US20090068821A1 - Charge-free low-temperature method of forming thin film-based nanoscale materials and structures on a substrate - Google Patents
Charge-free low-temperature method of forming thin film-based nanoscale materials and structures on a substrate Download PDFInfo
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- US20090068821A1 US20090068821A1 US12/154,374 US15437408A US2009068821A1 US 20090068821 A1 US20090068821 A1 US 20090068821A1 US 15437408 A US15437408 A US 15437408A US 2009068821 A1 US2009068821 A1 US 2009068821A1
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Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/0021—Reactive sputtering or evaporation
- C23C14/0026—Activation or excitation of reactive gases outside the coating chamber
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C59/00—Surface shaping of articles, e.g. embossing; Apparatus therefor
- B29C59/14—Surface shaping of articles, e.g. embossing; Apparatus therefor by plasma treatment
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y10/00—Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/12—Chemical modification
- C08J7/123—Treatment by wave energy or particle radiation
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L29/00—Semiconductor devices adapted for rectifying, amplifying, oscillating or switching, or capacitors or resistors with at least one potential-jump barrier or surface barrier, e.g. PN junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
- H01L29/02—Semiconductor bodies ; Multistep manufacturing processes therefor
- H01L29/06—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by their shape; characterised by the shapes, relative sizes, or dispositions of the semiconductor regions ; characterised by the concentration or distribution of impurities within semiconductor regions
- H01L29/0657—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by their shape; characterised by the shapes, relative sizes, or dispositions of the semiconductor regions ; characterised by the concentration or distribution of impurities within semiconductor regions characterised by the shape of the body
- H01L29/0665—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by their shape; characterised by the shapes, relative sizes, or dispositions of the semiconductor regions ; characterised by the concentration or distribution of impurities within semiconductor regions characterised by the shape of the body the shape of the body defining a nanostructure
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L29/00—Semiconductor devices adapted for rectifying, amplifying, oscillating or switching, or capacitors or resistors with at least one potential-jump barrier or surface barrier, e.g. PN junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
- H01L29/02—Semiconductor bodies ; Multistep manufacturing processes therefor
- H01L29/06—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by their shape; characterised by the shapes, relative sizes, or dispositions of the semiconductor regions ; characterised by the concentration or distribution of impurities within semiconductor regions
- H01L29/0657—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by their shape; characterised by the shapes, relative sizes, or dispositions of the semiconductor regions ; characterised by the concentration or distribution of impurities within semiconductor regions characterised by the shape of the body
- H01L29/0665—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by their shape; characterised by the shapes, relative sizes, or dispositions of the semiconductor regions ; characterised by the concentration or distribution of impurities within semiconductor regions characterised by the shape of the body the shape of the body defining a nanostructure
- H01L29/0669—Nanowires or nanotubes
- H01L29/0673—Nanowires or nanotubes oriented parallel to a substrate
Definitions
- the invention relates to the formation of nanostructured materials on a substrate. More particularly, the invention relates to growth of thin films on substrates to form such nanostructures. Even more particularly, the invention relates to growth of films on substrates using energetic neutral atom beam lithography and epitaxy to form such nanostructures.
- the present invention meets these and other needs by providing a method of fabricating nanoscale materials at low temperatures using energetic neutral atom beam lithography and epitaxy (also referred to herein as “ENABLE”). This technique uses a flux of neutral atoms to form nanostructures, such as thin films, on a substrate.
- one aspect of the invention is to provide a method of forming at least one nanoscale material on a substrate.
- the at least one nanoscale material comprises at least one of an oxide and a nitride.
- the method comprises the steps of: providing the substrate; providing a flux of at least one element to a surface of the substrate, wherein the at least one element is an element other than oxygen and nitrogen; introducing at least one of nitrogen and oxygen into a plasma within a plasma source, wherein the plasma dissociates, heats, and energizes the at least one of nitrogen and oxygen; extracting a collimated flux of energetic neutral atoms and molecules of at least one of nitrogen and oxygen from the plasma source; and directing the collimated flux from the plasma source onto the surface of the substrate, wherein the at least one element reacts with the energetic neutral atoms to form the at least one nanoscale material.
- the thin film comprises at least one of an oxide and a nitride.
- the method comprises the steps of: providing the substrate; providing a flux of at least one element to a surface of the substrate, wherein the at least one element is selected from the group consisting of silicon, germanium, gallium, indium, aluminum, zinc, magnesium, manganese, cobalt, tin, iron, and titanium; introducing at least one of nitrogen and oxygen into a plasma within a plasma source, wherein the plasma dissociates, heats, and energizes the at least one of nitrogen and oxygen; extracting a collimated flux of energetic neutral atoms and molecules of at least one of nitrogen and oxygen from the plasma source; and directing the collimated flux from the plasma source onto the surface of the substrate, wherein the at least one element reacts with the energetic neutral atoms to form the thin film on the surface.
- Still another aspect of the invention is to provide a nanoscale material disposed on a substrate.
- the nanoscale material comprises at least one of an oxide and a nitride and is formed by: providing the substrate; providing a flux of at least one element to a surface of a substrate, wherein the at least one element is an element other than oxygen and nitrogen; introducing at least one of nitrogen and oxygen into a plasma within a plasma source, wherein the plasma dissociates, heats, and energizes the at least one of nitrogen and oxygen; extracting a collimated flux of energetic neutral atoms and molecules of at least one of nitrogen and oxygen from the plasma source; and directing the collimated flux from the plasma source onto the surface of the substrate, wherein the at least one element reacts with the energetic neutral atoms to form the nanoscale material on the surface.
