JP2011070980A - Polymer electrolyte of solid polymer fuel cell, method for manufacturing the same, membrane-electrode assembly containing polymer electrolyte, and method for manufacturing the same membrane-electrode assembly - Google Patents

Polymer electrolyte of solid polymer fuel cell, method for manufacturing the same, membrane-electrode assembly containing polymer electrolyte, and method for manufacturing the same membrane-electrode assembly Download PDF

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JP2011070980A
JP2011070980A JP2009221843A JP2009221843A JP2011070980A JP 2011070980 A JP2011070980 A JP 2011070980A JP 2009221843 A JP2009221843 A JP 2009221843A JP 2009221843 A JP2009221843 A JP 2009221843A JP 2011070980 A JP2011070980 A JP 2011070980A
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JP5454050B2 (en
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Masafumi Ota
雅史 太田
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Toppan Inc
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    • 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
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    • 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
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a method for manufacturing a polymer electrolyte which has high proton conductivity and high gas permeability without changing a structure of the polymer electrolyte, and a solid polymer fuel cell having a membrane-electrode assembly including the polymer electrolyte. <P>SOLUTION: In the manufacturing method for a polymer electrolyte, a polymer electrolyte ink including a polymer electrolyte dispersion solution, a solvent, and an organic object wherein dipole moment is 2.0 D or more is produced, a coated film is formed by applying the polymer electrolyte ink to a base material, and the organic object in the film attained by drying the coated film is removed with acid treatment. Thus, the polymer electrolyte having high proton conductivity and high gas permeability can be attained. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

本発明は、高分子電解質の製造方法およびこの高分子電解質を含む膜電極接合体を備えてなる固体高分子形燃料電池に関するものである。   The present invention relates to a method for producing a polymer electrolyte and a solid polymer fuel cell comprising a membrane electrode assembly containing the polymer electrolyte.

燃料電池は、水素を含有する燃料ガスと、酸素を含む酸化剤ガスとを、触媒を含む電極で水の電気分解の逆反応を起こさせ、熱と同時に電気を生み出す発電システムである。この発電システムは、従来の発電方式と比較して高効率で低環境負荷、低騒音などの特徴を有し、将来のクリーンなエネルギー源として注目されている。用いるイオン伝導体の種類によってタイプがいくつかあり、イオン伝導性高分子膜を用いたものは、固体高分子形燃料電池と呼ばれる。   A fuel cell is a power generation system that generates electricity simultaneously with heat by causing a reverse reaction of electrolysis of water between a fuel gas containing hydrogen and an oxidant gas containing oxygen at an electrode containing a catalyst. This power generation system has features such as high efficiency, low environmental load, and low noise as compared with conventional power generation methods, and is attracting attention as a clean energy source in the future. There are several types depending on the type of ion conductor used, and those using an ion conductive polymer membrane are called solid polymer fuel cells.

燃料電池の中でも固体高分子形燃料電池は、室温程度でも使用可能なことから、車搭載源や家庭据置用電源などへの使用が有望視されており、近年、様々な研究開発が行われている。固体高分子形燃料電池は、膜電極接合体(Membrance and Electrolyte Assembly;MEA)と呼ばれる高分子電解質の両面に一対の電極触媒層を配置させた接合体を、前記電極の一方に水素を含有する燃料ガスを供給し、前記電極の他方に酸素を含む酸化剤ガスを供給するためのガス流路を形成した一対のセパレータ板で挟持した電池である。ここで、燃料ガスを供給する電極を燃料極、酸化剤ガスを供給する電極を空気極と呼ぶ。これらの電極は、白金系の貴金属などの触媒物質を担持したカーボン粒子と高分子電解質を積層してなる電極触媒層とガス通気性および電子伝導性を兼ね備えたガス拡散層からなる。   Among fuel cells, polymer electrolyte fuel cells can be used at room temperature, so they are expected to be used for on-vehicle sources and household stationary power sources. In recent years, various research and development have been conducted. Yes. A polymer electrolyte fuel cell is a membrane / electrode assembly (MEA) called a membrane electrode assembly, in which a pair of electrocatalyst layers are arranged on both sides of a polymer electrolyte, and one of the electrodes contains hydrogen. It is a battery that is sandwiched between a pair of separator plates that are provided with a gas flow path for supplying a fuel gas and supplying an oxidant gas containing oxygen to the other electrode. Here, the electrode for supplying the fuel gas is called a fuel electrode, and the electrode for supplying the oxidant gas is called an air electrode. These electrodes are composed of an electrode catalyst layer formed by laminating carbon particles carrying a catalyst substance such as a platinum-based noble metal and a polymer electrolyte, and a gas diffusion layer having both gas permeability and electron conductivity.

車搭載源として固体高分子燃料電池の高分子電解質を利用するためには、120℃20%RHで0.1S/cmのプロトン伝導度が必要とされており、高分子電解質膜には、耐熱性、高プロトン伝導性が要求され、さらに触媒電極層に含まれる高分子電解質には、ガス透過性が要求されることとなる。   Proton conductivity of 0.1 S / cm at 120 ° C. and 20% RH is required to use the polymer electrolyte of the solid polymer fuel cell as a vehicle-mounted source. Therefore, the polymer electrolyte contained in the catalyst electrode layer is required to have gas permeability.

