CN106698408B - A kind of concave structure single crystal graphene and preparation method thereof - Google Patents

A kind of concave structure single crystal graphene and preparation method thereof Download PDF

Info

Publication number
CN106698408B
CN106698408B CN201611256637.2A CN201611256637A CN106698408B CN 106698408 B CN106698408 B CN 106698408B CN 201611256637 A CN201611256637 A CN 201611256637A CN 106698408 B CN106698408 B CN 106698408B
Authority
CN
China
Prior art keywords
gas
single crystal
graphene
copper foil
passed
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201611256637.2A
Other languages
Chinese (zh)
Other versions
CN106698408A (en
Inventor
涂溶
张翅腾飞
章嵩
张联盟
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wuhan University of Technology WUT
Original Assignee
Wuhan University of Technology WUT
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Wuhan University of Technology WUT filed Critical Wuhan University of Technology WUT
Priority to CN201611256637.2A priority Critical patent/CN106698408B/en
Publication of CN106698408A publication Critical patent/CN106698408A/en
Application granted granted Critical
Publication of CN106698408B publication Critical patent/CN106698408B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B29/00Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/02Elements
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B25/00Single-crystal growth by chemical reaction of reactive gases, e.g. chemical vapour-deposition growth
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B29/00Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/60Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape characterised by shape
    • C30B29/64Flat crystals, e.g. plates, strips or discs
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2204/00Structure or properties of graphene
    • C01B2204/20Graphene characterized by its properties
    • C01B2204/32Size or surface area
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00Crystal-structural characteristics
    • C01P2002/80Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70
    • C01P2002/82Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70 by IR- or Raman-data
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/01Particle morphology depicted by an image
    • C01P2004/03Particle morphology depicted by an image obtained by SEM
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/60Particles characterised by their size
    • C01P2004/61Micrometer sized, i.e. from 1-100 micrometer

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Carbon And Carbon Compounds (AREA)
  • Crystals, And After-Treatments Of Crystals (AREA)

Abstract

The present invention discloses a kind of preparation method of concave structure single crystal graphene the following steps are included: 1) using acetic acid and acetone ultrasonic cleaning copper foil substrate, then carries out pre-anneal treatment;2) pre-oxidation treatment is carried out to the copper foil substrate after annealing;3) chemical gas deposition is carried out on the copper foil after step 2) pre-oxidation treatment using chemical vapour deposition technique, it is cooling up to the concave structure single crystal graphene.Preparation process of the present invention is simple and convenient to operate, favorable repeatability, by controlling reaction atmosphere, prepare the single crystal graphene with spill (internal single layer periphery is double-deck) structure, and the cost being related to is low, reproducible, has a good application prospect in fields such as optics, microwave diode and sensors.

