JP2014037578A - Copper foil for producing graphene and method for producing graphene using the same - Google Patents
Copper foil for producing graphene and method for producing graphene using the same Download PDFInfo
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 116
- 229910021389 graphene Inorganic materials 0.000 title claims abstract description 106
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims abstract description 90
- 239000011889 copper foil Substances 0.000 title claims abstract description 70
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 35
- 239000013078 crystal Substances 0.000 claims abstract description 29
- 238000005096 rolling process Methods 0.000 claims abstract description 20
- 239000010949 copper Substances 0.000 claims description 23
- 229910052802 copper Inorganic materials 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 17
- 238000010438 heat treatment Methods 0.000 claims description 16
- 239000007789 gas Substances 0.000 claims description 12
- 239000000956 alloy Substances 0.000 claims description 9
- 229910045601 alloy Inorganic materials 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 238000005530 etching Methods 0.000 claims description 8
- 229910052709 silver Inorganic materials 0.000 claims description 4
- 229910052718 tin Inorganic materials 0.000 claims description 4
- 238000007747 plating Methods 0.000 claims description 3
- 238000010030 laminating Methods 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 239000010408 film Substances 0.000 description 20
- 239000003921 oil Substances 0.000 description 20
- 238000005097 cold rolling Methods 0.000 description 15
- 239000000758 substrate Substances 0.000 description 11
- 238000005259 measurement Methods 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- 239000000463 material Substances 0.000 description 7
- 238000000137 annealing Methods 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 3
- 239000010731 rolling oil Substances 0.000 description 3
- 230000003746 surface roughness Effects 0.000 description 3
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 2
- 229920002799 BoPET Polymers 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 241001391944 Commicarpus scandens Species 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000012377 drug delivery Methods 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910003465 moissanite Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
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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
-
- 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
-
- 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]
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C9/00—Alloys based on copper
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/08—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2204/00—Structure or properties of graphene
- C01B2204/20—Graphene characterized by its properties
- C01B2204/32—Size or surface area
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- Engineering & Computer Science (AREA)
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- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- General Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Composite Materials (AREA)
- Inorganic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Metal Rolling (AREA)
- Carbon And Carbon Compounds (AREA)
Abstract
Description
本発明は、グラフェンを製造するための銅箔基材、及びそれを用いたグラフェンの製造方法に関する。 The present invention relates to a copper foil base material for producing graphene, and a method for producing graphene using the same.
グラファイトは平らに並んだ炭素6員環の層がいくつも積み重なった層状構造をもつが、その単原子層〜数原子層程度のものはグラフェン又はグラフェンシートと呼ばれる。グラフェンシートは独自の電気的、光学的及び機械的特性を有し、特にキャリア移動速度が高速である。そのため、グラフェンシートは、例えば、燃料電池用セパレータ、透明電極、表示素子の導電性薄膜、無水銀蛍光灯、コンポジット材、ドラッグデリバリーシステム(DDS)のキャリアーなど、産業界での幅広い応用が期待されている。 Graphite has a layered structure in which a number of flat carbon 6-membered ring layers are stacked, and those having a single atomic layer to several atomic layers are called graphene or graphene sheets. Graphene sheets have unique electrical, optical and mechanical properties, and in particular have a high carrier moving speed. Therefore, graphene sheets are expected to have a wide range of applications in the industry, such as fuel cell separators, transparent electrodes, conductive thin films for display elements, mercury-free fluorescent lamps, composite materials, and drug delivery system (DDS) carriers. ing.
グラフェンシートを製造する方法として、グラファイトを粘着テープで剥がす方法が知られているが、得られるグラフェンシートの層数が一定でなく、大面積のグラフェンシートが得難く、大量生産にも適さないという問題がある。
そこで、シート状の単結晶グラファイト化金属触媒上に炭素系物質を接触させた後、熱処理することによりグラフェンシートを成長させる技術(化学気相成長(CVD)法)が開発されている(特許文献1)。この単結晶グラファイト化金属触媒としては、Ni、Cu、Wなどの金属基板が記載されている。
同様に,NiやCuの金属箔やSi基板上に形成した銅層上に化学気相成長法でグラフェンを製膜する技術が報告されている.なお,グラフェンの製膜は1000℃程度で行われるのが一般的であるが(非特許文献1)、マイクロ波プラズマ等を使用することにより400℃程度の温度で製膜する技術も報告されている(特許文献2,3)。
As a method of producing a graphene sheet, a method of peeling graphite with an adhesive tape is known, but the number of layers of the obtained graphene sheet is not constant, it is difficult to obtain a large area graphene sheet, and it is not suitable for mass production There's a problem.
Thus, a technique (chemical vapor deposition (CVD) method) has been developed in which a graphene sheet is grown by bringing a carbon-based material into contact with a sheet-like single crystal graphitized metal catalyst and then performing heat treatment (Patent Literature). 1). As this single crystal graphitized metal catalyst, a metal substrate of Ni, Cu, W or the like is described.
Similarly, a technique for forming graphene by chemical vapor deposition on a copper layer formed on a Ni or Cu metal foil or Si substrate has been reported. Although graphene film formation is generally performed at about 1000 ° C. (Non-patent Document 1), a technique for forming a film at a temperature of about 400 ° C. by using microwave plasma or the like has also been reported. (Patent Documents 2 and 3).
