JPS62126557A - Thin battery - Google Patents

Thin battery

Info

Publication number
JPS62126557A
JPS62126557A JP26691985A JP26691985A JPS62126557A JP S62126557 A JPS62126557 A JP S62126557A JP 26691985 A JP26691985 A JP 26691985A JP 26691985 A JP26691985 A JP 26691985A JP S62126557 A JPS62126557 A JP S62126557A
Authority
JP
Japan
Prior art keywords
positive electrode
current collector
positive
active material
ink
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
JP26691985A
Other languages
Japanese (ja)
Inventor
Kenji Matsumoto
研二 松本
Masanori Suzuki
正則 鈴木
Yoshihiro Hino
好弘 日野
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.)
Toppan Inc
Original Assignee
Toppan Printing 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 Toppan Printing Co Ltd filed Critical Toppan Printing Co Ltd
Priority to JP26691985A priority Critical patent/JPS62126557A/en
Publication of JPS62126557A publication Critical patent/JPS62126557A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/06Electrodes for primary cells
    • H01M4/08Processes of manufacture
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/66Selection of materials
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/66Selection of materials
    • H01M4/661Metal or alloys, e.g. alloy coatings
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/66Selection of materials
    • H01M4/668Composites of electroconductive material and synthetic resins

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Composite Materials (AREA)
  • Manufacturing & Machinery (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

PURPOSE:To make performance uniform and improve adhesion of positive active material with a current collector by making ink with a positive mix and organic solvent, inking a current collector, and drying to form a positive electrode. CONSTITUTION:A positive mix ink is applied to a positive current collector 2 by screen printing, and dried to form a positive electrode 4. The current collector 2 is required to be stable against positive active material, electrolyte, and organic solvent. therefore, for example, a film obtained by laminating an aluminum foil on a conductive film prepared by dispersing carbon filler in polyolefin resin is used as the current collector. Thereby, adhesion of positive active material with current collector is increased and performance of the battery is made uniform.

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明は薄型電池で、特に丁ぐれた性能?有するIE礪
会合剤関するものである。
[Detailed Description of the Invention] <Industrial Application Field> The present invention is a thin battery with particularly excellent performance. The present invention relates to an IE clumping agent having the following properties.

〈従来技術〉 近年1時計、成卓、カメラ、玩具等のエレクトロニクス
化に伴って電池の小型化、薄型化が進められており、ボ
タン型電池や平板状電池が市販されるにいたっている。
<Prior Art> In recent years, as watches, desks, cameras, toys, etc. have become more electronic, batteries have become smaller and thinner, and button-shaped batteries and flat batteries have come on the market.

中でもアルミSと導電性プラスチックフィルムよりなる
=A4体?用いた薄型電池は金A4a’JAボタン北池
とくらべて可撓性があり、さらに大面積化や任意の形状
のもの2作つや丁い等の44々の利点?有している。
Among them, an A4 body made of aluminum S and conductive plastic film? The thin battery used is more flexible than the gold A4a' JA Button Kitaike, and has 44 other advantages such as a larger area and the ability to make two types of arbitrary shapes. have.

電池の薄型化は単に小型化へのニーズからだけでなく、
デノスプレー、印刷物、写真フィルム等の薄型製品との
一体化した利用法の点からも大いに期待される。
The thinning of batteries is not only due to the need for smaller size;
It is also highly anticipated from the point of view of its integrated use with thin products such as denosprays, printed matter, and photographic films.

従来tli型庖池では、漏電体と正極合剤層との間に圧
力がかからないので東成体と正極合剤層との密yft 
x保つためエーテル化デンプン、ヒドロキシエチルセル
ロース、ホリビニルアルコール等の水溶性高分子、酢酸
ビニルエマルジョン、アクリル酸エステルエマルジョン
等のエマルジョンm II!。
In the conventional TLI type tube, no pressure is applied between the leakage body and the positive electrode mixture layer, so the tightness between the Tosei body and the positive electrode mixture layer is reduced.
x To maintain the quality of water, emulsions such as etherified starch, hydroxyethyl cellulose, water-soluble polymers such as hollyvinyl alcohol, vinyl acetate emulsions, and acrylic acid ester emulsions m II! .

