JPH0636364B2 - Non-aqueous electrolyte battery - Google Patents

Non-aqueous electrolyte battery

Info

Publication number
JPH0636364B2
JPH0636364B2 JP61009345A JP934586A JPH0636364B2 JP H0636364 B2 JPH0636364 B2 JP H0636364B2 JP 61009345 A JP61009345 A JP 61009345A JP 934586 A JP934586 A JP 934586A JP H0636364 B2 JPH0636364 B2 JP H0636364B2
Authority
JP
Japan
Prior art keywords
positive electrode
aqueous electrolyte
cupric oxide
battery
active material
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.)
Expired - Lifetime
Application number
JP61009345A
Other languages
Japanese (ja)
Other versions
JPS62168345A (en
Inventor
親典 石橋
和郎 森脇
修弘 古川
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.)
Sanyo Electric Co Ltd
Original Assignee
Sanyo Electric 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 Sanyo Electric Co Ltd filed Critical Sanyo Electric Co Ltd
Priority to JP61009345A priority Critical patent/JPH0636364B2/en
Publication of JPS62168345A publication Critical patent/JPS62168345A/en
Publication of JPH0636364B2 publication Critical patent/JPH0636364B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/48Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/483Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides for non-aqueous cells
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Description

【発明の詳細な説明】 イ、産業上の利用分野 本発明はリチウム又はリチウム化合物を活物質とする負
極と、非水電解液と、酸化第二銅を活物質とする正極と
を備えた非水電解液電池に関する。
DETAILED DESCRIPTION OF THE INVENTION A. Field of Industrial Application The present invention provides a non-aqueous electrolyte comprising a negative electrode using lithium or a lithium compound as an active material, a non-aqueous electrolyte, and a positive electrode using cupric oxide as an active material. A water electrolyte battery.

ロ、従来の技術 リチウム又はリチウム化合物を活物質とする負極を用い
た非水電解液電池は高エネルギー密度を有し且自己放電
が少ないという利点を有する。そして、例えば特公昭5
6−40471号公報に開示されているように酸化第二
銅を正極活物質として組合せば電池電圧は約1.5Vと
なり既存のアルカリ乾電池、水銀電池、銀電池などのと
互換使用しうる利点がある。
B. Conventional Technique A non-aqueous electrolyte battery using a negative electrode containing lithium or a lithium compound as an active material has the advantages of high energy density and low self-discharge. And, for example, Japanese Patent Publication Sho 5
As disclosed in JP-A-6-40471, when cupric oxide is combined as a positive electrode active material, the battery voltage becomes about 1.5 V, which is advantageous in that it can be used interchangeably with existing alkaline dry batteries, mercury batteries, silver batteries and the like. is there.

ハ、発明が解決しようとする問題点 従来のリチウム一酸化第二銅系非水電解液電池において
は酸化第二銅は粉末状のものが用いられていた。ところ
が酸化第二銅粉末は表面積が小さく、この粉末を成型し
た正極は多孔度が小さいため含液率が低くその効果とし
て保存に伴ない内部抵抗が上昇するという問題があっ
た。
C. Problems to be Solved by the Invention In conventional lithium cupric monoxide-based non-aqueous electrolyte batteries, powdery cupric oxide was used. However, the cupric oxide powder has a small surface area, and the positive electrode formed from this powder has a small porosity, so that the liquid content is low, and as a result, there is a problem that the internal resistance increases with storage.

ニ、問題点を解決するための手段 本発明は正極活物質として繊維状の酸化第二銅を用いる
ことを特徴とする。
D. Means for Solving the Problems The present invention is characterized by using fibrous cupric oxide as the positive electrode active material.

ホ、作 用 粉末状酸化第二銅の表面積は1m2/g以下であるのに対
し繊維状酸化第二銅のそれは約5m2/gと極めて大き
い。それ故、繊維状酸化第二銅を成型した正極の多孔度
は大きく含液率が高くなるため正極内の電解液量が増し
負極活物質であるリチウムイオンが拡散しやすく内部抵
抗を感じることができる。
E. The surface area of powdered cupric oxide used is less than 1 m 2 / g, while that of fibrous cupric oxide is extremely large, about 5 m 2 / g. Therefore, the porosity of the positive electrode molded of fibrous cupric oxide is large and the liquid content is high, so that the amount of the electrolytic solution in the positive electrode is increased and lithium ions, which are the negative electrode active material, easily diffuse and the internal resistance is felt. it can.

又、繊維状酸化第二銅を活物質として用いることにより
放電時における正極の膨張を抑制しうる。即ち、正極膨
張の原因は放電反応によって生成せる金属銅が超微粉末
であり嵩高となるためである。繊維状酸化第二銅を用い
た場合には前述した如く電気の多孔度が大、充いかえれ
ば電極内の空隙が大なるためこの空隙部によって金属銅
の嵩高を吸収することができ、その結果として正極自身
の膨張を抑制しうる。
Further, by using fibrous cupric oxide as an active material, expansion of the positive electrode during discharge can be suppressed. That is, the cause of the positive electrode expansion is that the metallic copper produced by the discharge reaction is an ultrafine powder and becomes bulky. When fibrous cupric oxide is used, the porosity of electricity is large as described above, and if filled, the voids in the electrode become large, so the bulkiness of metallic copper can be absorbed by this void portion. As a result, expansion of the positive electrode itself can be suppressed.

ヘ、実施例 以下本発明の実施例につき詳述する。F. Examples Examples of the present invention will be described in detail below.