- FIG. 1 is a flow chart for a method of making a nanoscale material on a substrate
- FIG. 2 is a schematic representation of the application of energetic neutral atom beam lithography and epitaxy (ENABLE) to form oxide or nitride thin film materials;
- FIG. 3 is a series of scanning electron microscopy (SEM) images showing: a) a template polymer substrate; b) a stoichiometric aluminum nitride (AlN) film grown onto the patterned substrate shown in FIG. 3 a by evaporating aluminum metal with simultaneous exposure to a N-atom beam flux; and c) the resulting template-defined array of AlN wires, formed after dissolving the polymer template;
- SEM scanning electron microscopy
- FIG. 4 is a schematic representation of the formation of a continuous beam of energetic neutral nitrogen atoms created by extracting the constituents of a laser sustained N-plasma discharge through a supersonic nozzle;
- FIG. 5 is a series of ⁇ -2 ⁇ x-ray diffraction scans of GaN films grown on bare sapphire at ambient, 100° C., 200° C. and 300° C. substrate temperatures;
- FIG. 6 is a plot of electro-luminescent (EL) output for a GaN film grown by a method of the present invention and current-voltage (I-V) properties of a p-n junction prepared by growing gallium nitride (GaN) using the ENABLE method at a substrate temperature of 300° C. (inset); and
- FIG. 7 is: a) a ⁇ -2 ⁇ x-ray diffraction scan obtained for a GaN film grown at 500° C. on a sapphire substrate without a buffer layer; and b) a high-resolution cross-sectional transmission electron microscopy image of a GaN film grown at 500° C. on a sapphire substrate.
- nanoscale material is understood to include any material, structure, or feature that is formed by addition of a material to the substrate, wherein such features have at least one dimension (e.g., length, diameter, width, or depth) of less than about 100 nm.
- dimensions e.g., length, diameter, width, or depth
- nanoscale materials include, but are not limited to, thin films, wire, rods, sheets, ribbons, and the like.
- individual nanoscale materials have features with at least one dimension of at least 20 nm. In another embodiment, features as small as 1 nm may be achieved.
- the at least one nanoscale material is formed by providing materials—such as either metals or semiconducting materials—directly onto the substrate in the presence of the collimated flux of energetic neutral nitrogen or oxygen atoms to form either oxide or nitride materials.
- materials such as either metals or semiconducting materials
- Such metals and semiconducting materials include, but are not limited to, silicon, germanium, gallium, indium, aluminum, zinc, titanium, magnesium, manganese, tin, cobalt, iron, and the like.
- a substrate is provided.
- the substrate is usually a crystalline material upon which a thin film of the nanoscale material is epitaxially grown.
- Substrate crystallinity usually determines the quality and crystallinity of the nitride or oxide thin film, which in turn determine at least one of the electrical properties, optical properties, and general quality of the thin film.
- Typical crystalline substrates include, but are not limited to, sapphire (Al 2 O 3 ), silicon, zinc oxide, silicon carbide, and the like.
- the substrate crystalline lattice match to the thin film grown on the substrate can determine the final quality of the thin film.
- the thin film of nanoscale material is commonly grown on either the (0001) crystallographic face of sapphire, the (0001) face of silicon carbide, the (0001) face of zinc oxide, or the (111) face of silicon.
- the substrate is a polymeric substrate.
- polymeric substrates include, but are not limited to, polyimides, polymethyl methacrylate (PMMA), Shipley SU-8 photoresist, polycarbonates, perfluorinated cyclobutane (PFCB), and combinations thereof.
- the substrate may comprise highly oriented pyrolytic carbon (HOPC), glassy carbon, diamond, and combinations thereof.
- a flux of at least one element in gaseous form is provided to a surface of the substrate in Step 120 .
- the flux of the at least one element may be generated, for example, by either e-beam evaporation or thermal evaporation.
- neutral atoms and molecules of least one of nitrogen and oxygen are introduced into a plasma within a plasma source.
- a collimated flux or beam of energetic neutral atoms and molecules are then extracted from the plasma source (Step 140 ) and directed onto the surface of the substrate (Step 150 ).
- the flux of at least one element and the collimated flux of energetic neutral atoms and molecules react at or near the surface to form the nanoscale material (Step 160 ).
- the energetic neutral atoms and molecules in the plasma have an average kinetic energy in a range from about 1 eV to about 5 eV.
- the collimated flux is at least 10 14 neutral atoms and molecules/cm 2 -sec. In another embodiment, the collimated flux is in a range from about 10 14 neutral atoms and molecules m 2 sec to about 10 18 neutral atoms and molecules/cm 2 sec.
- the use of neutral atomic species with energies on the order of chemical bond strengths offers many advantages over more conventional approaches for materials processing involving thin film growth and etching.
- the high kinetic energy of the atoms and molecules in the collimated flux circumvent the need for thermal activation of the substrate, and allow the nanoscale materials and structures to be formed at lower substrate temperatures. These advantages in turn permit the use of some substrates, such as the polymeric substrates described herein, which would otherwise sustain substantial damage due to high processing temperatures.
- the substrate is heated up to about 800° C. during processing. In a second embodiment, the substrate is heated to about 500° C.
- the substrate is heated to a temperature in a range from about 20° C. to about 100° C. during processing.
- the substrate is maintained at near ambient (i.e., about 30° C.) temperature.
- Energetic Neutral Atom Beam Lithography and Epitaxy (also referred to herein as “ENABLE”), schematically illustrated in FIG. 2 , is capable of providing the necessary flux of atomic species.
- ENABLE utilizes a neutral atomic beam source that produces energetic species (O or N atoms) with kinetic energies in a range from about 0.5 eV to about 5 eV and a collimated flux of about 10 17 atoms/cm 2 sec (which is equivalent to about 100 monolayers/sec) over an area of approximately 20 cm 2 .
- energetic species O or N atoms
- collimated flux of about 10 17 atoms/cm 2 sec (which is equivalent to about 100 monolayers/sec) over an area of approximately 20 cm 2 .
- Nanostructures etched into polymer films on crystalline substrates can be used as templates for growing thin films nanoscale materials where the template determines their nanoscale dimensions.
- a method of etching such polymer films using ENABLE is described in the U.S. patent application Ser. No. ______, entitled “Charge-Free Method of Forming Nanostructures on a Substrate,” by Mark A. Hoffbauer et al., filed on Nov. 21, 2006, the contents of which are incorporated by reference herein in their entirety.
- polymer substrate surfaces In order to be suitable for ENABLE etching, polymer substrate surfaces must first be patterned with a mask material that does not react with energetic O-atoms to form volatile reaction products.
- a variety of techniques known in the art including photolithography, e-beam lithography, nanosphere lithography, and the like may be used for masking polymeric substrates.
- the unprotected areas are anisotropically etched away, leaving the underlying masked polymer substrate intact.
- etching represents a top-down approach for nanofabrication
- the invention offers the capability for bottom-up assembly of nanoscale materials in the same system.
