure as measured from its top end portion, divided by the length of the nanostructure.
  • FIG. 1A illustrates a single crystal semiconductor nanowire core (hereafter “nanowire”) 100 .
  • FIG. 1A shows a nanowire 100 that is a uniformly doped single crystal nanowire.
  • Such single crystal nanowires can be doped into either p- or n-type semiconductors in a fairly controlled way.
  • Doped nanowires such as nanowire 100 exhibit improved electronic properties. For instance, such nanowires can be doped to have carrier mobility levels comparable to bulk single crystal materials.
  • FIG. 1B shows a nanowire 110 having a core-shell structure.
  • Surface scattering can be reduced by forming an outer layer of the nanowire, such as by the passivation annealing of nanowires, and/or the use of core-shell structures with nanowires.
  • An insulating layer such as an oxide coating, can be formed on a nanowire as the shell layer.
  • the annealing of the nanowires in hydrogen (H 2 ) can greatly reduce surface states.
  • the core-shell combination is configured to satisfy the following constraints: (1) the shell energy level should be higher than the core energy level, so that the conducting carriers are confined in the core; and (2) the core and shell materials should have good lattice match, with few surface states and surface charges.
  • Other more complex NW core-shell structures may also be used to include a core of single crystal semiconductor, an inner-shell of gate dielectric, and an outer-shell of conformal gate. This can be realized by depositing a layer of TaAlN, WN, or highly-doped amorphous silicon around the Si/SiO x core-shell structure (described above) as the outer-gate shell, for example.
  • the valence band of the insulating shell can be lower than the valence band of the core for p-type doped wires, or the conduction band of the shell can be higher than the core for n-type doped wires.
  • the core nanostructure can be made from any metallic or semiconductor material, and the one or more shell layers deposited on the core can be made from the same or a different material.
  • the first core material can comprise a first semiconductor selected from the group consisting of: a Group II-VI semiconductor, a Group III-V semiconductor, a Group IV semiconductor, and an alloy thereof.
  • the second material of the one or more shell layers can comprise an oxide layer, a second semiconductor, the same as or different from the first semiconductor, e.g., selected from the group consisting of: a Group II-VI semiconductor, a Group III-V semiconductor, a Group IV semiconductor, and an alloy thereof.
  • Example semiconductors include, but are not limited to, CdSe, CdTe, InP, InAs, CdS, ZnS, ZnSe, ZnTe, HgTe, GaN, GaP, GaAs, GaSb, InSb, Si, Ge, AlAs, AlSb, PbSe, PbS, and PbTe.
  • metallic materials such as gold, chromium, tin, nickel, aluminum etc. and alloys thereof can be used as the core material, and the metallic core can be overcoated with an appropriate shell material such as silicon dioxide or other insulating materials, which may in turn may be coated with one or more additional shell layers of the materials described above to form more complex core-shell-shell nanowire structures.
  • Nanostructures can be fabricated and their size can be controlled by any of a number of convenient methods that can be adapted to different materials. For example, synthesis of nanocrystals of various composition is described in, e.g., Peng et al. (2000) “Shape Control of CdSe Nanocrystals” Nature 404, 59-61; Puntes et al. (2001) “Colloidal nanocrystal shape and size control: The case of cobalt” Science 291, 2115-2117; U.S. Pat. No. 6,306,736 to Alivisatos et al. (Oct. 23, 2001) entitled “Process for forming shaped group III-V semiconductor nanocrystals, and product formed using process”; U.S.
  • nanowires having various aspect ratios including nanowires with controlled diameters, is described in, e.g., Gudiksen et al (2000) “Diameter-selective synthesis of semiconductor nanowires” J. Am. Chem. Soc. 122, 8801-8802; Cui et al. (2001) “Diameter-controlled synthesis of single-crystal silicon nanowires” Appl. Phys. Lett. 78, 2214-2216; Gudiksen et al. (2001) “Synthetic control of the diameter and length of single crystal semiconductor nanowires” J. Phys. Chem. B 105, 4062-4064; Morales et al.
  • branched nanowires e.g., nanotetrapods, tripods, bipods, and branched tetrapods
  • FIG. 1 “Controlled synthesis of multi-armed CdS nanorod architectures using monosurfactant system” J. Am. Chem. Soc. 123, 5150-5151; and Manna et al. (2000) “ Synthesis of Soluble and Processable Rod -, Arrow -, Teardrop -, and Tetrapod - Shaped CdSe Nanocrystals” J. Am. Chem. Soc. 122, 12700-12706.
  • core-shell nanostructure heterostructures namely nanocrystal and nanowire (e.g., nanorod) core-shell heterostructures
  • core-shell nanostructure heterostructures namely nanocrystal and nanowire (e.g., nanorod) core-shell heterostructures
  • core-shell nanostructure heterostructures namely nanocrystal and nanowire (e.g., nanorod) core-shell heterostructures
  • Peng et al. 1997) “Epitaxial growth of highly luminescent CdSe/CdS core/shell nanocrystals with photostability and electronic accessibility” J. Am. Chem. Soc. 119, 7019-7029
  • Dabbousi et al. 1997 “(CdSe)ZnS core-shell quantum dots: Synthesis and characterization of a size series of highly luminescent nanocrysallites” J. Phys. Chem.
  • nanowire heterostructures in which the different materials are distributed at different locations along the long axis of the nanowire is described in, e.g., U.S. Pat. No. 6,882,051; Gudiksen et al. (2002) “Growth of nanowire superlattice structures for nanoscale photonics and electronics” Nature 415, 617-620; Bjork et al. (2002) “One-dimensional steeplechase for electrons realized” Nano Letters 2, 86-90; Wu et al. (2002) “Block-by-block growth of single-crystalline Si/SiGe superlattice nanowires” Nano Letters 2, 83-86; and U.S. Pat. No. 7,067,867. Similar approaches can be applied to growth of other heterostructures.
  • High-quality single crystalline nanowires such as silicon nanowires are commonly grown by metal-catalyzed chemical vapor deposition (CVD).
  • CVD metal-catalyzed chemical vapor deposition
  • nanosized metal catalysts such as gold nucleating particles, are used to catalyze the decomposition of a precursor gas such as silane (SiH 4 ).
  • SiH 4 silane
  • a liquid Au—Si alloy is formed and when supersaturation is reached, silicon precipitates out to form a silicon nanowire of diameter similar to that of the catalyst particle.
  • the preferred nanowire growth direction for this method may comprise ⁇ 111>, ⁇ 110> and ⁇ 112>.
  • vertically aligned nanowire growth is highly desirable to produce devices such as transistors with consistent performance characteristics.
  • Such orientation may be realized by epitaxial growth on single-crystalline substrates with suitable crystal structure (e.g., Si (111) wafers).
  • Epitaxial growth requires a clean interface between the nucleating particles (e.g., Au particles) and the substrate.
  • the native oxide (SiOx) may be removed prior to growth with a hydrofluoric (HF) acid etch as is known in the art.
  • HF hydrofluoric
  • the silicon added to the sidewall of the nanowires can be a combination of polysilicon, amorphous silicon, and/or epitaxial silicon depending on the growth conditions. Forms of silicon other than epitaxial silicon are undesirable since they can spoil the intrinsic electronic properties of the wires. It is desirable to be able to grow nanowires such as silicon nanowires that have reduced taper in order to produce devices based on such wires with consistent performance characteristics.
  • FIG. 2 is a flowchart of method 200 for preparing nanowires using a hydrogen chloride pre-clean step according to an embodiment of the invention.
  • Method 200 begins in step 201 .
  • the surface of a wafer such as a silicon wafer, is first passivated with a hydrofluoric acid gas etchant to remove the native oxide (e.g., SiOx) from the wafer surface prior to depositing nucleating particles on the substrate surface.
  • a hydrofluoric acid gas etchant to remove the native oxide (e.g., SiOx) from the wafer surface prior to depositing nucleating particles on the substrate surface.
  • one or more nucleating particles suitably metal catalysts such as Au colloid particles, are deposited on a substrate material to create nucleation sites for nanowire growth.
  • step 204 following deposition of the nucleating particles on the substrate, the substrate is heated to a first temperature in a reaction chamber and an etchant gas, e.g., hydrogen chloride gas, is introduced into the reaction chamber to clean the substrate surface coated with the nucleating particles.
  • the etchant gas aids in cleaning both the substrate surface as well as the nucleating particles on the substrate surface.
  • heating of the nucleating particles to a second temperature (which may be the same as or lower than the first temperature) and contacting the nucleating particles with a first precursor gas (e.g., silane), creates a liquid alloy droplet and initiates nanowire growth, which is indicated by label 206 , until they reach the desired size and orientation, as shown in step 208 .
  • a first precursor gas e.g., silane
  • the substrate material on which the nanowires are grown is a crystallographic substrate.
  • crystallographic substrate includes any substrate material which comprises atoms situated in a repeating or periodic array over large atomic distances, typically on the order of 10 or more angstroms ( ⁇ ). Such crystallographic substrates may be polycrystalline or may comprise single crystals.
  • the crystallographic substrate utilized in the processes of the present invention is silicon (Si).
  • suitable crystallographic materials include, but are not limited to, germanium (Ge), gallium arsenide (GaAs), gallium nitride (GaN), sapphire, quartz, and silicon germanium (SiGe).
  • the substrate material may comprise an amorphous material. Suitable amorphous substrate materials which may be used in the practice of the present invention include, but are not limited to SiO 2 , Si 3 N 4 and alumina.
  • the methods of the present invention comprise first depositing nucleating particles on a substrate material.
  • Nucleating particles that may be used in the practice of the present invention include metal catalysts and can be any metal that reacts with the precursor gas to form a eutectic phase. Such a mixture has a minimum melting point at which all components are in solution.
  • precursor gas molecules e.g., silicon
  • a saturation point on the eutectic phase diagram is reached such that semiconductor particles (e.g., Si) begin to precipitate out of the metal alloy, thereby creating a growing nanowire.
  • Continuous addition of precursor gas will continue to saturate the eutectic, thereby generating additional material for nanowire growth.
  • the nucleating particles will be metal catalysts and can comprise any of the transition metals from the Periodic Table, including, but not limited to, copper, silver, gold, nickel, palladium, platinum, cobalt, rhodium, iridium, indium, iron, ruthenium, tin, osmium, manganese, chromium, molybdenum, tungsten, vanadium, niobium, tantalum, titanium, zirconium and gallium, including mixtures of one or more of these metals.
  • the metal catalyst can comprise a gold (Au) colloid (i.e., a Au nanoparticle) or Au film.
  • 20 to 150 nanometer (nm) diameter gold colloids can be used.
  • the target is to achieve a uniform deposition of gold nanoparticles with density between about 0.14 to 6 particles per square micrometer ( ⁇ m).
  • a key is minimized gold particle cluster formation.
  • the clusters can result in undesired larger diameter nanowire growth.
  • Spin coating and self assembly methods can be explored for the deposition (see, e.g., U.S. Pat. No. 7,067,867 which is incorporated by reference herein in its entirety).
  • Spin coating is a fairly straightforward process.
  • a deposition density can be controlled through variation of the gold particle concentration in the precursor colloids, manipulation of surface chemistry of the silicon wafer, and changing the spin speed.
  • a drawback of spin coating can be low utilization efficiency of gold colloid solution.
  • a recycling process in the production stage can be used if warranted.
  • Self assembly involves some use of well established chemistry.
  • the surface of 4 inch silicon oxide coated wafer is functionalized with either (3-aminopropyl)-trimethoxysilane (APTES) or (3-mercaptopropyl)-trimethoxysilane (MPTES), then contacted with gold colloid solution.
  • APTES (3-aminopropyl)-trimethoxysilane
  • MPTES (3-mercaptopropyl)-trimethoxysilane
  • the gold particles are assembled on the surface. The difference between two different chemistries are compared, and the possibility of controlling the density of gold particles by control of the contact time and gold particle concentration in the contact solution can be used.
  • the nucleating particles used to practice the present invention can also be formed on a substrate surface by heating a gold film coating layer on the surface.
  • the present invention comprises heating the first precursor gas to a temperature at which 1) the gas dissociates into its free component atoms, and 2) the nucleating particles (e.g. metal catalyst) melts to a liquid.
  • the free gas molecules can then diffuse into the metal catalyst to form a liquid alloy droplet.
  • CVD chemical vapor deposition
  • the first precursor gas may be selected from, but not limited to, SiH 4 or Si 2 H 6 . Heating these Si precursor gases above the temperature at which the thermal energy is sufficient to break the bond energies between the gaseous molecules generates free Si atoms (e.g., Si—H bond: 93 kcal/mole, Si—Cl bond: 110 kcal/mole, Si—Si bond; 77 kcal/mole, see M. T. Swihart and R. W. Can, J. Phys Chem A 102:1542-1549 (1998).) Provided that this temperature is also high enough to liquefy the metal catalyst, the free Si atoms will diffuse into the metal and generate a eutectic phase. Dissociation temperatures for Si 2 H 6 and SiH 4 are between about 300° C. to 500° C., respectively, and preferably growth occurs at a temperature of about 600° C. to produce vertically oriented epitaxial wires.
  • the precursor gas used during any of the nanowire growth processes may further comprise one or more doping gases.
  • suitable doping gases include, but are not limited to, B 2 H 6 , POCl 3 and PH 3 .
  • in situ doping is necessary for complementary metal oxide semiconductor (CMOS) device fabrication.
  • wires can be grown using the same doping gas in each of the precursor gas mixtures. In such embodiments, the entire resulting wire will be either p-type or n-type, depending on the choice of dopant.
  • different doping gases can be introduced throughout the process as components of the precursor gas.
  • wire growth can be initiated using a precursor gas comprising an n-type dopant (e.g., P, As or Sb) and then continued using a precursor gas using a p-type dopant (e.g., B, Al or In).
  • a p-type doing gas will be used during initiation and then an n-type doping gas during growth.
  • the type of doping gas can be switched multiple times throughout the growth process as the precursor gases are switched, e.g., for axial modulation doping of the wires.
  • the resulting nanowires therefore can comprise several different dopant portions throughout their length.
  • a nanowire produced via the present invention may comprise an n-type base where electrical contact to a source electrode can be made, a p-type middle section, and an n-type top where electrical contact to a drain electrode may be made, or any suitable combination as envisioned by the ordinarily skilled artisan.
  • Such embodiments of the present invention would allow for an n-type wire to be grown on a p-type substrate, and vice versa.
  • the VLS growth method lends itself well to axial modulation of dopant to allow, e.g., for the doping of only certain portions of the wires (and not the entire length of the wire), e.g., at its ends, with a dopant species such as boron.
  • the first precursor gas can comprise SiH 4 and suitably a carrier gas, such as H 2 , He, Ar, or other inert gas. Heating this gas mixture to a sufficiently high temperature, e.g., about 600° C., generates free Si atoms.
  • the first precursor gas may comprise one or more dopant gases selected from those described throughout the application.
