WO2015001719A1 - 非水電解質二次電池 - Google Patents
非水電解質二次電池 Download PDFInfo
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- WO2015001719A1 WO2015001719A1 PCT/JP2014/003086 JP2014003086W WO2015001719A1 WO 2015001719 A1 WO2015001719 A1 WO 2015001719A1 JP 2014003086 W JP2014003086 W JP 2014003086W WO 2015001719 A1 WO2015001719 A1 WO 2015001719A1
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- positive electrode
- negative electrode
- mixture layer
- electrolyte secondary
- secondary battery
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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
- H01M10/058—Construction or manufacture
- H01M10/0587—Construction or manufacture of accumulators having only wound construction elements, i.e. wound positive electrodes, wound negative electrodes and wound separators
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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
- H01M4/139—Processes of manufacture
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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
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
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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
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/50—Current conducting connections for cells or batteries
- H01M50/572—Means for preventing undesired use or discharge
- H01M50/574—Devices or arrangements for the interruption of current
- H01M50/578—Devices or arrangements for the interruption of current in response to pressure
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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
- H01M2200/00—Safety devices for primary or secondary batteries
- H01M2200/20—Pressure-sensitive devices
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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
- H01M2220/00—Batteries for particular applications
- H01M2220/20—Batteries in motive systems, e.g. vehicle, ship, plane
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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
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/50—Current conducting connections for cells or batteries
- H01M50/572—Means for preventing undesired use or discharge
- H01M50/584—Means for preventing undesired use or discharge for preventing incorrect connections inside or outside the batteries
- H01M50/586—Means for preventing undesired use or discharge for preventing incorrect connections inside or outside the batteries inside the batteries, e.g. incorrect connections of electrodes
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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
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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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Definitions
- the present invention relates to an on-vehicle non-aqueous electrolyte secondary battery.
- Non-aqueous electrolyte secondary batteries for in-vehicle use used as power sources for driving electric vehicles (EV) and hybrid electric vehicles (HEV, PHEV) have a pressure detection type current interruption mechanism in addition to an explosion-proof safety valve. Yes.
- the pressure detection type current interruption mechanism is provided to prevent the battery from rupturing or igniting by being activated by a gas that is rapidly generated inside the battery in the event of an abnormality, and interrupting the current flowing to the outside.
- nonaqueous electrolyte secondary batteries it is known to increase the charging voltage as one of the methods for increasing the battery capacity.
- tert-amylbenzene, biphenyl see Patent Document 1
- a cycloalkylbenzene compound a cycloalkylbenzene compound
- a benzene ring adjacent to the benzene ring are included in the nonaqueous electrolyte.
- an overcharge inhibitor such as a compound having quaternary carbon (see Patent Document 2).
- the overcharge inhibitor decomposes even at the voltage set as the normal use range, and the battery characteristics are reduced after the charge / discharge cycle. There is concern about a decline and a reduction in safety.
- Li 2 CO 3 lithium carbonate
- Patent Document 3 When lithium carbonate is added to the positive electrode mixture of a non-aqueous electrolyte secondary battery, carbon dioxide gas is generated from the positive electrode plate when a high voltage is applied to the battery, such as during overcharging, thereby ensuring an explosion-proof safety valve.
- the pressure detection type current interrupting mechanism can be activated earlier than that.
- the positive electrode plate and the negative electrode plate have a wound electrode body wound in a state of being insulated from each other by a separator.
- the ends of the positive electrode plate on the winding start side and the winding end side are covered with a separator. Since the separator is flexible, the ends of the positive electrode plate on the winding start side and the winding end side are densely covered with the separator.
- the positive electrode mixture layer contains lithium carbonate, and at least one of the positive electrode mixture at the winding start side end and the winding end side end of the positive electrode plate.
- An insulating tape is applied on the agent layer at a position facing the separator along the width direction of the positive electrode mixture layer. Due to the presence of the insulating tape, a step is generated between the positive electrode mixture layer and the separator, and a ventilation channel is formed in the winding axis direction of the flat wound electrode body based on the step. Thereby, the carbon dioxide gas generated by the decomposition of the lithium carbonate in the positive electrode mixture layer in the overcharged state easily flows to the outside of the flat spirally wound electrode body through the vent flow path based on the step.
- carbon dioxide gas hardly stays on the surface of the positive electrode mixture layer, so that the temperature inside the battery rises and abnormalities such as smoke, ignition, and explosion occur.
