WO2014045569A1 - 密閉型二次電池 - Google Patents
密閉型二次電池 Download PDFInfo
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- WO2014045569A1 WO2014045569A1 PCT/JP2013/005505 JP2013005505W WO2014045569A1 WO 2014045569 A1 WO2014045569 A1 WO 2014045569A1 JP 2013005505 W JP2013005505 W JP 2013005505W WO 2014045569 A1 WO2014045569 A1 WO 2014045569A1
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- Prior art keywords
- battery
- battery case
- sealed secondary
- secondary battery
- thin portion
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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
- 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
- H01M50/543—Terminals
- H01M50/552—Terminals characterised by their shape
- H01M50/559—Terminals adapted for cells having curved cross-section, e.g. round, elliptic or button cells
- H01M50/56—Cup shaped terminals
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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
- H01M50/10—Primary casings; Jackets or wrappings
- H01M50/102—Primary casings; Jackets or wrappings characterised by their shape or physical structure
- H01M50/107—Primary casings; Jackets or wrappings characterised by their shape or physical structure having curved cross-section, e.g. round or elliptic
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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
- H01M10/04—Construction or manufacture in general
- H01M10/0431—Cells with wound or folded electrodes
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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
- H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
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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
- H01M2004/026—Electrodes composed of, or comprising, active material characterised by the polarity
- H01M2004/028—Positive electrodes
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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
- H01M4/131—Electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
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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
- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
- H01M4/525—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
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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
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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
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T10/00—Road transport of goods or passengers
- Y02T10/60—Other road transportation technologies with climate change mitigation effect
- Y02T10/70—Energy storage systems for electromobility, e.g. batteries
Definitions
- the present invention relates to a sealed secondary battery provided with a safety valve that exhausts gas generated in the battery to the outside of the battery when the pressure in the battery increases.
- lithium-ion secondary batteries as drive power sources for portable electronic devices such as mobile phones, portable personal computers, portable music players, and also for hybrid electric vehicles (HEV) and electric vehicles (EV) Sealed secondary batteries such as non-aqueous electrolyte secondary batteries are used.
- a sealed secondary battery when an internal short circuit or an external short circuit occurs, or when abnormal heating or abnormal shock occurs, rapid gas generation occurs due to rapid charge / discharge reaction or chemical reaction inside the battery. Thereby, there exists a possibility that a battery case may expand
- a safety valve explosion-proof mechanism
- Patent Document 1 a sealed secondary battery including a safety valve by a sealing body provided with a valve body and a safety valve by a battery case provided with a thin wall portion is described.
- the breaking pressure of the thin wall portion is larger than the breaking pressure of the valve body, when the gas generation rate is slow, the gas can be easily exhausted only by breaking the valve body. Temperature rise can be suppressed.
- the thin portion of the battery case is broken, so that the gas can be quickly exhausted and the battery case can be prevented from bursting.
- An object of the present invention is to solve the above-described problems, and a sealed secondary battery in which cracking is suppressed in a battery case even in a sealed secondary battery having a high energy density. It is to provide.
- a sealed secondary battery of the present invention includes a bottomed cylindrical battery case having an opening, a sealing body that seals the opening of the battery case, a positive electrode plate, and a negative electrode plate.
- a wound electrode group wound via a separator, and an annular thin portion is formed at the bottom of the battery case, and is surrounded by the annular thin portion with respect to the area of the bottom of the battery case
- the area ratio of the region is 10% or more, and the volume energy density is 500 Wh / L or more.
- the ratio of the area of the region surrounded by the annular thin portion to the area of the bottom of the battery case is more preferably 20% or more.
- the annular thin portion may have a circular shape such as a perfect circle or an ellipse in a plan view, or may have a polygonal shape or a track shape.
- a circular thin part is particularly preferable, and a perfect circular thin part is more preferable.
