WO2001073874A1 - Cathode de batterie secondaire a ion lithium, liant pour cathode de batterie secondaire a ion lithium, et batterie secondaire a ion lithium correspondante - Google Patents
Cathode de batterie secondaire a ion lithium, liant pour cathode de batterie secondaire a ion lithium, et batterie secondaire a ion lithium correspondante Download PDFInfo
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- WO2001073874A1 WO2001073874A1 PCT/JP2001/002610 JP0102610W WO0173874A1 WO 2001073874 A1 WO2001073874 A1 WO 2001073874A1 JP 0102610 W JP0102610 W JP 0102610W WO 0173874 A1 WO0173874 A1 WO 0173874A1
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- secondary battery
- ion secondary
- lithium ion
- negative electrode
- binder
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- 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
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
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- 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
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
- H01M4/621—Binders
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- 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
- H01M4/133—Electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
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- 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
- H01M4/58—Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
- H01M4/583—Carbonaceous material, e.g. graphite-intercalation compounds or CFx
- H01M4/587—Carbonaceous material, e.g. graphite-intercalation compounds or CFx for inserting or intercalating light metals
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- 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
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
- H01M4/621—Binders
- H01M4/622—Binders being polymers
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- 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
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- 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
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- 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 a negative electrode for a lithium ion secondary battery, a binder for the negative electrode for a lithium ion secondary battery, and a lithium ion secondary battery using them.
- a negative electrode for a lithium ion secondary battery a binder for the negative electrode for a lithium ion secondary battery
- a lithium ion secondary battery using them.
- the surface energy power 3 O m J m one more for a lithium ion secondary battery using polymer materials to the binder one negative electrode and lithium Umuion negative electrode binder for a secondary battery.
- lithium ion rechargeable batteries are lightweight and have high energy density, and are being researched and industrialized as power sources for driving these portable devices.
- a carbon-containing active material containing graphite is mainly used from the viewpoint of safety and the like.
- This graphite is an active material that forms an interlayer compound with lithium.
- lithium is electrochemically transferred into and out of the black ship layer contained in the negative electrode active material in the electrolyte (intercalation // deintercalation). Charging and discharging are being performed. What is important when electrochemically transferring lithium into and out of the black layer (intercalation / deintercalation) is that side reactions other than the transfer of lithium (intercalation / deintercalation), for example, Decomposition of electrolyte occurs That is not.
- an electrolyte mainly comprising an organic solvent is used because lithium reacts with water.
- EC ethylene carbonate
- ether-based solvent a mixed electrolyte of ethylene carbonate (hereinafter, referred to as EC) and an ether-based solvent is used for lithium secondary batteries that use a carbon material, including Kurofune, as the negative electrode active material. It is mainly used as an electrolyte.
- the ether-based electrolyte since the ether-based electrolyte has a low boiling point, it cannot be used in a high-temperature atmosphere, and has a disadvantage that it is weak against self-heating of the battery. Therefore, it is unsuitable for long-time use such as notebook computers and portable video cameras. Therefore, development of an electrolyte solution that is resistant to high-temperature atmosphere and self-heating is desired.
- PC has excellent characteristics in this respect, there still remains a problem that it is decomposed by reacting with the negative electrode active material made of graphite as described above.
- the present invention has been made in order to solve the above problems, and it is possible to use a PC as an electrolyte, a negative electrode for a lithium ion secondary battery made of a carbon material containing graphite, and a lithium ion secondary battery.
- An object of the present invention is to provide a binder for a negative electrode and a lithium ion secondary battery using the same. Disclosure of the invention
- the present inventors have considered that by preventing direct contact between the PC of the electrolyte and the graphite in the negative electrode active material, it is possible to suppress the decomposition reaction of the PC, By controlling the surface energy of a binder made of a polymer material that binds graphite and controlling the interfacial energy between the black bell and the binder, the inventors have found that the decomposition reaction of PC is suppressed, and completed the present invention.