しかしながら、特許文献1のように単結晶の金属基板を製造することは容易でなく極めて高コストであり、又、大面積の基板が得られ難く、ひいては大面積のグラフェンシートが得難いという問題がある。一方,非特許文献1には、Cuを基板として使用することが記載されているが,Cu箔上では短時間にグラフェンが面方向に成長せず,Si基板上に形成したCu層を焼鈍で粗大粒として基板としている。この場合、グラフェンの大きさはSi基板サイズに制約され,製造コストも高い。
すなわち、本発明は、大面積のグラフェンを低コストで生産可能なグラフェン製造用銅箔及びそれを用いたグラフェンの製造方法の提供を目的とする。
However, as in Patent Document 1, it is not easy to manufacture a single crystal metal substrate, which is extremely expensive, and it is difficult to obtain a large-area substrate, and thus it is difficult to obtain a large-area graphene sheet. . On the other hand, Non-Patent Document 1 describes that Cu is used as a substrate, but graphene does not grow in the surface direction in a short time on the Cu foil, and the Cu layer formed on the Si substrate is annealed. The substrate is formed as coarse particles. In this case, the size of graphene is limited by the Si substrate size, and the manufacturing cost is high.
That is, an object of the present invention is to provide a copper foil for producing graphene capable of producing large-area graphene at low cost and a method for producing graphene using the same.
本発明のグラフェン製造用銅箔は、圧延平行方向及び圧延直角方向の60度光沢度が共に500%以上であり、400℃で10分間加熱後の平均結晶粒径が30μm以上である。 The copper foil for producing graphene of the present invention has a 60 ° glossiness in both the rolling parallel direction and the perpendicular direction of rolling of 500% or more, and the average crystal grain size after heating at 400 ° C. for 10 minutes is 30 μm or more.
前記平均結晶粒径が120μm以上であることが好ましく、表面の算術平均粗さRaが0.07μm以下であることが好ましい。
JIS−H3100(合金番号:C1100)に規格するタフピッチ銅、JIS-H3510(合金番号:C1011)若しくはJIS−H3100(合金番号:C1020)に規格する無酸素銅、又は該タフピッチ銅若しくは無酸素銅に対し、Sn及びAgの群から選ばれる1種以上の元素を0.0001〜0.050質量%含有することが好ましい。
The average crystal grain size is preferably 120 μm or more, and the arithmetic average roughness Ra of the surface is preferably 0.07 μm or less.
Tough pitch copper standardized to JIS-H3100 (alloy number: C1100), oxygen-free copper standardized to JIS-H3510 (alloy number: C1011) or JIS-H3100 (alloy number: C1020), or tough pitch copper or oxygen-free copper On the other hand, it is preferable to contain 0.0001-0.050 mass% of 1 or more types of elements chosen from the group of Sn and Ag.
本発明のグラフェンの製造方法は、前記グラフェン製造用銅箔を用いて300℃以上400℃以下で行い、所定の室内に、加熱した前記グラフェン製造用銅箔を配置すると共に炭素含有ガスを供給し、前記グラフェン製造用銅箔又は前記銅めっき層の表面にグラフェンを形成するグラフェン形成工程と、前記グラフェンの表面に転写シートを積層し、前記グラフェンを前記転写シート上に転写しながら、前記グラフェン製造用銅箔をエッチング除去するグラフェン転写工程と、を有する。 The graphene production method of the present invention is performed at 300 ° C. or more and 400 ° C. or less using the graphene production copper foil, the heated copper foil for graphene production is placed in a predetermined chamber, and a carbon-containing gas is supplied. A graphene forming step of forming graphene on the surface of the copper foil for graphene production or the copper plating layer, and a graphene production process while laminating a transfer sheet on the surface of the graphene and transferring the graphene onto the transfer sheet And a graphene transfer step of etching away the copper foil for use.
本発明によれば、大面積のグラフェンを低コストで生産可能とする銅箔が得られる。 ADVANTAGE OF THE INVENTION According to this invention, the copper foil which can produce a large area graphene at low cost is obtained.
以下、本発明の実施形態に係るグラフェン製造用銅箔について説明する。なお、本発明において%とは、特に断らない限り、質量%を示すものとする。 Hereinafter, the copper foil for graphene manufacture which concerns on embodiment of this invention is demonstrated. In the present invention, “%” means “% by mass” unless otherwise specified.
<組成>
グラフェン製造用銅箔としては、JIS-H3100(合金番号:C1100)に規格するタフピッチ銅(TPC)、又はJIS-H3510(合金番号:C1011)若しくはJIS-H3100(合金番号:C1020)に規格する無酸素銅(OFC)を用いることができる。
又、これらタフピッチ銅又は無酸素銅に対し、Sn及びAgの群から選ばれる1種以上の元素を0.0001〜0.050質量%含有する組成を用いることもできる。上記元素を含有すると、銅箔の強度が向上し適度な伸びを有すると共に、結晶粒径を大きくすることができる。上記元素の含有割合が0.0001質量%未満であると、含有割合が小さいためその含有割合を制御することが困難になる場合がある。上記元素の含有割合が0.050質量%を超えると強度は更に向上するものの、伸びが低下して加工性が悪化すると共に結晶粒径の成長が抑制され、後述する400℃で10分間加熱後の平均結晶粒径が30μm未満となる。より好ましくは上記元素の含有割合が0.040質量%以下である。
また、グラフェン製造用銅箔としては、タフピッチ銅又は無酸素銅に対し、結晶粒径の大きさに大きな影響を与えない範囲の含有割合(例えば0.050質量%以下)で、Sn、Ag、In、Ti、Zn、Zr、Fe、P、Ni、Si、Te、Cr、Nb、B、及びVの群から選ばれる一種以上の元素を添加してもよいが、添加元素はこれらに限られない。
<Composition>
The copper foil for producing graphene is tough pitch copper (TPC) standardized to JIS-H3100 (alloy number: C1100), or JIS-H3510 (alloy number: C1011) or JIS-H3100 (alloy number: C1020). Oxygen copper (OFC) can be used.
