JPS58111275A - Organic electrolyte secondary battery - Google Patents

Organic electrolyte secondary battery

Info

Publication number
JPS58111275A
JPS58111275A JP56211782A JP21178281A JPS58111275A JP S58111275 A JPS58111275 A JP S58111275A JP 56211782 A JP56211782 A JP 56211782A JP 21178281 A JP21178281 A JP 21178281A JP S58111275 A JPS58111275 A JP S58111275A
Authority
JP
Japan
Prior art keywords
charge
battery
secondary battery
graphite
organic electrolyte
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
JP56211782A
Other languages
Japanese (ja)
Inventor
Takashi Sakai
貴史 酒井
Sanehiro Furukawa
古川 修弘
Kazuo Moriwaki
森脇 和郎
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
Sanyo Denki Co Ltd
Original Assignee
Sanyo Electric Co Ltd
Sanyo Denki 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, Sanyo Denki Co Ltd filed Critical Sanyo Electric Co Ltd
Priority to JP56211782A priority Critical patent/JPS58111275A/en
Publication of JPS58111275A publication Critical patent/JPS58111275A/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
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • 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
    • H01M4/583Carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • H01M4/587Carbonaceous material, e.g. graphite-intercalation compounds or CFx for inserting or intercalating light metals
    • 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)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Inorganic Chemistry (AREA)
  • Secondary Cells (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

PURPOSE:To improve conductivity to lower voltage in an initial stage of charge and enable to charge at constant current by mixing a conductive mass to polyacethylene which forms positive and negative eledctrodes. CONSTITUTION:90pts.wt. polyacethylene powder and 10pts.wt. graphite of a conductive mass are mixed and compressed to form a positive electrode and a negative electrode. These electrodes are combined with an organic eledtrolyte prepared by dissolving lithium perchlorete in an equal volume mixture solvent of polypropylene carbonate and 1, 2 dimethoxy ethane to form a secondary battery. Therefore, when the battery is charged, part of lithium ion is doped in graphite, and this lithium ion is used in discharge. Thereby conductivity is increased to lower voltage in an initial stage of charge and enable to charge at constant current.

Description

【発明の詳細な説明】 本発明は有機電解質二次電池Kllする・一般にこの種
電池の形態としてはリチウム、ナトリウム等の軽金属か
らなる負極と、プロピレンカーボネート、γ−ブチルラ
クトン等の有機溶媒に過塩素酸リチウム(btcloa
)、ホラすッ化リチウム(LiBF4)等の溶質を溶解
した有機電解質と、三酸化モリブデン、五酸化バナジウ
ム等を活物質とする正極とで構成される瞥モ。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an organic electrolyte secondary battery. Generally, this type of battery has a negative electrode made of a light metal such as lithium or sodium, and an organic solvent such as propylene carbonate or γ-butyl lactone. Lithium chlorate (btcloa)
), an organic electrolyte in which a solute such as lithium difluorosulfide (LiBF4) is dissolved, and a positive electrode containing molybdenum trioxide, vanadium pentoxide, etc. as an active material.

而して、近年に至っては例えば特開昭56−13646
9号公報に開示されている工うに、正、負極tポリアセ
チレンで構成し、溶質として過塩素酸リチウムを用いる
新規な二次電池が提案されている・ ポリアセチレン((CH)χ〕はそれ自身、 10−’
Ω−1・3−1から100 ・1 の電気伝導度【有す
るものであるがイオン種tドーピングすることに19、
その電気伝導fr!10.Ω ・1と上昇し金属的性質
を帯びる工うになるOそして、この電池の充放電反応機
構は次式で表さて、この電池の問題点は、前述したLう
にイオン種tドーピングする前のポリアセチレンの電気
伝導度が低いため、充電初期における電池電圧が高く(
IIE1図参照)、足電流充電が困難であると共に有機
溶媒を分解(通常、分解電圧は約5.0v)してしまう
ことでTo本。
In recent years, for example, Japanese Patent Application Laid-Open No. 56-13646
9, a new secondary battery has been proposed in which the positive and negative electrodes are composed of polyacetylene and lithium perchlorate is used as the solute. Polyacetylene ((CH)χ) itself is 10-'
It has an electrical conductivity of Ω-1.3-1 to 100.1; however, when doping with ionic species,
The electrical conduction fr! 10. The charge/discharge reaction mechanism of this battery is expressed by the following equation.The problem with this battery is that the polyacetylene before doping with ion species T Because of its low electrical conductivity, the battery voltage at the beginning of charging is high (
(See Figure IIE1), it is difficult to charge the current, and the organic solvent is decomposed (usually the decomposition voltage is about 5.0V), which leads to problems.

本発明は上記問題点を解消すべくなされたものであり、
その要旨とするところは導電剤を混合せしめて電気伝導
ft改養せるポリアセチレンで正、負極tagすること
にある。
The present invention has been made to solve the above problems,
The gist of this is to tag the positive and negative electrodes with polyacetylene that can be mixed with a conductive agent to improve electrical conductivity.

以下本発明の実施例について詳述する 実施例1 ポリアセチレン粉末90重量部と導電剤としてのグラフ
了イト10重量部とを混合した混合物を加圧成型したも
のt正、負極とする・ 有機電解質は1aビレyカーポネ・−トと1.2ジメト
キシエタンとの等体積混合溶媒に過塩素酸リチウムを溶
解したものであり、セパレ・1夕はポリプロピレン不織
布管用いて直径24■、高さ5゜0−の電池(A)t−
作成した・ 実施例2 実施例1において、導電剤として銅粉末を用いるととt
除いて、他は実施例1と同様の電池(lllt作成し友
@ 尚、比較の究めに導電剤tS合せずポリアセチレン単独
で構成した正、負極を用いる比較電Ak (C)を作成
した。
Examples of the present invention will be described in detail below. Example 1 A mixture of 90 parts by weight of polyacetylene powder and 10 parts by weight of graphite as a conductive agent was pressure molded. Positive and negative electrodes were used. Organic electrolyte was Lithium perchlorate is dissolved in a mixed solvent of equal volumes of 1a carbonate and 1.2 dimethoxyethane, and the separate part is made using a polypropylene non-woven tube with a diameter of 24cm and a height of 5°. battery (A)t-
Created Example 2 In Example 1, when copper powder is used as the conductive agent,
Except for this, the battery was otherwise the same as in Example 1 (Illt was prepared by a friend@).For comparison purposes, a comparative cell Ak (C) was prepared using positive and negative electrodes composed of polyacetylene alone without the conductive agent tS.

これらの電池を光電電lL2mAで20時間充電し、放
電電fi2mムで放電し’Jt a 第1図は充電特性
図、第2図は放電特性図を夫々示す。
These batteries were charged with a photoelectric current of 1L 2 mA for 20 hours and discharged with a discharge current of fi 2 mm. Fig. 1 shows a charging characteristic diagram, and Fig. 2 shows a discharging characteristic diagram.

第1図19ポリアセチレン単独で構成しt正、負極【用
いt電池(C)では充電初期の電池電圧が高く、初期の
み足電圧充電を行なわねばならず、且通常の有aSS媒
の分解電圧(約S、OV >以上の電圧を有している@ これに対して本発明電池(〜(S)では正、負極の電気
型導度が改善されている友め光電初期工9定電流の充電
が可能なるものである・ 又、jI2図を参照すると、導電剤としてグラファイト
e用いt場合に容量が増大することが伺える・これはグ
ラファイトが層間化合物であるため、充電時に一部のL
l イオン又はClO4イオンがグラファイトにドープ
され、このL1イオン又ハC4r)a  イオンも放電
に利用しつる究めである。
Figure 1 19 In the battery (C) used, the battery voltage is high at the initial stage of charging, and the voltage charging must be carried out only in the initial stage, and the decomposition voltage of the normal aSS medium ( On the other hand, in the battery of the present invention (~(S), the electrical type conductivity of the positive and negative electrodes is improved. Also, referring to Figure 2, it can be seen that the capacity increases when graphite is used as a conductive agent.This is because graphite is an intercalation compound, so some of the L
Graphite is doped with l ions or ClO4 ions, and this L1 ion or C4r)a ion is also utilized for discharge.