特開2006−24389号公報JP 2006-24389 A

Electrochimica Acta 54 4328−4333 2009年Electrochimica Acta 54 4328-4333 2009

上述の問題を解決するために、特許文献1では、フッ素系高分子電解質膜やフッ素系高分子電解質は、イオン交換基1個当たりの平均分子量に相当するEW(Equivalent Weight、等価質量)を小さくし、スルホン酸基密度を高める試みをしている。しかしながら、スルホン酸基密度を高めることにより、フッ素系高分子電解質が膨潤しやすくなり、安定的に発電できないものであった。   In order to solve the above problem, in Patent Document 1, the fluorinated polymer electrolyte membrane and the fluorinated polymer electrolyte have a small EW (Equivalent Weight) equivalent to the average molecular weight per ion-exchange group. And attempts to increase the sulfonic acid group density. However, by increasing the sulfonic acid group density, the fluorine-based polymer electrolyte easily swells and cannot stably generate power.

また、非特許文献1では、炭化水素系高分子電解質を用いて電極触媒の比活性(mass activity)を求めている。しかし、炭化水素系高分子電解質はガス透過性がフッ素系高分子電解質に比較して悪いため、高い比活性が得られないという課題があった。   Further, in Non-Patent Document 1, the specific activity (mass activity) of an electrode catalyst is determined using a hydrocarbon-based polymer electrolyte. However, since the hydrocarbon polymer electrolyte has poor gas permeability compared to the fluorine polymer electrolyte, there is a problem that high specific activity cannot be obtained.

本発明は、このような従来の課題を解決しようとするものであり、分子構造を変化させることなく、プロトン伝導度とガス透過性を向上させた高分子電解質の製造方法を提供し、この高分子電解質を電解質膜や触媒電極層内の高分子電解質に用いることで、さまざまな条件下で高い発電性能を有する固体高分子形燃料電池を提供することを目的とするものである。   The present invention is intended to solve such conventional problems, and provides a method for producing a polymer electrolyte with improved proton conductivity and gas permeability without changing the molecular structure. An object of the present invention is to provide a polymer electrolyte fuel cell having high power generation performance under various conditions by using a molecular electrolyte as a polymer electrolyte in an electrolyte membrane or a catalyst electrode layer.

上記目的を達成するために、本発明の請求項1記載の発明は、高分子電解質分散溶液と溶媒と双極子モーメントが、2.0D以上である有機物とを含む高分子電解質インクを作製し、基材上に高分子電解質インクを塗布して塗膜を形成し、塗膜を乾燥させることにより得られる膜中の有機物を酸処理により除去することを特徴とする高分子電解質の製造方法とするものである。   In order to achieve the above object, the invention according to claim 1 of the present invention is to produce a polymer electrolyte ink comprising a polymer electrolyte dispersion solution, a solvent, and an organic substance having a dipole moment of 2.0D or more, A method for producing a polymer electrolyte, comprising: applying a polymer electrolyte ink on a substrate to form a coating film; and drying the coating film to remove organic substances in the film by acid treatment. Is.

本発明の請求項2記載の発明は、有機物が、モノエチレングリコールまたは尿素であることを特徴とする請求項1に記載の高分子電解質の製造方法とするものである。   The invention according to claim 2 of the present invention is the method for producing a polymer electrolyte according to claim 1, wherein the organic substance is monoethylene glycol or urea.

本発明の請求項3記載の発明は、高分子電解質インクはスルホン酸を含み、有機物が、高分子電解質インクのスルホン酸基当量に対して2倍以上であることを特徴とする請求項1または2に記載の高分子電解質の製造方法とするものである。   The invention according to claim 3 of the present invention is characterized in that the polymer electrolyte ink contains a sulfonic acid, and the organic substance is at least twice the sulfonic acid group equivalent of the polymer electrolyte ink. The method for producing a polymer electrolyte described in 2 is used.

本発明の請求項4記載の発明は、請求項1乃至3のいずれかに記載の製造方法で作製されることを特徴とする高分子電解質とするものである。   According to a fourth aspect of the present invention, there is provided a polymer electrolyte produced by the production method according to any one of the first to third aspects.

本発明の請求項5記載の発明は、高分子電解質膜と、高分子電解質膜を挟持する電極触媒層と、からなる膜電極接合体であって、請求項4に記載の高分子電解質が、高分子電解質膜または電極触媒層として用いられることを特徴とする膜電極接合体とするものである。   The invention according to claim 5 of the present invention is a membrane electrode assembly comprising a polymer electrolyte membrane and an electrode catalyst layer sandwiching the polymer electrolyte membrane, wherein the polymer electrolyte according to claim 4 comprises: The membrane / electrode assembly is used as a polymer electrolyte membrane or an electrode catalyst layer.