- Metals or semiconductors such as, but not limited to, silicon, germanium, gallium, indium, aluminum, zinc, magnesium, titanium, manganese, cobalt, tin, iron, and the like, may be evaporated directly onto a substrate in the presence of energetic atomic oxygen or nitrogen species to form oxide or nitride materials, as illustrated in FIG. 2 .
- the elevated substrate temperatures often required for growing thin film materials by other methods e.g., metal organic chemical vapor deposition (MOCVD), molecular beam epitaxy (MBE), and atomic layer deposition (ALD)
- MOCVD metal organic chemical vapor deposition
- MBE molecular beam epitaxy
- ALD atomic layer deposition
- FIG. 3 b is a scanning electron microscopy (SEM) image of a 700 nm thick stoichiometric aluminum nitride (AlN) film that was grown at a rate of about 10 nm/min onto the patterned substrate shown in FIG. 3 a by evaporating Al metal with simultaneous exposure to a N-atom beam flux having an energy of about 0.8 eV.
- the resulting template-defined array of AlN wires shown in FIG. 3 c was formed after dissolving and removing the polymer template.
- the low-temperature fabrication approach of the invention may be used to produce 2- and 3-dimensional nanostructures and devices with multiple functionalities.
- GaN gallium nitride
- AlN aluminum nitride
- InN indium nitride
- Si 3 N 4 silicon nitride
- oxides such as aluminum oxide (Al 2 O3), titanium oxide (TiO 2 ), zinc oxide (ZnO), and silica (SiO 2 ) may be formed using these methods.
- a continuous beam of energetic neutral nitrogen or oxygen atoms is created by extracting the constituents of a laser sustained N- or O-based plasma discharge through a supersonic nozzle.
- the effective source temperature and final kinetic energy of the extracted species may be adjusted by translating the lens forward (i.e., toward the nozzle) to move the laser focus—and thus the plasma discharge—into the nozzle orifice.
- Very efficient ion-electron recombination in the constricted nozzle and in the high-density supersonic expansion region yields an energetic neutral beam flux consisting primarily of (i.e., often greater than 98%) atomic species.
- the atom beam velocity may be increased by seeding the plasma with a lower molecular weight gas such as, for example, helium or the like, by varying the plasma position relative to the nozzle, and/or varying the pressure within the laser-sustained plasma region.
- a lower molecular weight gas such as, for example, helium or the like
- nitrogen atoms having a mean kinetic energy of about 1.0 eV to about 2.0 eV or oxygen atoms having a mean kinetic energy of about 2.0 eV to about 3.0 eV are produced.
- Energy distribution ( ⁇ E/E) of the atomic species is typically about 30%.
- a neutral beam flux in a range from about 10 14 neutral atoms and molecules/cm 2 ⁇ sec to about 1018 neutral atoms and molecules/cm 2 ⁇ sec.
- the neutral beam flux is about 1 ⁇ 10 17 neutral atoms and molecules/cm 2 ⁇ sec.
- the neutral beam flux is uniform over an area of approximately 15 cm 2 at a distance 50 cm from the source nozzle with a divergence of less than 2°.
- the atomic beam velocity, energy, composition, and flux are directly measured using time-of-flight mass spectroscopy.
- gallium metal is provided by e-beam or thermal evaporation at rates ranging from about 0.1 ⁇ m/hr to 4.0 ⁇ m/hr. Evaporation rates of up to 10 ⁇ m/hr may be achieved.
- the GaN growth rate is limited by the Ga evaporation rate, since a large excess of active N is supplied to the surface.
- the growth chamber is maintained at a base pressure of about 5 ⁇ 10 ⁇ 9 torr or less, while the background pressure, which consists mostly of background N 2 and He, reaches about 2 ⁇ 10 ⁇ 6 torr during film growth.
- as-received c-axis oriented sapphire (0001) substrate pieces were moved into vacuum, heated to the GaN growth temperatures, and exposed to the atomic N beam with kinetic energies ranging from 0.8 eV to 2.0 eV for 5 minutes to clean and pre-nitride the substrate surface.
- Gallium nitride film growth at rate of approximately 1 ⁇ m/hr was initiated by opening a shutter to deliver the Ga flux.
- XRD x-ray diffraction
- FIG. 5 The ⁇ -2 ⁇ x-ray diffraction (XRD) scans of GaN films grown on bare sapphire at ambient, 100° C., 200° C. and 300° C. substrate temperatures are shown in FIG. 5 .
- RT ambient temperature
- GaN growth results in an amorphous film
- clear evidence for polycrystalline GaN films is observed at growth temperatures above 100° C.
- GaN films grown at 100° C. and 200° C. show similar degrees of crystallinity.
- a pronounced increase in the crystallographic alignment of the GaN film is observed in XRD scans obtained for films grown at 300° C., indicating that about 80% of the film is c-axis oriented.
- the electrical properties of the low-temperature GaN films also improve as growth temperature increases. GaN films grown at temperatures below 200° C. are highly insulating. Resistivity decreases sharply at growth temperatures above 200° C., resulting in n-type GaN films with an intrinsic carrier density ranging from 2.1 ⁇ 10 17 to 4.7 ⁇ 10 18 carriers/cm 3 .
- the inset in FIG. 6 shows the current-voltage (I-V) properties of a p-n junction prepared by growing 1 ⁇ m of ENABLE-grown GaN at a substrate temperature of 300° C. and a growth rate of about 1 ⁇ m/hr on top of a MOCVD grown p(Mg)-GaN substrate.
- I-V scans of the p-n junction show diodic behavior with forward conduction commencing at a bias of 3.0 ⁇ 0.1 V, accompanied by the room-temperature electro-luminescent (EL) output shown in FIG. 6 .
- FIG. 7 a shows the ⁇ -2 ⁇ XRD scan of a 400 nm thick GaN film grown at 500° C. on a bare c-plane (0001) sapphire substrate without a buffer layer. The resulting GaN film was found to be exclusively c-axis oriented.
- the FWHM of the ⁇ 002> GaN peak measures 0.28°, with the single crystal sapphire substrate ⁇ 006> peak FWHM of 0.21°, representing the instrumental contribution to peak broadening.
- a shift of 0.037° is observed in the position of the GaN ⁇ 002> peak due to the compressive strain resulting from the 13.8% lattice mismatch of the GaN film and the sapphire substrate.