  • the first precursor gas mixture is passed over the nucleating particles, suitably metal-catalyst particles (e.g., gold nanoparticles) deposited on the substrate material at a total pressure between about 5 to about 50 Torr, while the nucleating particles are heated up to a temperature of about 600° C.
  • the gas pressure may be increased or decreased, thereby requiring a modification in the temperature required to dissociate the precursor gas mixture.
  • Si and B will diffuse into the metal catalyst and generate a liquid alloy droplet. This eutectic phase of metal catalyst and precursor gases will continue to exist as precursor gas is solvated in the metal catalyst. Once an over-saturation is reached, Si/B atoms will precipitate out and initiate nanowire growth. In order to continue nanowire growth, a continuous supply of Si precursor gas and doping gas are required.
  • dopant gases such as diborane and phosphine affects the thermal decomposition rate of silane. Indeed, diborane has been shown to increase and phosphine decrease the thermal decomposition rate of silane. Diborane can thus induce substantial uncatalysed silicon growth on the nanowire sidewalls during growth of the wires which can result in a significant increase in the taper rate along the wires during wire growth and dopant incorporation.
  • an etchant gas such as hydrogen chloride may also be introduced into the reaction chamber during growth of the nanowires and/or during dopant incorporation.
  • Steps 301 , 302 , 304 , 306 , and 308 in FIG. 3 are the same as those corresponding steps 201 , 202 , 204 , 206 and 208 of FIG. 2 .
  • FIG. 3 also includes the additional step 310 of adding etchant gas, such as HCL, during the wire growth process 306 .
  • the HCl will produce a relatively low etch rate of the wires at the growth temperature of the wires (e.g., about 600° C.).
  • the growth temperature range of about 600° C. required to grow vertically aligned epitaxial silicon nanowires it has been observed that the etch rate of silicon with HCl is relatively low, and that the surface of the silicon nanowires may be covered with one or more monolayers of Cl and H.
  • Such a passivation layer can help to minimize sidewall deposition of silicon thus leading to wires with low taper, and can further sterically hinder lattice incorporation of boron (or other dopant gases) into the nanowire sidewalls thus promoting axial dopant incorporation (versus sidewall dopant incorporation which is less desirable).
  • the etchant gas such as hydrogen chloride
  • the partial pressure of HCl during the preclean step is higher (e.g., about 1.0 Torr) than the partial pressure of HCl introduced into the reaction chamber during the nanowire growth process (e.g., about 0.15 Torr) to minimize over-etching of the wires during growth.
  • the quality of the nanowires is dependent on the quality of gold nanoparticles, etchant gas concentration, control of gold nanoparticle distribution on the substrate and growth condition including temperature, ratio of dopant to precursor gas, partial pressure of the precursor gas, and resident time of precursor gases in the reactor.
  • the methods of the present invention provide nanowires having very low taper along their length, for example, have a taper rate of less than about 2 nm/micron, e.g., less than about 1 nm/micron, e.g., less than about 0.5 nm/micron, e.g., less than about 0.3 nm/micron.
  • the processes of the present invention can be accomplished using a computer controlled 8′′ semiconductor furnace.
  • 4A and 4B are a TEMs showing a base ( 4 A) and corresponding tip ( 4 B) of a 21 micron long nanowire having a taper rate of about 0.2 nm/micron grown using a combination of an HCl preclean step and introduction of HCl during the nanowire growth process according to the methods of the present invention.
  • High quality single-crystalline nanowire heterostructures such as silicon/germanium nanowires can also be grown using the teachings of the present invention.
  • Such wires are commonly grown by metal-catalyzed chemical vapor deposition (CVD), which is based on a vapor-liquid-solid (VLS) growth process.
  • CVD metal-catalyzed chemical vapor deposition
  • VLS vapor-liquid-solid growth process.
  • the process gases e.g., SiH 4 and GeH 4
  • Si (Ge) diffuses in the catalyst, and then when supersaturation occurs, the silicon (germanium) precipitates out at the catalyst-substrate interface to form a silicon/germanium nanowire of diameter similar to that of the catalyst.
  • Si and Ge The main difference between Si and Ge is that vertically aligned epitaxial germanium nanowires can be grown at temperatures approximately 200° C. lower than that for silicon nanowires. This can cause problems when growing Si/Ge and Si x Ge 1-x axially modulated structures where uncatalysed thermal decomposition of the GeH4 would lead to sidewall growth producing tapered nanowires at temperatures required for silicon nanowire growth.
  • the germanium added to the sidewall of the nanowire is undesirable since it would result in a radial as well as axial compositional modulation. This would degrade the electronic properties of this compositionally modulated wire.
  • This VLS growth technique lends itself well to axial modulation of Si and Ge where the transition would be controlled by intermittently introducing and stopping the SiH 4 (GeH 4 ) to create the axial modulated growth.
  • controlled amounts of HCl can be provided during growth of the Si/Ge nanowires to enable axial Si/Ge and Si x Ge 1-x modulation of vertical nanowires without sidewall growth of the precursor gas species.
  • the growth temperature range e.g., approximately 600° C.
  • the etch rate of silicon is very low and the surface of the Si/Ge naowire is covered with a monolayer of Cl and H.
  • Such a passivation layer prevents the sidewall decomposition of silane (and/or germanium gas). This prevents sidewall deposition on the segment of the nanowire previously grown with a different solid composition of Si x Ge 1-x . This allows a controlled axial modulation without encasing the nanowire radially with material of a different, undesirable composition.
  • the precursor gas that is introduced in any of the processes of the present invention may be introduced via Plasma Enhanced Sputter Deposition (or Plasma Enhanced Chemical Vapor Deposition (PECVD)).
  • Plasma Enhanced Sputter Deposition or Plasma Enhanced Chemical Vapor Deposition (PECVD)
  • PECVD Plasma Enhanced Chemical Vapor Deposition
  • the diameter distribution of silicon nanowires of these certain embodiments of the present invention is determined by that of the nucleating particles, e.g., metal (suitably gold) nanoparticles.
  • metal suitableably gold
  • gold colloids can have a diameter distribution of ⁇ 10%. The same distribution can be attained in the nanowires.
  • Gold nanoparticles can be split into smaller ones resulting in smaller diameter nanowires, depending on the growth condition. Growth conditions can be optimized to minimize this event. Given a growth condition, the length of nanowires can be controlled by varying duration of the growth. Crystallinity of silicon nanowires and dopant concentration are also growth condition dependent. They can be optimized and controlled together with other important nanowire characteristics.
  • the nanowires produced according to any of the processes of the present invention will suitably grow out of the plane of the substrate material.
  • Such growth includes nanowires that project out of the plane of the substrate material at any angle with respect to the substrate.
  • nanowires can grow at an angle of about 1° to about 90°, and any angle in between these values, relative to the plane of the substrate material.
  • the nanowires produced by the processes described herein must project out of the plane of the substrate. That is, the nanowires produced by the processes of the present invention must extend off of the plane of the substrate material a distance greater than the dimension of a single molecule.
  • the nanowires produced according to the present invention are distinct from structures such as thin films and quantum dots, which spread on the surface of a substrate material, rather than growing in a manner such that they project out of the plane of the substrate a distance that exceeds the atomic diameter of a single Si molecule for instance.
  • the nanowires produced according to any of the processes of the present invention will project out of the plane of the substrate material so as to attain a final length of about 100 nm to less than about 50 ⁇ m, e.g., between about 15 ⁇ m to about 25 ⁇ m.
  • the nanowires of the present invention will suitably be at least about 1 nm to less than about 1 ⁇ m in diameter.
  • the nanowires of the present invention will have a diameter of about a few nms to 100's of nms, so as to allow them to be harvested and utilized in an electronic device (See U.S. Application No. 60/754,520, filed Dec. 29, 2005, for a description of nanowire harvesting which is incorporated herein by reference.)
  • the nanowires when growing on a crystalline substrate (whether polycrystalline or single crystal) will preferably grow epitaxially.
  • the present invention also embodies growth on crystalline substrates wherein the nanowires do not grow in an epitaxial orientation.
  • epitaxial as it refers to the growth of nanowires means that the nanowires have the same crystallographic characteristic(s) as the substrate material on which they are growing.
  • the orientation of the substrate material can be any crystallographic orientation known to the ordinarily skilled artisan, including, but not limited to, ⁇ 111>, ⁇ 110>, ⁇ 100> and ⁇ 211>.
  • the nanowires produced by the processes of the present invention can be grown in any crystallographic orientation, and suitably in the same orientation as the substrate material, including those orientations discussed throughout and as known to the ordinarily skilled artisan.
  • the crystallographic plane of the substrate material can be off axis of the 0° horizontal plane.
  • the nanowires growing on the surface of such a substrate material can project out of the substrate material at an angle such that the wires can be normal to the crystallographic plane (i.e., 90° with respect to the crystallographic plane) or can be off axis relative to the crystallographic plane such that they can be normal to a 0° horizontal plane.
  • the nanowires produced according to the processes of the present invention will not grow epitaxially, as the amorphous material does not comprise a crystallographic orientation.
  • the nanowires grown on such substrates may project out of the plane of the substrate at any angle relative to the horizontal plane.
  • the processes of the present invention produce nanowires that may carry electrons between two points in space and thus act to transfer charge.
  • the nanowires of the present invention are further distinct from nanodots and in their size and orientation, are distinct from semiconductor films.
  • the present invention also provides for electronic circuits comprising the nanowires produced by any of the processes of the present invention.
  • Suitably collections of nanowires produced according to the processes of the present invention are useful building blocks for high performance electronics.
  • a collection of nanowires orientated in substantially the same direction will have a high mobility value.
  • nanowires can be flexibly processed in solution to allow for inexpensive manufacture. Collections of nanowires can be easily assembled onto any type of substrate from solution to achieve a thin film of nanowires.
  • a thin film of nanowires used in a semiconductor device can be formed to include 2, 5, 10, 100, and any other number of nanowires between or greater than these amounts, for use in high performance electronics.
  • Nanowires of the present invention can also be used to make high performance composite materials when combined with polymers/materials such as organic semiconductor materials, which can be flexibly spin-cast on any type of substrate. Nanowire/polymer composites can provide properties superior to a pure polymer materials.
  • Collections or thin films of nanowires of the present invention can be aligned into being substantially parallel to each other, or can be left non-aligned or random.
  • Non-aligned collections or thin films of nanowires provide electronic properties comparable or superior to polysilicon materials, which typically have mobility values in the range of 1-10 cm 2 /V ⁇ s.
  • Aligned thin films of nanowires of the present invention can be obtained in a variety of ways.
  • aligned thin films of nanowires can be produced by using the following techniques: (a) Langmuir-Blodgett film alignment; (b) fluidic flow approaches, such as described in U.S. Pat. No. 6,872,645, and incorporated herein by reference in its entirety; (c) application of mechanical shear force; and (d) use of AC electric fields as described in U.S. Patent Application Publication 20080224123.
  • Aligned thin films of nanowires/polymer composites can be obtained using these techniques, followed by a spin-casting of the desired polymer onto the created thin film of nanowires.
  • nanowires can be deposited in a liquid polymer solution, alignment can then be performed according to one of these or other alignment processes, and the aligned nanowires can then be cured (e.g., UV cured, crosslinked, etc.).
  • An aligned thin film of nanowires/polymer composite can also be obtained by mechanically stretching a randomly oriented thin film of nanowires/polymer composite.
  • P-doped nanowires and n-doped nanowires produced by the processes of the present invention can be separately fabricated, and deposited in a homogeneous mixture onto a surface, such as a macroelectronic substrate. On a macroscopic level, the resulting material appears to contain a high concentration of both n- and p-dopants.
  • macroelectronic devices can be fabricated that respond as if they are both n- and p-doped.
  • a resulting thin film of nanowires that includes both n-doped and p-doped nanowires can exhibit characteristics of both n-doped and p-doped nanowires.
  • diode, transistor, and other known electrical devices can be fabricated to include a combination of p-doped nanowires and n-doped nanowires.
  • Nanowires produced by the processes of the present invention can also be used to produce electrical devices such as p-n diodes, transistors, and other electrical device types, using nanowire heterostructures as described herein.
  • Nanowire heterostructures include a plurality of p-n junctions along the length of the nanowire and can include alternating portions or segments along their lengths that are differently doped.
  • Numerous electronic devices and systems can incorporate semiconductor or other type devices with thin films of nanowires produced by the methods of the present invention.
  • Some example applications for the present invention are described below or elsewhere herein for illustrative purposes, and are not limiting.
  • the applications described herein can include aligned or non-aligned thin films of nanowires, and can include composite or non-composite thin films of nanowires.
  • Semiconductor devices can be coupled to signals of other electronic circuits, and/or can be integrated with other electronic circuits.
  • Semiconductor devices can be formed on large substrates, which can be subsequently separated or diced into smaller substrates. Furthermore, on large substrates (i.e., substrates substantially larger than conventional semiconductor wafers), semiconductor devices formed thereon can be interconnected.
  • the nanowires produced by the processes of the present invention can also be incorporated in applications requiring a single semiconductor device, and to multiple semiconductor devices.
  • the nanowires produced by the processes of the present invention are particularly applicable to large area, macro electronic substrates on which a plurality of semiconductor devices are formed.
  • Such electronic devices can include display driving circuits for active matrix liquid crystal displays (LCDs), organic LED displays, and field emission displays.
  • LCDs liquid crystal displays
  • Other active displays can be formed from a nanowire-polymer, quantum dots-polymer composite (the composite can function both as the emitter and active driving matrix).
  • the nanowires produced by the processes of the present invention are also applicable to smart libraries, credit cards, large area array sensors, and radio-frequency identification (RFID) tags, including smart cards, smart inventory tags, and the like.
  • RFID radio-frequency identification
  • the nanowires produced by the processes of the present invention are also applicable to digital and analog circuit applications.
  • the nanowires produced by the processes of the present invention are useful in applications that require ultra large-scale integration on a large area substrate.
  • a thin film of nanowires produced by the processes of the present invention can be implemented in logic circuits, memory circuits, processors, amplifiers, and other digital and analog circuits.
  • a clear conducting substrate is used to enhance the photovoltaic properties of the particular photovoltaic device.
  • a clear conducting substrate can be used as a flexible, large-area replacement for indium tin oxide (ITO) or the like.
  • ITO indium tin oxide
  • a substrate can be coated with a thin film of nanowires that is formed to have a large bandgap, i.e., greater than visible light so that it would be non-absorbing, but would be formed to have either the HOMO or LUMO bands aligned with the active material of a photovoltaic device that would be formed on top of it.
  • Clear conductors can be located on two sides of the absorbing photovoltaic material to carry away current from the photovoltaic device.
  • Two different nanowire materials can be chosen, one having the HOMO aligned with that of the photovoltaic material HOMO band, and the other having the LUMO aligned with the LUMO band of the photovoltaic material.
  • the bandgaps of the two nanowires materials can be chosen to be much larger than that of the photovoltaic material.