Description

A kind of concave structure single crystal graphene and preparation method thereof
Technical field
The present invention relates to a kind of concave structure single crystal graphene and preparation method thereof more particularly to a kind of middle part single layer peripheries The controllable preparation of the single crystal graphene of double-layer structure.
Background technique
Since two thousand four, people achieve huge breakthrough to the research of graphene property and application, are corresponding to it Graphene technology of preparing also in rapid progress, search out a kind of quickly cheap mode is to prepare high-quality graphene All graphene researcher focus of attention.So far, people have been developed that mechanical stripping method, silicon carbide epitaxy method, Liquid phase stripping method, oxidation-reduction method, the preparation methods such as chemical vapour deposition technique and from bottom to top synthetic method.These methods respectively have excellent Gesture, suitable for different occasions, wherein chemical vapour deposition technique is considered as the preparation method of most prospect.
With the further investigation to graphene, people have obtained a series of graphene of special constructions, their special knots Structure and performance can satisfy the demand of many special industries, obtain there are mainly two types of the methods of the graphene of these special constructions: Photoetching and chemical vapor deposition.Wherein, it is needed by the graphene that photoetching process obtains object construction by spin coating, production mask Plate, photoetching and except glue, cost is very high.The present invention is made by methane partial pressure, depositing temperature and the collaboration of pre-oxidation It is low in cost with having obtained the graphene of " recessed " shape structure, it is reproducible.
Summary of the invention
The object of the present invention is to provide a kind of preparation method of concave structure single crystal graphene, the present invention passes through methane point The mono-crystalline structures that graphene made from pressure, depositing temperature and the synergistic effect of pre-oxidation has middle part single layer, periphery double-deck, and relate to And it is reproducible, to graphene monocrystalline research have important progradation.
To achieve the above object, the technical solution adopted by the present invention are as follows:
A kind of preparation method of concave structure single crystal graphene, includes the following steps:
1) it is cleaned by ultrasonic copper foil substrate using acetic acid and acetone, then carries out pre-anneal treatment;
2) gained copper foil substrate will be handled through step 1) carry out pre-oxidation treatment;
3) chemical vapor deposition is carried out on the copper foil after step 2) pre-oxidation treatment using chemical vapour deposition technique, it is cold But up to the concave structure single crystal graphene.
In above scheme, the ultrasonic cleaning step are as follows: method for suppersonic cleaning is used, with acetic acid (purity 99.5wt%) 20~40min is cleaned to copper foil respectively with acetone (purity 99.5wt%).Wherein acetic acid can wash the oxidation of copper foil surface Layer makes copper atom be exposed to most surface layer, promotes catalytic performance.Acetone can wash the residual organic impurities of copper foil surface, have Conducive to graphene nucleation density is reduced, make cleaning more thorough by way of ultrasonic cleaning, guarantees graphene growth environment Cleaning.
In above scheme, the pre-anneal treatment uses normal pressure annealing process, the specific steps are as follows: pass first into 500~ The Ar gas of 1000sccm drains air, is then passed through the H of 50~100sccm simultaneously2Gas is again heated to 1050~1080 DEG C, moves back 90~120min of fire closes H2Gas.The present invention can further remove the impurity of copper foil surface using annealing process, can also make Copper domain is grown up, and the surface of atomically flating is obtained, and is conducive to the nucleation for controlling graphene.
In above scheme, the pre-oxidation treatment technique are as follows: keep Ar gas be passed through flow be 500~1000sccm side by side H to the greatest extent2Gas, then it is passed through the O of 3~5sccm simultaneously2Gas, oxidizing temperature are 1050~1080 DEG C, and oxidization time is 5~10min, are closed O2Gas.The present invention is passivated copper foil using pre-oxidation treatment technique, so that oxygen atom is occupied the nucleation site of graphene, further decreases Graphene nucleation density is conducive to growing up for graphene monocrystalline.
In above scheme, the chemistry gas deposition step are as follows: the flow that is passed through of Ar gas is kept to be 500~1000sccm and lead to Enter the H of 300~500sccm2, while being passed through the CH of 1~1.5sccm4, depositing temperature is 1050~1080 DEG C, sedimentation time 60 ~90min.Internal single layer periphery double-layer structure can be obtained by the synergistic effect of pre-oxidation, atmosphere and depositing temperature in this step Single crystal graphene, it is low in cost, it is reproducible.
The flow that is passed through that Ar gas is kept in above scheme, in cooling step described in step 3) is 500~1000sccm, is closed Close CH4, and adjust H2Flow is 50~100sccm's, is down to 100 DEG C hereinafter, closing Ar, H to temperature2.This step is passed through 500 The H of the Ar and 50~100sccm of~1000sccm2, so that gained graphene film is stablized cooling under protective atmosphere, ensure that institute The quality for obtaining graphene film, obtaining single crystal graphene is double-deck structure (concave structure single crystal graphene) in middle part single layer periphery.
According to concave structure single crystal graphene prepared by above scheme, its laminated structure double-deck in middle part single layer periphery (middle part is single-layer graphene, and periphery is bilayer graphene, forms concave structure of the middle part to lower recess), single crystal graphene etc. Imitating diameter is 10~80 μm.Wherein, the single-layer graphene at middle part has semimetallic characteristic, peripheral bilayer graphene structure tool There is the characteristic of semiconductor, schottky junction can be formed in the two interface, can be applied to the fields such as microwave diode.
The present invention has obtained novel concave structure by methane partial pressure, depositing temperature and the synergistic effect of pre-oxidation for the first time Single crystal graphene.Field effect transistor, which is fabricated to, using this single crystal graphene is desired to have excellent performance;Additionally due to Inhomogeneities of the concave structure single crystal graphene in number of plies distribution, can be applied to microwave diode and sensor etc., It has broad application prospects.
The invention has the benefit that preparation method of the present invention is simple, and it is easy to operate, in methane partial pressure, deposition At temperature and the synergistic effect of pre-oxidation, the sheet concave structure single crystal graphite of middle part single layer, peripheral double-layer structure can be obtained Alkene, it is low in cost, it is reproducible, and inhomogeneities of the products therefrom in number of plies distribution, in optics, microwave diode and sensing The fields such as device have a good application prospect.
