JP2006040652A - Storage element - Google Patents
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- JP2006040652A JP2006040652A JP2004216774A JP2004216774A JP2006040652A JP 2006040652 A JP2006040652 A JP 2006040652A JP 2004216774 A JP2004216774 A JP 2004216774A JP 2004216774 A JP2004216774 A JP 2004216774A JP 2006040652 A JP2006040652 A JP 2006040652A
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- 238000003860 storage Methods 0.000 title claims abstract description 23
- 238000007789 sealing Methods 0.000 claims abstract description 20
- 238000004804 winding Methods 0.000 claims abstract description 6
- 239000000463 material Substances 0.000 claims description 13
- 239000007774 positive electrode material Substances 0.000 claims description 6
- 230000005611 electricity Effects 0.000 claims description 5
- 239000007773 negative electrode material Substances 0.000 claims description 4
- 238000003466 welding Methods 0.000 abstract description 22
- 238000004519 manufacturing process Methods 0.000 abstract description 7
- 238000012423 maintenance Methods 0.000 abstract description 3
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 abstract 2
- 230000000052 comparative effect Effects 0.000 description 13
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 10
- 229910001416 lithium ion Inorganic materials 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 238000007689 inspection Methods 0.000 description 8
- -1 nickel metal hydride Chemical class 0.000 description 8
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 6
- 230000007547 defect Effects 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
- 239000002033 PVDF binder Substances 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 230000002950 deficient Effects 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 4
- 239000003125 aqueous solvent Substances 0.000 description 3
- 239000006258 conductive agent Substances 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 2
- 229910013870 LiPF 6 Inorganic materials 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- 229910021383 artificial graphite Inorganic materials 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000011889 copper foil Substances 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 229910052987 metal hydride Inorganic materials 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- VAYTZRYEBVHVLE-UHFFFAOYSA-N 1,3-dioxol-2-one Chemical compound O=C1OC=CO1 VAYTZRYEBVHVLE-UHFFFAOYSA-N 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 1
- 229910013063 LiBF 4 Inorganic materials 0.000 description 1
- 229910015118 LiMO Inorganic materials 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- OJIJEKBXJYRIBZ-UHFFFAOYSA-N cadmium nickel Chemical compound [Ni].[Cd] OJIJEKBXJYRIBZ-UHFFFAOYSA-N 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000005678 chain carbonates Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000005676 cyclic carbonates Chemical class 0.000 description 1
- HHNHBFLGXIUXCM-GFCCVEGCSA-N cyclohexylbenzene Chemical compound [CH]1CCCC[C@@H]1C1=CC=CC=C1 HHNHBFLGXIUXCM-GFCCVEGCSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 229910001496 lithium tetrafluoroborate Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 229910021382 natural graphite Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 239000011255 nonaqueous electrolyte Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000009751 slip forming Methods 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
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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
-
- 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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- Secondary Cells (AREA)
- Connection Of Batteries Or Terminals (AREA)
- Battery Electrode And Active Subsutance (AREA)
Abstract
Description
本発明は、高出力に好適な蓄電素子に関するものであり、より詳しくは内部抵抗を低減しつつ工程不良の判別が容易な集電構造に関する。 The present invention relates to a power storage element suitable for high output, and more particularly to a current collection structure that can easily determine a process failure while reducing internal resistance.