- a pole figure XRD scan of the ⁇ 101> GaN Bragg peak shown in the inset of FIG. 7 a indicates excellent epitaxial alignment between the lattice mismatched substrate and the nitride film with a mosaic spread of 2.8° to 3.0°.
- mosaic spreads for a GaN film grown on a buffer layer at 1050° C. by MOCVD are typically between 2.8° and 3.2°.
- TEM transmission electron microscopy
- the invention also includes a thin film having at least one nanostructure disposed on a substrate formed by the methods described herein.
- the nanostructure is formed by providing a substrate; providing a flux of at least one element to a surface of a substrate, wherein the at least one element is an element other than nitrogen or oxygen (in one embodiment, the element is selected from the group consisting of silicon, germanium, gallium, indium, aluminum, zinc, magnesium, manganese, tin, iron, and titanium); introducing at least one of nitrogen and oxygen into a plasma within a plasma source, wherein the plasma heats, dissociates, and energizes at least one of nitrogen and oxygen; extracting a collimated flux of energetic neutral atoms and molecules of at least one of nitrogen and oxygen from the plasma source; and directing the collimated flux from the plasma source onto the surface of the substrate, wherein the at least one element reacts with the energetic neutral atoms to form the nanostructure on the surface.
- FIGS. 3 b and 3 c Examples of such nanostructures are shown in FIGS. 3 b and 3 c.
- FIG. 3 b is a SEM image of an aluminum nitride thin film grown onto a template ( FIG. 3 a ) formed by O-atom etching of a masked polyimide using ENABLE
- FIG. 3 c is a SEM image of AlN nanowires formed from the thin film shown in FIG. 3 b by removing the template.
Abstract
A method of forming a nanostructure at low temperatures. A substrate that is reactive with one of atomic oxygen and nitrogen is provided. A flux of neutral atoms of least one of nitrogen and oxygen is generated within a laser-sustained-discharge plasma source and a collimated beam of energetic neutral atoms and molecules is directed from the plasma source onto a surface of the substrate to form the nanostructure. The energetic neutral atoms and molecules in the plasma have an average kinetic energy in a range from about 1 eV to about 5 eV.
Description
- This application is a divisional application of U.S. patent application Ser. No. 11/603,517, filed Nov. 21, 2006.
- This invention was made with government support under Contract No. DE-AC 52-06 NA 25396, awarded by the U.S. Department of Energy. The government has certain rights in the invention.
- The invention relates to the formation of nanostructured materials on a substrate. More particularly, the invention relates to growth of thin films on substrates to form such nanostructures. Even more particularly, the invention relates to growth of films on substrates using energetic neutral atom beam lithography and epitaxy to form such nanostructures.
- Growing thin film materials and nanoscale structures for use in semiconducting, mechanical, and optical devices presents considerable challenges, especially when the active regions of such structures approach critical dimensions of only a few nanometers. Problems associated with charge deposition and structural damage from sputtering and related processes pose significant limitations for fabricating nanoscale structures and devices. In addition, the high substrate temperatures typically required for thin film growth often rule out many combinations of materials that could otherwise be used for novel device structures.
- Currently, the aggressive growth and processing conditions commonly used in fabricating nanoscale materials and structures often result in substantial damage and compromises the properties of such materials and structures. Moreover, high processing temperatures often preclude the use of certain materials. Therefore, what is needed is a damage-free method for fabricating nanoscale materials and structures. What is also needed. is a method of making nanoscale materials and structures that does not require high substrate temperatures.
- The present invention meets these and other needs by providing a method of fabricating nanoscale materials at low temperatures using energetic neutral atom beam lithography and epitaxy (also referred to herein as “ENABLE”). This technique uses a flux of neutral atoms to form nanostructures, such as thin films, on a substrate.
- Accordingly, one aspect of the invention is to provide a method of forming at least one nanoscale material on a substrate. The at least one nanoscale material comprises at least one of an oxide and a nitride. The method comprises the steps of: providing the substrate; providing a flux of at least one element to a surface of the substrate, wherein the at least one element is an element other than oxygen and nitrogen; introducing at least one of nitrogen and oxygen into a plasma within a plasma source, wherein the plasma dissociates, heats, and energizes the at least one of nitrogen and oxygen; extracting a collimated flux of energetic neutral atoms and molecules of at least one of nitrogen and oxygen from the plasma source; and directing the collimated flux from the plasma source onto the surface of the substrate, wherein the at least one element reacts with the energetic neutral atoms to form the at least one nanoscale material.
- Another aspect of the invention is to provide a method of forming a thin film on a substrate. The thin film comprises at least one of an oxide and a nitride. The method comprises the steps of: providing the substrate; providing a flux of at least one element to a surface of the substrate, wherein the at least one element is selected from the group consisting of silicon, germanium, gallium, indium, aluminum, zinc, magnesium, manganese, cobalt, tin, iron, and titanium; introducing at least one of nitrogen and oxygen into a plasma within a plasma source, wherein the plasma dissociates, heats, and energizes the at least one of nitrogen and oxygen; extracting a collimated flux of energetic neutral atoms and molecules of at least one of nitrogen and oxygen from the plasma source; and directing the collimated flux from the plasma source onto the surface of the substrate, wherein the at least one element reacts with the energetic neutral atoms to form the thin film on the surface.
- Still another aspect of the invention is to provide a nanoscale material disposed on a substrate. The nanoscale material comprises at least one of an oxide and a nitride and is formed by: providing the substrate; providing a flux of at least one element to a surface of a substrate, wherein the at least one element is an element other than oxygen and nitrogen; introducing at least one of nitrogen and oxygen into a plasma within a plasma source, wherein the plasma dissociates, heats, and energizes the at least one of nitrogen and oxygen; extracting a collimated flux of energetic neutral atoms and molecules of at least one of nitrogen and oxygen from the plasma source; and directing the collimated flux from the plasma source onto the surface of the substrate, wherein the at least one element reacts with the energetic neutral atoms to form the nanoscale material on the surface.
- These and other aspects, advantages, and salient features of the present invention will become apparent from the following detailed description, the accompanying drawings, and the appended claims.