本発明の請求項6記載の発明は、高分子電解質分散溶液と溶媒と双極子モーメントが、2.0D以上である有機物とを含む高分子電解質インクを作製し、基材上に高分子電解質インクを塗布して塗膜を形成し、塗膜を乾燥させることにより得られる膜を電極触媒層で狭持し、膜中の有機物を酸処理により除去して高分子電解質膜を形成することを特徴とする膜電極接合体の製造方法とするものである。   According to a sixth aspect of the present invention, there is provided a polymer electrolyte ink comprising a polymer electrolyte dispersion solution, a solvent, and an organic substance having a dipole moment of 2.0 D or more, and the polymer electrolyte ink is formed on a substrate. A film is formed by coating the film, and the film obtained by drying the film is sandwiched between the electrode catalyst layers, and organic substances in the film are removed by acid treatment to form a polymer electrolyte membrane. The method for producing a membrane electrode assembly is as follows.

本発明の請求項7記載の発明は、有機物が、モノエチレングリコールまたは尿素であることを特徴とする請求項6に記載の膜電極接合体の製造方法とするものである。   The invention according to claim 7 of the present invention is the process for producing a membrane electrode assembly according to claim 6, wherein the organic substance is monoethylene glycol or urea.

本発明の請求項8記載の発明は、高分子電解質インクはスルホン酸を含み、有機物が、高分子電解質インクのスルホン酸基当量に対して2倍以上であることを特徴とする請求項6または7に記載の膜電極接合体の製造方法とするものである。   The invention according to claim 8 of the present invention is characterized in that the polymer electrolyte ink contains a sulfonic acid, and the organic substance is at least twice the sulfonic acid group equivalent of the polymer electrolyte ink. 7. The method for producing a membrane / electrode assembly according to claim 7 is used.

本発明に係る高分子電解質の製造方法によれば、有機物を混合・酸処理することによって作製した高分子電解質が、スルホン酸基の集合によって形成されるクラスターサイズを大きくすることができるため、さまざまな湿度環境下において、プロトン伝導度が高く、またガス透過性の高い高分子電解質を提供できる。また、本発明に係る高分子電解質を用いた膜電極接合体を備える固体高分子形燃料電池を提供できる。   According to the method for producing a polymer electrolyte according to the present invention, a polymer electrolyte produced by mixing and acid-treating an organic substance can increase the cluster size formed by an assembly of sulfonic acid groups. It is possible to provide a polymer electrolyte having high proton conductivity and high gas permeability in a high humidity environment. Moreover, a polymer electrolyte fuel cell provided with the membrane electrode assembly using the polymer electrolyte concerning this invention can be provided.

本発明に係る高分子電解質の製造方法の説明図である。It is explanatory drawing of the manufacturing method of the polymer electrolyte which concerns on this invention. 本発明に係る固体高分子形燃料電池の分解模式図である。1 is an exploded schematic view of a polymer electrolyte fuel cell according to the present invention.

以下、本発明の実施の形態を、図1および図2に基づいて説明する。なお、本発明は、以下に記載する各実施の形態に限定されうるものではなく、当業者の知識に基づいて設計の変更等の変形を加えることも可能であり、そのような変形が加えられた実施の形態も本発明の範囲に含まれうるものである。   Hereinafter, embodiments of the present invention will be described with reference to FIGS. 1 and 2. Note that the present invention is not limited to the embodiments described below, and modifications such as design changes can be made based on the knowledge of those skilled in the art, and such modifications are added. The embodiments may be included in the scope of the present invention.

(高分子電解質の製造方法)
本発明に係る高分子電解質の製造方法を、図1を参照して説明する。本発明の高分子電解質の製造方法にあっては、高分子電解質分散溶液とモノエチレングリコール(MEG)または尿素(Urea)を混合し、1時間混合することにより、スルホン酸基の集合体から構成されるクラスター内に、モノエチレングリコールまたは尿素が取り込まれるので、クラスターサイズを大きくすることができる。(図1の工程1)
(Polymer electrolyte production method)
A method for producing a polymer electrolyte according to the present invention will be described with reference to FIG. In the method for producing a polymer electrolyte of the present invention, a polymer electrolyte dispersion solution and monoethylene glycol (MEG) or urea (Urea) are mixed and mixed for 1 hour to form a sulfonic acid group aggregate. Since monoethylene glycol or urea is taken into the cluster to be formed, the cluster size can be increased. (Step 1 in Fig. 1)

次に、ガラス基材上にPTFEシートを配置し、PTFE上に工程1で作製した高分子電解質インクを塗布し、アプリケータによって塗工する(図1の工程2)。さらに、塗工した高分子電解質を乾燥させ、残留溶剤を除去し(図1の工程3)、剥離する(図1の工程4)。最後に得られた高分子電解質をホットプレスし、大きくなったクラスターを固定する(図1の工程5)。 Next, a PTFE sheet is placed on the glass substrate, the polymer electrolyte ink prepared in Step 1 is applied on PTFE, and applied with an applicator (Step 2 in FIG. 1). Further, the coated polymer electrolyte is dried, the residual solvent is removed (step 3 in FIG. 1), and the polymer electrolyte is peeled off (step 4 in FIG. 1). Finally, the obtained polymer electrolyte is hot-pressed to fix the enlarged cluster (step 5 in FIG. 1).