- the negative electrode for a lithium ion secondary battery of the present invention uses a carbon material having a d 002 of 0.3370 nm or less as a part of the active material among the X-ray parameters obtained by the Gakushin method, and has a surface energy y S However, it is characterized in that a polymer material of 30 mjm- 2 or more is used as a binder.
- d 002 is 0.3370 nm or less, natural black supply, artificial black forceps, resin charcoal, It is preferable to use one or a combination of two or more of natural carbides, petroleum coal, coal coke, pitch coal, and mesocarbon microbeads. In particular, it is preferable to contain either natural graphite or artificial graphite. Thereby, a negative electrode for a lithium ion secondary battery having high safety and high capacity can be obtained.
- a carbon material with d 002 of 0.3370 ⁇ m or less has a degree of black ship formation of 0.4 or more, and is a region in which the lithium interaction process is dominant. Become.
- the negative electrode for a lithium ion secondary battery of the present invention has the following formulas (1), (2), and (3) obtained by measuring the surface energy -vs, contact angle at room temperature using water and methylene iodide as test liquids. This is a value calculated using equation (3).
- 0 is the contact angle at each test liquid
- y S d and y L d is the dispersion component of the surface energy of each the polymer material testing liquid
- T / S p and y L p is, respectively it polymeric material
- the polar component of the surface energy of the test liquid is, respectively it polymeric material
- the surface energy values of water and methylene iodide are
- the polymer material is a polymer material having an electrochemically active carbonyl group in a main chain or a side chain thereof; It is preferable that the content of the carbonyl group represented by the formula (1) in the polymer material is 0.05 or more.
- the polymer material is a combination of one or more of polyimide, polyamide, and polyamide.
- polyamide imides, and polyamides in particular, aromatic polyamides, aromatic polyamide imides, and combinations of two or more of aromatic polyamides are preferred. Les ,.
- a metal or a compound containing a metal can be used as the other material in the active material.
- a negative electrode for a lithium ion secondary battery using a carbon material containing graphite as a part of the active material without decomposing PC of the electrolytic solution can be obtained.
- the binder of the negative electrode for a lithium ion secondary battery of the present invention was obtained from the following formulas (1), (2), and (3) based on contact angle measurement at room temperature using water and methylene iodide as test liquids.
- the calculated surface energy gamma s with the, 3 Om J m - is a polymeric material which is a value of 2 or more.
- ⁇ is the contact angle of each test liquid
- ys d and ⁇ are the dispersion components of the surface energy of the polymer material and test liquid, respectively
- YS p and YL p are the surface energies of the polymer material and test liquid, respectively. Is a polar component.
- the surface energy values of water and methylene iodide are
- VL d 48. 5mJm- 2
- the surface E energy ys carbon material e.g., natural graphite 12 Om Jm one 2 about
- the surface E energy ys carbon material can small Kusuru the difference between, reduce interfacial energy To stabilize and increase the bonding work.
- the polymer material is a polymer material having an electrochemically active carbonyl group in a main chain or a side chain thereof; (4) the carbonizole group represented by It is preferable that the content in the polymer material is 0.05 or more.
- the capacity can be increased by using a material having a capacity of 0.05 or more, preferably 0.10 or more.
- the polymer material is a combination of one or more of polyimide, polyamide, and polyamide.
- polyimides polyamide imides, and polyamides, in particular, aromatic polyamides, aromatic polyamide imides, and combinations of two or more of aromatic polyamides are preferred.
- the present invention is a lithium ion secondary battery using the negative electrode for a lithium ion secondary battery and the binder of the negative electrode for a lithium ion secondary battery.
- FIG. 1 is a view showing contact angles of water (0 W ) and methylene iodide ( ⁇ MI) used for measuring the surface energy 7 S of the binder used in Examples and Comparative Examples.
- FIG. 2 is a diagram showing charging curves of the secondary batteries in the example and the comparative example.
