JPH0377651B2 - - Google Patents
Info
- Publication number
- JPH0377651B2 JPH0377651B2 JP10984083A JP10984083A JPH0377651B2 JP H0377651 B2 JPH0377651 B2 JP H0377651B2 JP 10984083 A JP10984083 A JP 10984083A JP 10984083 A JP10984083 A JP 10984083A JP H0377651 B2 JPH0377651 B2 JP H0377651B2
- Authority
- JP
- Japan
- Prior art keywords
- aluminum foil
- cathode material
- conductive metal
- sec
- aluminum
- 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
Links
Landscapes
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Electrolytic Production Of Metals (AREA)
- Physical Vapour Deposition (AREA)
Description
産業上の利用分野
この発明は電解コンデンサ用陰極材料の製造方
法に関する。
この明細書において、アルミニウムという語は
純アルミニウムのほかにアルミニウム合金も含む
ものとする。
従来の技術
従来、電解コンデンサ用陰極材料は、アルミニ
ウム箔にエツチングを施して表面積を拡大するこ
とによつて製造されていた。
発明が解決しようとする課題
ところが、従来の陰極材料では、アルミニウム
箔の材質、熱処理条件、エツチング条件などによ
つて陰極材料としての性能、主として静電容量に
ばらつきが生じるという問題があつた。また、エ
ツチングは湿式処理であるため廃液処理の問題が
あり、処理設備が必要となつてコストが高くなる
とともに、作業が面倒になるという問題があつ
た。
そこで、本出願人は、先に、アルミニウム箔の
表面をエツチングにより粗面化した後、この粗面
に上記アルミニウム箔よりも高純度のアルミニウ
ムを真空中で蒸着させる電解コンデンサ用アルミ
ニウム箔の製造方法を提案した。しかしながら、
この方法でも、エツチング工程が含まれるので、
エツチング工程を実施することによる上記問題は
以前として存在する。また、エツチングにより粗
面化した後に、アルミニウムを真空中で蒸着させ
ると、アルミニウム箔の粗面が平滑化されて表面
積増大効果は少なくなる。
この発明は、上記のような問題を一挙に解決
し、静電容量等性能のばらつきが少なく、コスト
が安く、しかも表面が多孔質性で表面積が著しく
増大した電解コンデンサ用陰極材料の製造方法を
提供することを目的とするものである。
問題点を解決するための手段
この発明の電解コンデンサ用陰極材料の製造方
法は、アルミニウム箔の表面に、このアルミニウ
ム箔よりも誘電率の高い導電性金属を蒸着させる
にあたり、アルミニウム箔と、上記導電性金属を
具備した蒸発源との距離を10〜100cmとし、不活
性ガス雰囲気中において、蒸着速度10〜5000Å/
secで蒸着させることを特徴とするものである。
上記において、アルミニウム箔よりも誘電率の
高い導電性金属としてはAu、Ag、Ti、Cr、Zn、
Al、Si、Ge、Co、Sn、Ta、Fe、Cu、Pb、Ni、
Bi、Mn等またはこれらの合金が使用されるが、
その中でもAu、Ag、Ti、Crが代表的である。
蒸着膜を形成する方法としては、イオンプレー
テイング法および真空蒸着法などがある。
蒸着膜の形成は、アルゴン、ヘリウム等の不活
性ガス雰囲気中で行なうべきである。不活性ガス
雰囲気中で蒸着膜の形成を行なうと、金属蒸気を
散乱させ、蒸着結晶寸法を小さくさせることがで
きる。したがつて、得られた蒸着膜は、多孔質状
となり、その表面に微細な凹部が均一かつ高密度
に形成されて陰極材料の表面積が拡大され、静電
容量が増大する。
アルミニウム箔よりも誘電率の高い導電性金属
を、アルミニウム箔に蒸着させるさいのアルミニ
ウム箔と、上記高導電性金属を具備した蒸発源と
アルミニウム箔との距離は10〜100cmとすべきで
あるが、その理由は次の通りである。すなわち、
上記距離が10cm未満であれば、アルミニウム箔が
蒸発源に近付きすぎることになつて、アルミニウ
ム箔が金属を蒸発させるさいの加熱により溶ける
おそれがあるとともに、アルミニウム箔が高温に
なり、アルミニウム箔表面に到達した蒸発粒子に
より構成される金属物質が溶け広がつて蒸着膜が
多孔質状とならず、100cmを越えると成膜効率が
悪くなるからである。
また、蒸着速度は10〜5000Å/secとすべきで
あるが、その理由は次の通りである。すなわち、
10Å/sec未満では生産性が悪くなり、5000Å/
secを越えるには上記導電性金属をかなり高温に
加熱する必要があるために、アルミニウム箔が金
属を蒸発させるさいの加熱により溶けるおそれが
あるとともに、アルミニウム箔が高温になり、ア
ルミニウム箔表面に到達した蒸発粒子により構成
される金属物質が溶け広がつて蒸着膜が多孔質状
とならないからである。
実施例
つぎに、この発明の実施例を比較例とともに示
す。
実施例
アルゴンガス圧9×10-4Torrに保つた真空槽
内の上部に、表面をクリーニングした厚さ0.1mm
のA1100−H製アルミニウム箔を配置しておい
た。一方、真空槽内の下部でかつアルミニウム箔
の下方にスズからなる蒸着物質を備えた蒸発源を
配置しておいた。アルミニウム箔と蒸発源との距
離は25cmであつた。そして、イオンプレーテイン