- the pressure inside the battery can be quickly raised to ensure that the pressure-sensitive current interruption mechanism can be operated, and the safety at the time of overcharging becomes very good.
- FIG. 1A is a plan view of the nonaqueous electrolyte secondary battery of the embodiment, and FIG. 1B is a front view of the same.
- 2A is a partial sectional view taken along line IIA-IIA in FIG. 1A
- FIG. 2B is a partial sectional view taken along line IIB-IIB in FIG. 2A
- FIG. 2C is taken along line IIC-IIC in FIG.
- FIG. 3A is a plan view of a positive electrode plate used in the nonaqueous electrolyte secondary battery of the embodiment
- FIG. 3B is a plan view of the negative electrode plate.
- 4A is a perspective view in which a winding end end side of the flat wound electrode body of the embodiment is developed, and FIG.
- FIG. 4B is an enlarged cross-sectional view of a portion along the line IVB-IVB in FIG. 4A after the winding is finished. It is. It is a top view of the positive electrode plate corresponding to a comparative example.
- FIG. 6A is a perspective view in which a winding end end side of a flat wound electrode body of a comparative example is developed
- FIG. 6B is an enlarged cross-sectional view of a portion along the VIB-VIB line of FIG. It is. It is sectional drawing of the nonaqueous electrolyte secondary battery provided with the forced short circuit mechanism.
- FIG. 8A is a diagram illustrating a state before the operation of the forced short-circuit mechanism
- FIG. 8B is a diagram illustrating a state after the operation of the forced short-circuit mechanism.
- the nonaqueous electrolyte secondary battery 10 includes a flat wound electrode body 14 in which a positive electrode plate 11 and a negative electrode plate 12 are wound in a state of being insulated from each other via a separator 13. have.
- the outermost surface side of the flat wound electrode body 14 is covered with the separator 13, but the negative electrode plate 12 is arranged on the outer peripheral side of the positive electrode plate 11.
- the positive electrode plate 11 has positive electrode cores on both sides of a positive electrode core made of aluminum or aluminum alloy foil having a thickness of about 10 to 20 ⁇ m along one end in the width direction.
- the positive electrode mixture layer 11a is formed so as to be exposed in a strip shape.
- the portion of the positive electrode core body exposed in the belt shape becomes the positive electrode core body exposed portion 15.
- an insulating tape 11b is attached along the width direction of the positive electrode mixture layer 11a on the positive electrode mixture layer 11a on both sides and at a position facing the separator 13. Has been. The specific configuration and operation of the insulating tape 11b will be described later.
- the negative electrode plate 12 has negative electrode cores on both sides of a negative electrode core made of copper or copper alloy foil having a thickness of about 5 to 15 ⁇ m along one end in the width direction.
- the negative and positive electrode mixture layer 12a is formed so as to be exposed in a strip shape.
- the negative electrode core portion exposed in the band shape becomes the negative electrode core exposed portion 16.
- the positive electrode core exposed portion 15 to the negative electrode core exposed portion 16 may be formed along both end portions in the width direction of the positive electrode plate 11 to the negative electrode plate 12, respectively.
- the positive electrode plate 11 and the negative electrode plate 12 are shifted so that the positive electrode core exposed portion 15 and the negative electrode core exposed portion 16 do not overlap with the electrode mixture layers facing each other, and are insulated from each other with the separator 13 interposed therebetween.
- the flat wound electrode body 14 is produced by winding in a flat shape. As shown in FIGS. 2A, 2B, and 4A, the flat wound electrode body 14 includes a plurality of stacked positive electrode core exposed portions 15 at one end, and a plurality at the other end. A negative electrode core exposed portion 16 is provided.
- a microporous membrane made of polyolefin is used by folding two sheets or one long sheet, the width of which can cover the positive electrode mixture layer 11a and the negative electrode mixture layer. Something larger than the width is used.
- a plurality of stacked positive electrode core exposed portions 15 are electrically connected to a positive electrode terminal 18 via a positive electrode current collector 17. Between the positive electrode current collector 17 and the positive electrode terminal 18, a current interruption mechanism 27 that is operated by a gas pressure generated inside the battery is provided. A plurality of laminated negative electrode core exposed portions 16 are electrically connected to the negative electrode terminal 20 via a negative electrode current collector 19.
- the positive electrode terminal 18 and the negative electrode terminal 20 are fixed to the sealing body 23 via insulating members 21 and 22, respectively, as shown in FIGS. 1A, 1B, and 2A.