- a lead electrically connected to the positive electrode plate or the negative electrode plate is connected to the battery inner surface side of the region surrounded by the annular thin portion, and the melting point of the lead is 1000 ° C. or higher. It is preferable that According to this configuration, even when the internal pressure of the battery rises and the annular thin portion provided at the bottom of the battery case breaks, the lead is connected to the region surrounded by the annular thin portion, Since the lead is not melted by the gas, the portion surrounded by the annular thin portion can be prevented from being violently scattered outside the battery.
- the lead having a melting point of 1000 ° C. or higher preferably contains nickel, a nickel alloy, copper, or a copper alloy.
- the positive electrode plate contains a positive electrode active material
- the positive electrode active material has a general formula Li x Ni y M 1-y O 2 (x: 0.95 ⁇ x ⁇ 1.15, 0.6 ⁇ y ⁇ 1, and M is preferably a lithium nickel composite oxide represented by Co, Mn, Cr, Fe, W, Mg, Zr, Ti, and Al).
- the lithium nickel composite oxide When the lithium nickel composite oxide is used as the positive electrode active material, a battery having a higher energy density can be obtained than when lithium cobaltate is used. However, if the lithium nickel composite oxide is used as the positive electrode active material, the amount of gas generated inside the battery at the time of battery abnormality increases, and the battery internal pressure tends to rise more rapidly. Problems such as cracks are likely to occur. Therefore, the present invention is particularly effective when the lithium nickel composite oxide is used as the positive electrode active material.
- the thin portion is preferably formed by providing a notch on the battery outer surface side of the bottom of the battery case.
- the cross-sectional shape of the notch is preferably substantially V-shaped.
- the said sealing body contains the filter which has an opening part, and the area of the opening part of the said filter is 30 mm ⁇ 2 > or more.
- the area of the opening of the filter is the area of the opening in plan view of the filter.
- the total area of all the openings is preferably 30 mm 2 or more.
- the battery case is preferably made of iron, and the thickness of the cylindrical part of the battery case is preferably 0.1 mm to 0.4 mm. According to such a structure, it can prevent more effectively that a crack arises in the cylindrical part of a battery case.
- a nickel layer is preferably formed on the surface of the iron battery case.
- a wire is connected to a region surrounded by a thin portion on the battery outer surface side at the bottom of the battery case.
- a conductive member is connected to the battery case of each sealed secondary battery in order to electrically connect the sealed secondary batteries to each other.
- the plate-like conductive member is connected to the battery case, the effect of the present invention can be obtained, but there is a possibility that breakage of the annular thin portion accompanying increase in the battery internal pressure may be hindered.
- the wire is connected as the conductive member to the battery outer surface side of the region surrounded by the annular thin portion at the bottom of the battery case, the fracture of the annular thin portion is difficult to be inhibited.
- the holding body for holding each battery has a shape that covers the cylindrical part (side surface part) of the sealed secondary battery. It is preferable to use it.
- FIG. 1 is a perspective view of a sealed secondary battery in an embodiment of the present invention.
- FIG. 2 is a cross-sectional view of a sealed secondary battery in an example of the present invention.
- FIG. 3 is a bottom view of the outer surface side of the sealed secondary battery according to the embodiment of the present invention.
- FIG. 4 is a bottom view of the battery inner surface side of the sealed secondary battery in the embodiment of the present invention.
- FIG. 5 is a bottom view of the battery outer surface side of the sealed secondary battery in the comparative example of the present invention.
- an electrode group 4 in which a positive electrode plate 1 and a negative electrode plate 2 are wound through a separator 3 is housed in a bottomed cylindrical battery case 15 together with a non-aqueous electrolyte (not shown).
- a ring-shaped insulating plate 7 and an insulating plate 8 are disposed above and below the electrode group 4, the positive plate 1 is joined to the filter 12 through the positive lead 5, and the negative plate 2 is connected through the negative lead 6. And joined to the bottom of the battery case 15 which also serves as a negative electrode terminal.
- the filter 12 is provided with an opening 12a.
- the area of the opening 12a when the filter 12 is viewed from above is preferably 30 mm 2 .
