US20140230733A1 - Graphene defect alteration - Google Patents
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- US20140230733A1 US20140230733A1 US14/265,991 US201414265991A US2014230733A1 US 20140230733 A1 US20140230733 A1 US 20140230733A1 US 201414265991 A US201414265991 A US 201414265991A US 2014230733 A1 US2014230733 A1 US 2014230733A1
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/15—Nano-sized carbon materials
- C01B32/182—Graphene
- C01B32/184—Preparation
- C01B32/186—Preparation by chemical vapour deposition [CVD]
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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
- B82Y40/00—Manufacture or treatment of nanostructures
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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
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/15—Nano-sized carbon materials
- C01B32/182—Graphene
- C01B32/194—After-treatment
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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
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
Definitions
- PCT Patent Application No. PCT/US2011/_______ (Attorney Docket Number 1574-0041), entitled “GRAPHENE DEFECT DETECTION” naming Seth Miller as inventor, filed DATE, MONTH, YEAR, which is currently co-pending; and PCT/US2011/_______ (Attorney Docket Number 1574-0042), entitled “ALTERATION OF GRAPHENE DEFECTS”, naming Seth Miller and Thomas Yager as inventors, filed DATE, MONTH, YEAR, which is currently co-pending.
- Graphene is a material that generally may include a one atom thick layer of bonded carbon atoms. Graphene may be formed by growing carbon atoms on top of another material such as copper. The copper may be inserted into a quartz tube, heated, and annealed. A gas mixture of CH 4 and H 2 may then be flowed into the tube and the copper may then be cooled with flowing H 2 to form graphene.
- a method for at least partially altering a defect area in a layer on a substrate may include receiving the layer, where the layer may include at least some graphene and at least some defect areas in the graphene.
- the method may further include exposing the layer to a gas where exposure of the layer to the gas may at least partially alter the defect area.
- the gas may include hydrogen and at least one of Boron (B), Aluminum (Al), Gallium (Ga), Indium (In) and/or Thallium (Tl).
- a system effective to alter a defect area in a layer on a substrate may include a chamber and a container arranged in communication with the chamber.
- the chamber may be configured effective to receive a layer, where the layer may include at least some defect areas in the graphene.
- the chamber and the container may be configured effective to expose the layer to a gas where exposure of the layer to the gas may be effective to at least partially alter the defect area.
- the gas may include hydrogen and at least one of Boron (B), Aluminum (Al), Gallium (Ga), Indium (In) and/or Thallium (Tl).
- a chamber effective to at least partially alter a defect area in a layer on a substrate is generally described.
- the chamber includes a layer, where the layer may include at least some graphene.
- the chamber may further include a gas where exposure of the layer to the gas may be effective to at least partially alter the defect.
- the gas may include hydrogen and at least one of Boron (B), Aluminum (Al), Gallium (Ga), Indium (In) and/or Thallium (Tl).
- FIG. 1 illustrates an example system that can be utilized to implement graphene defect alteration
- FIG. 2 depicts a flow diagram for an example process for implementing graphene defect alteration
- FIG. 3 illustrates a computer program product that can be utilized to implement graphene defect alteration
- FIG. 4 is a block diagram illustrating an example computing device that is arranged to implement graphene defect alteration
- This disclosure is generally drawn, inter alia, to systems, methods, materials and apparatus related to graphene defect alteration.
- An example method may include receiving and heating the layer to produce a heated layer and exposing the heated layer to a first gas to produce a first exposed layer, where the first gas may include an amine.
- the method may further include exposing the first exposed layer to a first inert gas to produce a second exposed layer and exposing the second exposed layer to a second gas to produce a third exposed layer where the second gas may include an alane or a borane. Exposure of the second exposed layer to the second gas may at least partially alter the defect area.
- FIG. 1 illustrates an example system that can be utilized to implement graphene defect alteration in accordance with at least some embodiments described herein.
- An example graphene defect alteration system 100 may include one or more chambers 112 , one or more containers 118 , 126 , 128 , one or more heaters 174 and/or one or more pumps 170 . At least some of the elements of the defect alteration system 100 may be arranged in communication with a processor 184 through a communication link 186 .
- processor 184 may be adapted in communication with a memory 188 that may include instructions 180 stored therein.
- Processor 184 may be configured, such as by instructions 180 , to control at least some of the operations/actions/functions described below.
- defects or defect areas may form on a layer 102 including graphene 106 .
- Such defects may result from impurities in the graphene formation process.
- chemical oxidation defects such as epoxides, carboxylic acid functionalities, alcohols, and/or ketones may form on graphene 106 which may degrade an operation of the graphene in some applications.
- an electrical conductivity, chemical inertness or mechanical properties of the graphene may be decreased due to the presence of the defects.
- a layer 102 on a substrate 104 including graphene 106 may include defect areas 108 and/or 110 .
- layer 102 may be exposed to a group IIIA hydride material in the gas phase which may be effective to at least partially alter defects 108 and/or 110 .
- layer 102 may be placed, such as by hand or machine, in a chamber 112 .
- Layer 102 may be placed on a substrate 104 .
- Chamber 112 may include ports 114 , 116 and chamber 112 may be in communication with pump 170 such as through valve 192 , heater 174 and/or containers 118 , 126 , and/or 128 such as through valve 190 .
- Chamber 112 may be any appropriate chamber such as, for example, a chemical vapor deposition chamber or a molecular vapor deposition chamber, such as a MVD 100 E chamber.
- Container 118 along with pump 170 , may be configured (e.g., under control by a controller such as processor 184 ) effective to expose layer 102 to a gas 120 .
- Gas 120 may include an amine such as pyrrolidine, piperidine, diethylamine, etc.
- layer 102 may be exposed to gas 120 at a pressure in a range between about 1 mtorr and about 1 atmosphere, such as 0.1 atmospheres, at a temperature in a range of about 35 degrees Celsius to about 150 degrees Celsius for a time interval in a range of about 30 seconds to about 10 minutes.
- container 126 may be configured to at least partially remove gas 120 from chamber 112 .
- these elements may be controlled to vacuum out chamber 112 and then pump gas 122 into chamber 112 through port 116 to push gas 120 out of chamber 114 .
- gas 122 may include an inert gas such as helium, neon, nitrogen, argon, krypton, xenon, radon, etc.
- container 128 may be configured effective to expose layer 102 to a gas 124 where exposure of the defect areas to the gas may be effective to alter the defect areas into compounds more like graphene such as by increasing the number of carbon atoms participating in carbon-carbon double bonds, and produce altered defect areas 146 , 148 .
- Pump 170 may be configured to generate (or control) pressure in chamber 112 that may be less than one atmosphere such as, for example, in a range of about 1 mtorr to about 1 atmosphere, such as 0.1 atmospheres.
- Heater 174 may be configured (e.g., via a controller such as processor 184 ) to heat chamber 112 to a temperature in a range of about 80 degrees Celsius to about 250 degrees Celsius.
- Gas 124 may include hydrogen and a material selected from column IIIA of the Periodic Table of Chemical Elements such as Boron (B), Aluminum (Al), Gallium (Ga) Indium (In) and/or Thallium (Tl).
- gas 124 may include a borane (B—H), or an alane (A-H), such as diborane (B 2 H 6 ), diisobutylaluminium hydride (“DIBALH”), 9-Borabicyclo(3.3.1)nonane (“9-BBN”), and/or aluminum hydride (AlH 3 ).
- Exposure of a borane or alane gas to the defect areas 108 , 110 may allow for the reduction of ketones, carboxylic acids, alcohols and/or epoxide defects in the graphene 106 of layer 102 .
- Adding gas 124 into chamber 112 may increase a pressure in chamber 112 to about 0.1 atmospheres.
- container 126 and with pump 170 may be configured, such as via a controller such as processor 184 to at least partially remove gas 124 from chamber 112 .
- these elements may be controlled to vacuum out chamber 112 and then pump gas 122 into chamber 112 through port 116 to push gas 120 out of chamber 114 .
- heater 174 may be configured (e.g., via a controller such as processor 184 ) effective to heat chamber 112 to a temperature in a range of about 150 degrees Celsius to about 300 degrees Celsius at a pressure of in a range of about 1 mtorr to about 1 atmosphere, such as 0.1 atmospheres, for a time interval of about 1 minute to about 15 minutes.
- an exposure of gas 122 and/or heat from heater 174 may be effective to remove amine and/or borate on layer 102 that may be remaining from the processes described at 138 and/or 142 .
- heater 174 may be configured (e.g., via a controller such as processor 184 ) effective to heat layer 102 to a temperature in a range of about 80 degrees Celsius to about 150 degrees Celsius to reduce water in layer 102 .
- Pump 170 may be configured effective to generate a vacuum in chamber 112 , for example, a pressure in a range of 1 mtorr to about 1 atmosphere, such as 0.1 atmospheres.
- Container 118 may be effective to store an amine gas 120 , such as piperidine, at a temperature in a range of about 15 degrees Celsius to about 25 degrees Celsius.