グ法により、蒸着速度1000Å/secでアルミニウ
ム箔の表面にスズからなる厚さ1.0μmの蒸着膜を
形成した。こうしてアルミニウム箔の表面にスズ
製蒸着膜を形成してなる陰極材料を得た。この蒸
着膜の表面には微細な凹部が均一かつ高密度に形
成されていた。
比較例
厚さ0.1mmの純度99.8wt%のアルミニウム箔を、
液温60℃で2wt%塩酸溶液中でD.C.20A/50cm2の
電流密度で300秒間エツチングして陰極材料を得
た。
上記のようにして得た2種の陰極材料の静電容
量を、それぞれ液温30℃の10wt%ホウ酸アンモ
ニウム溶液中で測定した。その結果を下表にまと
めて示す。
INDUSTRIAL APPLICATION FIELD This invention relates to a method for manufacturing a cathode material for an electrolytic capacitor. In this specification, the term aluminum includes not only pure aluminum but also aluminum alloys. Prior Art Conventionally, cathode materials for electrolytic capacitors have been manufactured by etching aluminum foil to increase its surface area. Problems to be Solved by the Invention However, with conventional cathode materials, there has been a problem in that the performance as a cathode material, mainly in capacitance, varies depending on the material of the aluminum foil, heat treatment conditions, etching conditions, etc. Furthermore, since etching is a wet process, there is a problem in waste liquid treatment, which requires treatment equipment, which increases costs and makes the work troublesome. Therefore, the present applicant has developed a method for manufacturing aluminum foil for electrolytic capacitors, in which the surface of the aluminum foil is first roughened by etching, and then aluminum of higher purity than the aluminum foil is vapor-deposited on the rough surface in vacuum. proposed. however,
This method also includes an etching process, so
The above-mentioned problems with performing the etching process still exist. Furthermore, if aluminum is deposited in vacuum after the surface has been roughened by etching, the rough surface of the aluminum foil will be smoothed and the effect of increasing the surface area will be reduced. This invention solves the above-mentioned problems at once, and provides a method for manufacturing a cathode material for electrolytic capacitors that has less variation in performance such as capacitance, is low in cost, and has a porous surface with a significantly increased surface area. The purpose is to provide Means for Solving the Problems The method for producing a cathode material for an electrolytic capacitor of the present invention involves depositing a conductive metal having a higher dielectric constant than the aluminum foil on the surface of the aluminum foil. The distance to the evaporation source containing a reactive metal is 10 to 100 cm, and the evaporation rate is 10 to 5000 Å/in an inert gas atmosphere.