- the filter 12 is connected to the inner cap 11, and the protrusion of the inner cap 11 is joined to the metal valve body 10. Furthermore, the valve body 10 is connected to a sealing plate 9 that also serves as a positive electrode terminal.
- the sealing plate 9, the valve body 10, the inner cap 11, and the filter 12 form a sealing body 20 and seal the opening of the battery case 15 through the gasket 13.
- the sealing body 20 does not need to include all of the sealing plate 9, the valve body 10, the inner cap 11, and the filter 12, as long as the opening of the battery case 15 can be sealed.
- the valve body 10 and the inner cap 11 are formed with a thin portion 10a and a thin portion 11a that are broken when the pressure in the battery reaches a predetermined value.
- the sealing plate 9 is formed with an exhaust hole 9 a for exhausting the gas generated in the battery to the outside of the battery through the broken valve body 10 and the inner cap 11.
- the valve body 10, the inner cap 11, and the exhaust hole 9a constitute a safety valve.
- it is not necessary to provide a safety valve on the sealing body but it is preferable to provide a safety valve on the sealing body.
- a circular thin portion 15a that is broken when the pressure in the battery reaches a predetermined value is formed at the bottom of the battery case 15.
- a safety valve is constituted by a circular thin portion 15 a formed at the bottom of the battery case 15.
- the breaking pressure of the thin portion 15a formed at the bottom of the battery case 15 is larger than the breaking pressure of the thin portion 10a formed in the valve body 10. . That is, the operating pressure of the safety valve provided at the bottom of the battery case is preferably set higher than the operating pressure of the safety valve provided at the sealing body.
- the dried electrode plate is compressed with a roller press so that the thickness becomes 163 ⁇ m, and then cut so that the exposed portion of the positive electrode core body in which no active material layer is formed remains, and a positive electrode having a width of 58 mm and a length of 660 mm A plate 1 was produced. Thereafter, the positive electrode lead 5 made of aluminum was connected to the core exposed portion of the positive electrode plate 1 by ultrasonic welding.
- Graphite as a negative electrode active material, styrene butadiene rubber as a binder, and carboxymethyl cellulose as a thickener are mixed at 98.4: 0.6: 1 (mass ratio), and this mixture is dispersed in water. And made a paste.
- This paste was uniformly applied on both sides of a negative electrode core made of a copper foil having a thickness of 10 ⁇ m and dried by heating to produce a dry electrode plate having an active material layer formed on the copper foil.
- the dried electrode plate is compressed by a roller press so as to have a thickness of 164 ⁇ m, and then cut so as to leave a negative electrode core exposed portion in which no active material layer is formed, and a negative electrode having a width of 59 mm and a length of 730 mm Plate 2 was prepared. Thereafter, the negative electrode lead 6 made of nickel was connected to the core exposed portion of the negative electrode plate 2 by ultrasonic welding.
- the electrode group 4 was prepared by winding the positive electrode plate 1, the negative electrode plate 2, and the polyethylene microporous separator 3 (thickness 20 ⁇ m) so that the positive electrode plate 1 and the negative electrode plate 2 were insulated by the separator 3. .
- a plate material having nickel plated on the surface of an iron base was drawn to produce a bottomed cylindrical battery case 15.
- the plate thickness of the cylindrical portion of the battery case 15 was 0.25 mm
- the plate thickness of the bottom portion of the battery case 15 was 0.3 mm.
- the thickness of the thin part was 0.25 mm.
- the ratio of the area of the region surrounded by the annular thin portion 15a to the area of the bottom portion (battery outer surface side) of the battery case 15 is 25%.
- the electrode group 4 was inserted into the battery case 15 so that the polypropylene disk-shaped insulating plate 8 was positioned between the electrode group 4 and the bottom of the battery case 15. Then, the negative electrode lead 6 was connected to the bottom of the battery case 15 by resistance welding. Thereby, the weld 6a was formed. At this time, as shown in FIG. 3, the tip of the negative electrode lead 6 was disposed so as to be within the region surrounded by the thin portion 15a. Since the tip of the negative electrode lead 6 is set to a length and a width that do not interfere with the thin portion 15a, it is difficult to hinder the operation of the safety valve. In addition, gas can be discharged smoothly.
