WO2008072460A1 - 非水電解質二次電池用負極とその製造方法およびそれを用いた非水電解質二次電池 - Google Patents
非水電解質二次電池用負極とその製造方法およびそれを用いた非水電解質二次電池 Download PDFInfo
- Publication number
- WO2008072460A1 WO2008072460A1 PCT/JP2007/072714 JP2007072714W WO2008072460A1 WO 2008072460 A1 WO2008072460 A1 WO 2008072460A1 JP 2007072714 W JP2007072714 W JP 2007072714W WO 2008072460 A1 WO2008072460 A1 WO 2008072460A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- columnar body
- negative electrode
- current collector
- body portion
- secondary battery
- Prior art date
Links
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
- H01M4/13—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
-
- 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
-
- 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
- H01M4/04—Processes of manufacture in general
-
- 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
-
- 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
- H01M2004/021—Physical characteristics, e.g. porosity, surface area
-
- 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
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49002—Electrical device making
- Y10T29/49108—Electric battery cell making
Definitions
- Anode for non-aqueous electrolyte secondary battery method for producing the same, and non-aqueous electrolyte secondary battery using the same
- the present invention relates to a nonaqueous electrolyte secondary battery excellent in charge / discharge characteristics, and more specifically, a negative electrode for a nonaqueous electrolyte secondary battery excellent in capacity retention, high rate characteristics and low temperature characteristics, and a method for producing the same
- the present invention relates to a non-aqueous electrolyte secondary battery using the same.
- Lithium ion secondary batteries which are representative of nonaqueous electrolyte secondary batteries, are characterized by high energy density with high electromotive force while being lightweight. Therefore, the demand for lithium ion secondary batteries as driving power sources for various types of portable electronic devices such as mobile phones, digital cameras, video cameras, and notebook computers and mobile communication devices is increasing.
- a lithium ion secondary battery is composed of a positive electrode made of a lithium-containing composite oxide, a negative electrode containing a negative electrode active material that occludes and releases lithium metal, a lithium alloy, or lithium ions, and an electrolyte. .
- the volume of these elements increases when occluding lithium ions during charging.
- the negative electrode active material is Si
- it is represented by Li Si when the maximum amount of lithium ions is occluded, and the volume changes from Si to Li Si.
- the current collector is made of a thin film of the above element, particularly by CVD or sputtering.
- a negative electrode active material is formed by depositing on the negative electrode active material, the negative electrode active material expands and contracts due to insertion and extraction of lithium ions, and the adhesion between the negative electrode active material and the negative electrode current collector decreases during repeated charge / discharge cycles. There was a possibility of peeling due to.
- Patent Document 1 a method is provided in which a surface of a current collector is provided with irregularities, a negative electrode active material thin film is deposited thereon, and voids are formed in the thickness direction by etching (eg, Patent Document 1). Reference).
- Patent Document 2 a method has been proposed in which a mesh is disposed above the current collector and a negative electrode active material thin film is deposited through the mesh, thereby suppressing deposition of the negative electrode active material in a region corresponding to the mesh frame ( For example, see Patent Document 2).
- the secondary batteries shown in Patent Document 1 and Patent Document 2 have a structure in which a thin film of a negative electrode active material is formed in a columnar shape, and voids are formed between the columns to prevent peeling and wrinkling.
- the metal surface of the current collector may be exposed through the gap.
- the exposed current collector faces the positive electrode during charging, so that lithium metal was deposited and immediately caused safety and reduced capacity.
- the tip (open side) of the columnar negative electrode active material is particularly a current collector.
- the negative electrode active material expands greatly as charging progresses compared to the vicinity of the current collector.
- columnar negative electrode active materials were brought into contact with each other in the vicinity of the tip and pressed against each other, and there was a problem that wrinkles occurred in the current collector when the current collector and the negative electrode active material were separated. For this reason, peeling of the current collector from the negative electrode active material could not simultaneously prevent generation of wrinkles in the current collector and increase the capacity.
- the electrolyte is confined in the space between the expanded and contacted columnar negative electrode active materials, the movement of lithium ions is hindered in the early stage of discharge, particularly high rate discharge (hereinafter referred to as “high rate discharge”) and low temperature. There were problems with the discharge characteristics in the environment.
- the negative electrode active material 53 formed with an inclination ( ⁇ ) is used to prevent the current collector 51 from being exposed and to deposit lithium metal. In advance You can power to prevent.
- the negative electrode active material 53 expands greatly as the charging progresses as compared to the vicinity of the current collector 51. As a result, the current collector 51 and the negative electrode active material 53 were peeled from each other and the current collector 51 was wrinkled. Furthermore, since the negative electrode active material is formed obliquely, it can be formed only on the two surfaces in the longitudinal direction of the convex portion of the current collector.
- Patent Document 1 Japanese Patent Laid-Open No. 2003-17040
- Patent Document 2 Japanese Patent Laid-Open No. 2002-279974
- Patent Document 3 Japanese Patent Laid-Open No. 2005-196970
- the present invention is a negative electrode for a non-aqueous electrolyte secondary battery that reversibly occludes / releases lithium ions, a current collector having a recess and a protrusion formed on at least one surface, and a protrusion of the current collector.
- the columnar body part in which the content ratio of the elements formed obliquely on the part changes sequentially in the longitudinal direction of the current collector, is stacked in n (n ⁇ 2) stages, and the content ratio of the odd-numbered and even-numbered elements
- Columnar bodies having columnar body portions with different directions of change, and the columnar shape on the side where the crossing angle between the center line in the vertical direction of each columnar body portion and the center line in the thickness direction of the current collector forms an obtuse angle
- a plurality of projecting bodies are provided on the surface of the body part, and a gap is provided in the columnar body by the projecting bodies of the stacked columnar body parts.
- the method for producing a negative electrode for a nonaqueous electrolyte secondary battery according to the present invention reversibly converts lithium ions.
- a method for producing a negative electrode for a non-aqueous electrolyte secondary battery that occludes / releases in a negative manner wherein the first step forms at least one concave portion and a convex portion on one side of the current collector, and the first-stage projecting body on the convex portion.
- the third step to be formed, the second step, and the third step are repeated to change the slanting direction of the odd-numbered and even-numbered columnar body portions, and the n-th (n ⁇ 2) stages are formed. And a fourth step of forming a columnar body having a gap.
- a nonaqueous electrolyte secondary battery of the present invention includes the above-described negative electrode for a nonaqueous electrolyte secondary battery, a positive electrode capable of reversibly occluding and releasing lithium ions, and a nonaqueous electrolyte. As a result, a non-aqueous electrolyte secondary battery having high safety and excellent reliability is manufactured.
- FIG. 1 is a cross-sectional view of a nonaqueous electrolyte secondary battery in an embodiment of the present invention.
- FIG. 2A is a partial schematic cross-sectional view showing the structure of a negative electrode in an embodiment of the present invention.
- FIG. 2B is a schematic diagram for explaining the change in the value of X in the width direction of the active material of the same embodiment.
- FIG. 3A is a partial schematic cross-sectional view showing in detail the structure of the negative electrode before charging in the embodiment of the present invention.
- FIG. 3B is a partial schematic cross-sectional view showing in detail the structure of the negative electrode after charging in the same embodiment.
- FIG. 4A is a partial cross-sectional schematic view showing a state before charging of the nonaqueous electrolyte secondary battery in the embodiment of the present invention.
- FIG. 4B is a partial cross-sectional schematic diagram showing a state after charging of the nonaqueous electrolyte secondary battery in the same embodiment.
- FIG. 5A shows a state before charging of the columnar body of the negative electrode in the embodiment of the present invention.
- FIG. 5B is a partial cross-sectional schematic view showing a state after charging of the columnar body of the negative electrode in the same embodiment.
- FIG. 6A is a schematic partial cross-sectional view illustrating a method for forming a columnar body provided with a protruding body of a negative electrode for a nonaqueous electrolyte secondary battery in an embodiment of the present invention.
- FIG. 6B is a partial schematic cross-sectional view illustrating a method for forming a columnar body provided with a protruding body of a negative electrode for a nonaqueous electrolyte secondary battery in an embodiment of the present invention.
- FIG. 6C is a partial cross-sectional schematic diagram for explaining a method of forming a columnar body provided with a protruding body of a negative electrode for a nonaqueous electrolyte secondary battery in an embodiment of the present invention.
- FIG. 6D is a partial cross-sectional schematic diagram for explaining a method of forming a columnar body provided with a protruding body of a negative electrode for a nonaqueous electrolyte secondary battery in an embodiment of the present invention.
