Carbon nanotubes are often used in conventional electron sources given their robust physical, chemical and electrical properties. For example, carbon nanotubes (CNTs) generally have high aspect ratios providing a low turn-on field, thereby enabling CNTs to emit electrons well. The CNTs are generally grown on a metal catalyst disposed on a non-metal substrate such as silicon dioxide.
Despite the ability to produce conventional electron sources with CNTs, the functionality of conventional electron sources is limited given the limitations of applying the metal catalyst to the non-metal substrate. For example, it is difficult to apply the metal catalyst in a precise pattern to the non-metal substrate. As such, the spacing of CNT groupings grown on respective regions of metal substrate is often non-uniform and difficult to control, thereby reducing the effectiveness of conventional electron sources. Further, the density of the CNTs in each of the groupings is difficult to control.
Additionally, the process of applying the metal catalyst to the non-metal substrate, e.g., metal catalyst deposition, is relatively expensive. As such, the cost of producing conventional electron sources is increased due to the relatively high cost of applying the metal catalyst to the non-metal substrate.
Accordingly, a need exists for a carbon nanotube (CNT) electron source with improved effectiveness. More specifically, a need exists for a CNT electron source with improved patterning of CNT groupings. A need also exists for a CNT electron source with a CNT density which can be more precisely controlled during manufacturing. Further, a need exists for a CNT electron source which can be produced more cheaply than conventional electron sources. Embodiments of the present invention provide novel solutions to these needs and others as described below.
Embodiments are directed to a CNT electron source, a method of manufacturing a CNT electron source, and a solar cell utilizing a patterned CNT sculptured substrate. More specifically, embodiments utilize a metal substrate which enables CNTs to be grown directly from the substrate. An inhibitor may be applied to the metal substrate to inhibit growth of CNTs from the metal substrate. The inhibitor may be precisely applied to the metal substrate in any pattern (e.g., using photolithography, nanoimprinting with a patterned stamp, bubble jet printing, etc.), thereby enabling the positioning of the CNT groupings to be more precisely controlled. The surface roughness of the metal substrate may be varied (e.g., by polishing or roughening the metal substrate before growing the CNTs) to control the density of the CNTs within each CNT grouping. Further, an absorber layer and an acceptor layer may be applied to the CNT electron source to form a solar cell, where a voltage potential may be generated between the acceptor layer and the metal substrate in response to sunlight exposure.
In one embodiment, a method of manufacturing an electron source includes accessing a metal substrate. An inhibitor is applied to a first plurality of regions of the metal substrate, wherein the inhibitor is operable to inhibit growth of carbon nanotubes in the first plurality of regions of the metal substrate. The carbon nanotubes are grown on the metal substrate in a second plurality of regions separate from the first plurality of regions. Applying an inhibitor may be done by applying photoresist to the metal substrate and exposing a portion of the photoresist to ultraviolet light using a photolithography process, wherein the portion of the photoresist is disposed on the second plurality of regions. Unexposed portions of the photoresist disposed on the first plurality of regions of the metal substrate may be removed. The inhibitor may be applied to the metal substrate and the portion of the photoresist. Additionally, the portion of the photoresist may be removed leaving the inhibitor disposed on the first plurality of regions of the metal substrate.
Alternatively, the inhibitor may include a polymer, and wherein applying an inhibitor may be done by applying a polymer to the metal substrate. The polymer may be patterned using a patterned stamp, wherein the patterned stamp includes features corresponding to the first plurality of regions. The polymer may be cured while the patterned stamp is in place. And in another embodiment, applying the inhibitor may be done by applying the inhibitor using a bubble jet printing process
In one embodiment, an electron source includes a metal substrate, an inhibitor disposed on a first plurality of regions of the metal substrate, and carbon nanotubes disposed on the metal substrate in a second plurality regions separate from the first plurality of regions. The metal substrate may include nickel chromium with an RMS surface roughness of less than approximately 5 nanometers. The carbon nanotubes may include a plurality of groupings of carbon nanotubes, and wherein each of the plurality of groupings of carbon nanotubes are physically separated from one another.