-
FIG. 1 is a flow chart for a method of making a nanoscale material on a substrate; -
FIG. 2 is a schematic representation of the application of energetic neutral atom beam lithography and epitaxy (ENABLE) to form oxide or nitride thin film materials; -
FIG. 3 is a series of scanning electron microscopy (SEM) images showing: a) a template polymer substrate; b) a stoichiometric aluminum nitride (AlN) film grown onto the patterned substrate shown inFIG. 3 a by evaporating aluminum metal with simultaneous exposure to a N-atom beam flux; and c) the resulting template-defined array of AlN wires, formed after dissolving the polymer template; -
FIG. 4 is a schematic representation of the formation of a continuous beam of energetic neutral nitrogen atoms created by extracting the constituents of a laser sustained N-plasma discharge through a supersonic nozzle; -
FIG. 5 is a series of θ-2θ x-ray diffraction scans of GaN films grown on bare sapphire at ambient, 100° C., 200° C. and 300° C. substrate temperatures; -
FIG. 6 is a plot of electro-luminescent (EL) output for a GaN film grown by a method of the present invention and current-voltage (I-V) properties of a p-n junction prepared by growing gallium nitride (GaN) using the ENABLE method at a substrate temperature of 300° C. (inset); and -
FIG. 7 is: a) a θ-2θ x-ray diffraction scan obtained for a GaN film grown at 500° C. on a sapphire substrate without a buffer layer; and b) a high-resolution cross-sectional transmission electron microscopy image of a GaN film grown at 500° C. on a sapphire substrate. - In the following description, like reference characters designate like or corresponding parts throughout the several views shown in the figures. It is also understood that terms such as “top,” “bottom,” “outward,” “inward,” and the like are words of convenience and are not to be construed as limiting terms. In addition, whenever a group is described as either comprising or consisting of at least one of a group of elements and combinations thereof, it is understood that the group may comprise or consist of any number of those elements recited, either individually or in combination with each other.
- Referring to the drawings in general and to
FIG. 1 in particular, it will be understood that the illustrations are for the purpose of describing a particular embodiment of the invention and are not intended to limit the invention thereto. Turning toFIG. 1 , a flow chart for a method of making at least one nanoscale material on a substrate is shown. As used herein, the term “nanoscale material” is understood to include any material, structure, or feature that is formed by addition of a material to the substrate, wherein such features have at least one dimension (e.g., length, diameter, width, or depth) of less than about 100 nm. Examples of such nanoscale materials include, but are not limited to, thin films, wire, rods, sheets, ribbons, and the like. In one embodiment, individual nanoscale materials have features with at least one dimension of at least 20 nm. In another embodiment, features as small as 1 nm may be achieved. - In
method 100, the at least one nanoscale material is formed by providing materials—such as either metals or semiconducting materials—directly onto the substrate in the presence of the collimated flux of energetic neutral nitrogen or oxygen atoms to form either oxide or nitride materials. Such metals and semiconducting materials include, but are not limited to, silicon, germanium, gallium, indium, aluminum, zinc, titanium, magnesium, manganese, tin, cobalt, iron, and the like. -
Step 110, a substrate is provided. For thin film growth, the substrate is usually a crystalline material upon which a thin film of the nanoscale material is epitaxially grown. Substrate crystallinity usually determines the quality and crystallinity of the nitride or oxide thin film, which in turn determine at least one of the electrical properties, optical properties, and general quality of the thin film. Typical crystalline substrates include, but are not limited to, sapphire (Al2O3), silicon, zinc oxide, silicon carbide, and the like. The substrate crystalline lattice match to the thin film grown on the substrate can determine the final quality of the thin film. The thin film of nanoscale material is commonly grown on either the (0001) crystallographic face of sapphire, the (0001) face of silicon carbide, the (0001) face of zinc oxide, or the (111) face of silicon. - Use of the ENABLE technique allows thin films of nanoscale materials such as GaN to be grown on substrates at low temperatures. Thus, in another embodiment, the substrate is a polymeric substrate. Non-limiting examples of such polymeric substrates include, but are not limited to, polyimides, polymethyl methacrylate (PMMA), Shipley SU-8 photoresist, polycarbonates, perfluorinated cyclobutane (PFCB), and combinations thereof. Alternatively, the substrate may comprise highly oriented pyrolytic carbon (HOPC), glassy carbon, diamond, and combinations thereof.
- A flux of at least one element in gaseous form is provided to a surface of the substrate in
Step 120. The flux of the at least one element may be generated, for example, by either e-beam evaporation or thermal evaporation. InStep 130, neutral atoms and molecules of least one of nitrogen and oxygen are introduced into a plasma within a plasma source. A collimated flux or beam of energetic neutral atoms and molecules are then extracted from the plasma source (Step 140) and directed onto the surface of the substrate (Step 150). The flux of at least one element and the collimated flux of energetic neutral atoms and molecules react at or near the surface to form the nanoscale material (Step 160). The energetic neutral atoms and molecules in the plasma have an average kinetic energy in a range from about 1 eV to about 5 eV. In one embodiment, the collimated flux is at least 1014 neutral atoms and molecules/cm2-sec. In another embodiment, the collimated flux is in a range from about 1014 neutral atoms and molecules m2 sec to about 1018 neutral atoms and molecules/cm2 sec. - Due to their energy, charge neutrality, and chemical specificity, the use of neutral atomic species with energies on the order of chemical bond strengths (i.e., a few electron volts (eVs)) offers many advantages over more conventional approaches for materials processing involving thin film growth and etching. The high kinetic energy of the atoms and molecules in the collimated flux circumvent the need for thermal activation of the substrate, and allow the nanoscale materials and structures to be formed at lower substrate temperatures. These advantages in turn permit the use of some substrates, such as the polymeric substrates described herein, which would otherwise sustain substantial damage due to high processing temperatures. In one embodiment, the substrate is heated up to about 800° C. during processing. In a second embodiment, the substrate is heated to about 500° C. In a third embodiment, the substrate is heated to a temperature in a range from about 20° C. to about 100° C. during processing. In yet another embodiment, the substrate is maintained at near ambient (i.e., about 30° C.) temperature. To achieve high etch or growth rates over large areas, a high flux of atomic species is required. Energetic Neutral Atom Beam Lithography and Epitaxy (also referred to herein as “ENABLE”), schematically illustrated in
FIG. 2 , is capable of providing the necessary flux of atomic species. ENABLE utilizes a neutral atomic beam source that produces energetic species (O or N atoms) with kinetic energies in a range from about 0.5 eV to about 5 eV and a collimated flux of about 1017 atoms/cm2 sec (which is equivalent to about 100 monolayers/sec) over an area of approximately 20 cm2. - The generation of the collimated flux of energetic neutral atoms and molecules by ENABLE is described in U.S. Pat. No. 4,780,608 by Jon B. Cross et al., entitled “Laser Sustained Discharge Nozzle Apparatus for the Production of an Intense Beam of High Kinetic Energy Atomic Species,” issued Oct. 25, 1988; U.S. Pat. No. 5,271,800 by Steven L. Koontz et al., entitled “Method for Anisotropic Etching in the Manufacture of Semiconductor Devices,” issued Dec. 21, 1993; and U.S. Pat. No. 6,68,967 by Mark A. Hoffbauer et al., entitled “Reduction of Surface Leakage Current by Surface Passivation of CdZnTe and Related Materials using Hyperthermal Oxygen Atoms,” issued Jan. 2, 2001; and U.S. patent application Ser. No. 10/102,303 by A. Mueller et al., entitled “Colloidal Quantum Dot Light Emitting Diodes,” filed Mar. 25, 2004, the contents of which are incorporated by reference herein in their entirety.