次に、工程5で得られた高分子電解質を70℃の純水中、3%過酸化水素水溶液、1M硫酸水溶液、再度純水で洗浄する(図1の工程6〜9)。最後に乾燥してクラスターサイズが拡大された高分子電解質を得ることができる。 Next, the polymer electrolyte obtained in step 5 is washed with pure water at 70 ° C., a 3% hydrogen peroxide aqueous solution, a 1M sulfuric acid aqueous solution, and pure water again (steps 6 to 9 in FIG. 1). Finally, a polymer electrolyte having an expanded cluster size can be obtained by drying.

本発明の高分子電解質において、混合される有機物としては、双極子相互作用が大きいものが好ましい。具体的には、水素結合性基を有し、双極子モーメントが2.0D(デバイ)以上であるモノエチレングリコールや尿素などが好ましい。この理由は、双極子モーメントが2.0Dより小さい有機物であると、高分子電解質内のスルホン酸基と水素結合しにくく、クラスターサイズが大きくなりにくいためである。 In the polymer electrolyte of the present invention, the organic substance to be mixed preferably has a large dipole interaction. Specifically, monoethylene glycol, urea or the like having a hydrogen bonding group and a dipole moment of 2.0 D (Debye) or more is preferable. This is because if the organic substance has a dipole moment of less than 2.0D, it is difficult to hydrogen bond with the sulfonic acid group in the polymer electrolyte, and the cluster size is difficult to increase.

本発明の高分子電解質において、混合される有機物の量としては、高分子電解質のスルホン酸基当量に対して2倍以上であることが好ましい。その理由は、2倍より少ないと、有機物の量が少なく、スルホン酸基と水素結合する確率が低下するので、クラスターサイズが大きくなりにくいためである。 In the polymer electrolyte of the present invention, the amount of the organic substance to be mixed is preferably twice or more with respect to the sulfonic acid group equivalent of the polymer electrolyte. The reason is that if it is less than 2 times, the amount of organic substances is small, and the probability of hydrogen bonding with the sulfonic acid group decreases, so that the cluster size is difficult to increase.

次に、本発明の高分子電解質を用いた膜電極接合体(MEA)及びその製造方法、また、本発明の固体高分子形燃料電池についてさらに詳細を説明する。 Next, the membrane electrode assembly (MEA) using the polymer electrolyte of the present invention, a method for producing the same, and the polymer electrolyte fuel cell of the present invention will be described in more detail.

(電極触媒インク)
本発明の電極触媒インクの分散媒として使用される溶媒は、触媒粒子や高分子電解質または有機物を混合、酸処理して得られた高分子電解質を侵食することなく、高分子電解質の流動性の高い状態で溶解または微細ゲルとして分散できるもので特に制限はない。しかし、揮発性の液体有機溶媒が少なくとも含まれることが望ましく、特に限定されるものではないが、メタノール、エタノール、1−プロパノ―ル、2−プロパノ―ル、1−ブタノ−ル、2−ブタノ−ル、イソブチルアルコール、tert−ブチルアルコール、ペンタノ−ル等のアルコール類、アセトン、メチルエチルケトン、ペンタノン、メチルイソブチルケトン、へプタノン、シクロヘキサノン、メチルシクロヘキサノン、アセトニルアセトン、ジイソブチルケトンなどのケトン系溶剤、テトラヒドロフラン、ジオキサン、ジエチレングリコールジメチルエーテル、アニソール、メトキシトルエン、ジブチルエーテル等のエーテル系溶剤、その他ジメチルホルムアミド、ジメチルアセトアミド、N−メチルピロリドン、エチレングリコール、ジエチレングリコール、ジアセトンアルコール、1−メトキシ−2−プロパノール等の極性溶剤等が使用されてもよい。また、これらの溶剤のうち二種以上を混合させたものを使用してもよい。
(Electrocatalyst ink)
The solvent used as a dispersion medium for the electrode catalyst ink of the present invention is a fluidity of the polymer electrolyte without eroding the polymer electrolyte obtained by mixing and acid-treating catalyst particles, polymer electrolyte or organic matter. There is no particular limitation as long as it can be dissolved or dispersed as a fine gel in a high state. However, it is desirable to include at least a volatile liquid organic solvent, and is not particularly limited, but is not limited to methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol. Alcohols such as alcohol, isobutyl alcohol, tert-butyl alcohol, pentanole, ketone solvents such as acetone, methyl ethyl ketone, pentanone, methyl isobutyl ketone, heptanone, cyclohexanone, methylcyclohexanone, acetonyl acetone, diisobutyl ketone, tetrahydrofuran , Dioxane, diethylene glycol dimethyl ether, anisole, methoxytoluene, dibutyl ether and other ether solvents, dimethylformamide, dimethylacetamide, N-methylpyrrolidone, ethylene glycol Le, diethylene glycol, diacetone alcohol, polar solvents such as 1-methoxy-2-propanol may be used. Moreover, you may use what mixed 2 or more types among these solvents.