- Container 128 may be effective to store a borane gas 124 , such as 9-BBN, at a temperature in a range of about 80 degrees Celsius to about 100 degrees Celsius at a pressure in a range of 1 mtorr to about 1 atmosphere, such as 0.1 atmospheres.
- Container 118 may be configured effective to expose piperidine gas 120 to layer 102 for a time interval of about 30 seconds to about 5 minutes.
- container 126 may be configured (e.g., via a controller such as processor 184 ) effective to at least partially remove gas 120 from chamber 112 .
- these elements may be controlled to vacuum out chamber 112 and then pump gas 122 , such as nitrogen, into chamber 112 through port 116 to push gas 120 out of chamber 114 for a time interval of about 30 seconds to about 3 minutes.
- these elements may operate at a pressure in a range between about 1 mtorr and about 1 atmosphere, such as 0.1 atmospheres, at a temperature in a range of about 35 degrees Celsius to about 150 degrees Celsius
- container 128 may be configured effective to expose borane gas 124 to layer 102 for a time interval that is in a range of about 2 minutes to about 10 minutes.
- container 126 may be configured effective to expose gas 122 to layer 102 for a time interval that is in a range of about 30 seconds to about 3 minutes.
- Heater 174 may be configured effective to heat chamber 112 to a temperature in a range of about 150 degrees Celsius to about 300 degrees Celsius.
- defect areas 108 , 110 include carboxylic acid functionalities
- these acids may be reduced to aldehydes using a DIBALH gas or to alcohols using 9-BBN or DIBALH.
- Alcohols may react with borohydrides to produce borate esters which, in turn, may form alkenes when heated.
- defect areas 108 , 110 include ketones
- a reaction of the ketone with an amine, such as pyrrolidine may form an enamine.
- Reaction of the enamine with 9-BBN may produce an amine-boron adduct. The adduct may then be removed through the application of heat to produce a desired alkene.
- a borane may be exposed to the epoxy to produce a borate ester.
- the borate ester may be cleaved to produce a double bond in response to the application of heat.
- a system arranged in accordance with the present disclosure may be used to at least partially alter defect areas in a layer on a substrate. Defect areas in the layer may be altered even after graphene has been transferred from a location from where the graphene was grown.
- Graphene may be used in applications that may be sensitive to voids or cracks such as technologies where graphene is used in lithography as may occur in displays, microelectronic circuits, electronic interconnects, and optical applications.
- a system arranged in accordance with the present disclosure may be implemented without toxic and/or flammable materials. As a gas may be used, less impurities may be exposed to a layer than if a liquid or solvent were used.
- Described gases using boranes and alanes may be used to alter a defect area in graphene and the gases may avoid reacting with a substrate such as SiO 2 .
- FIG. 2 depicts a flow diagram for an example process 200 for altering a defect area in a layer in accordance with at least some embodiments described herein.
- the process in FIG. 2 could be implemented using, for example, system 100 discussed above, where processor 184 may be adapted, via instructions, to control and facilitate the various processing operations through interfaces as will be further described with respect to FIG. 2 .
- An example process may include one or more operations, actions, or functions as illustrated by one or more of blocks S2, S4, S6, S8, S10, S12 and/or S14. Although illustrated as discrete blocks, various blocks may be divided into additional blocks, combined into fewer blocks, or eliminated, depending on the desired implementation.
- Process 200 may begin at block S2, “Receive the layer, the layer may include at least some graphene and at least some defect areas in the graphene.”
- a chamber may be configured effective to receive a layer including at least some graphene and at least some defect areas in the graphene.
- Processing may continue from block S2 to block S4, “Heat the layer to produce a heated layer.”
- the chamber may be configured, such as via heater 174 under control by a controller such as processor 184 , to heat the layer.
- the layer may be heated to a temperature in a range of about 80 degrees Celsius to about 150 degrees Celsius.
- Processing may continue from block S4 to block S6, “Expose the heated layer to a first gas to produce a first exposed layer.”
- the chamber along with valves and a container including the first gas may be configured, such as, via control by a controller such as processor 184 , to expose the heated layer to a first gas.
- the first gas may include an amine.
- the first gas may include at least one of pyrrolidine, piperidine or diethylamine.
- Processing may continue from block S6 to block S8, “Expose the first exposed layer to a first inert gas to produce a second exposed layer.”
- the chamber along with valves and a container including the inert gas may be configured, such as via control by a controller such as processor 184 , to expose the first exposed layer to a first inert gas.
- Processing may continue from block S8 to block S10, “Expose the second exposed layer to a second gas to produce a third exposed layer.”
- the chamber along with valves and a container including the second gas may be configured, such as via control by a controller such as processor 184 , to expose the second exposed layer to a second gas.
- the second gas may include a borane, an alane, diborane, 9-borabicyclo(3.3.1)nonane, diisobutylaluminium hydride, or aluminum hydride.
- Processing may continue from block S10 to block S12, “Expose the third exposed layer to a second inert gas to produce a fourth exposed layer.”
- the chamber along with valves and a container including the second inert gas may be configured, such as via control by a controller such as processor 184 , to expose the third exposed layer to a second inert gas to produce a fourth exposed layer.
- Processing may continue from block S12 to block S14, “Heat the fourth exposed layer.”
- the chamber may be configured, such as via heater 174 under control by controller such as processor 184 , to heat the fourth exposed layer.
- the chamber may be configured to heat the fourth exposed layer to a temperature in a range of about 150 degrees to Celsius to about 300 degrees Celsius.
- FIG. 3 illustrates a computer program product that can be utilized to implement graphene defect alteration in accordance with at least some embodiments described herein.
- Program product 300 may include a signal bearing medium 302 .
- Signal bearing medium 302 may include one or more instructions 304 that, when executed by, for example, a processor, may provide the functionality described above with respect to FIGS. 1-2 .
- processor 184 may undertake one or more of the blocks shown in FIG. 3 in response to instructions 304 conveyed to the system 100 by medium 302 .
- signal bearing medium 302 may encompass a computer-readable medium 306 , such as, but not limited to, a hard disk drive, a Compact Disc (CD), a Digital Video Disk (DVD), a digital tape, memory, etc.
- signal bearing medium 302 may encompass a recordable medium 308 , such as, but not limited to, memory, read/write (R/W) CDs, R/W DVDs, etc.
- signal bearing medium 302 may encompass a communications medium 310 , such as, but not limited to, a digital and/or an analog communication medium (e.g., a fiber optic cable, a waveguide, a wired communications link, a wireless communication link, etc.).
- program product 300 may be conveyed to one or more modules of the system 100 by an RF signal bearing medium 302 , where the signal bearing medium 302 is conveyed by a wireless communications medium 310 (e.g., a wireless communications medium conforming with the IEEE 802.11 standard).
- a wireless communications medium 310 e.g., a wireless communications medium conforming with the IEEE 802.11 standard.
- FIG. 4 is a block diagram illustrating an example computing device that is arranged to implement graphene defect alteration according to at least some embodiments described herein.
- computing device 400 typically includes one or more processors 404 and a system memory 406 .
- a memory bus 408 may be used for communicating between processor 404 and system memory 406 .
- processor 404 may be of any type including but not limited to a microprocessor ( ⁇ P), a microcontroller ( ⁇ C), a digital signal processor (DSP), or any combination thereof.
- Processor 404 may include one more levels of caching, such as a level one cache 410 and a level two cache 412 , a processor core 414 , and registers 416 .
- An example processor core 414 may include an arithmetic logic unit (ALU), a floating point unit (FPU), a digital signal processing core (DSP Core), or any combination thereof.
- An example memory controller 418 may also be used with processor 404 , or in some implementations memory controller 418 may be an internal part of processor 404 .
- system memory 406 may be of any type including but not limited to volatile memory (such as RAM), non-volatile memory (such as ROM, flash memory, etc.) or any combination thereof.
- System memory 406 may include an operating system 420 , one or more applications 422 , and program data 424 .
- Application 422 may include a graphene defect alteration algorithm 426 that is arranged to perform the various functions/actions/operations as described herein including at least those described with respect to system 100 of FIGS. 1-3 .
- Program data 424 may include graphene defect alteration data 428 that may be useful for implementing graphene defect alteration as is described herein.
- application 422 may be arranged to operate with program data 424 on operating system 420 such that graphene defect alteration may be provided.
- This described basic configuration 402 is illustrated in FIG. 4 by those components within the inner dashed line.
- Computing device 400 may have additional features or functionality, and additional interfaces to facilitate communications between basic configuration 402 and any required devices and interfaces.
- a bus/interface controller 430 may be used to facilitate communications between basic configuration 402 and one or more data storage devices 432 via a storage interface bus 434 .
- Data storage devices 432 may be removable storage devices 436 , non-removable storage devices 438 , or a combination thereof. Examples of removable storage and non-removable storage devices include magnetic disk devices such as flexible disk drives and hard-disk drives (HDD), optical disk drives such as compact disk (CD) drives or digital versatile disk (DVD) drives, solid state drives (SSD), and tape drives to name a few.
- Example computer storage media may include volatile and nonvolatile, removable and non-removable media implemented in any method or technology for storage of information, such as computer readable instructions, data structures, program modules, or other data.