繊維径約1〜10μの繊維状酸化第二銅85重量%に導
電剤としての黒鉛10重量%、結着剤としてのフッ素樹
脂粉末5重量%を加えて混合した後、この混合物を約2
トン/cm2の圧力で加圧成型して径15.0mm、厚み
1.1mmの成型体を得、この成型体を200〜300℃
の温度で熱処理して正極とする。
To 85% by weight of fibrous cupric oxide having a fiber diameter of about 1 to 10 μm, 10% by weight of graphite as a conductive agent and 5% by weight of fluororesin powder as a binder were added and mixed.
Pressure molding is performed at a pressure of ton / cm 2 to obtain a molded body having a diameter of 15.0 mm and a thickness of 1.1 mm, and this molded body is at 200 to 300 ° C.
Heat treatment is carried out at a temperature of to obtain a positive electrode.

負極はリチウム圧延板を約0.6mmの厚みに圧延し、こ
のリチウム圧延板を径15.0mmに打抜いたものであ
る。電解液はプロピレンカーボネートと1.2−ジメト
キシエタンとの混合溶媒に過塩素酸リチウムを1モル/
溶解させたものを用い、又セパレータとしてポリプロ
ピン不織布を用いて直径20.0mm、厚み2.5mmの本
発明電池(A)を作成した。
The negative electrode is obtained by rolling a rolled lithium plate to a thickness of about 0.6 mm and punching the rolled lithium plate to a diameter of 15.0 mm. The electrolyte is 1 mol / liter of lithium perchlorate in a mixed solvent of propylene carbonate and 1.2-dimethoxyethane.
A battery (A) of the present invention having a diameter of 20.0 mm and a thickness of 2.5 mm was prepared using the melted product and a polypropyne nonwoven fabric as a separator.

一方、比較のために正極活物質として市販特級の粉末状
酸化第二銅を用いることを除いて他は本発明電池と同様
の従来電池(B)を作成した。
On the other hand, for comparison, a conventional battery (B) similar to the battery of the present invention was prepared except that a commercially available special grade cupric oxide powder was used as the positive electrode active material.

第1図はこれら電池を温度60℃、湿度90%の条件下
で保存した時の内部抵抗の経時変化を示し、又第2図は
電池組立後、60℃で3ケ月保存したのち20℃、1K
Ω負荷での放電特性を示す。
Fig. 1 shows the changes in internal resistance over time when these batteries were stored under the conditions of a temperature of 60 ° C and a humidity of 90%, and Fig. 2 shows that after the batteries were assembled, they were stored at 60 ° C for 3 months and then at 20 ° C. 1K
Shows discharge characteristics under Ω load.

第1図及び第2図より本発明電池(A)は従来電池
(B)に比して保存特性が改善されているのがわかる。
It can be seen from FIGS. 1 and 2 that the battery (A) of the present invention has improved storage characteristics as compared with the conventional battery (B).

ト、発明の効果 上述した如く、繊維状の酸化第二銅を活物質とした正極
を用いれば多孔度が大で含液率が高くなるため正極内の
電解液量が増し、保存に伴う液量不足を因とする内部抵
抗の上昇を抑制でき電池の保存特性を改善することがで
きる。
As described above, when the positive electrode using fibrous cupric oxide as the active material is used, the porosity is large and the liquid content is high, so that the amount of the electrolytic solution in the positive electrode is increased and the liquid accompanying storage is increased. It is possible to suppress an increase in internal resistance due to insufficient amount and improve the storage characteristics of the battery.

又、多孔度が大であるため放電反応によって酸化第二銅
から金属銅への変化に伴う嵩高を多孔部の空隙で吸収し
正極自身の膨張を抑えることができ、依って電池の膨張
・変形を抑制しうる。
Also, since the porosity is large, the bulkiness due to the change from cupric oxide to metallic copper due to the discharge reaction can be absorbed in the voids of the porous part and the expansion of the positive electrode itself can be suppressed. Can be suppressed.

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

第1図及び第2図は本発明電池と従来電池との特性比較
図であって、第1図は高温、高湿下における内部抵抗の
経時変化、第2図は高温下での保存後における放電特性
を夫々示す。 (A)……本発明電池、(B)……従来電池。
1 and 2 are characteristic comparison diagrams of the battery of the present invention and a conventional battery. FIG. 1 shows changes in internal resistance with time at high temperature and high humidity, and FIG. 2 shows results after storage at high temperature. The discharge characteristics are shown respectively. (A) ... Battery of the present invention, (B) ... Conventional battery.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】リチウム又はリチウム化合物を活物質とす
る負極と、非水電解液と、繊維状の酸化第二銅を活物質
とする正極とを備えた非水電解液電池。
1. A non-aqueous electrolyte battery comprising a negative electrode containing lithium or a lithium compound as an active material, a non-aqueous electrolyte solution, and a positive electrode containing fibrous cupric oxide as an active material.
JP61009345A 1986-01-20 1986-01-20 Non-aqueous electrolyte battery Expired - Lifetime JPH0636364B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61009345A JPH0636364B2 (en) 1986-01-20 1986-01-20 Non-aqueous electrolyte battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61009345A JPH0636364B2 (en) 1986-01-20 1986-01-20 Non-aqueous electrolyte battery

Publications (2)

Publication Number Publication Date
JPS62168345A JPS62168345A (en) 1987-07-24
JPH0636364B2 true JPH0636364B2 (en) 1994-05-11

Family

ID=11717880

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61009345A Expired - Lifetime JPH0636364B2 (en) 1986-01-20 1986-01-20 Non-aqueous electrolyte battery

Country Status (1)

Country Link
JP (1) JPH0636364B2 (en)

Also Published As

Publication number Publication date
JPS62168345A (en) 1987-07-24

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