- Nanostructures etched into polymer films on crystalline substrates can be used as templates for growing thin films nanoscale materials where the template determines their nanoscale dimensions. A method of etching such polymer films using ENABLE is described in the U.S. patent application Ser. No. ______, entitled “Charge-Free Method of Forming Nanostructures on a Substrate,” by Mark A. Hoffbauer et al., filed on Nov. 21, 2006, the contents of which are incorporated by reference herein in their entirety. In order to be suitable for ENABLE etching, polymer substrate surfaces must first be patterned with a mask material that does not react with energetic O-atoms to form volatile reaction products. A variety of techniques known in the art, including photolithography, e-beam lithography, nanosphere lithography, and the like may be used for masking polymeric substrates. When the sample is exposed to the incident collimated beam of atomic oxygen, the unprotected areas are anisotropically etched away, leaving the underlying masked polymer substrate intact.
- While etching represents a top-down approach for nanofabrication, the invention offers the capability for bottom-up assembly of nanoscale materials in the same system. Metals or semiconductors such as, but not limited to, silicon, germanium, gallium, indium, aluminum, zinc, magnesium, titanium, manganese, cobalt, tin, iron, and the like, may be evaporated directly onto a substrate in the presence of energetic atomic oxygen or nitrogen species to form oxide or nitride materials, as illustrated in
FIG. 2 . Since the energy of the atomic species can overcome thermal activation barriers associated with oxidation and nitridation reactions, the elevated substrate temperatures often required for growing thin film materials by other methods (e.g., metal organic chemical vapor deposition (MOCVD), molecular beam epitaxy (MBE), and atomic layer deposition (ALD)) can be reduced or eliminated. As a result, high-quality nitride or oxide films can be grown at relatively low substrate temperatures even on very delicate materials such as polymers. - The invention allows nitride or other thin film materials to be directly grown onto polymeric films to form templated nanostructures. For example,
FIG. 3 b is a scanning electron microscopy (SEM) image of a 700 nm thick stoichiometric aluminum nitride (AlN) film that was grown at a rate of about 10 nm/min onto the patterned substrate shown inFIG. 3 a by evaporating Al metal with simultaneous exposure to a N-atom beam flux having an energy of about 0.8 eV. The resulting template-defined array of AlN wires shown inFIG. 3 c was formed after dissolving and removing the polymer template. The low-temperature fabrication approach of the invention may be used to produce 2- and 3-dimensional nanostructures and devices with multiple functionalities. - The formation of highly crystalline gallium nitride (GaN) films by the methods described herein serves to illustrate the features and advantages of the invention. While the formation of GaN is described, it is understood that nanoscale material and structures comprising other nitrides, oxides, or particular crystallographic structures thereof may be formed using these methods. For example, other Group III nitrides such as aluminum nitride (AlN) and indium nitride (InN), silicon nitride (Si3N4), and oxides, such as aluminum oxide (Al2O3), titanium oxide (TiO2), zinc oxide (ZnO), and silica (SiO2) may be formed using these methods.
- As illustrated in
FIG. 4 , a continuous beam of energetic neutral nitrogen or oxygen atoms is created by extracting the constituents of a laser sustained N- or O-based plasma discharge through a supersonic nozzle. The effective source temperature and final kinetic energy of the extracted species may be adjusted by translating the lens forward (i.e., toward the nozzle) to move the laser focus—and thus the plasma discharge—into the nozzle orifice. Very efficient ion-electron recombination in the constricted nozzle and in the high-density supersonic expansion region yields an energetic neutral beam flux consisting primarily of (i.e., often greater than 98%) atomic species. The atom beam velocity may be increased by seeding the plasma with a lower molecular weight gas such as, for example, helium or the like, by varying the plasma position relative to the nozzle, and/or varying the pressure within the laser-sustained plasma region. Typically, nitrogen atoms having a mean kinetic energy of about 1.0 eV to about 2.0 eV or oxygen atoms having a mean kinetic energy of about 2.0 eV to about 3.0 eV are produced. Energy distribution (ΔE/E) of the atomic species is typically about 30%. Subsequent collimation of the atom beam by a series of apertures results in a neutral beam flux in a range from about 1014 neutral atoms and molecules/cm2·sec to about 1018 neutral atoms and molecules/cm2·sec. In one embodiment, the neutral beam flux is about 1×1017 neutral atoms and molecules/cm2·sec. The neutral beam flux is uniform over an area of approximately 15 cm2 at a distance 50 cm from the source nozzle with a divergence of less than 2°. The atomic beam velocity, energy, composition, and flux are directly measured using time-of-flight mass spectroscopy. - Along with energetic nitrogen atoms, a collimated flux of gallium metal is simultaneously supplied to the substrate surface to initiate GaN film growth. In one embodiment, gallium metal is provided by e-beam or thermal evaporation at rates ranging from about 0.1 μm/hr to 4.0 μm/hr. Evaporation rates of up to 10 μm/hr may be achieved. The GaN growth rate is limited by the Ga evaporation rate, since a large excess of active N is supplied to the surface. The growth chamber is maintained at a base pressure of about 5×10−9 torr or less, while the background pressure, which consists mostly of background N2 and He, reaches about 2×10−6 torr during film growth.