- Computer storage media includes, but is not limited to, RAM, ROM, EEPROM, flash memory or other memory technology, CD-ROM, digital versatile disks (DVD) or other optical storage, magnetic cassettes, magnetic tape, magnetic disk storage or other magnetic storage devices, or any other medium which may be used to store the desired information and which may be accessed by computing device 400 . Any such computer storage media may be part of computing device 400 .
- Computing device 400 may also include an interface bus 440 for facilitating communication from various interface devices (e.g., output devices 442 , peripheral interfaces 444 , and communication devices 446 ) to basic configuration 402 via bus/interface controller 430 .
- Example output devices 442 include a graphics processing unit 448 and an audio processing unit 450 , which may be configured to communicate to various external devices such as a display or speakers via one or more A/V ports 452 .
- Example peripheral interfaces 444 include a serial interface controller 454 or a parallel interface controller 456 , which may be configured to communicate with external devices such as input devices (e.g., keyboard, mouse, pen, voice input device, touch input device, etc.) or other peripheral devices (e.g., printer, scanner, etc.) via one or more I/O ports 458 .
- An example communication device 446 includes a network controller 460 , which may be arranged to facilitate communications with one or more other computing devices 462 over a network communication link via one or more communication ports 464 .
- the network communication link may be one example of a communication media.
- Communication media may typically be embodied by computer readable instructions, data structures, program modules, or other data in a modulated data signal, such as a carrier wave or other transport mechanism, and may include any information delivery media.
- a “modulated data signal” may be a signal that has one or more of its characteristics set or changed in such a manner as to encode information in the signal.
- communication media may include wired media such as a wired network or direct-wired connection, and wireless media such as acoustic, radio frequency (RF), microwave, infrared (IR) and other wireless media.
- RF radio frequency
- IR infrared
- the term computer readable media as used herein may include both storage media and communication media.
- Computing device 400 may be implemented as a portion of a small-form factor portable (or mobile) electronic device such as a cell phone, a personal data assistant (PDA), a personal media player device, a wireless web-watch device, a personal headset device, an application specific device, or a hybrid device that include any of the above functions.
- a small-form factor portable (or mobile) electronic device such as a cell phone, a personal data assistant (PDA), a personal media player device, a wireless web-watch device, a personal headset device, an application specific device, or a hybrid device that include any of the above functions.
- PDA personal data assistant
- Computing device 400 may also be implemented as a personal computer including both laptop computer and non-laptop computer configurations.
- a range includes each individual member.
- a group having 1-3 cells refers to groups having 1, 2, or 3 cells.
- a group having 1-5 cells refers to groups having 1, 2, 3, 4, or 5 cells, and so forth.
Abstract
Technologies are generally described for a method and system configured effective to alter a defect area in a layer on a substrate including graphene. An example method may include receiving and heating the layer to produce a heated layer and exposing the heated layer to a first gas to produce a first exposed layer, where the first gas may include an amine. The method may further include exposing the first exposed layer to a first inert gas to produce a second exposed layer and exposing the second exposed layer to a second gas to produce a third exposed layer where the second gas may include an alane or a borane. Exposure of the second exposed layer to the second gas may at least partially alter the defect area.
Description
- The present application is related to the following listed application(s): PCT Patent Application No. PCT/US2011/______ (Attorney Docket Number 1574-0041), entitled “GRAPHENE DEFECT DETECTION” naming Seth Miller as inventor, filed DATE, MONTH, YEAR, which is currently co-pending; and PCT/US2011/______ (Attorney Docket Number 1574-0042), entitled “ALTERATION OF GRAPHENE DEFECTS”, naming Seth Miller and Thomas Yager as inventors, filed DATE, MONTH, YEAR, which is currently co-pending.
- Unless otherwise indicated herein, the materials described in this section are not prior art to the claims in this application and are not admitted to be prior art by inclusion in this section.
- Graphene is a material that generally may include a one atom thick layer of bonded carbon atoms. Graphene may be formed by growing carbon atoms on top of another material such as copper. The copper may be inserted into a quartz tube, heated, and annealed. A gas mixture of CH4 and H2 may then be flowed into the tube and the copper may then be cooled with flowing H2 to form graphene.
- In some examples, a method for at least partially altering a defect area in a layer on a substrate is generally described. In some examples, the method may include receiving the layer, where the layer may include at least some graphene and at least some defect areas in the graphene. The method may further include exposing the layer to a gas where exposure of the layer to the gas may at least partially alter the defect area. The gas may include hydrogen and at least one of Boron (B), Aluminum (Al), Gallium (Ga), Indium (In) and/or Thallium (Tl).
- In some examples, a system effective to alter a defect area in a layer on a substrate is generally described. In some examples, the system may include a chamber and a container arranged in communication with the chamber. The chamber may be configured effective to receive a layer, where the layer may include at least some defect areas in the graphene. The chamber and the container may be configured effective to expose the layer to a gas where exposure of the layer to the gas may be effective to at least partially alter the defect area. The gas may include hydrogen and at least one of Boron (B), Aluminum (Al), Gallium (Ga), Indium (In) and/or Thallium (Tl).
- In some examples, a chamber effective to at least partially alter a defect area in a layer on a substrate is generally described. In some examples, the chamber includes a layer, where the layer may include at least some graphene. The chamber may further include a gas where exposure of the layer to the gas may be effective to at least partially alter the defect. The gas may include hydrogen and at least one of Boron (B), Aluminum (Al), Gallium (Ga), Indium (In) and/or Thallium (Tl).
- The foregoing summary is illustrative only and is not intended to be in any way limiting. In addition to the illustrative aspects, embodiments, and features described above, further aspects, embodiments, and features will become apparent by reference to the drawings and the following detailed description.
- The foregoing and other features of this disclosure will become more fully apparent from the following description and appended claims, taken in conjunction with the accompanying drawings. Understanding that these drawings depict only several embodiments in accordance with the disclosure and are, therefore, not to be considered limiting of its scope, the disclosure will be described with additional specificity and detail through use of the accompanying drawings, in which:
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FIG. 1 illustrates an example system that can be utilized to implement graphene defect alteration; -
FIG. 2 depicts a flow diagram for an example process for implementing graphene defect alteration; -
FIG. 3 illustrates a computer program product that can be utilized to implement graphene defect alteration; and -
FIG. 4 is a block diagram illustrating an example computing device that is arranged to implement graphene defect alteration; - all arranged according to at least some embodiments described herein.
- In the following detailed description, reference is made to the accompanying drawings, which form a part hereof. In the drawings, similar symbols typically identify similar components, unless context dictates otherwise. The illustrative embodiments described in the detailed description, drawings, and claims are not meant to be limiting. Other embodiments may be utilized, and other changes may be made, without departing from the spirit or scope of the subject matter presented herein. It will be readily understood that the aspects of the present disclosure, as generally described herein, and illustrated in the Figures, can be arranged, substituted, combined, separated, and designed in a wide variety of different configurations, all of which are explicitly contemplated herein.
- This disclosure is generally drawn, inter alia, to systems, methods, materials and apparatus related to graphene defect alteration.
- Briefly stated, technologies are generally described for a method and system configured effective to alter a defect area in a layer on a substrate including graphene. An example method may include receiving and heating the layer to produce a heated layer and exposing the heated layer to a first gas to produce a first exposed layer, where the first gas may include an amine. The method may further include exposing the first exposed layer to a first inert gas to produce a second exposed layer and exposing the second exposed layer to a second gas to produce a third exposed layer where the second gas may include an alane or a borane. Exposure of the second exposed layer to the second gas may at least partially alter the defect area.
- It will also be understood that any compound, material or substance which is expressly or implicitly disclosed in the specification and/or recited in a claim as belonging to a group or structurally, compositionally and/or functionally related compounds, materials or substances, includes individual representatives of the group and all combinations thereof.