また、溶媒として低級アルコールを用いたものは発火の危険性が高く、このような溶媒を用いる際は水との混合溶媒にするのが好ましい。高分子電解質となじみがよい水が含まれていてもよい。水の添加量は、高分子電解質が分離して白濁を生じたり、ゲル化したりしない程度であれば特に制限はない。 In addition, those using lower alcohol as the solvent have a high risk of ignition, and when using such a solvent, it is preferable to use a mixed solvent with water. Water that is compatible with the polymer electrolyte may be contained. The amount of water added is not particularly limited as long as the polymer electrolyte is not separated to cause white turbidity or gelation.

電極触媒インク中の固形分含有量は、50質量%より多いと電極触媒インクの粘度が高くなるため、電極触媒層表面にクラックが入りやすくなり、また逆に1質量%より少ないと成膜レートが非常に遅く、生産性が低下してしまうため、1質量%以上50質量%以下であることが好ましい。 If the solid content in the electrode catalyst ink is more than 50% by mass, the viscosity of the electrode catalyst ink becomes high, so that the surface of the electrode catalyst layer tends to crack, and conversely if it is less than 1% by mass, the film formation rate is increased. However, since productivity will fall very slowly, it is preferable that they are 1 mass% or more and 50 mass% or less.

(電極触媒層)
本発明に係る高分子電解質を用いて作製した膜電極接合体の製造方法において、有機物を混合、酸処理により除去した本発明の高分子電解質、または高分子電解質で包埋した触媒担持炭素粒子は、触媒担持炭素粒子と、高分子電解質を溶媒に分散させた電極触媒インクを転写シートに塗布し、乾燥させることで得てもよい。
(Electrode catalyst layer)
In the method for producing a membrane / electrode assembly produced using the polymer electrolyte according to the present invention, the polymer electrolyte of the present invention in which organic substances are mixed and removed by acid treatment, or catalyst-supported carbon particles embedded with the polymer electrolyte are: Alternatively, the catalyst-supporting carbon particles and the electrode catalyst ink in which the polymer electrolyte is dispersed in a solvent may be applied to a transfer sheet and dried.

このとき、塗布方法としては、ドクターブレード法、ディッピング法、スクリーン印刷法、ロールコーティング法、スプレー法などを用いてもよい。 At this time, as a coating method, a doctor blade method, a dipping method, a screen printing method, a roll coating method, a spray method, or the like may be used.

本発明の電極触媒層の製造方法における基材としては、ガス拡散層、転写シート、もしくは本発明の有機物を混合、酸処理により除去した高分子電解質膜、または高分子電解質膜を用いてもよい。ガス拡散層としては、ガス拡散性と導電性とを有する材質のものを用いてもよい。また転写シートとしては、転写性がよい材質であればよい。 As a substrate in the method for producing an electrode catalyst layer of the present invention, a gas diffusion layer, a transfer sheet, a polymer electrolyte membrane obtained by mixing and removing the organic matter of the present invention by acid treatment, or a polymer electrolyte membrane may be used. . As the gas diffusion layer, a material having gas diffusibility and conductivity may be used. The transfer sheet may be any material that has good transferability.

基材として転写シートを用いた場合には、高分子電解質膜に電極触媒層を接合後に転写シートを剥離し、高分子電解質膜の両面に電極触媒層を備える膜電極接合体とすることができる。 When a transfer sheet is used as the substrate, the transfer sheet is peeled after the electrode catalyst layer is bonded to the polymer electrolyte membrane, and a membrane electrode assembly having electrode catalyst layers on both sides of the polymer electrolyte membrane can be obtained. .

有機物の酸処理洗浄による除去は、有機物が含有した高分子電解質を用いて作製した高分子電解質膜、電極触媒層を作製し、膜電極接合体を作製した後に行ってもよい。   The removal of the organic substance by acid treatment cleaning may be performed after producing a polymer electrolyte membrane and an electrode catalyst layer produced using a polymer electrolyte containing the organic substance and producing a membrane electrode assembly.

ガス拡散層およびセパレータとしては、通常の燃料電池に用いられているものを用いてもよい。具体的にはガス拡散層としてはカーボンクロス、カーボンペーパー、不織布などのポーラスカーボン材を用いてもよい。セパレータとしては、カーボンタイプあるいは金属タイプのものなどを用いてもよい。燃料電池としては、ガス供給装置、冷却装置などその他付随する装置を組み立てることにより製造される。 As the gas diffusion layer and the separator, those used in ordinary fuel cells may be used. Specifically, a porous carbon material such as carbon cloth, carbon paper, and nonwoven fabric may be used as the gas diffusion layer. As the separator, a carbon type or a metal type may be used. The fuel cell is manufactured by assembling other accompanying devices such as a gas supply device and a cooling device.

