JPH09283149A - Collector for battery plate and battery using this collector - Google Patents

Collector for battery plate and battery using this collector

Info

Publication number
JPH09283149A
JPH09283149A JP8114107A JP11410796A JPH09283149A JP H09283149 A JPH09283149 A JP H09283149A JP 8114107 A JP8114107 A JP 8114107A JP 11410796 A JP11410796 A JP 11410796A JP H09283149 A JPH09283149 A JP H09283149A
Authority
JP
Japan
Prior art keywords
battery
current collector
thin film
collector
electrode plate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP8114107A
Other languages
Japanese (ja)
Inventor
Hisashi Tsukamoto
寿 塚本
Hiroaki Yoshida
吉田  浩明
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Japan Storage Battery Co Ltd
Original Assignee
Japan Storage Battery Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Japan Storage Battery Co Ltd filed Critical Japan Storage Battery Co Ltd
Priority to JP8114107A priority Critical patent/JPH09283149A/en
Publication of JPH09283149A publication Critical patent/JPH09283149A/en
Pending legal-status Critical Current

Links

Classifications

    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Abstract

PROBLEM TO BE SOLVED: To provide a collector, which is effective for the weight reduction and non-combustible characteristic of a battery, by forming a collector for holding the active material or the host material in a battery of a specified layered body. SOLUTION: An organic electrolyte battery such as an organic liquid- electrolyte battery and a high molecular electrolyte battery is desirable. In this battery 1, a collector for holding the active material or the host material of electrodes 3, 4 is formed of a layered body of a resin film made of the thermoplastic resin such as polyethylene terephthalate and PP, of which thermal deforming temperature is lower than the igniting point of the organic electrolyte, and an electron conductive thin film made of the metal, to which non-electrolyte plating or deposition, is performed. A thin film of the collector of the positive electrode is desirably made of Al, and a thin film of the collector of the negative electrode is desirably made of Cu or Ni.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、リチウム二次電池
用極板等の電池用極板の集電体及びその集電体を用いた
電池に属する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a current collector of a battery electrode plate such as a lithium secondary battery electrode plate and a battery using the current collector.

【0002】[0002]

【従来の技術】近年、携帯用無線電話、携帯用パソコ
ン、携帯用ビデオカメラ等の電子機器が開発され、各種
電子機器が携帯可能な程度に小型化されている。それに
伴って、内蔵される電池としても、高エネルギー密度を
有し、且つ軽量なものが採用されている。そのような要
求を満たす典型的な電池は、特にリチウム金属やリチウ
ム合金等の活物質、リチウムイオンをホスト物質(ここ
でホスト物質とは、リチウムイオンを吸蔵及び放出でき
る物質をいう。)である炭素に吸蔵させたインターカレ
ーション等のリチウム系を負極材料とし、LiCI
4、LiPF6等のリチウム塩を溶解した非プロトン性
の有機溶媒を電解液とするリチウム二次電池である。
2. Description of the Related Art In recent years, electronic devices such as a portable radio telephone, a portable personal computer, and a portable video camera have been developed, and various electronic devices have been reduced in size to be portable. Along with this, as a built-in battery, a battery having a high energy density and being lightweight is adopted. A typical battery satisfying such requirements is an active material such as lithium metal or a lithium alloy, and a lithium ion host material (here, the host material means a material capable of inserting and extracting lithium ion). LiCI such as intercalation occluded in carbon is used as a negative electrode material, and LiCI
The lithium secondary battery uses an aprotic organic solvent in which a lithium salt such as O 4 or LiPF 6 is dissolved as an electrolytic solution.