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FIG. 1 illustrates an example system that can be utilized to implement graphene defect alteration in accordance with at least some embodiments described herein. An example graphenedefect alteration system 100 may include one ormore chambers 112, one ormore containers more heaters 174 and/or one ormore pumps 170. At least some of the elements of thedefect alteration system 100 may be arranged in communication with aprocessor 184 through acommunication link 186. In some examples,processor 184 may be adapted in communication with amemory 188 that may includeinstructions 180 stored therein.Processor 184 may be configured, such as byinstructions 180, to control at least some of the operations/actions/functions described below. - During a graphene formation process, defects or defect areas may form on a
layer 102 includinggraphene 106. Such defects may result from impurities in the graphene formation process. For example, chemical oxidation defects such as epoxides, carboxylic acid functionalities, alcohols, and/or ketones may form ongraphene 106 which may degrade an operation of the graphene in some applications. For example, an electrical conductivity, chemical inertness or mechanical properties of the graphene may be decreased due to the presence of the defects. In an example, as shown at 136, alayer 102 on asubstrate 104 includinggraphene 106 may includedefect areas 108 and/or 110. As discussed in more detail below,layer 102 may be exposed to a group IIIA hydride material in the gas phase which may be effective to at least partially alterdefects 108 and/or 110. - As shown at 138,
layer 102 may be placed, such as by hand or machine, in achamber 112.Layer 102 may be placed on asubstrate 104.Chamber 112 may includeports chamber 112 may be in communication withpump 170 such as throughvalve 192,heater 174 and/orcontainers valve 190.Chamber 112 may be any appropriate chamber such as, for example, a chemical vapor deposition chamber or a molecular vapor deposition chamber, such as a MVD 100E chamber.Container 118, along withpump 170, may be configured (e.g., under control by a controller such as processor 184) effective to exposelayer 102 to agas 120.Gas 120 may include an amine such as pyrrolidine, piperidine, diethylamine, etc. In an example,layer 102 may be exposed togas 120 at a pressure in a range between about 1 mtorr and about 1 atmosphere, such as 0.1 atmospheres, at a temperature in a range of about 35 degrees Celsius to about 150 degrees Celsius for a time interval in a range of about 30 seconds to about 10 minutes. As shown at 140, after exposure oflayer 102 withgas 120,container 126, along withpump 170, may be configured to at least partially removegas 120 fromchamber 112. For example, these elements may be controlled to vacuum outchamber 112 and then pumpgas 122 intochamber 112 throughport 116 to pushgas 120 out ofchamber 114. For example,gas 122 may include an inert gas such as helium, neon, nitrogen, argon, krypton, xenon, radon, etc. - As shown at 142,
container 128, along withpump 170, may be configured effective to exposelayer 102 to agas 124 where exposure of the defect areas to the gas may be effective to alter the defect areas into compounds more like graphene such as by increasing the number of carbon atoms participating in carbon-carbon double bonds, and produce altereddefect areas chamber 112 that may be less than one atmosphere such as, for example, in a range of about 1 mtorr to about 1 atmosphere, such as 0.1 atmospheres.Heater 174 may be configured (e.g., via a controller such as processor 184) toheat chamber 112 to a temperature in a range of about 80 degrees Celsius to about 250 degrees Celsius.Gas 124 may include hydrogen and a material selected from column IIIA of the Periodic Table of Chemical Elements such as Boron (B), Aluminum (Al), Gallium (Ga) Indium (In) and/or Thallium (Tl). For example,gas 124 may include a borane (B—H), or an alane (A-H), such as diborane (B2H6), diisobutylaluminium hydride (“DIBALH”), 9-Borabicyclo(3.3.1)nonane (“9-BBN”), and/or aluminum hydride (AlH3). Exposure of a borane or alane gas to thedefect areas graphene 106 oflayer 102. Addinggas 124 intochamber 112 may increase a pressure inchamber 112 to about 0.1 atmospheres. - As shown at 144, after exposure of
gas 124,container 126 and withpump 170 may be configured, such as via a controller such asprocessor 184 to at least partially removegas 124 fromchamber 112. For example, these elements may be controlled to vacuum outchamber 112 and then pumpgas 122 intochamber 112 throughport 116 to pushgas 120 out ofchamber 114. During the exposure ofgas 122 at 144,heater 174 may be configured (e.g., via a controller such as processor 184) effective to heatchamber 112 to a temperature in a range of about 150 degrees Celsius to about 300 degrees Celsius at a pressure of in a range of about 1 mtorr to about 1 atmosphere, such as 0.1 atmospheres, for a time interval of about 1 minute to about 15 minutes. In an example, an exposure ofgas 122 and/or heat fromheater 174 may be effective to remove amine and/or borate onlayer 102 that may be remaining from the processes described at 138 and/or 142. - In an example, focusing again at 138,
heater 174 may be configured (e.g., via a controller such as processor 184) effective toheat layer 102 to a temperature in a range of about 80 degrees Celsius to about 150 degrees Celsius to reduce water inlayer 102. Pump 170 may be configured effective to generate a vacuum inchamber 112, for example, a pressure in a range of 1 mtorr to about 1 atmosphere, such as 0.1 atmospheres.Container 118 may be effective to store anamine gas 120, such as piperidine, at a temperature in a range of about 15 degrees Celsius to about 25 degrees Celsius.Container 128 may be effective to store aborane gas 124, such as 9-BBN, at a temperature in a range of about 80 degrees Celsius to about 100 degrees Celsius at a pressure in a range of 1 mtorr to about 1 atmosphere, such as 0.1 atmospheres.Container 118 may be configured effective to exposepiperidine gas 120 to layer 102 for a time interval of about 30 seconds to about 5 minutes. - At 140,
container 126 may be configured (e.g., via a controller such as processor 184) effective to at least partially removegas 120 fromchamber 112. For example, these elements may be controlled to vacuum outchamber 112 and then pumpgas 122, such as nitrogen, intochamber 112 throughport 116 to pushgas 120 out ofchamber 114 for a time interval of about 30 seconds to about 3 minutes. In an example, these elements may operate at a pressure in a range between about 1 mtorr and about 1 atmosphere, such as 0.1 atmospheres, at a temperature in a range of about 35 degrees Celsius to about 150 degrees Celsius At 142,container 128 may be configured effective to exposeborane gas 124 to layer 102 for a time interval that is in a range of about 2 minutes to about 10 minutes. At 144,container 126 may be configured effective to exposegas 122 to layer 102 for a time interval that is in a range of about 30 seconds to about 3 minutes.Heater 174 may be configured effective to heatchamber 112 to a temperature in a range of about 150 degrees Celsius to about 300 degrees Celsius. - In an example where
defect areas defect areas defect areas - Among other potential benefits, a system arranged in accordance with the present disclosure may be used to at least partially alter defect areas in a layer on a substrate. Defect areas in the layer may be altered even after graphene has been transferred from a location from where the graphene was grown. Graphene may be used in applications that may be sensitive to voids or cracks such as technologies where graphene is used in lithography as may occur in displays, microelectronic circuits, electronic interconnects, and optical applications. A system arranged in accordance with the present disclosure may be implemented without toxic and/or flammable materials. As a gas may be used, less impurities may be exposed to a layer than if a liquid or solvent were used. As the processes described herein can take place at relatively low temperatures below 300 degrees Celsius, there is less chance of damaging a graphene layer by generating a carbon vacancy. Described gases using boranes and alanes may be used to alter a defect area in graphene and the gases may avoid reacting with a substrate such as SiO2.
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FIG. 2 depicts a flow diagram for anexample process 200 for altering a defect area in a layer in accordance with at least some embodiments described herein. The process inFIG. 2 could be implemented using, for example,system 100 discussed above, whereprocessor 184 may be adapted, via instructions, to control and facilitate the various processing operations through interfaces as will be further described with respect toFIG. 2 . An example process may include one or more operations, actions, or functions as illustrated by one or more of blocks S2, S4, S6, S8, S10, S12 and/or S14. Although illustrated as discrete blocks, various blocks may be divided into additional blocks, combined into fewer blocks, or eliminated, depending on the desired implementation. -
Process 200 may begin at block S2, “Receive the layer, the layer may include at least some graphene and at least some defect areas in the graphene.” At block S2, a chamber may be configured effective to receive a layer including at least some graphene and at least some defect areas in the graphene. - Processing may continue from block S2 to block S4, “Heat the layer to produce a heated layer.” At block S4, the chamber may be configured, such as via
heater 174 under control by a controller such asprocessor 184, to heat the layer. For example, the layer may be heated to a temperature in a range of about 80 degrees Celsius to about 150 degrees Celsius. - Processing may continue from block S4 to block S6, “Expose the heated layer to a first gas to produce a first exposed layer.” At block S6, the chamber along with valves and a container including the first gas, may be configured, such as, via control by a controller such as
processor 184, to expose the heated layer to a first gas. In an example, the first gas may include an amine. In an example the first gas may include at least one of pyrrolidine, piperidine or diethylamine. - Processing may continue from block S6 to block S8, “Expose the first exposed layer to a first inert gas to produce a second exposed layer.” At block S8, the chamber along with valves and a container including the inert gas, may be configured, such as via control by a controller such as
processor 184, to expose the first exposed layer to a first inert gas. - Processing may continue from block S8 to block S10, “Expose the second exposed layer to a second gas to produce a third exposed layer.” At block S10, the chamber along with valves and a container including the second gas, may be configured, such as via control by a controller such as
processor 184, to expose the second exposed layer to a second gas. For example the second gas may include a borane, an alane, diborane, 9-borabicyclo(3.3.1)nonane, diisobutylaluminium hydride, or aluminum hydride. - Processing may continue from block S10 to block S12, “Expose the third exposed layer to a second inert gas to produce a fourth exposed layer.” At block S12, the chamber along with valves and a container including the second inert gas may be configured, such as via control by a controller such as
processor 184, to expose the third exposed layer to a second inert gas to produce a fourth exposed layer. - Processing may continue from block S12 to block S14, “Heat the fourth exposed layer.” At block S14, the chamber may be configured, such as via
heater 174 under control by controller such asprocessor 184, to heat the fourth exposed layer. In an example, the chamber may be configured to heat the fourth exposed layer to a temperature in a range of about 150 degrees to Celsius to about 300 degrees Celsius. -