  • the nanowires, according to this embodiment can be lightly doped to decrease the resistance of the thin films of nanowires, while permitting the substrate to remain mostly non-absorbing.
  • such goods can include personal computers, workstations, servers, networking devices, handheld electronic devices such as PDAs and palm pilots, telephones (e.g., cellular and standard), radios, televisions, electronic games and game systems, home security systems, automobiles, aircraft, boats, other household and commercial appliances, and the like.
  • PDAs and palm pilots e.g., cellular and standard
  • telephones e.g., cellular and standard
  • radios e.g., televisions, electronic games and game systems, home security systems, automobiles, aircraft, boats, other household and commercial appliances, and the like.

Abstract

The present invention is directed to systems and methods for nanowire growth. In an embodiment, methods for nanowire growth and doping are provided, including methods for epitaxial vertically oriented nanowire growth including providing a substrate material having one or more nucleating particles deposited thereon in a reaction chamber, introducing an etchant gas into the reaction chamber at a first temperature which gas aids in cleaning the surface of the substrate material, contacting the nucleating particles with at least a first precursor gas to initiate nanowire growth, and heating the alloy droplet to a second temperature, whereby nanowires are grown at the site of the nucleating particles. The etchant gas may also be introduced into the reaction chamber during growth of the wires to provide nanowires with low taper.

Description

    CROSS REFERENCE TO RELATED APPLICATIONS
  • This application is a divisional of U.S. patent application Ser. No. 11/935,884, filed Nov. 6, 2007, which application claims the benefit of the filing date of U.S. Provisional Patent Application No. 60/857,450, filed Nov. 7, 2006, which is incorporated herein by reference in its entirety.
  • BACKGROUND OF THE INVENTION
  • The present invention relates to nanowires, and more particularly, to improved methods for nanowire growth.
  • Nanostructures, and in particular, nanowires have the potential to facilitate a whole new generation of electronic devices. A major impediment to the emergence of this new generation of electronic devices based on nanostructures is the ability to effectively grow nanowires and other nanostructures that have consistent characteristics. Current approaches to growing nanowires do not facilitate mass production and typically do not yield consistent nanowire performance characteristics.
  • What are needed are systems and methods to grow nanowires that have consistent performance characteristics.
  • SUMMARY OF THE INVENTION
  • The present invention provides methods for producing vertically aligned epitaxial nanowires (e.g., silicon nanowires) with uniform characteristics such as low taper, comprising providing a substrate material having one or more nucleating particles deposited thereon in a reaction chamber, introducing an etchant gas into the reaction chamber at a first temperature which gas aids in cleaning the surface of the substrate material (and the nucleating particles), contacting the nucleating particles with at least a first precursor gas to initiate nanowire growth, and heating the substrate material to a second temperature, whereby nanowires are grown at the site of the nucleating particles. The substrate material utilized in the processes of the present invention preferably is crystallographic, but may be amorphous. Suitably, the substrate material comprises crystallographic silicon, either polycrystalline or single crystalline. In other embodiments, the substrate may be amorphous SiO2, Si3N4, or alumina.
  • In one presently preferred embodiment, the precursor gas comprises SiH4, but may also comprise other precursor gases such as Si2H6. In certain suitable embodiments, the first temperature at which the etchant gas is introduced to clean the substrate surface is higher than the second temperature at which nanowire growth occurs in the presence of the precursor gas. Suitably, the first temperature may be at least about 100° C. higher than the second temperature, e.g., about 200° C. higher than the second temperature, and may occur at a temperature of about 800° C., for example. In other embodiments, the first temperature at which the etchant gas is introduced to clean the substrate surface may be about the same as the second temperature at which nanowire growth occurs in the presence of the precursor gas. For example, the first and second temperatures may be about 600° C. The nucleating particles used in the practice of the present invention will suitably be a metal catalyst and will comprise a metal that reacts with the first precursor gas to form a eutectic from which Si may precipitate. Suitable metal catalysts comprise Au, Al, Pt, Fe, Ti, Ga, Ni, Sn or In and in certain such embodiments, may be a Au colloid or Au film.
  • High quality single crystalline silicon nanowires may then be grown by metal-catalyzed chemical vapor deposition (CVD), for example, which is based on a vapor-liquid solid (VLS) growth process. During growth, the precursor gas (e.g., SiH4) decomposes at the nucleating particle catalyst surface, Si diffuses in the catalyst, then when supersaturation occurs, the Si atoms precipitate out at the catalyst-substrate interface to form a silicon nanowire of diameter similar to that of the catalyst nucleating particle.
  • In embodiments where crystalline substrates are utilized, the wires growing on the substrate material can preferably grow epitaxially from the substrate. Nanowires produced according to the processes of the present invention grow out of the plane of the substrate material in an axially aligned vertical orientation, and are capable of transporting electrical charge. It has been found that the methods of the present invention provide nanowires having very low taper along their length, for example, have a taper rate of less than about 2 nm/micron, e.g., less than about 1.5 nm/micron, e.g., less than about 1.0 nm/micron, e.g., less than about 0.5 nm/micron, e.g., less than about 0.3 nm/micron along their length.
  • The first precursor gas utilized in the processes of the present invention will suitably comprise SiH4 (or Si2H6) and may further comprise one or more dopant gases such as B2H6, POCl3 or PH3. The precursor gas used in the processes of the present invention may suitably be introduced via plasma enhanced sputter deposition. Sputter deposition can be accomplished via any method known to the ordinarily skilled artisan, for example, diode, radio frequency and direct current deposition.
  • In another suitable embodiment of the invention, to fully exploit the bottom-up potential of this nanowire growth method, in-situ doping, such as axial dopant modulation, is desirable for complementary metal oxide semiconductor (CMOS) device fabrication. For example, the VLS growth method lends itself well to axial modulation of dopant to allow, e.g., for the doping of only certain portions of the wires (and not the entire length of the wire), e.g., at its ends, with a dopant species such as boron or phosphorus. For example, for building CMOS devices such as transistors using nanowires, in certain cases it is desirable to grow the wires with doped ends where electrode contacts to the wires will be made to improve ohmic contact to the wires. However, it has been shown that the introduction of dopant gases such as diborane and phosphine affects the decomposition rate of silane. Indeed, diborane has been shown to increase and phosphine decrease the decomposition rate of silane. Diborane can thus induce substantial uncatalysed Si deposited on the nanowire sidewalls during growth of the wires which can result in a significant increase in the taper rate along the wires during growth and dopant incorporation.
  • Accordingly, in another suitable embodiment of the invention, an etchant gas such as hydrogen chloride may also be introduced into the reaction chamber during growth of the nanowires and/or during dopant incorporation. The HCl will produce a relatively low etch rate of the wires at the growth temperature of the wires (e.g., about 600° C. for vertically oriented epitaxial wires), and lead to a passivation layer of Cl on the wires which inhibits the sidewall growth of Si thereby providing good control of wire uniformity (e.g., wires with low taper), and further sterically hindering sidewall incorporation of dopant allowing for axially modulated electronic doping of the vertically aligned epitaxial wires. In the embodiment whereby the etchant gas, such as hydrogen chloride, is introduced into the reaction chamber both in the preclean step noted above as well as during growth of the wires and/or dopant incorporation, typically the partial pressure of HCl during the preclean step is higher (e.g., about 1.0 Torr) than the partial pressure of HCl introduced into the reaction chamber during the nanowire growth process (e.g., about 0.15 Torr) to minimize over-etching of the wires during growth.
  • By way of further example, according to another aspect of the invention, the teachings of the present invention further allow the synthesis of nanowires with different materials longitudinally along the length of the nanowire, such as would be the case with alternating or periodic segments of different materials or multi-segmented nanowires where at least two of the segments comprise different materials. An example of this would be where adjacent segments have different chemical compositions, such as Si, Ge and/or SiGe. The use of HCl during the nanowire growth process of these different segments will produce a very low etch rate and lead to a passivation layer of Cl which inhibits the sidewall decomposition of SiH4 or GeH4, providing improved control of the Si/Ge and SixGe(1-x) axial modulation of vertically aligned heterostructure nanowires with very low taper. It will be appreciated that various other nanowire structures using different semiconductor materials (e.g., such as PbSe) can also be grown using different precursor gases for those other materials.
  • Further embodiments, features, and advantages of the invention, as well as the structure and operation of the various embodiments of the invention are described in detail below with reference to accompanying drawings.
  • BRIEF DESCRIPTION OF THE FIGURES
  • The invention is described with reference to the accompanying drawings. In the drawings, like reference numbers indicate identical or functionally similar elements. The drawing in which an element first appears is indicated by the left-most digit in the corresponding reference number.
  • FIG. 1A is a diagram of a single crystal semiconductor nanowire.
  • FIG. 1B is a diagram of a nanowire doped according to a core-shell structure.
  • FIG. 2 is a flowchart of a method for preparing nanowires using an HCl preclean according to an embodiment of the invention.
  • FIG. 3 is a flowchart of a method for preparing nanowires using a combination of an HCl preclean step and introduction of HCl during the nanowire growth process, according to an embodiment of the invention.
  • FIGS. 4A and 4B are TEMs showing a base (4A) and corresponding tip (4B) of a 21 micron long nanowire having a taper rate of about 0.2 nm/micron grown using a combination of an HCl preclean step and introduction of HCl during the nanowire growth process according to the methods of the present invention.
  • DETAILED DESCRIPTION OF THE INVENTION
  • It should be appreciated that the particular implementations shown and described herein are examples of the invention and are not intended to otherwise limit the scope of the present invention in any way. Indeed, for the sake of brevity, conventional electronics, manufacturing, semiconductor devices, and nanowire (NW), nanorod, nanotube, and nanoribbon technologies and other functional aspects of the systems (and components of the individual operating components of the systems) may not be described in detail herein. Furthermore, for purposes of brevity, the invention is frequently described herein as pertaining to nanowires.
  • It should be appreciated that although nanowires are frequently referred to, the techniques described herein may also be applicable to other nanostructures, such as nanorods, nanotubes, nanotetrapods, nanoribbons and/or combinations thereof. It should further be appreciated that the manufacturing techniques described herein could be used to create any semiconductor device type, and other electronic component types. Further, the techniques would be suitable for application in electrical systems, optical systems, consumer electronics, industrial electronics, wireless systems, space applications, or any other application.
  • As used herein, an “aspect ratio” is the length of a first axis of a nanostructure divided by the average of the lengths of the second and third axes of the nanostructure, where the second and third axes are the two axes whose lengths are most nearly equal to each other. For example, the aspect ratio for a perfect rod would be the length of its long axis divided by the diameter of a cross-section perpendicular to (normal to) the long axis.
  • The term “heterostructure” when used with reference to nanostructures refers to nanostructures characterized by at least two different and/or distinguishable material types. Typically, one region of the nanostructure comprises a first material type, while a second region of the nanostructure comprises a second material type. In certain embodiments, the nanostructure comprises a core of a first material and at least one shell of a second (or third etc.) material, where the different material types are distributed radially about the long axis of a nanowire, a long axis of an arm of a branched nanocrystal, or the center of a nanocrystal, for example. A shell need not completely cover the adjacent materials to be considered a shell or for the nanostructure to be considered a heterostructure. For example, a nanocrystal characterized by a core of one material covered with small islands of a second material is a heterostructure. In other embodiments, the different material types are distributed at different locations within the nanostructure. For example, material types can be distributed along the major (long) axis of a nanowire or along a long axis or arm of a branched nanocrystal. Different regions within a heterostructure can comprise entirely different materials, or the different regions can comprise a same base material.
  • As used herein, a “nanostructure” is a structure having at least one region or characteristic dimension with a dimension of less than about 500 nm, e.g., less than about 200 nm, less than about 100 nm, less than about 50 nm, or even less than about 20 nm. Typically, the region or characteristic dimension will be along the smallest axis of the structure. Examples of such structures include nanowires, nanorods, nanotubes, branched nanocrystals, nanotetrapods, tripods, bipods, nanocrystals, nanodots, quantum dots, nanoparticles, branched tetrapods (e.g., inorganic dendrimers), and the like. Nanostructures can be substantially homogeneous in material properties, or in certain embodiments can be heterogeneous (e.g., heterostructures). Nanostructures can be, for example, substantially crystalline, substantially monocrystalline, polycrystalline, amorphous, or a combination thereof. In one aspect, each of the three dimensions of the nanostructure has a dimension of less than about 500 nm, for example, less than about 200 nm, less than about 100 nm, less than about 50 nm, or even less than about 20 nm.
  • As used herein, the term “nanowire” generally refers to any elongated conductive or semiconductive material (or other material described herein) that includes at least one cross sectional dimension that is less than 500 nm, and preferably, less than 100 nm, and has an aspect ratio (length:width) of greater than 10, preferably greater than 50, and more preferably, greater than 100.
  • The nanowires of this invention can be substantially homogeneous in material properties, or in certain embodiments can be heterogeneous (e.g. nanowire heterostructures). The nanowires can be fabricated from essentially any convenient material or materials, and can be, e.g., substantially crystalline, substantially monocrystalline, polycrystalline, or amorphous. Nanowires can have a variable diameter or can have a substantially uniform diameter, that is, a diameter that shows a variance less than about 20% (e.g., less than about 10%, less than about 5%, or less than about 1%) over the region of greatest variability and over a linear dimension of at least 5 nm (e.g., at least 10 nm, at least 20 nm, or at least 50 nm). Typically the diameter is evaluated away from the ends of the nanowire (e.g. over the central 20%, 40%, 50%, or 80% of the nanowire). A nanowire can be straight or can be e.g. curved or bent, over the entire length of its long axis or a portion thereof. In certain embodiments, a nanowire or a portion thereof can exhibit two- or three-dimensional quantum confinement. Nanowires according to this invention can expressly exclude carbon nanotubes, and, in certain embodiments, exclude “whiskers” or “nanowhiskers”, particularly whiskers having a diameter greater than 100 nm, or greater than about 200 nm.
  • Examples of such nanowires include semiconductor nanowires as described in Published International Patent Application Nos. WO 02/17362, WO 02/48701, and WO 01/03208, carbon nanotubes, and other elongated conductive or semiconductive structures of like dimensions, which are incorporated herein by reference.
  • As used herein, the term “nanorod” generally refers to any elongated conductive or semiconductive material (or other material described herein) similar to a nanowire, but having an aspect ratio (length:width) less than that of a nanowire. Note that two or more nanorods can be coupled together along their longitudinal axis so that the coupled nanorods span all the way between electrodes. Alternatively, two or more nanorods can be substantially aligned along their longitudinal axis, but not coupled together, such that a small gap exists between the ends of the two or more nanorods. In this case, electrons can flow from one nanorod to another by hopping from one nanorod to another to traverse the small gap. The two or more nanorods can be substantially aligned, such that they form a path by which electrons can travel between electrodes.