【0003】リチウム二次電池は、上記の負極材料をそ
の支持体である負極集電体に保持してなる負極板、リチ
ウムコバルト複合酸化物のようにリチウムイオンと可逆
的に電気化学反応をする正極活物質をその支持体である
正極集電体に保持してなる正極板、電解液を保持すると
ともに負極板と正極板との間に介在して両極の短絡を防
止するセパレータからなっている。
A lithium secondary battery has a negative electrode plate in which the above-mentioned negative electrode material is held by a negative electrode current collector as a support, and reversibly electrochemically reacts with lithium ions like a lithium cobalt composite oxide. It consists of a positive electrode plate holding the positive electrode active material on a positive electrode current collector as its support, and a separator that holds an electrolytic solution and intervenes between the negative electrode plate and the positive electrode plate to prevent a short circuit between both electrodes. .

【0004】そして、短冊形状又は円筒形状の電池の場
合、上記正極板、セパレータ及び負極板は、いずれも薄
いシートないし箔状に成形されたものを順に積層し、螺
旋状に巻いて電池容器に収納される。従って、極板は、
一般に活物質又はホスト物質に有機結着剤、導電剤及び
溶剤を混合してペースト状にし、それを支持体表面に塗
布し乾燥後、支持体とともに厚さ方向に加圧成形するこ
とによって製造される。従来、極板の集電体としては、
それ自体の導電性が必要であることから、銅、アルミニ
ウムなどの金属の箔が用いられていた。
In the case of a rectangular or cylindrical battery, the positive electrode plate, the separator and the negative electrode plate are each formed by laminating thin sheets or foils in order, and spirally wound into a battery container. Is stored. Therefore, the plates are
Generally, an active material or a host material is mixed with an organic binder, a conductive agent and a solvent to form a paste, which is applied to the surface of the support, dried, and then pressure-formed together with the support in the thickness direction. You. Conventionally, as the collector of the electrode plate,
Metallic foils such as copper and aluminum have been used because of their need for electrical conductivity.

【0005】[0005]

【発明が解決しようとする課題】リチウム電池に限らず
電池を電源とする機器の場合、機器全体の軽量化及び不
燃化の要請は尽きることがない。従って、電池性能が同
じで有れば軽いほど且つ安全であるほどユーザーに好ま
れる。
In the case of a device that uses a battery as a power source, not limited to a lithium battery, the demands for weight reduction and nonflammability of the entire device are endless. Therefore, the lighter and safer the battery performance is, the more the user likes it.

【0006】しかし、金属箔を薄くするにも生産上及び
取り扱い上の限界がある。また、機器破損等の対策とし
て、PTC素子、保護回路、電流遮断機構等が施されて
いるが、火元となる電極自体を不燃化する対策は提案さ
れていない。
However, there is a limit in production and handling even if the metal foil is thin. Further, although PTC elements, protection circuits, current interrupting mechanisms, etc. are provided as measures against equipment damage, no measures have been proposed to make the electrodes themselves that are the sources of fire non-combustible.

【0007】それ故、本発明の目的は、従来の集電体に
対するコンセプトから脱却し、従来の集電体と全く異な
る構成により、電池の軽量化及び不燃化に有効な集電体
並びにそのような集電体を用いた電池を提供することに
ある。
Therefore, an object of the present invention is to move away from the concept of a conventional current collector and to have a structure which is completely different from that of the conventional current collector, and which is effective in reducing the weight and incombustibility of the battery and the current collector. Another object is to provide a battery using a different current collector.

【0008】[0008]

【課題を解決するための手段】その目的を達成するため
に、本発明の電池用極板の集電体は、樹脂膜と、電子伝
導性の薄膜との層状体であることを特徴とする。
In order to achieve the object, the current collector of the battery electrode plate of the present invention is characterized by being a layered body of a resin film and an electron conductive thin film. .