FIG. 3 illustrates a computer program product that can be utilized to implement graphene defect alteration in accordance with at least some embodiments described herein.Program product 300 may include a signal bearing medium 302. Signal bearing medium 302 may include one ormore instructions 304 that, when executed by, for example, a processor, may provide the functionality described above with respect toFIGS. 1-2 . Thus, for example, referring tosystem 100,processor 184 may undertake one or more of the blocks shown inFIG. 3 in response toinstructions 304 conveyed to thesystem 100 by medium 302. - In some implementations, signal bearing medium 302 may encompass a computer-
readable medium 306, such as, but not limited to, a hard disk drive, a Compact Disc (CD), a Digital Video Disk (DVD), a digital tape, memory, etc. In some implementations, signal bearing medium 302 may encompass arecordable medium 308, such as, but not limited to, memory, read/write (R/W) CDs, R/W DVDs, etc. In some implementations, signal bearing medium 302 may encompass acommunications medium 310, such as, but not limited to, a digital and/or an analog communication medium (e.g., a fiber optic cable, a waveguide, a wired communications link, a wireless communication link, etc.). Thus, for example,program product 300 may be conveyed to one or more modules of thesystem 100 by an RF signal bearing medium 302, where the signal bearing medium 302 is conveyed by a wireless communications medium 310 (e.g., a wireless communications medium conforming with the IEEE 802.11 standard). -
FIG. 4 is a block diagram illustrating an example computing device that is arranged to implement graphene defect alteration according to at least some embodiments described herein. In a very basic configuration 402,computing device 400 typically includes one ormore processors 404 and asystem memory 406. A memory bus 408 may be used for communicating betweenprocessor 404 andsystem memory 406. - Depending on the desired configuration,
processor 404 may be of any type including but not limited to a microprocessor (μP), a microcontroller (μC), a digital signal processor (DSP), or any combination thereof.Processor 404 may include one more levels of caching, such as a level onecache 410 and a level twocache 412, aprocessor core 414, and registers 416. Anexample processor core 414 may include an arithmetic logic unit (ALU), a floating point unit (FPU), a digital signal processing core (DSP Core), or any combination thereof. Anexample memory controller 418 may also be used withprocessor 404, or in someimplementations memory controller 418 may be an internal part ofprocessor 404. - Depending on the desired configuration,
system memory 406 may be of any type including but not limited to volatile memory (such as RAM), non-volatile memory (such as ROM, flash memory, etc.) or any combination thereof.System memory 406 may include anoperating system 420, one ormore applications 422, andprogram data 424.Application 422 may include a graphene defect alteration algorithm 426 that is arranged to perform the various functions/actions/operations as described herein including at least those described with respect tosystem 100 ofFIGS. 1-3 .Program data 424 may include graphenedefect alteration data 428 that may be useful for implementing graphene defect alteration as is described herein. In some embodiments,application 422 may be arranged to operate withprogram data 424 onoperating system 420 such that graphene defect alteration may be provided. This described basic configuration 402 is illustrated inFIG. 4 by those components within the inner dashed line. -
Computing device 400 may have additional features or functionality, and additional interfaces to facilitate communications between basic configuration 402 and any required devices and interfaces. For example, a bus/interface controller 430 may be used to facilitate communications between basic configuration 402 and one or moredata storage devices 432 via a storage interface bus 434.Data storage devices 432 may beremovable storage devices 436,non-removable storage devices 438, or a combination thereof. Examples of removable storage and non-removable storage devices include magnetic disk devices such as flexible disk drives and hard-disk drives (HDD), optical disk drives such as compact disk (CD) drives or digital versatile disk (DVD) drives, solid state drives (SSD), and tape drives to name a few. Example computer storage media may include volatile and nonvolatile, removable and non-removable media implemented in any method or technology for storage of information, such as computer readable instructions, data structures, program modules, or other data. -
System memory 406,removable storage devices 436 andnon-removable storage devices 438 are examples of computer storage media. Computer storage media includes, but is not limited to, RAM, ROM, EEPROM, flash memory or other memory technology, CD-ROM, digital versatile disks (DVD) or other optical storage, magnetic cassettes, magnetic tape, magnetic disk storage or other magnetic storage devices, or any other medium which may be used to store the desired information and which may be accessed by computingdevice 400. Any such computer storage media may be part ofcomputing device 400. -
Computing device 400 may also include an interface bus 440 for facilitating communication from various interface devices (e.g.,output devices 442,peripheral interfaces 444, and communication devices 446) to basic configuration 402 via bus/interface controller 430.Example output devices 442 include agraphics processing unit 448 and anaudio processing unit 450, which may be configured to communicate to various external devices such as a display or speakers via one or more A/V ports 452. Exampleperipheral interfaces 444 include aserial interface controller 454 or aparallel interface controller 456, which may be configured to communicate with external devices such as input devices (e.g., keyboard, mouse, pen, voice input device, touch input device, etc.) or other peripheral devices (e.g., printer, scanner, etc.) via one or more I/O ports 458. An example communication device 446 includes anetwork controller 460, which may be arranged to facilitate communications with one or moreother computing devices 462 over a network communication link via one ormore communication ports 464. - The network communication link may be one example of a communication media. Communication media may typically be embodied by computer readable instructions, data structures, program modules, or other data in a modulated data signal, such as a carrier wave or other transport mechanism, and may include any information delivery media. A “modulated data signal” may be a signal that has one or more of its characteristics set or changed in such a manner as to encode information in the signal. By way of example, and not limitation, communication media may include wired media such as a wired network or direct-wired connection, and wireless media such as acoustic, radio frequency (RF), microwave, infrared (IR) and other wireless media. The term computer readable media as used herein may include both storage media and communication media.
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Computing device 400 may be implemented as a portion of a small-form factor portable (or mobile) electronic device such as a cell phone, a personal data assistant (PDA), a personal media player device, a wireless web-watch device, a personal headset device, an application specific device, or a hybrid device that include any of the above functions.Computing device 400 may also be implemented as a personal computer including both laptop computer and non-laptop computer configurations. - The present disclosure is not to be limited in terms of the particular embodiments described in this application, which are intended as illustrations of various aspects. Many modifications and variations can be made without departing from its spirit and scope, as will be apparent to those skilled in the art. Functionally equivalent methods and apparatuses within the scope of the disclosure, in addition to those enumerated herein, will be apparent to those skilled in the art from the foregoing descriptions. Such modifications and variations are intended to fall within the scope of the appended claims. The present disclosure is to be limited only by the terms of the appended claims, along with the full scope of equivalents to which such claims are entitled. It is to be understood that this disclosure is not limited to particular methods, reagents, compounds compositions or biological systems, which can, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting.
- With respect to the use of substantially any plural and/or singular terms herein, those having skill in the art can translate from the plural to the singular and/or from the singular to the plural as is appropriate to the context and/or application. The various singular/plural permutations may be expressly set forth herein for sake of clarity.
- It will be understood by those within the art that, in general, terms used herein, and especially in the appended claims (e.g., bodies of the appended claims) are generally intended as “open” terms (e.g., the term “including” should be interpreted as “including but not limited to,” the term “having” should be interpreted as “having at least,” the term “includes” should be interpreted as “includes but is not limited to,” etc.). It will be further understood by those within the art that if a specific number of an introduced claim recitation is intended, such an intent will be explicitly recited in the claim, and in the absence of such recitation no such intent is present. For example, as an aid to understanding, the following appended claims may contain usage of the introductory phrases “at least one” and “one or more” to introduce claim recitations. However, the use of such phrases should not be construed to imply that the introduction of a claim recitation by the indefinite articles “a” or “an” limits any particular claim containing such introduced claim recitation to embodiments containing only one such recitation, even when the same claim includes the introductory phrases “one or more” or “at least one” and indefinite articles such as “a” or “an” (e.g., “a” and/or “an” should be interpreted to mean “at least one” or “one or more”); the same holds true for the use of definite articles used to introduce claim recitations. In addition, even if a specific number of an introduced claim recitation is explicitly recited, those skilled in the art will recognize that such recitation should be interpreted to mean at least the recited number (e.g., the bare recitation of “two recitations,” without other modifiers, means at least two recitations, or two or more recitations). Furthermore, in those instances where a convention analogous to “at least one of A, B, and C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, and C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). In those instances where a convention analogous to “at least one of A, B, or C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, or C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). It will be further understood by those within the art that virtually any disjunctive word and/or phrase presenting two or more alternative terms, whether in the description, claims, or drawings, should be understood to contemplate the possibilities of including one of the terms, either of the terms, or both terms. For example, the phrase “A or B” will be understood to include the possibilities of “A” or “B” or “A and B.”
- In addition, where features or aspects of the disclosure are described in terms of Markush groups, those skilled in the art will recognize that the disclosure is also thereby described in terms of any individual member or subgroup of members of the Markush group.