あるいはポリテトラフルオロエチレンデイスハージョン
等のディスパージョンバインダーが用いられてきた。
Alternatively, dispersion binders such as polytetrafluoroethylene dispersion have been used.

く本発明が解決しようとする間頓点〉 化した場合、該インキの溶媒として水?用いるため正極
合剤の分散性が悪く電池性能の不均一性が生じた。また
エマルジョン樹脂あるいは、ディスパージョンバインダ
ーに用いると、正極合剤と混、凍しインキ化する場合に
エマルジョ/やディスパージョンが破壊され凝集しやす
くなり集成体上に均一な膜厚で載置できな(なってしま
っていた。
The problem that the present invention is trying to solve Because of this, the dispersibility of the positive electrode mixture was poor, resulting in non-uniformity in battery performance. In addition, if it is used in an emulsion resin or dispersion binder, when it is mixed with a positive electrode mixture and frozen to form an ink, the emulsion/dispersion is likely to be destroyed and aggregated, making it impossible to place it on the assembly with a uniform film thickness. (It had become.

さらに正極合剤?インキ化する溶媒として水γ用いてい
るため前記の様な水溶性、高分子やエマルジョンあるい
はディスパージョン以外のバインダー?用いることがで
きず正極活物質?還元せずかつdot体と接着性のよい
バインダー?使用することができない欠点?有していた
More positive electrode mixture? Since water γ is used as a solvent for ink formation, is there a binder other than water-soluble, polymer, emulsion, or dispersion as mentioned above? Cathode active material that cannot be used? A binder that does not reduce and has good adhesion to dot bodies? The downside of not being able to use it? had.

特に化学的に安定なポリオレフィン樹lI&¥主成分と
して炭素フィラー暑分散させて作成した体積固有抵抗1
05Ω・α以下の導電性フィルムとアルミ4のラミネー
トフィルム¥:集成体に用いた場合は、電池封口時成気
的に絶@?保ちヒートシールすることにより完全に密閉
され耐漏液性の優れた電池が作成可能である。しかし、
従来提案されている水溶性高分子やエマルジョン、サス
ペンションバインダーも水?用いインキ化し該it体上
に載置した場合、該インキが該集成体上ではじかれ均一
に塗布できなく、かつ集成体とバインダーの接着性が極
めて悪い性′tr有している。
Particularly chemically stable polyolefin resin lI & Volume resistivity 1 created by hot dispersing carbon filler as the main component
A laminate film of conductive film of 05Ω・α or less and aluminum 4: When used in an assembly, it will be completely vaporized when sealing the battery. By holding and heat sealing, it is possible to create a battery that is completely sealed and has excellent leakage resistance. but,
Are conventionally proposed water-soluble polymers, emulsions, and suspension binders also water-based? When the ink is made into an ink and placed on the IT body, the ink is repelled by the assemblage and cannot be applied uniformly, and the adhesiveness between the assemblage and the binder is extremely poor.

く間領点r解決するための手段〉 本発明は以上の現状に対しなされたものであり。Means to solve the problem The present invention has been made in response to the above-mentioned current situation.

E4活物質および有機バインダーχ含むIE極合剤?有
機廐剤r用いインキ化し4成本上に載置後乾燥して正極
電$i、γ作成することにより、正極合剤が極めて良好
に分散されかつ均一に塗布され、集成体と接着性が良好
で電池性能が均一で経時劣化の少ない薄型電池?提供す
るものである。
IE polar mixture containing E4 active material and organic binder χ? By making an ink using an organic lubricant, placing it on a four-component book, and drying it to create a positive electrode, the positive electrode mixture is extremely well dispersed and uniformly applied, and has good adhesion to the assembly. A thin battery with uniform battery performance and little deterioration over time? This is what we provide.

〈実施例〉 以下本発明?図面¥銹照しながら一実施例により詳細に
説明する。
<Example> What follows is the present invention? An embodiment will be described in detail with reference to the drawings.

下記に本実施例で用いた正極合剤?有機溶剤によりイン
キ化した正極合剤9ンキの配合例?示す。
The positive electrode mixture used in this example is shown below. A formulation example of 9 positive electrode mixtures made into ink using organic solvents? show.