- FIG. 7A is a partial cross-sectional schematic diagram illustrating a method for forming a columnar body including n-stage columnar body portions of the negative electrode for a nonaqueous electrolyte secondary battery in accordance with the exemplary embodiment of the present invention.
- FIG. 7B is a partial cross-sectional schematic diagram illustrating a method of forming a columnar body including n-stage columnar body portions of the negative electrode for a nonaqueous electrolyte secondary battery in accordance with the exemplary embodiment of the present invention.
- FIG. 7C is a partial cross-sectional schematic diagram illustrating a method of forming a columnar body including n-stage columnar body portions of the negative electrode for a nonaqueous electrolyte secondary battery in accordance with the exemplary embodiment of the present invention.
- FIG. 7D is a partial schematic cross-sectional view illustrating a method for forming a columnar body including n-stage columnar body portions of the negative electrode for a nonaqueous electrolyte secondary battery in accordance with the exemplary embodiment of the present invention.
- FIG. 7E is a partial schematic cross-sectional view illustrating a method for forming a columnar body composed of n-stage columnar body portions of the negative electrode for a nonaqueous electrolyte secondary battery in accordance with the exemplary embodiment of the present invention.
- FIG. 8 is a schematic diagram for explaining a manufacturing apparatus for producing a columnar body composed of n-stage columnar body portions of the negative electrode for a nonaqueous electrolyte secondary battery in the embodiment of the present invention.
- FIG. 9A is a partial cross-sectional schematic view showing another example of the structure of the negative electrode in the embodiment of the present invention.
- FIG. 9B is a schematic diagram for explaining a change in the value of X in the width direction of the active material of the same embodiment.
- FIG. 10A shows another example of the nonaqueous electrolyte secondary battery in the embodiment of the present invention. It is a partial cross section schematic diagram which shows the state before charge.
- FIG. 10B is a partial cross-sectional schematic view showing a state after charging in another example of the nonaqueous electrolyte secondary battery in the same embodiment.
- FIG. 11 is a diagram showing an example of charge / discharge cycle characteristics in the samples of the example and the comparative example.
- FIG. 12A is a partial cross-sectional schematic diagram showing the structure of a conventional negative electrode before charging.
- FIG. 12B is a partial cross-sectional schematic diagram showing the structure of a conventional negative electrode after charging.
- FIG. 1 is a cross-sectional view of a nonaqueous electrolyte secondary battery in an embodiment of the present invention.
- a laminated nonaqueous electrolyte secondary battery (hereinafter sometimes referred to as a “battery”) includes a negative electrode 1 described in detail below, and a negative electrode 1 that is in contact with the negative electrode 1 during discharge. It comprises an electrode group 4 composed of a positive electrode 2 for reducing ions and a porous separator 3 interposed between them to prevent direct contact between the negative electrode 1 and the positive electrode 2.
- the electrode group 4 and an electrolyte (not shown) having lithium ion conductivity are accommodated in the exterior case 5.
- the separator 3 is impregnated with an electrolyte having lithium ion conductivity.
- the positive electrode 2 is composed of a positive electrode current collector 2a and a positive electrode mixture layer 2b carried on the positive electrode current collector 2a.
- the negative electrode 1 includes a negative electrode current collector 1 a having a concave portion and a convex portion (hereinafter referred to as “current collector”), and at least a longitudinal direction of the convex portion.
- current collector a negative electrode current collector 1 a having a concave portion and a convex portion
- the columnar body lb is provided with a gap by a projecting body formed in a plurality of columnar body portions.
- the projecting body includes the center line in the oblique direction of each columnar body portion and the negative electrode current collector. At least on the surface of the columnar body portion on the side where the crossing angle with the center line in the thickness direction forms an obtuse angle.
- the columnar body portions are formed by sequentially changing the content ratio of the elements constituting them in the longitudinal direction in which the convex portions of the current collector are provided. Further, the columnar body portion formed by stacking n (n ⁇ 2) stages is formed so that the changing directions of the content ratios of the odd-numbered and even-numbered elements are different.
- the two surfaces of the convex portion mean a surface in a cross section when a protruding portion of the convex portion is cut in the longitudinal direction.
- the convex portion when it is a rectangular parallelepiped, it has a total of five surfaces including the top surface and the side surface of the convex portion, excluding the bottom surface of the convex portion. Therefore, the surface covered with the first-stage columnar body portion is one of the upper surface of the convex portion and the side surface of the convex portion.
- the columnar body portion is formed in a direction orthogonal to the side surface of the convex portion, it is formed as one surface, and when it is not orthogonal, it is formed as two surfaces.
- the formation surface of the columnar body portion is the upper surface and the side surface of the convex portion, and the surface covered by the first columnar body portion is Convex part Becomes part of the top and side surfaces.
- the positive electrode mixture layer 2b is LiCoO, LiNiO 2, Li MnO, or a mixture thereof.
- a lithium-containing composite oxide such as a composite compound is included as a positive electrode active material.
- Lithium nitrate can also be used. Furthermore, a part of these lithium-containing compounds may be substituted with a different element.
- the surface may be treated with a metal oxide, a lithium oxide, a conductive agent or the like, or the surface may be subjected to a hydrophobic treatment.
- the positive electrode mixture layer 2b further includes a conductive agent and a binder.
- Conductive agents include natural graphite and artificial graphite graphite, acetylene black, ketjen black, channel black, furnace black, lamp black, thermal black and other carbon blacks, and conductive fibers such as carbon fiber and metal fiber.
- binder for example, PVDF, polytetrafluoroethylene, polyethylene, polypropylene, ramid, woody effect, polyamide, polyimide, polyamide, imide, polyclinole linole, polyacrylic acid , Polyacrylic acid methyl ester, polyacrylic acid ethyl ester, polyacrylic acid hexyl ester, polymethacrylic acid, polymethacrylic acid methyl ester, polymethacrylic acid ethyl ester, polymethacrylic acid hexyl ester, poly (butyl acetate), poly (vinyl pyrrolidone), poly Ether, polyether sulfone, hexafluoropolypropylene, styrene butad
- a copolymer of two or more materials selected from leolomethinolevinoleetenore, acrylic acid, and hexagen may be used. You can also use a mixture of two or more selected from these.
- the positive electrode current collector 2a used for the positive electrode aluminum (A1), carbon, conductive resin, or the like can be used. Further, any of these materials may be surface treated with carbon or the like.
- an electrolyte solution in which a solute is dissolved in an organic solvent, or a so-called polymer electrolyte layer containing these and non-fluidized with a polymer can be applied.
- a separator 3 such as a nonwoven fabric or a microporous membrane made of polyethylene, polypropylene, aramid resin, amideimide, polyphenylene sulfide, polyimide, etc. is used between the positive electrode 2 and the negative electrode 1. It is preferable to impregnate the electrolyte solution.
- the inside or the surface of the separator 3 may contain a heat resistant filler such as anolemina, magnesia, silica, titania or the like.
- a heat-resistant layer composed of these fillers and the same binder used for the positive electrode 2 and the negative electrode 1 may be provided.
- the nonaqueous electrolyte material is selected based on the redox potential of each active material.
- Solutes preferably used for non-aqueous electrolytes include LiPF, LiBF, LiClO, LiAlCl, LiS
- Salts commonly used in lithium batteries such as NLi and lithium tetraphenylborate can be applied.
- the organic solvent for dissolving the salt includes ethylene carbonate (EC), propylene carbonate, butylene carbonate, vinylene carbonate, dimethylolate carbonate (DMC), jetinole carbonate, ethinoremethinolecarbonate ( EMC), dipropino carbonate, methyl formate, methyl acetate, methyl propionate, ethyl propionate, dimethoxymethane, ⁇ -butyrolatatane, ⁇ -valerolataton, 1,2-diethoxyethane, 1,2-dimethoxyethane, ethoxymethoxyethane, Tetrahydrofuran derivatives such as trimethoxymethane, tetrahydrofuran and 2-methyltetrahydrofuran, dimethyl sulfoxide, dioxolane derivatives such as 1,3-dioxolane, 4-methyl-1,3-dioxolane, formamide and alcohol Amide, dimethylformamide,
- vinylene carbonate, cyclohexyl benzene, biphenyl, diphenyl ether, butyl ethylene carbonate, dibutyl ethylene carbonate, phenylene carbonate carbonate, diallyl carbonate, fluoroethylene carbonate, force teconol carbonate, acetic acid Contains additives such as bur, ethylene sulfite, propane sultone, trifluoropropylene carbonate, dibenisofuran, 2,4-difluoroanisole, ⁇ -terfeninole, m-terphenyl, and so on! .
