JPS6164066A - Silver oxide battery - Google Patents

Silver oxide battery

Info

Publication number
JPS6164066A
JPS6164066A JP18603784A JP18603784A JPS6164066A JP S6164066 A JPS6164066 A JP S6164066A JP 18603784 A JP18603784 A JP 18603784A JP 18603784 A JP18603784 A JP 18603784A JP S6164066 A JPS6164066 A JP S6164066A
Authority
JP
Japan
Prior art keywords
silver
active material
oxide
silver oxide
positive
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
JP18603784A
Other languages
Japanese (ja)
Inventor
Hiroyoshi Yoshihisa
吉久 洋悦
Toshiyuki Iba
伊庭 利行
Tadao Takahashi
忠雄 高橋
Hiroshi Yufu
宏 油布
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.)
Yuasa Corp
Original Assignee
Yuasa Battery Corp
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 Yuasa Battery Corp filed Critical Yuasa Battery Corp
Priority to JP18603784A priority Critical patent/JPS6164066A/en
Publication of JPS6164066A publication Critical patent/JPS6164066A/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

Landscapes

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

Abstract

PURPOSE:To stably control the voltage of a silver oxide battery be bringing the silver layer of the positive active material into electric contact with the inner bottom surface of the positive case and adjusting the ratio of the amount of silver to that of silver oxide in the positive active material to at least a specified level. CONSTITUTION:A silver layer 2 is reliably brought into electric contact with the inner bottom surface of a positive case 1. It can be formed by such a method as follows: (1) stamping a sheet from silver foil before placing the sheet in a positive case 1; (2) weighing a necessary amount of silver powder before fixing it to the inner bottom surface of the positive case 1 by pressure; (3) reducing the bottom surface of a positive active material 3 composed of silver oxide alone or a mixture consisting of silver oxide and argentous oxide before the positive active material 3 is placed in the positive case 1. It is necessary that silver always exists in the positive case in spite of equilibrium reaction. Regardless of the proportions of argentous oxide and silver oxide in the positive active material 3, the voltage of the battery can be completely controlled by using at least 0.05g of silver per 1g of silver oxide in the positive active material.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は小型携帯電子機器などに用いる酸化第二銀また
は酸化銀と酸化第二銀との混合物を正極活物質とする酸
化第二銀電池に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a ferric oxide battery using ferric oxide or a mixture of silver oxide and ferric oxide as a positive electrode active material for use in small portable electronic devices, etc. It is.

従来技術とその間r点 小型携帯電子機器の普及に伴い、小型で大容士の酸化銀
M!池が広く用いられるようになってきているが、正極
活物質として単位体積当りの放電容量が酸化銀より大き
い酸化第二銀を、単独または酸化銀と混合させて用いる
場合、その放電反応は酸化第二銀が酸化銀に還元される
電位の1.8vと、酸化銀が銀に還元される電位の1.
5vとの2段階になるという欠点があった。
Conventional technology and the r-point between them With the spread of small portable electronic devices, small and large size silver oxide M! However, when ferric oxide, which has a higher discharge capacity per unit volume than silver oxide, is used alone or in combination with silver oxide as a positive electrode active material, the discharge reaction is caused by oxidation. 1.8V, the potential at which ferric silver is reduced to silver oxide, and 1.8V, the potential at which silver oxide is reduced to silver.
There was a drawback that it was in two stages with 5V.

この欠点を解消する考え方は、正極活物質中の酸化第二
銀を正極集電体を兼ねる正極容器に直1&Jfi?触さ
せないようにすることである。
The idea to eliminate this drawback is to directly transfer the silver oxide in the positive electrode active material to the positive electrode container, which also serves as the positive electrode current collector. It is important not to let them touch it.

その方法は例えば菊閥昭52−62629号、特開昭5
5−j6233号各公報に示された・如く、陽極合剤と
陽極缶との間にtA層を設けたり、特公昭56−977
6号、56−29831号、56−29852号各公報
に示された如く、陽極合剤の陰極対向面を口元して銀ま
たは銀と酸化銀との混合物から成る75Mを設けたりす
ることである。
For example, Kikufutsu No. 52-62629, Japanese Unexamined Patent Publication No. 5
As shown in each publication No. 5-j6233, a tA layer is provided between the anode mixture and the anode can, and
6, 56-29831, and 56-29852, 75M made of silver or a mixture of silver and silver oxide is provided at the mouth of the anode mixture facing the cathode. .

しかしながら前者の方法は陽極合剤と陽極缶とを物理的
に接触させるだけであるため、電池電圧の制御が不安定
になり、後者の方法は薄層の厚み分だけ正極活物質の景
が減少し、電池の小型化仙向に対し、容量のi保が困難
になるという欠点は克服できなかった。
However, since the former method only physically contacts the anode mixture and the anode can, control of the battery voltage becomes unstable, and the latter method reduces the visibility of the cathode active material by the thickness of the thin layer. However, with the trend toward smaller batteries, it has been difficult to maintain the capacity, which has not been overcome.

発明の目的 本発明は正極活物質に酸化第二銀を単独または酸化銀と
混合させて用いる酸化第二銀電池に関するもので、その
目的は電池電圧の制御を安定にすることにある。
OBJECTS OF THE INVENTION The present invention relates to a ferric oxide battery that uses ferric oxide alone or in combination with silver oxide as a positive electrode active material, and its purpose is to stabilize control of battery voltage.

発明の構成 本発明は上記の如き酸化第二銀電池における電池電圧の
制御は、正極集電体を兼ねる正極容器内に設けられた銀
層が該正極容器に確実に接触しているとともに銀の量に
依存していることに着目してなされたものである。すな
わち正極活物質中の酸化第二銀は前記銀層を酸化して酸
化銀に変化させ、同時に自らも還元されて酸化銀となる
。こうして生成された酸化銀は放電により還元されて銀
になり、再度正極活物質中の酸化第二銀により酸化され
て酸化銀になる平衡反応により電池電圧の制御が行なわ
れる。この平衡反応の過程において銀が常時正極容器内
に存在していることが必要条件である。
Structure of the Invention The present invention is directed to controlling the battery voltage in the above-described silver oxide battery by ensuring that the silver layer provided in the positive electrode container, which also serves as a positive electrode current collector, is in reliable contact with the positive electrode container, and that the silver layer is in contact with the positive electrode container. This was done by focusing on the fact that it depends on quantity. That is, the second silver oxide in the positive electrode active material oxidizes the silver layer and changes it into silver oxide, and at the same time is itself reduced to become silver oxide. The silver oxide thus produced is reduced to silver by discharge, and is oxidized again by the second silver oxide in the positive electrode active material to become silver oxide, thereby controlling the battery voltage through an equilibrium reaction. It is a necessary condition that silver is always present in the positive electrode container during the course of this equilibrium reaction.

実施例 第1図は本発明に関る酸化第二銀電池の断面図で、1は
正極集電体を兼ねる正極容器、2は正極容器の内側底面
に電気的に確実に接触するように設けられた銀層、5は
酸化第二鎖単独または酸化第二銀と酸化銀との混合物か
ら成る正極活物質、4は負極集電体を兼ねる負極容器、
5は負極活物質、6はプラスチック製半透膜、セロハン
を複数枚積層してなる七パレータS7は不純布から成る
電解液保持層、8はガスケットである。銀層2は、銀箔
を打ち抜き、正極容器1内に挿入する方法、銀粉末を必
要員秤量し、挿入、圧着する方法、正極活物質5の底面
を還元し、正極容器1内に挿入する方法等により設ける
ことができる。
Embodiment FIG. 1 is a cross-sectional view of a silver oxide battery according to the present invention, in which 1 is a positive electrode container that also serves as a positive electrode current collector, and 2 is a positive electrode container that is provided to ensure electrical contact with the inner bottom surface of the positive electrode container. 5 is a positive electrode active material consisting of a second oxidized chain alone or a mixture of second silver oxide and silver oxide; 4 is a negative electrode container that also serves as a negative electrode current collector;
5 is a negative electrode active material, 6 is a plastic semipermeable membrane, 7 is a pallet made of a plurality of layers of cellophane, and 7 is an electrolyte retaining layer made of impure cloth. 8 is a gasket. The silver layer 2 can be formed by punching out silver foil and inserting it into the cathode container 1, by weighing the necessary amount of silver powder, inserting it, and pressing it together, or by reducing the bottom surface of the cathode active material 5 and inserting it into the cathode container 1. It can be provided by etc.