- the sealing body 23 is also provided with a gas discharge valve 28 that is opened when a gas pressure higher than the operating pressure of the current interrupt mechanism 27 is applied.
- the negative electrode current collector 19 and the negative electrode terminal 20 are made of copper or a copper alloy, respectively.
- the flat wound electrode body 14 is inserted into a rectangular exterior body 25 having one surface open with an insulating sheet 24 formed of a resin material interposed around the periphery of the sealing body 23 except for the sealing body 23 side.
- an insulating sheet 24 formed of a resin material interposed around the periphery of the sealing body 23 except for the sealing body 23 side.
- aluminum or aluminum alloy is used for the rectangular outer package 25.
- the sealing body 23 is fitted into the opening of the rectangular exterior body 25, and the fitting portion between the sealing body 23 and the rectangular exterior body 25 is laser-welded.
- a nonaqueous electrolytic solution is injected into the rectangular outer casing 25 from an electrolytic solution injection port 26, and the electrolytic solution injection port 26 is sealed with, for example, a blind rivet.
- the non-aqueous electrolyte secondary battery 10 is used alone or in a plurality of types connected in series, parallel, or series-parallel.
- a positive external terminal and a negative external terminal may be separately provided and each battery connected by a bus bar. .
- the flat wound electrode body 14 used in the nonaqueous electrolyte secondary battery 10 of the embodiment is used for applications requiring a high capacity and a high output characteristic with a battery capacity of 20 Ah or more.
- the number of windings of the positive electrode plate 11 is 43, that is, the total number of stacked positive electrode plates 11 is as large as 86. If the number of windings is 15 times or more, that is, if the total number of stacked sheets is 30 or more, the battery capacity can be easily increased to 20 Ah or more without increasing the battery size more than necessary.
- the positive electrode current collector 17 is formed on the positive electrode core exposed portion 15 and the negative electrode current collector 19 is formed on the negative electrode core exposed portion 16.
- a large welding current is required to form welding marks 15a, 16a penetrating over all the laminated portions of the positive electrode core exposed portion 15 or the negative electrode core exposed portion 16 which are stacked. is required.
- the plurality of positive electrode core exposed portions 15 wound and stacked are converged to the central portion in the thickness direction and further divided into two, Converging is centered on 1/4 of the thickness of the flat wound electrode body, and the intermediate member 30 for the positive electrode is disposed therebetween.
- the positive electrode intermediate member 30 a plurality of, for example, two conductive positive electrode conductive members 29 are held on a base made of a resin material.
- the positive electrode conductive member 29 for example, a cylindrical member is used, and a truncated cone-shaped protrusion that acts as a projection is formed on the side facing each of the stacked positive electrode core exposed portions 15.
- the plurality of negative electrode core body exposed portions 16 wound and stacked are converged to the center side in the thickness direction and further divided into 1 ⁇ 4 of the thickness of the flat wound electrode body.
- the negative electrode intermediate member 32 is disposed therebetween.
- a plurality of negative electrode conductive members 31, here two, are held on a base made of a resin material.
- a cylindrical member is used as the negative electrode conductive member 31, and a truncated cone-shaped protrusion that acts as a projection is formed on the side facing each of the laminated negative electrode core exposed portions 16.
- the positive electrode current collectors 17 are disposed on the outermost surfaces on both sides of the positive electrode core exposed portion 15 located on both sides of the positive electrode conductive member 29, and the negative electrode located on both sides of the negative electrode conductive member 31.
- a negative electrode current collector 19 is disposed on each of the outermost surfaces of the core body exposed portion 16.
- the positive electrode conductive member 29 is preferably made of aluminum or aluminum which is the same material as the positive electrode core
- the negative electrode conductive member 31 is preferably made of copper or copper alloy which is the same material as the negative electrode core.
- the shapes of the positive electrode conductive member 29 and the negative electrode conductive member 31 may be the same or different.
- FIG. 2A shows two welding marks 33 formed by resistance welding on the positive electrode current collector 17, and also shows two welding marks 34 on the negative electrode current collector 19.
- a lithium nickel cobalt manganese composite oxide represented by LiNi 0.35 Co 0.35 Mn 0.30 O 2 was used as the positive electrode active material.
- This lithium nickel cobalt manganese composite oxide, carbon powder as a conductive agent, and polyvinylidene fluoride ( PVdF) and lithium carbonate are weighed in a mass ratio of 92: 0.9: 5: 1.5, and mixed with N-methyl-2-pyrrolidone (NMP) as a dispersion medium. A mixture slurry was prepared.