In yet another embodiment, a solar cell may include a metal substrate, an inhibitor disposed on a first plurality of regions of the metal substrate, and carbon nanotubes disposed on the metal substrate in a second plurality of regions separate from the first plurality of regions. An absorber layer is disposed on the inhibitor and the carbon nanotubes. Further, an acceptor layer is disposed on the absorber layer, the acceptor layer for generating a voltage potential with respect to the metal substrate in response to light exposure therewith.
The present invention is illustrated by way of example, and not by way of limitation, in the figures of the accompanying drawings and in which like reference numerals refer to similar elements.
Reference will now be made in detail to embodiments of the present invention, examples of which are illustrated in the accompanying drawings. While the present invention will be discussed in conjunction with the following embodiments, it will be understood that they are not intended to limit the present invention to these embodiments alone. On the contrary, the present invention is intended to cover alternatives, modifications, and equivalents which may be included with the spirit and scope of the present invention as defined by the appended claims. Furthermore, in the following detailed description of the present invention, numerous specific details are set forth in order to provide a thorough understanding of the present invention. However, embodiments of the present invention may be practiced without these specific details. In other instances, well-known methods, procedures, components, and circuits have not been described in detail so as not to unnecessarily obscure aspects of the present invention.
Embodiments of the present invention are generally directed to an electron source with a metal substrate which enables carbon nanotubes (CNTs) to be grown directly from the substrate. An inhibitor may be applied to the metal substrate to inhibit growth of CNTs from the metal substrate, thereby enabling the CNTs to be precisely positioned and/or patterned on the metal substrate. The inhibitor may be applied to the metal substrate using the following: photolithography (e.g., as discussed with respect to
As shown in
In one embodiment, preparation of the metal substrate (e.g., 110) may include an HDMS treatment of the metal substrate to remove impurities (e.g., water, solvents, etc.). For example, a primer (e.g., MCC primer 80/20 produced by MicroChem Corporation of Newton, Mass.) may be applied (e.g., puddled) onto the metal substrate (e.g., 110) and spun-dry (e.g., for approximately 30 seconds at approximately 4,500 rpm). The metal substrate may then be heated or baked (e.g., at approximately 110 degrees Celsius for approximately two minutes).
Step 220 involves applying photoresist (e.g., 120) to the metal substrate (e.g., 110). The photoresist may include UV-60.6 in one embodiment. Additionally, the photoresist may be applied to the metal substrate using a spin-on process in one embodiment. Further, the photoresist may be heated or baked (e.g., at approximately 130 degrees Celsius for approximately one minute).
As shown in
Mask 130 may include a transmission electron microscopy (TEM) grid. Alternatively, mask 130 may include a stencil mask, photolithography mask, or the like.
Step 240 involves heating or baking the photoresist (e.g., 110). In one embodiment, the post-exposure bake may include heating the photoresist (e.g., 110) at 140 degree Celsius for approximately 90 seconds.
As shown in
As shown in
Step 260 involves applying an inhibitor (e.g., 162 and 165) to the remaining photoresist (e.g., exposed portions 125 of photoresist 120, unexposed portions 122 of photoresist 120 where exposed portions 125 are removed in step 250, etc.) and the metal substrate (e.g., 110). The inhibitor may be used to inhibit the growth of CNTs in the regions of the metal substrate on which the inhibitor is disposed. Additionally, the inhibitor (e.g., 162 and 165) may include any material that inhibits the growth of CNTs. For example, the inhibitor (e.g., 162 and 165) may include a non-metal, a polymer, and a metal (e.g., Mo, Al, Cr, etc.). And in one embodiment, the inhibitor (e.g., 162 and 165) may include IBS molybdenum.
As shown in
Step 280 involves treating the metal substrate (e.g., 110) and the remaining metal inhibitor (e.g., 165). In one embodiment, the metal substrate (e.g., 110) and the remaining metal inhibitor (e.g., 165) may be washed with de-ionized water and cleaned with methanol.