- the non-aqueous electrolyte is a polymer material such as polyethylene oxide, polypropylene oxide, polyphosphazene, polyaziridine, polyethylene sulfide, polybutyl alcohol, polyvinylidene fluoride, and polyhexafluoropropylene.
- Mixed seeds or more may be mixed with a compound or the like and used as a solid electrolyte. Further, it may be used in a gel form by mixing with the above organic solvent.
- a gel-like nonaqueous electrolyte may be disposed between the negative electrode 1 and the positive electrode 2 instead of the separator 3.
- the gel-like nonaqueous electrolyte may be disposed adjacent to the separator 3.
- the current collector la of the negative electrode 1 is made of a metal foil such as stainless steel, nickel, copper, or titanium, or a thin film of carbon or conductive resin. Furthermore, surface treatment may be performed with carbon, nickel, titanium, or the like.
- the columnar body part constituting the columnar body lb of the negative electrode 1 has a theoretical capacity density of 833 mAh / reversibly occluding and releasing lithium ions such as silicon (Si) and tin (Sn).
- An active material exceeding cm 3 can be used. With such an active material, it is possible to exert the effects of the present invention even if it is! /, Or a deviation of a composite active material including a simple substance, an alloy, a compound, a solid solution, and a silicon-containing material or a tin-containing material. It is.
- Si silicon-containing material
- Si Ox (0 ⁇ x ⁇ 2.0)
- Tin-containing materials include Ni Sn, Mg Sn, SnOx (0 ⁇ x ⁇ 2.
- active materials may be constituted singly or may be constituted by plural kinds of active materials.
- the active material include a compound containing Si, oxygen, and nitrogen, and a composite of a plurality of compounds containing Si and oxygen and having different constituent ratios of Si and oxygen.
- FIG. 2A is a partial cross-sectional schematic diagram showing the structure of the negative electrode in the embodiment of the present invention
- FIG. 2B is a schematic diagram for explaining the change in the value of X in the width direction of the active material in the embodiment. It is.
- FIG. 2A is a partial cross-sectional schematic diagram showing the structure of the negative electrode in the embodiment of the present invention
- FIG. 2B is a schematic diagram for explaining the change in the value of X in the width direction of the active material in the embodiment. It is.
- FIG. 3A is a partial schematic cross-sectional view showing in detail the structure of the negative electrode before charging in the embodiment of the present invention
- FIG. 3B shows the detailed structure of the negative electrode in the embodiment after charging. It is a partial section schematic diagram shown. Note that FIGS. 3A and 3B are shown in any scale to facilitate understanding of the voids of the columnar bodies formed by the protrusions of the plurality of columnar body portions.
- a recess 12 and a protrusion 13 are provided on at least the upper surface of the current collector 11 made of a conductive metal material such as a copper (Cu) foil.
- the active material represented by SiOx constituting the columnar body 15 is folded in a zigzag manner by an oblique vapor deposition method using, for example, a sputtering method or a vacuum vapor deposition method.
- it is formed in the shape of a columnar body 15 made up of n (n ⁇ 2) columnar body portions having different obliquely inclined directions in odd and even stages.
- the first-stage columnar body portion 151 constituting the columnar body 15 is arranged in the oblique direction as described below with reference to FIGS. 5A and 5B and FIGS. 6A and 6B.
- the crossing angle ⁇ between the center line (A—A) and the thickness direction center line (AA—AA) of current collector 11 forms an obtuse angle (180 ⁇ ).
- a plurality of protrusions 16 are provided on the 10 10 side.
- the second-stage columnar body portion 152 is formed in a direction different from the oblique direction of the first-stage columnar body portion 151, and the projecting body 16 is formed on the obtuse angle side.
- the projecting body 16 is oriented in the direction of the force away from the current collector 11 in the direction of the angle ⁇ between the vertical center line (A A) of the columnar body 15 and its perpendicular.
- the columnar body parts 153 to 158 are formed in the same direction as the columnar body part 151 for the odd-numbered stages and the columnar body part 152 for the even-numbered stages, for example. It may be formed in different directions as long as productivity and the configuration of the manufacturing apparatus allow.
- a plurality of columnar body portions are formed by being folded in a zigzag manner, thereby being stacked via the protrusions 16 formed in each columnar body portion, and a gap portion 17 as shown in FIG. 2A.
- a columnar body 15 is formed.
- the columnar body portion 151 of the columnar body 15 is not separated from the center line (A) in the oblique direction of the columnar body portion 151 on at least the convex portion 13 of the current collector 11. It is formed so as to form a crossing angle (hereinafter referred to as “an oblique angle”) 6 i with the center line (AA—AA) in the thickness direction of the electric body 11. Then, the columnar body portion 152 of the columnar body 15 covers the projecting body 161 of the columnar body portion 151 and the center line (B) in the oblique direction and the center line (AA—) in the thickness direction of the current collector 11. AA) and the oblique angle ⁇ are formed. Further, the columnar body portion 153 of the columnar body 15 is a columnar body.
- the center line (C) in the oblique direction and the center line (AA—AA) in the thickness direction of the current collector 11 form an oblique angle ⁇ so as to cover the protrusion 162 of the part 152 Has been.
- the 15 columnar body parts 154 cover the projecting body 163 of the columnar body part 153 with the center line (D) in the oblique direction and the center line (AA—AA) in the thickness direction of the current collector 11. To form an oblique angle ⁇
- the columnar body portion 155 of the columnar body 15 is formed so that the oblique line center line (E) and the thickness direction center line (AA) of the current collector 11 (AA) cover the projecting body 164 of the columnar body portion 154. — AA) and an oblique angle ⁇ , and a projecting body 165 is formed on the obtuse angle side.
- a porous gap portion 17 is formed in the center portion of the columnar body 15 by the protruding body of each columnar body portion.
- the protrusions are formed entirely on the obtuse angled surface inclined to each columnar part, but depending on the vapor deposition conditions, the protrusions can be formed only near the upper part of the obtuse angle side surface. Monkey.
- the protruding body 165 of the columnar body portion 155 is not necessarily required and may not be formed. Further, the oblique angles ⁇ , ⁇ , ⁇ , ⁇ , ⁇ are not necessarily required and may not be formed. Further, the oblique angles ⁇ , ⁇ , ⁇ , ⁇ , ⁇ are not necessarily required and may not be formed. Further, the oblique angles ⁇ , ⁇ , ⁇ , ⁇ , ⁇ are
- the columnar body parts 151, 152, 153, 154, 155, 156, 157, and 15 8 constituting the columnar body 15 are, for example, odd-numbered columnar body parts as schematically shown in FIG. 2B.
- 151, 153, 155, 1 57 and even-numbered columnar body parts 152, 154, 156, 158 Content ratio of elements in the width direction, for example
- the direction in which the value of x changes is different. That is, the value of X is sequentially increased from the oblique angle side forming the acute angle of the columnar body parts 151, 153, 155, and 157 toward the obtuse angle side.
- the force S is shown to change linearly with the value of x, but is not limited to this.
- the stress generated between the columnar body portions due to the expansion and contraction of each columnar body portion of the columnar body can be relieved by the porous void portion formed by the projecting body formed in the central portion of the columnar body.
- the portions where the respective columnar body portions are stacked and folded have different element composition ratios, and therefore are liable to be peeled off due to stress due to expansion and contraction and have low reliability.
- the stress can be relieved and the occurrence of peeling or the like can be greatly reduced.
- a highly reliable negative electrode with excellent long-term stability such as a charge / discharge cycle can be realized.
- the columnar body 15 having the five-stage columnar body portion is inclined on the convex portion 13 of the current collector 11, so that the columnar body When 15 is projected from the positive electrode 18, the concave portion 12 of the current collector 11 is partially shielded by the columnar body 15 from the positive electrode 18. Therefore, the lithium ions released from the positive electrode 18 during charging are blocked from reaching the concave portion 12 of the current collector 11 directly by the negative columnar body 15, and most of the lithium ions are occluded in the columnar body 15. Is suppressed. As the lithium ion is occluded, the tilting angle of the five-stage columnar body portion increases, and finally the columnar body 15 becomes almost upright with respect to the current collector 11. Note that the tilt angle is 90 ° or more due to design factors such as the number of columnar body parts that do not necessarily stand upright. Underneath, it may be folded, but it is preferable to design at an oblique angle of 90 °.
- the columnar body 15 formed of the five-stage columnar body portion expanded by charging is in an upright state with respect to the current collector 11. Become. Therefore, the electrolytic solution 19 between the adjacent columnar bodies 15 can easily move through the columnar bodies 15 as indicated by arrows in the drawing. Since the electrolytic solution 19 between the columnar bodies 15 can be easily convected through the gaps between the columnar bodies 15, the movement of lithium ions and the like are not hindered. As a result, it is possible to significantly improve the discharge characteristics at the time of no-discharge discharge and low temperature.