  • A wide range of types of materials for nanowires, nanorods, nanotubes and nanoribbons can be used, including semiconductor material selected from, e.g., Si, Ge, Sn, Se, Te, B, C (including diamond), P, B—C, B—P(BP6), B—Si, Si—C, Si—Ge, Si—Sn and Ge—Sn, SiC, BN/BP/BAs, AlN/AlP/AlAs/AlSb, GaN/GaP/GaAs/GaSb, InN/InP/InAs/InSb, ZnO/ZnS/ZnSe/ZnTe, CdS/CdSe/CdTe, HgS/HgSe/HgTe, BeS/BeSe/BeTe/MgS/MgSe, GeS, GeSe, GeTe, SnS, SnSe, SnTe, PbO, PbS, PbSe, PbTe, CuF, CuCl, CuBr, CuI, AgF, AgCl, AgBr, AgI, BeSiN2, CaCN2, ZnGeP2, CdSnAs2, ZnSnSb2, CuGeP3, CuSi2P3, (Cu, Ag)(Al, Ga, In, Tl, Fe)(S, Se, Te)2, Si3N4, Ge3N4, Al2O3, (Al, Ga, In)2 (S, Se, Te)3, Al2CO, and an appropriate combination of two or more such semiconductors.
  • The nanowires can also be formed from other materials such as metals such as gold, nickel, palladium, iradium, cobalt, chromium, aluminum, titanium, tin and the like, metal alloys, polymers, conductive polymers, ceramics, and/or combinations thereof. Other now known or later developed conducting or semiconductor materials can be employed.
  • In certain aspects, the semiconductor may comprise a dopant from a group consisting of: a p-type dopant from Group III of the periodic table; an n-type dopant from Group V of the periodic table; a p-type dopant selected from a group consisting of: B, Al and In; an n-type dopant selected from a group consisting of: P, As and Sb; a p-type dopant from Group II of the periodic table; a p-type dopant selected from a group consisting of: Mg, Zn, Cd and Hg; a p-type dopant from Group IV of the periodic table; a p-type dopant selected from a group consisting of: C and Si.; or an n-type dopant selected from a group consisting of: Si, Ge, Sn, S, Se and Te. Other now known or later developed dopant materials can be employed.
  • Additionally, the nanowires or nanoribbons can include carbon nanotubes, or nanotubes formed of conductive or semiconductive organic polymer materials, (e.g., pentacene, and transition metal oxides).
  • Hence, although the term “nanowire” is referred to throughout the description herein for illustrative purposes, it is intended that the description herein also encompass the use of nanotubes (e.g., nanowire-like structures having a hollow tube formed axially therethrough). Nanotubes can be formed in combinations/thin films of nanotubes as is described herein for nanowires, alone or in combination with nanowires, to provide the properties and advantages described herein.
  • As used herein, the term “taper rate” refers to the diameter of an elongated nanostructure (such as a nanowire) as measured from its bottom end portion less the diameter of the nanostructure as measured from its top end portion, divided by the length of the nanostructure.
  • It should be understood that the spatial descriptions (e.g., “above”, “below”, “up”, “down”, “top”, “bottom,” etc.) made herein are for purposes of illustration only, and that devices of the present invention can be spatially arranged in any orientation or manner.
  • Types of Nanowires and their Synthesis
  • FIG. 1A illustrates a single crystal semiconductor nanowire core (hereafter “nanowire”) 100. FIG. 1A shows a nanowire 100 that is a uniformly doped single crystal nanowire. Such single crystal nanowires can be doped into either p- or n-type semiconductors in a fairly controlled way. Doped nanowires such as nanowire 100 exhibit improved electronic properties. For instance, such nanowires can be doped to have carrier mobility levels comparable to bulk single crystal materials.
  • FIG. 1B shows a nanowire 110 having a core-shell structure. Surface scattering can be reduced by forming an outer layer of the nanowire, such as by the passivation annealing of nanowires, and/or the use of core-shell structures with nanowires. An insulating layer, such as an oxide coating, can be formed on a nanowire as the shell layer. Furthermore, for example, for silicon nanowires having an oxide coating, the annealing of the nanowires in hydrogen (H2) can greatly reduce surface states. In embodiments, the core-shell combination is configured to satisfy the following constraints: (1) the shell energy level should be higher than the core energy level, so that the conducting carriers are confined in the core; and (2) the core and shell materials should have good lattice match, with few surface states and surface charges. Other more complex NW core-shell structures may also be used to include a core of single crystal semiconductor, an inner-shell of gate dielectric, and an outer-shell of conformal gate. This can be realized by depositing a layer of TaAlN, WN, or highly-doped amorphous silicon around the Si/SiOx core-shell structure (described above) as the outer-gate shell, for example.
  • The valence band of the insulating shell can be lower than the valence band of the core for p-type doped wires, or the conduction band of the shell can be higher than the core for n-type doped wires. Generally, the core nanostructure can be made from any metallic or semiconductor material, and the one or more shell layers deposited on the core can be made from the same or a different material. For example, the first core material can comprise a first semiconductor selected from the group consisting of: a Group II-VI semiconductor, a Group III-V semiconductor, a Group IV semiconductor, and an alloy thereof. Similarly, the second material of the one or more shell layers can comprise an oxide layer, a second semiconductor, the same as or different from the first semiconductor, e.g., selected from the group consisting of: a Group II-VI semiconductor, a Group III-V semiconductor, a Group IV semiconductor, and an alloy thereof. Example semiconductors include, but are not limited to, CdSe, CdTe, InP, InAs, CdS, ZnS, ZnSe, ZnTe, HgTe, GaN, GaP, GaAs, GaSb, InSb, Si, Ge, AlAs, AlSb, PbSe, PbS, and PbTe. As noted above, metallic materials such as gold, chromium, tin, nickel, aluminum etc. and alloys thereof can be used as the core material, and the metallic core can be overcoated with an appropriate shell material such as silicon dioxide or other insulating materials, which may in turn may be coated with one or more additional shell layers of the materials described above to form more complex core-shell-shell nanowire structures.
  • Nanostructures can be fabricated and their size can be controlled by any of a number of convenient methods that can be adapted to different materials. For example, synthesis of nanocrystals of various composition is described in, e.g., Peng et al. (2000) “Shape Control of CdSe Nanocrystals” Nature 404, 59-61; Puntes et al. (2001) “Colloidal nanocrystal shape and size control: The case of cobalt” Science 291, 2115-2117; U.S. Pat. No. 6,306,736 to Alivisatos et al. (Oct. 23, 2001) entitled “Process for forming shaped group III-V semiconductor nanocrystals, and product formed using process”; U.S. Pat. No. 6,225,198 to Alivisatos et al. (May 1, 2001) entitled “Process for forming shaped group II-VI semiconductor nanocrystals, and product formed using process”; U.S. Pat. No. 5,505,928 to Alivisatos et al. (Apr. 9, 1996) entitled “Preparation of III-V semiconductor nanocrystals”; U.S. Pat. No. 5,751,018 to Alivisatos et al. (May 12, 1998) entitled “Semiconductor nanocrystals covalently bound to solid inorganic surfaces using self-assembled monolayers”; U.S. Pat. No. 6,048,616 to Gallagher et al. (Apr. 11, 2000) entitled “Encapsulated quantum sized doped semiconductor particles and method of manufacturing same”; and U.S. Pat. No. 5,990,479 to Weiss et al. (Nov. 23, 1999) entitled “Organo luminescent semiconductor nanocrystal probes for biological applications and process for making and using such probes.”
  • Growth of nanowires having various aspect ratios, including nanowires with controlled diameters, is described in, e.g., Gudiksen et al (2000) “Diameter-selective synthesis of semiconductor nanowires” J. Am. Chem. Soc. 122, 8801-8802; Cui et al. (2001) “Diameter-controlled synthesis of single-crystal silicon nanowires” Appl. Phys. Lett. 78, 2214-2216; Gudiksen et al. (2001) “Synthetic control of the diameter and length of single crystal semiconductor nanowires” J. Phys. Chem. B 105, 4062-4064; Morales et al. (1998) “A laser ablation method for the synthesis of crystalline semiconductor nanowires” Science 279, 208-211; Duan et al. (2000) “General synthesis of compound semiconductor nanowires” Adv. Mater. 12, 298-302; Cui et al. (2000) “Doping and electrical transport in silicon nanowires” J. Phys. Chem. B 104, 5213-5216; Peng et al. (2000) “Shape control of CdSe nanocrystals” Nature 404, 59-61; Puntes et al. (2001) “Colloidal nanocrystal shape and size control: The case of cobalt” Science 291, 2115-2117; U.S. Pat. No. 6,306,736 to Alivisatos et al. (Oct. 23, 2001) entitled “Process for forming shaped group III-V semiconductor nanocrystals, and product formed using process”; U.S. Pat. No. 6,225,198 to Alivisatos et al. (May 1, 2001) entitled “Process for forming shaped group II-VI semiconductor nanocrystals, and product formed using process”; U.S. Pat. No. 6,036,774 to Lieber et al. (Mar. 14, 2000) entitled “Method of producing metal oxide nanorods”; U.S. Pat. No. 5,897,945 to Lieber et al. (Apr. 27, 1999) entitled “Metal oxide nanorods”; U.S. Pat. No. 5,997,832 to Lieber et al. (Dec. 7, 1999) “Preparation of carbide nanorods”; Urban et al. (2002) “Synthesis of single-crystalline perovskite nanowires composed of barium titanate and strontium titanate” J. Am. Chem. Soc., 124, 1186; and Yun et al. (2002) “Ferroelectric Properties of Individual Barium Titanate Nanowires Investigated by Scanned Probe Microscopy” Nanoletters 2, 447.
  • Growth of branched nanowires (e.g., nanotetrapods, tripods, bipods, and branched tetrapods) is described in, e.g., Jun et al. (2001) “Controlled synthesis of multi-armed CdS nanorod architectures using monosurfactant system” J. Am. Chem. Soc. 123, 5150-5151; and Manna et al. (2000) “Synthesis of Soluble and Processable Rod-, Arrow-, Teardrop-, and Tetrapod-Shaped CdSe Nanocrystals” J. Am. Chem. Soc. 122, 12700-12706.
  • Synthesis of nanoparticles is described in, e.g., U.S. Pat. No. 5,690,807 to Clark Jr. et al. (Nov. 25, 1997) entitled “Method for producing semiconductor particles”; U.S. Pat. No. 6,136,156 to El-Shall, et al. (Oct. 24, 2000) entitled “Nanoparticles of silicon oxide alloys”; U.S. Pat. No. 6,413,489 to Ying et al. (Jul. 2, 2002) entitled “Synthesis of nanometer-sized particles by reverse micelle mediated techniques”; and Liu et al. (2001) “Sol-Gel Synthesis of Free-Standing Ferroelectric Lead Zirconate Titanate Nanoparticles” J. Am. Chem. Soc. 123, 4344. Synthesis of nanoparticles is also described in the above citations for growth of nanocrystals, nanowires, and branched nanowires, where the resulting nanostructures have an aspect ratio less than about 1.5.
  • Synthesis of core-shell nanostructure heterostructures, namely nanocrystal and nanowire (e.g., nanorod) core-shell heterostructures, are described in, e.g., U.S. Pat. No. 6,882,051; Peng et al. (1997) “Epitaxial growth of highly luminescent CdSe/CdS core/shell nanocrystals with photostability and electronic accessibility” J. Am. Chem. Soc. 119, 7019-7029; Dabbousi et al. (1997) “(CdSe)ZnS core-shell quantum dots: Synthesis and characterization of a size series of highly luminescent nanocrysallites” J. Phys. Chem. B 101, 9463-9475; Manna et al. (2002) “Epitaxial growth and photochemical annealing of graded CdS/ZnS shells on colloidal CdSe nanorods” J. Am. Chem. Soc. 124, 7136-7145; and Cao et al. (2000) “Growth and properties of semiconductor core/shell nanocrystals with InAs cores” J. Am. Chem. Soc. 122, 9692-9702. Similar approaches can be applied to growth of other core-shell nanostructures.
  • Growth of nanowire heterostructures in which the different materials are distributed at different locations along the long axis of the nanowire is described in, e.g., U.S. Pat. No. 6,882,051; Gudiksen et al. (2002) “Growth of nanowire superlattice structures for nanoscale photonics and electronics” Nature 415, 617-620; Bjork et al. (2002) “One-dimensional steeplechase for electrons realized” Nano Letters 2, 86-90; Wu et al. (2002) “Block-by-block growth of single-crystalline Si/SiGe superlattice nanowires” Nano Letters 2, 83-86; and U.S. Pat. No. 7,067,867. Similar approaches can be applied to growth of other heterostructures.
  • Epitaxial-Oriented Nanowire Growth Using an Etchant Pre-Clean Step
  • High-quality single crystalline nanowires such as silicon nanowires are commonly grown by metal-catalyzed chemical vapor deposition (CVD). During this vapor-liquid-solid (VLS) growth process, nanosized metal catalysts, such as gold nucleating particles, are used to catalyze the decomposition of a precursor gas such as silane (SiH4). A liquid Au—Si alloy is formed and when supersaturation is reached, silicon precipitates out to form a silicon nanowire of diameter similar to that of the catalyst particle. The preferred nanowire growth direction for this method may comprise <111>, <110> and <112>.
  • For many processes, vertically aligned nanowire growth is highly desirable to produce devices such as transistors with consistent performance characteristics. Such orientation may be realized by epitaxial growth on single-crystalline substrates with suitable crystal structure (e.g., Si (111) wafers). Epitaxial growth requires a clean interface between the nucleating particles (e.g., Au particles) and the substrate. The native oxide (SiOx) may be removed prior to growth with a hydrofluoric (HF) acid etch as is known in the art. Unfortunately, in most cases, low yield epitaxial growth of vertically oriented silicon nanowires nucleated from gold nanoparticles is observed and other surface cleaning treatments are necessary.
  • In addition, at growth temperatures required for epitaxial silicon nanowire growth, uncatalysed thermal decomposition of the silane occurs leading to sidewall growth of silicon producing tapered nanowires. The silicon added to the sidewall of the nanowires can be a combination of polysilicon, amorphous silicon, and/or epitaxial silicon depending on the growth conditions. Forms of silicon other than epitaxial silicon are undesirable since they can spoil the intrinsic electronic properties of the wires. It is desirable to be able to grow nanowires such as silicon nanowires that have reduced taper in order to produce devices based on such wires with consistent performance characteristics.
  • FIG. 2 is a flowchart of method 200 for preparing nanowires using a hydrogen chloride pre-clean step according to an embodiment of the invention. Method 200 begins in step 201. In step 201, the surface of a wafer, such as a silicon wafer, is first passivated with a hydrofluoric acid gas etchant to remove the native oxide (e.g., SiOx) from the wafer surface prior to depositing nucleating particles on the substrate surface. In step 202, one or more nucleating particles, suitably metal catalysts such as Au colloid particles, are deposited on a substrate material to create nucleation sites for nanowire growth. As shown in step 204, following deposition of the nucleating particles on the substrate, the substrate is heated to a first temperature in a reaction chamber and an etchant gas, e.g., hydrogen chloride gas, is introduced into the reaction chamber to clean the substrate surface coated with the nucleating particles. The etchant gas aids in cleaning both the substrate surface as well as the nucleating particles on the substrate surface. Next, heating of the nucleating particles to a second temperature (which may be the same as or lower than the first temperature) and contacting the nucleating particles with a first precursor gas (e.g., silane), creates a liquid alloy droplet and initiates nanowire growth, which is indicated by label 206, until they reach the desired size and orientation, as shown in step 208.
