JPH0729576A - Manufacture of electrode for fuel cell - Google Patents

Manufacture of electrode for fuel cell

Info

Publication number
JPH0729576A
JPH0729576A JP5197729A JP19772993A JPH0729576A JP H0729576 A JPH0729576 A JP H0729576A JP 5197729 A JP5197729 A JP 5197729A JP 19772993 A JP19772993 A JP 19772993A JP H0729576 A JPH0729576 A JP H0729576A
Authority
JP
Japan
Prior art keywords
paste
electrode
gas supply
fuel cell
supply layer
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
JP5197729A
Other languages
Japanese (ja)
Inventor
Junko Shimizu
純子 清水
Taizo Yamamoto
泰三 山本
Hirohiko Koseki
宏彦 小関
Masataka Ueno
正隆 上野
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.)
Aisin AW Co Ltd
Equos Research Co Ltd
Original Assignee
Aisin AW Co Ltd
Equos Research 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 Aisin AW Co Ltd, Equos Research Co Ltd filed Critical Aisin AW Co Ltd
Priority to JP5197729A priority Critical patent/JPH0729576A/en
Publication of JPH0729576A publication Critical patent/JPH0729576A/en
Pending 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
    • Y02E60/30Hydrogen technology
    • Y02E60/50Fuel cells

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  • Inert Electrodes (AREA)

Abstract

PURPOSE:To enhance the performance of the fuel cell comprising an electrode composed of a reactive layer and a gas supply layer, by providing a state of bond therebetween in which the both layers are partially permeated one into the other, unlike a conventional state of bond therebetween in which a line of bond is in the form of a straight line, and thereby uniformly supplying a gas into the catalyst in the reactive layer through the gas supply layer. CONSTITUTION:Catalyst, ion-conductive polymer solution, and water are mixed with each other to prepare a paste. When coating this paste onto a porous sheet fixed within a predetermined reactive-paste coating frame, this coating is performed while suction is being conducted from a rear-face side of the porous sheet. As a result, a state wherein the paste has been permeated into the porous sheet is obtained. Thereafter, the paste is desiccated and hardened, whereupon there is produced an electrode 1 wherein a reactive layer 2 consisting of the paste material and a gas supply layer 3 consisting of the porous sheet are bonded together in such a manner as to partially permeate one into the other.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は燃料電池用電極の製造方
法に関し、特に塗布法による燃料電池用電極の製造方法
に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for manufacturing a fuel cell electrode, and more particularly to a method for manufacturing a fuel cell electrode by a coating method.

【0002】[0002]

【従来の技術】燃料電池において、触媒を含む反応層の
外側に、カーボンシート等の多孔質体よりなるガス供給
層を設けることにより、ガス(水素または酸素)を均等
に拡散しながら反応層に供給して電池反応の効率化を図
ることが行われている。
2. Description of the Related Art In a fuel cell, a gas supply layer made of a porous material such as a carbon sheet is provided outside a reaction layer containing a catalyst so that the gas (hydrogen or oxygen) is uniformly diffused in the reaction layer. In order to improve the efficiency of the battery reaction by supplying it.

【0003】ガス供給層に反応層を接合させる方法とし
ては、一般に両側より圧接する方法が採用されている
が、圧接による場合は接合面を均一に加圧することが困
難であった。また、圧接の際の高圧によって反応層中の
ガス導入路が破壊され、反応層へのガス供給を妨げてし
まうという欠点もあった。
As a method for joining the reaction layer to the gas supply layer, a method in which pressure is applied from both sides is generally adopted. However, in the case of pressure contact, it was difficult to uniformly press the joint surface. Further, there is a drawback that the gas introduction path in the reaction layer is destroyed by the high pressure during the pressure contact, and the gas supply to the reaction layer is hindered.

【0004】これらの欠点を解消すべく、特開平4−3
29264号公報には、反応層を形成する混合成分をア
ルコールでペースト状にしたものをガス供給層上に塗布
し、高温にて焼成することにより接合する方法が提案さ
れている。
In order to eliminate these drawbacks, JP-A-4-3
Japanese Patent No. 29264 proposes a method in which a paste containing mixed components forming a reaction layer is applied onto a gas supply layer, and the mixture is fired at a high temperature to join them.