- a disk-shaped insulating plate 7 made of polypropylene was disposed on the electrode group 4. Then, a groove portion 15b having a U-shaped cross section of 1.0 mm in width and 1.5 mm in depth was formed in the circumferential direction in a portion of the cylindrical portion of the battery case 15 on the opening side of the insulating plate 7. Thereby, the protrusion part which protrudes inside is formed in the inner surface side of the cylindrical part of the battery case 15 over the perimeter. Thereafter, a nonaqueous electrolytic solution was injected into the battery case 15. The positive electrode lead 5 is connected to the filter 12 constituting the sealing body 20 by laser welding, and the positive electrode lead 5 is folded so that the sealing body 20 is formed on the inner surface side of the cylindrical portion of the battery case 15.
- the sealed secondary battery of Example 1 was fabricated by placing the cylindrical part near the opening of the battery case 15 and crimping the cylindrical part.
- This sealed secondary battery has a cylindrical shape with a diameter of 18 mm and a height of 65 mm.
- the volume of the sealed secondary battery was 0.0165L.
- the battery capacity of this sealed secondary battery was 3200 mAh, and the energy capacity was 11.5 Wh.
- the volume energy density was 697 Wh / L.
- the battery capacity was obtained by the following method.
- the sealed secondary battery was charged to 4.2 V at a current of 1.0 A, and then charged at a constant voltage of 4.2 V for 4 hours. Subsequently, the battery was discharged to 2.5 V with a constant current of 0.6A. The discharge capacity at this time was defined as the battery capacity.
- Comparative Example 1 A sealed secondary battery of Comparative Example 1 was produced in the same manner as in the example, except that a battery case having a circular thin part with a diameter of 5 mm formed at the bottom of the battery case was used.
- the ratio of the area of the region surrounded by the annular thin portion to the area of the bottom of the battery case is 8%.
- Comparative Example 2 As the battery case, as shown in FIG. 5, the sealed type two of Comparative Example 2 was used in the same manner as in the example except that a battery case 25 having a C-shaped thin portion 25 a having a diameter of 9 mm was formed at the bottom. A secondary battery was produced.
- Example 1 Ten sealed secondary batteries of Example 1, Comparative Example 1 and Comparative Example 2 were produced, respectively, and a heating test was performed under the following conditions. First, the battery was charged at a current of 1500 mA in a 25 ° C. environment until the battery voltage reached 4.2V. The sealed secondary battery after charging was placed on a hot plate set at 200 ° C. so that the cylindrical part of the battery case was in contact with the hot plate, and heated at 200 ° C. And the presence or absence of the scattering of a sealing body and the crack of a battery case was confirmed. The results are shown in Table 1.
- Example 1 in which a circular thin portion having a diameter of 9 mm was provided at the bottom of the battery case, the thin portion at the bottom of the battery case opened and the gas inside the battery was smoothly discharged, so that the sealing body was not scattered, The battery case did not crack.
- Comparative Example 1 in which a circular thin part with a diameter of 5 mm was provided at the bottom of the battery case, and in Comparative Example 2 in which a C-shaped thin part with a diameter of 9 mm was provided in the bottom of the battery case, there was no scattering of the sealing body. However, a crack occurred in the battery case.
- the crack occurrence rate of the battery case was 80% in Comparative Example 1 and 30% in Comparative Example 2.
- the gas generated inside the battery cannot be smoothly discharged to the outside of the battery, so it is considered that a crack occurred in the cylindrical part of the battery case.
- the sealed secondary battery of the present invention by defining the shape of the thin portion provided at the bottom of the battery case and the ratio of the area of the region surrounded by the thin portion to the area of the bottom of the battery case, It is possible to prevent the cylindrical portion from being cracked, and to provide a sealed secondary battery that is more excellent in safety.
- a lithium ion secondary battery which is a nonaqueous electrolyte secondary battery has been described as a sealed secondary battery, but the same effect can be obtained with a sealed secondary battery such as an alkaline storage battery other than the nonaqueous electrolyte secondary battery. Is obtained.