Detailed description of the invention
Fig. 1 is that the SEM of 1 products therefrom of the embodiment of the present invention schemes;
Fig. 2 is 1 products therefrom of the embodiment of the present invention in SiO2(a) Raman test result and (b) optics on/Si substrate is aobvious Structure chart under micro mirror;
Fig. 3 is the SAED figure of the double layer area of 1 products therefrom of the embodiment of the present invention.
Fig. 4 is that the SEM of comparative example products therefrom of the present invention schemes.
Specific embodiment
To make the objectives, technical solutions, and advantages of the present invention more comprehensible, with reference to embodiments, to the present invention into Row is further described.It should be appreciated that described herein, specific examples are only used to explain the present invention, is not used to limit The present invention.
Embodiment 1
A kind of concave structure single crystal graphene, preparation method include the following steps:
1) copper foil that area is 2cm × 2cm is cut, successively using acetic acid (purity 99.5wt%) and acetone, (concentration is 99.5wt%) by copper foil ultrasonic cleaning 20min;Copper foil after cleaning is put into quartz ampoule, quartz tube 6cm, it is long Degree is 100cm, is passed through the Ar of 500sccm, keeps 30min, it is ensured that drains the air in quartz ampoule, then is passed through 50sccm's simultaneously H2, 1050 DEG C are risen to the speed of 15 DEG C/min, is kept 90min (annealing), H is closed2
2) the Ar throughput in step 1) is kept to drain H in quartz ampoule2, then it is passed through the O of 3sccm2Pre-oxidation treatment is carried out, 5min is kept, oxidizing temperature is 1050 DEG C, closes O2;Keep the flow of Ar in step 2) constant, H2Flow increase to 300sccm, and it is passed through the CH of 1sccm4, chemical vapor deposition is carried out at a temperature of 1050 DEG C, growth is kept the temperature on copper foil 60min;
3) it keeps the flow of Ar in step 2) constant, closes CH4, H2Flow is decreased to 50sccm, is down to 100 DEG C to temperature Hereinafter, closing Ar, H2, sample is taken out to get the concave structure single crystal graphene.
Fig. 1 is the SEM structure chart of the present embodiment products therefrom, and products therefrom diameter is 10~80 μm;Fig. 2 is embodiment institute Product is obtained in SiO2Structure chart under (a) optical microscopy and (b) Raman test result on/Si substrate, wherein No. 1 region I2D: IG> 2, i.e. No. 1 region is single layer region, the I in No. 2 regions2D: IG< 1, i.e., No. 2 regions are double layer area, illustrate products therefrom In double-deck concave structure in internal single layer, periphery.Fig. 3 is the SAED figure of the double layer area of embodiment products therefrom, I in figure1-210: I1-100> 2, i.e. shooting area is double layer area.
The present embodiment products therefrom is applied to prepare microwave diode, shows good service performance.
Embodiment 2
A kind of concave structure single crystal graphene, preparation method include the following steps:
1) copper foil that area is 2cm × 2cm is cut, successively using acetic acid (purity 99.5wt%) and acetone, (concentration is 99.5wt%) by copper foil ultrasonic cleaning 30min;Copper foil after cleaning is put into quartz ampoule, quartz tube 6cm, it is long Degree is 100cm, is passed through the Ar of 750sccm, keeps 30min, it is ensured that drains the air in quartz ampoule, then is passed through 75sccm's simultaneously H2, 1065 DEG C are risen to the speed of 15 DEG C/min, keeps 100min, closes H2(annealing);
2) Ar throughput in step 1) is kept to drain H in quartz ampoule2, then it is passed through the O of 4sccm2, keep 7min, oxidizing temperature 1065 DEG C, close O2;Keep the flow of Ar in step 2) constant, H2Flow increase to 400sccm, and be passed through 1.2sccm's CH4, chemical vapor deposition is carried out at a temperature of 1065 DEG C, the heat preservation growth 70min on copper foil;
4) it keeps the flow of Ar in step 3) constant, closes CH4, H2Flow is decreased to 75sccm, is down to 100 DEG C to temperature Hereinafter, closing Ar, H2, sample is taken out to get the concave structure single crystal graphene.
The present embodiment products therefrom is applied to prepare microwave diode, shows good service performance.
Embodiment 3
A kind of concave structure single crystal graphene, preparation method include the following steps:
1) copper foil that area is 2cm × 2cm is cut, successively using acetic acid (purity 99.5wt%) and acetone, (concentration is 99.5wt%) by copper foil ultrasonic cleaning 40min;Copper foil after cleaning is put into quartz ampoule, quartz tube 6cm, it is long Degree is 100cm, is passed through the Ar of 1000sccm, keeps 30min, it is ensured that drains the air in quartz ampoule, then is passed through 100sccm simultaneously H2, 1080 DEG C are risen to the speed of 15 DEG C/min, is kept 120min (annealing), H is closed2
2) Ar throughput in step 1) is kept to drain H in quartz ampoule2, then it is passed through the O of 5sccm2Pre-oxidation treatment is carried out, is protected 10min is held, oxidizing temperature is 1080 DEG C, closes O2;Keep the flow of Ar in step 2) constant, H2Flow increase to 500sccm, and it is passed through the CH of 1.5sccm4, chemical vapor deposition is carried out at a temperature of 1080 DEG C, heat preservation growth is (heavy on copper foil Product) 90min;
3) it keeps the flow of Ar in step 2) constant, closes CH4, H2Flow is decreased to 100sccm, is down to 100 DEG C to temperature Hereinafter, closing Ar, H2, sample is taken out to get the concave structure single crystal graphene.
The present embodiment products therefrom is applied to prepare microwave diode, shows good service performance.
Comparative example
A kind of single crystal graphene, preparation method include the following steps:
1) copper foil that area is 2cm × 2cm is cut, successively using acetic acid (purity 99.5wt%) and acetone, (concentration is 99.5wt%) by copper foil ultrasonic cleaning 40min;Copper foil after cleaning is put into quartz ampoule, quartz tube 6cm, it is long Degree is 100cm, is passed through the Ar of 1000sccm, keeps 30min, it is ensured that drain the air in quartz ampoule, then be passed through 100sccm's H2, 1080 DEG C are risen to the speed of 15 DEG C/min, keeps 120min, closes H2
2) Ar throughput in step 1) is kept to drain H in quartz ampoule2, then it is passed through the O of 5sccm2, keep 10min, oxidation temperature Degree is 1080 DEG C, closes O2;Keep the flow of Ar in step 2) constant, H2Flow reduce to 50sccm, and be passed through 1sccm's CH4, chemical vapor deposition is carried out at a temperature of 1080 DEG C, the heat preservation growth 60min on copper foil;
3) it keeps the flow of Ar in step 2) constant, closes CH4, H2Flow increases to 100sccm, is down to 100 DEG C to temperature Hereinafter, closing Ar, H2, take out sample.Gained sample is no longer concave structure single crystal graphene.
Fig. 4 is the SEM structure chart of this comparative example products therefrom, and gained graphene monocrystalline is in uniform laminated structure.
Above-described embodiment is just for the sake of clearly demonstrating the present invention, not to the limitation of embodiment, while here without It needs also be exhaustive all embodiments.For those of ordinary skill in the art, the present invention is not being departed from Under the premise of concept, amplified it is obvious it is several improvement and variation still in the invention protection scope it It is interior.