【0009】本発明の集電体は、樹脂膜を芯としている
ので、同じ厚さの金属箔からなる集電体よりも軽い。し
かも、樹脂の多くは、その熱変形温度が有機電解質の発
火点よりも低いので、短絡により発熱しても有機電解液
や高分子電解質等の有機電解質が発火する前に樹脂膜が
熱収縮するか溶けて、電流が遮断される。この点、金属
箔の場合、その融点が有機電解質の発火点よりも高いか
ら、短絡により発熱すると、電極温度が金属箔の融点に
達する前に有機電解質が発火して危険な状態となるのと
異なり、本発明集電体は電流遮断機能を兼ね備える。そ
して、樹脂の多くは絶縁性であるが、本発明の集電体
は、樹脂膜の表面に電子伝導性の薄膜が密着しているの
で、その薄膜を電流が流れる。
Since the current collector of the present invention has the resin film as the core, it is lighter than the current collector made of the metal foil having the same thickness. Moreover, since the thermal deformation temperature of many resins is lower than the ignition point of the organic electrolyte, even if heat is generated due to a short circuit, the resin film undergoes thermal contraction before the organic electrolyte such as the organic electrolyte solution or the polymer electrolyte ignites. It melts and the current is cut off. In this regard, in the case of metal foil, since the melting point is higher than the ignition point of the organic electrolyte, if heat is generated due to short-circuit, the organic electrolyte will ignite before the electrode temperature reaches the melting point of the metal foil, resulting in a dangerous state. Differently, the current collector of the present invention has a current interruption function. Although most of the resin is insulative, the current collector of the present invention has an electron-conductive thin film in close contact with the surface of the resin film, so that a current flows through the thin film.

【0010】このように、本発明の集電体は、軽くて電
流遮断機能を有するので、これを用いた本発明の電池も
軽くて安全である。もちろん、有機電解質電池に限ら
ず、一次電池及び二次電池の区別無く、アルカリ電池、
Ni−Cd電池、Ni−HM電池、鉛電池など電池全般
において軽量化及び安全化が期待できることは言うまで
もない。更に、金属箔からなる従来の集電体を所定の大
きさに切断加工する際は、切断面に短絡の原因となるバ
リを生じることがあったが、本発明の集電体は、樹脂膜
を芯としているので、切断性に優れ、バリを生じない。
As described above, since the current collector of the present invention is light and has the function of blocking current, the battery of the present invention using the current collector is also light and safe. Of course, it is not limited to organic electrolyte batteries, and there is no distinction between primary batteries and secondary batteries, alkaline batteries,
It goes without saying that weight reduction and safety can be expected in all batteries such as Ni-Cd batteries, Ni-HM batteries, and lead batteries. Further, when a conventional current collector made of a metal foil is cut into a predetermined size, burrs may be generated on the cut surface, which may cause a short circuit. The core is excellent in cutting property and does not generate burrs.

【0011】[0011]

【発明の実施の形態】上記の電流遮断機能を確実にする
ために、有機電解質電池の場合、樹脂膜としては、集電
体が用いられる電池の有機電解質の発火点よりも低い熱
変形温度を有するものが好ましい。発火点の測定法とし
ては、定速加熱法及び定温加熱法の2種類が知られてい
るが、現実に即した方を選択すると良い。どちらが現実
に即しているか不明の場合は、低い測定値を選択するほ
うが安全である。樹脂膜の材質例としては、ポリエチレ
ンテレフタレート(PET)、ポリプロピレン(PP)
等の熱可塑性樹脂が挙げられる。
BEST MODE FOR CARRYING OUT THE INVENTION In order to ensure the above-mentioned current interruption function, in the case of an organic electrolyte battery, a resin film is formed with a heat deformation temperature lower than the ignition point of the organic electrolyte of a battery using a current collector. Are preferred. There are two known methods for measuring the ignition point: a constant speed heating method and a constant temperature heating method. If you are uncertain which is realistic, it is safer to choose a lower measurement. Examples of the material of the resin film include polyethylene terephthalate (PET) and polypropylene (PP).
And the like.