- As will be understood by one skilled in the art, for any and all purposes, such as in terms of providing a written description, all ranges disclosed herein also encompass any and all possible subranges and combinations of subranges thereof. Any listed range can be easily recognized as sufficiently describing and enabling the same range being broken down into at least equal halves, thirds, quarters, fifths, tenths, etc. As a non-limiting example, each range discussed herein can be readily broken down into a lower third, middle third and upper third, etc. As will also be understood by one skilled in the art all language such as “up to,” “at least,” “greater than,” “less than,” and the like include the number recited and refer to ranges which can be subsequently broken down into subranges as discussed above. Finally, as will be understood by one skilled in the art, a range includes each individual member. Thus, for example, a group having 1-3 cells refers to groups having 1, 2, or 3 cells. Similarly, a group having 1-5 cells refers to groups having 1, 2, 3, 4, or 5 cells, and so forth.
- While various aspects and embodiments have been disclosed herein, other aspects and embodiments will be apparent to those skilled in the art. The various aspects and embodiments disclosed herein are for purposes of illustration and are not intended to be limiting, with the true scope and spirit being indicated by the following claims.
Claims (24)
1. A system for at least partially altering one or more defects in a layer on a substrate, wherein the layer comprises graphene, the system comprising:
a chamber configured to receive the layer, wherein the layer comprises one or more defects in the graphene; and
a container configured to be in communication with the chamber;
wherein the chamber and the container are configured to expose the layer to a gas, wherein the gas comprises hydrogen and at least one of Boron (B), Aluminum (Al), Gallium (Ga), Indium (In) and Thallium (Tl); and
wherein exposure of the layer to the gas at least partially alter the one or more defects in the graphene.
2. The system of claim 1 , wherein the chamber and the container are configured to expose the layer to the gas, wherein the gas comprises one or more of a borane and an alane.
3. The system of claim 1 , wherein:
the gas is a first gas; and
wherein the chamber and the container are configured to
expose the layer to a second gas to produce an exposed layer, wherein the second gas comprises an amine; and
expose the exposed layer to the first gas.
4. The system of claim 1 , wherein:
the gas is a first gas; and
wherein the chamber and the container are configured to
expose the layer to a second gas to produce an exposed layer, wherein the second gas comprises an amine; and
expose the exposed layer to the first gas, wherein the first gas comprises one or more of a borane and an alane.
5. The system of claim 1 , wherein:
the gas is a first gas; and
wherein the chamber and the container are configured to
expose the layer to a second gas to produce an exposed layer, wherein the second gas comprises one or more of pyrrolidine, piperidine and diethylamine; and
expose the exposed layer to the first gas, wherein the first gas comprises one or more of a borane and an alane.
6. The system of claim 1 , wherein the chamber and the container are configured to expose the layer to the gas, wherein the gas comprises at least one of diborane, 9-borabicyclo(3.3.1)nonane, diisobutylaluminium hydride, and aluminum hydride.
7. The system of in claim 1 , wherein the chamber and the container are configured to
expose the layer to piperidine to produce an exposed layer; and
expose the exposed layer to 9-borabicyclo(3.3.1)nonane.
8. The system of claim 1 , wherein the chamber and the container are configured to
expose the layer to a second gas to produce a first exposed layer, wherein the second gas comprises an amine;
expose the first exposed layer to a first inert gas to produce a second exposed layer;
expose the second exposed layer to the first gas to produce a third exposed layer; and
expose the third exposed layer to a second inert gas to produce a fourth exposed layer.
9. The system of claim 1 , further comprising:
a heater in communication with the chamber, wherein the heater is configured to heat the layer to a temperature of about 150 degrees Celsius to about 300 degrees Celsius.
10. The system of claim 1 , wherein the gas is a first gas and the system further comprises:
a heater in communication with the chamber, wherein the heater is configured to heat the layer to a temperature of about 80 degrees Celsius to about 150 degrees Celsius to produce a heated layer; and
the chamber and the container are configured to
expose the heated layer to a second gas to produce a first exposed layer, wherein the second gas comprises an amine;
expose the first exposed layer to a first inert gas to produce a second exposed layer;
expose the second exposed layer to the first gas to produce a third exposed layer;
expose the third exposed layer to a second inert gas to produce a fourth exposed layer; and
the heater is configured to heat the fourth exposed layer to a temperature of about 150 degrees Celsius to about 300 degrees Celsius.
11. The system of claim 1 , wherein the gas is a first gas and the system further comprises:
a heater in communication with the chamber, wherein the heater is configured to heat the layer to a temperature of about 80 degrees Celsius to about 150 degrees Celsius to produce a heated layer;
the chamber and the container are configured to
expose the heated layer to a second gas to produce a first exposed layer, wherein the second gas comprises an amine;
expose the first exposed layer to a first inert gas to produce a second exposed layer;
expose the second exposed layer to the first gas to produce a third exposed layer, wherein the first gas comprises one or more of an alane and a borane;
expose the third exposed layer to a second inert gas to produce a fourth exposed layer; and
the heater is configured to heat the fourth exposed layer to a temperature of about 150 degrees Celsius to about 300 degrees Celsius.
12. The system of claim 1 , wherein the gas is a first gas and the system further comprises:
a heater in communication with the chamber, wherein the heater is configured to heat the layer to a temperature of about 80 degrees Celsius to about 150 degrees Celsius to produce a heated layer;
wherein the chamber and the container are configured to
expose the heated layer to a second gas to produce a first exposed layer, wherein the second gas comprises an amine;
expose the first exposed layer to a first inert gas to produce a second exposed layer;
expose the second exposed layer to the first gas to produce a third exposed layer, wherein the first gas comprises at least one of diborane, 9-borabicyclo(3.3.1)nonane, diisobutylaluminium hydride, and aluminum hydride;
expose the third exposed layer to a second inert gas to produce a fourth exposed layer; and
the heater is configured to heat the fourth exposed layer to a temperature of about 150 degrees Celsius to about 300 degrees Celsius.
13. A chamber for at least partially altering one or more defects in a layer on a substrate, wherein the layer comprises graphene, the chamber comprising:
an inlet port configured to receive a gas into the chamber, wherein the gas comprises hydrogen and at least one of Boron (B), Aluminum (Al), Gallium (Ga), Indium (In) and Thallium (Tl),
wherein the chamber is configured to receive the layer, the layer comprising one or more defects in the graphene, and to expose the layer to the gas to at least partially alter the one or more defects in the graphene.
14. The chamber of claim 13 , further comprising the substrate and the layer on the substrate.
15. The chamber of claim 13 , further comprising the gas.
16. The chamber of claim 13 , further configured to be in communication with a container, wherein the chamber and the container are configured to expose the layer to the gas.
17. The chamber of claim 13 , further configured to be in communication with a heater, wherein the heater is configured to heat the layer to a temperature of about 150 degrees Celsius to about 300 degrees Celsius.
18. The chamber of claim 13 , wherein the gas comprises one or more of a borane and an alane.
19. The chamber of claim 13 , wherein the gas comprises at least one of diborane, 9-borabicyclo(3.3.1)nonane, diisobutylaluminium hydride, and aluminum hydride.
20. The chamber of claim 13 , wherein the gas is a first gas and the inlet port is further configured to receive a second gas into the chamber, wherein the second gas comprises an amine, and wherein exposure of the layer to the second gas produces an exposed layer.
21. The chamber of claim 18 , wherein the gas is a first gas and the inlet port is further configured to receive a second gas into the chamber, wherein the second gas comprises an amine, and wherein exposure of the layer to the second gas produces an exposed layer.
22. The chamber of claim 18 , wherein the gas is a first gas and the inlet port is further configured to receive a second gas into the chamber, wherein the second gas comprises one or more of pyrrolidine, piperidine and diethylamine, and wherein exposure of the layer to the second gas produces an exposed layer.
23. The chamber of claim 13 , wherein the gas is a first gas and is 9-borabicyclo(3.3.1)nonane and the inlet port is further configured to receive a second gas into the chamber, wherein the second gas comprises piperidine, and wherein exposure of the layer to the second gas produces an exposed layer.
24. The chamber of claim 13 , wherein the gas is a first gas and the inlet port is further configured to receive:
a second gas into the chamber, wherein the second gas comprises an amine, and wherein exposure of the layer to the second gas produces a first exposed layer;
a first inert gas into the chamber, wherein exposure of the first exposed layer to the first inert gas produces a second exposed layer, and wherein exposure of the second exposed layer to the first gas produces a third exposed layer; and
a second inert gas into the chamber, wherein exposure of the third exposed layer to the second inert gas produces a fourth exposed layer.