- NMP N-methyl-2-pyrrolidone
- Lithium carbonate is preferably contained in an amount of 0.1 to 5.0% by mass with respect to the positive electrode mixture.
- the content of lithium carbonate in the positive electrode mixture is less than 0.1% by mass, the generation of carbon dioxide gas from lithium carbonate is small, and it becomes difficult to quickly activate the current interruption mechanism.
- the content of lithium carbonate in the positive electrode mixture exceeds 5.0% by mass, the proportion of lithium carbonate not involved in the electrode reaction is excessively increased, and the battery capacity is greatly reduced.
- the positive electrode core body an aluminum foil having a thickness of 15 ⁇ m was used, and the positive electrode mixture slurry produced by the above method was applied to both surfaces of the positive electrode core body by a die coater. However, the slurry was not applied to one end portion along the longitudinal direction of the positive electrode core (end portions in the same direction on both surfaces), and the core body was exposed to form the positive electrode core exposed portion 15. Next, drying was performed to remove NMP as a dispersion medium, and compression was performed to a predetermined thickness by a roll press, and the obtained electrode plate was cut into a predetermined dimension.
- polypropylene (PP) having a predetermined constant width along the width direction of the positive electrode mixture layer 11a on both surfaces of the positive electrode plate 11 facing the separator 13 at the end of winding.
- An insulating tape 11b was attached.
- the respective insulating tapes 11b were pasted so as to extend outward (left side in FIG. 3A) from the positive electrode mixture layer 11a, and the extended portions were bonded to each other.
- the length of the insulating tape 11b is the same as the width of the positive electrode mixture layer 11a of the positive electrode plate 11, but may be shorter or longer than the width of the positive electrode mixture layer 11a.
- the configuration of the positive electrode plate 11 thus manufactured is as shown in FIG. 3A.
- the negative electrode plate was produced as follows. A negative electrode mixture slurry was prepared by dispersing 98 parts by mass of graphite powder, 1 part by mass of carboxymethyl cellulose (CMC) as a thickener, and 1 part by mass of styrene-butadiene rubber (SBR) as a binder in water. The negative electrode mixture slurry was applied to both surfaces of a negative electrode current collector made of a copper foil having a thickness of 10 ⁇ m by a die coater and dried to form a negative electrode mixture layer on both surfaces of the negative electrode current collector. Next, it was dried and compressed to a predetermined thickness using a compression roller, and the obtained electrode plate was cut into a predetermined size.
- CMC carboxymethyl cellulose
- SBR styrene-butadiene rubber
- the negative electrode mixture layer is formed at one end in the width direction of the electrode plate such that the negative electrode core exposed portion 16 in which the negative positive electrode mixture layer is not formed on both sides with a constant width over the entire length direction is formed. It peeled.
- the configuration of the negative electrode plate 12 produced in this way is as shown in FIG. 3B.
- LiPF 6 is used as an electrolyte salt in a mixed solvent in which ethylene carbonate (EC) and methyl ethyl carbonate (MEC) are mixed at a volume ratio (25 ° C., 1 atm) in a ratio of 3: 7. It added so that it might become 1 mol / L, and also what added 0.3 mass% of vinylene carbonate VC with respect to the total nonaqueous electrolyte mass was used.
- EC ethylene carbonate
- MEC methyl ethyl carbonate
- the gap between the positive electrode mixture layer 11a and the separator 13 and between the insulating tape 11b and the separator 13 is not limited.
- a sufficient gap is formed in the winding axis direction of the flat wound electrode body 14 (direction perpendicular to the paper surface in FIG. 4B).
- the air permeability between the positive electrode mixture layer 11a and the outside of the flat wound electrode body 14 is ensured satisfactorily. Therefore, when the nonaqueous electrolyte secondary battery 10 is overcharged and lithium carbonate is decomposed in the positive electrode mixture layer 11a to generate carbon dioxide, the carbon dioxide is generated outside the flat wound electrode body 14. It becomes easy to slip out.
- the nonaqueous electrolyte secondary battery 10 of the embodiment since the carbon dioxide gas does not easily stay on the surface of the positive electrode mixture layer 11a, the temperature inside the battery rises and an abnormal state such as smoke, ignition, or explosion occurs. Before arriving, the pressure inside the battery is quickly raised, and the pressure-sensitive current interruption mechanism 27 (see FIG. 2A) can be reliably operated. When the current interrupting mechanism 27 is activated, the generation of carbon dioxide is stopped because no charging current flows, so that the internal pressure of the nonaqueous electrolyte secondary battery 10 does not increase, and safety during overcharge is improved. Very good.