- the present invention is particularly effective in the case of a nonaqueous electrolyte secondary battery.
- the shape of the thin part provided in the bottom part of a battery case was circular, it is good also as polygonal shape etc.
- Lithium transition metal composite oxide includes lithium cobalt composite oxide, lithium nickel composite oxide, lithium nickel cobalt composite oxide, lithium nickel cobalt manganese composite oxide, spinel type lithium manganese composite oxide, and these compounds A compound obtained by substituting a part of the transition metal element with another metal element (Zr, Mg, Ti, Al, W, etc.) is preferable.
- the lithium transition metal phosphate compound having an olivine structure is preferably lithium iron phosphate. These can be used alone, or can be used in combination of two or more.
- a material capable of reversibly occluding and releasing lithium ions can be used as the negative electrode active material.
- carbon materials such as natural graphite, artificial graphite, non-graphitizable carbon (hard carbon), graphitizable carbon (soft carbon), metal oxides such as tin oxide and silicon oxide, silicon containing such as silicon and silicide A compound or the like can be used.
- a polyolefin-based material as the separator, and it is more preferable to use a combination of a polyolefin-based material and a heat-resistant material.
- the polyolefin-based material include porous films such as polyethylene, polypropylene, and ethylene-propylene copolymer. These can be used independently and can also be used in combination of 2 or more type.
- a porous film made of a heat resistant resin such as aramid, polyimide, polyamideimide, or a mixture of a heat resistant resin and an inorganic filler can be used.
- nonaqueous solvent for the nonaqueous electrolyte cyclic carbonates such as ethylene carbonate, propylene carbonate, butylene carbonate, and chain carbonates such as dimethyl carbonate, ethyl methyl carbonate, dimethyl carbonate, and dinormal butyl carbonate are used.
- Lactones such as ⁇ -butyrolactone and ⁇ -valerolactone, carboxylic acid esters such as methyl pivalate, ethyl pivalate, methyl isobutyrate, methyl propionate, etc. may be used singly or in combination. preferable.
- electrolyte salts of non-aqueous electrolytes include LiClO 4 , LiCF 3 SO 3 , LiPF 6 , LiBF 4 , LiAsF 6 , LiN (CF 3 SO 2 ) 2 , LiN (CF 2 CF 3 SO 2 ) 2, etc. It is preferable to use 1 type or in mixture of multiple types.