It is characterized by being deposited at sec. In the above, conductive metals with higher permittivity than aluminum foil include Au, Ag, Ti, Cr, Zn,
Al, Si, Ge, Co, Sn, Ta, Fe, Cu, Pb, Ni,
Bi, Mn, etc. or their alloys are used, but
Among them, Au, Ag, Ti, and Cr are representative. Methods for forming a deposited film include an ion plating method and a vacuum deposition method. Formation of the vapor deposited film should be performed in an inert gas atmosphere such as argon or helium. When a deposited film is formed in an inert gas atmosphere, metal vapor can be scattered and the size of deposited crystals can be reduced. Therefore, the obtained vapor-deposited film becomes porous, and fine recesses are uniformly and densely formed on its surface, expanding the surface area of the cathode material and increasing the capacitance. When a conductive metal with a higher dielectric constant than the aluminum foil is evaporated onto the aluminum foil, the distance between the aluminum foil and the evaporation source containing the above-mentioned highly conductive metal should be 10 to 100 cm. , The reason is as follows. That is,
If the above distance is less than 10cm, the aluminum foil will be too close to the evaporation source, and there is a risk that the aluminum foil will melt due to the heat generated during evaporation of the metal, and the aluminum foil will become hot, causing the surface of the aluminum foil to This is because the metal substance constituted by the evaporated particles that have arrived will melt and spread, preventing the evaporated film from becoming porous, and if the thickness exceeds 100 cm, the film formation efficiency will deteriorate. Further, the deposition rate should be 10 to 5000 Å/sec, and the reason is as follows. That is,
If it is less than 10Å/sec, productivity will be poor, and if it is less than 5000Å/sec,
To exceed sec, it is necessary to heat the conductive metal to a considerably high temperature, so there is a risk that the aluminum foil will melt due to the heating when the metal is evaporated, and the aluminum foil will become hot enough to reach the surface of the aluminum foil. This is because the metal substance formed by the evaporated particles will not melt and spread and the evaporated film will not become porous. Examples Next, examples of the present invention will be shown together with comparative examples. Example: A 0.1 mm thick surface with a cleaned surface was placed on the top of a vacuum chamber maintained at an argon gas pressure of 9×10 -4 Torr.
An aluminum foil made of A1100-H was placed. On the other hand, an evaporation source containing an evaporation substance made of tin was placed in the lower part of the vacuum chamber and below the aluminum foil. The distance between the aluminum foil and the evaporation source was 25 cm. Then, by ion plating, a 1.0 μm thick vapor deposition film of tin was formed on the surface of the aluminum foil at a vapor deposition rate of 1000 Å/sec. In this way, a cathode material was obtained in which a vapor-deposited tin film was formed on the surface of an aluminum foil. Fine depressions were uniformly and densely formed on the surface of this deposited film. Comparative example: Aluminum foil with a purity of 99.8wt% and a thickness of 0.1mm,
A cathode material was obtained by etching in a 2 wt % hydrochloric acid solution at a liquid temperature of 60° C. at a current density of DC 20 A/50 cm 2 for 300 seconds. The capacitances of the two types of cathode materials obtained as described above were each measured in a 10 wt % ammonium borate solution at a liquid temperature of 30°C. The results are summarized in the table below.