- FIGS. 5 and 6 A specific configuration of the nonaqueous electrolyte secondary battery of the comparative example will be described with reference to FIGS. 5 and 6.
- the specific configuration of the nonaqueous electrolyte secondary battery of the comparative example is substantially the same as the nonaqueous electrolyte secondary battery 10 of the embodiment except for the configuration of the positive electrode plate. 1 and FIG. 2 are used as appropriate, and the same components as those of the nonaqueous electrolyte secondary battery 10 of the embodiment are given the same reference numerals, and detailed description thereof is omitted.
- the nonaqueous electrolyte secondary battery of the comparative example is the positive electrode plate of the embodiment except that the positive electrode plate 11 ⁇ / b> A does not have the insulating tape 11 b in the positive electrode plate 11 of the embodiment. 11 has the same configuration.
- the configuration of the winding end end side of the flat wound electrode body 14A of the comparative example is as shown in FIG. 6A.
- the positional relationship between the positive electrode mixture layer 11a and the separator 13 in the positive electrode plate 11 when the flat wound electrode body 14A is formed is as shown in FIG. 6B.
- the separator 13 is soft, so the gap between the positive electrode plate 11 and the separator 13 becomes very narrow.
- the nonaqueous electrolyte secondary battery of the comparative example when lithium carbonate is decomposed in the positive electrode mixture layer 11a and carbon dioxide gas is generated in the overcharged state, the carbon dioxide gas is generated in the positive electrode mixture layer 11a. It tends to stay on the surface side. Therefore, the pressure detection type current interruption mechanism cannot be sufficiently operated. Therefore, according to the nonaqueous electrolyte secondary battery of the comparative example, the safety is insufficient as compared with the nonaqueous electrolyte secondary battery 10 of the embodiment.
- the insulating tape 11b In the nonaqueous electrolyte secondary battery 10 of the embodiment, an example in which PP is used as the insulating tape 11b has been shown, but polyethylene (PE), polyimide, polyamide, polyester, etc. are commonly used as insulating tape. It can be used by appropriately selecting from the above. As the thickness of the insulating tape 11b increases, the step becomes larger and the gap formed between the separator 13 and the separator 13 becomes larger. However, since the unevenness becomes conspicuous on the surface of the flat wound electrode body 14 as the level difference increases, the thickness of the edge tape 11b is preferably equal to or less than the thickness of the positive electrode mixture layer 11a.
- the insulating tape 11b is provided only at the winding end side end portion of the positive electrode plate 11 is shown, but it may be formed only at the winding start side end portion.
- the winding end side end and the winding start side end may be provided at both ends.
- the air permeability of the flat wound electrode body 14 in the winding axis direction becomes better, and thus the above effect is further improved. It will be played well.
- the example in which the insulating tape 11b is attached on both sides of the positive electrode mixture layer 11a is shown, but only one side may be used. Furthermore, in the nonaqueous electrolyte secondary battery 10 according to the embodiment, the insulating tape 11b attached to the positive electrode mixture layer 11a on both sides extends outward from the positive electrode mixture layer 11a and is bonded to each other. However, it may be affixed only to the surface of the positive electrode mixture layer 11a.
- the positive electrode active material that can be used in the non-aqueous electrolyte secondary battery of the present invention can be appropriately selected and used as long as it is a compound capable of reversibly occluding and releasing lithium ions.
- lithium transition metal composite oxidation represented by LiMO 2 (wherein M is at least one of Co, Ni, and Mn) capable of reversibly occluding and releasing lithium ions.
- the solvent for the nonaqueous electrolyte is not particularly limited, and a solvent that has been conventionally used for nonaqueous electrolyte secondary batteries can be used.
- cyclic carbonates such as ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate, vinylene carbonate (VC); chain carbonates such as dimethyl carbonate (DMC), methyl ethyl carbonate (MEC), and diethyl carbonate (DEC)
- DMC dimethyl carbonate
- MEC methyl ethyl carbonate
- DEC diethyl carbonate
- esters such as methyl acetate, ethyl acetate, propyl acetate, methyl propionate, ethyl propionate and ⁇ -butyrolactone
- compounds containing sulfone groups such as propane sultone
- 1,2-dimethoxyethane 1,2- Compounds containing ethers such as diethoxyethane, tetrahydrofur
- a solvent in which a part of these H is substituted with F is preferably used. Further, these can be used alone or in combination, and a solvent in which a cyclic carbonate and a chain carbonate are combined, and a solvent in which a compound containing a small amount of nitrile or an ether is further combined with these is preferable. .