図2に本発明の実施の形態に係る固体高分子形燃料電池の分解模式図を示した。本発明の固体高分子形燃料電池にあっては、膜電極接合体12の電極触媒層2および電極触媒層の3と対向して空気極側のガス拡散層4および燃料極側のガス拡散層5が配置される。これによりそれぞれ空気極(カソード)6及び燃料極(アノード)7が構成される。そしてガス流通用のガス流路8を備え、相対する主面に冷却水流通用の冷却水流路9を備えた導電性でかつ不透過性の材料よりなる一組のセパレータ10が配置される。燃料極7側のセパレータ10のガス流路8からは燃料ガスとして、例えば水素ガスが供給される。一方、空気極6側のセパレータ10のガス流路8からは、酸化剤ガスとして、例えば酸素を含むガスが供給される。そして、燃料ガスの水素と酸素ガスとを触媒の存在下で電極反応させることにより、燃料極と空気極との間に起電力を生じさせることができる。   FIG. 2 shows an exploded schematic view of the polymer electrolyte fuel cell according to the embodiment of the present invention. In the polymer electrolyte fuel cell of the present invention, the gas diffusion layer 4 on the air electrode side and the gas diffusion layer on the fuel electrode side are opposed to the electrode catalyst layer 2 and the electrode catalyst layer 3 of the membrane electrode assembly 12. 5 is arranged. As a result, an air electrode (cathode) 6 and a fuel electrode (anode) 7 are formed. A pair of separators 10 made of a conductive and impermeable material is disposed, which includes a gas flow path 8 for gas flow and a cooling water flow path 9 for cooling water flow on the opposing main surface. For example, hydrogen gas is supplied as a fuel gas from the gas flow path 8 of the separator 10 on the fuel electrode 7 side. On the other hand, a gas containing oxygen, for example, is supplied as an oxidant gas from the gas flow path 8 of the separator 10 on the air electrode 6 side. An electromotive force can be generated between the fuel electrode and the air electrode by causing electrode reaction between hydrogen and oxygen gas of the fuel gas in the presence of the catalyst.

図2に示した固体高分子形燃料電池は一組のセパレータに固体高分子電解質膜1、電極触媒層2、3、ガス拡散層4、5が狭持されている。いわゆる単セル構造の固体高分子形燃料電池であるが、本発明にあっては、セパレータ10を介して複数のセルを積層して燃料電池としてもよい。   In the solid polymer fuel cell shown in FIG. 2, the solid polymer electrolyte membrane 1, the electrode catalyst layers 2, 3, and the gas diffusion layers 4, 5 are sandwiched between a pair of separators. Although it is a so-called single cell polymer electrolyte fuel cell, in the present invention, a plurality of cells may be stacked via a separator 10 to form a fuel cell.

以下に、実施例および比較例について説明する。   Examples and comparative examples will be described below.

(高分子電解質分散溶液)
20質量%高分子電解質分散溶液(ナフィオン:Nafion(登録商標)、Dupont社製)を高分子電解質分散溶液として用いた。
(Polymer electrolyte dispersion)
A 20% by mass polymer electrolyte dispersion solution (Nafion: Nafion (registered trademark), manufactured by Dupont) was used as the polymer electrolyte dispersion solution.

(実施例1)
(高分子電解質の作製)
10mlのガラス容器に20質量%高分子電解質分散溶液と高分子電解質のスルホン酸基当量に対して6.6倍のモノエチレングリコールを混合し、1時間撹拌した。次に、ガラス上に粘着剤を介して貼り合わせた高分子フィルム(PTFE)上に高分子電解質インクを塗布し、膜厚が約25μm程度になるようにドクターブレードにより、塗工した。その後、60℃で5分間乾燥させて高分子フィルムから剥離した。その後、高分子電解質を130℃で30分間ホットプレスした。
Example 1
(Production of polymer electrolyte)
In a 10 ml glass container, 6.6 times as much monoethylene glycol as the sulfonic acid group equivalent of the 20% by mass polymer electrolyte dispersion and polymer electrolyte was mixed and stirred for 1 hour. Next, a polymer electrolyte ink was applied onto a polymer film (PTFE) bonded to glass via an adhesive, and was applied with a doctor blade so that the film thickness was about 25 μm. Then, it was made to dry for 5 minutes at 60 degreeC, and it peeled from the polymer film. Thereafter, the polymer electrolyte was hot pressed at 130 ° C. for 30 minutes.

(高分子電解質からのモノエチレングリコールの除去)
高分子電解質をそれぞれ70℃の純水、3wt%の過酸化水素水溶液、1Mの硫酸水溶液、純水に1時間浸漬させ、モノエチレングリコールを除去した。その後、80℃で1時間真空乾燥させることにより、高分子電解質を作製した。
(Removal of monoethylene glycol from polymer electrolyte)
The polymer electrolyte was immersed in pure water at 70 ° C., 3 wt% hydrogen peroxide aqueous solution, 1 M sulfuric acid aqueous solution and pure water for 1 hour to remove monoethylene glycol. Then, the polymer electrolyte was produced by making it vacuum-dry at 80 degreeC for 1 hour.