【表】
以上の結果から明らかなように、この発明の方
法で製造された電解コンデンサ用陰極材料は、従
来の陰極材料に比較して静電容量が大きくなつて
いる。
発明の効果
この発明の電解コンデンサ用陰極材料製造方法
によれば、アルミニウム箔の表面に、このアルミ
ニウム箔よりも誘電率の高い導電性金属を蒸着さ
せるにあたり、アルミニウム箔と、上記導電性金
属を具備した蒸発源との距離を10〜100cmとし、
不活性ガス雰囲気中において、蒸着速度10〜5000
Å/secで蒸着させるので、得られた導電性金属
からなる蒸着膜が多孔質状となつて、その表面に
微細な凹部が均一かつ高密度に形成されることに
なり、製造された陰極材料の表面積が著しく増大
する。また、この発明の方法によれば、アルミニ
ウム箔の材質に無関係に、箔の表面に誘電率の大
きな導電性金属蒸着膜を形成しうる。したがつ
て、上記表面積増大効果と相俟つて、製造された
陰極材料の静電容量が著しく増大する。しかも、
製造された陰極材料には、性能、主として、静電
容量のばらつきが生じることはない。さらに、ア
ルミニウム箔の材質を適宜選択することにより得
られた陰極材料の機械的強度を大きくできる。
また、従来のようにエツチング処理を行なう必
要がないので、廃液処理の問題もなく、コストが
安くなるとともに作業が容易になる。[Table] As is clear from the above results, the electrolytic capacitor cathode material produced by the method of the present invention has a larger capacitance than conventional cathode materials. Effects of the Invention According to the method for producing a cathode material for an electrolytic capacitor of the present invention, when depositing a conductive metal having a higher dielectric constant than the aluminum foil on the surface of the aluminum foil, the aluminum foil and the conductive metal are provided. The distance to the evaporation source is 10 to 100 cm.
Deposition rate 10-5000 in inert gas atmosphere
Because the vapor deposition is performed at a rate of Å/sec, the resulting vapor-deposited film made of conductive metal becomes porous, with fine depressions uniformly and densely formed on its surface, which improves the quality of the produced cathode material. surface area increases significantly. Further, according to the method of the present invention, a conductive metal vapor deposition film having a large dielectric constant can be formed on the surface of the aluminum foil, regardless of the material of the aluminum foil. Therefore, together with the surface area increasing effect, the capacitance of the produced cathode material increases significantly. Moreover,
The produced cathode materials are free from variations in performance, primarily capacitance. Furthermore, by appropriately selecting the material of the aluminum foil, the mechanical strength of the resulting cathode material can be increased. Further, since there is no need to perform etching treatment as in the conventional method, there is no problem of waste liquid treatment, resulting in lower costs and easier work.
Claims (1)
箔よりも誘電率の高い導電性金属を蒸着させるに
あたり、アルミニウム箔と、上記導電性金属を具
備した蒸発源との距離を10〜100cmとし、不活性
ガス雰囲気中において、蒸着速度10〜5000Å/
secで蒸着させることを特徴とする電解コンデン
サ用陰極材料の製造方法。1. When depositing a conductive metal with a higher dielectric constant than the aluminum foil on the surface of the aluminum foil, the distance between the aluminum foil and the evaporation source containing the conductive metal is set at 10 to 100 cm, and an inert gas atmosphere is set. In the middle, the deposition rate is 10~5000Å/
A method for producing a cathode material for an electrolytic capacitor, characterized by vapor deposition using sec.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10984083A JPS601826A (en) | 1983-06-17 | 1983-06-17 | Cathode material for electrolytic condenser |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10984083A JPS601826A (en) | 1983-06-17 | 1983-06-17 | Cathode material for electrolytic condenser |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS601826A JPS601826A (en) | 1985-01-08 |
| JPH0377651B2 true JPH0377651B2 (en) | 1991-12-11 |
Family
ID=14520530
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10984083A Granted JPS601826A (en) | 1983-06-17 | 1983-06-17 | Cathode material for electrolytic condenser |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS601826A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61180420A (en) * | 1985-02-05 | 1986-08-13 | 昭和アルミニウム株式会社 | Cathode material for electrolytic capacitor |
| WO2001020625A1 (en) | 1999-09-10 | 2001-03-22 | Matsushita Electric Industrial Co., Ltd. | Solid electrolytic capacitor and production method thereof, and conductive polymer polymerizing oxidizing agent solution |
-
1983
- 1983-06-17 JP JP10984083A patent/JPS601826A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS601826A (en) | 1985-01-08 |
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