蓄電素子、とりわけリチウムイオン電池やニッケル水素電池などの二次電池は、携帯電話を始めとする各種コードレス機器の主電源として用いられている。しかし近年、電気自動車や電動工具などの駆動用電源としての実用化検討が活発化する中、高エネルギー密度に加え軽量なリチウムイオン電池が注目されている。コードレス機器の主電源に用いられる二次電池は、一般的に図1のような構造を有する。すなわち、正極集電体に正極材料を塗着し、その長尺方向の一端に集電用リード1aを溶接した帯状の正極板1と、負極集電体に負極合剤を塗着し、その長尺方向の一端に集電用リード2aを溶接した帯状の負極板2とを、セパレータ3を介して渦巻状に捲回して極板群とした後、この電極群を有底缶に挿入し、正極集電用リード1aを、開口部側に配置された封口板の端子に溶接し、負極集電用リード2aを、端子を兼ねた有底缶の底部に溶接した後、封口するというものである(例えば特許文献1)。この方法は簡便であり、製造コストを低減できるという利点を有している一方、正負極とも集電用リードのみで電子伝導性を確保するため集電効率が低く、内部抵抗が高くなるという課題を有する。
Power storage elements, particularly secondary batteries such as lithium ion batteries and nickel metal hydride batteries, are used as main power sources for various cordless devices such as mobile phones. However, in recent years, as lithium ion batteries that are light in addition to high energy density are attracting attention, as practical studies for driving power sources for electric vehicles and electric tools are activated. A secondary battery used for a main power source of a cordless device generally has a structure as shown in FIG. That is, a positive electrode material is applied to a positive electrode current collector, a strip-like positive electrode plate 1 having a current collecting lead 1a welded to one end in the longitudinal direction, and a negative electrode mixture is applied to the negative electrode current collector, A strip-shaped
そこで電動工具用などの高出力を必要とする二次電池は、集電効率を高めるため、図4のような構造に改良されている。すなわち、正極集電体に正極材料を塗着し、その長尺方向に極板材料が付着されていない集電体露出部1bを連続的に設けた帯状の正極板1と、負極集電体に負極合剤を塗着し、その長尺方向に極板材料が付着されていない集電体露出部2bを連続的に設けた帯状の負極板2とを、セパレータ3を介して渦巻状に捲回し、一方から正極板1の集電体露出部1bを、他方から負極板2の集電体露出部2bを突出させて極板群とした後、集電体露出部1bおよび2bと集電端子板4とを集合溶接し、この極板群を有底缶に挿入した。底部側の集電端子板4と一体化された負極集電用リード2aを、端子を兼ねた有底缶の底部に溶接し、開口部側の集電端子板4と一体化された正極集電用リード1aを、封口板の端子に溶接した後、封口するというものである(例えば特許文献2)。この集電構造は電極の各部位から電子を取り出せるため、図1の構造と比べて集電効率が向上しており、高出力用途に適している。
しかしながら特許文献2の構造では、上述したように、電極群を有底缶に挿入した後で底部側の集電端子板と有底缶の底部とを溶接せざるを得ない。このような場合、溶接時のスパークによるセパレータの溶融など、工程管理の不十分が原因で起こる不具合を目視で判別できないため、溶接工程の管理に気付かぬまま、後工程である短絡検査(電圧測定)にて相当量の不良電池を排出するという課題を有していた。
そこで本発明は、上述した課題を解決し、溶接工程での不良品を目視判別することにより生産歩留が向上でき、かつ高い集電効率を有する、高出力用蓄電素子を提供することを目的とする。
However, in the structure of
SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to solve the above-described problems and to provide a high-output power storage device that can improve production yield by visually determining defective products in a welding process and has high current collection efficiency. And
前記の課題を解決するために、本発明の請求項1は、帯状の正極板および負極板とセパレータとを捲回して構成される電極群を有底缶に挿入し、開口部を封口板にて封口してなる蓄電素子について、正極板あるいは負極板のいずれか一方の電極板の長尺方向に極板材料が付着されていない集電体露出部を連続的に設け、この集電体露出部と集電端子板とを集合溶接し、この集電端子板を有底缶の底側に配置し、集電用リードによりこの集電端子板と端子を有する封口板とを電気的に接続することを特徴とする。
また本発明の請求項4は、帯状の正極板および負極板とセパレータとを捲回して構成される電極群を有底缶に挿入し、開口部を封口板にて封口してなる蓄電素子について、正極板および負極板の長尺方向に極板材料が付着されていない集電体露出部を連続的に設け、この集電体露出部と集電端子板とを集合溶接し、有底缶の底部側の集電端子板を集電用リードにより端子を有する封口板と電気的に接続し、この封口板と接続された集電用リードを電極群の外縁に沿って配置したことを特徴とする。
有底缶に挿入する前に、集電体露出部と集電端子板とを集合溶接しうる構造を採ることにより、高出力を維持しつつ生産歩留の高い蓄電素子を提供することができる。
In order to solve the above-mentioned problem, the present invention provides a first aspect in which an electrode group constituted by winding a belt-like positive electrode plate and a negative electrode plate and a separator is inserted into a bottomed can, and the opening is used as a sealing plate. For the electricity storage device that is sealed, a current collector exposed portion to which no electrode plate material is attached is continuously provided in the longitudinal direction of either the positive electrode plate or the negative electrode plate. The current collector terminal plate and the current collecting terminal plate are welded together, and this current collecting terminal plate is arranged on the bottom side of the bottomed can, and the current collecting terminal plate and the sealing plate having the terminals are electrically connected by a current collecting lead. It is characterized by doing.