  • In suitable embodiments, the substrate material on which the nanowires are grown is a crystallographic substrate. The term “crystallographic substrate” includes any substrate material which comprises atoms situated in a repeating or periodic array over large atomic distances, typically on the order of 10 or more angstroms (Å). Such crystallographic substrates may be polycrystalline or may comprise single crystals. Suitably, the crystallographic substrate utilized in the processes of the present invention is silicon (Si). Other suitable crystallographic materials include, but are not limited to, germanium (Ge), gallium arsenide (GaAs), gallium nitride (GaN), sapphire, quartz, and silicon germanium (SiGe). In other embodiments of the present invention, the substrate material may comprise an amorphous material. Suitable amorphous substrate materials which may be used in the practice of the present invention include, but are not limited to SiO2, Si3N4 and alumina.
  • As outlined in FIG. 2, in certain embodiments, the methods of the present invention comprise first depositing nucleating particles on a substrate material. Nucleating particles that may be used in the practice of the present invention include metal catalysts and can be any metal that reacts with the precursor gas to form a eutectic phase. Such a mixture has a minimum melting point at which all components are in solution. Upon addition of precursor gas molecules (e.g., silicon) a saturation point on the eutectic phase diagram is reached such that semiconductor particles (e.g., Si) begin to precipitate out of the metal alloy, thereby creating a growing nanowire. Continuous addition of precursor gas will continue to saturate the eutectic, thereby generating additional material for nanowire growth.
  • In suitable embodiments, the nucleating particles will be metal catalysts and can comprise any of the transition metals from the Periodic Table, including, but not limited to, copper, silver, gold, nickel, palladium, platinum, cobalt, rhodium, iridium, indium, iron, ruthenium, tin, osmium, manganese, chromium, molybdenum, tungsten, vanadium, niobium, tantalum, titanium, zirconium and gallium, including mixtures of one or more of these metals. In preferred embodiments of the present invention, the metal catalyst can comprise a gold (Au) colloid (i.e., a Au nanoparticle) or Au film. In certain such embodiments, 20 to 150 nanometer (nm) diameter gold colloids can be used. The target is to achieve a uniform deposition of gold nanoparticles with density between about 0.14 to 6 particles per square micrometer (μm). A key is minimized gold particle cluster formation. The clusters can result in undesired larger diameter nanowire growth. Spin coating and self assembly methods can be explored for the deposition (see, e.g., U.S. Pat. No. 7,067,867 which is incorporated by reference herein in its entirety).
  • Spin coating is a fairly straightforward process. A deposition density can be controlled through variation of the gold particle concentration in the precursor colloids, manipulation of surface chemistry of the silicon wafer, and changing the spin speed. A drawback of spin coating can be low utilization efficiency of gold colloid solution. A recycling process in the production stage can be used if warranted.
  • Self assembly involves some use of well established chemistry. The surface of 4 inch silicon oxide coated wafer is functionalized with either (3-aminopropyl)-trimethoxysilane (APTES) or (3-mercaptopropyl)-trimethoxysilane (MPTES), then contacted with gold colloid solution. The gold particles are assembled on the surface. The difference between two different chemistries are compared, and the possibility of controlling the density of gold particles by control of the contact time and gold particle concentration in the contact solution can be used.
  • The nucleating particles used to practice the present invention can also be formed on a substrate surface by heating a gold film coating layer on the surface.
  • In one embodiment, the present invention comprises heating the first precursor gas to a temperature at which 1) the gas dissociates into its free component atoms, and 2) the nucleating particles (e.g. metal catalyst) melts to a liquid. The free gas molecules can then diffuse into the metal catalyst to form a liquid alloy droplet. This process is commonly known to those of ordinary skill in the art as chemical vapor deposition (CVD).
  • In suitable embodiments of the present invention, the first precursor gas may be selected from, but not limited to, SiH4 or Si2H6. Heating these Si precursor gases above the temperature at which the thermal energy is sufficient to break the bond energies between the gaseous molecules generates free Si atoms (e.g., Si—H bond: 93 kcal/mole, Si—Cl bond: 110 kcal/mole, Si—Si bond; 77 kcal/mole, see M. T. Swihart and R. W. Can, J. Phys Chem A 102:1542-1549 (1998).) Provided that this temperature is also high enough to liquefy the metal catalyst, the free Si atoms will diffuse into the metal and generate a eutectic phase. Dissociation temperatures for Si2H6 and SiH4 are between about 300° C. to 500° C., respectively, and preferably growth occurs at a temperature of about 600° C. to produce vertically oriented epitaxial wires.
  • In all embodiments of the present invention, the precursor gas used during any of the nanowire growth processes may further comprise one or more doping gases. Examples of suitable doping gases that may be used in the practice of the present invention include, but are not limited to, B2H6, POCl3 and PH3. In many applications of the wires, in situ doping is necessary for complementary metal oxide semiconductor (CMOS) device fabrication. In suitable embodiments of the present invention, wires can be grown using the same doping gas in each of the precursor gas mixtures. In such embodiments, the entire resulting wire will be either p-type or n-type, depending on the choice of dopant. In other embodiments of the present invention, different doping gases can be introduced throughout the process as components of the precursor gas. For example, wire growth can be initiated using a precursor gas comprising an n-type dopant (e.g., P, As or Sb) and then continued using a precursor gas using a p-type dopant (e.g., B, Al or In). In other embodiments, a p-type doing gas will be used during initiation and then an n-type doping gas during growth.
  • In other embodiments, the type of doping gas can be switched multiple times throughout the growth process as the precursor gases are switched, e.g., for axial modulation doping of the wires. The resulting nanowires therefore can comprise several different dopant portions throughout their length. For example, a nanowire produced via the present invention may comprise an n-type base where electrical contact to a source electrode can be made, a p-type middle section, and an n-type top where electrical contact to a drain electrode may be made, or any suitable combination as envisioned by the ordinarily skilled artisan. Such embodiments of the present invention would allow for an n-type wire to be grown on a p-type substrate, and vice versa.
  • As discussed above, the VLS growth method lends itself well to axial modulation of dopant to allow, e.g., for the doping of only certain portions of the wires (and not the entire length of the wire), e.g., at its ends, with a dopant species such as boron. In one embodiment of the present invention, for example, the first precursor gas can comprise SiH4 and suitably a carrier gas, such as H2, He, Ar, or other inert gas. Heating this gas mixture to a sufficiently high temperature, e.g., about 600° C., generates free Si atoms. In suitable such embodiments, the first precursor gas may comprise one or more dopant gases selected from those described throughout the application. When a dopant gas such as B2H6 is present in the precursor gas mixture, B atoms will also be generated. The first precursor gas mixture is passed over the nucleating particles, suitably metal-catalyst particles (e.g., gold nanoparticles) deposited on the substrate material at a total pressure between about 5 to about 50 Torr, while the nucleating particles are heated up to a temperature of about 600° C. In other embodiments of the present invention, the gas pressure may be increased or decreased, thereby requiring a modification in the temperature required to dissociate the precursor gas mixture.
  • Si and B will diffuse into the metal catalyst and generate a liquid alloy droplet. This eutectic phase of metal catalyst and precursor gases will continue to exist as precursor gas is solvated in the metal catalyst. Once an over-saturation is reached, Si/B atoms will precipitate out and initiate nanowire growth. In order to continue nanowire growth, a continuous supply of Si precursor gas and doping gas are required. However, it has been shown that the introduction of dopant gases such as diborane and phosphine affects the thermal decomposition rate of silane. Indeed, diborane has been shown to increase and phosphine decrease the thermal decomposition rate of silane. Diborane can thus induce substantial uncatalysed silicon growth on the nanowire sidewalls during growth of the wires which can result in a significant increase in the taper rate along the wires during wire growth and dopant incorporation.
  • Accordingly, in another suitable embodiment of the invention as shown in FIG. 3, an etchant gas such as hydrogen chloride may also be introduced into the reaction chamber during growth of the nanowires and/or during dopant incorporation. Steps 301, 302, 304, 306, and 308 in FIG. 3 are the same as those corresponding steps 201, 202, 204, 206 and 208 of FIG. 2. FIG. 3 also includes the additional step 310 of adding etchant gas, such as HCL, during the wire growth process 306.
  • The HCl will produce a relatively low etch rate of the wires at the growth temperature of the wires (e.g., about 600° C.). In the growth temperature range of about 600° C. required to grow vertically aligned epitaxial silicon nanowires, it has been observed that the etch rate of silicon with HCl is relatively low, and that the surface of the silicon nanowires may be covered with one or more monolayers of Cl and H. Such a passivation layer can help to minimize sidewall deposition of silicon thus leading to wires with low taper, and can further sterically hinder lattice incorporation of boron (or other dopant gases) into the nanowire sidewalls thus promoting axial dopant incorporation (versus sidewall dopant incorporation which is less desirable). In the embodiment whereby the etchant gas, such as hydrogen chloride, is introduced into the reaction chamber both in the preclean step noted above in FIG. 2 as well as during growth of the wires and/or dopant incorporation, typically the partial pressure of HCl during the preclean step is higher (e.g., about 1.0 Torr) than the partial pressure of HCl introduced into the reaction chamber during the nanowire growth process (e.g., about 0.15 Torr) to minimize over-etching of the wires during growth.
  • Continuously supplying the precursor gas will allow the nanowire to continue growing until termination by desire or death caused by local condition change. The quality of the nanowires is dependent on the quality of gold nanoparticles, etchant gas concentration, control of gold nanoparticle distribution on the substrate and growth condition including temperature, ratio of dopant to precursor gas, partial pressure of the precursor gas, and resident time of precursor gases in the reactor. It has been found that the methods of the present invention provide nanowires having very low taper along their length, for example, have a taper rate of less than about 2 nm/micron, e.g., less than about 1 nm/micron, e.g., less than about 0.5 nm/micron, e.g., less than about 0.3 nm/micron. In suitable embodiments of the present invention, the processes of the present invention can be accomplished using a computer controlled 8″ semiconductor furnace. FIGS. 4A and 4B are a TEMs showing a base (4A) and corresponding tip (4B) of a 21 micron long nanowire having a taper rate of about 0.2 nm/micron grown using a combination of an HCl preclean step and introduction of HCl during the nanowire growth process according to the methods of the present invention.
  • High quality single-crystalline nanowire heterostructures such as silicon/germanium nanowires can also be grown using the teachings of the present invention. Such wires are commonly grown by metal-catalyzed chemical vapor deposition (CVD), which is based on a vapor-liquid-solid (VLS) growth process. During growth, the process gases (e.g., SiH4 and GeH4) decompose at the catalyst surface, Si (Ge) diffuses in the catalyst, and then when supersaturation occurs, the silicon (germanium) precipitates out at the catalyst-substrate interface to form a silicon/germanium nanowire of diameter similar to that of the catalyst. The main difference between Si and Ge is that vertically aligned epitaxial germanium nanowires can be grown at temperatures approximately 200° C. lower than that for silicon nanowires. This can cause problems when growing Si/Ge and SixGe1-x axially modulated structures where uncatalysed thermal decomposition of the GeH4 would lead to sidewall growth producing tapered nanowires at temperatures required for silicon nanowire growth. The germanium added to the sidewall of the nanowire is undesirable since it would result in a radial as well as axial compositional modulation. This would degrade the electronic properties of this compositionally modulated wire.
  • This VLS growth technique lends itself well to axial modulation of Si and Ge where the transition would be controlled by intermittently introducing and stopping the SiH4 (GeH4) to create the axial modulated growth. According to the teachings of the present invention, controlled amounts of HCl can be provided during growth of the Si/Ge nanowires to enable axial Si/Ge and SixGe1-x modulation of vertical nanowires without sidewall growth of the precursor gas species. In the growth temperature range (e.g., approximately 600° C.) required to grow vertically aligned epitaxial silicon nanowires, the etch rate of silicon is very low and the surface of the Si/Ge naowire is covered with a monolayer of Cl and H. Such a passivation layer prevents the sidewall decomposition of silane (and/or germanium gas). This prevents sidewall deposition on the segment of the nanowire previously grown with a different solid composition of SixGe1-x. This allows a controlled axial modulation without encasing the nanowire radially with material of a different, undesirable composition.
  • In suitable embodiments, the precursor gas that is introduced in any of the processes of the present invention may be introduced via Plasma Enhanced Sputter Deposition (or Plasma Enhanced Chemical Vapor Deposition (PECVD)). (See Hofmann et al., “Gold Catalyzed Growth of Silicon Nanowires by Plasma Enhanced Chemical Vapor Deposition,” J. Appl. Phys. 94:6005-6012 (2003).) The diameter distribution of silicon nanowires of these certain embodiments of the present invention is determined by that of the nucleating particles, e.g., metal (suitably gold) nanoparticles. Commercially available gold colloids can have a diameter distribution of ±10%. The same distribution can be attained in the nanowires. Gold nanoparticles can be split into smaller ones resulting in smaller diameter nanowires, depending on the growth condition. Growth conditions can be optimized to minimize this event. Given a growth condition, the length of nanowires can be controlled by varying duration of the growth. Crystallinity of silicon nanowires and dopant concentration are also growth condition dependent. They can be optimized and controlled together with other important nanowire characteristics.
  • The nanowires produced according to any of the processes of the present invention will suitably grow out of the plane of the substrate material. Such growth includes nanowires that project out of the plane of the substrate material at any angle with respect to the substrate. For example, nanowires can grow at an angle of about 1° to about 90°, and any angle in between these values, relative to the plane of the substrate material. It is a requirement of the present invention that the nanowires produced by the processes described herein must project out of the plane of the substrate. That is, the nanowires produced by the processes of the present invention must extend off of the plane of the substrate material a distance greater than the dimension of a single molecule. As such, the nanowires produced according to the present invention are distinct from structures such as thin films and quantum dots, which spread on the surface of a substrate material, rather than growing in a manner such that they project out of the plane of the substrate a distance that exceeds the atomic diameter of a single Si molecule for instance.
  • Suitably, the nanowires produced according to any of the processes of the present invention will project out of the plane of the substrate material so as to attain a final length of about 100 nm to less than about 50 μm, e.g., between about 15 μm to about 25 μm. The nanowires of the present invention will suitably be at least about 1 nm to less than about 1 μm in diameter. For use in electronic devices, the nanowires of the present invention will have a diameter of about a few nms to 100's of nms, so as to allow them to be harvested and utilized in an electronic device (See U.S. Application No. 60/754,520, filed Dec. 29, 2005, for a description of nanowire harvesting which is incorporated herein by reference.)