- FIGS. 4A and 4B a mechanism in which the columnar body 15 reversibly changes the oblique angle due to insertion and extraction of lithium ions will be described with reference to FIGS. 4A and 4B.
- a columnar body composed of one columnar body portion will be described as an example in order to facilitate the description.
- an n-stage configuration works with the same mechanism.
- FIG. 5A is a partial cross-sectional schematic diagram showing a state before charging of the negative electrode columnar body according to the embodiment of the present invention
- FIG. 5B shows a state after charging of the negative electrode columnar body according to the same embodiment. It is a partial cross section schematic diagram.
- the columnar body 15 shown in FIGS. 5A and 5B has a columnar shape from the lower side 15a in which the center line (A—A) of the columnar body 15 and the center line (AA—AA) of the current collector 11 form an acute angle.
- the element content ratio of the active material made of SiOx is changed so that the value of X continuously increases toward the upper side 15b forming the obtuse angle of the body 15.
- an active material composed of SiOx decreases in the amount of expansion due to occlusion of lithium ions as the value of X increases from 0 to 2.
- the expansion stress generated by expansion due to occlusion of lithium ions during charging is changed from the expansion stress F1 on the lower side 15a of the columnar body 15 to the expansion stress F2 on the upper side 15b. And continuously smaller.
- the tilt angle ⁇ 1 ⁇ force formed by the center line (A—A) of the columnar body 15 and the center line (AA—AA) of the current collector 11 also changes to ⁇ .
- the columnar body 15 rises in the direction indicated by the arrow.
- the expansion stress is reduced by contraction due to the release of lithium ions during discharge.
- the oblique angle of the columnar body 15 changes to ⁇ force ⁇ force ⁇ , and the columnar body 15 moves in the direction indicated by the arrow in FIG. 5B. Will be transformed.
- the tilt angle of the columnar body 15 reversibly changes due to insertion and extraction of lithium ions.
- the stress due to expansion / contraction of each columnar body part constituting the columnar body is provided by providing a porous space at the center of the columnar body composed of n-stage columnar body parts. Can be greatly relaxed.
- the columnar body formed in an inclined manner is lowered in height and the columnar body is formed in a plurality of stages, the columnar body can be formed into a substantially upright shape, so that it can be seen during occlusion / release of lithium ions. Only the height (thickness) of the columnar body changes. Therefore, a large gap between adjacent columnar bodies can be maintained.
- the stress due to expansion / contraction is remarkably reduced while realizing a high capacity using an active material with large expansion / contraction due to insertion / extraction of lithium ions.
- the negative electrode structure it is possible to realize a non-aqueous electrolyte secondary battery excellent in capacity retention, high rate characteristics, and low temperature characteristics.
- FIGS. 6A to 6D a method for producing a columnar body of a negative electrode for a non-aqueous electrolyte secondary battery according to an embodiment of the present invention will be described with reference to FIGS. 6A to 6D, FIGS. 7A to 7E, and FIG.
- FIGS. 6A to 6D are partial cross-sectional schematic diagrams illustrating a method for forming a columnar body provided with a projecting body of a negative electrode for a nonaqueous electrolyte secondary battery in an embodiment of the present invention.
- a columnar body composed of one columnar body portion will be described as an example in order to facilitate explanation of the force that is composed of columnar body portions of columnar body strength steps.
- the n-stage configuration works with the same mechanism.
- the columnar body 15 is formed in a state where the value of X of SiOx to be formed is sequentially changed with respect to the moving direction of the current collector 11.
- the value of X on the right side of the drawing is small and the value of X on the left side of the drawing is large.
- the convex portion 13 of the current collector is shown enlarged to help understanding.
- the force S that the columnar body 15 grows on the convex portion 13 of the current collector 11 causes the protrusion 16 to be formed on the left side in the drawing where the value of X is large. It is formed.
- the projecting body 16 is bonded to oxygen gas while Si, which is an evaporated particle forming the columnar body 15, flies and is formed on the current collector 11. It is thought to result from being disrupted by a collision. Therefore, the protrusions 16 are not always formed, but are strongly dependent on the film forming speed and the degree of vacuum. For example, in the case of 10 nm / S or less, since the scattering component increases, only the columnar body 15 is easily formed. However, this condition is not uniquely determined and varies in relation to other conditions such as the degree of vacuum.
- the columnar body 15 having the projecting bodies 16 is formed at a predetermined oblique angle ⁇ to produce a negative electrode.
- the evaporated particles from the vapor deposition source are obliquely applied to the current collector 11.
- a method of incidence is known.
- the columnar body 15 grows macroscopically at an angle between the normal direction of the current collector 11 and the incident direction of the evaporated particles. That is, in the growth process of the columnar body 15, at the initial stage of the growth, the projections of the adjacent current collectors and the columnar body 15 itself develop a shadow effect on the evaporated particles as the columnar body 15 grows.
- the evaporated particles flying from the evaporation source may be combined with oxygen gas having a short mean free process distance.
- a component that is scattered by a collision or the like (a component in which evaporated particles are deflected to an angle different from the incident angle) is generated.
- the majority of the evaporated particles It is taken into the columnar body by growth and is formed as a continuously grown columnar body.
- the growing shadow portion of the columnar body described above is not exposed to the evaporated particles having an incident angle where the majority of the columnar bodies fly.
- the scattering components of the evaporated particles at least the evaporated particles in the direction toward the columnar body fly and grow at a predetermined angle with respect to the surface of the shadowed portion of the columnar body.
- the scattering component of the evaporated particles is smaller than the number of evaporated particles forming the columnar body, it does not grow on the continuum film, but grows discretely, so that the protrusions are formed. .
- the inclined angle of the formed protrusions depends on the angle at which the scattering component of the evaporated particles flies, similarly to the inclined angle of the columnar bodies, and depends on the formation surface of the columnar protrusions. In contrast, it is formed at a predetermined oblique angle.
- the protrusion is formed by the scattering component of the evaporated particles, it can be controlled by the degree of vacuum, the film forming speed, the type and flow rate of the introduced gas, the shape of the convex portion of the current collector, and the like. Is.
- FIGS. 7A to 7E are partial cross-sectional schematic diagrams illustrating a method for forming a columnar body including n-stage columnar body portions of the negative electrode for a nonaqueous electrolyte secondary battery in the embodiment of the present invention.
- 8 is a schematic diagram for explaining the manufacturing apparatus.
- the gas introduction pipe 42 includes a nozzle 45 that releases oxygen gas into the vacuum vessel 41, and a fixing base 43 that fixes the current collector is installed above the nozzle 45.
- an evaporation source 46 that is deposited on the surface of the current collector to form a columnar body is installed below the fixed base 43 vertically.
- the positional relationship between the current collector and the vapor deposition source 46 can be changed depending on the angle of the fixed base 43. That is, the oblique direction of each step of the columnar body composed of n steps is controlled by changing the angle ⁇ formed by the normal direction and the horizontal direction of the surface of the current collector by the fixed base 43.
- this manufacturing apparatus shows an example in which a columnar body is formed by forming a columnar body portion of ⁇ steps on one side of a current collector, but in actuality, both sides of the current collector are shown.
- a device configuration for producing a columnar body is used.
- the concave portion 12 and the convex portion 13 are formed on the surface by a plating method.
- a current collector 11 having a height 7. ⁇ ⁇ ⁇ ⁇ width 10 111 and an interval of 20 ⁇ is manufactured. Then, the current collector 11 is installed on the fixed base 43 shown in FIG.
- the fixing base 43 is disposed at an angle ⁇ (for example, 60 °) with respect to the normal direction of the current collector 1 1.
- an active material such as Si (scrap silicon: purity 99.999%) is evaporated by heating with an electron beam, and is incident on the convex portion 13 of the current collector 11 from the direction of the arrow in FIG. 7B.
- oxygen (O) gas is introduced from the gas introduction pipe 42 and supplied from the nozzle 45 toward the current collector 11.
- the interior of the empty container 41 was an oxygen atmosphere with a pressure of 3.5 Pa.
- the active material force of SiOx in which Si and oxygen are combined for example, at a predetermined height (thickness) at an angle ⁇ on the convex portion 13 of the current collector 11 placed on the fixed base 43 arranged at an angle ⁇ .
- a first columnar body portion 151 having a thickness of 10 m in the oblique direction and having a protruding body (not shown) is formed.
- the columnar body portion 151 is formed in a state where the value of X of SiO X to be formed is sequentially changed in the width direction of the current collector 11. For example, in FIG.