According to a fourth aspect of the present invention, there is provided an electricity storage device in which an electrode group formed by winding a belt-like positive electrode plate and negative electrode plate and a separator is inserted into a bottomed can and the opening is sealed with a sealing plate. A collector exposed portion to which no electrode plate material is attached is continuously provided in the longitudinal direction of the positive electrode plate and the negative electrode plate, and the collector exposed portion and the current collector terminal plate are collectively welded to form a bottomed can The current collecting terminal plate on the bottom side of the electrode is electrically connected to a sealing plate having a terminal by a current collecting lead, and the current collecting lead connected to the sealing plate is arranged along the outer edge of the electrode group. And
By adopting a structure in which the current collector exposed portion and the current collector terminal plate can be collectively welded before being inserted into the bottomed can, it is possible to provide a power storage element with a high production yield while maintaining a high output. .
本発明によれば、高出力用途に適した蓄電素子を、高い生産歩留で提供することができる。 ADVANTAGE OF THE INVENTION According to this invention, the electrical storage element suitable for a high output use can be provided with a high production yield.
ここでは蓄電素子の一例として、リチウムイオン電池についての詳細な形態および構成手順を、図1および図2を用いて示す。 Here, as an example of the storage element, a detailed form and a configuration procedure of a lithium ion battery will be described with reference to FIGS.
正極活物質には一般式LiMO2あるいはLiM2O4で表されるリチウム複合酸化物を用いることができる。上記一般式におけるMにはコバルト、ニッケル、マンガンなどの遷移金属元素を、1種あるいは数種を複合して選択できる。また遷移金属元素の一部をアルミニウム、マグネシウムなどの典型金属元素に置換することもできる。 As the positive electrode active material, a lithium composite oxide represented by a general formula LiMO 2 or LiM 2 O 4 can be used. M in the above general formula can be selected from one or more transition metal elements such as cobalt, nickel, and manganese. Further, a part of the transition metal element can be replaced with a typical metal element such as aluminum or magnesium.
これら正極活物質を、導電剤(正極電位下で安定な黒鉛・カーボンブラック・金属粉末などが用いられる)および結着剤(正極電位下で安定なポリフッ化ビニリデン(PVDF)・ポリテトラフルオロエチレン(PTFE)などが用いられる)と混練し、集電体(アルミニウムの箔・穿孔体などが用いられる)に塗着することにより帯状の正極板1が作製される。 These positive electrode active materials are mixed with a conductive agent (graphite, carbon black, metal powder, etc. stable under the positive electrode potential) and a binder (polyvinylidene fluoride (PVDF), polytetrafluoroethylene (stable under the positive electrode potential) ( PTFE) or the like is used, and is applied to a current collector (aluminum foil or perforated body is used) to produce a strip-like positive electrode plate 1.