【0012】樹脂膜の表面に形成される薄膜としては、
無電解メッキされたNi、Cu又は蒸着されたCu、A
lなどの金属が好ましい。特に、正極の集電体の薄膜は
アルミニウムAlが好ましい。アルミニウムは耐食性に
優れ、正極が高電位となる充電時においても電解液中に
溶け出さないからである。一方、負極の集電体の薄膜と
して特に好ましいのは、銅Cu又はニッケルNiであ
る。銅は、蒸着により膜厚を極めて薄くし、集電体を軽
量にすることができる。また、銅は、3.7〜3.9V
vs. Li/Li+付近で溶けてしまうことが実験的に知
られている。従って、適正な放電電圧は3Vまでであっ
て、それ以下は過放電となる。これに対して、Niは
4.0〜4.2V vs. Li/Li+まで溶けないので、
0Vまで放電できる。
As the thin film formed on the surface of the resin film,
Electroless plated Ni, Cu or evaporated Cu, A
Metals such as 1 are preferred. In particular, the thin film of the positive electrode current collector is preferably aluminum Al. This is because aluminum has excellent corrosion resistance and does not dissolve into the electrolyte even during charging when the positive electrode has a high potential. On the other hand, copper Cu or nickel Ni is particularly preferable as the thin film of the current collector of the negative electrode. Copper can be made extremely thin by vapor deposition to reduce the weight of the current collector. Moreover, copper is 3.7-3.9V.
It is experimentally known that it melts in the vicinity of vs. Li / Li + . Therefore, the proper discharge voltage is up to 3V, and below that is overdischarge. On the other hand, Ni does not melt up to 4.0 to 4.2 V vs. Li / Li + ,
Can discharge to 0V.

【0013】層状体の層構成は、樹脂膜と薄膜との2層
でも又は薄膜、樹脂膜及び薄膜の順の3層でも良い。層
状にする手段としては、蒸着やメッキを含めて種々の公
知の手段が適用可能である。また、樹脂膜と薄膜とは全
面密着していても良いし、一部が密着していても良い。
電極全体の形状も渦巻き状に限定されない。
The layer structure of the layered body may be two layers of a resin film and a thin film, or three layers of a thin film, a resin film and a thin film in this order. As a means for forming a layer, various known means including vapor deposition and plating can be applied. Moreover, the resin film and the thin film may be in close contact with each other over the entire surface, or a part thereof may be in close contact.
The shape of the entire electrode is not limited to a spiral shape.

【0014】[0014]

【実施例】【Example】

−実施例1− 本発明の実施例を図面とともに説明する。図1は、実施
例の有機電解質電池の分解斜視図である。有機電解質電
池1は、正極板3、負極板4及びセパレータ5からなる
電極群2が非水系の電解液(図示省略)とともに電池ケ
ース6に収納された角形リチウム二次電池である。
-Example 1-An example of the present invention will be described with reference to the drawings. FIG. 1 is an exploded perspective view of an organic electrolyte battery of an example. The organic electrolyte battery 1 is a prismatic lithium secondary battery in which an electrode group 2 including a positive electrode plate 3, a negative electrode plate 4, and a separator 5 is housed in a battery case 6 together with a non-aqueous electrolyte (not shown).

【0015】正極板3は、集電体に活物質としてリチウ
ムコバルト複合酸化物部が保持されたものである。集電
体は、厚さ20μmのPET膜の表面に真空蒸着により
厚さ2μmのアルミニウム薄膜を密着させることによっ
て得られたものである。正極板3は、結着剤であるポリ
フッ化ビニリデン8部と導電剤であるアセチレンブラッ
ク5部とを活物質87部とともに混合してペースト状に
調製した後、その集電体材料の両面に塗布、乾燥するこ
とによって製作された。
The positive electrode plate 3 has a lithium cobalt composite oxide portion as an active material held on a current collector. The current collector was obtained by bringing a 2 μm thick aluminum thin film into close contact with the surface of a 20 μm thick PET film by vacuum deposition. The positive electrode plate 3 is prepared by mixing 8 parts of polyvinylidene fluoride as a binder and 5 parts of acetylene black as a conductive agent together with 87 parts of an active material to prepare a paste, and then applying the paste to both surfaces of the current collector material , Made by drying.