- For the results described herein, as-received c-axis oriented sapphire (0001) substrate pieces, measuring about 1 cm2, were moved into vacuum, heated to the GaN growth temperatures, and exposed to the atomic N beam with kinetic energies ranging from 0.8 eV to 2.0 eV for 5 minutes to clean and pre-nitride the substrate surface. Gallium nitride film growth at rate of approximately 1 μm/hr was initiated by opening a shutter to deliver the Ga flux.
- The θ-2θ x-ray diffraction (XRD) scans of GaN films grown on bare sapphire at ambient, 100° C., 200° C. and 300° C. substrate temperatures are shown in
FIG. 5 . At ambient temperature (labeled “RT” inFIG. 5 ), GaN growth results in an amorphous film, whereas clear evidence for polycrystalline GaN films is observed at growth temperatures above 100° C. GaN films grown at 100° C. and 200° C. show similar degrees of crystallinity. A pronounced increase in the crystallographic alignment of the GaN film is observed in XRD scans obtained for films grown at 300° C., indicating that about 80% of the film is c-axis oriented. - The electrical properties of the low-temperature GaN films also improve as growth temperature increases. GaN films grown at temperatures below 200° C. are highly insulating. Resistivity decreases sharply at growth temperatures above 200° C., resulting in n-type GaN films with an intrinsic carrier density ranging from 2.1×1017 to 4.7×1018 carriers/cm3. The inset in
FIG. 6 shows the current-voltage (I-V) properties of a p-n junction prepared by growing 1 μm of ENABLE-grown GaN at a substrate temperature of 300° C. and a growth rate of about 1 μm/hr on top of a MOCVD grown p(Mg)-GaN substrate. I-V scans of the p-n junction show diodic behavior with forward conduction commencing at a bias of 3.0±0.1 V, accompanied by the room-temperature electro-luminescent (EL) output shown inFIG. 6 . The spectrum shows that the EL emission is centered at 415 nm (2.98 eV, FWHM=41 nm), matching the energy gap between the Mg dopant level of the p-GaN and the conduction band edge of the ENABLE n-GaN. - Increasing the GaN film growth temperature to 500° C. significantly increases film crystallinity.
FIG. 7 a shows the θ-2θ XRD scan of a 400 nm thick GaN film grown at 500° C. on a bare c-plane (0001) sapphire substrate without a buffer layer. The resulting GaN film was found to be exclusively c-axis oriented. The FWHM of the <002> GaN peak measures 0.28°, with the single crystal sapphire substrate <006> peak FWHM of 0.21°, representing the instrumental contribution to peak broadening. A shift of 0.037° is observed in the position of the GaN <002> peak due to the compressive strain resulting from the 13.8% lattice mismatch of the GaN film and the sapphire substrate. A pole figure XRD scan of the <101> GaN Bragg peak shown in the inset ofFIG. 7 a indicates excellent epitaxial alignment between the lattice mismatched substrate and the nitride film with a mosaic spread of 2.8° to 3.0°. For comparison, mosaic spreads for a GaN film grown on a buffer layer at 1050° C. by MOCVD are typically between 2.8° and 3.2°. - The high-resolution cross-sectional transmission electron microscopy (TEM) image shown in
FIG. 7 b for a GaN film 710 grown on a sapphire substrate 720 at 500° C. shows an atomically abrupt GaN film/sapphire interface 700. Similar results have been reported for GaN grown by plasma assisted molecular beam epitaxy (MBE) at 800° C. with extensive substrate preparation. A larger field image of the same film shows a columnar microstructure with grain sizes of about 50 nm. This microstructure likely has a detrimental effect on electron mobilities in GaN films due to carrier scattering at defect sites. The maximum mobility measured at room temperature was about 9.7 cm/V sec. Significantly higher mobilities for doped GaN films grown by the ENABLE method may be achieved when lattice mismatch is mitigated using either buffer layers or better lattice-matched substrates. - The invention also includes a thin film having at least one nanostructure disposed on a substrate formed by the methods described herein. In one embodiment, the nanostructure is formed by providing a substrate; providing a flux of at least one element to a surface of a substrate, wherein the at least one element is an element other than nitrogen or oxygen (in one embodiment, the element is selected from the group consisting of silicon, germanium, gallium, indium, aluminum, zinc, magnesium, manganese, tin, iron, and titanium); introducing at least one of nitrogen and oxygen into a plasma within a plasma source, wherein the plasma heats, dissociates, and energizes at least one of nitrogen and oxygen; extracting a collimated flux of energetic neutral atoms and molecules of at least one of nitrogen and oxygen from the plasma source; and directing the collimated flux from the plasma source onto the surface of the substrate, wherein the at least one element reacts with the energetic neutral atoms to form the nanostructure on the surface. Examples of such nanostructures are shown in
FIGS. 3 b and 3 c.FIG. 3 b is a SEM image of an aluminum nitride thin film grown onto a template (FIG. 3 a) formed by O-atom etching of a masked polyimide using ENABLE, whereasFIG. 3 c is a SEM image of AlN nanowires formed from the thin film shown inFIG. 3 b by removing the template. - While typical embodiments have been set forth for the purpose of illustration, the foregoing description should not be deemed to be a limitation on the scope of the invention. Accordingly, various modifications, adaptations, and alternatives may occur to one skilled in the art without departing from the spirit and scope of the present invention.
Claims (8)
1. A nanoscale material disposed on a substrate, the nanoscale material comprising at least one of an oxide and a nitride, wherein the nanoscale material is formed by:
a. providing the substrate;
b. providing a flux of at least one element to a surface of a substrate, wherein the at least one element is an element other than oxygen and nitrogen;
c. introducing at least one of nitrogen and oxygen into a plasma within a plasma source, wherein the plasma dissociates, heats, and energizes the at least one of nitrogen and oxygen;
d. extracting a collimated flux of energetic neutral atoms and molecules of at least one of nitrogen and oxygen from the plasma source; and
e. directing the collimated flux from the plasma source onto the surface of the substrate, wherein the at least one element reacts with the energetic neutral atoms to form the nanoscale material on the surface.