  • In suitable embodiments of the present invention, the nanowires, when growing on a crystalline substrate (whether polycrystalline or single crystal) will preferably grow epitaxially. However, the present invention also embodies growth on crystalline substrates wherein the nanowires do not grow in an epitaxial orientation. As used herein, the term epitaxial as it refers to the growth of nanowires means that the nanowires have the same crystallographic characteristic(s) as the substrate material on which they are growing. For example, the orientation of the substrate material can be any crystallographic orientation known to the ordinarily skilled artisan, including, but not limited to, <111>, <110>, <100> and <211>. In suitable embodiments then, the nanowires produced by the processes of the present invention can be grown in any crystallographic orientation, and suitably in the same orientation as the substrate material, including those orientations discussed throughout and as known to the ordinarily skilled artisan.
  • In other suitable embodiments of the present invention, the crystallographic plane of the substrate material can be off axis of the 0° horizontal plane. The nanowires growing on the surface of such a substrate material can project out of the substrate material at an angle such that the wires can be normal to the crystallographic plane (i.e., 90° with respect to the crystallographic plane) or can be off axis relative to the crystallographic plane such that they can be normal to a 0° horizontal plane.
  • In embodiments of the present invention where amorphous substrates are utilized, the nanowires produced according to the processes of the present invention will not grow epitaxially, as the amorphous material does not comprise a crystallographic orientation. However, as noted above, the nanowires grown on such substrates may project out of the plane of the substrate at any angle relative to the horizontal plane.
  • The processes of the present invention produce nanowires that may carry electrons between two points in space and thus act to transfer charge. In this way, the nanowires of the present invention are further distinct from nanodots and in their size and orientation, are distinct from semiconductor films.
  • The present invention also provides for electronic circuits comprising the nanowires produced by any of the processes of the present invention. Suitably collections of nanowires produced according to the processes of the present invention are useful building blocks for high performance electronics. A collection of nanowires orientated in substantially the same direction will have a high mobility value. Furthermore, nanowires can be flexibly processed in solution to allow for inexpensive manufacture. Collections of nanowires can be easily assembled onto any type of substrate from solution to achieve a thin film of nanowires. For example a thin film of nanowires used in a semiconductor device can be formed to include 2, 5, 10, 100, and any other number of nanowires between or greater than these amounts, for use in high performance electronics.
  • The nanowires of the present invention can also be used to make high performance composite materials when combined with polymers/materials such as organic semiconductor materials, which can be flexibly spin-cast on any type of substrate. Nanowire/polymer composites can provide properties superior to a pure polymer materials.
  • Collections or thin films of nanowires of the present invention can be aligned into being substantially parallel to each other, or can be left non-aligned or random. Non-aligned collections or thin films of nanowires provide electronic properties comparable or superior to polysilicon materials, which typically have mobility values in the range of 1-10 cm2/V·s.
  • Aligned thin films of nanowires of the present invention can be obtained in a variety of ways. For example, aligned thin films of nanowires can be produced by using the following techniques: (a) Langmuir-Blodgett film alignment; (b) fluidic flow approaches, such as described in U.S. Pat. No. 6,872,645, and incorporated herein by reference in its entirety; (c) application of mechanical shear force; and (d) use of AC electric fields as described in U.S. Patent Application Publication 20080224123. Aligned thin films of nanowires/polymer composites can be obtained using these techniques, followed by a spin-casting of the desired polymer onto the created thin film of nanowires. For example, nanowires can be deposited in a liquid polymer solution, alignment can then be performed according to one of these or other alignment processes, and the aligned nanowires can then be cured (e.g., UV cured, crosslinked, etc.). An aligned thin film of nanowires/polymer composite can also be obtained by mechanically stretching a randomly oriented thin film of nanowires/polymer composite.
  • P-doped nanowires and n-doped nanowires produced by the processes of the present invention can be separately fabricated, and deposited in a homogeneous mixture onto a surface, such as a macroelectronic substrate. On a macroscopic level, the resulting material appears to contain a high concentration of both n- and p-dopants. By creating such a mixture of p- and n-doped nanowires, macroelectronic devices can be fabricated that respond as if they are both n- and p-doped. For example, a resulting thin film of nanowires that includes both n-doped and p-doped nanowires can exhibit characteristics of both n-doped and p-doped nanowires. For example, diode, transistor, and other known electrical devices can be fabricated to include a combination of p-doped nanowires and n-doped nanowires.
  • Nanowires produced by the processes of the present invention can also be used to produce electrical devices such as p-n diodes, transistors, and other electrical device types, using nanowire heterostructures as described herein. Nanowire heterostructures include a plurality of p-n junctions along the length of the nanowire and can include alternating portions or segments along their lengths that are differently doped.
  • Use of Nanowires of the Present Invention in Exemplary Devices and Applications
  • Numerous electronic devices and systems can incorporate semiconductor or other type devices with thin films of nanowires produced by the methods of the present invention. Some example applications for the present invention are described below or elsewhere herein for illustrative purposes, and are not limiting. The applications described herein can include aligned or non-aligned thin films of nanowires, and can include composite or non-composite thin films of nanowires.
  • Semiconductor devices (or other type devices) can be coupled to signals of other electronic circuits, and/or can be integrated with other electronic circuits. Semiconductor devices can be formed on large substrates, which can be subsequently separated or diced into smaller substrates. Furthermore, on large substrates (i.e., substrates substantially larger than conventional semiconductor wafers), semiconductor devices formed thereon can be interconnected.
  • The nanowires produced by the processes of the present invention can also be incorporated in applications requiring a single semiconductor device, and to multiple semiconductor devices. For example, the nanowires produced by the processes of the present invention are particularly applicable to large area, macro electronic substrates on which a plurality of semiconductor devices are formed. Such electronic devices can include display driving circuits for active matrix liquid crystal displays (LCDs), organic LED displays, and field emission displays. Other active displays can be formed from a nanowire-polymer, quantum dots-polymer composite (the composite can function both as the emitter and active driving matrix). The nanowires produced by the processes of the present invention are also applicable to smart libraries, credit cards, large area array sensors, and radio-frequency identification (RFID) tags, including smart cards, smart inventory tags, and the like.
  • The nanowires produced by the processes of the present invention are also applicable to digital and analog circuit applications. In particular, the nanowires produced by the processes of the present invention are useful in applications that require ultra large-scale integration on a large area substrate. For example, a thin film of nanowires produced by the processes of the present invention can be implemented in logic circuits, memory circuits, processors, amplifiers, and other digital and analog circuits.
  • The nanowires produced by the processes of the present invention can be applied to photovoltaic applications. In such applications, a clear conducting substrate is used to enhance the photovoltaic properties of the particular photovoltaic device. For example, such a clear conducting substrate can be used as a flexible, large-area replacement for indium tin oxide (ITO) or the like. A substrate can be coated with a thin film of nanowires that is formed to have a large bandgap, i.e., greater than visible light so that it would be non-absorbing, but would be formed to have either the HOMO or LUMO bands aligned with the active material of a photovoltaic device that would be formed on top of it. Clear conductors can be located on two sides of the absorbing photovoltaic material to carry away current from the photovoltaic device. Two different nanowire materials can be chosen, one having the HOMO aligned with that of the photovoltaic material HOMO band, and the other having the LUMO aligned with the LUMO band of the photovoltaic material. The bandgaps of the two nanowires materials can be chosen to be much larger than that of the photovoltaic material. The nanowires, according to this embodiment, can be lightly doped to decrease the resistance of the thin films of nanowires, while permitting the substrate to remain mostly non-absorbing.
  • Hence, a wide range of military and consumer goods can incorporate the nanowires produced by the processes of the present invention. For example, such goods can include personal computers, workstations, servers, networking devices, handheld electronic devices such as PDAs and palm pilots, telephones (e.g., cellular and standard), radios, televisions, electronic games and game systems, home security systems, automobiles, aircraft, boats, other household and commercial appliances, and the like.
  • CONCLUSION
  • Exemplary embodiments of the present invention have been presented. The invention is not limited to these examples. These examples are presented herein for purposes of illustration, and not limitation. Alternatives (including equivalents, extensions, variations, deviations, etc., of those described herein) will be apparent to persons skilled in the relevant art(s) based on the teachings contained herein. Such alternatives fall within the scope and spirit of the invention.
  • All publications, patents and patent applications mentioned in this specification are indicative of the level of skill of those skilled in the art to which this invention pertains, and are herein incorporated by reference to the same extent as if each individual publication, patent or patent application was specifically and individually indicated to be incorporated by reference.

Claims (7)

1. A population of at least four semiconductor nanowires each having a taper rate along a length of the nanowire of less than about 2 nm/micron.
2. The population of semiconductor nanowires of claim 1, wherein the taper rate along the length of each of the nanowires is length than about 1 nm/micron.
3. The population of semiconductor nanowires of claim 2, wherein the taper rate along the length of each of the nanowires is length than about 0.5 nm/micron.
4. The population of semiconductor nanowires of claim 3, wherein the taper rate along the length of each of the nanowires is length than about 0.3 nm/micron.
5. The population of semiconductor nanowires of claim 3, wherein the nanowires comprise silicon.
6. The population of semiconductor nanowires of claim 3, wherein the nanowires comprise silicon and germanium.
7. The population of semiconductor nanowires of claim 5, wherein the nanowires comprise a core made from silicon and one or more shell layers disposed about the core made from an oxide.
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110315953A1 (en) * 2010-06-28 2011-12-29 International Business Machines Corporation Method of forming compound semiconductor

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8958917B2 (en) 1998-12-17 2015-02-17 Hach Company Method and system for remote monitoring of fluid quality and treatment
US9056783B2 (en) 1998-12-17 2015-06-16 Hach Company System for monitoring discharges into a waste water collection system
US7454295B2 (en) 1998-12-17 2008-11-18 The Watereye Corporation Anti-terrorism water quality monitoring system
US8920619B2 (en) 2003-03-19 2014-12-30 Hach Company Carbon nanotube sensor
EP2171761A4 (en) * 2007-07-19 2011-11-02 California Inst Of Techn Structures of ordered arrays of semiconductors
JP2010538464A (en) * 2007-08-28 2010-12-09 カリフォルニア インスティテュート オブ テクノロジー Polymer embedded semiconductor rod array
KR101445877B1 (en) * 2008-03-24 2014-09-29 삼성전자주식회사 Method for Manufacturing Zinc Oxide Nanowires
CN102084467A (en) 2008-04-14 2011-06-01 班德加普工程有限公司 Process for fabricating nanowire arrays
KR101475524B1 (en) * 2008-08-05 2014-12-23 삼성전자주식회사 Nanowire comprising silicon rich oxide and method for producing the same
US8029851B2 (en) 2008-08-29 2011-10-04 Korea University Research And Business Foundation Nanowire fabrication
JP5598805B2 (en) * 2008-09-26 2014-10-01 独立行政法人物質・材料研究機構 Organic polymer nanowire and manufacturing method thereof
US8247325B2 (en) * 2008-10-10 2012-08-21 Uchicago Argonne, Llc Direct growth of metal nanoplates on semiconductor substrates
CN101649491A (en) * 2009-07-17 2010-02-17 宁波工程学院 Method for directionally growing SiC monocrystal nanowire array
US9059344B2 (en) * 2009-08-24 2015-06-16 Shih-Ping Bob Wang Nanowire-based photovoltaic energy conversion devices and related fabrication methods
US8274138B2 (en) * 2009-09-30 2012-09-25 Eastman Kodak Company II-VI semiconductor nanowires
US20110076841A1 (en) * 2009-09-30 2011-03-31 Kahen Keith B Forming catalyzed ii-vi semiconductor nanowires
WO2011066570A2 (en) * 2009-11-30 2011-06-03 California Institute Of Technology Semiconductor wire array structures, and solar cells and photodetectors based on such structures
US9263612B2 (en) 2010-03-23 2016-02-16 California Institute Of Technology Heterojunction wire array solar cells
JP2013527831A (en) * 2010-05-05 2013-07-04 シュパウント プライベート ソシエテ ア レスポンサビリテ リミテ Nanowires produced from novel precursors and methods for producing the same
CN102971452B (en) * 2010-05-11 2017-03-29 昆南诺股份有限公司 The vapor- phase synthesis of line
FR2965280A1 (en) * 2010-09-29 2012-03-30 Commissariat Energie Atomique Fabricating boron-doped silicon wire for semiconductor structures that are useful in electronic, photonic/photovoltaic devices, by depositing catalyst pads on substrate, and performing catalytic growth of wire in absence of boron precursor