As shown in
Accordingly, exemplary process 200 may be used to produce an electron source (e.g., 190) with a metal substrate (e.g., 110). The electron source (e.g., 190) may be produced without metal catalyst deposition in one embodiment. Additionally, the CNTs may be grown (e.g., in step 290) directly from the substrate (e.g., instead of from a metal catalyst deposited on another substrate layer). Further, it should be appreciated that the electron source (e.g., 190) produced in accordance with process 200 may be used in any application where lighting suitable to its characteristics is required such as for backlighting of a liquid crystal display (LCD) and/or other lighting applications (e.g., as a light source or light bulb). The electron source (e.g., 190) produced in accordance with process 200 may also be used in other applications, for instance, as part of a solar cell (e.g., as discussed with respect to
Although
As shown in
Step 420 involves applying inhibitor (e.g., 320) to the metal substrate (e.g., 110). The inhibitor (e.g., 320) may include a thermoset polymer in one embodiment. The thermoset polymer may be curable using heat, light, chemical reactions, drying, etc.
As shown in
Step 430 also involves curing the inhibitor while the stamp is in place (e.g., pressed against inhibitor 320 and/or metal substrate 110). The inhibitor may be cured using heat, light, a chemical reaction, drying, etc. Accordingly, the inhibitor features (e.g., 325) may be maintained or locked in place after the inhibitor is cured in step 430.
As shown in
Accordingly, exemplary process 400 may be used to produce an electron source (e.g., 390) with a metal substrate (e.g., 110). The electron source (e.g., 390) may be produced without metal catalyst deposition in one embodiment. Additionally, the CNTs may be grown (e.g., in step 440) directly from the substrate (e.g., instead of from a metal catalyst deposited on another substrate layer). Further, it should be appreciated that the electron source (e.g., 390) produced in accordance with process 400 may be used in any application where lighting suitable to its characteristics is required such as for backlighting of a liquid crystal display (LCD) and/or other lighting applications (e.g., as a light source or light bulb). The electron source (e.g., 390) produced in accordance with process 400 may also be used in other applications, for instance, as part of a solar cell (e.g., as discussed with respect to
Although
As shown in
Step 620 involves applying inhibitor (e.g., 525) to the metal substrate (e.g., 110) using bubble jet printing. The inhibitor (e.g., 525) may include a polymer in one embodiment. Additionally, the inhibitor (e.g., 525) may be applied to the metal substrate (e.g., 110) by a nozzle (e.g., 580) as shown in
As shown in
Step 640 involves growing CNTs (e.g., 170) in regions of the metal substrate without inhibitor disposed thereon (e.g., in regions 175). Step 640 may be performed analogously to step 290 of
Accordingly, exemplary process 600 may be used to produce an electron source (e.g., 590) with a metal substrate (e.g., 110). The electron source (e.g., 590) may be produced without metal catalyst deposition in one embodiment. Additionally, the CNTs may be grown (e.g., in step 640) directly from the substrate (e.g., instead of from a metal catalyst deposited on another substrate layer). Further, it should be appreciated that the electron source (e.g., 590) produced in accordance with process 600 may be used in any application where lighting suitable to its characteristics is required such as for backlighting of a liquid crystal display (LCD) and/or other lighting applications (e.g., as a light source or light bulb). The electron source (e.g., 590) produced in accordance with process 600 may also be used in other applications, for instance, as part of a solar cell (e.g., as discussed with respect to
Although
As shown in
Step 820 involves disposing an absorber layer on the patterned CNT sculptured substrate. For example, as shown in
As shown in
Accordingly, process 800 may be used to produce a solar cell (e.g., 795) using a patterned CNT sculptured substrate (e.g., 790) with a metal substrate (e.g., 110). The solar cell (e.g., 795) may be used to generate a voltage potential between the metal substrate (e.g., 110) and the acceptor layer (e.g., 730) when exposed to sunlight.
In one embodiment, the metal substrate (e.g., 110) may function as an anode while the acceptor layer (e.g., 730) may function as a cathode, where the metal substrate (e.g., 110) may release electrons to the acceptor layer (e.g., 730) when exposed to sunlight. In this manner, the patterned CNT sculptured substrate (e.g., 790) may function as an electron donor.