【0005】[0005]

【発明が解決しようとする課題】ところが、圧接法ある
いは焼成法のいずれによって接合しても、反応層とガス
供給層とがほぼ整然と二分されてしまう(図4)ため、
反応層中のすべての触媒に均等にガスを供給することが
困難である。すなわち、ガス供給層から離れた位置にあ
る触媒の活性が低下してしまう。
However, the reaction layer and the gas supply layer are divided into two parts in an orderly manner, regardless of whether they are joined by the pressure welding method or the firing method (FIG. 4).
It is difficult to supply gas evenly to all the catalysts in the reaction layer. That is, the activity of the catalyst located at a position away from the gas supply layer is reduced.

【0006】[0006]

【課題を解決するための手段】本発明は、反応層とガス
供給層とからなる電極を得るに当たってこれら層同士の
接合状態を良好にし、ガス供給層を介して行われるガス
の供給を反応層中のほぼすべての触媒に対して満遍なく
行われるようにし、反応層における触媒の活性の偏りを
解消することを目的とする。
DISCLOSURE OF THE INVENTION According to the present invention, in obtaining an electrode composed of a reaction layer and a gas supply layer, the bonding state between these layers is made good, and the gas supplied through the gas supply layer is supplied to the reaction layer. The purpose of the present invention is to disperse the catalyst evenly in almost all the catalysts therein, and to eliminate the bias of the activity of the catalysts in the reaction layer.

【0007】この目的を達成するため、本発明は塗布法
による燃料電池用電極の製造方法を採用する。燃料電池
またはそのための電極の製造を塗布法によって行うこと
は従来より提案されている。たとえば特開平5−290
05号公報には、イオン導電性ポリマー等よりなる電解
質板上に電極触媒用のペーストをスクリーン印刷により
塗布して電極−電解質接合体を製造することが記載され
ている。しかしながら、ガス供給層に反応層を接合する
際に単に塗布法を適用しただけでは、上記したと同様に
これらの層が整然と二分された構造体となり、課題を解
決することができない。
To achieve this object, the present invention employs a method for manufacturing a fuel cell electrode by a coating method. It has been conventionally proposed to manufacture a fuel cell or an electrode therefor by a coating method. For example, Japanese Patent Laid-Open No. 5-290
Japanese Patent Publication No. 05 discloses that an electrode-catalyst paste is applied by screen printing onto an electrolyte plate made of an ion-conductive polymer or the like to produce an electrode-electrolyte assembly. However, if the coating method is simply applied when the reaction layer is joined to the gas supply layer, then these layers become a structure in which these layers are properly divided into two, and the problem cannot be solved.

【0008】そこで、本発明は、ガス供給層に反応層を
接合するための手法として塗布法を採用しつつ、塗布の
際に接合面とは反対側から吸引することにより反応層ペ
ーストをガス供給層に浸透させた状態とすることを想起
し、完成に至ったものである。
Therefore, the present invention adopts the coating method as a method for bonding the reaction layer to the gas supply layer, and at the time of coating, the reaction layer paste is gas-supplied by sucking from the side opposite to the bonding surface. It was completed by recalling that it was infiltrated into the layers.

【0009】すなわち本発明による燃料電池用電極の製
造方法は、触媒と溶剤と水を少なくとも含んで調製され
たペーストよりなる反応層をガス供給層上に形成するに
際して、ガス供給層の背面側より吸引しながら形成する
ことによりペーストをガス供給層に浸透せしめることを
特徴とする。
That is, in the method for producing a fuel cell electrode according to the present invention, when a reaction layer made of a paste prepared by containing at least a catalyst, a solvent and water is formed on the gas supply layer, the reaction layer is applied from the back side of the gas supply layer. It is characterized in that the paste is permeated into the gas supply layer by forming it while sucking.

【0010】ペーストのガス供給層への浸透深さは、ガ
ス供給層の細孔径および吸引の強さを調節することによ
ってコントロールされる。
The depth of penetration of the paste into the gas supply layer is controlled by adjusting the pore size and suction strength of the gas supply layer.