Moreover, the composition containing 0.0001-0.050 mass% of 1 or more types of elements chosen from the group of Sn and Ag with respect to these tough pitch copper or oxygen-free copper can also be used. When the above elements are contained, the strength of the copper foil is improved, the film has an appropriate elongation, and the crystal grain size can be increased. When the content ratio of the element is less than 0.0001% by mass, it may be difficult to control the content ratio because the content ratio is small. When the content of the above elements exceeds 0.050% by mass, the strength is further improved, but the elongation is lowered and the workability is deteriorated and the growth of the crystal grain size is suppressed, and the average after heating at 400 ° C. described later for 10 minutes. The crystal grain size is less than 30 μm. More preferably, the content ratio of the element is 0.040% by mass or less.
In addition, as the copper foil for producing graphene, Sn, Ag, in a content ratio (for example, 0.050% by mass or less) in a range that does not greatly affect the crystal grain size with respect to tough pitch copper or oxygen-free copper. One or more elements selected from the group of In, Ti, Zn, Zr, Fe, P, Ni, Si, Te, Cr, Nb, B, and V may be added, but the additive elements are not limited to these. Absent.
<厚み>
グラフェン製造用銅箔の厚みは特に制限されないが、一般的には5〜150μmである。さらに、ハンドリング性を確保しつつ、後述するエッチング除去を容易に行うため、銅箔の厚みを12〜50μmとすると好ましい。グラフェン製造用銅箔の厚みが12μm未満であると、破断し易くなってハンドリング性に劣り、厚みが50μmを超えるとエッチング除去がし難くなる場合がある。
<Thickness>
The thickness of the graphene-producing copper foil is not particularly limited, but is generally 5 to 150 μm. Furthermore, it is preferable to set the thickness of the copper foil to 12 to 50 μm in order to easily perform the etching removal described later while ensuring the handleability. When the thickness of the copper foil for producing graphene is less than 12 μm, it is easy to break and the handling property is inferior, and when the thickness exceeds 50 μm, it may be difficult to remove by etching.
<60度光沢度>
グラフェン製造用銅箔の圧延平行方向及び圧延直角方向の60度光沢度(JIS Z 8741)が共に500%以上である。
後述するように、本発明のグラフェン製造用銅箔を用いてグラフェンを製造した後、銅箔から転写シートへグラフェンを転写する必要があるが、銅箔の表面が粗いと転写がし難く、グラフェンが破損することがわかった。そこで、銅箔の表面凹凸を表す指標として、60度光沢度を規定する。
圧延平行方向及び圧延直角方向の60度光沢度のいずれかが500%未満であると、転写の際にグラフェンが破損する。圧延平行方向及び圧延直角方向の60度光沢度の上限は特に制限されないが、実用上、900%程度が上限である。
又、このように転写シートへグラフェンを転写し易くするため、JIS B0601に規格するグラフェン製造用銅箔表面の算術平均粗さRaが0.05μm以下であることが好ましい。
<60 degree gloss>
Both the 60-degree glossiness (JIS Z 8741) in the rolling parallel direction and the perpendicular direction of rolling of the copper foil for producing graphene is 500% or more.
As will be described later, after producing graphene using the copper foil for producing graphene of the present invention, it is necessary to transfer the graphene from the copper foil to the transfer sheet. However, if the surface of the copper foil is rough, transfer is difficult. Was found to be damaged. Therefore, 60 degree glossiness is defined as an index representing the surface roughness of the copper foil.
If any of the 60 ° gloss in the direction parallel to rolling and the direction perpendicular to rolling is less than 500%, the graphene is damaged during transfer. The upper limit of the 60 degree glossiness in the rolling parallel direction and the direction perpendicular to the rolling direction is not particularly limited, but about 900% is practically the upper limit.
In order to facilitate the transfer of graphene to the transfer sheet as described above, the arithmetic average roughness Ra of the surface of the copper foil for producing graphene specified in JIS B0601 is preferably 0.05 μm or less.
<平均結晶粒径>
グラフェン製造用銅箔を400℃で10分間加熱後の平均結晶粒径が30μm以上である。
グラフェン製造用銅箔の平均結晶粒径が30μmより小さいと、グラフェン製造用銅箔の表面にグラフェンを成長させる際の障害となり、面方向にグラフェンが成長し難くなる。これは、結晶粒界がグラフェンの成長の障害となるためと考えられる。特に、グラフェン製造用銅箔の平均結晶粒径が120μm以上であると好ましい。銅箔の平均結晶粒径の上限は特に限定されないが、例えば500μm以下、好ましくは450μm以下、より好ましくは400μm以下、最も好ましくは300μm以下である。
なお、400℃で10分間の加熱は、グラフェンを製造する際、プラズマアシストCVD法により加熱する条件を模したものである。
又、平均結晶粒径は、JIS H0501の切断法により、グラフェン製造用銅箔を測定する。
<Average crystal grain size>
The average crystal grain size after heating the graphene-producing copper foil at 400 ° C. for 10 minutes is 30 μm or more.