(実施例2)
(高分子電解質の作製)
10mlのガラス容器に20質量%高分子電解質分散溶液と高分子電解質のスルホン酸基当量に対して2.2倍の尿素を混合し、1時間撹拌した。次に、ガラス上に粘着剤を介して貼り合わせた高分子フィルム(PTFE)上に高分子電解質インクを塗布し、膜厚が約25μm程度になるようにドクターブレードにより、塗工した。その後、60℃で5分間乾燥させて高分子フィルムから剥離した。その後、高分子電解質を130℃で30分間ホットプレスした。
(Example 2)
(Production of polymer electrolyte)
In a 10 ml glass container, 20% by mass of the polymer electrolyte dispersion solution and 2.2 times of urea with respect to the sulfonic acid group equivalent of the polymer electrolyte were mixed and stirred for 1 hour. Next, a polymer electrolyte ink was applied onto a polymer film (PTFE) bonded to glass via an adhesive, and was applied with a doctor blade so that the film thickness was about 25 μm. Then, it was made to dry for 5 minutes at 60 degreeC, and it peeled from the polymer film. Thereafter, the polymer electrolyte was hot pressed at 130 ° C. for 30 minutes.

(高分子電解質からの尿素の除去)
高分子電解質をそれぞれ70℃の純水、3wt%の過酸化水素水溶液、1Mの硫酸水溶液、純水に1時間浸漬させ、尿素を除去した。その後、80℃で1時間真空乾燥させることにより、高分子電解質を作製した。
(Removal of urea from polymer electrolyte)
Each of the polymer electrolytes was immersed in 70 ° C. pure water, 3 wt% aqueous hydrogen peroxide solution, 1M sulfuric acid aqueous solution and pure water for 1 hour to remove urea. Then, the polymer electrolyte was produced by making it vacuum-dry at 80 degreeC for 1 hour.

(比較例)
(高分子電解質の作製)
ガラス上に粘着剤を介して貼り合わせた高分子フィルム(PTFE)上に20質量%高分子分散溶液を塗布し、膜厚が約25μm程度になるようにドクターブレードにより、塗工した。その後、60℃で5分間乾燥させて高分子フィルムから剥離した。その後、高分子電解質を130℃で30分間ホットプレスした。
(Comparative example)
(Production of polymer electrolyte)
A 20% by mass polymer dispersion solution was applied on a polymer film (PTFE) bonded to glass via an adhesive, and was coated with a doctor blade so that the film thickness was about 25 μm. Then, it was made to dry for 5 minutes at 60 degreeC, and it peeled from the polymer film. Thereafter, the polymer electrolyte was hot pressed at 130 ° C. for 30 minutes.

(高分子電解質の洗浄)
高分子電解質をそれぞれ70℃の純水、3wt%の過酸化水素水溶液、1Mの硫酸水溶液、純水に1時間浸漬させた。その後、80℃で1時間真空乾燥させることにより、高分子電解質を作製した。
(Polymer electrolyte cleaning)
The polymer electrolytes were immersed in pure water at 70 ° C., 3 wt% aqueous hydrogen peroxide, 1 M sulfuric acid, and pure water for 1 hour, respectively. Then, the polymer electrolyte was produced by making it vacuum-dry at 80 degreeC for 1 hour.

(電極触媒インクの調整)
白金担持量が50質量%である白金担持カーボン触媒(商品名:TEC10E50E、田中貴金属工業製)と、20質量%高分子電解質分散溶液(ナフィオン:Nafion(登録商標)、Dupont社製)を溶媒中で混合し、遊星ボールミル(商品名:Pulverisette7、Fritsch社製)で分散処理を行った。ボールミルのポット、ボールにはジルコニア製のものを用いた。出発原料の組成比を白金担持カーボン粒子とナフィオン(Nafion(登録商標)、Dupont社製)の質量比で2:1としたものを電極触媒インクとした。
(Adjustment of electrode catalyst ink)
A platinum-supported carbon catalyst (trade name: TEC10E50E, manufactured by Tanaka Kikinzoku Kogyo Co., Ltd.) with a platinum-supported amount of 50% by mass and a 20% by mass polymer electrolyte dispersion (Nafion: Nafion (registered trademark), manufactured by Dupont) in a solvent. And dispersion treatment was performed using a planetary ball mill (trade name: Pulverisette 7, manufactured by Fritsch). Ball mill pots and balls made of zirconia were used. The electrode catalyst ink was prepared by setting the composition ratio of the starting material to 2: 1 by mass ratio of platinum-supporting carbon particles and Nafion (Nafion (registered trademark), manufactured by Dupont).

