WO2012002380A1 - 電解銅箔、リチウムイオン二次電池用電解銅箔、該電解銅箔を用いたリチウムイオン二次電池用電極、該電極を使用したリチウムイオン二次電池 - Google Patents
電解銅箔、リチウムイオン二次電池用電解銅箔、該電解銅箔を用いたリチウムイオン二次電池用電極、該電極を使用したリチウムイオン二次電池 Download PDFInfo
- Publication number
- WO2012002380A1 WO2012002380A1 PCT/JP2011/064797 JP2011064797W WO2012002380A1 WO 2012002380 A1 WO2012002380 A1 WO 2012002380A1 JP 2011064797 W JP2011064797 W JP 2011064797W WO 2012002380 A1 WO2012002380 A1 WO 2012002380A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- copper foil
- lithium ion
- secondary battery
- ion secondary
- active material
- Prior art date
Links
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/66—Selection of materials
- H01M4/661—Metal or alloys, e.g. alloy coatings
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D3/00—Electroplating: Baths therefor
- C25D3/02—Electroplating: Baths therefor from solutions
- C25D3/38—Electroplating: Baths therefor from solutions of copper
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D7/00—Electroplating characterised by the article coated
- C25D7/06—Wires; Strips; Foils
- C25D7/0614—Strips or foils
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
- H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
- H01M4/134—Electrodes based on metals, Si or alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/38—Selection of substances as active materials, active masses, active liquids of elements or alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/66—Selection of materials
- H01M4/661—Metal or alloys, e.g. alloy coatings
- H01M4/662—Alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/70—Carriers or collectors characterised by shape or form
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Definitions
- the present invention relates to an electrolytic copper foil.
- the present invention also provides a lithium ion secondary battery comprising a positive electrode, a negative electrode having a negative electrode current collector formed on the surface of the negative electrode current collector, and a non-aqueous electrolyte. And an electrolytic copper foil for a lithium secondary battery current collector constituting the current collector of the electrode.
- a lithium ion secondary battery comprising a positive electrode and a negative electrode current collector made of copper foil having a smooth surface, coated with carbon particles as a negative electrode active material layer, further pressed, and a non-aqueous electrolyte is currently a mobile phone. It is used for notebook type personal computers.
- a so-called “untreated electrolytic copper foil” manufactured by electrolysis is subjected to a rust prevention treatment.
- the electrolytic copper foil with a small difference in surface roughness between the glossy surface and the rough surface as described above is suitable for various electrolytes such as various water-soluble polymer substances, various surfactants, various organic sulfur compounds, and chloride ions.
- Manufactured by selecting and adding For example, a method for producing an electrolytic copper foil using a compound having a mercapto group added to an electrolytic solution, chloride ions, a low molecular weight glue having a molecular weight of 10,000 or less, and a high molecular weight polysaccharide is disclosed. (See Patent Document 2)
- the electrolytic copper foil produced by the above production method is coated with carbon particles on the surface of the copper foil and further pressed to form a negative electrode.
- lithium has been used as a negative electrode active material in the form of powder (primary particles), such as germanium, silicon, and tin, which are electrochemically alloyed with lithium during charging, in order to increase the capacity of lithium ion secondary batteries.
- primary particles such as germanium, silicon, and tin
- An ion secondary battery has been proposed (see Patent Document 3).
- An electrode (negative electrode) for a lithium ion secondary battery for the purpose of increasing the capacity is obtained by depositing, for example, silicon on an amorphous silicon thin film or microcrystalline silicon thin film on a current collector such as a copper foil by CVD or sputtering. As it is deposited and formed. Since the thin film layer of the active material prepared by such a method is in close contact with the current collector, it has been found that it exhibits good charge / discharge cycle characteristics (see Patent Document 4).
- Patent Document 6 discloses that the carbon-based active material is composed of secondary particles obtained by applying amorphous carbon to the surface of crystalline carbon primary particles.
- Patent Document 7 proposes an active material composed of secondary particles in which silicon, tin, and copper are mixed to form a melt alloy, which is then pulverized and composited with carbon.
- the active material consisting of secondary particles is granulated into a single aggregate of primary particles by a spray dryer method, in which the thickener, conductive additive and binder (binder) are precisely mixed with the primary active material. ing.
- the secondary particles are mixed with the binder, the thickener or the conductive auxiliary agent, so that the expansion of the primary particles occurs in the aggregate (secondary particles), and the aggregate (secondary particles) It is characterized by a small volume change because it is absorbed inside.
- these secondary particles as an active material, it is said that the phenomenon that the active material is miniaturized during the charge / discharge action (described later) and the current collecting function is reduced can be suppressed.
- Patent Documents 6 and 7, etc. a detailed examination is not made on a current collector that is compatible with a secondary processed active material, that is, a copper foil.
- These secondary processing active materials are easy to apply because the shape of the particles is large, but have a disadvantage of being inferior in productivity because a complicated process for forming secondary particles is added.
- the active material absorbs lithium ions during charging as a battery, so that the volume expands up to about 4 times and discharges lithium ions during discharging. Shrink. Therefore, a phenomenon in which the active material is pulverized and peeled off from the current collector due to expansion and contraction of the active material layer volume accompanying charging / discharging is observed. Further, since the active material layer is in close contact with the current collector, there is a problem that a large stress is applied to the current collector when the volume of the active material layer expands and contracts due to repeated charge and discharge.
- the active material consisting of primary particles such as silicon and tin has a small particle size, it is difficult to apply a uniform thickness and good adhesion when applied in a slurry form on the negative electrode current collector. It is. In particular, if the current collector has a large difference in surface roughness, it becomes more difficult to apply the active material to the front and back surfaces with a uniform thickness, which adversely affects the output characteristics and cycle characteristics of the battery.
- the present invention relates to a lithium ion secondary battery using a negative electrode in which an active material mainly composed of silicon, germanium, or tin, for example, is deposited on a current collector, and the current collector is free from wrinkles.
- an active material mainly composed of silicon, germanium, or tin for example, is deposited on a current collector, and the current collector is free from wrinkles.
- the electrolytic copper foil of the present invention is provided with an uneven surface roughening layer of copper or copper alloy having a particle size of 3 ⁇ m or less by roughening treatment by electrolytic plating on both surfaces of the untreated copper foil,
- the surface roughness Rz of the roughened layer is 1.0 to 5 ⁇ m, or Ra is 0.25 to 0.7 ⁇ m, and the difference between the front and back surface roughness Rz is within 3 ⁇ m, or the difference in Ra is within 0.3 ⁇ m. It is an electrolytic copper foil.
- the untreated copper foil is a copper foil made of granular crystals.
- the roughening copper alloy is preferably Cu, the main component of which is Mo, Fe, Ni, Co, W, As, Zn, or an alloy containing one or more thereof.
- the electrolytic copper foil for a lithium ion secondary battery of the present invention is provided with an uneven surface roughening treatment layer of copper or copper alloy having a particle size of 3 ⁇ m or less by roughening treatment by electrolytic plating on both surfaces of the untreated copper foil.
- the surface roughness Rz of the rough surface treatment layer on both surfaces is 1.0 to 5 ⁇ m, or Ra is 0.25 to 0.7 ⁇ m, and the difference in roughness Rz between the front and back surfaces is within 3 ⁇ m, or Ra It is an electrolytic copper foil for a lithium ion secondary battery having a difference within 0.3 ⁇ m.
- the electrolytic copper foil for lithium ion secondary batteries of this invention is an uneven surface roughening process layer which consists of copper or a copper alloy whose particle size is 3 micrometers or less by the roughening process by electrolytic plating on both surfaces of untreated copper foil.
- the surface roughness Rz of the both roughened surface treatment layers is 1.0 to 5 ⁇ m, or Ra is 0.25 to 0.7 ⁇ m, and the difference between the front and back surface roughness Rz is within 3 ⁇ m, or Ra
- the difference between the convex surfaces of adjacent rough surfaces is larger than the average particle size of the primary particles of the lithium ion secondary battery, and the average active material for the lithium ion secondary battery electrode It is the electrolytic copper foil for lithium ion secondary batteries characterized by being smaller than or equal to a particle size.
- the surface area ratio after the roughening treatment is preferably 2 to 6 times.
- the active material deposited on the surface of the electrolytic copper foil for lithium ion secondary batteries is a primary particle of silicon, germanium, tin, or an alloy compound thereof, or secondary particles obtained by processing the primary particles. It is.
- the lithium ion secondary battery of the present invention is a lithium ion secondary battery using the electrode for a lithium ion secondary battery as an electrode.
- the electrolytic copper foil or the electrolytic copper foil for a lithium ion secondary battery of the present invention when the copper foil is used as a current collector, wrinkles and the like can be prevented from being generated by charging and discharging.