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Citations (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3561920A (en) * | 1968-05-31 | 1971-02-09 | Varian Associates | Chemical vapor deposition of thick deposits of isotropic boron nitride |
US4923717A (en) * | 1989-03-17 | 1990-05-08 | Regents Of The University Of Minnesota | Process for the chemical vapor deposition of aluminum |
US6517800B1 (en) * | 1999-06-16 | 2003-02-11 | Institute Of Metal Research Of The Chinese Academy Of Sciences | Production of single-walled carbon nanotubes by a hydrogen arc discharge method |
US20040043569A1 (en) * | 2002-08-28 | 2004-03-04 | Ahn Kie Y. | Atomic layer deposited HfSiON dielectric films |
US20040144980A1 (en) * | 2003-01-27 | 2004-07-29 | Ahn Kie Y. | Atomic layer deposition of metal oxynitride layers as gate dielectrics and semiconductor device structures utilizing metal oxynitride layers |
US20060024517A1 (en) * | 2004-08-02 | 2006-02-02 | Applied Materials, Inc. | Coating for aluminum component |
US20060128168A1 (en) * | 2004-12-13 | 2006-06-15 | Micron Technology, Inc. | Atomic layer deposited lanthanum hafnium oxide dielectrics |
US20060141155A1 (en) * | 2002-11-15 | 2006-06-29 | Havard University | Atomic layer deposition using metal amidinates |
US20070037392A1 (en) * | 2005-08-08 | 2007-02-15 | Thompson Jeffery S | Atomic layer deposition of ruthenium-containing films using surface-activating agents and novel ruthenium complexes |
US20070037391A1 (en) * | 2005-08-08 | 2007-02-15 | Thompson Jeffery S | Atomic layer deposition of metal-containing films using surface-activating agents |
US20070048926A1 (en) * | 2005-08-31 | 2007-03-01 | Micron Technology, Inc. | Lanthanum aluminum oxynitride dielectric films |
US20070184190A1 (en) * | 2003-08-27 | 2007-08-09 | Mineo Hiramatsu | Method for producing carbon nanowalls, carbon nanowall, and apparatus for producing carbon nanowalls |
US20070187831A1 (en) * | 2006-02-16 | 2007-08-16 | Micron Technology, Inc. | Conductive layers for hafnium silicon oxynitride films |
US20080057659A1 (en) * | 2006-08-31 | 2008-03-06 | Micron Technology, Inc. | Hafnium aluminium oxynitride high-K dielectric and metal gates |
WO2009099707A1 (en) * | 2008-02-05 | 2009-08-13 | Crain, John, M. | Printed electronics |
US20090235721A1 (en) * | 2008-03-20 | 2009-09-24 | The Government Of The United States Of America, As Represented By The Secretary Of The Navy | Reduced graphene oxide film |
WO2010002896A1 (en) * | 2008-07-01 | 2010-01-07 | Vorbeck Materials Corp. | Articles having a compositional gradient and methods for their manufacture |
US20100028681A1 (en) * | 2008-07-25 | 2010-02-04 | The Board Of Trustees Of The Leland Stanford Junior University | Pristine and Functionalized Graphene Materials |
WO2010022164A1 (en) * | 2008-08-19 | 2010-02-25 | William Marsh Rice University | Preparation of graphene nanoribbons from carbon nanotubes |
US20100221424A1 (en) * | 2009-02-27 | 2010-09-02 | Lockheed Martin Corporation | Low temperature cnt growth using gas-preheat method |
US20100239869A1 (en) * | 2009-03-20 | 2010-09-23 | Northwestern University | Method of forming a film of graphite oxide single layers, and applications of same |
US20100317790A1 (en) * | 2009-03-03 | 2010-12-16 | Sung-Yeon Jang | Graphene composite nanofiber and preparation method thereof |
WO2011007323A1 (en) * | 2009-07-14 | 2011-01-20 | L'air Liquide Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude | Deposition of group iv metal-containing films at high temperature |
WO2011016889A2 (en) * | 2009-05-22 | 2011-02-10 | William Marsh Rice University | Highly oxidized graphene oxide and methods for production thereof |
CN102001642A (en) * | 2009-09-02 | 2011-04-06 | 中国科学院金属研究所 | Method for producing graphene belts in controllable macroscopic quantity by chemically cutting grapheme |
US20110091647A1 (en) * | 2009-10-21 | 2011-04-21 | Board Of Regents, The University Of Texas System | Graphene synthesis by chemical vapor deposition |
US20110088931A1 (en) * | 2009-04-06 | 2011-04-21 | Vorbeck Materials Corp. | Multilayer Coatings and Coated Articles |
US20110318257A1 (en) * | 2009-12-16 | 2011-12-29 | Georgia Tech Research Corporation | Production of graphene sheets and features via laser processing of graphite oxide/ graphene oxide |
US20120021224A1 (en) * | 2010-07-23 | 2012-01-26 | Clean Energy Labs, Llc | Graphene/graphene oxide platelet composite membranes and methods and devices thereof |
US20120074387A1 (en) * | 2010-09-23 | 2012-03-29 | Sean King | Microelectronic transistor having an epitaxial graphene channel layer |
WO2012061603A2 (en) * | 2010-11-03 | 2012-05-10 | Massachusetts Institute Of Technology | Compositions comprising and methods for forming functionalized carbon-based nanostructures |
US20120121891A1 (en) * | 2009-09-24 | 2012-05-17 | Sang Ouk Kim | 3-dimensional nanostructure having nanomaterials stacked on graphene substrate and fabrication method thereof |
US20120136601A1 (en) * | 2010-11-30 | 2012-05-31 | Charlene Chen | Method and System of Improved Uniformity Testing |
WO2012125854A1 (en) * | 2011-03-15 | 2012-09-20 | Peerless Worldwide, Llc | Facile synthesis of graphene, graphene derivatives and abrasive nanoparticles and their various uses, including as tribologically-beneficial lubricant additives |
US20130040283A1 (en) * | 2011-02-11 | 2013-02-14 | Alexander Star | Graphene composition, method of forming a graphene composition and sensor system comprising a graphene composition |
Family Cites Families (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5023451B2 (en) * | 2004-08-25 | 2012-09-12 | 株式会社Sumco | Silicon wafer manufacturing method, silicon single crystal growth method |
CN101547858B (en) | 2006-10-18 | 2013-06-12 | 新加坡科技研究局 | Method of functionalizing a carbon material |
KR101622306B1 (en) * | 2009-10-29 | 2016-05-19 | 삼성전자주식회사 | Graphene sheet, substrate comprising graphene sheet and process for preparing these materials |
US9156701B2 (en) | 2008-01-03 | 2015-10-13 | National University Of Singapore | Functionalised graphene oxide |
AU2009204141B2 (en) | 2008-01-08 | 2014-06-26 | William Marsh Rice University | Graphene compositions and drilling fluids derived therefrom |
US8409450B2 (en) * | 2008-03-24 | 2013-04-02 | The Regents Of The University Of California | Graphene-based structure, method of suspending graphene membrane, and method of depositing material onto graphene membrane |
GB0812320D0 (en) | 2008-07-04 | 2008-08-13 | Imp Innovations Ltd | Activation |
US20100218801A1 (en) * | 2008-07-08 | 2010-09-02 | Chien-Min Sung | Graphene and Hexagonal Boron Nitride Planes and Associated Methods |
WO2010096646A2 (en) * | 2009-02-20 | 2010-08-26 | University Of Florida Research Foundation, Inc. | Graphene processing for device and sensor applications |
US20110135884A1 (en) * | 2009-04-06 | 2011-06-09 | Vorbeck Materials Corp. | Bent Coated Articles |
US8226801B2 (en) | 2009-07-27 | 2012-07-24 | Nanotek Instruments, Inc. | Mass production of pristine nano graphene materials |
KR101119916B1 (en) | 2009-08-24 | 2012-03-13 | 삼성전자주식회사 | Electronic device utilizing graphene electrodes and organic/inorganic hybrid composites and method for manufacturing the same |
US8164089B2 (en) | 2009-10-08 | 2012-04-24 | Xerox Corporation | Electronic device |
KR20110042952A (en) * | 2009-10-20 | 2011-04-27 | 삼성전자주식회사 | Method of healing defect of graphene using laser beam and manufacturing electronic device using the same |
KR101660413B1 (en) * | 2009-11-02 | 2016-09-28 | 삼성전자주식회사 | Layered structure of graphene and organic materials having conjugated system, and process for preparing the same |
JP5471351B2 (en) | 2009-11-20 | 2014-04-16 | 富士電機株式会社 | Film formation method of graphene thin film |
KR101279606B1 (en) * | 2009-12-11 | 2013-07-05 | 한국전자통신연구원 | Method for depositing graphene film |
US8808810B2 (en) * | 2009-12-15 | 2014-08-19 | Guardian Industries Corp. | Large area deposition of graphene on substrates, and products including the same |
US8426842B2 (en) | 2010-02-02 | 2013-04-23 | The Invention Science Fund I, Llc | Doped graphene electronic materials |
JP2011178617A (en) | 2010-03-02 | 2011-09-15 | Panasonic Corp | Method for forming graphene film |
US20130230722A1 (en) * | 2010-11-24 | 2013-09-05 | Fuji Electric Co., Ltd. | Conductive thin film and transparent conductive film comprising graphene |