【0011】塗布用のペーストは、燃料電池の電解質を
構成すると同一のイオン導電性ポリマーの溶液を結着剤
として調製され得る。このイオン導電性ポリマー溶液中
のアルコール溶剤分は、塗布後の乾燥工程により除去す
ることができる。
The paste for coating can be prepared by using as a binder a solution of the same ion conductive polymer that constitutes the electrolyte of the fuel cell. The alcohol solvent content in the ion conductive polymer solution can be removed by a drying step after coating.

【0012】好ましくは、ペーストを塗布する前に該ペ
ーストを加熱乾燥することによりペースト中のアルコー
ル溶剤分のみを任意量除去し、該ペーストを塗布に適し
た粘度に調整する。
[0012] Preferably, the paste is heated and dried before the paste is applied to remove an arbitrary amount of the alcohol solvent content in the paste, and the paste is adjusted to have a viscosity suitable for application.

【0013】[0013]

【作用】反応層を形成すべきペーストをガス供給層を形
成すべき多孔質シート上に塗布するに際して、多孔質シ
ートの塗布面とは反対側から吸引しながら該塗布が行わ
れるので、ペーストが多孔質シートに少なくとも部分的
に浸透した状態が得られる。
When the paste for forming the reaction layer is applied to the porous sheet on which the gas supply layer is to be formed, the paste is applied while sucking from the side opposite to the application surface of the porous sheet. A state in which the porous sheet is at least partially penetrated is obtained.

【0014】[0014]

【実施例】触媒(Pt)を担持するカーボンブラック、
イオン導電性ポリマー(ナフィオン−登録商標)溶液お
よび水を1:13.3:4.0の割合で混合し、15分
間超音波撹拌した後、65℃の加熱条件に1時間保持し
て粘度調製して、塗布用ペーストを調製する。
Example: Carbon black supporting a catalyst (Pt),
The ion conductive polymer (Nafion-registered trademark) solution and water were mixed at a ratio of 1: 13.3: 4.0, ultrasonically stirred for 15 minutes, and then maintained at 65 ° C for 1 hour under heating conditions to adjust the viscosity. Then, a coating paste is prepared.

【0015】この塗布用ペーストを、塗布用の枠内に固
定した撥水処理済みのシート状多孔質体(カーボンシー
ト、金属発泡体等)上に塗布するが、その際、多孔質シ
ートの背面側より吸引しつつ塗布を行う。これにより、
塗布されるペーストが多孔質シート内に十分に浸透され
る。ペーストの多孔質体への浸透深さは、多孔質体の細
孔径および吸引の強さを調節することによりコントロー
ルする。
This coating paste is applied onto a water-repellent sheet-like porous body (carbon sheet, metal foam, etc.) fixed in a coating frame, with the back surface of the porous sheet at that time. Apply while sucking from the side. This allows
The applied paste penetrates well into the porous sheet. The penetration depth of the paste into the porous body is controlled by adjusting the pore size and suction strength of the porous body.

【0016】吸引しつつ塗布を終了した後、室温にて約
1時間乾燥して、ナフィオン溶液中のアルコール溶剤を
乾燥除去し、印刷用ペーストによる反応層を多孔質シー
トからなるガス供給層の上に積層形成する。上記のよう
に塗布用ペーストは多孔質シート内に浸透された状態で
乾燥固化されるので、このようにして得られる電極1に
おいては、反応層2が部分的にガス供給層3に入り込ん
だ接合状態が得られる(図1)。この接合状態より明ら
かなように、反応層2中の触媒担持量を減少させること
なくその実質的な厚みを薄くすることができ、コンパク
ト化が図られる。また、反応層2はガス供給層3と交絡
した構造となるため、これらの接合表面積が平面同士の
接合に比べて増大し、電極の抵抗値が低減される。
After the application is completed while sucking, the coating is dried at room temperature for about 1 hour to dry and remove the alcohol solvent in the Nafion solution, and the reaction layer formed by the printing paste is placed on the gas supply layer made of a porous sheet. To be laminated. As described above, since the coating paste is dried and solidified in a state of being permeated into the porous sheet, in the electrode 1 thus obtained, the reaction layer 2 partially joins the gas supply layer 3 and is bonded. The state is obtained (Fig. 1). As is apparent from this joined state, the substantial thickness of the reaction layer 2 can be reduced without reducing the amount of catalyst supported in the reaction layer 2, and the size can be reduced. Further, since the reaction layer 2 has a structure in which it is entangled with the gas supply layer 3, the bonding surface area of these is increased as compared with the bonding between flat surfaces, and the resistance value of the electrode is reduced.

