JPS59108269A - Organic electrolyte battery - Google Patents

Organic electrolyte battery

Info

Publication number
JPS59108269A
JPS59108269A JP57218611A JP21861182A JPS59108269A JP S59108269 A JPS59108269 A JP S59108269A JP 57218611 A JP57218611 A JP 57218611A JP 21861182 A JP21861182 A JP 21861182A JP S59108269 A JPS59108269 A JP S59108269A
Authority
JP
Japan
Prior art keywords
discharge
cuxfes2
organic electrolyte
positive terminal
batteries
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.)
Granted
Application number
JP57218611A
Other languages
Japanese (ja)
Other versions
JPH0326504B2 (en
Inventor
Takafumi Fujii
隆文 藤井
Nobuo Eda
江田 信夫
Teruyoshi Morita
守田 彰克
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP57218611A priority Critical patent/JPS59108269A/en
Publication of JPS59108269A publication Critical patent/JPS59108269A/en
Publication of JPH0326504B2 publication Critical patent/JPH0326504B2/ja
Granted 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
    • H01M4/58Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
    • H01M4/581Chalcogenides or intercalation compounds thereof
    • 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)

Abstract

PURPOSE:To improve voltage flatness by using CuxFeS2 (0<x<1) as the positive active substance. CONSTITUTION:Mixtures mixing powders of Cu, Fe and S in various rates are sealed in the vacuumed quartz glass tube, CuxFeS2 obtained by thermal reaction for 5hr at 700 deg.C, acetylene black used as the conductive material and polytetrafluoric ethylene used as a binder are mixed in the weight ratio of 100:5:7. It is then pressurizingly filled in the expanded metal made of nickel. Thereby, an electrode sheet in the thickness of 0.35mm. can be formed and it is then punched in diameter of 5.8mm. for the use as the positive terminal. With such positive terminal, a button type battery has been assembled. As is apparent from the discharge curve when discharge is carried out through a constant resistor of 50kOMEGA at 20 deg.C, the batteries by this invention B(X=0.75), C(X=0.5) and D(X=0.25) are all superior in the voltage flatness characteristic to the conventional CuFe S2A and FeS2E.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、有機電解液電池にかかり、特にその正極活物
質の改良に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to organic electrolyte batteries, and particularly to improvements in positive electrode active materials thereof.

従来例の構成とその問題点 F e S 2やCu F e S 2を正極活物質と
する有機電解液電池は、それらの単位体積当たりの理論
電気容量が犬ぎく、またリチウム負極と組み合わせたと
きの放電々圧が1.4〜1.5Vで、従来の酸化銀電池
などと互換性があるなどの特長を有している。
Structures of conventional examples and their problems Organic electrolyte batteries using F e S 2 or Cu F e S 2 as positive electrode active materials have very low theoretical electric capacity per unit volume, and when combined with a lithium negative electrode. Its discharge voltage is 1.4 to 1.5V, and it has features such as being compatible with conventional silver oxide batteries.

したかつ−C1電子ウォッチなどの電源として注目され
ている。
Shikatsu-C1 is attracting attention as a power source for electronic watches.

電子ウォッチは、使用される電池電圧の変動がその精蕨
に大きな影響を与える。このため、放電々圧の変化がよ
り少ない電池が必要となる。
Fluctuations in the battery voltage used in electronic watches have a major impact on their performance. Therefore, a battery with less variation in discharge pressure is required.

しかし、F e b 2やCu F e S 2を正極
活物質として用いた有機電解液リチウム電池は放電々圧
の平坦性に問題がある。すなわち、F e S 2の場
合、この放電機構はFeS  +4Li→L4zFeS
2+2Li→2Li2S+Feで、放電曲線が二段とな
り、前述のようなウォッチの精度面での問題を有してい
た。
However, organic electrolyte lithium batteries using Fe b 2 or Cu Fe S 2 as positive electrode active materials have a problem in flatness of discharge pressure. That is, in the case of FeS 2, this discharge mechanism is FeS +4Li→L4zFeS
2+2Li→2Li2S+Fe, the discharge curve becomes two steps, and there is a problem in terms of accuracy of the watch as described above.

Cu F e S 2の放電曲線はF e S 2とは
異なり一段の曲線となるが、電圧の平坦性に乏しく、F
 e S 2と同様な問題を有していた。
Unlike Fe S 2, the discharge curve of Cu Fe S 2 is a single-stage curve, but the voltage flatness is poor, and F
It had the same problem as eS2.