負極活物質としては、天然黒鉛、人造黒鉛、アルミニウムやそれを主体とする種々の合金、酸化スズなどの金属酸化物、金属窒化物を用いることができる。これら負極活物質を、導電剤(負極電位下で安定な黒鉛・カーボンブラック・金属粉末などが用いられる)および結着剤(負極電位下で安定なスチレン−ブタジエン共重合体ゴム(SBR)・カルボキシメチルセルロース(CMC)などが用いられる)と混練し、集電体(銅箔・銅穿孔体などが用いられる)に塗着することにより帯状の負極板2が作製される。
As the negative electrode active material, natural graphite, artificial graphite, aluminum, various alloys mainly composed thereof, metal oxides such as tin oxide, and metal nitrides can be used. These negative electrode active materials are made of a conductive agent (graphite, carbon black, metal powder, etc. stable under negative electrode potential) and a binder (styrene-butadiene copolymer rubber (SBR) / carboxy stable under negative electrode potential). A belt-like
ここで帯状の正負極板1あるいは2の少なくとも一方は、本願の集電構造を成立させるため、長尺方向に極板材料が付着されていない集電体露出部1bあるいは2bが連続的に設けられている必要がある。この集電体露出部1bあるいは2bは、集電端子板4と集合溶接される。集合溶接の方法としては、接触抵抗低減の観点からレーザー溶接や抵抗溶接を用いることが好ましい。
Here, at least one of the strip-like positive and
ここで図1のように一方の電極板(ここでは負極板2)のみに集電体露出部2bを設ける場合、集電端子板4は有底缶の底側に配置され、この集電端子板4と一体化された負極集電用リード2aが、電極群の外縁または電極群の捲回中心部に存在する空間に沿って開口部に向かうよう配置される。正極板1からは、集電用リード1aのみが開口部に向かうよう配置される。これら集電用リード1aおよび2aは各々封口板に設けられた端子と溶接された後、有底缶に挿入され、封口されることにより本願の蓄電素子となる。
仮に集電端子板4を正極板1の集電体露出部1bと集合溶接し、有底缶の開口部側に配置した場合、図5のように負極板2の集電用リード2aを、封口板の端子と溶接させるために長くする必要がある。負極板2は集電端子板4を用いていないため正極板1よりも集電効率が低い上に、集電用リード2aが延長されることにより、さらに集電効率が低下するので好ましくない。
Here, when the current collector exposed
If the current
また図2のように両方の電極板に集電体露出部1bおよび2bを設ける場合、有底缶の底側に配置された方の集電端子板4と一体化された負極集電用リード2aは、電極群の外縁に沿って開口部に向かうよう配置され、集電端子板4と一体化された正極集電用リード1aともども、封口板に設けられた端子と溶接された後、有底缶に挿入され、封口されることにより本願の蓄電素子となる。
Further, when the collector exposed
上述した極板群に含浸させる非水電解液は、溶質と非水溶媒とからなる。溶質として、六フッ化リン酸リチウム(LiPF6)、四フッ化ホウ酸リチウム(LiBF4)などのリチウム塩が挙げられる。非水溶媒としては、エチレンカーボネート、プロピレンカーボネートなどの環状カーボネート類や、ジメチルカーボネート、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などの鎖状カーボネート類などが好ましいが、これらに限定されない。非水溶媒は、1種を単独で用いてもよいが、2種以上を組み合わせてもよい。また、添加剤としては、ビニレンカーボネート、シクロヘキシルベンゼン、ジフェニルエーテルなどが挙げられる。 The nonaqueous electrolytic solution impregnated in the electrode plate group described above is composed of a solute and a nonaqueous solvent. Examples of the solute include lithium salts such as lithium hexafluorophosphate (LiPF 6 ) and lithium tetrafluoroborate (LiBF 4 ). As the non-aqueous solvent, cyclic carbonates such as ethylene carbonate and propylene carbonate, and chain carbonates such as dimethyl carbonate, diethyl carbonate, and ethyl methyl carbonate are preferable, but not limited thereto. The non-aqueous solvent may be used alone or in combination of two or more. Examples of the additive include vinylene carbonate, cyclohexyl benzene, and diphenyl ether.
なお上述したのはリチウムイオン電池の形態および構成手順であったが、ニッケル水素蓄電池やニッケルカドミウム蓄電池などの二次電池や、電気二重層キャパシタなどを構成する場合も、一般的に用いられる材料を駆使することにより、上述内容と同様に本発明の効果を活用することができる。さらに図1〜2では負極板の方を有底缶の底部になるよう配置したが、正極板と負極板の配置を逆転させても、同様の効果が得られる。 In addition, although what was mentioned above was a form and structure procedure of a lithium ion battery, also when constructing secondary batteries, such as a nickel metal hydride storage battery and a nickel cadmium storage battery, or an electric double layer capacitor, the material generally used is used. By making full use, the effects of the present invention can be utilized in the same manner as described above. Further, in FIGS. 1 and 2, the negative electrode plate is arranged to be the bottom of the bottomed can, but the same effect can be obtained even if the arrangement of the positive electrode plate and the negative electrode plate is reversed.