US9011968B2 (en) * | 2011-09-16 | 2015-04-21 | Empire Technology Development Llc | Alteration of graphene defects |
US8889997B2 (en) * | 2012-05-01 | 2014-11-18 | Tyco Electronics Corporation | Methods for improving corrosion resistance and applications in electrical connectors |
-
2011
- 2011-09-16 KR KR1020127013781A patent/KR101405256B1/en not_active IP Right Cessation
- 2011-09-16 DE DE112011100116T patent/DE112011100116T5/en not_active Withdrawn
- 2011-09-16 WO PCT/US2011/051870 patent/WO2013039506A1/en active Application Filing
- 2011-09-16 US US13/377,971 patent/US8747947B2/en not_active Expired - Fee Related
-
2012
- 2012-01-20 TW TW101102497A patent/TWI455877B/en not_active IP Right Cessation
-
2014
- 2014-04-30 US US14/265,991 patent/US20140230733A1/en not_active Abandoned
Patent Citations (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3561920A (en) * | 1968-05-31 | 1971-02-09 | Varian Associates | Chemical vapor deposition of thick deposits of isotropic boron nitride |
US4923717A (en) * | 1989-03-17 | 1990-05-08 | Regents Of The University Of Minnesota | Process for the chemical vapor deposition of aluminum |
US6517800B1 (en) * | 1999-06-16 | 2003-02-11 | Institute Of Metal Research Of The Chinese Academy Of Sciences | Production of single-walled carbon nanotubes by a hydrogen arc discharge method |
US20040043569A1 (en) * | 2002-08-28 | 2004-03-04 | Ahn Kie Y. | Atomic layer deposited HfSiON dielectric films |
US20060141155A1 (en) * | 2002-11-15 | 2006-06-29 | Havard University | Atomic layer deposition using metal amidinates |
US20040144980A1 (en) * | 2003-01-27 | 2004-07-29 | Ahn Kie Y. | Atomic layer deposition of metal oxynitride layers as gate dielectrics and semiconductor device structures utilizing metal oxynitride layers |
US20070184190A1 (en) * | 2003-08-27 | 2007-08-09 | Mineo Hiramatsu | Method for producing carbon nanowalls, carbon nanowall, and apparatus for producing carbon nanowalls |
US20060024517A1 (en) * | 2004-08-02 | 2006-02-02 | Applied Materials, Inc. | Coating for aluminum component |
US20060128168A1 (en) * | 2004-12-13 | 2006-06-15 | Micron Technology, Inc. | Atomic layer deposited lanthanum hafnium oxide dielectrics |
US20070037392A1 (en) * | 2005-08-08 | 2007-02-15 | Thompson Jeffery S | Atomic layer deposition of ruthenium-containing films using surface-activating agents and novel ruthenium complexes |
US20070037391A1 (en) * | 2005-08-08 | 2007-02-15 | Thompson Jeffery S | Atomic layer deposition of metal-containing films using surface-activating agents |
US20070048926A1 (en) * | 2005-08-31 | 2007-03-01 | Micron Technology, Inc. | Lanthanum aluminum oxynitride dielectric films |
US20070187831A1 (en) * | 2006-02-16 | 2007-08-16 | Micron Technology, Inc. | Conductive layers for hafnium silicon oxynitride films |
US20080057659A1 (en) * | 2006-08-31 | 2008-03-06 | Micron Technology, Inc. | Hafnium aluminium oxynitride high-K dielectric and metal gates |
WO2009099707A1 (en) * | 2008-02-05 | 2009-08-13 | Crain, John, M. | Printed electronics |
US20090235721A1 (en) * | 2008-03-20 | 2009-09-24 | The Government Of The United States Of America, As Represented By The Secretary Of The Navy | Reduced graphene oxide film |
WO2010002896A1 (en) * | 2008-07-01 | 2010-01-07 | Vorbeck Materials Corp. | Articles having a compositional gradient and methods for their manufacture |
US20100028681A1 (en) * | 2008-07-25 | 2010-02-04 | The Board Of Trustees Of The Leland Stanford Junior University | Pristine and Functionalized Graphene Materials |
WO2010022164A9 (en) * | 2008-08-19 | 2010-06-17 | William Marsh Rice University | Preparation of graphene nanoribbons from carbon nanotubes |
US20100105834A1 (en) * | 2008-08-19 | 2010-04-29 | Tour James M | Methods for Preparation of Graphene Nanoribbons From Carbon Nanotubes and Compositions, Thin Films and Devices Derived Therefrom |
WO2010022164A1 (en) * | 2008-08-19 | 2010-02-25 | William Marsh Rice University | Preparation of graphene nanoribbons from carbon nanotubes |
US20100221424A1 (en) * | 2009-02-27 | 2010-09-02 | Lockheed Martin Corporation | Low temperature cnt growth using gas-preheat method |
US20100317790A1 (en) * | 2009-03-03 | 2010-12-16 | Sung-Yeon Jang | Graphene composite nanofiber and preparation method thereof |
US20100239869A1 (en) * | 2009-03-20 | 2010-09-23 | Northwestern University | Method of forming a film of graphite oxide single layers, and applications of same |
US20110088931A1 (en) * | 2009-04-06 | 2011-04-21 | Vorbeck Materials Corp. | Multilayer Coatings and Coated Articles |
WO2011016889A2 (en) * | 2009-05-22 | 2011-02-10 | William Marsh Rice University | Highly oxidized graphene oxide and methods for production thereof |
US20120129736A1 (en) * | 2009-05-22 | 2012-05-24 | William Marsh Rice University | Highly oxidized graphene oxide and methods for production thereof |
WO2011007323A1 (en) * | 2009-07-14 | 2011-01-20 | L'air Liquide Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude | Deposition of group iv metal-containing films at high temperature |
US20120175751A1 (en) * | 2009-07-14 | 2012-07-12 | Julien Gatineau | Deposition of group iv metal-containing films at high temperature |
CN102001642A (en) * | 2009-09-02 | 2011-04-06 | 中国科学院金属研究所 | Method for producing graphene belts in controllable macroscopic quantity by chemically cutting grapheme |
US20120121891A1 (en) * | 2009-09-24 | 2012-05-17 | Sang Ouk Kim | 3-dimensional nanostructure having nanomaterials stacked on graphene substrate and fabrication method thereof |
US20110091647A1 (en) * | 2009-10-21 | 2011-04-21 | Board Of Regents, The University Of Texas System | Graphene synthesis by chemical vapor deposition |
US20110318257A1 (en) * | 2009-12-16 | 2011-12-29 | Georgia Tech Research Corporation | Production of graphene sheets and features via laser processing of graphite oxide/ graphene oxide |
US20120021224A1 (en) * | 2010-07-23 | 2012-01-26 | Clean Energy Labs, Llc | Graphene/graphene oxide platelet composite membranes and methods and devices thereof |
US20120074387A1 (en) * | 2010-09-23 | 2012-03-29 | Sean King | Microelectronic transistor having an epitaxial graphene channel layer |
US20120116094A1 (en) * | 2010-11-03 | 2012-05-10 | Massachusetts Institute Of Technology | Compositions comprising and methods for forming functionalized carbon-based nanostructures |
WO2012061607A2 (en) * | 2010-11-03 | 2012-05-10 | Massachusetts Institute Of Technology | Compositions comprising functionalized carbon-based nanostructures and related methods |
WO2012061603A2 (en) * | 2010-11-03 | 2012-05-10 | Massachusetts Institute Of Technology | Compositions comprising and methods for forming functionalized carbon-based nanostructures |
US20120171093A1 (en) * | 2010-11-03 | 2012-07-05 | Massachusetts Institute Of Technology | Compositions comprising functionalized carbon-based nanostructures and related methods |
US20120136601A1 (en) * | 2010-11-30 | 2012-05-31 | Charlene Chen | Method and System of Improved Uniformity Testing |
US20130040283A1 (en) * | 2011-02-11 | 2013-02-14 | Alexander Star | Graphene composition, method of forming a graphene composition and sensor system comprising a graphene composition |
WO2012125854A1 (en) * | 2011-03-15 | 2012-09-20 | Peerless Worldwide, Llc | Facile synthesis of graphene, graphene derivatives and abrasive nanoparticles and their various uses, including as tribologically-beneficial lubricant additives |
Non-Patent Citations (7)
Title |
---|
US 61180505 22.05.2009 (Pr. Doc.) * |
US 61185640 10.06.2009 (Pr. Doc.) * |
US 61452781 15.03.2011 (Pr. Doc.) * |
US 61491633 31.05.2011 (Pr. Doc.) * |
US 61503203 30.06.2011 (Pr. Doc.) * |
V. Singh et al. "Graphene Based Materials: Past, Present and Future." Prog. Mater. Sci. 56 (2011). pp. 1178-1271. * |
W. S. Hummers et al. "Preparation of Graphitic Oxide." J. Am. Chem. Soc., Vol. 80, No. 1937 (1958). p. 1339. * |
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WO2013039506A1 (en) | 2013-03-21 |
KR20130039315A (en) | 2013-04-19 |
KR101405256B1 (en) | 2014-06-10 |
US20130071564A1 (en) | 2013-03-21 |
DE112011100116T5 (en) | 2013-12-24 |
TWI455877B (en) | 2014-10-11 |
TW201313608A (en) | 2013-04-01 |
US8747947B2 (en) | 2014-06-10 |
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