- Lithium ion secondary that can increase the energy density per volume of the secondary battery, and does not break the current collector (copper foil), and has high adhesion between the active material and the current collector for long periods of time.
- a battery electrode and a lithium ion secondary battery can be provided.
- the lithium ion secondary battery of the present invention uses the electrolytic copper foil for the negative electrode of the battery, the current collector does not generate wrinkles or the like due to charge / discharge, and the energy density per volume of the lithium ion secondary battery is reduced. In addition, since the current collector is not broken and the adhesion between the active material and the current collector is high, a lithium ion secondary battery having stable performance for a long time can be provided.
- the electrolytic copper foil of the present invention or the electrolytic copper foil for a lithium ion secondary battery is subjected to an uneven surface roughening treatment made of copper or a copper alloy having a particle size of 3 ⁇ m or less by electrolytic plating on both surfaces of the untreated electrolytic copper foil. Is done.
- the surface of the untreated copper foil is roughened by electrolytic plating, particles are deposited and grown in a dendritic shape on the surface of the untreated copper foil. Then, the surface of the electrolytic plating deposited and grown in this dendritic form is overlaid, and at this time, if the size of the copper or copper alloy particles is 3 ⁇ m or more, Rz of the roughened surface is 5 ⁇ m, or Ra is 0.1.
- the size of the particle to be roughened is preferably as fine as possible.
- the size of particles deposited by electrolytic plating is 3 ⁇ m or less.
- the particles are deposited and grown in a dendritic shape on the surface of the untreated copper foil, and when the next step is overlaid, Rz is 1 ⁇ m to 5 ⁇ m, or Ra is 0.25 ⁇ m to 0
- the surface becomes 0.7 ⁇ m, the adhesiveness between the copper foil (current collector) and the active material is good, and the cycle characteristics of the battery can be improved.
- the surface roughness of the roughened surface of the electrolytic copper foil of the present invention is 1.0 to 5 ⁇ m for Rz, or 0.25 to 0.7 ⁇ m for Ra, and the difference between the surface roughness Rz is within 3 ⁇ m. Or the difference of Ra is within 0.3 ⁇ m.
- Rz is 1.0 to 5 ⁇ m, or Ra is 0.25 to 0.7 ⁇ m, and the difference between the front and back roughness Rz is within 3 ⁇ m, or the difference in Ra is within 0.3 ⁇ m This is because the roughening improves the adhesion to the active material and absorbs the volume change accompanying the expansion and contraction of the battery by the space generated by the roughening.
- the electrolytic copper foil of the present invention exhibits an excellent effect as a current collector for a lithium ion secondary battery.
- the electrolytic copper foil should be used for applications with severe expansion and contraction other than the current collector for a lithium ion secondary battery. Of course you can.
- an example in which the electrolytic copper foil is used as a current collector for a lithium ion secondary battery will be described below.
- the untreated copper foil is preferably made of granular crystals. Because the untreated copper foil is a granular crystal, the difference in roughness between both surfaces in the state of the untreated copper foil can be reduced, and the difference in roughness after the roughening treatment can be further reduced. . This is because when the untreated copper foil is made of columnar crystals, the difference in roughness between both surfaces in the state of the untreated copper foil becomes large, and it is difficult to eliminate the difference even after the roughening treatment.
- the roughening treatment is preferably formed from Mo, Fe, Ni, Co, W, As, Zn, or an alloy containing one or more of them containing Cu as a main component.
- the copper foil is untreated and has a surface roughness of 0.8 to 2.0 ⁇ m.
- the crystal structure at room temperature is a granular crystal structure having a crystal grain size of 5 ⁇ m or less, and the tensile strength is 300 N at room temperature.
- An electrolytic copper foil having an elongation of / mm 2 or more, an elongation of 4.0% or more, and a tensile strength after 150 ° C. ⁇ 15 hours of 250 N / mm 2 or more is preferable.
- the tensile strength of the foil decreases and the elongation tends to increase.
- germanium, silicon, tin, etc. are used for the negative electrode active material, if the foil strength is low, the current collector can absorb the expansion and contraction of the battery regardless of the roughening treatment. Without breaking the foil.
- the tensile strength is preferably 300 N / mm 2 or more and the elongation is about 4.0% or more, and the crystal grain size at that time is preferably 5 ⁇ m or less.
- the negative electrode current collector for a lithium ion secondary battery has a drying step in the manufacturing process, and if this drying is insufficient, the characteristics of the battery deteriorate.
- the drying conditions at this time are generally about 100 to 200 ° C. and about 5 to 20 hours. At this time, if the copper foil as the current collector is softened, the foil breaks during charge / discharge as described above, so the strength of the foil after drying is also an important factor.
- the additive concentration in the electrolyte during the production of the untreated copper foil is MPS (3-mercapto 1-propanesulfonic acid sodium): 3 to 10 ppm, HEC ( Hydroxyethyl cellulose / polymer polysaccharide): 15 to 20 ppm, glue: 30 to 70 ppm.
- the surface area ratio after the roughening treatment is preferably 2 to 6 times.
- the surface area ratio is obtained by measuring an area of 50 ⁇ m ⁇ 50 ⁇ m using VK-8500 manufactured by KEYENCE, and expressing this value as a ratio around 2500 ⁇ m 2 . That is, a product having a surface area ratio of 1 is completely smooth, and if it is 5000 ⁇ m 2 , the surface area ratio is doubled.
- the roughness Rz of both surfaces of the untreated copper foil on the surface (glossy surface or S surface) in contact with the titanium roll (cathode) and the surface in contact with the electrolyte (matt surface or M surface) is 0.
- a low one of 8 ⁇ m to 2.0 ⁇ m is adopted, and the untreated copper foil is subjected to a roughening treatment.
- roughened particles having a particle diameter of 0.1 to 3 ⁇ m are used to form a roughened surface with Rz of 1.0 to 5 ⁇ m or Ra of 0.25 to 0.7 ⁇ m by subsequent overplating.
- the surface area ratio can be made 2 to 6 times. When the surface area ratio is 2 times or less, the contact area of the active material is extremely reduced, and as a battery, heat is generated and deterioration is accelerated. The larger the surface area, the larger the contact area with the active material layer and the lower the interface resistance.
- the current collector has a large surface area.
- the surface area ratio exceeds six times, the Rz of the roughened surface becomes too large, and as a result, the active material layer reaches the depth (bottom) of the roughened (unevenness). It does not reach, and a gap is formed between the copper foil and the active material layer, the adhesion is poor, the electrical conductivity is lowered, the battery is heated, and the battery is rapidly deteriorated.
- the tensile strength and elongation are values measured by a method defined in Japanese Industrial Standard (JIS K 6251).
- the surface roughnesses Rz and Ra are a ten-point average roughness and an arithmetic surface roughness defined in Japanese Industrial Standards (JIS B 0601-1994), for example, values measured with a surface roughness meter.
- the untreated copper foil used for the electrolytic copper foil for a lithium ion secondary battery of the present invention comprises an insoluble anode made of titanium coated with a white metal element or an oxide element thereof, using an aqueous solution of sulfuric acid and copper sulfate as an electrolyte, and the anode. Copper is deposited on the surface of the cathode drum by supplying a direct current between both electrodes while supplying the electrolyte solution to a titanium cathode drum provided oppositely and rotating the cathode drum at a constant speed. In this case, the deposited copper is peeled off from the surface of the cathode drum and continuously wound.
- the untreated copper foil used for the electrolytic copper foil for the lithium ion secondary battery of the present invention is composed of a compound having a mercapto group in a sulfuric acid-copper sulfate electrolytic solution, chloride ions, and a low molecular weight glue and a high molecular weight polysaccharide having a molecular weight of 10,000 kg or less. It can manufacture by adding.
- the surface of the untreated electrolytic copper foil is roughened.
- an electrolytic plating method can be suitably employed.
- the electrolytic plating method is a method of roughening the surface by forming a thin film layer having irregularities on the surface of the untreated electrolytic copper foil.
- a plating film mainly composed of copper such as copper or copper alloy is formed on the surface of the untreated electrolytic copper foil by electrolytic plating.
- a method for roughening the surface of the untreated electrolytic copper foil by electrolytic plating for example, disclosed in Patent Document 5 (Japanese Patent Publication No. 53-39376) is used by plating used for copper foils for printed circuits.
- a roughening method is preferably used. That is, after forming a granular copper plating layer by so-called “bake plating”, “cover plating” is performed on the granular copper plating layer so as not to impair the uneven shape, thereby substantially smoothing.
- a plated layer is deposited to make the granular copper into a so-called bumpy copper layer.