- FIG. 3 is a diagram showing the relationship between the type of binder, capacity, and charge / discharge efficiency.
- d 002 is 0.3370 nm or less.
- one or a combination of two or more of the Bonbon microbeads is used.
- the material contains either natural graphite or artificial graphite.
- a carbon material with d 002 of 0.3370 nm or less has a degree of graphitization of 0.4 or more and supports the lithium intercalation process. It is a layout area.
- binders that bind these carbon materials were calculated using the following formulas (1), (2), and (3) from contact angle measurements at room temperature using water and methylene iodide as test liquids. those surface energy y s is 3 Om J m-2 or more polymeric materials are preferred.
- theta is the contact angle at each test liquid
- y S d and y L d is the dispersion component of the surface energy of each the polymer material testing liquid
- y S p and y L p is their respective polymeric materials
- the polar component of the surface energy of the test liquid is the surface energy values of water and methylene iodide.
- the surface E energy of the carbon material e.g., natural graphite 12 Om J m one 2 about
- the surface E energy of the carbon material can small Kusuru the difference between the interfacial energy It can reduce and stabilize and increase the bonding work.
- the polymer material is: A polymer material having an electrochemically active carbonyl group in a main chain or a side chain, wherein the content of the carboxy group represented by the following formula (4) in the polymer material: Is preferably 0.05 or more.
- the content of the carbonyl group represented by the formula (4) in the polymer material is preferably at least 0.05. It is possible to increase the capacity by using a capacitor of 0.10 or more.
- the polymer material used in the present invention can be synthesized by a known method, for example, a low-temperature polycondensation method depending on the compound, and the method is not particularly limited.
- a known method for example, a low-temperature polycondensation method depending on the compound, and the method is not particularly limited.
- polyimide, polyamide imide, and polyamide are preferably used, and more preferably, polyimide and polyamide imide are used.
- aromatic polyimides particularly preferred are aromatic polyimides, aromatic polyamides, aromatic polyamides, and combinations thereof, and particularly preferred are aromatic polyimides.
- aromatic polyimides By including these aromatic groups, electron transfer can be performed relatively easily.
- aromatic polyimides, aromatic polyamides, aromatic polyamides, and the like can also be synthesized by a known method, for example, a low-temperature polycondensation method.
- polyimide, polyamide imide, and polyamide can be synthesized by reacting tetracarboxylic dianhydride or acid chloride with diamine.
- the tetracarboxylic dianhydride used is pyromellitic dianhydride, 3, 3 ', 4, 4'-diphenyltetracarboxylic dianhydride, 2, 2', 3, 3 ' —Diphenyltetracarboxylic dianhydride, 3,4,9,10—Perylenetetracarboxylic dianhydride, bis (3,4-dicarboxyphenyl) ether dianhydride, benzene— 1,2,3,4-tetracarboxylic dianhydride, 3,4,3 ', 4'-benzophenonetetracarboxylic dianhydride, 2,3,2', 3-benzophenonetetracarboxylic acid Dianhydride, 2, 3, 3 ', 4' monobenzoph
- diamine compounds include 3,3'-diaminodiphenylmethane, 3,3'-diaminodiphenyl ether, 3,3'-diaminodiphenylenolesulfone, 3,3'-diaminodiphenylsnolefide, p -Phenylenediamine, m-phenylenediamine, 4,4'-diaminodiphenylpropane, 4,4'-diaminodiphenylmethane, 3,3'-diaminobenzophenone, 4,4'diaminodiphenyls Sulfide, 4,4'-diaminodiphenylsulfone, 4,4'-diaminodiphenylether, 3,4'-diaminodiphenylether,
- the solvent for synthesizing these is not particularly limited as long as the raw material resin and the produced polymer can be dissolved therein. From the viewpoint of the body, it is preferable to use N, N-dimethylformamide, N, N-dimethylacetamide, and N-methyl-2-pyrrolidone.