Claims (5)

1. a kind of preparation method of concave structure single crystal graphene, which comprises the steps of:
1) it is cleaned by ultrasonic copper foil substrate using acetic acid and acetone, then carries out pre-anneal treatment;
2) gained copper foil substrate will be handled through step 1) carry out pre-oxidation treatment;
3) chemical gas deposition is carried out on the copper foil after step 2) pre-oxidation treatment using chemical vapour deposition technique, cooling to obtain the final product The concave structure single crystal graphene;Its laminated structure double-deck in middle part single layer periphery, middle part is single-layer graphene, and periphery is Bilayer graphene;
The pre-oxidation treatment technique are as follows: the flow that is passed through of Ar gas is kept to be 500~1000sccm and drain H2Gas, then lead to simultaneously Enter the O of 3~5sccm2Gas, oxidizing temperature are 1050~1080 DEG C, and oxidization time is 5~10min, close O2Gas;
The chemistry gas deposition step are as follows: the flow that is passed through of Ar gas is kept to be 500~1000sccm and be passed through 300~500sccm H2, while being passed through the CH of 1~1.5sccm4, depositing temperature is 1050~1080 DEG C, and sedimentation time is 60~90min.
2. preparation method according to claim 1, which is characterized in that the ultrasonic cleaning step are as follows: clear using ultrasonic wave Washing method successively cleans 20~40min to copper foil respectively with acetic acid and acetone.
3. preparation method according to claim 1, which is characterized in that the pre-anneal treatment uses normal pressure annealing process, Specific step is as follows: the Ar gas for passing first into 500~1000sccm drains air, is then passed through the H of 50~100sccm simultaneously2 Gas is again heated to 1050~1080 DEG C, and anneal 90~120min, and annealing is completed to close H2Gas.
4. preparation method according to claim 1, which is characterized in that keep Ar gas in cooling step described in step 3) Being passed through flow is 500~1000sccm, closes CH4, and adjust H2Flow is 50~100sccm, to temperature be down to 100 DEG C with Under, close Ar, H2
5. concave structure single crystal graphene made from any one of Claims 1 to 4 preparation method, which is characterized in that described recessed The shape structure single crystal graphene laminated structure double-deck in middle part single layer, periphery, the equivalent diameter of single crystal graphene is 10~80 μm.
CN201611256637.2A 2016-12-30 2016-12-30 A kind of concave structure single crystal graphene and preparation method thereof Active CN106698408B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201611256637.2A CN106698408B (en) 2016-12-30 2016-12-30 A kind of concave structure single crystal graphene and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201611256637.2A CN106698408B (en) 2016-12-30 2016-12-30 A kind of concave structure single crystal graphene and preparation method thereof