When the average crystal grain size of the graphene-producing copper foil is smaller than 30 μm, it becomes an obstacle to growing graphene on the surface of the graphene-producing copper foil, and the graphene is difficult to grow in the plane direction. This is presumably because the crystal grain boundaries hinder the growth of graphene. In particular, the average crystal grain size of the copper foil for producing graphene is preferably 120 μm or more. The upper limit of the average crystal grain size of the copper foil is not particularly limited, but is, for example, 500 μm or less, preferably 450 μm or less, more preferably 400 μm or less, and most preferably 300 μm or less.
Note that the heating at 400 ° C. for 10 minutes simulates the conditions of heating by the plasma-assisted CVD method when producing graphene.
In addition, the average crystal grain size is measured for a graphene-producing copper foil by the cutting method of JIS H0501.
以上のように規定したグラフェン製造用銅箔を用いることで、大面積のグラフェンを低コストで、かつ高い歩留りで生産することができる。 By using the graphene-producing copper foil defined as described above, large-area graphene can be produced at a low cost and with a high yield.
<グラフェン製造用銅箔の製造>
本発明の実施形態に係るグラフェン製造用銅箔は、例えば以下のようにして製造することができる。まず、所定の組成の銅インゴットを製造し、熱間圧延を行った後、焼鈍と冷間圧延を繰り返し、圧延板を得る。この圧延板を焼鈍して再結晶させ,所定の厚みまで圧下率を80〜99.9%(好ましくは85〜99.9%、更に好ましくは90〜99.9%)として最終冷間圧延して銅箔を得る。
<Manufacture of copper foil for graphene production>
The copper foil for producing graphene according to the embodiment of the present invention can be produced, for example, as follows. First, after manufacturing the copper ingot of a predetermined composition and performing hot rolling, annealing and cold rolling are repeated and a rolled sheet is obtained. The rolled sheet is annealed and recrystallized, and finally cold-rolled to a predetermined thickness of 80 to 99.9% (preferably 85 to 99.9%, more preferably 90 to 99.9%). To obtain copper foil.
ここで、グラフェン製造用銅箔の60度光沢度を500%以上に制御することが重要である。その方法として、最終冷間圧延の最終パスと最終冷間圧延の最終パスの1つ前のパスの両方の油膜当量をいずれも18000以下とする。
圧延銅箔は、一般に油潤滑のもと高速で加工されるが、潤滑油膜が薄くなるほどせん断帯変形が支配的になりやすい。これは金属一般に共通する現象である。なお、せん断帯の存在は、焼鈍した場合の結晶粒の成長にとって好ましいとはいえない。そして、せん断帯の多少あるいは短深は銅箔表面の光沢度で表すことができる。具体的には、圧延時の現象として、ロールと材料の間に導入される油膜が厚いと圧延加工表面にオイルピット(凹凸)を生じるが、油膜が薄ければ材料表面で圧延ロールと接触する面積が増えて自由変形が制限され、オイルピットが発達せず、圧延ロールの平滑な表面プロフィルが転写され、平滑な表面が形成される。このようなことから、油膜を薄くする指標として、油膜当量を18000以下とする。油膜当量が18000を超えると、銅箔表面の60度光沢度が500%未満となる。
Here, it is important to control the 60 degree gloss of the copper foil for producing graphene to 500% or more. As the method, both oil film equivalents of the final pass of the final cold rolling and the pass before the final pass of the final cold rolling are set to 18000 or less.
The rolled copper foil is generally processed at high speed under oil lubrication, but the shear band deformation tends to become dominant as the lubricating oil film becomes thinner. This is a phenomenon common to metals in general. Note that the presence of a shear band is not preferable for the growth of crystal grains when annealed. And the some or short depth of a shear band can be represented by the glossiness of the copper foil surface. Specifically, as a phenomenon during rolling, if the oil film introduced between the roll and the material is thick, oil pits (unevenness) are formed on the rolled surface, but if the oil film is thin, it contacts the rolling roll on the material surface. The area increases and free deformation is limited, oil pits do not develop, the smooth surface profile of the rolling roll is transferred, and a smooth surface is formed. Therefore, the oil film equivalent is set to 18000 or less as an index for thinning the oil film. If the oil film equivalent exceeds 18000, the 60 degree glossiness of the copper foil surface will be less than 500%.
油膜当量は下記式で表される。
(油膜当量)={(圧延油粘度、40℃の動粘度;cSt)×(圧延速度;m/分)}/{(材料の降伏応力;kg/mm2)×(ロール噛込角;rad)}
油膜当量を18000以下とするためには、低粘度の圧延油を用いたり、通板速度を遅くしたりする等、公知の方法を用いればよい。
The oil film equivalent is represented by the following formula.
(Oil film equivalent) = {(rolling oil viscosity, kinematic viscosity at 40 ° C .; cSt) × (rolling speed; m / min)} / {(yield stress of material; kg / mm 2 ) × (roll biting angle; rad )}
In order to set the oil film equivalent to 18000 or less, a known method such as using a low-viscosity rolling oil or slowing the sheet passing speed may be used.