尚、有機電解質を構成する溶質としては実施例で示した
過塩素酸リチウム以外にホウフッ化リチウム(1,IB
F4)、6フツ化リンリチウム(LiPF4)、6フツ
化ヒ識リチウム(Liロア4)、4塩化アルミニウムリ
チウム(Liム1cla)等も利用できる・ 以上詳述したように、本発明はポリアセチレンで正、負
極tsscする有機電解質二次電池に関するものであり
、ポリアセチレンに導電剤tS合することに19、電気
伝導ft改善して充電初期にドける電池電圧1itt抑
え、足型I51光電を可能ならしめると共に1機溶媒の
分解を阻止するものである・ 又、導電剤として特にグラファイトを用いれば上記効果
に加えて電池容量の増大も計ることができ、この種電池
の性能同上に資するところ大なるものである。
In addition to the lithium perchlorate shown in the examples, lithium borofluoride (1, IB
F4), lithium phosphorus hexafluoride (LiPF4), lithium phosphorus hexafluoride (Liloa4), lithium aluminum tetrachloride (Limu1cla), etc. can also be used. As detailed above, the present invention can be applied to polyacetylene. This relates to an organic electrolyte secondary battery with positive and negative electrodes, and combining polyacetylene with a conductive agent tS improves electrical conduction ft, suppresses the battery voltage at the initial stage of charging by 1it, and makes foot-shaped I51 photoelectricity possible. In addition, if graphite is used as a conductive agent, it is possible to increase the battery capacity in addition to the above effects, which greatly contributes to the performance of this type of battery. It is.

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

図IIにいずれも本発明電池と比較電池との特性比較図
であり、第1!11は充電特性、II2図は放電特性を
夫々示す・ (Ji)(四・・・本発明電池、(C)・・・比較電池
0出願人三洋電機株式金社
Figure II is a comparison diagram of the characteristics of the present invention battery and the comparative battery. Figure 1!11 shows the charging characteristics, and Figure II2 shows the discharge characteristics. )... Comparative battery 0 Applicant Sanyo Electric Co., Ltd. Kinsha

Claims (1)

【特許請求の範囲】 前記圧、負極が導電剤【混合したポリアセチレンで構成
されていることt特徴とする有機電解質二次電池。 ■ 前記導電剤がグラファイトであること1*徴とする
特許請求の範囲篤■項記載の有機電解質二次電池。
[Scope of Claim] An organic electrolyte secondary battery characterized in that the pressure negative electrode is composed of polyacetylene mixed with a conductive agent. (2) The organic electrolyte secondary battery according to claim (1), characterized in that the conductive agent is graphite.
JP56211782A 1981-12-23 1981-12-23 Organic electrolyte secondary battery Pending JPS58111275A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56211782A JPS58111275A (en) 1981-12-23 1981-12-23 Organic electrolyte secondary battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56211782A JPS58111275A (en) 1981-12-23 1981-12-23 Organic electrolyte secondary battery

Publications (1)

Publication Number Publication Date
JPS58111275A true JPS58111275A (en) 1983-07-02

Family

ID=16611504

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56211782A Pending JPS58111275A (en) 1981-12-23 1981-12-23 Organic electrolyte secondary battery

Country Status (1)

Country Link
JP (1) JPS58111275A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6065478A (en) * 1983-09-21 1985-04-15 Hitachi Ltd Polymer secondary battery
EP0199175A2 (en) * 1985-04-19 1986-10-29 AlliedSignal Inc. Negative electrodes for non-aqueous secondary batteries composed of conjugated polymer and alkali metal alloying or inserting material

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6065478A (en) * 1983-09-21 1985-04-15 Hitachi Ltd Polymer secondary battery
JPH0460304B2 (en) * 1983-09-21 1992-09-25 Hitachi Seisakusho Kk
EP0199175A2 (en) * 1985-04-19 1986-10-29 AlliedSignal Inc. Negative electrodes for non-aqueous secondary batteries composed of conjugated polymer and alkali metal alloying or inserting material

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