Publications (2)

Publication Number Publication Date
CN106698408A CN106698408A (en) 2017-05-24
CN106698408B true CN106698408B (en) 2019-09-10

Family

ID=58905344

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201611256637.2A Active CN106698408B (en) 2016-12-30 2016-12-30 A kind of concave structure single crystal graphene and preparation method thereof

Country Status (1)

Country Link
CN (1) CN106698408B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108423659B (en) * 2018-05-30 2019-02-26 绍兴文理学院 A kind of preparation method of the grade single layer single crystal graphene based on polycrystalline copper foil

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101701237B1 (en) * 2013-05-21 2017-02-03 한양대학교 산학협력단 Lare-size Single-crystal Monolayer Graphene and Manufacturing Method Thereof
CN105439126B (en) * 2014-09-01 2017-12-22 华北电力大学 A kind of grade single crystal graphene preparation method
CN104498902B (en) * 2014-12-12 2016-10-19 中国科学院重庆绿色智能技术研究院 A kind of preparation method of aumospheric pressure cvd graphene film
CN104975344A (en) * 2015-07-09 2015-10-14 中国科学院上海微系统与信息技术研究所 Low nucleation density graphene single crystal preparation method based on cuprous oxide film substrate
CN105220214B (en) * 2015-11-13 2018-02-06 中国科学院上海高等研究院 A kind of preparation method of graphene film

Also Published As

Publication number Publication date
CN106698408A (en) 2017-05-24

Similar Documents

Publication Publication Date Title
Gong et al. Electronic and optoelectronic applications based on 2D novel anisotropic transition metal dichalcogenides
Podrezova et al. Comparison between ZnO nanowires grown by chemical vapor deposition and hydrothermal synthesis
CN103194729B (en) The preparation method of metal chalcogenide film
CN104389016B (en) Method for quickly preparing large-size single-crystal graphene
CN105734529B (en) A kind of synthetic method of molybdenum disulfide nano wall
CN110790313A (en) Preparation method of 3R phase transition metal chalcogenide two-dimensional nanosheet
Burton et al. Integrated wafer scale growth of single crystal metal films and high quality graphene
CN111987169B (en) Transistor based on two-dimensional gallium oxide thin film and preparation method
Segawa et al. Low-temperature crystallization of oriented ZnO film using seed layers prepared by sol–gel method
KR20210018855A (en) High efficiency chemical vapor deposition method graphene wrinkle removal method
CN107032331B (en) A kind of graphene preparation method based on dielectric base
CN102653401B (en) Structural graphene preparation method based on Ni film annealing
Wang et al. Epitaxy of hexagonal boron nitride thin films on sapphire for optoelectronics
CN104418387B (en) A kind of molybdenum disulfide nano thin slice and preparation method thereof
CN107188161A (en) Graphene and preparation method thereof
CN106698408B (en) A kind of concave structure single crystal graphene and preparation method thereof
CN104211054A (en) Method for controllably preparing graphene
Meng et al. Controlled synthesis of large scale continuous monolayer WS2 film by atmospheric pressure chemical vapor deposition
Smovzh et al. Synthesis of graphene by chemical vapor deposition and its transfer to polymer
JP2009283922A5 (en)
KR101466482B1 (en) Etching-free graphene growth method using oxidizable metal
JP2014034503A (en) Method for producing graphene film and graphene film
CN113410287A (en) Two-dimensional SnSe-SnSe2P-n heterojunction and preparation method thereof
CN112938946B (en) Preparation method of graphene
CN112593205B (en) Method for preparing large-area single-layer molybdenum disulfide with assistance of ammonia water

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant