JPH01283765A - Organic electrolyte cell - Google Patents
Organic electrolyte cellInfo
- Publication number
- JPH01283765A JPH01283765A JP63113916A JP11391688A JPH01283765A JP H01283765 A JPH01283765 A JP H01283765A JP 63113916 A JP63113916 A JP 63113916A JP 11391688 A JP11391688 A JP 11391688A JP H01283765 A JPH01283765 A JP H01283765A
- Authority
- JP
- Japan
- Prior art keywords
- aluminum
- lithium
- foaming substance
- discharge
- 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
Links
- 239000005486 organic electrolyte Substances 0.000 title claims abstract description 10
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 28
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 27
- 229910052744 lithium Inorganic materials 0.000 claims abstract description 18
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000006260 foam Substances 0.000 claims description 9
- 239000011149 active material Substances 0.000 claims description 3
- 239000003792 electrolyte Substances 0.000 abstract description 6
- 229910045601 alloy Inorganic materials 0.000 abstract description 5
- 239000000956 alloy Substances 0.000 abstract description 5
- 238000005275 alloying Methods 0.000 abstract description 3
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 abstract description 2
- 238000005187 foaming Methods 0.000 abstract 4
- 239000000126 substance Substances 0.000 abstract 4
- 230000006866 deterioration Effects 0.000 abstract 1
- 239000011888 foil Substances 0.000 description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 238000007789 sealing Methods 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 2
- 239000005751 Copper oxide Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910000431 copper oxide Inorganic materials 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- -1 polypropylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- MBMLMWLHJBBADN-UHFFFAOYSA-N Ferrous sulfide Chemical compound [Fe]=S MBMLMWLHJBBADN-UHFFFAOYSA-N 0.000 description 1
- QDDVNKWVBSLTMB-UHFFFAOYSA-N [Cu]=O.[Li] Chemical compound [Cu]=O.[Li] QDDVNKWVBSLTMB-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910000416 bismuth oxide Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- TYIXMATWDRGMPF-UHFFFAOYSA-N dibismuth;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Bi+3].[Bi+3] TYIXMATWDRGMPF-UHFFFAOYSA-N 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 150000002642 lithium compounds Chemical class 0.000 description 1
- MHCFAGZWMAWTNR-UHFFFAOYSA-M lithium perchlorate Chemical compound [Li+].[O-]Cl(=O)(=O)=O MHCFAGZWMAWTNR-UHFFFAOYSA-M 0.000 description 1
- 229910001486 lithium perchlorate Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000007773 negative electrode material Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 239000007774 positive electrode material Substances 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/06—Electrodes for primary cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/50—Methods or arrangements for servicing or maintenance, e.g. for maintaining operating temperature
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/14—Cells with non-aqueous electrolyte
- H01M6/16—Cells with non-aqueous electrolyte with organic electrolyte
Abstract
Description
【発明の詳細な説明】 産業上の利用分野 本発明は、有機電解質電池の改良に関するものである。[Detailed description of the invention] Industrial applications The present invention relates to improvements in organic electrolyte batteries.
従来の技術
リチウムを活物質とする有機電解質電池は、高エネルギ
ー密度を有するところから、電子ウォッチをはじめ各種
の小型電子機器用電源として注目されている。しかしな
がら、金属リチウムは、非常に活性なため、リチウム表
面へのリチウム化合物膜の形成による内部抵抗の上昇が
あり、さらに放電の進行に伴なってリチウム表面積の低
下による内部抵抗の上昇がみられる。このために、電子
ウォッチなどのパルス放電全行なうと、閉路電圧の低下
が大きくなり、電池容量を最後まで有効に使用できなく
なる。BACKGROUND OF THE INVENTION Organic electrolyte batteries using lithium as an active material have high energy density and are attracting attention as power sources for various small electronic devices including electronic watches. However, since metallic lithium is very active, the internal resistance increases due to the formation of a lithium compound film on the lithium surface, and furthermore, as the discharge progresses, the internal resistance increases due to a decrease in the lithium surface area. For this reason, when an electronic watch or the like performs full pulse discharge, the drop in closed circuit voltage increases, making it impossible to use the battery capacity effectively to the end.
このような欠点を解消するために、リチウム表面にアル
ミニウム箔をはりつけ1合金層の形成により発生する負
極の微細化状態やシワ状態により負極表面積を増大させ
、内部抵抗を低下させるという提案がなされている。In order to eliminate these drawbacks, a proposal has been made to attach aluminum foil to the lithium surface and increase the surface area of the negative electrode through the miniaturization and wrinkles of the negative electrode caused by the formation of a 1-alloy layer, thereby lowering the internal resistance. There is.