- an uneven surface roughening treatment layer made of copper or a copper alloy having a particle size of 0.1 ⁇ m to 3 ⁇ m is provided on both surfaces of the untreated copper foil by a roughening treatment by electrolytic plating.
- the distance between adjacent convex tips of the rough surface is smaller than or equal to the average particle diameter of the active material described later.
- the distance between the convex tips adjacent to each other on the rough surface can be adjusted to the particle size of the active material to be used by arbitrarily adjusting the treatment time or current density of “cover plating”.
- the active material layer in the present invention is a material that occludes / releases lithium, and is preferably an active material that occludes lithium by alloying.
- Examples of such an active material include silicon, germanium, tin, lead, zinc, magnesium, sodium, aluminum, potassium, and indium.
- silicon, germanium, and tin are preferably used because of their high theoretical capacity.
- the active material layer used in the present invention is preferably a layer containing silicon, germanium or tin as a main component, and particularly preferably a layer containing silicon as a main component.
- the active material layer in the present invention may be composed of primary particles composed of particles of the active material metal or its alloy itself, or may be composed of secondary particles processed into, for example, a spherical shape with the primary particles as the main component.
- the active material is preferably amorphous or microcrystalline.
- the primary particles are particularly preferably amorphous silicon or microcrystalline silicon.
- the active material layer in the present invention can be formed by a CVD method, a sputtering method, a vapor deposition method, a thermal spraying method, or a plating method when formed as a thin film.
- CVD method a chemical vapor deposition method
- a thermal spraying method a plating method when formed as a thin film.
- the active material is formed into a slurry together with a binder and a solvent, and is applied to the surface of a current collector (copper foil), dried and pressed.
- a current collector copper foil
- the current collector is preferably thin, and therefore is preferably a metal foil, particularly an electrolytic copper foil.
- the active material layer can be formed by being deposited on one side or both sides of the current collector.
- the surface roughness Rz on both sides of the current collector is 1.0 to 5 ⁇ m, or Ra is 0.25 to 0.7 ⁇ m, and both surfaces It is preferable that the difference in roughness (Rz) of (front and back) is within 3 ⁇ m, or the difference in Ra is within 0.3 ⁇ m.
- the thickness of the current collector is preferably about 8 ⁇ m for a thin one and about 20 ⁇ m for a thick one. This is because if the thickness is 8 ⁇ m or less, the strength of the foil cannot be maintained, and breakage occurs when the active material expands or contracts. On the other hand, if the thickness exceeds 20 ⁇ m, the battery characteristics can be satisfied, but the battery itself is large and heavy. When the Ra and Rz values are below the lower limit, the adhesion due to the anchor effect with the active material is poor. On the other hand, when the upper limit is exceeded, the active material layer does not enter the depth of the roughening, Adhesion is poor.
- the thickness of the active material will differ on both sides in the process of applying the active material to the surface of the copper foil (current collector), which will adversely affect the characteristics of the finished electrode. As much as possible, make sure there is no difference in roughness between the front and back sides.
- FIG. 1 is an enlarged schematic view of a cross section of a negative electrode showing an embodiment of the present invention.
- Electrolytic copper in which a roughened layer 2 composed of a brushed layer 2a and a covering layer 2b is provided on the surface of an untreated copper foil 1.
- An active material layer 20 is deposited on the foil 10.
- the electrolytic copper foil 10 having the roughening layer 2 for the negative electrode has a concave opening 3 in the roughening layer 2 (protrusions 4, 4 adjacent to the roughening of the roughening layer). Is formed larger than the average particle diameter of the particles 211 of the active material 21.
- a mixture of silicon (SiO), acetylene black, PVDF (polyvinylidene fluoride), and NMP (N-methyl-2-pyrrolidone) as a primary particle active material is applied to a current collector and dried.
- the binder 22 and the fine particle active material (smaller than the average particle size) enter the recess opening 3 into the recess opening 3 of the roughening treatment layer 2 by chiller coating, drying, and pressing, and the active material having large particles Are deposited across the protrusions 4.
- the active material 21 on the convex portion 4 of the roughened layer is attracted to the roughened layer convex portion 4 of the copper foil 10 to contribute to adhesion, and the active material 21 and the copper foil 10 conductivity and contributes to improvement of battery characteristics.
- the active material entering the opening 3 has a small particle diameter, its expansion and contraction is absorbed by the elongation of the copper foil and the binder, and the influence on the copper foil is suppressed to a small level.
- the secondary-processed active material is applied to the current collector together with the slurry or the like, dried, pressed and deposited, the secondary active material 212 straddles the convex portions 4 and 4 of the roughened layer as described above.
- the active material 212 is attracted to the roughened layer protrusion 4 of the copper foil 10 and contributes to adhesion, and contributes to the conductivity of the active material 21 and the copper foil 10 and the improvement of battery characteristics. . Further, the active material 211 having a small particle size separated from the active material that has become secondary particles enters the opening 3, but the active material 211 has a small particle diameter, so that its expansion and contraction is caused by the elongation of the copper foil and the binder. And the influence on the copper foil is kept small.
- lithium may be occluded or added in advance.
- Lithium may be added when forming the active material layer. That is, an active material layer containing lithium is formed in advance on the current collector surface. Further, after forming the active material layer, lithium may be occluded or added to the active material layer. Examples of a method for inserting or adding lithium into the active material layer include a method for electrochemically inserting or adding lithium.
- a lithium ion secondary battery of the present invention comprises a negative electrode comprising the lithium ion secondary battery electrode of the present invention, a positive electrode using a material that absorbs and releases lithium as an active material, and a nonaqueous electrolyte. .
- the nonaqueous electrolyte used in the lithium ion secondary battery of the present invention is an electrolyte in which a solute is dissolved in a solvent.
- the solvent for the non-aqueous electrolyte is not particularly limited as long as it is a solvent used for lithium ion secondary batteries.
- cyclic carbonates such as ethylene carbonate, propylene carbonate, butylene carbonate, vinylene carbonate, dimethyl carbonate, diethyl carbonate
- chain carbonates such as methyl ethyl carbonate.
- a mixed solvent of a cyclic carbonate and a chain carbonate is used.
- a mixed solvent of the above cyclic carbonate and an ether solvent such as 1,2-dimethoxyethane or 1,2-diethoxyethane, or a chain ester such as ⁇ -butyrolactone, sulfolane, or methyl acetate may be used. Good.
- the solute of the nonaqueous electrolyte is not particularly limited as long as it is a solute used for a lithium ion secondary battery.
- LiPF 6 , LiBF 4 , LiCF 3 SO 3 , LiN (CF 3 SO 2 ) 2 , LiN (C 2 F 5 SO 2 ) 2 , LiN (CF 3 SO 2 ) (C 4 F 9 SO 2 ), LiC (CF 3 SO 2 ) 3 , LiC (C 2 F 5 SO 2 ) 3 , LiAsF 6 examples thereof include LiClO 4 , Li 2 B 10 Cl 10 , and Li 2 B 12 Cl 12 .
- LiXFy (wherein X is P, As, Sb, B, Bi, Al, Ga, or In, y is 6 when X is P, As, or Sb, and X is B, Bi, Al) , Ga, or In, y is 4.) and lithium perfluoroalkylsulfonic acid imide LiN (C m F 2m + 1 SO 2 ) (C n F 2n + 1 SO 2 ), where m and n Are each independently an integer of 1 to 4.) or lithium perfluoroalkylsulfonic acid methide LiC (C p F 2p + 1 SO 2 ) (C q F 2q + 1 SO 2 ) (C r F 2r + 1 SO 2 ) (wherein p, q and r are each independently an integer of 1 to 4).
- a mixed solute of LiPF 6 and LiN (C 2 F 5 SO 2 ) 2 is particularly preferably used.
- a gel polymer electrolyte obtained by impregnating a polymer electrolyte such as polyethylene oxide, polyacrylonitrile, or polyvinylidene fluoride with an electrolytic solution, or an inorganic solid electrolyte such as LiI or Li 3 N can be used.
- a polymer electrolyte such as polyethylene oxide, polyacrylonitrile, or polyvinylidene fluoride
- an electrolytic solution or an inorganic solid electrolyte such as LiI or Li 3 N
- the electrolyte of the lithium ion secondary battery of the present invention is limited as long as the Li compound as a solute that develops ionic conductivity and the solvent that dissolves and retains it are not decomposed by the voltage at the time of charging, discharging or storing the battery. Can be used without any problem.
- lithium-containing transition metal oxides such as LiCoO 2 , LiNiO 2 , LiMn 2 O 4 , LiMnO 2 , LiCo 0.5 Ni 0.5 O 2 , LiNi 0.7 Co 0.2 Mn 0.1 O 2
- metal oxides such as MnO 2 that do not contain lithium.
- any substance that can occlude and release lithium electrochemically can be used without limitation.
- the current collector can be prevented from wrinkling or breaking due to charge / discharge, the energy density per volume of the lithium ion secondary battery is increased, and stable performance is maintained for a long time.
- a lithium ion secondary battery can be provided.
- chloride ion concentrations were adjusted to 30 ppm, the chloride ion concentration is appropriately changed depending on the electrolysis conditions, and is not limited to this concentration.
- a noble metal oxide-coated titanium electrode for the anode, and a titanium rotating drum for the cathode, and 10 ⁇ m thick untreated copper under the electrolysis conditions (current density, liquid temperature) shown in Table 1 The foil was produced by an electrolytic foil method. Table 2 shows the performance of the prepared copper foil.
- the thickness is a value measured with a micrometer
- the tensile strength and the elongation are values measured using a tensile tester (type 1122 manufactured by Instron).
- the surface roughness Ra, Rz was measured with a stylus type surface roughness meter (SE-3C type manufactured by Kosaka Laboratory).
- Cover plating (dense copper plating) conditions Copper sulfate 200g / L Sulfuric acid 90 ⁇ 130g / L Liquid temperature 30-60 °C Current density 10-30A / dm 2 Treatment time 2 to 20 seconds * Additive: An alloy containing one or more of Mo, Fe, Ni, Co, W, As, and Zn.
- the surface roughness Ra, Rz, Sm, the diameter of the roughened particles, and the surface area of the roughened surface after the roughening treatment were measured by the above-described measuring methods. was measured from the SEM image.
- the silicon (SiO) electrode is prepared by mixing silicon (SiO), acetylene black, PVDF (polyvinylidene fluoride), and NMP (N-methyl-2-pyrrolidone) on the current collectors X1 to X4 and Y3 to Y6. The slurry was applied, dried and pressed.
- a three-electrode beaker cell was prepared in a glove box under an argon gas atmosphere.
- the beaker cell was constructed by immersing a counter electrode, a working electrode, and a reference electrode in an electrolytic solution placed in a glass container.
- an electrolytic solution an electrolytic solution in which 1 mol / liter of LiPF 6 was dissolved in a solvent in which ethylene carbonate and diethyl carbonate were mixed at a volume ratio of 3: 7 was used.
- Lithium metal was used as the counter electrode and the reference electrode.
- Comparative Examples 1 and 2 used the same untreated copper foil as in Example 1, but both the differences in roughness Ra and Rz on both sides in the roughening treatment were large, and thus the discharge capacity after 100 cycles of charge / discharge efficiency. The retention rate was not satisfactory.
- Comparative Example 3 the same untreated copper foil as in Example 7 was used. However, since the difference in roughness Ra after roughening was large and the surface area was large, the discharge capacity retention after 100 cycles of charge / discharge efficiency could not be satisfied. It became a thing.
- Comparative Examples 4 to 6 since the crystal structure of the untreated copper foil was columnar, both the roughness Ra and Rz after the roughening were large, and the evaluation of the charge / discharge cycle characteristics in the beaker cell battery was all unsatisfactory. .
- Comparative Example 7 as in Comparative Example 4, the crystal structure of the untreated copper foil was columnar, and the surface area after the roughening treatment was large. Therefore, the evaluation of the charge / discharge cycle characteristics in the beaker cell battery was all unsatisfactory. It was.
- Comparative Example 8 the crystal grain size of the untreated copper foil was large, and the current collector after repeated charge and discharge for 300 cycles was broken.
- the present invention it is possible to suppress the occurrence of deformation such as wrinkles and breakage of the current collector due to charge and discharge by performing a roughening treatment on both sides of the copper foil and eliminating the difference in shape between both sides. It is possible to provide a lithium ion secondary battery that can increase the energy density per volume of the secondary battery and can be downsized with a long lifetime that does not cause a decrease in capacity even after repeated charge and discharge cycles.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Cell Electrode Carriers And Collectors (AREA)
- Battery Electrode And Active Subsutance (AREA)
Abstract
Description
また、本発明は正極と、表面が凹凸状に形成された負極集電体の表面に負極活物質層が形成された負極と、非水電解質とを備えるリチウムイオン二次電池、該二次電池に用いる電極、ならびに該電極の集電体を構成するリチウム二次電池集電体用電解銅箔に関するものである。
例えば、電解液にメルカプト基を持つ化合物、塩化物イオン、並びに分子量10000 以下の低分子量膠及び高分子多糖類を添加したものを用いた電解銅箔の製造方法が開示されている。(特許文献2参照)
上記製造方法で製造した電解銅箔は、その銅箔の表面にカーボン粒子が塗布され、さらにプレスされて負極電極とされる。
二次粒子からなる活物質は一次活物質に増粘剤、導電助剤とバインダー(結合剤)を精密に混合して、スプレードライヤー法で、一つの一次粒子の集合体となるよう造粒されている。このように二次粒子は、結合剤、増粘剤または導電助剤が混合されることで、一次粒子の膨張は集合体(二次粒子)の中で起こり、集合体(二次粒子)の中で吸収されるので体積変化が少ないことが特徴である。この二次粒子を活物質として採用することで(後述する)充放電作用中に活物質が微細化して集電機能が低下する現象を抑制できる、とされている。しかし、この特許文献6、7等には、二次加工した活物質に適合する集電体、即ち、銅箔については詳細な検討がなされていない。
これらの二次加工活物質は粒子の形状が大きくなるだけに塗布工程は容易になるが、二次粒子とするための複雑な工程が付加されるため、生産性に劣る欠点がある。
従って充放電に伴う活物質層体積の膨張及び収縮により、活物質が微粉化して集電体から剥離する現象が見られる。
また該活物質層が集電体と密着しているため、充放電の繰り返しにより活物質層の体積が膨張及び収縮すると、集電体に大きな応力が働くといった問題があった。
集電体にしわなどの変形が生じると、電池内における負極電極の占める体積が大きくなり、体積当りのエネルギー密度が低下する。また、集電体に破断が起こると長時間安定した電池性能を維持することができなくなる。
未処理銅箔の表面に電解めっきで凹凸粗面化処理を施すと、未処理銅箔の表面に粒子が樹枝状に堆積、成長する。次いでこの樹枝状に堆積、成長した電解めっき表面に被せめっきを施すが、この時銅または銅合金粒子の大きさが3μm以上であると、粗化処理面のRzが5μm、またはRaが0.7μmを超えてしまい、この面に活物質を堆積しても、銅箔(集電体)と活物質との密着性が悪く、電池の劣化を早めるため、好ましくないためである。なお、粗化処理する粒子の大きさは細かいほど好ましい。しかし、現実では銅または銅合金粒子を粒径0.1μm以下に細かくすることは困難である。
本発明では電解めっきで堆積する粒子の大きさを3μm以下としている。堆積する粒子の大きさを3μm以下として未処理銅箔表面に該粒子を樹枝状に堆積、成長させ、次工程で被せめっきを施すと、Rzが1μm~5μm、またはRaが0.25μm~0.7μmの表面となり、銅箔(集電体)と活物質との密着性が良く、電池のサイクル特性を向上することができる。
前記乾燥条件下での再結晶を抑制するためには、未処理銅箔製造時の電解液中の添加剤濃度が、MPS(3-メルカプト1-プロパンスルホン酸ナトリウム):3~10ppm、HEC(ヒドロキシエチルセルロース・高分子多糖類):15~20ppm、膠:30~70ppmであることが好ましい。
本発明では、チタンロール(カソード)に接していた面(光沢面またはS面)と電解液に接していた面を(マット面またはM面)における未処理銅箔の両面の粗度Rzが0.8μm~2.0μmと低いものを採用し、該未処理銅箔に粗化処理を施す。粗化処理は粒径0.1~3μmの粗化粒子を用いて、後の被せめっきで、Rzが1.0~5μmまたはRaが0.25~0.7μmの粗化面を形成する。表面粗度が低い未処理銅箔を使用することで表面積比2~6倍とすることが可能となる。
表面積比2倍以下では、活物質の接触面積が極端に少なくなり、電池として、発熱して、劣化が早まる結果となる。
表面積が大きいほど活物質層との接触面積が大きくなり、界面抵抗が低下する。これにより電子の移動がスムーズになり電池の容量・出力特性が向上する。このため集電体の表面積は大きい方が好ましいが、表面積比6倍を超えると、粗化表面のRzが大きくなり過ぎ、結果として、活物質層が粗化(凹凸)の奥(底)まで届かず、銅箔と活物質層の間に空隙ができ、密着性が悪く、導電率が落ち、電池の発熱を起こし、電池の劣化が早まる結果となる。
また、表面粗さRz及びRaは、日本工業規格(JIS B 0601-1994)に定められた十点平均粗さ及び算術表面粗さであり、例えば表面粗さ計により測定した値である。
電解めっき法は、未処理電解銅箔の表面に凹凸を有する薄膜層を形成することにより表面を粗面化する方法である。
未処理電解銅箔の表面を電解めっきにより粗面化する方法としては、例えば、特許文献5(特公昭53-39376号公報)に開示された、プリント回路用銅箔に用いられているめっきによる粗面化方法が好ましく用いられる。すなわち、いわゆる「やけめっき」により、粒粉状銅めっき層を形成した後、この粒粉状銅めっき層の上に、その凹凸形状を損なわないように「被せめっき」を行い、実質的に平滑なめっき層を堆積させて粒粉状銅をいわゆるコブ状銅層とする。
凹凸粗面の隣り合わせの凸状先端間距離は「被せめっき」の処理時間または電流密度を任意に調整することによって、使用する活物質の粒径にあわせることができる。
また塗布型タイプの場合には、活物質をバインダー、溶剤とともにスラリー状にして、集電体(銅箔)の表面に塗布、乾燥、プレスすることにより形成する。
二次粒子とする場合は、たとえば前記特許文献6、7等に開示されている方法で製造することができる。
なお、銅箔の表裏において表面粗度に大きな差があると、銅箔(集電体)表面に活物質を塗工する工程で活物質の厚みが両面で異なり、出来上がった電極の特性に悪影響を与えるため、できる限り表裏で粗度の差がないようにする。
例えば、一次粒子の活物質としてシリコン(SiO)とアセチレンブラック、PVDF(ポリフッ化ビニリデン)、NMP(N-メチル-2-ビロリドン)を混合してスラリーとしたものを集電体に塗布し、乾燥、プレスすると、スリラー塗布、乾燥、プレスにより、粗化処理層2の凹部開口3にバインダー22と粒子の細かい(平均粒径より小さい)活物質は凹部開口3内に入り込み、大きい粒子の活物質は凸部4に跨って堆積される。ついでバインダー22が硬化後、粗化処理層の凸部4にある活物質21は銅箔10の粗化処理層凸部4とお互い引き付けあって、密着性に寄与し、活物質21と銅箔10の導電性と、電池特性の向上に寄与する。また、開口3に入り込んだ活物質は粒子の径が小さいためにその膨張収縮は銅箔の伸びとバインダーとに吸収され、銅箔への影響が小さく抑えられる。
また、二次加工された活物質を集電体にスラリー等と共に塗布し、乾燥、プレスして堆積すると、前記同様、二次活物質212は粗化処理層の凸部4、4間に跨って堆積され、活物質212は銅箔10の粗化処理層凸部4とお互い引き付けあって、密着性に寄与し、活物質21と銅箔10の導電性と、電池特性の向上に寄与する。また、二次粒子となった活物質から離脱した粒径の小さい活物質211は開口3に入り入り込むが、活物質211は粒子の径が小さいためにその膨張収縮は銅箔の伸びとバインダーとに吸収され、銅箔への影響が小さく抑えられる。
〔実施例1~6及び比較例1~8〕
銅70~130g/l-硫酸80~140g/lの酸性銅電解浴に表1に示す組成の添加剤を添加した。表中、MPSは3-メルカプト1-プロパンスルホン酸ナトリウム、HEC(高分子多糖類)はヒドロキシエチルセルロース、膠は分子量3,000の低分子量膠である。MPS、HEC及び塩化物イオンを表1に示す濃度となるように、それぞれ添加し製箔用電解液を調製した。なお、塩化物イオン濃度を全て30ppmに調整したが、塩化物イオン濃度は電解条件により適宜変更するものであり、この濃度に限定されるものではない。
調製した電解液を用い、アノードには貴金属酸化物被覆チタン電極、カソードにはチタン製回転ドラムを用いて表1に示す電解条件(電流密度、液温)の下に、10μm厚みの未処理銅箔を電解製箔法によって製造した。作成した銅箔の性能を表2に示す。
前記条件で製箔した銅箔それぞれの両表面に下記条件で電解めっきにより銅のやけめっきを施し、粒粉状銅めっき層を形成し、さらに、該粒粉状銅めっき層の上にその凹凸形状を損なわないように、緻密な銅めっき(被せめっき)を行い、粒粉状銅と電解銅箔との密着性を向上させた表3に示す粗面化電解銅箔を作成した。
硫酸銅 80g/L
硫酸 110~160g/L
添加剤* 適量
液温 30~60℃
電流密度 10~50A/dm2
処理時間 2~20秒
硫酸銅 200g/L
硫酸 90~130g/L
液温 30~60℃
電流密度 10~30A/dm2
処理時間 2~20秒
*添加剤:Mo、Fe、Ni、Co、W、As、Znの内のそれらを一種以上含む合金。
シリコン(SiO)電極は、集電体X1~X4,Y3~Y6の上に、シリコン(SiO)とアセチレンブラック、PVDF(ポリフッ化ビニリデン)、NMP(N-メチル-2-ビロリドン)を混合してスラリーとしたものを塗布し、乾燥、プレスすることにより作製した。
上記の作用極(負極電極)を用い、アルゴンガス雰囲気下のグローブボックス中で、三電極式ビーカーセルを作成した。ビーカーセルは、ガラス容器内に入れられた電解液中に、対極、作用極、及び参照極を浸漬することにより構成した。電解液としては、エチレンカーボネートとジエチルカーボネートを体積比3:7の割合で混合した溶媒に対し、LiPF6を1モル/リットル溶解した電解液を用いた。対極及び参照極としてはリチウム金属を用いた。
上記のようにして作成したビーカーセルを、25℃にて4mAの定電流で、作用極の電位が0V(vs.Li/Li+)に達するまで充電した後、4mAの定電流で、作用極の電位が2V(vs.Li/Li+)に達するまで放電し充放電効率100サイクル後の放電容量保持率にて評価した。評価結果を表4に示す。
また300サイクル充放電を繰り返した後の銅箔の破断の有無についても表4中に示した。
比較例3は実施例7と同じ未処理銅箔を使用したが、粗化後の粗度Raの差が大きく、また表面積が大きいため、充放電効率100サイクル後の放電容量保持率が満足できないものとなった。
比較例7は比較例4と同様未処理銅箔の結晶組織が柱状であり、粗化処理後の表面積も大きかったために、ビーカーセル電池での充放電サイクル特性の評価は全て不満足の結果となった。
比較例8は未処理銅箔の結晶粒径が大きく、300サイクル充放電を繰り返した後の集電体に破断が見られた。
1 未処理銅箔
2 粗化処理層
3 粗化面の凹部
4 粗化面の凸部
20 活物質層
21 活物質
211 粒径の小さい活物質
212 粒径の大きい活物質、活物質が加工された二次粒子
22 バインダー
Claims (12)
- 未処理銅箔の両方の表面に電解めっきによる粗化処理で粒径が3μm以下の銅または銅合金の凹凸粗面化処理層が設けられ、該両表面の凹凸粗面化処理層の表面粗度Rzが1.0~5μmまたはRaが0.25~0.7μmであり、表裏の粗度Rzの差が3μm以内、またはRaの差が0.3μm以内である電解銅箔。
- 前記未処理銅箔が、粒状晶である請求項1に記載の電解銅箔。
- 前記粗化処理の銅合金は、Cuを主成分としMo、Fe、Ni、Co、W、As、Znまたはそれらを一種以上含む合金である請求項1に記載の電解銅箔。
- 未処理銅箔の両方の表面に電解めっきによる粗化処理で粒径が3μm以下の銅または銅合金の凹凸粗面化処理層が設けられ、該両表面の凹凸粗面化処理層の表面粗度Rzが1.0~5μm、またはRaが0.25~0.7μmであり、表裏の粗度Rzの差が3μm以内、またはRaの差が0.3μm以内であるリチウムイオン二次電池用電解銅箔。
- 未処理銅箔の両方の表面に電解めっきによる粗化処理で粒径が3μm以下の銅または銅合金からなる凹凸粗面化処理層が設けられ、該両凹凸粗面化処理層の表面粗度Rzが1.0~5μm、またはRaが0.25~0.7μmであり、表裏の粗度Rzの差が3μm以内、またはRaの差が0.3μm以内であり、前記凹凸粗面の隣り合わせの凸状先端間距離がリチウムイオン二次電池電極用活物質の一次粒子の平均粒径より大きく、且つ二次粒子の平均粒径より小さいもしくは等しいリチウムイオン二次電池用電解銅箔。
- 前記未処理銅箔が、粒状晶である請求項4または5に記載のリチウムイオン二次電池用電解銅箔。
- 前記粗化処理の銅合金は、Cuを主成分としMo、Fe、Ni、Co、W、As、Zn又はそれらを一種以上含む合金である請求項4または5に記載のリチウムイオン二次電池用電解銅箔。
- 前記粗化処理後の表面積比が2~6倍である請求項4~7のいずれかに記載のリチウムイオン二次電池用電解銅箔。
- 150℃×15時間加熱後の引張り強度が250N/mm2以上である請求項4~7のいずれかに記載のリチウムイオン二次電池用電解銅箔。
- 前記リチウムイオン二次電池用活物質の平均粒径は活物質そのもの(一次粒子)または活物質を加工したもの(二次粒子)である請求項5に記載のリチウムイオン二次電池用電解銅箔。
- 請求項4~10のいずれかに記載のリチウムイオン二次電池用電解銅箔の表面に、シリコン、ゲルマニウム、錫又はそれらの合金化合物またはそれらを主成分とする活物質が堆積されているリチウムイオン二次電池用電極。
- 請求項11に記載のリチウムイオン二次電池用電極を使用したリチウムイオン二次電池。
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP11800844.0A EP2587574A4 (en) | 2010-06-28 | 2011-06-28 | ELECTROLYTIC COPPER FOIL, ELECTROLYTIC COPPER FOIL FOR A LITHIUMION ACCUMULATOR, ELECTRODE FOR A LITHIUMION ACCUMULATOR WITH THE ELECTROLYTIC COPPER FOIL AND LITHIUMION ACCUMULATOR WITH THE ELECTRODE |
CN201180032555.9A CN102959775B (zh) | 2010-06-28 | 2011-06-28 | 电解铜箔、锂离子充电电池用电解铜箔、使用该电解铜箔的锂离子充电电池用电极、使用该电极的锂离子充电电池 |
KR1020137000921A KR20130030806A (ko) | 2010-06-28 | 2011-06-28 | 전해 동박, 리튬 이온 이차 전지용 전해 동박, 상기 전해 동박을 이용한 리튬 이온 이차 전지용 전극, 상기 전극을 사용한 리튬 이온 이차 전지 |
US13/807,137 US20130108922A1 (en) | 2010-06-28 | 2011-06-28 | Electrolytic copper foil, electrolytic copper foil for lithium ion secondary battery, electrode for lithium ion secondary battery using the electrolytic copper foil, and lithium ion secondary battery using the electrode |
KR1020167027093A KR101800993B1 (ko) | 2010-06-28 | 2011-06-28 | 전해 동박, 리튬 이온 이차 전지용 전해 동박, 상기 전해 동박을 이용한 리튬 이온 이차 전지용 전극, 상기 전극을 사용한 리튬 이온 이차 전지 |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2010145869 | 2010-06-28 | ||
JP2010-145869 | 2010-06-28 | ||
JP2011140270A JP5128695B2 (ja) | 2010-06-28 | 2011-06-24 | 電解銅箔、リチウムイオン二次電池用電解銅箔、該電解銅箔を用いたリチウムイオン二次電池用電極、該電極を使用したリチウムイオン二次電池 |
JP2011-140270 | 2011-06-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2012002380A1 true WO2012002380A1 (ja) | 2012-01-05 |
Family
ID=45402087
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2011/064797 WO2012002380A1 (ja) | 2010-06-28 | 2011-06-28 | 電解銅箔、リチウムイオン二次電池用電解銅箔、該電解銅箔を用いたリチウムイオン二次電池用電極、該電極を使用したリチウムイオン二次電池 |
Country Status (7)
Country | Link |
---|---|
US (1) | US20130108922A1 (ja) |
EP (1) | EP2587574A4 (ja) |
JP (1) | JP5128695B2 (ja) |
KR (2) | KR101800993B1 (ja) |
CN (1) | CN102959775B (ja) |
TW (1) | TWI570277B (ja) |
WO (1) | WO2012002380A1 (ja) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013002273A1 (ja) * | 2011-06-28 | 2013-01-03 | 古河電気工業株式会社 | リチウムイオン二次電池、該二次電池の負極電極を構成する集電体、並びに該負極電極集電体を構成する電解銅箔 |
KR20160137678A (ko) * | 2012-03-30 | 2016-11-30 | 제이엑스금속주식회사 | 금속박 |
EP2845251B1 (de) * | 2012-05-02 | 2017-08-30 | Hydro Aluminium Rolled Products GmbH | Texturierte stromableiterfolie |
WO2018088642A1 (ko) * | 2016-11-11 | 2018-05-17 | 일진머티리얼즈 주식회사 | 이차전지용 전해동박 및 그의 제조방법 |
EP3404755A4 (en) * | 2016-01-13 | 2019-09-18 | LS Mtron Ltd. | COPPER FOIL, ITS MANUFACTURING METHOD, ELECTRODE COMPRISING THE SAME, AND SECONDARY BATTERY COMPRISING THE SAME |
WO2023243554A1 (ja) * | 2022-06-16 | 2023-12-21 | 株式会社村田製作所 | 二次電池用電極および二次電池 |
Families Citing this family (48)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100285358A1 (en) | 2009-05-07 | 2010-11-11 | Amprius, Inc. | Electrode Including Nanostructures for Rechargeable Cells |
US8450012B2 (en) | 2009-05-27 | 2013-05-28 | Amprius, Inc. | Interconnected hollow nanostructures containing high capacity active materials for use in rechargeable batteries |
JP5306418B2 (ja) * | 2010-07-09 | 2013-10-02 | 日新製鋼株式会社 | 銅被覆鋼箔、負極用電極及び電池 |
KR102096193B1 (ko) | 2010-10-22 | 2020-04-02 | 암프리우스, 인코포레이티드 | 껍질에 제한된 고용량 활물질을 함유하는 복합 구조물 |
JP5751448B2 (ja) | 2011-05-25 | 2015-07-22 | 日産自動車株式会社 | リチウムイオン二次電池用負極活物質 |
CN103649378B (zh) * | 2011-06-30 | 2016-12-14 | 古河电气工业株式会社 | 电解铜箔、该电解铜箔的制造方法、以及将该电解铜箔作为集电体的锂离子二次电池 |
WO2013080988A1 (ja) * | 2011-11-29 | 2013-06-06 | 古河電気工業株式会社 | 電極用集電体、非水電解質二次電池用電極、非水電解質二次電池 |
WO2013129588A1 (ja) * | 2012-02-28 | 2013-09-06 | 古河電気工業株式会社 | リチウムイオン二次電池、該二次電池の負極電極を構成する集電体、ならびに該負極電極集電体を構成する電解銅箔 |
JP5718426B2 (ja) * | 2012-10-31 | 2015-05-13 | 古河電気工業株式会社 | 銅箔、非水電解質二次電池用負極および非水電解質二次電池 |
CN104813515B (zh) * | 2012-11-22 | 2017-12-01 | 日产自动车株式会社 | 电气设备用负极、及使用其的电气设备 |
CN104813513B (zh) | 2012-11-22 | 2017-06-16 | 日产自动车株式会社 | 电气设备用负极和使用了其的电气设备 |
KR101787513B1 (ko) * | 2013-01-29 | 2017-10-18 | 후루카와 덴키 고교 가부시키가이샤 | 전해 동박, 상기 전해 동박을 이용한 전지용 집전체, 상기 집전체를 이용한 이차전지용 전극, 상기 전극을 이용한 이차전지 |
JP6459023B2 (ja) * | 2013-06-18 | 2019-01-30 | 株式会社Gsユアサ | 蓄電素子及び蓄電モジュール |
CN105164838B (zh) * | 2013-07-10 | 2018-01-26 | 日立金属株式会社 | 锂离子二次电池用集电体以及锂离子二次电池用正极 |
EP3089183A4 (en) * | 2013-12-26 | 2017-04-05 | Sumitomo Electric Industries, Ltd. | Alkali metal ion capacitor |
KR101695236B1 (ko) * | 2013-12-30 | 2017-01-11 | 일진머티리얼즈 주식회사 | 동박, 이를 포함하는 전기부품 및 전지 |
KR20150077943A (ko) * | 2013-12-30 | 2015-07-08 | 일진머티리얼즈 주식회사 | 동박, 이를 포함하는 전기부품 및 전지 |
WO2015111189A1 (ja) | 2014-01-24 | 2015-07-30 | 日産自動車株式会社 | 電気デバイス |
EP3098892B1 (en) | 2014-01-24 | 2018-11-14 | Nissan Motor Co., Ltd | Electrical device |
WO2015175509A1 (en) | 2014-05-12 | 2015-11-19 | Amprius, Inc. | Structurally controlled deposition of silicon onto nanowires |
DE102014211298A1 (de) * | 2014-06-13 | 2015-12-17 | Robert Bosch Gmbh | Substrat mit einer Oberflächenbeschichtung und Verfahren zum Beschichten einer Oberfläche eines Substrates |
JP2016121394A (ja) * | 2014-12-23 | 2016-07-07 | エル エス エムトロン リミテッドLS Mtron Ltd. | 電解銅箔、これを含むfccl及びccl |
HUE059762T2 (hu) * | 2015-06-24 | 2022-12-28 | Sk Nexilis Co Ltd | Elektrolitos rézfólia, ugyanezen elektrolitos rézfóliát magában foglaló áramgyûjtõ, ugyanezen áramgyûjtõt magában foglaló elektród, ugyanezen elektródot magában foglaló másodlagos akkumulátor, és eljárás ugyanennek gyártására |