- a metal such as boron or silicon may be added to the negative electrode active material, followed by heat treatment. These are adjusted to a required particle size by a predetermined treatment such as pulverization and classification to be used as an active material of a negative electrode material for a secondary battery.
- a metal or a compound of a metal can be used as an active material other than the organic polymer.
- the metal include tin and silicon.
- the metal compound include oxides, chlorides, nitrides, borides, and phosphides of various metals.
- the amount of active material as a negative electrode can be reduced by using an aromatic polyimide, which is 0.10 or more, such as an aromatic polyimide, an aromatic polyimide, or an aromatic polyimide, more preferably, as the binder. Without this, the electric capacity of the aromatic polyimide, aromatic polyamide, and aromatic polyamide can be used as a secondary battery.
- the binder such as aromatic polyimide is not only used as a binder for the active material of the negative electrode for a secondary battery, but also as a binder for improving the adhesion to a current collector such as copper. Still works.
- an amorphous compound containing lithium on the negative electrode for a secondary battery by forming an amorphous compound containing lithium on the negative electrode for a secondary battery according to the present invention, the surface reaction of the negative electrode for a secondary battery can be suppressed, and the overall capacity can be increased.
- lithium hydroxide or the like is added to the gelled metal alkoxide together with the solution, and this is applied to the surface of the negative electrode for a lithium ion secondary battery according to the present invention. Thereafter, the solution is dried to obtain a higher capacity negative electrode for a secondary battery.
- a lithium ion secondary battery using the binder of the negative electrode for a lithium ion secondary battery and the negative electrode for a lithium ion secondary battery can be provided.
- an amorphous compound can be formed, it is not limited to a metal alkoxide.
- Fluorine-based polyimide (hereinafter referred to as 6 FDA-PDA) was used as the binder. This was added to a previously synthesized synthesis solvent, N, N-dimethylacetamide. 6-0-8 and N-dimethylacetamide synthesis solution were applied on a glass plate. After drying, the surface was washed with n-hexane and dried at 80 ° C. for 10 minutes, and each contact angle was measured at room temperature using water and methylene iodide as test liquids. After measuring each contact angle, the surface energy of the binder 6 FDA-PDA was calculated by the following formulas (1), (2) and (3). The surface energy determined from this was 35. lm jm- 2 .
- a binder is 10 mass%, average particle size 20 Myupaiiota, of X-ray parameters obtained by Gakushin method, a slurry scratch d 002 is added scaly natural graphite powder of 0. 3354 nm It was adjusted. Next, it is applied to the surface of a current collector made of copper foil with a thickness of 20 ⁇ m, and dried at 1.3 kPa and 135 ° C for 17 hours to obtain N, N-dimethylacetamide, a synthetic solvent. Removed.
- a conversion treatment of polyamide acid to polyimide is performed in an inert gas atmosphere at 300 for 1 hour, and after rolling, it is processed into a predetermined shape to obtain a desired negative electrode for a secondary battery.
- a three-electrode cell was assembled. Lithium metal was used for the counter electrode and the reference electrode.
- the electrolytic solution was used a mixture of the L i C 10 4 Imo lZ rate Torr containing ethylene carbonate Nei preparative ZPC (1/1 V o 1 %).
- Polyamide (hereinafter referred to as PA) was used as a binder. This was added to N, N dimethylacetamide, a synthesis solvent, to synthesize a synthesis solution.
- the surface energy y s was 42.8 mJm- 2 . Otherwise, in the same manner as in Example 1, a negative electrode for a secondary battery was obtained. .
- BPDA-PDA Polyimide
- a commercially available polyvinyl chloride powder (hereinafter, referred to as PVC) was used. This is synthesized with N, N dimethylacetamide And a synthesis solution was synthesized. Surface energy Y s was 40. 8m J m one 2. In other respects, a negative electrode for a secondary battery was formed in the same manner as in Example 1.