以下に、本発明の実施例を具体的に示す。
《実施例1》
(正極板の作製)
コバルト酸リチウム粉末85重量部、導電剤として炭素粉末10重量部、結着剤としてPVDF5重量部を、溶媒としてN−メチル−2−ピロリドン(以下NMPと記す)を用いて混合した。この混合物を厚み15μmのアルミニウム箔集電体に塗布、乾燥した後、厚みが100μmとなるよう圧延し、長尺方向の一端に集電用リード1aを溶接して帯状の正極板1を作製した。
(負極板の作製)
人造黒鉛粉末95重量部、結着剤としてPVDF5重量部を、NMPを用いて混合した。この混合物を厚み10μmの銅箔集電体に塗布、乾燥した後、厚みが110μmとなるよう圧延し、長尺方向の一方に極板材料が付着されていない集電体露出部2bを連続的に設けて帯状の負極板2を作製した。
(電池の作製)
セパレータ3として厚み25μmのポリプロピレン樹脂製微多孔フィルムを用い、図1に示す電極群を構成した。集電用リード1aおよび2aを封口板の端子にそれぞれ溶接した後、この電極群を有底缶に挿入した。この有底缶に、非水電解液としてエチレンカーボネートとエチルメチルカーボネートを体積比1:1で混合した非水溶媒に、六フッ化リン酸リチウム(LiPF6)が1mol/Lになるように溶解させたものを注入し、封口板を有底缶の開口部に嵌め込むことにより、直径26mm、高さ95mm、理論容量3000mAhの円筒形リチウムイオン電池を作製した。これを実施例1の電池とする。
《実施例2》
正極板1の長尺方向の一方に極板材料が付着されていない集電体露出部1bを連続的に設けて、図2に示す構造とした以外は、実施例1と同様の電池を作製した。これを実施例2の電池とする。
《比較例1》
負極板2の長尺方向の一端に集電用リード2aを溶接して、図3に示す構造とした以外は、実施例1と同様の電池を作製した。これを比較例1の電池とする。
《比較例2》
正極板1の長尺方向の一方に極板材料が付着されていない集電体露出部1bを連続的に設けて、図4に示す構造とした以外は、実施例1と同様の電池を作製した。これを比較例2の電池とする。
《比較例3》
正極板1の長尺方向の一方に極板材料が付着されていない集電体露出部1bを連続的に設け、かつ負極板2の長尺方向の一端に集電用リード2aを溶接して、図5に示す構造とした以外は、実施例1と同様の電池を作製した。これを比較例3の電池とする。
Examples of the present invention are specifically shown below.
Example 1
(Preparation of positive electrode plate)
85 parts by weight of lithium cobaltate powder, 10 parts by weight of carbon powder as a conductive agent, 5 parts by weight of PVDF as a binder, and N-methyl-2-pyrrolidone (hereinafter referred to as NMP) as a solvent were mixed. This mixture was applied to an aluminum foil current collector having a thickness of 15 μm, dried, then rolled to a thickness of 100 μm, and a current collecting lead 1a was welded to one end in the longitudinal direction to produce a belt-like positive electrode plate 1. .
(Preparation of negative electrode plate)
95 parts by weight of artificial graphite powder and 5 parts by weight of PVDF as a binder were mixed using NMP. This mixture is applied to a copper foil current collector having a thickness of 10 μm, dried, and then rolled to have a thickness of 110 μm, so that the current collector exposed
(Production of battery)
As the
Example 2
A battery similar to that of Example 1 was prepared except that a current collector exposed portion 1b to which no electrode plate material was attached was continuously provided on one side in the longitudinal direction of the positive electrode plate 1 to obtain the structure shown in FIG. did. This is referred to as the battery of Example 2.
<< Comparative Example 1 >>
A battery was prepared in the same manner as in Example 1 except that the current collecting lead 2a was welded to one end in the longitudinal direction of the
<< Comparative Example 2 >>
A battery similar to that of Example 1 was produced except that a current collector exposed portion 1b to which no electrode plate material was attached was continuously provided on one side in the longitudinal direction of the positive electrode plate 1 to obtain the structure shown in FIG. did. This is referred to as the battery of Comparative Example 2.