- the concentration of the electrolyte salt is preferably 0.5 to 2.0 M (mol / liter).
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- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Secondary Cells (AREA)
- Sealing Battery Cases Or Jackets (AREA)
- Gas Exhaust Devices For Batteries (AREA)
- Battery Electrode And Active Subsutance (AREA)
- Connection Of Batteries Or Terminals (AREA)
Description
正極活物質としてのLiNi0.8Co0.15Al0.05O2と、導電剤としてのアセチレンブラックと、結着剤としてのポリフッ化ビニリデンとを96:1.6:2.4(質量比)で混合し、この混合物をN-メチル-2-ピロリドンに分散してペーストとした。このペーストを、厚さ15μmのアルミニウム箔からなる正極芯体の両面に均一に塗布し、加熱乾燥して、アルミニウム箔上に活物質層が形成された乾燥極板を作製した。乾燥極板をローラープレス機で厚みが163μmになるように圧縮した後、一部に活物質層が形成されていない正極芯体露出部が残るように裁断して幅58mm、長さ660mmの正極板1を作製した。その後、正極板1の芯体露出部にアルミニウム製の正極リード5を超音波溶接により接続した。
負極活物質としての黒鉛と、結着剤としてのスチレンブタジエンゴムと、増粘剤としてのカルボキシメチルセルロースとを98.4:0.6:1(質量比)で混合し、この混合物を水に分散してペーストとした。このペーストを厚さ10μmの銅箔からなる負極芯体の両面に均一に塗布し、加熱乾燥して、銅箔上に活物質層が形成された乾燥極板を作製した。乾燥極板をローラープレス機で厚みが164μmになるように圧縮した後、一部に活物質層が形成されていない負極芯体露出部が残るように裁断して幅59mm、長さ730mmの負極板2を作製した。その後、負極板2の芯体露出部にニッケル製の負極リード6を超音波溶接により接続した。
電極群4は、上記正極板1と負極板2とポリエチレン製微多孔質セパレータ3(厚み20μm)とを、正極板1と負極板2がセパレータ3により絶縁されるように、巻回して作製した。
エチレンカーボネート、ジエチルカーボネートおよびエチルメチルカーボネートを体積比で20:20:60(25℃、1気圧)の割合で混合した非水溶媒に電解質塩として六フッ化リン酸リチウム(LiPF6)を1mol/Lとなるように溶解した。
鉄製の基材の表面にニッケルメッキを施した板材を絞り加工し、有底円筒状の電池ケース15を作製した。ここで、電池ケース15の筒状部の板厚は0.25mm、電池ケース15の底部の板厚は0.3mmとした。また、電池ケース15の底部は直径18mmとし、図3に示すように電池ケース15の底部には直径D=9mmの円状の薄肉部15aを設けた。薄肉部の板厚は0.25mmとした。ここで、電池ケース15の底部(電池外面側)の面積に対する環状の薄肉部15aにより囲まれた領域の面積の割合は25%である。
電極群4と電池ケース15の底部の間にポリプロピレン製の円板状の絶縁板8が位置するようにして、電極群4を電池ケース15に挿入した。そして、負極リード6を電池ケース15の底部に抵抗溶接により接続した。これにより溶接部6aが形成された。このとき、図3に示すように、負極リード6の先端部が、薄肉部15aにより囲まれた領域内に収まるように配置した。負極リード6の先端は薄肉部15aに干渉しない長さ、幅に設定されているため、安全弁の作動を阻害し難くなっている。また、ガスの排出も円滑となる。次に、電極群4の上部にポリプロピレン製の円板状の絶縁板7を配置した。そして、電池ケース15の筒状部における絶縁板7よりも開口側の部分に、断面がU字形の幅1.0mm、深さ1.5mmの溝部15bを円周方向に加工成形した。これにより、電池ケース15の筒状部の内面側に、全周にわたって内側に突出する突出部が形成される。その後、非水電解液を電池ケース15内に注入した。そして、正極リード5を、封口体20を構成するフィルタ12とレーザ溶接により接続し、正極リード5を折りたたんだ状態として、封口体20を電池ケース15の筒状部の内面側に形成された突出部上に配置し、電池ケース15の開口部近傍の筒状部をカシメることにより、実施例1の密閉型二次電池を作製した。この密閉型二次電池は、直径18mm、高さ65mmの円筒形である。この密閉型二次電池の体積は0.0165Lであった。また、この密閉型二次電池の電池容量は3200mAhであり、エネルギー容量は11.5Whであった。体積エネルギー密度は697Wh/Lであった。
電池ケースとして、電池ケースの底部に直径5mmの円状の薄肉部を形成したものを用いた以外は、実施例と同様の方法で比較例1の密閉型二次電池を作製した。ここで、電池ケースの底部の面積に対する環状の薄肉部により囲まれた領域の面積の割合は8%である。
電池ケースとして、図5に示すように電池ケース25の底部に直径9mmのC字状の薄肉部25aを形成したものを用いた以外は、実施例と同様の方法で比較例2の密閉型二次電池を作製した。
実施例1、比較例1および比較例2の密閉型二次電池をそれぞれ10個ずつ作製し、以下のような条件で加熱試験を行った。まず、25℃の環境下で1500mAの電流で電池電圧が4.2Vとなるまで充電した。充電後の密閉型二次電池を200℃に設定したホットプレートの上に電池ケースの筒状部がホットプレートと接するように配置し、200℃で加熱した。そして、封口体の飛散、電池ケースの亀裂の有無を確認した。その結果を表1に示す。