この時の銀の鼠は前述の平衡反応に対して、常時正極容
器内に存在しうる量だけが必要である。
At this time, only the amount of silver that can always be present in the positive electrode container is required for the above-mentioned equilibrium reaction.

表−1は正極容器の内側底面に、銀粉末を秤量すること
により酸化第二銀1gに対する銀の量を種々変化させて
銀層を形成するとともに、正極活物質の組成も種々変化
させて直径7J3「φ、高さ1.6鯰のボタン型の酸化
第二銀電池としたものを1各々100個製作し1電池電
圧の制御ができた個数を示したものである。
Table 1 shows that a silver layer was formed on the inner bottom surface of the positive electrode container by varying the amount of silver per 1 g of ferric oxide by weighing silver powder, and the composition of the positive electrode active material was also varied. 7J3 "100 button-shaped ferric oxide batteries with a diameter of 1.6 mm in height were manufactured, and the number of batteries for which the voltage of each battery could be controlled is shown.

表−1 表−1から正極活物質中の酸化第二銀1gに対する銀の
1を0.0.05g以上とすれば酸化銀と酸化第二銀と
の組成をどのようにしても電圧制御は完全になることが
わかる。
Table 1 From Table 1, if the ratio of silver to 1 g of silver oxide in the positive electrode active material is 0.0.05 g or more, voltage control is possible no matter what the composition of silver oxide and silver oxide is. I know it will become perfect.

発明の効果 実施例において詳述した如く、本発明は正極容器の内側
底面に設ける銀の量を、正極活物質中の酸化第二銀1g
当りの割合に換算するとともに、そのPを0.0.05
g以上とすれば、電圧制御が完全な酸化第二銀電池を得
ることができる。
Effects of the Invention As detailed in the Examples, the present invention has the advantage of reducing the amount of silver provided on the inner bottom surface of the positive electrode container to 1 g of silver oxide in the positive electrode active material.
Convert it to a hit ratio and convert the P to 0.0.05
g or more, a silver oxide battery with perfect voltage control can be obtained.

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

第1図は本発明に関る酸化第二銀電池の断面図である。 1・・・正極容器 2・・・銀層 5・・・正極活物質 FIG. 1 is a sectional view of a silver oxide battery according to the present invention. 1... Positive electrode container 2...Silver layer 5... Positive electrode active material

Claims (1)

【特許請求の範囲】[Claims] 正極容器の内側底面に電気的に接触させるとともに、正
極活物質中の酸化第二銀1gに対する量が0.05g以
上となるように銀を配したことを特徴とする酸化第二銀
電池。
A ferric oxide battery, characterized in that silver is placed in electrical contact with the inner bottom surface of a cathode container and in an amount of 0.05 g or more per 1 g of ferric oxide in the cathode active material.
JP18603784A 1984-09-05 1984-09-05 Silver oxide battery Pending JPS6164066A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18603784A JPS6164066A (en) 1984-09-05 1984-09-05 Silver oxide battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18603784A JPS6164066A (en) 1984-09-05 1984-09-05 Silver oxide battery

Publications (1)

Publication Number Publication Date
JPS6164066A true JPS6164066A (en) 1986-04-02

Family

ID=16181292

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18603784A Pending JPS6164066A (en) 1984-09-05 1984-09-05 Silver oxide battery

Country Status (1)

Country Link
JP (1) JPS6164066A (en)

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