- PVd F Polyvinylidene fluoride
- Ethylene propylene monogen rubber (hereinafter referred to as EPDM) was used as a binder. This was dissolved in cyclohexane to prepare a synthesis solution. The surface energy ys was 23.6 mJm- 2 . Otherwise, in the same manner as in Example 1, a negative electrode for a secondary battery was obtained.
- EPDM Ethylene propylene monogen rubber
- FIG. 1 shows the contact angles of water and methylene iodide used for measuring the surface energy y s of the binder used in Examples 1 to 4 and Comparative Examples 1 and 2.
- y s the surface energy of the binder used in Examples 1 to 4 and Comparative Examples 1 and 2.
- 0 Ml the contact angle of methylene iodide.
- the current density of the secondary batteries of Examples 1 to 4 and Comparative Examples 1 and 2 was 1.5 6111.
- Fig. 2 shows the charging curve.
- FIG. 2 in Examples 1 to 4, a flat area around 0 to 8 V due to decomposition of PC is not seen.
- the comparative example it can be seen that a flat area exists and PC is decomposed. ,
- the binder is included in the electrolyte. It can be seen that the PC does not come into direct contact with the carbon material, and that PC decomposition can be suppressed.
- Polyamide acid composed of pyromellitic dianhydride (hereinafter, referred to as PMDA) and: p-phenylenediamine (hereinafter, referred to as PDA) was used as the binder.
- PMDA pyromellitic dianhydride
- PDA p-phenylenediamine
- NMP N-methyl-2-pyrrolidone
- an average particle 'size of 20 mu m scaly black ship powder 95 g in the binder one is 5 g, i.e., so that the amount of the binder is 5 mass 0/0, by adding scaly graphite powder to the solution adjustment did.
- it was applied to the surface of a current collector made of a copper foil having a thickness of 20 xm, and dried to remove NMP.
- a conversion treatment of polyamic acid to polyimide was performed in an inert gas atmosphere, and after rolling, processed into a predetermined shape to obtain a desired negative electrode for a secondary battery. Using this negative electrode for a secondary battery, a three-electrode cell was assembled.
- Lithium metal was used for the counter and reference electrodes, charged to OV at 25 mA, and lithium intercalated into graphite. After that, it was discharged to 3 V and dintering was performed.
- Ethylene carbonate Ne over preparative the electrolytic solution lmo 1 Roh including L a L i C 10 4: dimethyl carbonate 1: Using a mixture of 1 (volume ratio). The charge capacity in the first cycle was 469 mAh / g, the discharge capacity was 396 mAh / g, and the discharge efficiency defined by these ratios was 84.4%.
- Example 5 A cell assembly and a charge / discharge test were performed in the same procedure as in Example 5, except that PDA was changed to diaminodiphenyl ether (hereinafter, DDE) in Example 5.
- the charge capacity in the first cycle was 424 mAh / g
- the discharge capacity was 368 mAh
- the discharge efficiency was 86.8%.
- the decrease in discharge capacity after 300 cycles was within 20%.
- a cell assembly and a charge / discharge test were performed in the same manner as in Example 5 except that the PDA was changed to 1,4-bis (4-aminophenoxy) benzene (hereinafter, referred to as BAP B) in Example 5.
- the charge capacity in the first cycle is 400 mAhZg
- the discharge capacity is 35 ZmAhZg
- the discharge efficiency is 88.0 ° /. It was.
- the decrease in discharge capacity after 300 cycles was within 20%.
- Example 5 The procedure of Example 5 was repeated except that PMDA was changed to 3,4,3 ', 4,4', 1-biphenyltetracarboxylic dianhydride (hereinafter referred to as BPDA).
- BPDA 3,4,3 ', 4,4', 1-biphenyltetracarboxylic dianhydride
- a discharge test was performed. In the first cycle, the charge capacity was 468 mAhZg, the discharge capacity was 405 mAh / g, and the discharge efficiency was 86.5%. The decrease in discharge capacity after 300 cycles was within 20%.