【0016】負極板4の集電体は、厚さ20μmのPE
T膜の表面に真空蒸着により厚さ2μmの銅薄膜を密着
させることによって得られた。負極板4は、その集電体
の両面に、ホスト物質としてのグラファイト(黒鉛)8
6部と結着剤としてのポリフッ化ビニリデン14部とを
混合しペースト状に調製したものを塗布、乾燥すること
によって製作された。
The collector of the negative electrode plate 4 is made of PE having a thickness of 20 μm.
It was obtained by bringing a copper thin film having a thickness of 2 μm into close contact with the surface of the T film by vacuum vapor deposition. The negative electrode plate 4 has graphite 8 as a host material on both sides of its current collector.
6 parts and 14 parts of polyvinylidene fluoride as a binder were mixed to prepare a paste, which was applied and dried.

【0017】セパレータ5は、ポリエチレン微多孔膜で
ある。また、電解液は、LiPF6を1mol/l含む
エチレンカーボネート:ジエチルカーボネート=1:1
(体積比)の混合液である。
The separator 5 is a polyethylene microporous film. Further, the electrolytic solution contains ethylene carbonate: diethyl carbonate = 1: 1 containing 1 mol / l of LiPF6.
(Volume ratio).

【0018】各々の寸法は、正極板3が厚さ180μ
m、幅29mmで、セパレータ5が厚さ25μm、幅3
3mmで、負極板4が厚さ220μm、幅31mmとな
っており、順に重ね合わせてポリエチレンの巻芯を中心
として、その周囲に長円渦状に巻いた後、電池ケース6
に収納されている。電池ケース6は、厚さ0.3mm、
内寸33.1×46.5×7.5mmの鉄製本体の表面
に厚さ5μmのニッケルメッキを施したものであり、側
部上部には電解液注入用の孔12が設けられている。
The respective dimensions are such that the positive electrode plate 3 has a thickness of 180 μm.
m, width 29 mm, separator 5 thickness 25 μm, width 3
3 mm, the negative electrode plate 4 has a thickness of 220 μm and a width of 31 mm. The negative electrode plate 4 is superposed in order and wound around the polyethylene core in an oval spiral shape.
It is stored in. The battery case 6 has a thickness of 0.3 mm,
The surface of an iron main body having an inner size of 33.1 × 46.5 × 7.5 mm is nickel-plated with a thickness of 5 μm, and a hole 12 for injecting an electrolyte is provided at an upper side portion.

【0019】なお、正極板3は、安全弁8と正極端子1
0とを設けたケース蓋7の端子10に正極リード11を
介して接続されている。負極板4は、蓋7の下面に溶接
された負極リード(図示省略)と接続している。そし
て、この電池は、ケース6に蓋7をレーザー溶接して封
口される。
The positive electrode plate 3 includes a safety valve 8 and a positive electrode terminal 1.
0 is connected via a positive electrode lead 11 to a terminal 10 of a case lid 7 provided with a zero. The negative electrode plate 4 is connected to a negative electrode lead (not shown) welded to the lower surface of the lid 7. Then, this battery is sealed by laser welding a lid 7 to the case 6.

【0020】完成した電池の重さは、16gであった。
この電池に1CmAで充電終止電圧4.1Vまで定電流
充電した後、電池1のケース6の側面より直径2.5m
mの鉄釘を貫通させ、暫く様子を観察したが、電解液は
発火しなかった。
The completed battery weighed 16 g.
This battery was charged at a constant current of 1 CmA to a final charge voltage of 4.1 V, and then 2.5 m in diameter from the side of the case 6 of the battery 1.
m was passed through an iron nail and observed for a while, but the electrolyte did not ignite.

【0021】−実施例2− 負極板4の集電体として、真空蒸着により銅薄膜をPE
T膜に密着させる代わりに無電解メッキにより厚さ8μ
mのニッケル薄膜をPET膜に密着させた以外は、実施
例1と同一条件で電池を製造した。
Example 2-As a collector of the negative electrode plate 4, a copper thin film PE was formed by vacuum deposition.
The thickness is 8μ by electroless plating instead of adhering to the T film.
A battery was manufactured under the same conditions as in Example 1, except that the nickel thin film of m was adhered to the PET film.