2. The nanoscale material according to claim 1 , wherein the element is selected from the group consisting of silicon, germanium, gallium, indium, aluminum, zinc, magnesium, manganese, cobalt, tin, iron, and titanium.
3. The nanoscale material according to claim 1 , wherein the nanoscale material comprises at least one of aluminum nitride, gallium nitride, indium nitride, silicon nitride, aluminum oxide, titanium oxide, zinc oxide, and silica.
4. The method according to claim 1 , wherein the substrate is one of silicon, sapphire, silicon carbide, and zinc oxide.
5. The method according to claim 3 , wherein the nanoscale material is epitaxially deposited on the substrate.
6. The method according to claim 1 , wherein the substrate is one of a polymeric substrate, highly oriented pyrolytic carbon, glassy carbon, and diamond.
7. The method according to claim 6 , wherein the polymeric substrate is templated.
8. The method according to claim 6 , wherein the polymeric substrate is one of a polyimide, polymethyl methacrylate, a polycarbonate, perfluorinated cyclobutane, and combinations thereof.
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US11/603,516 Expired - Fee Related US7759229B2 (en) | 2005-11-21 | 2006-11-21 | Charge-free method of forming nanostructures on a substrate |
US11/603,517 Expired - Fee Related US7393762B2 (en) | 2005-11-21 | 2006-11-21 | Charge-free low-temperature method of forming thin film-based nanoscale materials and structures on a substrate |
US12/154,374 Abandoned US20090068821A1 (en) | 2005-11-21 | 2008-05-22 | Charge-free low-temperature method of forming thin film-based nanoscale materials and structures on a substrate |
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US7759229B2 (en) * | 2005-11-21 | 2010-07-20 | Los Alamos National Security, Llc | Charge-free method of forming nanostructures on a substrate |
US7601430B2 (en) * | 2006-01-31 | 2009-10-13 | Los Alamos National Security, Llc | Biaxially oriented film on flexible polymeric substrate |
US20100181288A1 (en) * | 2009-01-21 | 2010-07-22 | Creatv Microtech, Inc. | Method of fabrication of micro- and nanofilters |
US8431815B2 (en) | 2009-12-22 | 2013-04-30 | Los Alamos National Security, Llc | Photovoltaic device comprising compositionally graded intrinsic photoactive layer |
US11175279B2 (en) | 2010-05-03 | 2021-11-16 | Creatv Microtech, Inc. | Polymer microfilters, devices comprising the same, methods of manufacturing the same, and uses thereof |
US10195570B2 (en) | 2011-01-07 | 2019-02-05 | Creative Micro Tech, Inc. | Fabrication of microfilters and nanofilters and their applications |
KR20120108324A (en) * | 2011-03-23 | 2012-10-05 | 한국기초과학지원연구원 | Method and apparatus for manufacturing light emit device using hyperthermal neutral beam |
JP6321455B2 (en) * | 2014-05-21 | 2018-05-09 | 東京応化工業株式会社 | Method for producing gallium nitride |
CN104498883B (en) * | 2014-11-27 | 2017-06-16 | 清华大学 | The method for depositing high c-axis orientation aluminium nitride film on flexible substrates |
US20240043989A1 (en) * | 2020-12-31 | 2024-02-08 | 3M Innovative Properties Company | Metallic Nanohole Arrays on Nanowells with Controlled Depth and Methods of Making the Same |
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US5858471A (en) * | 1994-04-08 | 1999-01-12 | Genus, Inc. | Selective plasma deposition |
US20040131718A1 (en) * | 2000-07-18 | 2004-07-08 | Princeton University | Lithographic apparatus for fluid pressure imprint lithography |
US6869671B1 (en) * | 2002-06-03 | 2005-03-22 | University Of Notre Dame | Enabling nanostructured materials via multilayer thin film precursor and applications to biosensors |
US6982519B2 (en) * | 2001-09-18 | 2006-01-03 | Ut-Battelle Llc | Individually electrically addressable vertically aligned carbon nanofibers on insulating substrates |
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US4780608A (en) | 1987-08-24 | 1988-10-25 | The United States Of America As Represented By The United States Department Of Energy | Laser sustained discharge nozzle apparatus for the production of an intense beam of high kinetic energy atomic species |
US4996187A (en) * | 1988-10-17 | 1991-02-26 | Allied-Signal Inc. | Epitaxial Ba-Y-Cu-O superconductor film |
US6320725B1 (en) * | 1989-11-27 | 2001-11-20 | Censtor Corporation | Hard disk drive having ring head with predominantly perpendicular media fields |
US5271800A (en) | 1991-07-12 | 1993-12-21 | The United States Of America As Represented By The Administrator Of National Aeronautics And Space Administration | Method for anisotropic etching in the manufacture of semiconductor devices |
US7717696B2 (en) * | 2000-07-18 | 2010-05-18 | Nanonex Corp. | Apparatus for double-sided imprint lithography |
US7649712B2 (en) * | 2004-08-31 | 2010-01-19 | Hitachi Global Storage Technologies Netherlands B.V. | Self aligned wrap around shield for perpendicular magnetic recording |
US7759229B2 (en) * | 2005-11-21 | 2010-07-20 | Los Alamos National Security, Llc | Charge-free method of forming nanostructures on a substrate |
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2006
- 2006-11-21 US US11/603,516 patent/US7759229B2/en not_active Expired - Fee Related
- 2006-11-21 US US11/603,517 patent/US7393762B2/en not_active Expired - Fee Related
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2008
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US5858471A (en) * | 1994-04-08 | 1999-01-12 | Genus, Inc. | Selective plasma deposition |
US20040131718A1 (en) * | 2000-07-18 | 2004-07-08 | Princeton University | Lithographic apparatus for fluid pressure imprint lithography |
US6982519B2 (en) * | 2001-09-18 | 2006-01-03 | Ut-Battelle Llc | Individually electrically addressable vertically aligned carbon nanofibers on insulating substrates |
US6869671B1 (en) * | 2002-06-03 | 2005-03-22 | University Of Notre Dame | Enabling nanostructured materials via multilayer thin film precursor and applications to biosensors |
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US20070114207A1 (en) | 2007-05-24 |
US20070114124A1 (en) | 2007-05-24 |
US7393762B2 (en) | 2008-07-01 |
US7759229B2 (en) | 2010-07-20 |
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