- a senoré assembly and charge / discharge test were performed in the same manner as in Example 8 except that the PDA was changed to DDE.
- the charge capacity in the first cycle is 4 5 1 mAh / g
- discharge capacity was 387 mAh / g
- discharge efficiency was 85.8%.
- the decrease in discharge capacity after 300 cycles was within 20%.
- a senoré assembly and charge / discharge test were performed in the same manner as in Example 8 except that the PDA was changed to BAPB in Example 8.
- the charge capacity in the first cycle was 459 mAh
- the discharge capacity was 389 mAhZg
- the discharge efficiency was 84.7%.
- the decrease in discharge capacity after 300 cycles is 20. /. Was within.
- Example 5 The assembly and charge / discharge test were performed in the same manner as in Example 5 except that the amount of the binder was changed to 10% by mass in Example 5.
- the charge capacity in the first cycle was 553 mAh / g
- the discharge capacity was 47 lmAhZg
- the discharge efficiency was 85.2%.
- the decrease in discharge capacity after 300 cycles was within 20%.
- a cell assembly and a charge / discharge test were performed in the same procedure as in Example 8, except that the amount of the binder was changed to 10% by mass in Example 8.
- the charge capacity in the first cycle was 567 mAh / g
- the discharge capacity was 51 OmAh / g
- the discharge efficiency was 89.9%.
- the decrease in discharge capacity after 300 cycles was within 20%.
- Example 5 a cell assembly and a charge / discharge test were performed in the same procedure as in Example 5, except that the same PVdF as in Comparative Example 1 was used as the binder.
- the charge capacity in the first cycle was 388 mAh / g
- the discharge capacity was 36 OmAh / g
- the discharge efficiency was 92.8%.
- the decrease in discharge capacity after 300 cycles was within 20%.
- Example 4 A cell assembly and a charge / discharge test were performed in the same manner as in Example 5 except that polystyrene was used as the binder in Example 5.
- the charge capacity in the first cycle was 376 mAh / g
- the discharge capacity was 347 mAh g
- the discharge efficiency was 92.3%.
- the decrease in discharge capacity after 300 cycles was within 20%.
- Examples 5 to 12 in which polyimide, polyamide, and polyamides were used as a part of the negative electrode active material according to the present invention were Comparative Examples 3 and 4 in which the conventional negative electrode active material was used.
- Comparative Example 4 it can be seen that the capacity was high. It can also be seen that the charge and discharge efficiency after 300 cycles is equal to or higher than that.
- the present invention is configured as described above, and even when PC is used as the electrolyte, the decomposition reaction of PC is suppressed, and the battery is heated for a long time by self-heating due to prolonged use, or Lithium with high charge / discharge efficiency that can be used even in a high temperature atmosphere.
- a binder for an anode for an on-secondary battery, a binder for an anode for a lithium-ion secondary battery, and a lithium ion secondary battery using these can be provided.