- the current collector 11 in which the first-stage columnar body portion 151 is formed on the convex portion 13 is fixed to the fixing base 43 as shown by the broken line in the drawing. Is rotated and placed at an angle (180- ⁇ ) (for example, 120 °) with respect to the normal direction of the current collector 11. Then, the active material such as Si (scrap silicon: purity 99. 999%) is evaporated, and the first columnar body portion 151 of the current collector 11 is placed in FIG. Incident from the direction of the arrow. At the same time, oxygen (O) gas is introduced from the gas introduction pipe 42 and is directed from the nozzle 45 to the current collector 11.
- O oxygen
- the SiOx active material in which Si and oxygen are combined has an angle ⁇ on the first columnar body portion 151 and the thickness (height) in the oblique direction 0 ⁇ 1 111 to 5111.
- a columnar body portion 152 having a not-shown shape is formed so as to cover the protruding body of the first-stage columnar body portion 151.
- the columnar body portion 152 is formed in a state in which the value of X of SiOx to be formed is sequentially changed in the width direction of the current collector 11.
- the value of X on the left side in the drawing is small and the value of X on the right side in the drawing is large.
- the first-stage columnar body portion 151 and the second-stage columnar body portion 152 are formed so that the change direction of the value of X is opposite to the width direction of the current collector 11, and Produced with different vertical and oblique directions.
- the fixing stage 43 is returned to the same state as in FIG. 7B, and the third stage so as to cover the projecting body of the second stage columnar body part 152.
- the columnar body portion 153 is formed with a thickness (height) in the oblique direction 0 ⁇ 1 111 to 5 111.
- the value of X on the right side in the drawing is small and the value of X on the left side in the drawing is large.
- the second-stage columnar body portion 152 and the third-stage columnar body portion 153 are formed so that the change direction of the X value is opposite to the width direction of the current collector 11 and It is made with different angle and oblique direction.
- the first-stage columnar body portion 151 and the third-stage columnar body portion 153 are formed in the same oblique direction.
- the thickness (height) in the oblique direction is 0.1 m to 5 except for the first-stage columnar body portion.
- a negative electrode 1 having a columnar body 15 composed of a columnar body portion made of m is produced.
- the columnar body portions of 2 m to 5 m are used.
- the odd-numbered columnar body portions 151, 153, 155, 157 and the several-stage columnar body portions 152, 154, 156, 158 are arranged as follows. It is formed opposite to the width direction, and is manufactured with different angles and directions.
- a columnar body composed of arbitrary n (n ⁇ 2) columnar body portions can be formed.
- a columnar body is formed on a current collector having a predetermined size.
- the present invention is not limited to this, and various apparatus configurations are possible.
- a roll-shaped current collector is placed between the feed roll and the take-up roll, and a plurality of film forming rolls are placed in series between the rolls, and the current collector is moved in one direction while being arranged in an n-stage column shape. You may make a body.
- the current collector may be inverted to form a columnar body on the other surface of the current collector. Thereby, a negative electrode can be produced with high productivity.
- the height of the first-stage columnar body portion 151 of the columnar body 15 is 10 ⁇ m, and the second-stage columnar body portion 152 is formed near the tip thereof.
- n 8 steps so as to cover three surfaces at least in the longitudinal section of the protruding portion of the protruding portion 13 of the current collector 11.
- All the columnar body parts 15;! To 158 may be similarly formed at a height of 2 m to 5 m.
- the height of all the columnar body portions may be set to 0 ⁇ 1 111 to 2 111 to increase the number of steps.
- the three surfaces of the convex portion are, for example, when the convex portion is a rectangular parallelepiped, the surface covered by the first-stage columnar body portion is the convex upper surface and the convex side surface. One or two sides. Therefore, if the columnar body part is formed in a direction orthogonal to the side surface of the convex part, it is formed as one surface, and if it is not orthogonal, it is formed in two surfaces.
- the surface covered with the second columnar body portion is at least one of the remaining three surfaces when the first columnar body portion covers one surface of the convex side surface.
- the first-stage columnar body covers two surfaces of the convex side surface, it is formed on the remaining two surfaces.
- the convex shape is an ellipse or a cylinder when the convex portion is viewed from the top surface
- the formation surface of the body part is the upper surface and the side surface of the convex part
- the surface covered with the first columnar body part is the upper surface and part of the side surface of the convex part.
- the surface covered by the second columnar body portion is the remaining part of the side surface of the convex portion.
- the columnar body of the negative electrode was produced using the manufacturing apparatus shown in FIG.
- a strip-shaped electrolytic copper foil having a thickness of 30 m and a convex portion formed on the surface with a width of 10 m, a height of 7.5 m, and an interval of 20 m was used by using the Mekking method. It was.
- Si was used as the active material for the negative electrode, and an oxygen gas having a purity of 99.7% was obtained from Nozure 45 using a vapor deposition unit (a unit of vapor deposition source, crucible, and electron beam generator).
- a columnar body was produced by introducing it into a vacuum vessel and changing the value of X in the width direction made of SiOx.
- the inside of the vacuum vessel was in an oxygen atmosphere with a pressure of 3.5 Pa.
- the electron beam generated by the electron beam generator was deflected by the deflection yoke and irradiated to the deposition source.
- scrap material scrap silicon: purity 99.999%) generated when forming a semiconductor wafer was used.
- the columnar body was formed at a film formation rate of about 8 nm / s by adjusting the angle of the fixed base so that the angle ⁇ was 60 °.
- a first-stage columnar body for example, height ⁇ cross-sectional area 150 11 m 2
- the columnar body for example, height 3111, cross-sectional area 150 ⁇ 2
- the angle of the columnar body in the negative electrode with respect to the center line of the current collector was evaluated by cross-sectional observation using a scanning electron microscope (S-4700, manufactured by Hitachi). The angle was about 41 °. At this time, the formed columnar body had a thickness (height) of 31 Hm.
- EPMA electron beam microprobe analyzer
- the oxygen distribution was examined by measuring the line distribution in the cross-sectional direction of the columnar body portion of each stage constituting the negative pole columnar body. As a result, in the width direction of each columnar body part, the oxygen concentration (value of X) continuously increased from the oblique angle ⁇ side to the (180- ⁇ ) direction. The increasing direction of the oxygen concentration (X value) was in the opposite direction between the odd-numbered columnar body portions and the even-numbered columnar body portions. The range of X at this time was 0.;! ⁇ 2 and the average was 0.6.
- a positive electrode having a positive electrode active material capable of inserting and extracting lithium ions was produced by the following method.
- the pack was mixed with 4 parts by weight.
- NMP N-methyl-2-pyrrolidone
- PVDF polyvinylidene fluoride
- An appropriate amount of NMP was added to this mixture to prepare a positive electrode mixture paste.
- This positive electrode mixture paste was applied to both sides of the current collector using a doctor blade method on a positive electrode current collector (thickness 15 m) with aluminum (A1) foil strength, and the density of the positive electrode mixture layer was 3 ⁇ Rolled to 5 g / cc and 160 m thick, dried sufficiently at 85 ° C, and cut this to produce a positive electrode.
- the exposed part was provided on the A1 foil without facing the negative electrode on the inner peripheral side of the positive electrode, and an A1 positive electrode lead was welded.
- the negative electrode and the positive electrode produced as described above were laminated via a separator made of porous polypropylene having a thickness of 25 m to form a 40 mm x 30 mm square electrode group. Then, in the electrode group, an electrolyte solution of LiPF ethylene carbonate / jetyl carbonate is mixed.
- a negative electrode was produced in the same manner as in Example 1 except that the angle of the fixing base was adjusted so that the angle ⁇ force became 70 °.
- the oblique angle of the columnar body portion of each step was about 54 °, and the thickness (height) of the formed columnar body was 31 m.
- the oxygen concentration (value of X) continuously increased from the oblique angle ⁇ side to the (180- ⁇ ) direction.
- the increasing direction of the oxygen concentration (X value) was in the opposite direction between the odd-numbered columnar body portions and the even-numbered columnar body portions.
- the range of X at this time was 0. !!-2, with an average of 0.6.
- a nonaqueous electrolyte secondary battery produced by the same method as in Example 1 was used except that the above negative electrode was used.
- a negative electrode was produced in the same manner as in Example 1 except that the angle of the fixing base was adjusted so that the angle ⁇ force was 50 °.
- the oblique angle of the columnar body portion of each step was about 31 °, and the thickness (height) of the formed columnar body was 31 m.
- the oxygen concentration (value of X) continuously increased from the oblique angle ⁇ side to the (180- ⁇ ) direction.