- an ionic liquid can also be used as the non-aqueous solvent for the non-aqueous electrolyte.
- the cation species and the anion species are not particularly limited, but low viscosity, electrochemical stability, and hydrophobic properties. From the viewpoint, a combination using a pyridinium cation, an imidazolium cation, or a quaternary ammonium cation as the cation and a fluorine-containing imide anion as the anion is particularly preferable.
- a solute used for the non-aqueous electrolyte a known lithium salt that is conventionally used in a non-aqueous electrolyte secondary battery can be used.
- a lithium salt a lithium salt containing one or more elements among P, B, F, O, S, N, and Cl can be used.
- LiPF 6 LiBF 4 , LiCF 3 SO 3 , LiN (FSO 2 ) 2 , LiN (CF 3 SO 2 ) 2 , LiN (C 2 F 5 SO 2 ) 2 , LiN (CF 3 SO 2 ) (C 4 F 9 SO 2 ), Lithium salts such as LiC (C 2 F 5 SO 2 ) 3 , LiAsF 6 , LiClO 4 , LiPF 2 O 2 and mixtures thereof can be used.
- LiPF 6 is preferably used in order to enhance the high rate charge / discharge characteristics and durability of the nonaqueous electrolyte secondary battery.
- a lithium salt having an oxalato complex as an anion can also be used.
- a lithium salt having an oxalato complex as an anion in addition to LiBOB (lithium-bisoxalate borate), a lithium salt having an anion in which C 2 O 4 2 ⁇ is coordinated to a central atom, for example, Li [M (C 2 O 4 ) x R y ] (wherein M is a transition metal, an element selected from Groups 13, 14, and 15 of the periodic table, R is selected from a halogen, an alkyl group, and a halogen-substituted alkyl group) Group, x is a positive integer, and y is 0 or a positive integer).
- Li [B (C 2 O 4 ) F 2 ] Li [P (C 2 O 4 ) F 4 ] Li [P (C 2 O 4 ) 2 F 2 ]
- LiBOB Li [B (C 2 O 4 ) F 2 ]
- the above solutes may be used alone or in combination of two or more.
- the concentration of the solute is not particularly limited, but is preferably 0.8 to 1.7 mol per liter of the non-aqueous electrolyte. Furthermore, in applications that require discharging with a large electric current, the concentration of the solute is desirably 1.0 to 1.6 mol per liter of the non-aqueous electrolyte.
- the negative electrode active material used for the negative electrode is not particularly limited as long as it can reversibly occlude and release lithium.
- a carbon material, lithium metal, A metal or alloy material alloyed with lithium, a metal oxide, or the like can be used.
- a carbon material for the negative electrode active material For example, natural graphite, artificial graphite, mesophase pitch-based carbon fiber (MCF), mesocarbon microbeads (MCMB), coke, hard carbon Etc. can be used.
- MCF mesophase pitch-based carbon fiber
- MCMB mesocarbon microbeads
- coke hard carbon Etc.
- a carbon material obtained by coating a graphite material with low crystalline carbon as the negative electrode active material.
- separator As the separator, a known separator that has been conventionally used in nonaqueous electrolyte secondary batteries can be used. Specifically, not only a separator made of polyethylene but also a material in which a layer made of polypropylene is formed on the surface of polyethylene or a material in which an aramid resin is applied on the surface of a polyethylene separator may be used.
- a layer containing a conventionally used inorganic filler can be formed at the interface between the positive electrode and the separator or the interface between the negative electrode and the separator.
- this filler it is also possible to use an oxide or a phosphoric acid compound that uses titanium, aluminum, silicon, magnesium, etc., which has been used conventionally, or a material whose surface is treated with a hydroxide or the like. it can.
- the filler layer is formed by a method in which a filler-containing slurry is directly applied to a positive electrode, a negative electrode, or a separator, or a method in which a sheet formed with a filler is attached to a positive electrode, a negative electrode, or a separator. be able to.
- a nonaqueous electrolyte secondary battery in which a pressure-sensitive current interruption mechanism is provided in at least one of a conductive path between the positive electrode plate and the positive electrode terminal and a conductive path between the negative electrode plate and the negative electrode terminal will be described. did.
- a non-aqueous electrolyte secondary battery provided with a pressure-sensitive forced short-circuit mechanism instead of the pressure-sensitive current interruption mechanism may be considered.