発明が解決しようとする課題
しかしながら1通常のアルミニウム箔を使用するとアル
ミニウム箔の体積分の電解液が減少するため、電池の反
応効率が落ち、容量低下をまねくばかりでなく、放電末
期ではパルス放電特性の低下がおこる。また、通常のア
ルミニウム箔では、リチウムとの接触面積が小さいため
、合金化が均一に進まず、正極との対向面の合金層は粒
子が粗く、負極表面積の増加も少ないため、パルス特性
も満足いくものが得られない。さらにはアルミニウム箔
の厚みが厚くなると、アルミニウムが合金化されずに残
り、リチウムの反応を阻害して放電容量を低下させる等
の問題があった。Problems to be Solved by the Invention However, 1. If ordinary aluminum foil is used, the electrolyte will be reduced by the volume of the aluminum foil, which will not only reduce the reaction efficiency of the battery and cause a decrease in capacity, but also cause the pulse discharge characteristics to deteriorate at the end of discharge. A decrease occurs. In addition, with ordinary aluminum foil, the contact area with lithium is small, so alloying does not proceed uniformly, and the alloy layer on the surface facing the positive electrode has coarse particles, and the increase in the negative electrode surface area is small, so the pulse characteristics are also satisfactory. I can't get anything. Furthermore, when the thickness of the aluminum foil becomes thicker, there is a problem that aluminum remains unalloyed, inhibits the reaction of lithium, and reduces the discharge capacity.
本発明は上記のような問題点を解消し、電解液の減少を
少なくし1合金化を均一にして内部抵抗が低く、パルス
放電にすぐれた有機電解質電池を提供することを目的と
する。It is an object of the present invention to solve the above-mentioned problems, to provide an organic electrolyte battery that reduces the loss of electrolyte solution, uniformly forms a single alloy, has low internal resistance, and is excellent in pulse discharge.
課題を解決するための手段
このような問題点を解決するために本発明は、アルミニ
ウム発泡体を、負極のリチウム反応表面に載置して電池
を構成したものである。Means for Solving the Problems In order to solve these problems, the present invention constructs a battery by placing an aluminum foam on the lithium reaction surface of the negative electrode.
作用
このアルミニウム発泡体を使用して電池を構成すること
により、アルミニウム発泡体中に、電解液が浸透し、電
解液の減少を防いで、反応効率の低下を防ぐ。また、ア
ルミニウム発泡体では1表面積が通常の板状あるいは箔
状のアルミニウムに比べ1表面積が増大する。そのため
に、アルミニウムと、リチウムとの合金化のスピードが
早く。Function: By constructing a battery using this aluminum foam, the electrolyte permeates into the aluminum foam, preventing the electrolyte from decreasing and reducing reaction efficiency. Moreover, the surface area of aluminum foam is larger than that of ordinary plate-shaped or foil-shaped aluminum. Therefore, the speed of alloying of aluminum and lithium is fast.
均一で、微細な粒子状の合金層を得ることができ。A uniform, finely grained alloy layer can be obtained.
アルミニウム層を厚くする場合においても1合金化され
ないアルミニウム部分が発生することがなくなり、内部
抵抗が低くパルス放電特性にすぐれ。Even when the aluminum layer is made thicker, there are no aluminum parts that are not alloyed, resulting in low internal resistance and excellent pulse discharge characteristics.
安定した放電特性を得ることが可能となる。It becomes possible to obtain stable discharge characteristics.
実施例 以下、本発明の詳細な説明する。Example The present invention will be explained in detail below.
第1図はリチウム−酸化銅系のボタン型有機電解質電池
を示す。第1図において、1は厚さ02MMの片面にニ
ッケルメッキしたステンレス鋼板を打ち抜き加工した正
極ケース、2は厚さ0.2MMの片面ニッケルメッキを
施したステンレス鋼製封口板、3は負極活物質の金属リ
チウムで、封口板2の内面の凹凸部に圧着固定されてい
る。4は酸化銅を主成分とする活物質に導電材としての
黒鉛と結着剤とを混合して成形し、これを正極ケースに
位置させ、断面り字状のステンレス製正極リング6とと
もに加圧圧着した正極、6は本発明によるアルミニウム
発泡体で、厚みは100μmを使用し、一部がリチウム
金属内に埋没するよう圧力を加えてリチウムの反応面側
に載置した。7はポリプロピレン製のセパレータ、 8
ij:ポリプロピレン展のガスケットである。電解液に
は、炭酸プロピレンと、1−2ジメトキシエタンとの混
合有機溶媒に、過塩素酸リチウムを溶解した液を使用し
、電池サイズは、外径9.5ff、高さ2.7MMとし
た。FIG. 1 shows a button-type organic electrolyte battery based on lithium-copper oxide. In Figure 1, 1 is a positive electrode case made by punching a stainless steel plate with a thickness of 02 mm and nickel plated on one side, 2 is a stainless steel sealing plate with a thickness of 0.2 mm and nickel plated on one side, and 3 is a negative electrode active material. The metal lithium is crimped and fixed to the uneven portion of the inner surface of the sealing plate 2. 4 is formed by mixing an active material containing copper oxide as a main component with graphite as a conductive material and a binder, placing this in a positive electrode case, and pressurizing it together with a stainless steel positive electrode ring 6 having an angular cross section. The deposited positive electrode 6 was an aluminum foam according to the present invention having a thickness of 100 μm, and was placed on the lithium reaction surface side under pressure so that a portion of the positive electrode was buried in the lithium metal. 7 is a polypropylene separator, 8
ij: Polypropylene gasket. The electrolyte used was a solution in which lithium perchlorate was dissolved in a mixed organic solvent of propylene carbonate and 1-2 dimethoxyethane, and the battery size was 9.5 ff in outer diameter and 2.7 mm in height. .
第2図は上記サイズの電池を温度20′C下で30にΩ
の負荷をつないで放電した場合の特性を示す。図中ムは
1本発明のアルミニウム発泡体を使用した電池、Bは通
常のアルミニウム箔を使用した電池、C[アルミニウム
箔を使用しない電池の放電曲線である。Figure 2 shows a battery of the above size with a resistance of 30 Ω at a temperature of 20'C.
This shows the characteristics when a load is connected and discharged. In the figure, M is a battery using the aluminum foam of the present invention, B is a battery using a normal aluminum foil, and C is a discharge curve of a battery using no aluminum foil.
第3図は、−10°C下で6にΩの負荷を毎秒7.8m
5s・Cかけ、72時間後の閉路電圧を放電深度別に示
したもので1図中ムは本発明のアルミニウム発泡体を使
用した電池、Bは通常のアルミニウム箔を使用した電池
、C[アルミニウム箔を使用しない電池である。Figure 3 shows a load of 6 Ω at 7.8 m/s at -10°C.
The closed-circuit voltage after 72 hours of 5s・C is shown by depth of discharge. It is a battery that does not use.
なお実施例では、正極活物質に酸化銅を使用した例につ
いて述べたが、正極にフッ化炭素、二酸化マンガン、硫
化鉄、酸化ビスマス等を使用した場合でも同様な効果が
得らnた。In the examples, an example was described in which copper oxide was used as the positive electrode active material, but similar effects were obtained when carbon fluoride, manganese dioxide, iron sulfide, bismuth oxide, etc. were used in the positive electrode.
発明の効果
以上のように、アルミニウム発泡体を、負極リチウムの
反応表面に載置することによって、放電中の内部抵抗が
低く、パルス特性にすぐれた有機電解質電池が得られた
。Effects of the Invention As described above, by placing an aluminum foam on the reaction surface of the lithium negative electrode, an organic electrolyte battery with low internal resistance during discharge and excellent pulse characteristics was obtained.
第1図は本発明の実施例による有機電解質電池の縦断面
図、第2図は放電カーブを示す図、第3図は放電深度別
の閉路電圧を示す図である。
1・・・・・・正極ケース、2・・・・・・封口板、3
・・・・・・負極。
4・・・・・・正極、6・・・・・・正極リング、6・
・・・・・アルミニウム発泡体、7・・・・・・セパレ
ータ、8・・・・・・ガスケット。
代理人の氏名 弁理士 中 尾 敏 男 ほか1名1−
−−ケース
2−−一辷T絨
5・−正本iリソグ
E−−−アルミ:つ4貞55浜本
7−−−でハ′″L−タ
8−一一乃′入ケ、ト
第3図
放iうま崖(泪FIG. 1 is a longitudinal cross-sectional view of an organic electrolyte battery according to an embodiment of the present invention, FIG. 2 is a diagram showing a discharge curve, and FIG. 3 is a diagram showing closed circuit voltage depending on the depth of discharge. 1...Positive electrode case, 2...Sealing plate, 3
・・・・・・Negative electrode. 4...Positive electrode, 6...Positive electrode ring, 6.
... Aluminum foam, 7 ... Separator, 8 ... Gasket. Name of agent: Patent attorney Toshio Nakao and 1 other person1-
--Case 2--One side T carpet 5・-Original i lithog E---Aluminum: Tsu 4 Tei 55 Hamamoto 7---Ha'''L-ta 8-11' insert, To 3rd Tuhoi Uma Cliff (Tears)
Claims (1)
とからなる電池であって、負極の反応側表面に、アルミ
ニウム発泡体を載置したことを特徴とする有機電解質電
池。An organic electrolyte battery comprising a negative electrode containing lithium as an active material, an organic electrolyte, and a positive electrode, characterized in that an aluminum foam is placed on the reaction side surface of the negative electrode.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63113916A JPH01283765A (en) | 1988-05-11 | 1988-05-11 | Organic electrolyte cell |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63113916A JPH01283765A (en) | 1988-05-11 | 1988-05-11 | Organic electrolyte cell |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01283765A true JPH01283765A (en) | 1989-11-15 |
Family
ID=14624404
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63113916A Pending JPH01283765A (en) | 1988-05-11 | 1988-05-11 | Organic electrolyte cell |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01283765A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH042050A (en) * | 1990-04-18 | 1992-01-07 | Matsushita Electric Ind Co Ltd | Organic electrolyte primary battery |
-
1988
- 1988-05-11 JP JP63113916A patent/JPH01283765A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH042050A (en) * | 1990-04-18 | 1992-01-07 | Matsushita Electric Ind Co Ltd | Organic electrolyte primary battery |
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