該正極合剤インキタスクリーン印刷により第1図に示す
E@a心体(2)に200μの厚みに塗布し、乾燥する
ことにより正極電極14)2作成する。ここで正翫東成
体(2)は、正極活物質、亀解夜有機溶剤に安定である
必要があるため本実施例ではポリオレフィン樹脂に炭素
フィラーr分散させ作成した導電性フィルムにアルミ店
?ラミネートしたフィルム?用いた。
The positive electrode mixture is applied to the E@a core body (2) shown in FIG. 1 to a thickness of 200 μm by ink screen printing, and is dried to form a positive electrode 14) 2. Here, the positive electrode active material (2) needs to be stable to organic solvents, so in this example, a conductive film made by dispersing carbon filler in a polyolefin resin was used. Laminated film? Using.

該導電性フィルムは眠気化学的に安定であるばかりでな
く電池封口時ヒートシールにより電池?完全に密閉でき
る長所?有している。
The conductive film is not only chemically stable, but also heat-sealed when sealing the battery. What is the advantage of being completely sealed? have.

上記正極合剤インキ配合例中の粉末状正極活物質として
本実施例では、 100mesh 、’!通過した電解
二酸化マンガン?用い、該導電剤としてアセチレンブラ
ック馨用いた。該有機バインダーは、集電体の材質や正
極活物質の植頌、用いる有機溶剤の種類により選定され
る必要がある。該有機バインダーは、圧填活物質問の結
着性がありかつ集成体との接着性が良好で市極活物質?
還元しないもの¥:選ぶ必要があり1本実施例でt・ま
エチルセルロースと低塩素化ポリオレフィン?ブレンド
したもの?用いた。
In this example, the powdered positive electrode active material in the above positive electrode mixture ink formulation example was 100mesh,'! Passed electrolytic manganese dioxide? Acetylene black was used as the conductive agent. The organic binder needs to be selected depending on the material of the current collector, the type of positive electrode active material, and the type of organic solvent used. The organic binder has the binding properties of the compressed active material and has good adhesion to the aggregate, and is the active material of the city.
Non-reducing ¥: It is necessary to choose one example: t・ma ethyl cellulose or low chlorinated polyolefin? Blended? Using.

次に有機溶剤は、前記正4后物質に対し安定で。Next, the organic solvent is stable to the above-mentioned positive substance.

前記LE極合剤?均一に分散できるものでかつ前記有機
バインダー?溶解することのできるものであれば良い。
Said LE polar mixture? Is it something that can be uniformly dispersed and the organic binder? Any material that can be dissolved may be used.

本実施例では、スクリーン印刷により該E4合剤インキ
?東成体に塗布したため、スクリーン印刷にも適するd
剤としてジエチレングリコール、ジエチルエーテル?用
いた。
In this example, the E4 mixture ink was printed by screen printing. Since it is applied to the Tosei body, it is also suitable for screen printing.
Diethylene glycol or diethyl ether as an agent? Using.

さらに第2図に示すように、上述の如くして構成した正
1永α4(41Y用いて瀦梨亀池Nγ作成した。
Furthermore, as shown in FIG. 2, a tanari-kameike Nγ was prepared using the regular one-year α4 (41Y) constructed as described above.

丁なわち該傅型電池は、該正極電極(4)に過塩素酸炬
鉛水g[からなる心解rL?含浸させたポリエステル不
織布よりなるセパレーター(5)¥介し、唾鉛粉末とバ
インダーよりなる負1i合剤I6)が負極at体17)
K塗布されてなる負極電極と対向し心池周縁部?ポリエ
チレン/ポリエチレンテレフタレート/ポリエチレンか
らなる三層構造の絶縁フィルムで密閉することにより作
成されたものである。
In other words, in this double-type battery, the positive electrode (4) is made of perchlorate and lead water. A separator (5) made of impregnated polyester nonwoven fabric is inserted, and a negative 1i mixture I6) made of salivary lead powder and a binder is used as a negative electrode at body 17).
The periphery of the core pond facing the negative electrode coated with K? It is made by sealing with a three-layer insulating film consisting of polyethylene/polyethylene terephthalate/polyethylene.