- FIG. 8 is an enlarged view of a portion where the forced short-circuit mechanism 50 of FIG. 7 is provided.
- FIG. 8A shows a state before the operation of the forced short-circuit mechanism 50
- FIG. 8B shows a state after the operation of the forced short-circuit mechanism 50.
- the metal sealing body 23 has a valve portion 51 electrically connected to the positive electrode plate 11, and a plate shape electrically connected to the negative electrode plate 12 outside the valve portion 51.
- the conductive member 52 is arranged.
- the valve portion 51 is made of metal and may be formed integrally with the sealing body 23. Further, a valve part 51 that is separate from the sealing body 23 may be connected to the sealing body 23.
- the conductive member 52 is connected to the negative electrode terminal 20, and is electrically connected to the negative electrode plate 12 via the negative electrode current collector 19.
- the conductive member 52, the negative electrode terminal 20, and the negative electrode current collector 19 are electrically insulated from the sealing member 23 by the insulating member 22.
- valve portion 51 When the battery is overcharged and the pressure inside the battery exceeds a predetermined value, the valve portion 51 is deformed outward (upward in FIG. 8B) and contacts the conductive member 52 as shown in FIG. 8B. Since the valve portion 51 is made of metal and is electrically connected to the positive electrode plate 11 and the conductive member 52 is electrically connected to the negative electrode plate 12, the positive electrode plate 11 is brought into contact with the valve portion 51 and the conductive member 52. And the negative electrode plate 12 is short-circuited. Thereby, charging current can be prevented from flowing into the electrode body. Moreover, the energy in the electrode body can be quickly released. In this way, safety can be ensured when the battery is overcharged.
- Electroconductive member for positive electrodes 30 ... Intermediate member for positive electrodes 31 .
- Conductive member for negative electrodes 32 ...
- Intermediate members for negative electrodes 33, 34 ...
- Weld mark 50 ... Forced short-circuit mechanism 51 .
- Valve part 52 ... Conductive member
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- Secondary Cells (AREA)
- Battery Electrode And Active Subsutance (AREA)
- Sealing Battery Cases Or Jackets (AREA)
- Connection Of Batteries Or Terminals (AREA)
- Gas Exhaust Devices For Batteries (AREA)
Abstract
Description
正極芯体上に正極合剤層が形成された正極板と、
負極芯体上に負極合剤層が形成された負極板と、
前記正極板及び前記負極板がセパレータを挟んで互いに絶縁された状態で偏平状に巻回された偏平状の巻回電極体と、
非水電解質と、
外装体と、を有し、