【0017】以上のようにして同一構成の電極を2個作
成し、電解質となるイオン導電性ポリマー(ナフィオ
ン)4をこれら電極1、1で挟み、ホットプレス(10
0kg/cm、130℃、90秒)により接合して、
電極−電解質−電極よりなる単電池5が製造される(図
2)。
As described above, two electrodes having the same structure were prepared, and an ion conductive polymer (Nafion) 4 serving as an electrolyte was sandwiched between these electrodes 1 and 1 and hot pressed (10).
0 kg / cm 2 , 130 ° C., 90 seconds),
A unit cell 5 composed of an electrode, an electrolyte and an electrode is manufactured (FIG. 2).

【0018】図3は、本発明および従来技術による単電
池における電池電圧(V)−電流密度(A/cm)カ
ーブの比較図である。この比較図より、電極における反
応層とガス供給層との接合をホットプレスにより行った
従来技術の単電池に比べて、本発明による単電池の電極
の電流密度は大幅に向上していることが分かる。
FIG. 3 is a comparison diagram of the battery voltage (V) -current density (A / cm 2 ) curves in the unit cells according to the present invention and the prior art. From this comparative diagram, it can be seen that the current density of the electrodes of the unit cell according to the present invention is significantly improved as compared with the conventional unit cell in which the reaction layer and the gas supply layer in the electrode are joined by hot pressing. I understand.

【0019】塗布用ペーストにおいては触媒の結着剤と
して、電解質に用いられるイオン導電性ポリマーと同一
組成物であるナフィオンの溶液が用いられる。このこと
は、本発明の電極を用いて製造される燃料電池において
はイオン導電性ポリマーが電解質のみならずその両側に
接する電極においても存在することとなって電池性能を
向上させると共に、塗布用ペーストの乾燥工程を簡素化
することを可能にする。
In the coating paste, a solution of Nafion having the same composition as the ion conductive polymer used in the electrolyte is used as the binder of the catalyst. This means that in the fuel cell manufactured by using the electrode of the present invention, the ion conductive polymer is present not only in the electrolyte but also in the electrodes in contact with both sides of the ion conductive polymer, thereby improving the cell performance and coating paste. It is possible to simplify the drying process of.

【0020】すなわち、本発明の塗布用ペーストには樹
脂の溶剤として低沸点かつ高揮発性の溶剤(主としてア
ルコール)が用いられ、従来塗布用ペーストの粘度調製
のために常用されてきたエチレングリコールやグリセリ
ン等の溶剤を含まない。
That is, in the coating paste of the present invention, a solvent having a low boiling point and a high volatility (mainly alcohol) is used as a solvent for the resin, and ethylene glycol, which has been conventionally used for adjusting the viscosity of the coating paste, is used. Does not contain solvents such as glycerin.

【0021】調製した塗布用ペーストはたとえば65
℃、1時間の条件にて乾燥処理され、これによりイオン
導電性ポリマーの樹脂溶液中のアルコールの一部が乾燥
除去されて該ペーストが所定の粘度とされる。この際の
乾燥処理条件を変えることによりペーストの粘度を自在
に調整し、塗布に適したペースト粘度(たとえば5〜
2,000ポイズ)とすることができる。
The prepared coating paste is, for example, 65
The paste is dried under the condition of 1 ° C. for 1 hour, whereby a part of the alcohol in the resin solution of the ion conductive polymer is removed by drying, and the paste has a predetermined viscosity. The viscosity of the paste can be freely adjusted by changing the drying treatment conditions at this time, and the paste viscosity suitable for application (for example, 5 to 5).
2,000 poise).