く作 用〉 上述の如く作成した薄at池Nと、アクリル酸メチル6
0部、メタクリル酸メチル40部?乳化重合して作成し
たエマルジョン?正画バインダーに用い水馨用いE+合
剤?インキ化し東成本に塗布後乾燥して作成した正極電
極と用いた以外は同一のl専準電池F3−、作成し、第
3図に示す如<60℃保存での内部抵抗の経時変化?測
定した。同図から明らかなように本発明の4威亀池Nは
、従来品の薄型Bに比較し電池内部抵抗の増大は生じな
い。これは正極活$!J質と集成体の密着性が優れ長期
間保存してもこの密着性が著しく変化しないことに起因
しているためである。
Effect〉 Thin at pond N prepared as described above and methyl acrylate 6
0 parts, 40 parts of methyl methacrylate? An emulsion created by emulsion polymerization? E+ mixture used by Mizukai for the original image binder? The same standard battery F3-, except that it was used with a positive electrode made from ink, applied to a Tonari book and dried, was prepared, and as shown in Fig. 3, the change in internal resistance over time when stored at <60°C? It was measured. As is clear from the figure, the battery internal resistance does not increase in the 4-way game pond N of the present invention compared to the conventional thin type B. This is positive electrode activity $! This is because the adhesion between the J quality and the aggregate is excellent and this adhesion does not change significantly even after long-term storage.

さらに前述の薄型電池N、137100個づつ作成し6
0°C20日保存117.5 KΩの定抵抗下で放電し
たときの放心利用ぷおよび利用率の分散度?第1表に示
す。
Furthermore, 137,100 pieces of the above-mentioned thin battery N were made 6
Storage at 0°C for 20 days Dispersion of eccentric utilization and utilization rate when discharging under constant resistance of 117.5 KΩ? Shown in Table 1.

第1表から明らかな様に本発明の薄型電池Nは従来品の
薄型電池Bに比較し利用名の変動が少ない。これは上極
合剤が有機溶剤により均一に分肢されるために電池性能
が一定になるとともにit体と正極合剤の密着性が長期
間保存しても変化しないことに起因しているためである
As is clear from Table 1, the usage name of the thin battery N of the present invention has less variation than that of the conventional thin battery B. This is because the upper electrode mixture is evenly divided by the organic solvent, so the battery performance remains constant, and the adhesion between the IT body and the positive electrode mixture does not change even after long-term storage. It is.

本実施例では、itd液として中性塩系水溶液2用いた
が1本発明は中性塩系水浴液?用いた薄型電池に限定さ
れろものではなく、非水溶媒?用いたりチウム−マンガ
ン電池等にも用いることが可能である。従来非水心媒系
成解液?用いた電池のバインダーとして主にポリテトラ
フルオロエチレンディスバージョン?用いているが本発
明に示した如く、E 4合剤?有@m媒馨用いインキ化
するため(重々のバインダーが使用可能であり従来の欠
点とされていたE4東電体およびE極合剤の密着性が改
良され区ミ乞性能が向上する。さらに正極合剤?水?用
いずに調整することが可能であるためIE、ifu合剤
の脱水工程が簡略化されろ利点も有する。
In this example, a neutral salt-based aqueous solution 2 was used as the ITD liquid, but the present invention is a neutral salt-based water bath solution. Is it not limited to the thin battery used, but is it a non-aqueous solvent? It can also be used in lithium-manganese batteries and the like. Conventional non-aqueous core medium decomposition liquid? Is polytetrafluoroethylene dispersion mainly used as a binder for batteries? However, as shown in the present invention, is E4 mixture used? Since the ink is made using a medium (multiple binders can be used, the adhesion of E4 TEPCO and E electrode mixture, which was considered a drawback in the past, is improved, and the performance of the positive electrode is improved. Since it is possible to prepare the mixture without using water, it also has the advantage that the dehydration process of the IE and ifu mixtures is simplified.