2 負極板
3 セパレータ
4 電極群
5 正極リード
6 負極リード
7、8 絶縁板
9 封口板
9a 排気孔
10 弁体
10a 薄肉部
11 インナーキャップ
11a 薄肉部
12 フィルタ
12a 開口部
13 ガスケット
15 電池ケース
15a 薄肉部
15b 溝部
20 封口体
Claims (8)
- 開口部を有する有底筒状の電池ケースと、
前記電池ケースの開口部を封止する封口体と、
正極板及び負極板がセパレータを介して巻回された巻回型電極群とを備え、
前記電池ケースの底部には、環状の薄肉部が形成され、前記電池ケースの底部の面積に対する前記環状の薄肉部により囲まれた領域の面積の割合が10%以上であり、体積エネルギー密度が500Wh/L以上である密閉型二次電池。 - 前記環状の薄肉部により囲まれた領域の電池内面側には、前記正極板又は前記負極板に電気的に接続されたリードが接続されており、前記リードの融点は1000℃以上である請求項1に記載の密閉型二次電池。
- 前記正極板には正極活物質が含有され、前記正極活物質は一般式LixNiyM1-yO2(x:0.95≦x≦1.15、0.6≦y≦1、MはCo、Mn、Cr、Fe、W、Mg、Zr、TiおよびAlの少なくとも1種類)で表されるリチウムニッケル複合酸化物である請求項1又は2に記載の密閉型二次電池。
- 前記薄肉部は、前記電池ケースの底部の電池外面側にノッチを設けることにより形成されている請求項1~3のいずれかに記載の密閉型二次電池。
- 前記封口体は開口部を有するフィルタを含み、前記フィルタの開口部の面積は30mm2以上である請求項1~4のいずれかに記載の密閉型二次電池。
- 前記環状の薄肉部は円状である請求項1~5のいずれかに記載の密閉型二次電池。
- 前記電池ケースは鉄製であり、前記電池ケースの筒状部の厚みは、0.1mm~0.4mmである請求項1~6のいずれかに記載の密閉型二次電池。
- 前記環状の薄肉部により囲まれた領域の電池外面側にワイヤーが接続されている請求項1~7のいずれかに記載の密閉型二次電池。
Priority Applications (3)
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|---|---|---|---|
| US14/397,703 US20150132625A1 (en) | 2012-09-24 | 2013-09-18 | Sealed secondary battery |
| CN201380010325.1A CN104126238B (zh) | 2012-09-24 | 2013-09-18 | 封闭式二次电池 |
| JP2014532140A JP5737481B2 (ja) | 2012-09-24 | 2013-09-18 | 密閉型非水電解質二次電池 |
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| Application Number | Priority Date | Filing Date | Title |
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| JP2012209480 | 2012-09-24 | ||
| JP2012-209480 | 2012-09-24 |
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| WO2014045569A1 true WO2014045569A1 (ja) | 2014-03-27 |
Family
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| PCT/JP2013/005505 Ceased WO2014045569A1 (ja) | 2012-09-24 | 2013-09-18 | 密閉型二次電池 |
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| Country | Link |
|---|---|
| US (1) | US20150132625A1 (ja) |
| JP (2) | JP5737481B2 (ja) |
| CN (1) | CN104126238B (ja) |
| WO (1) | WO2014045569A1 (ja) |
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| JP2025511567A (ja) * | 2022-05-12 | 2025-04-16 | ビーワイディー カンパニー リミテッド | バッテリ、バッテリ・モジュール、バッテリ・パック、および車両 |
| WO2024004627A1 (ja) | 2022-06-28 | 2024-01-04 | パナソニックエナジー株式会社 | 密閉電池 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPWO2014045569A1 (ja) | 2016-08-18 |
| JP5737481B2 (ja) | 2015-06-17 |
| JP2015135822A (ja) | 2015-07-27 |
| CN104126238A (zh) | 2014-10-29 |
| US20150132625A1 (en) | 2015-05-14 |
| CN104126238B (zh) | 2016-02-24 |
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