JP5002703B2 (en) * 2010-12-08 2012-08-15 株式会社東芝 Semiconductor light emitting device
US8834831B2 (en) 2011-01-11 2014-09-16 The United States Of America As Represented By The Secretary Of The Army Controlling morpholoy of titanium oxide using designed peptides
EP3978426A1 (en) 2011-07-26 2022-04-06 OneD Material, Inc. Nanostructured battery active materials and methods of producing same
WO2013052456A1 (en) 2011-10-05 2013-04-11 Nanosys, Inc. Silicon nanostructure active materials for lithium ion batteries and processes, compositions, components, and devices related thereto
US10026560B2 (en) 2012-01-13 2018-07-17 The California Institute Of Technology Solar fuels generator
US9545612B2 (en) 2012-01-13 2017-01-17 California Institute Of Technology Solar fuel generator
US9476129B2 (en) 2012-04-02 2016-10-25 California Institute Of Technology Solar fuels generator
WO2013126432A1 (en) 2012-02-21 2013-08-29 California Institute Of Technology Axially-integrated epitaxially-grown tandem wire arrays
WO2013152132A1 (en) 2012-04-03 2013-10-10 The California Institute Of Technology Semiconductor structures for fuel generation
CN103854971B (en) * 2012-12-04 2016-10-05 中芯国际集成电路制造(上海)有限公司 The manufacture method of nano wire, the manufacture method of nano-wire field effect transistor
FR3000612B1 (en) * 2012-12-28 2016-05-06 Commissariat Energie Atomique OPTOELECTRONIC MICROFILL OR NANOWIL DEVICE
US9553223B2 (en) 2013-01-24 2017-01-24 California Institute Of Technology Method for alignment of microwires
DE102013201608A1 (en) 2013-01-31 2014-07-31 Wacker Chemie Ag Method of depositing polycrystalline silicon
JP5999611B2 (en) * 2013-08-13 2016-09-28 国立大学法人北海道大学 Tunnel field effect transistor, manufacturing method thereof, and switch element
WO2016109516A1 (en) * 2014-12-29 2016-07-07 Georgia Tech Research Corporation Methods for the continuous, large-scale manufacture of functional nanostructures
CN105185879B (en) * 2015-10-10 2017-08-18 厦门市三安光电科技有限公司 A kind of iii-nitride light emitting devices of three-dimensional doping and preparation method thereof
US11728477B2 (en) 2016-07-15 2023-08-15 Oned Material, Inc. Manufacturing apparatus and method for making silicon nanowires on carbon based powders for use in batteries
US11139402B2 (en) 2018-05-14 2021-10-05 Synopsys, Inc. Crystal orientation engineering to achieve consistent nanowire shapes
CN109962010B (en) * 2018-11-08 2022-05-27 中国科学院半导体研究所 Wafer-level large-area semiconductor nanosheet and preparation method thereof
US11264458B2 (en) 2019-05-20 2022-03-01 Synopsys, Inc. Crystal orientation engineering to achieve consistent nanowire shapes
US11515147B2 (en) 2019-12-09 2022-11-29 Micron Technology, Inc. Material deposition systems, and related methods
KR102271030B1 (en) * 2019-12-20 2021-07-01 서울대학교산학협력단 Method of fabricating a CMOS device with selective area growth
CN111893454B (en) * 2020-07-08 2023-03-14 陕西科技大学 Preparation method of germanium tin nano material under normal pressure

Citations (90)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5252835A (en) * 1992-07-17 1993-10-12 President And Trustees Of Harvard College Machining oxide thin-films with an atomic force microscope: pattern and object formation on the nanometer scale
US5274602A (en) * 1991-10-22 1993-12-28 Florida Atlantic University Large capacity solid-state memory
US5332910A (en) * 1991-03-22 1994-07-26 Hitachi, Ltd. Semiconductor optical device with nanowhiskers
US5338430A (en) * 1992-12-23 1994-08-16 Minnesota Mining And Manufacturing Company Nanostructured electrode membranes
US5505928A (en) * 1991-11-22 1996-04-09 The Regents Of University Of California Preparation of III-V semiconductor nanocrystals
US5512131A (en) * 1993-10-04 1996-04-30 President And Fellows Of Harvard College Formation of microstamped patterns on surfaces and derivative articles
US5640343A (en) * 1996-03-18 1997-06-17 International Business Machines Corporation Magnetic memory array using magnetic tunnel junction devices in the memory cells
US5674592A (en) * 1995-05-04 1997-10-07 Minnesota Mining And Manufacturing Company Functionalized nanostructured films
US5690807A (en) * 1995-08-03 1997-11-25 Massachusetts Institute Of Technology Method for producing semiconductor particles
US5751018A (en) * 1991-11-22 1998-05-12 The Regents Of The University Of California Semiconductor nanocrystals covalently bound to solid inorganic surfaces using self-assembled monolayers
US5840435A (en) * 1993-07-15 1998-11-24 President And Fellows Of Harvard College Covalent carbon nitride material comprising C2 N and formation method
US5858862A (en) * 1996-09-25 1999-01-12 Sony Corporation Process for producing quantum fine wire
US5897945A (en) * 1996-02-26 1999-04-27 President And Fellows Of Harvard College Metal oxide nanorods
US5953595A (en) * 1995-09-29 1999-09-14 Sony Corporation Method of manufacturing thin film transistor
US5962863A (en) * 1993-09-09 1999-10-05 The United States Of America As Represented By The Secretary Of The Navy Laterally disposed nanostructures of silicon on an insulating substrate
US5976957A (en) * 1996-10-28 1999-11-02 Sony Corporation Method of making silicon quantum wires on a substrate
US5990479A (en) * 1997-11-25 1999-11-23 Regents Of The University Of California Organo Luminescent semiconductor nanocrystal probes for biological applications and process for making and using such probes
US5997832A (en) * 1997-03-07 1999-12-07 President And Fellows Of Harvard College Preparation of carbide nanorods
US6004444A (en) * 1997-11-05 1999-12-21 The Trustees Of Princeton University Biomimetic pathways for assembling inorganic thin films and oriented mesoscopic silicate patterns through guided growth
US6036774A (en) * 1996-02-26 2000-03-14 President And Fellows Of Harvard College Method of producing metal oxide nanorods
US6048616A (en) * 1993-04-21 2000-04-11 Philips Electronics N.A. Corp. Encapsulated quantum sized doped semiconductor particles and method of manufacturing same
US6128214A (en) * 1999-03-29 2000-10-03 Hewlett-Packard Molecular wire crossbar memory
US6136156A (en) * 1996-03-01 2000-10-24 Virginia Commonwealth University Nanoparticles of silicon oxide alloys
US6159742A (en) * 1998-06-05 2000-12-12 President And Fellows Of Harvard College Nanometer-scale microscopy probes
US6190634B1 (en) * 1995-06-07 2001-02-20 President And Fellows Of Harvard College Carbide nanomaterials
US6196396B1 (en) * 1999-10-10 2001-03-06 Erith Lestine Bennett Apparel accessories rack
US6207229B1 (en) * 1997-11-13 2001-03-27 Massachusetts Institute Of Technology Highly luminescent color-selective materials and method of making thereof
US6225198B1 (en) * 2000-02-04 2001-05-01 The Regents Of The University Of California Process for forming shaped group II-VI semiconductor nanocrystals, and product formed using process
US6235675B1 (en) * 1998-09-22 2001-05-22 Idaho Research Foundation, Inc. Methods of forming materials containing carbon and boron, methods of forming catalysts, filaments comprising boron and carbon, and catalysts
US6248674B1 (en) * 2000-02-02 2001-06-19 Hewlett-Packard Company Method of aligning nanowires
US6256767B1 (en) * 1999-03-29 2001-07-03 Hewlett-Packard Company Demultiplexer for a molecular wire crossbar network (MWCN DEMUX)
US6274007B1 (en) * 1999-11-25 2001-08-14 Sceptre Electronics Limited Methods of formation of a silicon nanostructure, a silicon quantum wire array and devices based thereon
US20010023986A1 (en) * 2000-02-07 2001-09-27 Vladimir Mancevski System and method for fabricating logic devices comprising carbon nanotube transistors
US6306736B1 (en) * 2000-02-04 2001-10-23 The Regents Of The University Of California Process for forming shaped group III-V semiconductor nanocrystals, and product formed using process
US6329214B1 (en) * 1997-09-05 2001-12-11 Yamaha Corporation Manufacture of field emission device
US6339281B2 (en) * 2000-01-07 2002-01-15 Samsung Sdi Co., Ltd. Method for fabricating triode-structure carbon nanotube field emitter array
US20020014667A1 (en) * 2000-07-18 2002-02-07 Shin Jin Koog Method of horizontally growing carbon nanotubes and field effect transistor using the carbon nanotubes grown by the method
US6380103B2 (en) * 1996-01-03 2002-04-30 Micron Technology, Inc. Rapid thermal etch and rapid thermal oxidation
US6383923B1 (en) * 1999-10-05 2002-05-07 Agere Systems Guardian Corp. Article comprising vertically nano-interconnected circuit devices and method for making the same
US6413489B1 (en) * 1997-04-15 2002-07-02 Massachusetts Institute Of Technology Synthesis of nanometer-sized particles by reverse micelle mediated techniques
US6438025B1 (en) * 1999-09-08 2002-08-20 Sergei Skarupo Magnetic memory device
US20020117659A1 (en) * 2000-12-11 2002-08-29 Lieber Charles M. Nanosensors
US6447663B1 (en) * 2000-08-01 2002-09-10 Ut-Battelle, Llc Programmable nanometer-scale electrolytic metal deposition and depletion
US20020127495A1 (en) * 2001-03-12 2002-09-12 Axel Scherer Method of fabricating nanometer-scale flowchannels and trenches with self-aligned electrodes and the structures formed by the same
US20020125192A1 (en) * 2001-02-14 2002-09-12 Lopez Gabriel P. Nanostructured devices for separation and analysis
US20020130353A1 (en) * 1999-07-02 2002-09-19 Lieber Charles M. Nanoscopic wire-based devices, arrays, and methods of their manufacture
US20020130311A1 (en) * 2000-08-22 2002-09-19 Lieber Charles M. Doped elongated semiconductors, growing such semiconductors, devices including such semiconductors and fabricating such devices
US6471761B2 (en) * 2000-04-21 2002-10-29 University Of New Mexico Prototyping of patterned functional nanostructures
US20020158342A1 (en) * 2001-03-14 2002-10-31 Mark Tuominen Nanofabrication
US20020163079A1 (en) * 2001-05-02 2002-11-07 Fujitsu Limited Integrated circuit device and method of producing the same
US20020175408A1 (en) * 2001-03-30 2002-11-28 The Regents Of The University Of California Methods of fabricating nanostructures and nanowires and devices fabricated therefrom
US20030012723A1 (en) * 2001-07-10 2003-01-16 Clarke Mark S.F. Spatial localization of dispersed single walled carbon nanotubes into useful structures
US20030044777A1 (en) * 1993-10-28 2003-03-06 Kenneth L. Beattie Flowthrough devices for multiple discrete binding reactions
US20030042562A1 (en) * 2001-08-30 2003-03-06 Carsten Giebeler Magnetoresistive device and electronic device
US20030071246A1 (en) * 2001-01-23 2003-04-17 Grigorov Leonid N. Quantum devices based on crystallized electron pairs and methods for their manufacture and use
US20030089899A1 (en) * 2000-08-22 2003-05-15 Lieber Charles M. Nanoscale wires and related devices
US6566704B2 (en) * 2000-06-27 2003-05-20 Samsung Electronics Co., Ltd. Vertical nano-size transistor using carbon nanotubes and manufacturing method thereof
US6586785B2 (en) * 2000-06-29 2003-07-01 California Institute Of Technology Aerosol silicon nanoparticles for use in semiconductor device fabrication
US20030121887A1 (en) * 2001-03-22 2003-07-03 Garvey James F. Multi-component substances and processes for preparation thereof
US20030186522A1 (en) * 2002-04-02 2003-10-02 Nanosys, Inc. Methods of positioning and/or orienting nanostructures
US20030189202A1 (en) * 2002-04-05 2003-10-09 Jun Li Nanowire devices and methods of fabrication
US20040005258A1 (en) * 2001-12-12 2004-01-08 Fonash Stephen J. Chemical reactor templates: sacrificial layer fabrication and template use
US20040026684A1 (en) * 2002-04-02 2004-02-12 Nanosys, Inc. Nanowire heterostructures for encoding information
US20040031975A1 (en) * 2002-03-18 2004-02-19 Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften E.V., A German Corporation Field effect transistor memory cell, memory device and method for manufacturing a field effect transistor memory cell
US20040036128A1 (en) * 2002-08-23 2004-02-26 Yuegang Zhang Multi-gate carbon nano-tube transistors
US20040061422A1 (en) * 2002-09-26 2004-04-01 International Business Machines Corporation System and method for molecular optical emission
US20040095658A1 (en) * 2002-09-05 2004-05-20 Nanosys, Inc. Nanocomposites
US20040112964A1 (en) * 2002-09-30 2004-06-17 Nanosys, Inc. Applications of nano-enabled large area macroelectronic substrates incorporating nanowires and nanowire composites
US6760245B2 (en) * 2002-05-01 2004-07-06 Hewlett-Packard Development Company, L.P. Molecular wire crossbar flash memory
US20040135951A1 (en) * 2002-09-30 2004-07-15 Dave Stumbo Integrated displays using nanowire transistors
US20040146560A1 (en) * 2002-09-05 2004-07-29 Nanosys, Inc. Oriented nanostructures and methods of preparing
US6773616B1 (en) * 2001-11-13 2004-08-10 Hewlett-Packard Development Company, L.P. Formation of nanoscale wires
US6798000B2 (en) * 2000-07-04 2004-09-28 Infineon Technologies Ag Field effect transistor
US6815760B2 (en) * 2001-10-02 2004-11-09 Mosel Vitelic, Inc. Nonvolatile memory structures and fabrication methods
US6815218B1 (en) * 1999-06-09 2004-11-09 Massachusetts Institute Of Technology Methods for manufacturing bioelectronic devices
US6831017B1 (en) * 2002-04-05 2004-12-14 Integrated Nanosystems, Inc. Catalyst patterning for nanowire devices
US6858455B2 (en) * 2001-05-25 2005-02-22 Ut-Battelle, Llc Gated fabrication of nanostructure field emission cathode material within a device
US20050064618A1 (en) * 2001-08-20 2005-03-24 Brown Simon Anthony Nanoscale electronic devices & frabrication methods
US20050066883A1 (en) * 2003-09-25 2005-03-31 Nanosys, Inc. Methods, devices and compositions for depositing and orienting nanostructures
US6878871B2 (en) * 2002-09-05 2005-04-12 Nanosys, Inc. Nanostructure and nanocomposite based compositions and photovoltaic devices
US20050079659A1 (en) * 2002-09-30 2005-04-14 Nanosys, Inc. Large-area nanoenabled macroelectronic substrates and uses therefor
US20050089467A1 (en) * 2003-10-22 2005-04-28 International Business Machines Corporation Control of carbon nanotube diameter using CVD or PECVD growth
US20050133476A1 (en) * 2003-12-17 2005-06-23 Islam M. S. Methods of bridging lateral nanowires and device using same
US20050145596A1 (en) * 2003-12-29 2005-07-07 Metz Matthew V. Method of fabricating multiple nanowires of uniform length from a single catalytic nanoparticle
US20050266662A1 (en) * 2004-05-28 2005-12-01 Yi Sung S Method of growing semiconductor nanowires with uniform cross-sectional area using chemical vapor deposition
US20050279274A1 (en) * 2004-04-30 2005-12-22 Chunming Niu Systems and methods for nanowire growth and manufacturing
US20060019472A1 (en) * 2004-04-30 2006-01-26 Nanosys, Inc. Systems and methods for nanowire growth and harvesting
US7087920B1 (en) * 2005-01-21 2006-08-08 Hewlett-Packard Development Company, L.P. Nanowire, circuit incorporating nanowire, and methods of selecting conductance of the nanowire and configuring the circuit
US20060175601A1 (en) * 2000-08-22 2006-08-10 President And Fellows Of Harvard College Nanoscale wires and related devices