発明の目的 本発明は、M機電解液′電池の放電特性、特に電圧平坦
性の改良を目的としたものである。
OBJECTS OF THE INVENTION The object of the present invention is to improve the discharge characteristics, particularly the voltage flatness, of M electrolyte batteries.

発明の構成 本発明は、正極活物質としてCuxFeS2(Oくx〈
1)を用いることを特徴とする。
Structure of the Invention The present invention uses CuxFeS2 (Ox
1) is used.

このCu xk’ e b 2はUu、Fe、Sの各粉
末の混合物を加熱反応させることにより、各種X値の化
合物として得られる。
This Cu xk' e b 2 is obtained as a compound with various X values by subjecting a mixture of powders of Uu, Fe, and S to a heating reaction.

実施例の説明 Cu、FeおよびS、の各粉末を各種の割合で混合した
混合物を石英ガラス管に真空封入し、7o。
Description of Examples A mixture of powders of Cu, Fe, and S in various proportions was vacuum sealed in a quartz glass tube, and then heated to 7o.

℃で5時間加熱反応させて各種X値のCuXFe52を
j4tた。得られた試料はX線回折で合成物の確認をし
た。
A heating reaction was carried out at ℃ for 5 hours to obtain CuXFe52 of various X values. The obtained sample was confirmed to be a compound by X-ray diffraction.

こh らCux” S2 と導電材のアセテレンフラノ
クと結着剤のポリ47ノ化エチレンとを1’OO:5ニ
アの重量比で混合し、これをニッケルからなるエキスパ
ンデッドメタルに加圧、充填し、厚さ0.35mmのシ
ート状電極を作り、これを直径5.8門にj″Jち抜い
て正極とする。
Here, Cux" S2, the conductive material acetelene furanok, and the binder poly(47-ethylene) were mixed at a weight ratio of 1'OO:5Nia, and this was added to the expanded metal made of nickel. A sheet-like electrode with a thickness of 0.35 mm was prepared by pressing and filling, and this was punched out to a diameter of 5.8 mm to form a positive electrode.

池を組み立てた。第1図において、1はニッケルメッキ
を施した厚さ0.15mのステンレス鋼からなる外径8
.50、高さ0.60m+nの封目板で、その粗面化し
た内面には直径6.5朋、厚さ0.25mmの金属リチ
ウムからなる負極2を圧着している。3はポリプロピレ
ン製不織布からなるセパレータで、F[プロピレン1,
2ニジメトキシエタンとを体積比で1=1の割合で混合
した溶媒に過塩素酸リチウムを1モル/を溶解させた電
解液を含浸している。4は前記の正極で、その片面には
集電体として前記エキスパンデッドメタル5を有する。
Assembled the pond. In Figure 1, 1 is an outer diameter 8 made of nickel-plated stainless steel with a thickness of 0.15 m.
.. 50, a sealing plate with a height of 0.60 m+n, and a negative electrode 2 made of metallic lithium with a diameter of 6.5 mm and a thickness of 0.25 mm is crimped onto its roughened inner surface. 3 is a separator made of polypropylene nonwoven fabric, F[propylene 1,
It is impregnated with an electrolytic solution in which 1 mole of lithium perchlorate is dissolved in a solvent mixed with 2 dimethoxyethane at a volume ratio of 1=1. 4 is the above-mentioned positive electrode, and one side thereof has the above-mentioned expanded metal 5 as a current collector.

6はニッケルメッキを施した厚さ0.15mmのステン
レス鋼よりなる外径9.5mm、高さ1.3喘のケース
、了はポリプロピレン製ガスケットである。
6 is a case made of nickel-plated stainless steel with a thickness of 0.15 mm and has an outer diameter of 9.5 mm and a height of 1.3 mm, and holder is a polypropylene gasket.

前記の各種正極を用いて作成した電池を20℃において
soKΩの定抵抗放電をしたときの放電曲線を第2図に
示す。なお、Eは正極活物質に市販のF’ e S 2
を用いた電池の特性を表す。
FIG. 2 shows discharge curves when batteries prepared using the various positive electrodes described above were subjected to constant resistance discharge of soKΩ at 20°C. In addition, E is commercially available F' e S 2 as a positive electrode active material.
represents the characteristics of a battery using

この図から明らかなように、CuXFe52(0くxく
1)は従来のCu F e S 2およびF’ e S
 2に比べて極めて電圧平坦性にすぐれていることがわ
かる。
As is clear from this figure, CuXFe52 (0 x x 1) is different from conventional Cu Fe S 2 and F' e S
It can be seen that the voltage flatness is extremely superior to that of 2.