<< Comparative Example 3 >>
A current collector exposed portion 1b to which no electrode plate material is attached is continuously provided on one side in the longitudinal direction of the positive electrode plate 1, and a
以上の電池に対し、以下に示す評価を行った。結果を(表1)に示す。
(溶接検査)
溶接用の銅製電極の先端に、酸化銅の粉末を被覆することにより、溶接工程における不具合が故意に起こるようにした。この状態で正負極の集電用リード1aおよび2aを各々の端子に溶接した。溶接時のスパークによるセパレータの溶融を目視で確認できた場合、銅製電極の先端を研磨し、溶接を再開した。このようにして、各実施例・比較例当り100個の電池を連続して作製し、目視確認できた不具合電池を排除した。
(短絡検査)
上述した溶接不良検査を通過した電池について、300mAで電圧が4.1Vに達するまで充電し、初期の開回路電圧V1を測定した。さらにこの電池を45℃環境下で7日間放置し、放置後の開回路電圧V2を測定した。この開回路電圧差(V1−V2)が0.3Vを上回った電池を、短絡不良電池として排除した。
(放電特性)
上述した短絡検査を通過した電池から5個を抜き取り、一旦300mAで電圧が3Vに達するまで放電した。続いて300mAで電圧が4.2Vに達するまで充電した後、300mAで電圧が3Vに達するまで放電し、低電流放電容量A1を得た。さらに300mAで電圧が4.2Vに達するまで充電した後、3000mAで電圧が3Vに達するまで放電し、高電流放電容量A2を得た。こうして得られた低電流放電容量と高電流放電容量の比率(A2/A1)の平均値を求めた。
The following evaluation was performed with respect to the above battery. The results are shown in (Table 1).
(Welding inspection)
By coating the tip of the copper electrode for welding with copper oxide powder, defects in the welding process occurred intentionally. In this state, positive and negative current collecting leads 1a and 2a were welded to the respective terminals. When melting of the separator due to spark during welding could be visually confirmed, the tip of the copper electrode was polished and welding was resumed. In this way, 100 batteries were continuously produced for each example and comparative example, and defective batteries that could be visually confirmed were excluded.
(Short-circuit inspection)
The battery that passed the above-described welding failure inspection was charged at 300 mA until the voltage reached 4.1 V, and the initial open circuit voltage V 1 was measured. Further, this battery was allowed to stand for 7 days in a 45 ° C. environment, and the open circuit voltage V 2 after the standing was measured. A battery in which the open circuit voltage difference (V 1 −V 2 ) exceeded 0.3 V was excluded as a short circuit defective battery.
(Discharge characteristics)
Five batteries were extracted from the battery that passed the short-circuit inspection described above, and discharged at 300 mA until the voltage reached 3V. Subsequently, the battery was charged at 300 mA until the voltage reached 4.2 V, and then discharged at 300 mA until the voltage reached 3 V to obtain a low current discharge capacity A 1 . The battery was further charged at 300 mA until the voltage reached 4.2 V, and then discharged at 3000 mA until the voltage reached 3 V to obtain a high current discharge capacity A 2 . The average value of the ratio (A 2 / A 1 ) between the low current discharge capacity and the high current discharge capacity thus obtained was determined.
一方、本願の発明である実施例1〜2、および比較例3は、有底缶に挿入する前の、目視可能な状態で溶接検査が行えたため、溶接不良(溶接時のスパークによるセパレータの溶融)を排除し、さらに適切なメンテナンス(銅製電極の先端研磨)を行った後に溶接を再開することができた。よってその後の溶接不良を抑止できたため、短絡不良を発生させることなく、高い歩留を確保できた。 On the other hand, in Examples 1 and 2 and Comparative Example 3 which are the inventions of the present application, since welding inspection was performed in a visible state before being inserted into the bottomed can, welding failure (melting of the separator due to spark during welding) was performed. ), And after proper maintenance (polishing of the copper electrode tip), welding could be resumed. Therefore, since subsequent welding defects could be suppressed, a high yield could be secured without causing short circuit defects.