〈発明の効果〉 本発明は以上の如くであり、E極合剤?有機溶剤により
インキ化し44体上にaii乾燥して得られる正極Kf
fl¥:薄型成池に用い電池とにより、王・4合剤の分
散性が良好で均一な電池特性?有しさらにiE濯活物鐙
と東成体の密着性が良好で保有安定性の浸れた。工業的
価(直の極めて大きい薄型電池が得られるものとなる。
<Effects of the Invention> The present invention is as described above, and the E polar mixture? Positive electrode Kf obtained by forming ink with an organic solvent and drying it on 44 bodies
fl¥: Due to the batteries used in thin-shaped ponds, the dispersibility of the King-4 mixture is good and the battery characteristics are uniform? Furthermore, the adhesion between the iE active material stirrup and the Tousei body was good, and the retention stability was improved. A thin battery with an extremely high industrial value can be obtained.

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

第1図は本発明美施例により得たIE極成極の断面図、
第2図は第1図に示した正極電極乞用いた4型成池、第
3図は本実施例で得た薄型電池と従来の薄型電池の60
℃雰囲気での保存特性馨示す表の図である。
FIG. 1 is a cross-sectional view of IE polarization obtained by a beautiful example of the present invention.
Figure 2 shows a 4-type battery using the positive electrode shown in Figure 1.
FIG. 2 is a table showing storage characteristics in a °C atmosphere.

Claims (1)

【特許請求の範囲】 1)正極活物質及び有機バインダーを含む正極合剤が集
電体上に載置後乾燥されてなる正極電極を有する薄型電
池において、 該正極合剤中にはインキ化するために有機溶剤が含まれ
ていることを特徴とする薄型電池。 2)前記有機バインダーは電解液に不溶で、かつ前記有
機溶剤に可溶であることを特徴とする特許請求の範囲第
1項記載の薄型電池。 3)前記集電体はポリオレフィン系樹脂に炭素フィラー
を分散させた導電性フィルムにアルミ箔がラミネートさ
れてなることを特徴とする特許請求の範囲第1項及び第
2項記載の薄型電池。
[Scope of Claims] 1) In a thin battery having a positive electrode in which a positive electrode mixture containing a positive electrode active material and an organic binder is placed on a current collector and then dried, the positive electrode mixture is formed into an ink. A thin battery characterized by containing an organic solvent. 2) The thin battery according to claim 1, wherein the organic binder is insoluble in the electrolyte and soluble in the organic solvent. 3) The thin battery according to claims 1 and 2, wherein the current collector is formed by laminating aluminum foil on a conductive film made of polyolefin resin with carbon filler dispersed therein.
JP26691985A 1985-11-27 1985-11-27 Thin battery Pending JPS62126557A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26691985A JPS62126557A (en) 1985-11-27 1985-11-27 Thin battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26691985A JPS62126557A (en) 1985-11-27 1985-11-27 Thin battery

Publications (1)

Publication Number Publication Date
JPS62126557A true JPS62126557A (en) 1987-06-08

Family

ID=17437496

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26691985A Pending JPS62126557A (en) 1985-11-27 1985-11-27 Thin battery

Country Status (1)

Country Link
JP (1) JPS62126557A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0352796A2 (en) * 1988-07-29 1990-01-31 Canon Kabushiki Kaisha Recording material
US8119278B2 (en) 2002-02-12 2012-02-21 Eveready Battery Company, Inc. Flexible thin printed battery and device and method of manufacturing same
US9027242B2 (en) 2011-09-22 2015-05-12 Blue Spark Technologies, Inc. Cell attachment method
US9444078B2 (en) 2012-11-27 2016-09-13 Blue Spark Technologies, Inc. Battery cell construction
US9693689B2 (en) 2014-12-31 2017-07-04 Blue Spark Technologies, Inc. Body temperature logging patch
US9782082B2 (en) 2012-11-01 2017-10-10 Blue Spark Technologies, Inc. Body temperature logging patch
US10849501B2 (en) 2017-08-09 2020-12-01 Blue Spark Technologies, Inc. Body temperature logging patch

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0352796A2 (en) * 1988-07-29 1990-01-31 Canon Kabushiki Kaisha Recording material
US8119278B2 (en) 2002-02-12 2012-02-21 Eveready Battery Company, Inc. Flexible thin printed battery and device and method of manufacturing same
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