前記偏平状の巻回電極体の一方の端部には巻回された正極芯体露出部が形成され、
前記偏平状の巻回電極体の他方の端部には巻回された負極芯体露出部が形成され、
前記巻回された正極芯体露出部は収束されて正極集電体が接続され、
前記巻回された負極芯体露出部は収束されて負極集電体が接続され、
前記正極集電体及び前記負極集電体の少なくとも一方に電気的に接続された圧力感応式の電流遮断機構が設けられており、
前記正極合剤層内には炭酸リチウムが含有されており、
前記正極板の巻き始め側端部及び巻き終り側端部の少なくとも一方の前記正極合剤層上であって、前記セパレータと対向する位置には、前記正極合剤層の幅方向に沿って、絶縁テープが貼付されている、
非水電解質二次電池が提供される。
最初に、実施形態の非水電解質二次電池を図1~図4を用いて説明する。この非水電解質二次電池10は、図4に示したように、正極板11と負極板12とがセパレータ13を介して互いに絶縁された状態で巻回された偏平状の巻回電極体14を有している。この偏平状の巻回電極体14の最外面側は、セパレータ13で被覆されているが、負極板12が正極板11よりも外周側となるようになされている。
正極活物質としては、LiNi0.35Co0.35Mn0.30O2で表されるリチウムニッケルコバルトマンガン複合酸化物を用いた。このリチウムニッケルコバルトマンガン複合酸化物と、導電剤としての炭素粉末と、結着剤としてのポリフッ化ビニリデン(
PVdF)と、炭酸リチウムとを、それぞれ質量比で92:0.9:5:1.5となるよ
うに秤量し、分散媒としてのN-メチル-2-ピロリドン(NMP)と混合して正極合剤
スラリーを調製した。
負極板は次のようにして作製した。黒鉛粉末98質量部、増粘剤としてのカルボキシメチルセルロース(CMC)1質量部、結着剤としてのスチレン-ブタジエンゴム(SBR)1質量部を水に分散させ負極合剤スラリーを調製した。この負極合剤スラリーを厚さ10μmの銅箔からなる負極集電体の両面にダイコーターによって塗布し、乾燥して負極集電体の両面に負極合剤層を形成した。次いで、乾燥し、圧縮ローラーを用いて所定厚さに圧縮し、得られた極板を予め定めた所定寸法に切り出した。その後、極板の幅方向の一方端に、長さ方向全体にわたって一定幅に負正極合剤層が両面ともに形成されていない負極芯体露出部16が形成されるように、負極合剤層を剥離した。このようにして作製された負極板12の構成は、図3Bに示したとおりである。
非水電解液としては、溶媒としてエチレンカーボネート(EC)とメチルエチルカーボネート(MEC)とを体積比(25℃、1気圧)で3:7の割合で混合した混合溶媒に電解質塩としてLiPF6を1mol/Lとなるように添加し、さらに全非水電解質質量に対してビニレンカーボネートVCを0.3質量%添加したものを用いた。
上述ようにして作製された負極板12及び正極板11を、最外面側が負極板12となるようにして、それぞれセパレータ13を介して互いに絶縁された状態で巻回した後、偏平状に成形して偏平状の巻回電極体14を作製した。偏平状の巻回電極体14の巻回終了端側の構成は図4Aに示したとおりである。また、偏平状の巻回電極体14は圧縮されているため、偏平状の巻回電極体14の形成時の正極板11における正極合剤層11aと、絶縁テープ11bと、セパレータ13との配置関係は、図4Bに示したとおりとなる。
比較例の非水電解質二次電池の具体的構成を図5及び図6を用いて説明する。比較例の非水電解質二次電池の具体的構成は、正極板の構成を除いて実質的に実施形態の非水電解質二次電池10と同様である。そこで、適宜図1及び図2を援用するとともに、実施形態の非水電解質二次電池10と同一の構成部分には同一の参照符号を付与してその詳細な説明は省略する。
11b…絶縁テープ 12…負極板 12a…負極合剤層
13…セパレータ 14、14A…偏平状の巻回電極体 15…正極芯体露出部
15a…溶接痕 16…負極芯体露出部 17…正極集電体
18…正極端子 19…負極集電体 20…負極端子
21、22…絶縁部材 23…封口体 24…絶縁シート
25…角形外装体 26…電解液注液口 27…電流遮断機構
28…ガス排出弁 29…正極用導電部材 30…正極用中間部材
31…負極用導電部材 32…負極用中間部材 33、34…溶接跡
50…強制短絡機構 51…弁部 52…導電部材
Claims (5)
- 正極芯体上に正極合剤層が形成された正極板と、
負極芯体上に負極合剤層が形成された負極板と、
前記正極板及び前記負極板がセパレータを挟んで互いに絶縁された状態で偏平状に巻回された偏平状の巻回電極体と、
非水電解質と、
外装体と、を有し、
前記偏平状の巻回電極体の一方の端部には巻回された正極芯体露出部が形成され、
前記偏平状の巻回電極体の他方の端部には巻回された負極芯体露出部が形成され、
前記巻回された正極芯体露出部は収束されて正極集電体が接続され、
前記巻回された負極芯体露出部は収束されて負極集電体が接続され、
前記正極集電体及び前記負極集電体の少なくとも一方に電気的に接続された圧力感応式の電流遮断機構が設けられており、
前記正極合剤層内には炭酸リチウムが含有されており、
前記正極板の巻き始め側端部及び巻き終り側端部の少なくとも一方の前記正極合剤層上であって、前記セパレータと対向する位置には、前記正極合剤層の幅方向に沿って、絶縁テープが貼付されている、
非水電解質二次電池。 - 前記正極合剤層は、前記正極芯体の両面に形成されており、前記絶縁テープは前記正極合剤層の両面に貼付されている、請求項1に記載の非水電解質二次電池。
- 前両面に貼付されているそれぞれの絶縁テープは、それぞれ前記正極合剤層よりも外方に延在して互いに張り合わされている、請求項2に記載の非水電解質二次電池。
- 前記正極合剤層中の炭酸リチウム濃度は前記正極合剤質量に対して0.1質量%以上5質量%以下である、請求項1~3のいずれかに記載の非水電解質二次電池。
- 前記外装体は角形である、請求項1~4のいずれかに記載の非水電解質二次電池。
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