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Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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EP01917579A EP1274141A4 (en) | 2000-03-29 | 2001-03-29 | LITHIUMION SECONDARY BATTERY CATHODE, BINDERS THEREFOR AND THIS USING LITHIUMION SECONDARY BATTERY CATHODE |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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JP2000-95287 | 2000-03-29 | ||
JP2000095287 | 2000-03-29 | ||
JP2000-310011 | 2000-10-11 | ||
JP2000310011 | 2000-10-11 |
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WO2001073874A1 true WO2001073874A1 (fr) | 2001-10-04 |
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PCT/JP2001/002610 WO2001073874A1 (fr) | 2000-03-29 | 2001-03-29 | Cathode de batterie secondaire a ion lithium, liant pour cathode de batterie secondaire a ion lithium, et batterie secondaire a ion lithium correspondante |
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US (1) | US20030049535A1 (ja) |
EP (1) | EP1274141A4 (ja) |
KR (1) | KR100716881B1 (ja) |
CN (1) | CN1213496C (ja) |
TW (1) | TW507394B (ja) |
WO (1) | WO2001073874A1 (ja) |
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US7816037B2 (en) * | 2002-01-25 | 2010-10-19 | Toyo Tanso Co., Ltd. | Anode material for lithium ion secondary battery |
WO2005089422A2 (en) | 2004-03-17 | 2005-09-29 | California Institute Of Technology | Methods for purifying carbon materials |
WO2006052313A1 (en) * | 2004-11-08 | 2006-05-18 | 3M Innovative Properties Company | Polyimide electrode binders |
CN100416897C (zh) * | 2005-01-17 | 2008-09-03 | 比亚迪股份有限公司 | 一种锂离子二次电池的负极及包括该负极的锂离子二次电池 |
US20060216596A1 (en) * | 2005-03-25 | 2006-09-28 | Michael Cheiky | PTFE copolymer and binding for coating cathode particles |
US7794880B2 (en) | 2005-11-16 | 2010-09-14 | California Institute Of Technology | Fluorination of multi-layered carbon nanomaterials |
US8232007B2 (en) | 2005-10-05 | 2012-07-31 | California Institute Of Technology | Electrochemistry of carbon subfluorides |
US20100221603A1 (en) * | 2006-03-03 | 2010-09-02 | Rachid Yazami | Lithium ion fluoride battery |
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JP3311402B2 (ja) * | 1992-11-19 | 2002-08-05 | 三洋電機株式会社 | 二次電池 |
JP3133530B2 (ja) * | 1992-12-28 | 2001-02-13 | 三洋電機株式会社 | 二次電池 |
JPH10188992A (ja) * | 1996-12-24 | 1998-07-21 | Sony Corp | 非水電解液電池 |
JPH1173968A (ja) * | 1997-08-29 | 1999-03-16 | Hitachi Chem Co Ltd | 二次電池 |
JPH1197028A (ja) * | 1997-09-16 | 1999-04-09 | Pi Gijutsu Kenkyusho:Kk | 二次電池 |
JPH11185751A (ja) * | 1997-12-16 | 1999-07-09 | Asahi Glass Co Ltd | 二次電源 |
EP0973180A3 (en) * | 1998-07-14 | 2003-11-19 | Asahi Glass Company Ltd. | Secondary power source |
US6632569B1 (en) * | 1998-11-27 | 2003-10-14 | Mitsubishi Chemical Corporation | Carbonaceous material for electrode and non-aqueous solvent secondary battery using this material |
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2001
- 2001-03-29 WO PCT/JP2001/002610 patent/WO2001073874A1/ja active Application Filing
- 2001-03-29 US US10/239,208 patent/US20030049535A1/en not_active Abandoned
- 2001-03-29 EP EP01917579A patent/EP1274141A4/en not_active Withdrawn
- 2001-03-29 CN CNB018075630A patent/CN1213496C/zh not_active Expired - Fee Related
- 2001-03-29 TW TW090107537A patent/TW507394B/zh not_active IP Right Cessation
- 2001-03-29 KR KR1020027012656A patent/KR100716881B1/ko not_active IP Right Cessation
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JPH05266880A (ja) * | 1992-03-18 | 1993-10-15 | Matsushita Electric Ind Co Ltd | 非水電解質二次電池用負極の製造法 |
JPH11158277A (ja) * | 1997-12-01 | 1999-06-15 | Kanegafuchi Chem Ind Co Ltd | 電池電極用バインダー樹脂とその製造方法 |
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Also Published As
Publication number | Publication date |
---|---|
EP1274141A1 (en) | 2003-01-08 |
KR20020093001A (ko) | 2002-12-12 |
EP1274141A4 (en) | 2009-02-18 |
TW507394B (en) | 2002-10-21 |
US20030049535A1 (en) | 2003-03-13 |
CN1422446A (zh) | 2003-06-04 |
CN1213496C (zh) | 2005-08-03 |
KR100716881B1 (ko) | 2007-05-09 |
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