上記のような方法により、グラフェン製造用銅箔の60度光沢度を500%以上に制御することができる。又、銅箔の60度光沢度が500%以上になると、焼鈍後の結晶粒径が大きくなりやすいことが判明している。これは、上記した油膜当量や最終冷間圧延中の材料温度を制御し、せん断帯変形を起きにくくすることで、焼鈍後の結晶成長が促進されるためと考えられる。
なお、グラフェン製造用銅箔の60度光沢度を500%以上に制御する方法は上記に限られるものではない。
By the above method, the 60 degree glossiness of the copper foil for producing graphene can be controlled to 500% or more. Further, it has been found that when the 60 ° glossiness of the copper foil is 500% or more, the crystal grain size after annealing tends to increase. This is presumably because crystal growth after annealing is promoted by controlling the oil film equivalent and the material temperature during the final cold rolling to make shear band deformation difficult to occur.
In addition, the method of controlling the 60 degree glossiness of the copper foil for producing graphene to 500% or more is not limited to the above.
<グラフェンの製造方法>
次に、図1を参照し、本発明の実施形態に係るグラフェンの製造方法について説明する。
まず、室(真空チャンバ等)100内に、上記した本発明のグラフェン製造用銅箔10を配置し、グラフェン製造用圧延銅箔10をヒータ104で加熱すると共に、室100内を減圧又は真空引きする。そしてガス導入口102から室100内に炭素含有ガスGを供給する(図1(a))。炭素含有ガスGとしては、一酸化炭素、メタン、エタン、プロパン、エチレン、アセチレン等が挙げられるがこれらに限定されず、これらのうち1種又は2種以上の混合ガスとしてもよい。そしてプラズマ発生装置106で炭素含有ガスGを励起(分解)する。又、グラフェン製造用銅箔10の加熱温度は300℃以上400℃程度とすることができる。
これにより、分解ガス(炭素ガス)がグラフェン製造用銅箔10の表面にグラフェン20を形成する(図1(b))。
<Graphene production method>
Next, with reference to FIG. 1, a method for producing graphene according to an embodiment of the present invention will be described.
First, the graphene producing copper foil 10 of the present invention described above is placed in a chamber (vacuum chamber or the like) 100, the rolled copper foil 10 for producing graphene is heated by the heater 104, and the inside of the chamber 100 is decompressed or evacuated. To do. Then, a carbon-containing gas G is supplied from the gas inlet 102 into the chamber 100 (FIG. 1 (a)). Examples of the carbon-containing gas G include carbon monoxide, methane, ethane, propane, ethylene, acetylene, and the like. However, the carbon-containing gas G is not limited to these, and may be one or two or more mixed gases. The plasma generator 106 excites (decomposes) the carbon-containing gas G. Moreover, the heating temperature of the copper foil 10 for graphene production can be about 300 ° C. or more and about 400 ° C.
Thereby, decomposition gas (carbon gas) forms the graphene 20 on the surface of the copper foil 10 for graphene manufacture (FIG.1 (b)).
そして、グラフェン製造用銅箔10を常温に冷却し、グラフェン20の表面に転写シート30を積層し、グラフェン20を転写シート30上に転写する。次に、この積層体をシンクロール120を介してエッチング槽110に連続的に浸漬し、グラフェン製造用銅箔10をエッチング除去する(図1(c))。このようにして、所定の転写シート30上に積層されたグラフェン20を製造することができる。
さらに、グラフェン製造用銅箔10が除去された積層体を引き上げ、グラフェン20の表面に基板40を積層し、グラフェン20を基板40上に転写しながら、転写シート30を剥がすと、基板40上に積層されたグラフェン20を製造することができる。
And the copper foil 10 for graphene manufacture is cooled to normal temperature, the transfer sheet 30 is laminated | stacked on the surface of the graphene 20, and the graphene 20 is transcribe | transferred on the transfer sheet 30. FIG. Next, this laminated body is continuously immersed in the etching tank 110 through the sink roll 120, and the copper foil 10 for graphene production is removed by etching (FIG. 1C). Thus, the graphene 20 laminated on the predetermined transfer sheet 30 can be manufactured.
Furthermore, when the laminated body from which the copper foil 10 for producing graphene is removed is pulled up, the substrate 40 is laminated on the surface of the graphene 20, and the transfer sheet 30 is peeled off while transferring the graphene 20 onto the substrate 40, The stacked graphene 20 can be manufactured.
転写シート30としては、各種樹脂シート(ポリエチレン、ポリウレタン等のポリマーシート)を用いることができる。グラフェン製造用銅箔10をエッチング除去するエッチング液としては、例えば硫酸溶液、過硫酸ナトリウム溶液、過酸化水素、及び過硫酸ナトリウム溶液又は過酸化水素に硫酸を加えた溶液を用いることができる。又、基板40としては、例えばSi、 SiC、Ni又はNi合金を用いることができる。 As the transfer sheet 30, various resin sheets (polymer sheets such as polyethylene and polyurethane) can be used. As an etching solution for etching and removing the copper foil 10 for producing graphene, for example, a sulfuric acid solution, a sodium persulfate solution, hydrogen peroxide, a sodium persulfate solution, or a solution obtained by adding sulfuric acid to hydrogen peroxide can be used. As the substrate 40, for example, Si, SiC, Ni, or Ni alloy can be used.