- the increasing direction of the oxygen concentration (X value) was in the opposite direction between the odd-numbered columnar body portions and the even-numbered columnar body portions.
- the range of X at this time was 0. !!-2, with an average of 0.6.
- Sample 3 was a non-aqueous electrolyte secondary battery produced by the same method as in Example 1 except that the above negative electrode was used.
- a negative electrode was produced in the same manner as in Example 1, except that a columnar body having 10 steps was formed and the thickness of the columnar body portion of each step was changed to 3 am.
- the oblique angle of the columnar body portion of each step was about 41 °, and the thickness (height) of the formed columnar body was 30 ⁇ m.
- Sample 4 was a nonaqueous electrolyte secondary battery produced by the same method as in Example 1 except that the above negative electrode was used.
- a negative electrode was produced in the same manner as in Example 1 except that a columnar body having 15 steps was formed and the thickness of the columnar body portion of each step was set to 2 ⁇ m.
- the oblique angle of the columnar body portion of each step was about 41 °, and the thickness (height) of the formed columnar body was 30 ⁇ m.
- the oxygen concentration (value of X) continuously increased from the oblique angle ⁇ side to the (180- ⁇ ) direction.
- the increasing direction of the oxygen concentration (X value) was in the opposite direction between the odd-numbered columnar body portions and the even-numbered columnar body portions.
- the range of X at this time was 0. !!-2, with an average of 0.6.
- a negative electrode was produced in the same manner as in Example 1 except that a columnar body having 30 steps was formed and the thickness of the columnar body portion of each step was changed to 1 am.
- the oblique angle of the columnar body portion of each step was about 41 °, and the thickness (height) of the formed columnar body was 30 ⁇ m.
- the oxygen concentration (value of X) increased continuously from the oblique angle ⁇ side to the (1 80- ⁇ ) direction.
- the increasing direction of the oxygen concentration (X value) was in the opposite direction between the odd-numbered columnar body portions and the even-numbered columnar body portions.
- the range of X at this time was 0. !!-2, with an average of 0.6.
- a negative electrode was produced in the same manner as in Example 1 except that the pressure inside the vacuum vessel was 1.7 Pa in an oxygen atmosphere, and the columnar body part had a thickness of 5 m and a 5-stage columnar body. .
- the oblique angle of the columnar body portion of each step was about 41 °, and the thickness (height) of the formed columnar body was 25 m.
- Sample 7 was a nonaqueous electrolyte secondary battery produced by the same method as in Example 1 except that the above negative electrode was used.
- a negative electrode was produced in the same manner as in Example 1 except that a columnar body composed of 60 steps was formed and the thickness of the columnar body portion of each step was changed to 0.5 am.
- the oblique angle of the columnar body portion of each step was about 41 °, and the thickness (height) of the formed columnar body was 30 ⁇ m.
- the oxygen concentration (value of X) continuously increased from the oblique angle ⁇ side to the (180- ⁇ ) direction.
- the increasing direction of the oxygen concentration (X value) was in the opposite direction between the odd-numbered columnar body portions and the even-numbered columnar body portions.
- the range of X at this time was 0. !!-2, with an average of 0.6.
- a negative electrode was produced in the same manner as in Example 1 except that a columnar body was formed by tilting in one step at a height (thickness) of 30.
- a columnar body was formed by tilting in one step at a height (thickness) of 30.
- a non-aqueous electrolyte secondary battery produced by the same method as in Example 1 except that the above negative electrode was used is referred to as Sample C1.
- Each non-aqueous electrolyte secondary battery was charged and discharged under the following conditions at an ambient temperature of 25 ° C.
- the battery voltage is at a constant current of 1.OC (21mA).
- the battery was charged until it reached 2V, and constant voltage charging was performed at a constant voltage of 4.2V to decay to a current value of 0 ⁇ 05C (1.05mA). Then, it rested for 30 minutes.
- the battery was discharged at a constant current at a current rate of 0.2C (4.2 mA) at a time rate until the battery voltage dropped to 3.0V.
- Each non-aqueous electrolyte secondary battery was repeatedly charged and discharged under the following conditions at an ambient temperature of 25 ° C.
- the battery is charged at a constant current of 1.OC (21mA) until the battery voltage reaches 4.2V, and the charging current is 4.2% at a constant voltage of 0V.
- the battery was charged until the current value dropped to 05C (1. 05mA). Then, after charging, it was paused for 30 minutes.
- the battery was discharged at a constant current until the battery voltage dropped to 3.0 V at a current rate of 0.2 C (4.2 mA). Then, after the discharge, it was paused for 30 minutes.
- the above charge / discharge cycle was defined as one cycle, which was repeated 500 times.
- the ratio of the discharge capacity at the 500th cycle to the discharge capacity at the first cycle is expressed as a percentage.
- the capacity retention rate (%) was used. In other words, the closer the capacity retention rate is to 100, the better the charge / discharge cycle characteristics.
- Fig. 11 shows the evaluation results of Sample 1 and Sample C1 as an example of charge / discharge cycle characteristics.
- the negative electrode including a columnar body having a plurality of columnar body portions on the convex portion of the current collector and having a porous void portion formed by the projecting body at the center thereof It was confirmed that a non-aqueous electrolyte secondary battery with significantly improved cycle characteristics can be realized by using.
- the present invention is not particularly limited as long as it is an element capable of reversibly occluding and releasing lithium ions.
- the active material may contain materials other than the above elements.
- transition metals and 2A group elements are included!
- the shape and interval of the protrusions formed on the current collector are not limited to the contents described in the above embodiments, and an oblique columnar body is formed. Any shape is possible as long as it is possible.
- the oblique angle formed by the center line of the columnar body and the centerline of the current collector, and the shape and dimensions of the columnar body are not limited to the above embodiment, It is appropriately changed depending on the required characteristics of the nonaqueous electrolyte secondary battery to be used.
- the negative electrode for a non-aqueous electrolyte secondary battery of the present invention can provide a non-aqueous electrolyte secondary battery excellent in high rate characteristics and charge / discharge cycle characteristics while enabling high capacity. Therefore, from portable electronic devices such as mobile phones and PDAs that are expected to be in great demand in the future. It is useful as a non-aqueous electrolyte secondary battery up to large electronic devices.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Battery Electrode And Active Subsutance (AREA)
- Secondary Cells (AREA)
- Cell Electrode Carriers And Collectors (AREA)