【0022】このようにして粘度調整されたペーストを
多孔質シート上にアスピレーター、ロータリーポンプ等
の減圧手段により吸引しつつ塗布した後に行われる乾燥
処理は、得られた電極を1時間程度室温に放置すること
により行うことができ、このような室温乾燥によってイ
オン導電性ポリマー溶液中に残留するアルコールを完全
に除去することができる。したがって、塗布用ペースト
中の溶剤分が電極中に残留することによる電極性能の低
下の問題は本発明では生じない。
The paste thus obtained is applied to the porous sheet while being sucked by a pressure reducing means such as an aspirator or a rotary pump, and the obtained electrode is left at room temperature for about 1 hour. By performing such room temperature drying, the alcohol remaining in the ion conductive polymer solution can be completely removed. Therefore, the problem of deterioration of the electrode performance due to the solvent content in the coating paste remaining in the electrode does not occur in the present invention.

【0023】電解質に用いられるイオン導電性ポリマー
は一般に熱に弱く、その分解温度は150℃近辺である
ものの、実際には130℃付近の加熱乾燥によっても熱
劣化してイオン導電性が悪化する。しかしながら本発明
においては、ペースト粘度調整のための乾燥処理温度は
65℃程度で十分であり、また電極を得た後のペースト
固化は室温放置で行うことが可能であるため、イオン導
電性ポリマーを熱劣化させることがなく、所期の電池性
能が損なわれることがない。
The ionic conductive polymer used for the electrolyte is generally weak to heat, and its decomposition temperature is around 150 ° C., but actually, it is thermally deteriorated by heating and drying at around 130 ° C. to deteriorate the ionic conductivity. However, in the present invention, a drying treatment temperature of about 65 ° C. for adjusting the paste viscosity is sufficient, and the paste solidification after obtaining the electrode can be carried out at room temperature. There is no thermal deterioration and the desired battery performance is not impaired.

【0024】[0024]

【発明の効果】本発明によれば、ガス供給層を介してガ
スが反応層中の触媒にまんべんなく供給され、触媒の活
性化が図られるため、燃料極および空気極のいずれにお
いても電極の性能が大幅に向上する。
According to the present invention, the gas is evenly supplied to the catalyst in the reaction layer through the gas supply layer to activate the catalyst, so that the performance of the electrode is improved in both the fuel electrode and the air electrode. Is greatly improved.

【0025】一方、反応層の厚みが薄くなるため、反応
ペーストに撥水剤を添加する必要がなくなり、電極性能
が向上する。
On the other hand, since the thickness of the reaction layer is thin, it is not necessary to add a water repellent agent to the reaction paste, and the electrode performance is improved.

【0026】また、本発明は塗布法により電極を製造す
るものであるが、塗布用ペーストに結着剤として、電解
質に用いられると同一のイオン導電性ポリマーを用いる
ため、電池全体のイオン導電性が向上され、またエチレ
ングリコールやグリセリン等の溶剤を含まないため、こ
れら溶剤が電極中に残留することによる電極性能の低下
を招くことがない。
Further, although the present invention manufactures an electrode by a coating method, since the same ion conductive polymer as that used in the electrolyte is used as a binder in the coating paste, the ion conductive property of the entire battery is improved. In addition, since the solvent does not contain a solvent such as ethylene glycol or glycerin, the solvent performance does not deteriorate due to the solvent remaining in the electrode.

【0027】更に、これら溶剤および撥水剤を含まない
ペーストを使用しているため、ペースト塗布後の乾燥が
室温で可能となり、イオン導電性ポリマーに対する熱劣
化が回避される。
Further, since the paste containing neither solvent nor water repellent is used, the paste can be dried at room temperature, and thermal deterioration of the ion conductive polymer can be avoided.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明により製造される電極における反応層と
ガス供給層との接合状態を示す模式図である。
FIG. 1 is a schematic diagram showing a bonded state of a reaction layer and a gas supply layer in an electrode manufactured according to the present invention.

【図2】図1の電極を用いて製造される単電池を示す模
式図である。
FIG. 2 is a schematic diagram showing a unit cell manufactured using the electrode of FIG.