<試料の作製>
表1、表2に示す組成の銅インゴットを製造し、熱間圧延を行った後、冷間圧延を行った。その後300〜800℃の温度に設定した焼鈍炉で焼鈍を行った後、冷間圧延を行い、1〜2mm厚の圧延板を得た。この圧延板を300〜800℃の温度に設定した焼鈍炉で焼鈍して再結晶させ,表1、表2に記載の厚み(箔厚)まで圧下率を95.0〜99.8%として最終冷間圧延し、実施例1〜27、比較例1〜10の銅箔を得た。
<Preparation of sample>
A copper ingot having the composition shown in Tables 1 and 2 was manufactured, hot-rolled, and then cold-rolled. Then, after annealing in an annealing furnace set to a temperature of 300 to 800 ° C., cold rolling was performed to obtain a rolled sheet having a thickness of 1 to 2 mm. This rolled sheet is annealed in an annealing furnace set to a temperature of 300 to 800 ° C. and recrystallized, and finally cold-rolled to a thickness (foil thickness) shown in Tables 1 and 2 with a reduction ratio of 95.0 to 99.8%. The copper foil of Examples 1-27 and Comparative Examples 1-10 was obtained.
ここで、最終冷間圧延の最終パスと最終冷間圧延の最終パスの1つ前のパスの両方の油膜当量をいずれも表1、表2に示す値に調整した。
油膜当量は下記式で表される。
(油膜当量)={(圧延油粘度、40℃の動粘度;cSt)×(圧延速度;m/分)}/{(材料の降伏応力;kg/mm2)×(ロール噛込角;rad)}
Here, the oil film equivalents of both the final pass of the final cold rolling and the pass before the final pass of the final cold rolling were adjusted to the values shown in Tables 1 and 2.
The oil film equivalent is represented by the following formula.
(Oil film equivalent) = {(rolling oil viscosity, kinematic viscosity at 40 ° C .; cSt) × (rolling speed; m / min)} / {(yield stress of material; kg / mm 2 ) × (roll biting angle; rad )}
<60度光沢度の測定>
実施例1〜27、比較例1〜10の銅箔について、最終冷間圧延後、及びその後に400℃で10分間加熱した後の表面の60度光沢度を測定した。
60度光沢度は、JIS−Z8741に準拠した光沢度計(日本電色工業製、商品名「PG-1M」)を使用して測定した。
<Measurement of 60 degree glossiness>
About the copper foil of Examples 1-27 and Comparative Examples 1-10, the 60 degree glossiness of the surface after the last cold rolling and after heating for 10 minutes at 400 degreeC was measured.
The 60 degree glossiness was measured using a gloss meter (trade name “PG-1M” manufactured by Nippon Denshoku Industries Co., Ltd.) in accordance with JIS-Z8741.
<表面粗さ(Ra,Rz,Sm)の測定>
実施例1〜27、比較例1〜10の銅箔について、最終冷間圧延後、及びその後に400℃で10分間加熱した後の表面粗さを測定した。
接触粗さ計(小坂研究所製、商品名「SE−3400」)を使用し、JIS−B0601に準拠した算術平均粗さ(Ra;μm)を測定し、オイルピット深さRzはJIS B0601−1994に準拠して十点平均粗さを測定した。測定基準長さ0.8mm、評価長さ4mm、カットオフ値0.8mm、送り速さ0.1mm/秒の条件で圧延方向と平行に測定位置を変えて10回行ない、各方向で10回の測定での値を求めた。また凹凸の平均間隔(Sm;mm)は、測定基準長さ0.8mm、評価長さ4mm、カットオフ値0.8mm、送り速さ0.1mm/秒の条件で圧延方向と平行に測定位置を変えて10回行ない、10回の測定での値を求めた。なお、Smは表面性状を輪郭曲線方式で表すJIS B0601−2001(ISO4287−1997準拠)において、凹凸の「凹凸の平均間隔」と規定されており、基準長さ内での各凹凸の輪郭長さの平均をいう。
<Measurement of surface roughness (Ra, Rz, Sm)>
About the copper foils of Examples 1 to 27 and Comparative Examples 1 to 10, the surface roughness after final cold rolling and after heating at 400 ° C. for 10 minutes was measured.
Using a contact roughness meter (trade name “SE-3400”, manufactured by Kosaka Laboratories), the arithmetic average roughness (Ra; μm) based on JIS-B0601 was measured, and the oil pit depth Rz was JIS B0601-. Ten-point average roughness was measured according to 1994. The measurement position is changed 10 times in parallel with the rolling direction under the conditions of a measurement standard length of 0.8 mm, an evaluation length of 4 mm, a cut-off value of 0.8 mm, and a feed rate of 0.1 mm / second, and 10 times in each direction. The value in the measurement was obtained. In addition, the average interval of unevenness (Sm; mm) is a measurement position parallel to the rolling direction under the conditions of a measurement reference length of 0.8 mm, an evaluation length of 4 mm, a cut-off value of 0.8 mm, and a feed rate of 0.1 mm / second. The measurement was repeated 10 times, and the values for 10 measurements were obtained. Note that Sm is defined as “average interval of unevenness” in JIS B0601-2001 (conforms to ISO 4287-1997) in which the surface property is expressed by a contour curve method, and the contour length of each unevenness within the reference length. The average of
<平均結晶粒径の測定>
実施例1〜27、比較例1〜10の銅箔について、最終冷間圧延後に400℃で10分間加熱した後に、JIS H0501の切断法により、表面の平均結晶粒径を測定した。
<Measurement of average crystal grain size>
About the copper foil of Examples 1-27 and Comparative Examples 1-10, after heating for 10 minutes at 400 degreeC after the last cold rolling, the average crystal grain diameter of the surface was measured by the cutting method of JISH0501.