時に前記Xの値が小さくなるとともに放電々圧ならびに
放電容量が向上する。これは(/ u XF e S 
2のCu含有量を低減させることにより、放電反応にお
けるリチウムイオンのCuxkeS2へのインター力レ
ーシ目ンがより円滑に進行することによるものと考えら
れる。
Sometimes, as the value of X becomes smaller, the discharge voltage and discharge capacity improve. This is (/ u XF e S
It is thought that this is because by reducing the Cu content of Cuxke S2, the interaction of lithium ions to Cuxke S2 in the discharge reaction proceeds more smoothly.

発明の効果 以上のように、本発明によれば、放電時の電圧平坦性に
優れ、電子ウォッチなどに好適な有機電解液電池を得る
ことができる0
Effects of the Invention As described above, according to the present invention, it is possible to obtain an organic electrolyte battery that has excellent voltage flatness during discharge and is suitable for electronic watches and the like.

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

第1図は本発明による電池の一部を断面した側面図、第
2図は各種正極を用いた電池の放電曲線を示す。 2・・・・・・負極、3・・・・・セパレータ、4・・
・・・・正極。 代理人の氏名 弁理士 中 尾 敏 男 ほか1名第1
FIG. 1 is a partially sectional side view of a battery according to the present invention, and FIG. 2 shows discharge curves of batteries using various positive electrodes. 2... Negative electrode, 3... Separator, 4...
...Positive electrode. Name of agent: Patent attorney Toshio Nakao and 1 other person No. 1
figure

Claims (1)

【特許請求の範囲】[Claims] Cu xF e 82 (0< x < 1 )を活物
質とする正極と軽金属を活物質とする負極、および有機
電解液からなる有機電解液電池。
An organic electrolyte battery comprising a positive electrode using Cu x Fe 82 (0<x<1) as an active material, a negative electrode using a light metal as an active material, and an organic electrolyte.
JP57218611A 1982-12-13 1982-12-13 Organic electrolyte battery Granted JPS59108269A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57218611A JPS59108269A (en) 1982-12-13 1982-12-13 Organic electrolyte battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57218611A JPS59108269A (en) 1982-12-13 1982-12-13 Organic electrolyte battery

Publications (2)

Publication Number Publication Date
JPS59108269A true JPS59108269A (en) 1984-06-22
JPH0326504B2 JPH0326504B2 (en) 1991-04-11

Family

ID=16722664

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57218611A Granted JPS59108269A (en) 1982-12-13 1982-12-13 Organic electrolyte battery

Country Status (1)

Country Link
JP (1) JPS59108269A (en)

Also Published As

Publication number Publication date
JPH0326504B2 (en) 1991-04-11

Similar Documents

Publication Publication Date Title
US3415687A (en) Electric current producing cell
Croce et al. Ambient Temperature Lithium Polymer Rocking‐Chair Batteries
US3380855A (en) Battery including methyl formate and lithium perchlorate
US4381258A (en) Electronic cell with a non-aqueous electrolyte
US4172927A (en) Organic electrolyte battery
JP2000311692A (en) Manufacture of electrochemical element
US4234667A (en) Battery and method for fabricating same
JPS59108269A (en) Organic electrolyte battery
JP2001068116A (en) Lithium battery and method of manufacturing therefor
JPH05325961A (en) Lithium battery
JP2812943B2 (en) Organic electrolyte battery
JPH0151854B2 (en)
JPS58194258A (en) Organic electrolytic battery
JPH0770315B2 (en) Non-aqueous electrolyte battery
JP2001185126A (en) Lithium secondary battery and manufacturing method thereof
JPH0338702B2 (en)
JPS5987764A (en) Manufacture of positive active material for organic electrolyte battery
JPH0326502B2 (en)
JPS58206056A (en) Organic electrolyte battery
JPS58181267A (en) Organic electrolyte battery
JPH0320861B2 (en)
JP2000012033A (en) Nonaqueous electrolyte battery
JPH04163861A (en) Secondary battery with non-aqueous electrolyte
JPS5820106B2 (en) Yuuki Denkai Shitsudenchi
JPS6352739B2 (en)