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/093,540 US20100291441A1 (en) | 2006-12-13 | 2007-11-26 | Negative electrode for non-aqueous electrolyte secondary battery, method of manufacturing the same, and non-aqueous electrolyte secondary battery using the same |
CN2007800013527A CN101356666B (zh) | 2006-12-13 | 2007-11-26 | 非水电解质二次电池用负极及其制造方法、以及采用该负极的非水电解质二次电池 |
EP07832439A EP2051317A4 (en) | 2006-12-13 | 2007-11-26 | NEGATIVE ELECTRODE FOR RECHARGEABLE BATTERY WITH NONAQUEOUS ELECTROLYTE, METHOD FOR MANUFACTURING THE NEGATIVE ELECTRODE, AND RECHARGEABLE BATTERY WITH NONAQUEOUS ELECTROLYTE USING THE NEGATIVE ELECTRODE |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006335410 | 2006-12-13 | ||
JP2006-335410 | 2006-12-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2008072460A1 true WO2008072460A1 (ja) | 2008-06-19 |
Family
ID=39511485
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2007/072714 WO2008072460A1 (ja) | 2006-12-13 | 2007-11-26 | 非水電解質二次電池用負極とその製造方法およびそれを用いた非水電解質二次電池 |
Country Status (6)
Country | Link |
---|---|
US (1) | US20100291441A1 (ja) |
EP (1) | EP2051317A4 (ja) |
JP (1) | JP2008171802A (ja) |
KR (1) | KR101038178B1 (ja) |
CN (1) | CN101356666B (ja) |
WO (1) | WO2008072460A1 (ja) |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009010758A2 (en) | 2007-07-17 | 2009-01-22 | Nexeon Limited | A method of fabricating structured particles composed of silicon or a silicon-based material and their use in lithium rechargeable batteries |
US7683359B2 (en) | 2002-11-05 | 2010-03-23 | Nexeon Ltd. | Structured silicon anode |
CN102197517A (zh) * | 2008-10-27 | 2011-09-21 | 日产自动车株式会社 | 蓄电装置用复合电极、其制造方法及蓄电装置 |
US8101298B2 (en) | 2006-01-23 | 2012-01-24 | Nexeon Ltd. | Method of fabricating fibres composed of silicon or a silicon-based material and their use in lithium rechargeable batteries |
US20120244441A1 (en) * | 2009-12-10 | 2012-09-27 | The University Of Tokyo | Silicon film and lithium secondary battery |
US8585918B2 (en) | 2006-01-23 | 2013-11-19 | Nexeon Ltd. | Method of etching a silicon-based material |
US8642211B2 (en) | 2007-07-17 | 2014-02-04 | Nexeon Limited | Electrode including silicon-comprising fibres and electrochemical cells including the same |
US8772174B2 (en) | 2010-04-09 | 2014-07-08 | Nexeon Ltd. | Method of fabricating structured particles composed of silicon or silicon-based material and their use in lithium rechargeable batteries |
US8945774B2 (en) | 2010-06-07 | 2015-02-03 | Nexeon Ltd. | Additive for lithium ion rechageable battery cells |
US8962183B2 (en) | 2009-05-07 | 2015-02-24 | Nexeon Limited | Method of making silicon anode material for rechargeable cells |
US9012079B2 (en) | 2007-07-17 | 2015-04-21 | Nexeon Ltd | Electrode comprising structured silicon-based material |
US9184438B2 (en) | 2008-10-10 | 2015-11-10 | Nexeon Ltd. | Method of fabricating structured particles composed of silicon or a silicon-based material and their use in lithium rechargeable batteries |
US9252426B2 (en) | 2007-05-11 | 2016-02-02 | Nexeon Limited | Silicon anode for a rechargeable battery |
US9608272B2 (en) | 2009-05-11 | 2017-03-28 | Nexeon Limited | Composition for a secondary battery cell |
US9647263B2 (en) | 2010-09-03 | 2017-05-09 | Nexeon Limited | Electroactive material |
US9853292B2 (en) | 2009-05-11 | 2017-12-26 | Nexeon Limited | Electrode composition for a secondary battery cell |
US9871248B2 (en) | 2010-09-03 | 2018-01-16 | Nexeon Limited | Porous electroactive material |
US11444285B2 (en) | 2020-02-28 | 2022-09-13 | Nissan North America, Inc. | Three-dimensional anode current collector for lithium batteries |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008218125A (ja) * | 2007-03-02 | 2008-09-18 | Matsushita Electric Ind Co Ltd | リチウムイオン二次電池用負極およびリチウムイオン二次電池 |
JP5326340B2 (ja) * | 2008-04-28 | 2013-10-30 | ソニー株式会社 | 二次電池用負極、二次電池および電子機器 |
JP4906886B2 (ja) * | 2009-05-18 | 2012-03-28 | 日産自動車株式会社 | 蓄電デバイス用複合電極、その製造方法及び蓄電デバイス |
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 |
JP5446612B2 (ja) | 2009-08-28 | 2014-03-19 | Tdk株式会社 | リチウムイオン二次電池 |
EP2630684A4 (en) | 2010-10-22 | 2015-12-23 | Amprius Inc | COMPOSITE STRUCTURES CONTAINING POROUS ACTIVE MATERIALS HIGH CAPACITY CONTRAINTS IN ENVELOPES |
GB2492167C (en) | 2011-06-24 | 2018-12-05 | Nexeon Ltd | Structured particles |
AT511668B1 (de) * | 2011-06-30 | 2015-05-15 | Avl List Gmbh | Wiederaufladbare elektrische batterie |
GB201117279D0 (en) * | 2011-10-06 | 2011-11-16 | Nexeon Ltd | Etched silicon structures, method of forming etched silicon structures and uses thereof |
WO2013114095A1 (en) | 2012-01-30 | 2013-08-08 | Nexeon Limited | Composition of si/c electro active material |
GB2499984B (en) | 2012-02-28 | 2014-08-06 | Nexeon Ltd | Composite particles comprising a removable filler |
GB2502625B (en) | 2012-06-06 | 2015-07-29 | Nexeon Ltd | Method of forming silicon |
GB2507535B (en) | 2012-11-02 | 2015-07-15 | Nexeon Ltd | Multilayer electrode |
US20160233490A1 (en) * | 2013-07-10 | 2016-08-11 | Umicore | Silicon-Based Powder and Electrode Containing the Same |
WO2015045341A1 (ja) * | 2013-09-27 | 2015-04-02 | 三洋電機株式会社 | 非水電解質二次電池用負極 |
KR101567203B1 (ko) | 2014-04-09 | 2015-11-09 | (주)오렌지파워 | 이차 전지용 음극 활물질 및 이의 방법 |
KR101604352B1 (ko) | 2014-04-22 | 2016-03-18 | (주)오렌지파워 | 음극 활물질 및 이를 포함하는 리튬 이차 전지 |
US9923201B2 (en) | 2014-05-12 | 2018-03-20 | Amprius, Inc. | Structurally controlled deposition of silicon onto nanowires |
GB2533161C (en) | 2014-12-12 | 2019-07-24 | Nexeon Ltd | Electrodes for metal-ion batteries |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002279974A (ja) | 2001-03-19 | 2002-09-27 | Sanyo Electric Co Ltd | 二次電池用電極の製造方法 |
JP2002313319A (ja) * | 2001-04-09 | 2002-10-25 | 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 |
JP2003017040A (ja) | 2001-06-28 | 2003-01-17 | Sanyo Electric Co Ltd | 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用電極 |
JP2005196970A (ja) | 2003-12-26 | 2005-07-21 | Matsushita Electric Ind Co Ltd | 非水電解質二次電池用負極とその製造方法ならびにそれを用いた非水電解質二次電池 |
JP2006269306A (ja) * | 2005-03-25 | 2006-10-05 | Sanyo Electric Co Ltd | リチウム二次電池用電極およびその製造方法 |
JP2006278104A (ja) * | 2005-03-29 | 2006-10-12 | Sanyo Electric Co Ltd | リチウム二次電池 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6887623B2 (en) * | 2001-04-09 | 2005-05-03 | Sanyo Electric Co., Ltd. | Electrode for rechargeable lithium battery and rechargeable lithium battery |
JP4994634B2 (ja) * | 2004-11-11 | 2012-08-08 | パナソニック株式会社 | リチウムイオン二次電池用負極、その製造方法、およびそれを用いたリチウムイオン二次電池 |
US8080334B2 (en) * | 2005-08-02 | 2011-12-20 | Panasonic Corporation | Lithium secondary battery |
EP1953850B1 (en) * | 2005-11-07 | 2011-03-23 | Panasonic Corporation | Electrode for lithium rechargeable battery, lithium rechargeable battery, and process for producing said lithium rechargeable battery |
CN101361209B (zh) * | 2006-02-14 | 2012-03-21 | 松下电器产业株式会社 | 非水电解质二次电池用电极及其制造方法以及具备该电极的非水电解质二次电池 |
US8734997B2 (en) * | 2006-10-10 | 2014-05-27 | Panasonic Corporation | Negative electrode for nonaqueous electrolyte secondary battery |
US8029933B2 (en) * | 2006-10-13 | 2011-10-04 | Panasonic Corporation | Negative electrode for non-aqueous electrolyte secondary battery, method for manufacturing the same, and non-aqueous electrolyte secondary battery using the same |
-
2007
- 2007-11-05 JP JP2007286986A patent/JP2008171802A/ja not_active Withdrawn
- 2007-11-26 US US12/093,540 patent/US20100291441A1/en not_active Abandoned
- 2007-11-26 EP EP07832439A patent/EP2051317A4/en not_active Withdrawn
- 2007-11-26 CN CN2007800013527A patent/CN101356666B/zh not_active Expired - Fee Related
- 2007-11-26 WO PCT/JP2007/072714 patent/WO2008072460A1/ja active Application Filing
- 2007-11-26 KR KR1020087011621A patent/KR101038178B1/ko not_active IP Right Cessation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002279974A (ja) | 2001-03-19 | 2002-09-27 | Sanyo Electric Co Ltd | 二次電池用電極の製造方法 |