KR101897474B1 (ko) * | 2015-06-26 | 2018-09-12 | 케이씨에프테크놀로지스 주식회사 | 리튬 이차전지용 전해동박 및 이를 포함하는 리튬 이차전지 |
KR102207524B1 (ko) * | 2016-09-01 | 2021-01-26 | 주식회사 엘지화학 | 리튬 이차전지용 전극의 제조방법 및 이로부터 제조된 리튬 이차전지용 전극 |
JP6773119B2 (ja) * | 2016-09-16 | 2020-10-21 | 株式会社村田製作所 | リチウムイオン二次電池用負極、リチウムイオン二次電池、電池パック、電動車両、電力貯蔵システム、電動工具および電子機器 |
KR101733409B1 (ko) * | 2016-11-11 | 2017-05-10 | 일진머티리얼즈 주식회사 | 이차전지용 전해동박 및 그의 제조방법 |
KR101734840B1 (ko) * | 2016-11-11 | 2017-05-15 | 일진머티리얼즈 주식회사 | 내굴곡성이 우수한 이차전지용 전해동박 및 그의 제조방법 |
KR101733410B1 (ko) * | 2016-11-11 | 2017-05-10 | 일진머티리얼즈 주식회사 | 저온 물성이 우수한 이차전지용 전해동박 및 그의 제조방법 |
JP7193915B2 (ja) * | 2017-02-03 | 2022-12-21 | Jx金属株式会社 | 表面処理銅箔並びにこれを用いた集電体、電極及び電池 |
US10529992B2 (en) | 2017-02-03 | 2020-01-07 | Jx Nippon Mining & Metals Corporation | Surface-treated copper foil, and current collector, electrode, and battery cell using the surface-treated copper foil |
JP6931293B2 (ja) * | 2017-03-28 | 2021-09-01 | 三洋電機株式会社 | 二次電池の製造方法 |
JP6543001B2 (ja) * | 2017-03-30 | 2019-07-10 | 古河電気工業株式会社 | 表面処理銅箔、並びにこれを用いた銅張積層板およびプリント配線板 |
US10205170B1 (en) * | 2017-12-04 | 2019-02-12 | Chang Chun Petrochemical Co., Ltd. | Copper foil for current collector of lithium secondary battery |
CN108677231B (zh) * | 2018-05-04 | 2021-05-07 | 瑞声光学解决方案私人有限公司 | 压延铜遮光圈片制备方法及压延铜遮光圈片 |
CN109065833B (zh) * | 2018-06-28 | 2021-04-02 | 合肥国轩高科动力能源有限公司 | 一种锂电池硅碳复合负极片的多孔集流体表面处理方法 |
KR20200102242A (ko) * | 2019-02-21 | 2020-08-31 | 에스케이이노베이션 주식회사 | 전극용 기재 및 이를 이용한 전극 제조 방법 |
US20220285692A1 (en) * | 2019-07-24 | 2022-09-08 | Board Of Regents, The University Of Texas System | Multilayered anode and associated methods and systems |
TWI700393B (zh) | 2019-08-27 | 2020-08-01 | 長春石油化學股份有限公司 | 電解銅箔以及包含其之電極與鋰離子電池 |
JP7470130B2 (ja) * | 2019-09-30 | 2024-04-17 | 三洋電機株式会社 | 二次電池の製造方法、及び二次電池 |
KR102348461B1 (ko) * | 2019-12-19 | 2022-01-10 | 일진머티리얼즈 주식회사 | 표면처리 동박, 이의 제조방법 및 이를 포함한 이차전지용 음극 |
CN111074317B (zh) * | 2019-12-30 | 2022-02-18 | 禹象铜箔(浙江)有限公司 | 一种铜箔的表面处理方法及铜箔材料 |
US10944113B1 (en) * | 2020-02-27 | 2021-03-09 | ZAF Energy Systems, Incorporated | Electrode having protective and locking layers on current collector |
CN112054208B (zh) * | 2020-03-17 | 2022-06-28 | 安徽理士新能源发展有限公司 | Cu3Pt铜网-锂金属电极及其制法及锂电池制法 |
CN112635772B (zh) * | 2020-12-18 | 2022-06-17 | 江西理工大学 | 一种锂电池用多孔铜箔及其制备方法和应用 |
WO2023057067A1 (en) * | 2021-10-07 | 2023-04-13 | Circuit Foil Luxembourg | Copper foil with high engery at break and secondary battery comprising the same |
LU502546B1 (en) * | 2022-07-21 | 2024-01-22 | Circuit Foil Luxembourg | Copper foil, secondary battery comprising the same and production method thereof |
CN115775865B (zh) * | 2023-02-03 | 2023-04-28 | 中创新航科技股份有限公司 | 一种锂离子电池 |
Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5339376B1 (ja) | 1971-08-03 | 1978-10-20 | ||
JPH09143785A (ja) * | 1995-09-22 | 1997-06-03 | Furukawa Circuit Foil Kk | ファインパターン用電解銅箔とその製造方法 |
JPH10255768A (ja) | 1997-03-11 | 1998-09-25 | Masataka Wakihara | 電極、及びリチウム二次電池 |
JPH11354122A (ja) | 1998-05-21 | 1999-12-24 | Samsung Display Devices Co Ltd | リチウム二次電池用負極活物質及びリチウム二次電池 |
JP2001357855A (ja) * | 2000-06-14 | 2001-12-26 | Shin Kobe Electric Mach Co Ltd | 非水電解液二次電池 |
JP2002083594A (ja) | 1999-10-22 | 2002-03-22 | Sanyo Electric Co Ltd | リチウム電池用電極並びにこれを用いたリチウム電池及びリチウム二次電池 |
JP2002319407A (ja) * | 2001-04-23 | 2002-10-31 | Sanyo Electric Co Ltd | リチウム二次電池用電極及びリチウム二次電池 |
JP3742144B2 (ja) | 1996-05-08 | 2006-02-01 | ソニー株式会社 | 非水電解液二次電池及び非水電解液二次電池用の平面状集電体 |
JP2007165061A (ja) | 2004-12-10 | 2007-06-28 | Canon Inc | リチウム二次電池用の電極構造体及び該電極構造体を有する二次電池 |
JP2008010320A (ja) * | 2006-06-29 | 2008-01-17 | Sony Corp | 電極集電体及びその検査方法、電池用電極及びその製造方法、並びに二次電池及びその製造方法 |
JP2008013847A (ja) * | 2006-06-07 | 2008-01-24 | Furukawa Circuit Foil Kk | 表面処理電解銅箔及びその製造方法、並びに回路基板 |
JP2008226800A (ja) * | 2007-03-16 | 2008-09-25 | Fukuda Metal Foil & Powder Co Ltd | リチウム二次電池負極集電体用銅箔およびその製造方法 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5339376A (en) | 1976-09-22 | 1978-04-11 | Nippon Telegraph & Telephone | Method of attaching of parts to be attached on to parts of synthetic resin |
JP2003007305A (ja) * | 2001-04-19 | 2003-01-10 | Sanyo Electric Co Ltd | リチウム二次電池用電極及びリチウム二次電池 |
JP4629969B2 (ja) * | 2003-11-11 | 2011-02-09 | 古河電気工業株式会社 | 電磁波シールド用銅箔、その製造方法、および該銅箔で作成した電磁波シールド体 |
JP2006103189A (ja) * | 2004-10-06 | 2006-04-20 | Furukawa Circuit Foil Kk | 表面処理銅箔並びに回路基板 |
JP4859380B2 (ja) * | 2005-03-17 | 2012-01-25 | 三洋電機株式会社 | リチウム二次電池用電極の製造方法及びリチウム二次電池 |
TWI414638B (zh) * | 2006-06-07 | 2013-11-11 | Furukawa Electric Co Ltd | A method for manufacturing a surface-treated electrolytic copper foil, and a circuit board |
WO2008132987A1 (ja) * | 2007-04-20 | 2008-11-06 | Nippon Mining & Metals Co., Ltd. | リチウム二次電池用電解銅箔及び該銅箔の製造方法 |
JP2009231072A (ja) * | 2008-03-24 | 2009-10-08 | Sanyo Electric Co Ltd | リチウム二次電池及びその製造方法 |
EP2544282A1 (en) * | 2010-03-01 | 2013-01-09 | Furukawa Electric Co., Ltd. | Surface treatment method for copper foil, surface treated copper foil and copper foil for negative electrode collector of lithium ion secondary battery |
-
2011
- 2011-06-24 JP JP2011140270A patent/JP5128695B2/ja active Active
- 2011-06-28 KR KR1020167027093A patent/KR101800993B1/ko active IP Right Grant
- 2011-06-28 TW TW100122796A patent/TWI570277B/zh active
- 2011-06-28 US US13/807,137 patent/US20130108922A1/en not_active Abandoned
- 2011-06-28 WO PCT/JP2011/064797 patent/WO2012002380A1/ja active Application Filing
- 2011-06-28 CN CN201180032555.9A patent/CN102959775B/zh active Active
- 2011-06-28 EP EP11800844.0A patent/EP2587574A4/en not_active Withdrawn
- 2011-06-28 KR KR1020137000921A patent/KR20130030806A/ko active Search and Examination
Patent Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5339376B1 (ja) | 1971-08-03 | 1978-10-20 | ||
JP3313277B2 (ja) | 1995-09-22 | 2002-08-12 | 古河サーキットフォイル株式会社 | ファインパターン用電解銅箔とその製造方法 |
JPH09143785A (ja) * | 1995-09-22 | 1997-06-03 | Furukawa Circuit Foil Kk | ファインパターン用電解銅箔とその製造方法 |
JP3742144B2 (ja) | 1996-05-08 | 2006-02-01 | ソニー株式会社 | 非水電解液二次電池及び非水電解液二次電池用の平面状集電体 |
JPH10255768A (ja) | 1997-03-11 | 1998-09-25 | Masataka Wakihara | 電極、及びリチウム二次電池 |
JPH11354122A (ja) | 1998-05-21 | 1999-12-24 | Samsung Display Devices Co Ltd | リチウム二次電池用負極活物質及びリチウム二次電池 |
JP2002083594A (ja) | 1999-10-22 | 2002-03-22 | Sanyo Electric Co Ltd | リチウム電池用電極並びにこれを用いたリチウム電池及びリチウム二次電池 |
JP2001357855A (ja) * | 2000-06-14 | 2001-12-26 | Shin Kobe Electric Mach Co Ltd | 非水電解液二次電池 |
JP2002319407A (ja) * | 2001-04-23 | 2002-10-31 | Sanyo Electric Co Ltd | リチウム二次電池用電極及びリチウム二次電池 |
JP2007165061A (ja) | 2004-12-10 | 2007-06-28 | Canon Inc | リチウム二次電池用の電極構造体及び該電極構造体を有する二次電池 |
JP2008013847A (ja) * | 2006-06-07 | 2008-01-24 | Furukawa Circuit Foil Kk | 表面処理電解銅箔及びその製造方法、並びに回路基板 |
JP2008010320A (ja) * | 2006-06-29 | 2008-01-17 | Sony Corp | 電極集電体及びその検査方法、電池用電極及びその製造方法、並びに二次電池及びその製造方法 |
JP2008226800A (ja) * | 2007-03-16 | 2008-09-25 | Fukuda Metal Foil & Powder Co Ltd | リチウム二次電池負極集電体用銅箔およびその製造方法 |
Non-Patent Citations (1)
Title |
---|
See also references of EP2587574A4 * |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013002273A1 (ja) * | 2011-06-28 | 2013-01-03 | 古河電気工業株式会社 | リチウムイオン二次電池、該二次電池の負極電極を構成する集電体、並びに該負極電極集電体を構成する電解銅箔 |
JP5158918B2 (ja) * | 2011-06-28 | 2013-03-06 | 古河電気工業株式会社 | リチウムイオン二次電池、該二次電池の負極電極を構成する集電体、並びに該負極電極集電体を構成する電解銅箔 |
KR20160137678A (ko) * | 2012-03-30 | 2016-11-30 | 제이엑스금속주식회사 | 금속박 |
KR102095619B1 (ko) * | 2012-03-30 | 2020-03-31 | 제이엑스금속주식회사 | 금속박 |
EP2845251B1 (de) * | 2012-05-02 | 2017-08-30 | Hydro Aluminium Rolled Products GmbH | Texturierte stromableiterfolie |
US9887044B2 (en) | 2012-05-02 | 2018-02-06 | Hydro Aluminium Rolled Products Gmbh | Textured current collector foil |
EP3404755A4 (en) * | 2016-01-13 | 2019-09-18 | LS Mtron Ltd. | COPPER FOIL, ITS MANUFACTURING METHOD, ELECTRODE COMPRISING THE SAME, AND SECONDARY BATTERY COMPRISING THE SAME |
WO2018088642A1 (ko) * | 2016-11-11 | 2018-05-17 | 일진머티리얼즈 주식회사 | 이차전지용 전해동박 및 그의 제조방법 |
US11380898B2 (en) | 2016-11-11 | 2022-07-05 | Iljin Materials Co., Ltd. | Electrolytic copper foil for secondary battery and method for producing the same |
WO2023243554A1 (ja) * | 2022-06-16 | 2023-12-21 | 株式会社村田製作所 | 二次電池用電極および二次電池 |
Also Published As
Publication number | Publication date |
---|---|
KR20160119269A (ko) | 2016-10-12 |
EP2587574A1 (en) | 2013-05-01 |
KR20130030806A (ko) | 2013-03-27 |
JP2012033475A (ja) | 2012-02-16 |
TWI570277B (zh) | 2017-02-11 |
JP5128695B2 (ja) | 2013-01-23 |
CN102959775B (zh) | 2015-03-25 |
KR101800993B1 (ko) | 2017-11-23 |
TW201213620A (en) | 2012-04-01 |
US20130108922A1 (en) | 2013-05-02 |
EP2587574A4 (en) | 2014-02-12 |
CN102959775A (zh) | 2013-03-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5128695B2 (ja) | 電解銅箔、リチウムイオン二次電池用電解銅箔、該電解銅箔を用いたリチウムイオン二次電池用電極、該電極を使用したリチウムイオン二次電池 | |
JP5276158B2 (ja) | リチウムイオン二次電池、該電池用負極電極、該電池負極集電体用電解銅箔 | |
WO2010110205A1 (ja) | リチウムイオン二次電池、該電池用電極、該電池電極用電解銅箔 | |
JP5437536B2 (ja) | 電極用集電体、非水電解質二次電池用負極、非水電解質二次電池 | |
JP5435519B2 (ja) | リチウムイオン二次電池負極電極用被覆層付き金属箔及びその製造方法、リチウムイオン二次電池負極用電極及びその製造方法、リチウムイオン二次電池 | |
JP2002319408A (ja) | リチウム二次電池用電極及びリチウム二次電池 | |
JP2013133514A (ja) | 銅箔、二次電池の電極、二次電池、並びにプリント回路基板 | |
JP2009266761A (ja) | 非水電解質二次電池及びその製造方法 | |
JP2005150039A (ja) | リチウム二次電池 | |
WO2012001856A1 (ja) | リチウムイオン二次電池用負極及びリチウムイオン二次電池 | |
US20090202913A1 (en) | Negative electrode for nonaqueous secondary battery | |
JP5981165B2 (ja) | 銅箔、二次電池の負極電極、二次電池、並びにプリント回路基板 | |
JP6067256B2 (ja) | 電解銅箔、リチウムイオン二次電池用負極電極及びリチウムイオン二次電池 | |
JP2015198020A (ja) | 負極電極用表面処理銅箔、負極電極およびそれを使用したリチウムイオン二次電池 | |
JP5873711B2 (ja) | 銅箔、二次電池の電極、二次電池、並びにプリント回路基板 | |
JP2013012450A (ja) | リチウムイオン二次電池電極の集電体用金属箔、該金属箔の製造方法、及び該金属箔を集電体としたリチウムイオン二次電池 | |
JP2008124036A (ja) | リチウム二次電池用負極及びリチウム二次電池 | |
JP2008047305A (ja) | 非水電解液二次電池 | |
CN117712386A (zh) | 复合铜箔及其制备方法、锂离子二次电池 | |
JP2014009365A (ja) | 電解銅箔、リチウムイオン二次電池負極電極、及びリチウムイオン二次電池 | |
US8563158B2 (en) | Lithium secondary battery |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 201180032555.9 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 11800844 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 13807137 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2011800844 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: 20137000921 Country of ref document: KR Kind code of ref document: A |