Alternatively, In one embodiment, the metal substrate (e.g., 110) may function as an cathode while the acceptor layer (e.g., 730) may function as a anode, where the acceptor layer (e.g., 730) may release electrons to the metal substrate (e.g., 110) when exposed to sunlight. In this manner, the patterned CNT sculptured substrate (e.g., 790) may function as an electron acceptor.
Although
In the foregoing specification, embodiments of the invention have been described with reference to numerous specific details that may vary from implementation to implementation. Thus, the sole and exclusive indicator of what is, and is intended by the applicant to be, the invention is the set of claims that issue from this application, in the specific form in which such claims issue, including any subsequent correction. Hence, no limitation, element, property, feature, advantage, or attribute that is not expressly recited in a claim should limit the scope of such claim in any way. Accordingly, the specification and drawings are to be regarded in an illustrative rather than a restrictive sense.
The present application claims the benefit of U.S. Provisional Patent Application No. 61/022,291, filed Jan. 18, 2008, entitled “SYSTEM AND METHOD FOR GROWING CARBON NANOTUBES ON METAL SUBSTRATES AND MODIFYING THE METAL SUBSTRATES TO CONTROL THE PROPERTIES OF THE CARBON NANOTUBES,” naming Cattien V. Nguyen as the inventor. That application is incorporated herein by reference in its entirety and for all purposes.
The inventions described herein were made by non-government employees, whose contributions were made in the performance of work under a NASA contract, and is subject to the provisions of Public Law 96-517 (35 U.S.C. §202). These inventions were made with Government support under contract NAS2-03144 awarded by NASA. The Government has certain rights in these inventions.
Number | Name | Date | Kind |
---|---|---|---|
6811957 | Mau et al. | Nov 2004 | B1 |
6866801 | Mau et al. | Mar 2005 | B1 |
7238594 | Fonash et al. | Jul 2007 | B2 |
20050147746 | Dublin et al. | Jul 2005 | A1 |
20060233692 | Scaringe et al. | Oct 2006 | A1 |
20070242202 | Kawase | Oct 2007 | A1 |
Number | Date | Country |
---|---|---|
2003510236 | Mar 2003 | JP |
1020050104650 | Mar 2005 | KR |
Entry |
---|
Bonard et al. “Carbon nanotube films as electron field emitters”, Carbon, vol. 40, pp. 1715-1728 Dec. 12, 2001. |
Hu et al. “Field emission of carbon nanotubes grown on nciekl substrate”, Science Direct, vol. 100, pp. 477-480, Jan. 25, 2006. |
“Direct Growth of Aligned Carbon Nanotubes on Bulk Metals”, Talapatra, et al. Department of Materials Science and Engineering, Rensselaer Polytechnic Institute, vol. 1 Nov. 2006 pp. 112-116. |
“Ultra-Low Threshold Field Electron Emission from Pillar Array of Aligned Carbon Nanotube Bundles”, Katayama, et al., Department of Electronic Engineering, Osaka University, May 28, 2004 pp. L774-L776. |
“Carbon Nanotube Films as Electron Field Emitters”, Bonard,e t al., Apr. 3, 2001, 2002 Elsvier Science Ltd. pp. 1715-1728. |
“Nanotechnology in the Development of Photovoltaic Cells”, Manna, et al., Center for Energy Systems Research Tennessee Tech University IEEE 2007 pp. 379-386. |
“Field Emission of Carbon Nanotubes Grown on Nickel Substrate”, Hu, et al., College of Materials Science and Engineering, Nanjing University of Technology, Jan. 25, 2006 pp. 477-480. |
International Search Report for PCT/US2009/000310; Filing Date: Jan. 16, 2009; Eloret Corporation et al; Submitted as a supporting document for JP 2003-510236 A, since English Abstract cannot be located. |
Number | Date | Country | |
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20090183770 A1 | Jul 2009 | US |
Number | Date | Country | |
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61022291 | Jan 2008 | US |