【0022】完成した電池の重さは、17gであった。
この電池に1CmAで充電終止電圧4.1Vまで定電流
充電した後、1CmAで放電したところ、放電終止電圧
0Vまで異常無く放電した。
The completed battery weighed 17 g.
This battery was charged with a constant current of 1 CmA to a charge end voltage of 4.1 V and then discharged at 1 CmA, and it was discharged to a discharge end voltage of 0 V without any abnormality.

【0023】−比較例− 正極板3の集電体として厚さ20μmのアルミニウム
箔、負極板4の集電体として厚さ20μmの銅箔を用い
た以外は、実施例1と同一条件で比較用電池を製造し
た。この電池の重さは、20gであった。この電池1の
ケース6の側面より直径2.5mmの鉄釘を貫通させた
ところ、30秒後に発煙した。
Comparative Example Comparison was made under the same conditions as in Example 1 except that a 20 μm thick aluminum foil was used as the collector of the positive electrode plate 3 and a 20 μm thick copper foil was used as the collector of the negative electrode plate 4. Batteries were manufactured. The weight of this battery was 20 g. When an iron nail having a diameter of 2.5 mm was passed through the side of the case 6 of the battery 1, smoke was emitted 30 seconds later.

【0024】[0024]

【発明の効果】以上のように、本発明によれば、電池を
軽くしかも安全なものとすることができるので、携帯用
電子機器の部品として有益である。
As described above, according to the present invention, the battery can be made light and safe, which is useful as a component of a portable electronic device.

【図面の簡単な説明】[Brief description of drawings]

【図1】実施例の有機電解質電池を示す分解斜視図であ
る。
FIG. 1 is an exploded perspective view showing an organic electrolyte battery of an example.

【符号の説明】[Explanation of symbols]

1 有機電解質電池 2 電極群 3 正極板 4 負極板 5 セパレータ 6 電池ケース 7 ケース蓋 1 organic electrolyte battery 2 electrode group 3 positive electrode plate 4 negative electrode plate 5 separator 6 battery case 7 case lid

Claims (10)

【特許請求の範囲】[Claims] 【請求項1】電池の中で、電極の活物質又はホスト物質
を保持する集電体において、 樹脂膜と、電子伝導性の薄膜との層状体であることを特
徴とする電池用極板の集電体。
1. A current collector for holding an active material of an electrode or a host material in a battery, which is a layered body of a resin film and an electronically conductive thin film. Current collector.
【請求項2】電池が有機電解液電池、高分子電解質電池
等の有機電解質電池である請求項1に記載の電池用極板
の集電体。
2. The current collector for a battery electrode plate according to claim 1, wherein the battery is an organic electrolyte battery such as an organic electrolyte battery or a polymer electrolyte battery.
【請求項3】樹脂膜が、前記有機電解質の発火点よりも
低い熱変形温度を有する請求項2に記載の電池用極板の
集電体。
3. The current collector for a battery electrode plate according to claim 2, wherein the resin film has a heat distortion temperature lower than the ignition point of the organic electrolyte.
【請求項4】前記樹脂膜がポリエチレンテレフタレート
(PET)、ポリプロピレン(PP)等の熱可塑性樹脂
からなる請求項2に記載の電池用極板の集電体。
4. The current collector for a battery electrode plate according to claim 2, wherein the resin film is made of a thermoplastic resin such as polyethylene terephthalate (PET) or polypropylene (PP).
【請求項5】前記薄膜が無電解メッキ又は蒸着された金
属からなる請求項1〜4のいずれかに記載の電池用極板
の集電体。
5. The current collector for a battery electrode plate according to claim 1, wherein the thin film is made of electroless plated or vapor-deposited metal.
【請求項6】前記層状体が、樹脂膜と薄膜との2層又は
薄膜、樹脂膜及び薄膜の順の3層である請求項1〜5の
いずれかに記載の電池用極板の集電体。
6. The current collector for a battery electrode plate according to claim 1, wherein the layered body has two layers of a resin film and a thin film or three layers of a thin film, a resin film and a thin film in this order. body.
【請求項7】請求項1〜6のいずれかに記載の集電体を
正負の電極に用いた電池。
7. A battery using the current collector according to claim 1 for positive and negative electrodes.
【請求項8】前記正極の集電体の薄膜がアルミニウムA
lである請求項7に記載の電池。
8. The thin film of the current collector of the positive electrode is aluminum A
The battery according to claim 7, wherein the battery is 1.
【請求項9】前記負極の集電体の薄膜が銅Cuである請
求項7又は8に記載の電池。
9. The battery according to claim 7, wherein the thin film of the current collector of the negative electrode is copper Cu.
【請求項10】前記負極の集電体の薄膜がニッケルNi
である請求項7又は8に記載の電池。
10. The thin film of the current collector of the negative electrode is nickel Ni.
The battery according to claim 7, which is
JP8114107A 1996-04-10 1996-04-10 Collector for battery plate and battery using this collector Pending JPH09283149A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8114107A JPH09283149A (en) 1996-04-10 1996-04-10 Collector for battery plate and battery using this collector

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8114107A JPH09283149A (en) 1996-04-10 1996-04-10 Collector for battery plate and battery using this collector

Publications (1)

Publication Number Publication Date
JPH09283149A true JPH09283149A (en) 1997-10-31

Family

ID=14629306

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8114107A Pending JPH09283149A (en) 1996-04-10 1996-04-10 Collector for battery plate and battery using this collector

Country Status (1)

Country Link
JP (1) JPH09283149A (en)

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000042669A1 (en) * 1999-01-14 2000-07-20 Fujitsu Limited Lithium secondary cell
JP2001085016A (en) * 1999-09-09 2001-03-30 Sony Corp Non-aqueous electrolyte battery
JP2005108835A (en) * 2003-09-26 2005-04-21 Samsung Sdi Co Ltd Rechargeable lithium-ion secondary battery
KR100585584B1 (en) * 1999-04-01 2006-06-07 삼성테크윈 주식회사 method and apparatus for manufacturing electric collector of battery
WO2009157263A1 (en) * 2008-06-23 2009-12-30 シャープ株式会社 Lithium ion secondary battery
JP2010282789A (en) * 2009-06-03 2010-12-16 Sharp Corp Nonaqueous electrolyte secondary battery
WO2012127561A1 (en) * 2011-03-18 2012-09-27 株式会社日立製作所 Non-aqueous electrolyte battery
CN103081205A (en) * 2010-08-27 2013-05-01 株式会社Lg化学 Cable type rechargeable battery
US9548497B2 (en) 2011-06-10 2017-01-17 Eaglepicher Technologies, Llc Layered composite current collector with plurality of openings, methods of manufacture thereof, and articles including the same
US10700339B2 (en) 2017-09-09 2020-06-30 Sateria Battery Innovation Group, Inc. Method of manufacture of an energy storage device having an internal fuse
US10763481B2 (en) 2017-09-09 2020-09-01 Soteria Battery Innovation Group Inc. Lithium storage device with improved safety architecture
US10854868B2 (en) 2017-09-09 2020-12-01 Soteria Battery Innovation Group, Inc. Lithium energy storage device with internal fuse
JP2020198290A (en) * 2019-05-31 2020-12-10 寧徳時代新能源科技股▲分▼有限公司Contemporary Amperex Technology Co., Limited Lithium ion secondary battery, cell and negative electrode sheet
US10957956B2 (en) 2017-09-09 2021-03-23 Soteria Battery Innovation Group, Inc. Energy storage device having a current collector with inherent current limitations
US11139510B2 (en) 2017-09-09 2021-10-05 Soteria Battery Innovation Group, Inc. Battery connections and metallized film components in energy storage devices having internal fuses
US11158860B2 (en) 2017-09-09 2021-10-26 Soteria Battery Innovation Group, Inc. Battery connections and metallized film components in energy storage devices having internal fuses
US11482711B2 (en) 2017-09-09 2022-10-25 Soteria Battery Innovation Group, Inc. Tabless cell utilizing metallized film current collectors
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Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000042669A1 (en) * 1999-01-14 2000-07-20 Fujitsu Limited Lithium secondary cell