JP2002313319A (ja) * | 2001-04-09 | 2002-10-25 | 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 |
JP2003017040A (ja) | 2001-06-28 | 2003-01-17 | Sanyo Electric Co Ltd | 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用電極 |
JP2005196970A (ja) | 2003-12-26 | 2005-07-21 | Matsushita Electric Ind Co Ltd | 非水電解質二次電池用負極とその製造方法ならびにそれを用いた非水電解質二次電池 |
JP2006269306A (ja) * | 2005-03-25 | 2006-10-05 | Sanyo Electric Co Ltd | リチウム二次電池用電極およびその製造方法 |
JP2006278104A (ja) * | 2005-03-29 | 2006-10-12 | Sanyo Electric Co Ltd | リチウム二次電池 |
Cited By (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8384058B2 (en) | 2002-11-05 | 2013-02-26 | Nexeon Ltd. | Structured silicon anode |
US7683359B2 (en) | 2002-11-05 | 2010-03-23 | Nexeon Ltd. | Structured silicon anode |
US7842535B2 (en) | 2002-11-05 | 2010-11-30 | Nexeon Ltd. | Structured silicon anode |
US8017430B2 (en) | 2002-11-05 | 2011-09-13 | Nexeon Ltd. | Structured silicon anode |
US9583762B2 (en) | 2006-01-23 | 2017-02-28 | Nexeon Limited | Method of fabricating fibres composed of silicon or a silicon-based material and their use in lithium rechargeable batteries |
US8597831B2 (en) | 2006-01-23 | 2013-12-03 | Nexeon Ltd. | Method of fabricating fibres composed of silicon or a silicon-based material and their use in lithium rechargeable batteries |
US8585918B2 (en) | 2006-01-23 | 2013-11-19 | Nexeon Ltd. | Method of etching a silicon-based material |
US8101298B2 (en) | 2006-01-23 | 2012-01-24 | Nexeon Ltd. | Method of fabricating fibres composed of silicon or a silicon-based material and their use in lithium rechargeable batteries |
US9871249B2 (en) | 2007-05-11 | 2018-01-16 | Nexeon Limited | Silicon anode for a rechargeable battery |
US9252426B2 (en) | 2007-05-11 | 2016-02-02 | Nexeon Limited | Silicon anode for a rechargeable battery |
US8870975B2 (en) | 2007-07-17 | 2014-10-28 | Nexeon Ltd. | Method of fabricating structured particles composed of silicon or a silicon-based material and their use in lithium rechargeable batteries |
EP2194596A3 (en) * | 2007-07-17 | 2010-11-17 | Nexeon Limited | A method of fabricating structured particles composed of silicon or a silicon-based material and their use in lithium rechargeable batteries |
JP4834814B2 (ja) * | 2007-07-17 | 2011-12-14 | ネグゼオン・リミテッド | シリコン又はシリコンベースの材料で構成される構造化粒子の製造方法及びリチウム蓄電池におけるそれらの使用 |
US8642211B2 (en) | 2007-07-17 | 2014-02-04 | Nexeon Limited | Electrode including silicon-comprising fibres and electrochemical cells including the same |
JP2010533637A (ja) * | 2007-07-17 | 2010-10-28 | ネグゼオン・リミテッド | シリコン又はシリコンベースの材料で構成される構造化粒子の製造方法及びリチウム蓄電池におけるそれらの使用 |
WO2009010758A2 (en) | 2007-07-17 | 2009-01-22 | Nexeon Limited | A method of fabricating structured particles composed of silicon or a silicon-based material and their use in lithium rechargeable batteries |
US8940437B2 (en) | 2007-07-17 | 2015-01-27 | Nexeon Limited | Method of fabricating structured particles composed of silicon or a silicon-based material and their use in lithium rechargeable batteries |
US9871244B2 (en) | 2007-07-17 | 2018-01-16 | Nexeon Limited | Method of fabricating structured particles composed of silicon or a silicon-based material and their use in lithium rechargeable batteries |
WO2009010758A3 (en) * | 2007-07-17 | 2009-03-12 | Nexeon Ltd | A method of fabricating structured particles composed of silicon or a silicon-based material and their use in lithium rechargeable batteries |
US9012079B2 (en) | 2007-07-17 | 2015-04-21 | Nexeon Ltd | Electrode comprising structured silicon-based material |
US9184438B2 (en) | 2008-10-10 | 2015-11-10 | Nexeon Ltd. | Method of fabricating structured particles composed of silicon or a silicon-based material and their use in lithium rechargeable batteries |
CN102197517A (zh) * | 2008-10-27 | 2011-09-21 | 日产自动车株式会社 | 蓄电装置用复合电极、其制造方法及蓄电装置 |
US8962183B2 (en) | 2009-05-07 | 2015-02-24 | Nexeon Limited | Method of making silicon anode material for rechargeable cells |
US9553304B2 (en) | 2009-05-07 | 2017-01-24 | Nexeon Limited | Method of making silicon anode material for rechargeable cells |
US10050275B2 (en) | 2009-05-11 | 2018-08-14 | Nexeon Limited | Binder for lithium ion rechargeable battery cells |
US9853292B2 (en) | 2009-05-11 | 2017-12-26 | Nexeon Limited | Electrode composition for a secondary battery cell |
US9608272B2 (en) | 2009-05-11 | 2017-03-28 | Nexeon Limited | Composition for a secondary battery cell |
US20120244441A1 (en) * | 2009-12-10 | 2012-09-27 | The University Of Tokyo | Silicon film and lithium secondary battery |
US8772174B2 (en) | 2010-04-09 | 2014-07-08 | Nexeon Ltd. | Method of fabricating structured particles composed of silicon or silicon-based material and their use in lithium rechargeable batteries |
US9368836B2 (en) | 2010-06-07 | 2016-06-14 | Nexeon Ltd. | Additive for lithium ion rechargeable battery cells |
US8945774B2 (en) | 2010-06-07 | 2015-02-03 | Nexeon Ltd. | Additive for lithium ion rechageable battery cells |
US9871248B2 (en) | 2010-09-03 | 2018-01-16 | Nexeon Limited | Porous electroactive material |
US9647263B2 (en) | 2010-09-03 | 2017-05-09 | Nexeon Limited | Electroactive material |
US9947920B2 (en) | 2010-09-03 | 2018-04-17 | Nexeon Limited | Electroactive material |
US11444285B2 (en) | 2020-02-28 | 2022-09-13 | Nissan North America, Inc. | Three-dimensional anode current collector for lithium batteries |
Also Published As
Publication number | Publication date |
---|---|
JP2008171802A (ja) | 2008-07-24 |
US20100291441A1 (en) | 2010-11-18 |
EP2051317A1 (en) | 2009-04-22 |
KR101038178B1 (ko) | 2011-05-31 |
EP2051317A4 (en) | 2012-04-25 |
CN101356666B (zh) | 2010-10-27 |
KR20080069604A (ko) | 2008-07-28 |
CN101356666A (zh) | 2009-01-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2008072460A1 (ja) | 非水電解質二次電池用負極とその製造方法およびそれを用いた非水電解質二次電池 | |
JP4164541B2 (ja) | 非水電解質二次電池用負極 | |
US8389156B2 (en) | Negative electrode for non-aqueous electrolyte secondary battery, method for producing the same, and non-aqueous electrolyte secondary battery | |
US8067115B2 (en) | Non-aqueous electrolyte secondary battery | |
JP5151343B2 (ja) | 非水電解質二次電池用負極とその製造方法およびそれを用いた非水電解質二次電池 | |
US8334073B2 (en) | Non-aqueous electrolyte secondary battery and method of manufacturing negative electrode thereof | |
WO2008029719A1 (fr) | Cellule secondaire électrolytique non aqueuse | |
CN101689628B (zh) | 电化学元件用电极和使用该电极的电化学元件 | |
JP2008192594A (ja) | 非水電解質二次電池用負極とその製造方法およびそれを用いた非水電解質二次電池 | |
JP2010073571A (ja) | リチウムイオン二次電池およびその製造方法 | |
JP5177153B2 (ja) | 非水電解質二次電池用負極の製造方法 | |
JP2008277256A (ja) | 電気化学素子用電極の製造方法 | |
JP5250998B2 (ja) | 電気化学素子用電極とその製造方法およびそれを用いた電気化学素子 | |
US8048569B2 (en) | Non-aqueous electrolyte secondary battery | |
US20080171263A1 (en) | Negative electrode for nonaqueous electrolyte secondary battery, its manufacturing method, and nonaqueous electrolyte secondary battery using the same | |
JP4594965B2 (ja) | リチウムイオン二次電池用負極集電体、リチウムイオン二次電池用負極およびリチウムイオン二次電池 | |
JP2008277255A (ja) | 電気化学素子用電極とそれを用いた電気化学素子 | |
JP4479769B2 (ja) | 非水電解質二次電池用負極とそれを用いた非水電解質二次電池 | |
JP2008258139A (ja) | 非水電解質二次電池用負極とその製造方法およびそれを用いた非水電解質二次電池 | |
JP2008124007A (ja) | 非水電解質二次電池と非水電解質二次電池用負極の製造方法 | |
JP2012009152A (ja) | リチウムイオン二次電池 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200780001352.7 Country of ref document: CN |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2007832439 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 12093540 Country of ref document: US |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1020087011621 Country of ref document: KR |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 07832439 Country of ref document: EP Kind code of ref document: A1 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |