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JPS5947432B2 - organic solvent battery - Google Patents
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JPS5947432B2 - organic solvent battery - Google Patents

organic solvent battery

Info

Publication number
JPS5947432B2
JPS5947432B2 JP53039040A JP3904078A JPS5947432B2 JP S5947432 B2 JPS5947432 B2 JP S5947432B2 JP 53039040 A JP53039040 A JP 53039040A JP 3904078 A JP3904078 A JP 3904078A JP S5947432 B2 JPS5947432 B2 JP S5947432B2
Authority
JP
Japan
Prior art keywords
battery
positive electrode
organic solvent
electrode active
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
Application number
JP53039040A
Other languages
Japanese (ja)
Other versions
JPS54131722A (en
Inventor
信太郎 鈴木
泰三郎 菊地
良康 青木
浩一 田中
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.)
FDK Twicell Co Ltd
Original Assignee
Toshiba 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 Toshiba Battery Co Ltd filed Critical Toshiba Battery Co Ltd
Priority to JP53039040A priority Critical patent/JPS5947432B2/en
Publication of JPS54131722A publication Critical patent/JPS54131722A/en
Publication of JPS5947432B2 publication Critical patent/JPS5947432B2/en
Expired 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

Landscapes

  • Battery Electrode And Active Subsutance (AREA)

Description

【発明の詳細な説明】 本発明はリチウム、ナトリウムなどのアルカリ金属を負
極として使用し、これらを溶解しない有機溶媒を用いた
電解液を使用し、正極活物質として五酸化リンを用いて
なる高エネルギー密度電池に関するものである。
Detailed Description of the Invention The present invention uses alkali metals such as lithium and sodium as the negative electrode, uses an electrolytic solution using an organic solvent that does not dissolve these metals, and uses phosphorus pentoxide as the positive electrode active material. It concerns energy density batteries.

従来、リチウム、ナトリウムなどのアルカリ金属を負極
として有機電解液を使用する電池は、適当な正極活物質
を用いることにより高電圧、高エネルギー密度を得られ
るので種々の正極活物質について検討されてきた。
Conventionally, batteries that use an alkali metal such as lithium or sodium as a negative electrode and an organic electrolyte have been studied for various positive electrode active materials because high voltage and high energy density can be obtained by using an appropriate positive electrode active material. .

これらの中の代表的なものとしては、Cl゛2、NiF
2、cUct3Agctなどの金属ハロゲン化物、Cr
2O3、cu2o2MnO2、MoO3などの金属酸化
物、(CF)nなどの層間化合物がある。
Typical of these are Cl゛2, NiF
2. Metal halides such as cUct3Agct, Cr
There are metal oxides such as 2O3, cu2o2MnO2, and MoO3, and interlayer compounds such as (CF)n.

しかし、自己放電が大きかつたり分極の大きいことによ
り放電性能が悪いものや、正極活物質そのものの安全性
に問題のあるものが多かつた。
However, there were many cases in which discharge performance was poor due to large self-discharge and large polarization, and there were problems with the safety of the positive electrode active material itself.

’本発明は、従来よりすぐれた正極を得るため、新たな
活物質を種々検討した結果、五酸化リンが特にすぐれて
いることを見出したことに基づくものである。五酸化リ
ンは吸湿性が非常に大きく水分により分解しやすいもの
の、電解液に対して漏れがよくかつ溶解度も小さく化学
的に安定である。
'The present invention is based on the fact that, as a result of investigating various new active materials in order to obtain a positive electrode superior to conventional ones, it was discovered that phosphorus pentoxide is particularly superior. Although phosphorus pentoxide has very high hygroscopicity and is easily decomposed by moisture, it leaks easily into the electrolyte, has low solubility, and is chemically stable.

また、リチウム負極と組合わせたときの実測開路電圧は
3.8Vとなつた。放電容量より放電反応は4電子反応
で、電池反応式はP2O5+ 4Li→P203+ 2
Li20で、正極はp2o5+4e−→P203+20
2−である。
Furthermore, the actually measured open circuit voltage when combined with a lithium negative electrode was 3.8V. According to the discharge capacity, the discharge reaction is a 4-electron reaction, and the battery reaction formula is P2O5+ 4Li→P203+ 2
With Li20, the positive electrode is p2o5+4e-→P203+20
It is 2-.

このときの理論エネルギー密度は3.911wh/cc
となり、水分に対する処理を十分行なえば高電圧、高エ
ネルギー密度の電池を得ることが期待できる。開路電圧
、エネルギー密度についての従来の正極活物質との比較
を表1に示す。次に、本発明の実施例を24.5−φ×
2.5□をのコイン電池に組立てた場合において図面に
基づいて説明する。
The theoretical energy density at this time is 3.911wh/cc
Therefore, if moisture is treated sufficiently, it can be expected that a battery with high voltage and high energy density can be obtained. Table 1 shows a comparison with conventional positive electrode active materials in terms of open circuit voltage and energy density. Next, the embodiment of the present invention will be described as 24.5-φ×
The case where 2.5□ is assembled into a coin battery will be explained based on the drawings.

第1図において、1は五酸化リンの正極活物質と導電材
として10%のグラフアイトを混合した正極合剤であり
、2t0n/Ciiの圧力で正極缶2中に直径2011
!、厚さ1.511に成形して充填したものである。
In Fig. 1, 1 is a positive electrode mixture consisting of a positive electrode active material of phosphorus pentoxide and 10% graphite as a conductive material, and is placed in a positive electrode can 2 with a diameter of 201 mm at a pressure of 2 tons/Cii.
! , formed to a thickness of 1.511 mm and filled.

この正極合剤1は、高真空に}いて十分乾燥させ水分を
除去した五酸化リンに同じく高真空で乾燥したグラフア
イトを水分及び酸素が5〜6再肛のアルゴン雰囲気ドラ
イボツクス内で混合したものである。他の電池組み立て
作業も上記ドライボツクス内で行なつた。3はポリプロ
ピレンの不織布からなるセパレータで、これに電解質と
して1モルのLictO4を含むプロピレンカーボネー
ト有機電解液を浸み込ませた電解質層を形成した。
This positive electrode mixture 1 was prepared by mixing phosphorus pentoxide, which had been sufficiently dried in a high vacuum to remove moisture, with graphite, which had also been dried in a high vacuum, in an argon atmosphere dry box with a moisture and oxygen content of 5 to 6 degrees. It is something. Other battery assembly operations were also performed in the dry box. Reference numeral 3 denotes a separator made of a polypropylene non-woven fabric, on which an electrolyte layer was formed by impregnating a propylene carbonate organic electrolyte solution containing 1 mol of LictO4 as an electrolyte.

4はリチウムの負極活物質である。4 is a lithium negative electrode active material.

5は負極封口板であり、6はパツキングである。5 is a negative electrode sealing plate, and 6 is a packing.

第2図は第1図の本発明の実施例に示す電池と従来の電
池とを30KΩの定抵抗で放電したときの放電容量に対
する端子電圧の特性を示した比較図である。
FIG. 2 is a comparison diagram showing the characteristics of terminal voltage with respect to discharge capacity when the battery shown in the embodiment of the present invention shown in FIG. 1 and the conventional battery are discharged with a constant resistance of 30 KΩ.

曲線Aは正極活物質に本発明による五酸化リンを用いた
場合、Bは二酸化マンガン、Cはフツ化カーボンを用い
た場合の放電曲線である。
Curve A is a discharge curve when phosphorus pentoxide according to the present invention is used as the positive electrode active material, curve B is a discharge curve when manganese dioxide is used, and curve C is a discharge curve when carbon fluoride is used.

第2図の放電曲線をもとにして単位体積当たりの放電容
量を求めると表2のごとくなり、本発明の電池は従来の
ものに比べて、単位体積当たりの放電容量が約35〜5
0%向上していることがわかる。以上のように本発明の
五酸化リンを用いた電池は従来電池よりも端子電圧が高
く、単位体積当たりの放電量も高いなど、その工業的価
値は極めて大なるものである。
Table 2 shows that the discharge capacity per unit volume is determined based on the discharge curve in Figure 2, and the battery of the present invention has a discharge capacity per unit volume of approximately 35 to 55% compared to the conventional battery.
It can be seen that there is an improvement of 0%. As described above, the battery using phosphorus pentoxide of the present invention has a higher terminal voltage and a higher discharge amount per unit volume than conventional batteries, and has extremely high industrial value.

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

第1図は本発明の実施例における有機溶媒電池の縦断面
図、第2図は本発明電池と従来の電池との放電特性比較
図である。 1・・・・・・正極合剤、2・・・・・・正極缶、3・
・・・・・セパレータ、4・・・・・・負極活物質、5
・・・・・・負極封口板、6・・・・・・パツキング。
FIG. 1 is a longitudinal sectional view of an organic solvent battery in an example of the present invention, and FIG. 2 is a comparison diagram of discharge characteristics between the battery of the present invention and a conventional battery. 1...Positive electrode mixture, 2...Positive electrode can, 3.
... Separator, 4 ... Negative electrode active material, 5
...Negative electrode sealing plate, 6... Packing.

Claims (1)

【特許請求の範囲】[Claims] 1 リチウム、ナトリウムなどのアルカリ金属よりなる
負極活物質と、正極活物質と、有機溶媒電解液とを備え
た電池において、該正極活物質が、水分を除去した五酸
化リン(P_2O_5)であることを特徴とする有機溶
媒電池。
1. In a battery comprising a negative electrode active material made of an alkali metal such as lithium or sodium, a positive electrode active material, and an organic solvent electrolyte, the positive electrode active material is phosphorus pentoxide (P_2O_5) from which water has been removed. An organic solvent battery featuring:
JP53039040A 1978-04-03 1978-04-03 organic solvent battery Expired JPS5947432B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP53039040A JPS5947432B2 (en) 1978-04-03 1978-04-03 organic solvent battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP53039040A JPS5947432B2 (en) 1978-04-03 1978-04-03 organic solvent battery

Publications (2)

Publication Number Publication Date
JPS54131722A JPS54131722A (en) 1979-10-13
JPS5947432B2 true JPS5947432B2 (en) 1984-11-19

Family

ID=12542001

Family Applications (1)

Application Number Title Priority Date Filing Date
JP53039040A Expired JPS5947432B2 (en) 1978-04-03 1978-04-03 organic solvent battery

Country Status (1)

Country Link
JP (1) JPS5947432B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59134561A (en) * 1983-01-24 1984-08-02 Nippon Telegr & Teleph Corp <Ntt> Lithium cell

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5242840B2 (en) * 1971-08-27 1977-10-26

Also Published As

Publication number Publication date
JPS54131722A (en) 1979-10-13

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