JP3696790B2 (en) * 1999-01-14 2005-09-21 富士通株式会社 Lithium secondary battery
KR100585584B1 (en) * 1999-04-01 2006-06-07 삼성테크윈 주식회사 method and apparatus for manufacturing electric collector of battery
JP2001085016A (en) * 1999-09-09 2001-03-30 Sony Corp Non-aqueous electrolyte battery
JP2005108835A (en) * 2003-09-26 2005-04-21 Samsung Sdi Co Ltd Rechargeable lithium-ion secondary battery
US7560192B2 (en) 2003-09-26 2009-07-14 Samsung Sdi Co., Ltd. Rechargeable lithium ion battery
US7736809B2 (en) 2003-09-26 2010-06-15 Samsung Sdi Co., Ltd. Rechargeable lithium ion battery
WO2009157263A1 (en) * 2008-06-23 2009-12-30 シャープ株式会社 Lithium ion secondary battery
JPWO2009157263A1 (en) * 2008-06-23 2011-12-08 シャープ株式会社 Lithium ion secondary battery
JP5371979B2 (en) * 2008-06-23 2013-12-18 シャープ株式会社 Lithium ion secondary battery
JP2010282789A (en) * 2009-06-03 2010-12-16 Sharp Corp Nonaqueous electrolyte secondary battery
JP2013538427A (en) * 2010-08-27 2013-10-10 エルジー・ケム・リミテッド Cable type secondary battery
CN103081205A (en) * 2010-08-27 2013-05-01 株式会社Lg化学 Cable type rechargeable battery
US8748032B2 (en) 2010-08-27 2014-06-10 Lg Chem, Ltd. Cable-type secondary battery
WO2012127561A1 (en) * 2011-03-18 2012-09-27 株式会社日立製作所 Non-aqueous electrolyte battery
US9548497B2 (en) 2011-06-10 2017-01-17 Eaglepicher Technologies, Llc Layered composite current collector with plurality of openings, methods of manufacture thereof, and articles including the same
US10854868B2 (en) 2017-09-09 2020-12-01 Soteria Battery Innovation Group, Inc. Lithium energy storage device with internal fuse
US10763481B2 (en) 2017-09-09 2020-09-01 Soteria Battery Innovation Group Inc. Lithium storage device with improved safety architecture
US10700339B2 (en) 2017-09-09 2020-06-30 Sateria Battery Innovation Group, Inc. Method of manufacture of an energy storage device having an internal fuse
US10957956B2 (en) 2017-09-09 2021-03-23 Soteria Battery Innovation Group, Inc. Energy storage device having a current collector with inherent current limitations
US11139510B2 (en) 2017-09-09 2021-10-05 Soteria Battery Innovation Group, Inc. Battery connections and metallized film components in energy storage devices having internal fuses
US11158860B2 (en) 2017-09-09 2021-10-26 Soteria Battery Innovation Group, Inc. Battery connections and metallized film components in energy storage devices having internal fuses
US11482711B2 (en) 2017-09-09 2022-10-25 Soteria Battery Innovation Group, Inc. Tabless cell utilizing metallized film current collectors
JP2020198290A (en) * 2019-05-31 2020-12-10 寧徳時代新能源科技股▲分▼有限公司Contemporary Amperex Technology Co., Limited Lithium ion secondary battery, cell and negative electrode sheet
US11611081B2 (en) 2019-05-31 2023-03-21 Contemporary Amperex Technology Co., Limited Lithium ion secondary battery, battery core, negative electrode plate, and apparatus
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