<グラフェンの製造>
各実施例、各比較例の銅箔(縦横100X100mm)を真空チャンバーに設置し、このチャンバーにメタンガスを供給する(供給ガス流量:10〜100cc/min)と共に、プラズマ発生装置を作動させた。その後、銅箔を400℃まで10分で昇温した後、10分間保持し、銅箔表面にグラフェンを成長させた。
各実施例について、上記条件でグラフェンの製造を10回行い、銅箔表面のグラフェンをPETフィルムに転写した後、4端子法によりグラフェンの抵抗値(シート抵抗:Ω/sq)を測定した。シート抵抗が1000Ω/sqを越えたものを不良とみなし、10回の製造のうち1000Ω/sqを越えた回数により以下の基準で歩留を評価した。評価が◎、○であれば実用上問題はない。
◎:10回の製造のうち、1000Ω/sqを越えた回数が1回以下
○:10回の製造のうち、1000Ω/sqを越えた回数が2回以上4回以下
×:10回の製造のうち、1000Ω/sqを越えた回数が5回以上
<Manufacture of graphene>
The copper foil (100 × 100 mm) in each example and each comparative example was placed in a vacuum chamber, methane gas was supplied to this chamber (supply gas flow rate: 10 to 100 cc / min), and the plasma generator was operated. Then, after heating up copper foil to 400 degreeC in 10 minutes, it hold | maintained for 10 minutes and made the graphene grow on the copper foil surface.
For each example, graphene was produced 10 times under the above conditions, and after the graphene on the surface of the copper foil was transferred to a PET film, the resistance value of the graphene (sheet resistance: Ω / sq) was measured by a four-terminal method. A sheet resistance exceeding 1000Ω / sq was regarded as defective, and the yield was evaluated according to the following criteria based on the number of times exceeding 1000Ω / sq out of 10 productions. If the evaluation is ◎ or ○, there is no practical problem.
A: The number of times exceeding 1000 Ω / sq is 10 times or less in 10 times of manufacture. ○: The number of times exceeding 1000 Ω / sq is 2 times or more and 4 times or less in 10 times of manufacturing. Of which, the number of times exceeding 1000Ω / sq is 5 times or more
得られた結果を表1、表2に示す。なお、表1、表2において、G60RD、G60TDはそれぞれ圧延平行方向及び圧延直角方向の60度光沢度を示す。又、GSは平均結晶粒径を示す。 The obtained results are shown in Tables 1 and 2. In Tables 1 and 2, G60 RD and G60 TD indicate 60 degree glossiness in the rolling parallel direction and the rolling perpendicular direction, respectively. GS represents an average crystal grain size.
表1、表2から明らかなように、銅箔の表面の60度光沢度が500%以上であり、400℃で10分間加熱後の平均結晶粒径が30μm以上である実施例1〜26の場合、グラフェンの製造歩留が優れていた。
特に、400℃で10分間加熱後の平均結晶粒径が120μm以上である実施例3、6、7、8、11、12、14、15、16、17、18、19、20、21、22、23、24、26、27の場合、グラフェンの製造歩留が最も優れていた。
As is apparent from Tables 1 and 2, the 60 degree glossiness of the surface of the copper foil is 500% or more, and the average crystal grain size after heating at 400 ° C. for 10 minutes is 30 μm or more. In the case, the production yield of graphene was excellent.
In particular, Examples 3, 6, 7, 8, 11, 12, 14, 15, 16, 17, 18, 19, 20, 21, 22 having an average crystal grain size of 120 μm or more after heating at 400 ° C. for 10 minutes. , 23, 24, 26, and 27, the graphene production yield was the best.
一方、最終冷間圧延の最終パスと最終冷間圧延の最終パスの1つ前のパスの両方の油膜当量が18000を超え、銅箔自身の表面の60度光沢度が500%未満となった比較例1、2,4〜10の場合、グラフェンの製造歩留が劣った。又、比較例1、2,4〜10の場合、400℃で10分間加熱後の平均結晶粒径が30μm未満となったが、これは、最終冷間圧延の油膜当量が多すぎ、せん断帯が生じて結晶粒の成長が抑制されたためと考えられる。
Agを0.050質量%を超えて含有する比較例3の場合、400℃で10分間加熱後の平均結晶粒径が30μm未満となり、グラフェンの製造歩留が劣った。なお、比較例3の場合、最終冷間圧延の最終パスと最終冷間圧延の最終パスの1つ前のパスの両方の油膜当量を18000以下としたので、銅箔の表面の60度光沢度が光沢度が500%以上となった。
On the other hand, the oil film equivalent of both the final cold rolling final pass and the pass immediately before the final cold rolling pass exceeded 18000, and the 60-degree glossiness of the surface of the copper foil itself was less than 500%. In Comparative Examples 1, 2, 4 to 10, the production yield of graphene was inferior. In the case of Comparative Examples 1, 2, 4 to 10, the average grain size after heating at 400 ° C. for 10 minutes was less than 30 μm. This is because the oil film equivalent of the final cold rolling is too much, and the shear band This is considered to be because the growth of crystal grains was suppressed.