【図3】図2の単電池の性能を従来例と比較して示す図
である。
FIG. 3 is a diagram showing the performance of the unit cell of FIG. 2 in comparison with a conventional example.

【図4】従来例による電極における反応層とガス供給層
との接合状態を示す模式図である。
FIG. 4 is a schematic view showing a joined state of a reaction layer and a gas supply layer in an electrode according to a conventional example.

【符号の説明】[Explanation of symbols]

1 電極 2 反応層 3 ガス供給層 4 イオン導電性ポリマー 5 単電池 1 Electrode 2 Reaction Layer 3 Gas Supply Layer 4 Ion Conductive Polymer 5 Single Cell

───────────────────────────────────────────────────── フロントページの続き (72)発明者 小関 宏彦 愛知県安城市藤井町高根10番地 アイシ ン・エィ・ダブリュ株式会社内 (72)発明者 上野 正隆 愛知県安城市藤井町高根10番地 アイシ ン・エィ・ダブリュ株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Hirohiko Ozeki 10 Takane, Fujii-cho, Anjo City, Aichi Prefecture Aisin AW Co., Ltd. (72) Masataka Ueno 10 Takane, Fujii-cho, Anjo City, Aichi Prefecture Aisin・ AW Co., Ltd.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 触媒と溶剤と水を少なくとも含んで調
製されたペーストよりなる反応層をガス供給層上に形成
するに際して、前記ガス供給層の背面側より吸引しなが
ら形成することにより前記ペーストを前記ガス供給層に
浸透せしめることを特徴とする、燃料電池用電極の製造
方法。
1. When forming a reaction layer composed of a paste prepared by containing at least a catalyst, a solvent and water on a gas supply layer, the paste is formed by sucking from the back side of the gas supply layer. A method of manufacturing an electrode for a fuel cell, which is characterized in that the gas supply layer is permeated.
【請求項2】 燃料電池の電解質を構成すると同一の
イオン導電性ポリマーの溶液を結着剤として前記ペース
トを調製し、前記乾燥工程において前記イオン導電性ポ
リマー溶液中のアルコール溶剤分を乾燥除去することを
特徴とする請求項1の燃料電池用電極の製造方法。
2. The paste is prepared by using the same ion conductive polymer solution as a binder to form an electrolyte of a fuel cell, and the alcohol solvent component in the ion conductive polymer solution is removed by drying in the drying step. The method for manufacturing an electrode for a fuel cell according to claim 1, wherein
【請求項3】 前記乾燥工程を室温にて行うことを特
徴とする請求項2の燃料電池用電極の製造方法。
3. The method for producing a fuel cell electrode according to claim 2, wherein the drying step is performed at room temperature.
【請求項4】 前記ペーストによる反応層を形成する
前に前記ペーストを加熱乾燥することにより前記ペース
ト中のアルコール溶剤分のみを任意量除去してその粘度
を調整することを特徴とする請求項2または3の燃料電
池用電極の製造方法。
4. The viscosity of the paste is adjusted by heating and drying the paste before forming a reaction layer of the paste to remove an arbitrary amount of the alcohol solvent in the paste. Alternatively, the method of manufacturing an electrode for a fuel cell according to 3).
JP5197729A 1993-07-16 1993-07-16 Manufacture of electrode for fuel cell Pending JPH0729576A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5197729A JPH0729576A (en) 1993-07-16 1993-07-16 Manufacture of electrode for fuel cell

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5197729A JPH0729576A (en) 1993-07-16 1993-07-16 Manufacture of electrode for fuel cell

Publications (1)

Publication Number Publication Date
JPH0729576A true JPH0729576A (en) 1995-01-31

Family

ID=16379376

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5197729A Pending JPH0729576A (en) 1993-07-16 1993-07-16 Manufacture of electrode for fuel cell

Country Status (1)

Country Link
JP (1) JPH0729576A (en)

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JP2002110202A (en) * 2000-10-02 2002-04-12 Asahi Glass Co Ltd Solid high polymer fuel cell and manufacturing method therefor
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