US20060193093A1 (en) * 2004-11-02 2006-08-31 Nantero, Inc. Nanotube ESD protective devices and corresponding nonvolatile and volatile nanotube switches

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5196396A (en) * 1991-07-16 1993-03-23 The President And Fellows Of Harvard College Method of making a superconducting fullerene composition by reacting a fullerene with an alloy containing alkali metal
EP0812434B1 (en) 1995-03-01 2013-09-18 President and Fellows of Harvard College Microcontact printing on surfaces and derivative articles
US6815750B1 (en) * 2002-05-22 2004-11-09 Hewlett-Packard Development Company, L.P. Field effect transistor with channel extending through layers on a substrate
EP1563555A4 (en) 2002-09-30 2009-08-26 Nanosys Inc Applications of nano-enabled large area macroelectronic substrates incorporating nanowires and nanowire composites
AU2003283973B2 (en) 2002-09-30 2008-10-30 Oned Material Llc Large-area nanoenabled macroelectronic substrates and uses therefor
WO2005023923A2 (en) 2003-09-04 2005-03-17 Nanosys, Inc. Methods of processing nanocrystals, and compositions, devices and systems including same
US20070037365A1 (en) 2005-08-15 2007-02-15 Ranganath Tirumala R Semiconductor nanostructures and fabricating the same
US20070186627A1 (en) * 2006-02-10 2007-08-16 Sungsoo Yi High aspect ratio AFM probe and method of making

Patent Citations (99)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5332910A (en) * 1991-03-22 1994-07-26 Hitachi, Ltd. Semiconductor optical device with nanowhiskers
US5274602A (en) * 1991-10-22 1993-12-28 Florida Atlantic University Large capacity solid-state memory
US5751018A (en) * 1991-11-22 1998-05-12 The Regents Of The University Of California Semiconductor nanocrystals covalently bound to solid inorganic surfaces using self-assembled monolayers
US5505928A (en) * 1991-11-22 1996-04-09 The Regents Of University Of California Preparation of III-V semiconductor nanocrystals
US5252835A (en) * 1992-07-17 1993-10-12 President And Trustees Of Harvard College Machining oxide thin-films with an atomic force microscope: pattern and object formation on the nanometer scale
US5338430A (en) * 1992-12-23 1994-08-16 Minnesota Mining And Manufacturing Company Nanostructured electrode membranes
US6048616A (en) * 1993-04-21 2000-04-11 Philips Electronics N.A. Corp. Encapsulated quantum sized doped semiconductor particles and method of manufacturing same
US5840435A (en) * 1993-07-15 1998-11-24 President And Fellows Of Harvard College Covalent carbon nitride material comprising C2 N and formation method
US5962863A (en) * 1993-09-09 1999-10-05 The United States Of America As Represented By The Secretary Of The Navy Laterally disposed nanostructures of silicon on an insulating substrate
US5512131A (en) * 1993-10-04 1996-04-30 President And Fellows Of Harvard College Formation of microstamped patterns on surfaces and derivative articles
US20030044777A1 (en) * 1993-10-28 2003-03-06 Kenneth L. Beattie Flowthrough devices for multiple discrete binding reactions
US5674592A (en) * 1995-05-04 1997-10-07 Minnesota Mining And Manufacturing Company Functionalized nanostructured films
US6190634B1 (en) * 1995-06-07 2001-02-20 President And Fellows Of Harvard College Carbide nanomaterials
US5690807A (en) * 1995-08-03 1997-11-25 Massachusetts Institute Of Technology Method for producing semiconductor particles
US5953595A (en) * 1995-09-29 1999-09-14 Sony Corporation Method of manufacturing thin film transistor
US6380103B2 (en) * 1996-01-03 2002-04-30 Micron Technology, Inc. Rapid thermal etch and rapid thermal oxidation
US6036774A (en) * 1996-02-26 2000-03-14 President And Fellows Of Harvard College Method of producing metal oxide nanorods
US5897945A (en) * 1996-02-26 1999-04-27 President And Fellows Of Harvard College Metal oxide nanorods
US6136156A (en) * 1996-03-01 2000-10-24 Virginia Commonwealth University Nanoparticles of silicon oxide alloys
US5640343A (en) * 1996-03-18 1997-06-17 International Business Machines Corporation Magnetic memory array using magnetic tunnel junction devices in the memory cells
US5858862A (en) * 1996-09-25 1999-01-12 Sony Corporation Process for producing quantum fine wire
US5976957A (en) * 1996-10-28 1999-11-02 Sony Corporation Method of making silicon quantum wires on a substrate
US5997832A (en) * 1997-03-07 1999-12-07 President And Fellows Of Harvard College Preparation of carbide nanorods
US6413489B1 (en) * 1997-04-15 2002-07-02 Massachusetts Institute Of Technology Synthesis of nanometer-sized particles by reverse micelle mediated techniques
US6329214B1 (en) * 1997-09-05 2001-12-11 Yamaha Corporation Manufacture of field emission device
US6004444A (en) * 1997-11-05 1999-12-21 The Trustees Of Princeton University Biomimetic pathways for assembling inorganic thin films and oriented mesoscopic silicate patterns through guided growth
US6322901B1 (en) * 1997-11-13 2001-11-27 Massachusetts Institute Of Technology Highly luminescent color-selective nano-crystalline materials
US6207229B1 (en) * 1997-11-13 2001-03-27 Massachusetts Institute Of Technology Highly luminescent color-selective materials and method of making thereof
US5990479A (en) * 1997-11-25 1999-11-23 Regents Of The University Of California Organo Luminescent semiconductor nanocrystal probes for biological applications and process for making and using such probes
US6159742A (en) * 1998-06-05 2000-12-12 President And Fellows Of Harvard College Nanometer-scale microscopy probes
US6235675B1 (en) * 1998-09-22 2001-05-22 Idaho Research Foundation, Inc. Methods of forming materials containing carbon and boron, methods of forming catalysts, filaments comprising boron and carbon, and catalysts
US6128214A (en) * 1999-03-29 2000-10-03 Hewlett-Packard Molecular wire crossbar memory
US6256767B1 (en) * 1999-03-29 2001-07-03 Hewlett-Packard Company Demultiplexer for a molecular wire crossbar network (MWCN DEMUX)
US6815218B1 (en) * 1999-06-09 2004-11-09 Massachusetts Institute Of Technology Methods for manufacturing bioelectronic devices
US20020130353A1 (en) * 1999-07-02 2002-09-19 Lieber Charles M. Nanoscopic wire-based devices, arrays, and methods of their manufacture
US6438025B1 (en) * 1999-09-08 2002-08-20 Sergei Skarupo Magnetic memory device
US6383923B1 (en) * 1999-10-05 2002-05-07 Agere Systems Guardian Corp. Article comprising vertically nano-interconnected circuit devices and method for making the same
US6196396B1 (en) * 1999-10-10 2001-03-06 Erith Lestine Bennett Apparel accessories rack
US6274007B1 (en) * 1999-11-25 2001-08-14 Sceptre Electronics Limited Methods of formation of a silicon nanostructure, a silicon quantum wire array and devices based thereon
US6339281B2 (en) * 2000-01-07 2002-01-15 Samsung Sdi Co., Ltd. Method for fabricating triode-structure carbon nanotube field emitter array
US6248674B1 (en) * 2000-02-02 2001-06-19 Hewlett-Packard Company Method of aligning nanowires
US6225198B1 (en) * 2000-02-04 2001-05-01 The Regents Of The University Of California Process for forming shaped group II-VI semiconductor nanocrystals, and product formed using process
US6306736B1 (en) * 2000-02-04 2001-10-23 The Regents Of The University Of California Process for forming shaped group III-V semiconductor nanocrystals, and product formed using process
US20010023986A1 (en) * 2000-02-07 2001-09-27 Vladimir Mancevski System and method for fabricating logic devices comprising carbon nanotube transistors
US6471761B2 (en) * 2000-04-21 2002-10-29 University Of New Mexico Prototyping of patterned functional nanostructures
US6566704B2 (en) * 2000-06-27 2003-05-20 Samsung Electronics Co., Ltd. Vertical nano-size transistor using carbon nanotubes and manufacturing method thereof
US6586785B2 (en) * 2000-06-29 2003-07-01 California Institute Of Technology Aerosol silicon nanoparticles for use in semiconductor device fabrication
US6798000B2 (en) * 2000-07-04 2004-09-28 Infineon Technologies Ag Field effect transistor
US20020014667A1 (en) * 2000-07-18 2002-02-07 Shin Jin Koog Method of horizontally growing carbon nanotubes and field effect transistor using the carbon nanotubes grown by the method
US6447663B1 (en) * 2000-08-01 2002-09-10 Ut-Battelle, Llc Programmable nanometer-scale electrolytic metal deposition and depletion
US20020130311A1 (en) * 2000-08-22 2002-09-19 Lieber Charles M. Doped elongated semiconductors, growing such semiconductors, devices including such semiconductors and fabricating such devices
US20060175601A1 (en) * 2000-08-22 2006-08-10 President And Fellows Of Harvard College Nanoscale wires and related devices
US20030089899A1 (en) * 2000-08-22 2003-05-15 Lieber Charles M. Nanoscale wires and related devices
US7129554B2 (en) * 2000-12-11 2006-10-31 President & Fellows Of Harvard College Nanosensors
US20020117659A1 (en) * 2000-12-11 2002-08-29 Lieber Charles M. Nanosensors
US20030071246A1 (en) * 2001-01-23 2003-04-17 Grigorov Leonid N. Quantum devices based on crystallized electron pairs and methods for their manufacture and use
US20020125192A1 (en) * 2001-02-14 2002-09-12 Lopez Gabriel P. Nanostructured devices for separation and analysis
US20020127495A1 (en) * 2001-03-12 2002-09-12 Axel Scherer Method of fabricating nanometer-scale flowchannels and trenches with self-aligned electrodes and the structures formed by the same
US20020158342A1 (en) * 2001-03-14 2002-10-31 Mark Tuominen Nanofabrication
US20030121887A1 (en) * 2001-03-22 2003-07-03 Garvey James F. Multi-component substances and processes for preparation thereof
US6882051B2 (en) * 2001-03-30 2005-04-19 The Regents Of The University Of California Nanowires, nanostructures and devices fabricated therefrom
US20020175408A1 (en) * 2001-03-30 2002-11-28 The Regents Of The University Of California Methods of fabricating nanostructures and nanowires and devices fabricated therefrom
US20020163079A1 (en) * 2001-05-02 2002-11-07 Fujitsu Limited Integrated circuit device and method of producing the same
US6858455B2 (en) * 2001-05-25 2005-02-22 Ut-Battelle, Llc Gated fabrication of nanostructure field emission cathode material within a device
US20030012723A1 (en) * 2001-07-10 2003-01-16 Clarke Mark S.F. Spatial localization of dispersed single walled carbon nanotubes into useful structures
US20050064618A1 (en) * 2001-08-20 2005-03-24 Brown Simon Anthony Nanoscale electronic devices & frabrication methods
US20030042562A1 (en) * 2001-08-30 2003-03-06 Carsten Giebeler Magnetoresistive device and electronic device
US6815760B2 (en) * 2001-10-02 2004-11-09 Mosel Vitelic, Inc. Nonvolatile memory structures and fabrication methods
US6773616B1 (en) * 2001-11-13 2004-08-10 Hewlett-Packard Development Company, L.P. Formation of nanoscale wires
US20040005258A1 (en) * 2001-12-12 2004-01-08 Fonash Stephen J. Chemical reactor templates: sacrificial layer fabrication and template use
US20040031975A1 (en) * 2002-03-18 2004-02-19 Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften E.V., A German Corporation Field effect transistor memory cell, memory device and method for manufacturing a field effect transistor memory cell
US20040026684A1 (en) * 2002-04-02 2004-02-12 Nanosys, Inc. Nanowire heterostructures for encoding information
US20030186522A1 (en) * 2002-04-02 2003-10-02 Nanosys, Inc. Methods of positioning and/or orienting nanostructures
US6872645B2 (en) * 2002-04-02 2005-03-29 Nanosys, Inc. Methods of positioning and/or orienting nanostructures
US6962823B2 (en) * 2002-04-02 2005-11-08 Nanosys, Inc. Methods of making, positioning and orienting nanostructures, nanostructure arrays and nanostructure devices
US20030189202A1 (en) * 2002-04-05 2003-10-09 Jun Li Nanowire devices and methods of fabrication
US6831017B1 (en) * 2002-04-05 2004-12-14 Integrated Nanosystems, Inc. Catalyst patterning for nanowire devices
US6760245B2 (en) * 2002-05-01 2004-07-06 Hewlett-Packard Development Company, L.P. Molecular wire crossbar flash memory
US20040036128A1 (en) * 2002-08-23 2004-02-26 Yuegang Zhang Multi-gate carbon nano-tube transistors
US20040036126A1 (en) * 2002-08-23 2004-02-26 Chau Robert S. Tri-gate devices and methods of fabrication
US20040095658A1 (en) * 2002-09-05 2004-05-20 Nanosys, Inc. Nanocomposites
US20040146560A1 (en) * 2002-09-05 2004-07-29 Nanosys, Inc. Oriented nanostructures and methods of preparing
US6878871B2 (en) * 2002-09-05 2005-04-12 Nanosys, Inc. Nanostructure and nanocomposite based compositions and photovoltaic devices
US20040061422A1 (en) * 2002-09-26 2004-04-01 International Business Machines Corporation System and method for molecular optical emission
US7051945B2 (en) * 2002-09-30 2006-05-30 Nanosys, Inc Applications of nano-enabled large area macroelectronic substrates incorporating nanowires and nanowire composites
US20050079659A1 (en) * 2002-09-30 2005-04-14 Nanosys, Inc. Large-area nanoenabled macroelectronic substrates and uses therefor
US20040135951A1 (en) * 2002-09-30 2004-07-15 Dave Stumbo Integrated displays using nanowire transistors
US20040112964A1 (en) * 2002-09-30 2004-06-17 Nanosys, Inc. Applications of nano-enabled large area macroelectronic substrates incorporating nanowires and nanowire composites
US20050066883A1 (en) * 2003-09-25 2005-03-31 Nanosys, Inc. Methods, devices and compositions for depositing and orienting nanostructures
US7067328B2 (en) * 2003-09-25 2006-06-27 Nanosys, Inc. Methods, devices and compositions for depositing and orienting nanostructures
US20050089467A1 (en) * 2003-10-22 2005-04-28 International Business Machines Corporation Control of carbon nanotube diameter using CVD or PECVD growth
US20050133476A1 (en) * 2003-12-17 2005-06-23 Islam M. S. Methods of bridging lateral nanowires and device using same
US20050145596A1 (en) * 2003-12-29 2005-07-07 Metz Matthew V. Method of fabricating multiple nanowires of uniform length from a single catalytic nanoparticle
US20060019472A1 (en) * 2004-04-30 2006-01-26 Nanosys, Inc. Systems and methods for nanowire growth and harvesting
US20050279274A1 (en) * 2004-04-30 2005-12-22 Chunming Niu Systems and methods for nanowire growth and manufacturing
US7105428B2 (en) * 2004-04-30 2006-09-12 Nanosys, Inc. Systems and methods for nanowire growth and harvesting
US20050266662A1 (en) * 2004-05-28 2005-12-01 Yi Sung S Method of growing semiconductor nanowires with uniform cross-sectional area using chemical vapor deposition
US20060193093A1 (en) * 2004-11-02 2006-08-31 Nantero, Inc. Nanotube ESD protective devices and corresponding nonvolatile and volatile nanotube switches
US7087920B1 (en) * 2005-01-21 2006-08-08 Hewlett-Packard Development Company, L.P. Nanowire, circuit incorporating nanowire, and methods of selecting conductance of the nanowire and configuring the circuit

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110315953A1 (en) * 2010-06-28 2011-12-29 International Business Machines Corporation Method of forming compound semiconductor
US8680510B2 (en) * 2010-06-28 2014-03-25 International Business Machines Corporation Method of forming compound semiconductor

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KR20090087467A (en) 2009-08-17
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US7776760B2 (en) 2010-08-17
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