ただし比較例3については、集電端子板4を用いていない負極板2の集電用リード2aが相当に長いため、集電効率の低下に伴う放電特性の劣化が認められた。よって本願発明の主幹である、溶接後に電極群を有底缶に挿入する構造を採るためには、底部から集電用リードを取り出す側の電極板は、集電端子板の活用とこれに応じた電極板構造の採用(集電体露出部の連続的な設置)が不可欠であることがわかった。
However, in Comparative Example 3, since the current collecting lead 2a of the
以上のように、本願発明の集電構造を活用することにより、高出力な蓄電素子を高い歩留で提供することができる。本発明による蓄電素子は、大電流充放電を要する電気自動車や電動工具などの駆動電源に好適である。 As described above, by using the current collecting structure of the present invention, a high-output power storage element can be provided with a high yield. The power storage device according to the present invention is suitable for a drive power source such as an electric vehicle or a power tool that requires large current charge / discharge.
1 正極板
1a 正極集電用リード
1b 正極集電体露出部
2 負極板
2a 負集電用リード
2b 負極集電体露出部
3 セパレータ
4 集電端子板
DESCRIPTION OF SYMBOLS 1 Positive electrode plate 1a Positive electrode collector lead 1b Positive electrode collector exposed
Claims (4)
(i)前記正極板あるいは前記負極板のいずれか一方の電極板は、長尺方向に極板材料が付着されていない集電体露出部が連続的に設けられており、
(ii)前記集電体露出部は、集電端子板と集合溶接されており、
(iii)前記集電端子板は、前記有底缶の底側に配置されており、
(iv)前記集電端子板は、集電用リードを介して端子を有する前記封口板と電気的に接続されていることを特徴とする蓄電素子。 An electrode group formed by winding a strip-like positive electrode plate with a positive electrode material attached to a positive electrode current collector, a belt-like negative electrode plate with a negative electrode material attached to a negative electrode current collector, and a separator, Is an electricity storage element that is inserted into the opening and sealed with a sealing plate,
(I) Either one of the positive electrode plate or the negative electrode plate is continuously provided with a collector exposed portion to which no electrode plate material is attached in the longitudinal direction;
(Ii) The current collector exposed portion is collectively welded to the current collector terminal plate,
(Iii) The current collector terminal plate is disposed on the bottom side of the bottomed can,
(Iv) The electricity storage element, wherein the current collecting terminal plate is electrically connected to the sealing plate having a terminal through a current collecting lead.
(i)前記正極板および前記負極板は、長尺方向に極板材料が付着されていない集電体露出部が連続的に設けられており、
(ii)前記集電体露出部は、集電端子板と集合溶接されており、
(iii)前記有底缶の底部に配置された側の前記集電端子板は、集電用リードを介して端子を有する前記封口板と電気的に接続されており、
(iv)前記封口板と接続された集電用リードが、前記電極群の外縁に沿って配置されていることを特徴とする蓄電素子。
An electrode group configured by winding a strip-like positive electrode plate with a positive electrode material attached to a positive electrode current collector, a belt-like negative electrode plate with a negative electrode material attached to a negative electrode current collector, and a separator, Is an electricity storage element that is inserted into the opening and sealed with a sealing plate,
(I) The positive electrode plate and the negative electrode plate are continuously provided with a current collector exposed portion to which no electrode plate material is attached in the longitudinal direction,
(Ii) The current collector exposed portion is collectively welded to the current collector terminal plate,
(Iii) The current collector terminal plate disposed on the bottom of the bottomed can is electrically connected to the sealing plate having a terminal through a current collecting lead,
(Iv) A power storage element, wherein a current collecting lead connected to the sealing plate is disposed along an outer edge of the electrode group.
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WO2013018473A1 (en) * | 2011-07-29 | 2013-02-07 | 古河電気工業株式会社 | Metal foil with coating layer and method for producing same, secondary cell electrode and method for producing same, and lithium ion secondary cell |
CN110465761A (en) * | 2019-07-11 | 2019-11-19 | 惠州市多科达科技有限公司 | A kind of column type battery capillary machine |
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JP2002075322A (en) * | 2000-08-31 | 2002-03-15 | Yuasa Corp | Sealed battery |
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WO2013018473A1 (en) * | 2011-07-29 | 2013-02-07 | 古河電気工業株式会社 | Metal foil with coating layer and method for producing same, secondary cell electrode and method for producing same, and lithium ion secondary cell |
CN110465761A (en) * | 2019-07-11 | 2019-11-19 | 惠州市多科达科技有限公司 | A kind of column type battery capillary machine |
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