In the case of Comparative Example 3 containing Ag in excess of 0.050 mass%, the average crystal grain size after heating at 400 ° C. for 10 minutes was less than 30 μm, and the graphene production yield was poor. In the case of Comparative Example 3, the oil film equivalent of both the final pass of the final cold rolling and the pass immediately before the final pass of the final cold rolling was set to 18000 or less, so the 60 degree glossiness of the surface of the copper foil However, the glossiness was 500% or more.
2 銅箔基材
4 銅めっき層
10 グラフェン製造用銅箔
20 グラフェン
30 転写シート
2 Copper foil base material 4 Copper plating layer 10 Copper foil for graphene production 20 Graphene 30 Transfer sheet
Claims (5)
所定の室内に、加熱した前記グラフェン製造用銅箔を配置すると共に炭素含有ガスを供給し、前記グラフェン製造用銅箔又は前記銅めっき層の表面にグラフェンを形成するグラフェン形成工程と、
前記グラフェンの表面に転写シートを積層し、前記グラフェンを前記転写シート上に転写しながら、前記グラフェン製造用銅箔をエッチング除去するグラフェン転写工程と、を有するグラフェンの製造方法。 It is a manufacturing method of graphene in 300 ° C or more and 400 ° C or less using the copper foil for graphene manufacture in any one of Claims 1-4,
A graphene forming step of arranging the heated copper foil for producing graphene in a predetermined chamber and supplying a carbon-containing gas, and forming graphene on the surface of the copper foil for producing graphene or the copper plating layer,
A graphene transfer process comprising: laminating a transfer sheet on the surface of the graphene; and transferring the graphene onto the transfer sheet while etching and removing the copper foil for producing graphene.
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JP2016003339A (en) * | 2014-06-13 | 2016-01-12 | Jx日鉱日石金属株式会社 | Rolled copper foil for production of two-dimensional hexagonal lattice compound and production method of two-dimensional hexagonal lattice compound |
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010227971A (en) * | 2009-03-27 | 2010-10-14 | Nippon Mining & Metals Co Ltd | Rolled copper foil |
WO2011046415A2 (en) * | 2009-10-16 | 2011-04-21 | 성균관대학교산학협력단 | Roll-to-roll transfer method of graphene, graphene roll produced by the method, and roll-to-roll transfer equipment for graphene |
JP2012183581A (en) * | 2011-02-18 | 2012-09-27 | Jx Nippon Mining & Metals Corp | Copper foil for graphene production and graphene production method using the same |
JP2012183583A (en) * | 2011-02-18 | 2012-09-27 | Jx Nippon Mining & Metals Corp | Copper foil for graphene production and graphene production method using the same |
WO2013065601A1 (en) * | 2011-11-04 | 2013-05-10 | Jx日鉱日石金属株式会社 | Copper foil for graphene production and production method therefor, and graphene production method |
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CN101760724B (en) * | 2010-01-26 | 2011-10-12 | 电子科技大学 | Method for preparing graphene membrane electrode with overlarge area and high quality |
WO2013065301A1 (en) * | 2011-10-31 | 2013-05-10 | 株式会社Jvcケンウッド | Video coding device, video coding method, video coding program, transmission device, transmission method, and transmission program, as well as video decoding device, video decoding method, video decoding program, reception device, reception method, and reception program |
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Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010227971A (en) * | 2009-03-27 | 2010-10-14 | Nippon Mining & Metals Co Ltd | Rolled copper foil |
WO2011046415A2 (en) * | 2009-10-16 | 2011-04-21 | 성균관대학교산학협력단 | Roll-to-roll transfer method of graphene, graphene roll produced by the method, and roll-to-roll transfer equipment for graphene |
JP2012183581A (en) * | 2011-02-18 | 2012-09-27 | Jx Nippon Mining & Metals Corp | Copper foil for graphene production and graphene production method using the same |
JP2012183583A (en) * | 2011-02-18 | 2012-09-27 | Jx Nippon Mining & Metals Corp | Copper foil for graphene production and graphene production method using the same |
WO2013065601A1 (en) * | 2011-11-04 | 2013-05-10 | Jx日鉱日石金属株式会社 | Copper foil for graphene production and production method therefor, and graphene production method |
Non-Patent Citations (1)
Title |
---|
JPN6015041592; LUO, Z. et al.: 'Effect of Substrate Roughness and Feedstock Concentration on Growth of Wafer-Scale Graphene at Atmos' Chem.Mater. Vol.23, No.6, 20110210, p. 1441-1447 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2015013797A (en) * | 2013-06-07 | 2015-01-22 | 独立行政法人産業技術総合研究所 | Manufacturing method of graphene transparent conductive film and graphene transparent conductive film manufactured therewith |
JP2016003339A (en) * | 2014-06-13 | 2016-01-12 | Jx日鉱日石金属株式会社 | Rolled copper foil for production of two-dimensional hexagonal lattice compound and production method of two-dimensional hexagonal lattice compound |
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