(電極触媒層の作製)
電極触媒層用インクをPTFE基材上に塗布し、ドクターブレードにより塗工した。塗工した電極触媒層を60℃で5分間乾燥させて作製した。また、電極触媒層の厚さは、白金担持量が約0.3mg/cmになるように調整し、電極触媒層の電極面積は5cmの正方形になるようにカッティングした。
(Production of electrode catalyst layer)
The electrode catalyst layer ink was applied onto a PTFE base material and applied with a doctor blade. The coated electrode catalyst layer was produced by drying at 60 ° C. for 5 minutes. The thickness of the electrode catalyst layer was adjusted so that the amount of platinum supported was about 0.3 mg / cm 2, and the electrode area of the electrode catalyst layer was cut so as to be a square of 5 cm 2 .

(膜電極接合体の作製)
5cmの正方形に切り抜かれた電極触媒層を高分子電解質膜の両面に対面するように転写シートを配置し、130℃の条件で15分間ホットプレスして膜電極接合体を作製した。
(Production of membrane electrode assembly)
A transfer sheet was placed so that the electrode catalyst layer cut into a 5 cm 2 square faced both surfaces of the polymer electrolyte membrane, and hot-pressed at 130 ° C. for 15 minutes to prepare a membrane electrode assembly.

(水素ガスリーク電流測定)
膜電極接合体にガス拡散層としてカーボンクロスを挟むように貼り合わせ、発電評価セル(エヌエフ回路設計ブロック社製)内に設置した。これを燃料電池測定装置(商品名:GFI−SG1、東陽テクニカ社製)を用いて、セル温度80℃で、加湿器は、アノード、カソードともに100%RHになるようにした。
(Measurement of hydrogen gas leak current)
The membrane electrode assembly was bonded so as to sandwich a carbon cloth as a gas diffusion layer, and installed in a power generation evaluation cell (manufactured by NF Circuit Design Block). Using a fuel cell measurement device (trade name: GFI-SG1, manufactured by Toyo Technica Co., Ltd.), the cell temperature was 80 ° C., and the humidifier was adjusted to 100% RH for both the anode and the cathode.

燃料ガスとしてアノード側は、200ml/minの水素または窒素、カソード側は、200ml/minの窒素を流した。   As fuel gas, 200 ml / min of hydrogen or nitrogen was flowed on the anode side, and 200 ml / min of nitrogen was flowed on the cathode side.

水素ガスリーク電流は、アノードに対極と参照電極を配置し、カソードに作用電極を配置してLSV(リニアスイープボルタンメトリー)測定により算出した。LSVとは、作用電極の電位を初期電位から終了電位まで順方向のみ走査させる測定である。測定の際は、走査速度1mV/secで0〜0.8mV vs. RHEの範囲で行った。水素ガスリーク電流の算出の際には、アノード、カソードともに窒素を流した場合のLSVとアノードに水素、カソードに窒素を流した場合のLSV測定を行い、バックグラウンド(Background)電流を差し引いて、水素ガスリーク電流とした。   The hydrogen gas leakage current was calculated by LSV (linear sweep voltammetry) measurement with a counter electrode and a reference electrode arranged on the anode and a working electrode arranged on the cathode. LSV is a measurement in which the potential of the working electrode is scanned only in the forward direction from the initial potential to the end potential. At the time of measurement, 0 to 0.8 mV vs. 1 at a scanning speed of 1 mV / sec. Performed in the RHE range. When calculating the hydrogen gas leakage current, LSV measurement is performed when nitrogen is supplied to both the anode and cathode, and LSV measurement is performed when hydrogen is supplied to the anode and nitrogen is supplied to the cathode, and the background current is subtracted to obtain hydrogen Gas leakage current was used.

下記の表1に0.5mV vs. RHEの場合の水素ガスリーク電流値を示す。
In Table 1 below, 0.5 mV vs. The hydrogen gas leak current value in the case of RHE is shown.

表1より、実施例と比較例とを比較すると、実施例1及び2によれば、尿素(Urea)、またはモノエチレングリコール(MEG)を混合、酸処理することにより、水素ガスリーク電流が高くなることが確認できた。   From Table 1, when Examples and Comparative Examples are compared, according to Examples 1 and 2, hydrogen gas leakage current is increased by mixing and acid-treating urea (Urea) or monoethylene glycol (MEG). I was able to confirm.

(プロトン伝導度測定)
膜の伝導度は、下記式のように膜抵抗と膜の寸法より算出する。
σ=(1/R)・(L/S)
σ:伝導度、R:電気抵抗、L:電極間距離、S:断面積
膜抵抗の測定は、交流インピーダンス法で行った。測定装置にはNF回路設計ブロック製のFRA 5080を用いた。測定周波数は10Hz〜2MHzとした。交流印加電圧は100mV、直流印加電圧は0Vとした。また、そのときの測定環境は、80℃で30、50、70、95%RHの条件で測定した。
(Proton conductivity measurement)
The conductivity of the film is calculated from the film resistance and the film size as in the following equation.
σ = (1 / R) · (L / S)
σ: conductivity, R: electrical resistance, L: distance between electrodes, S: cross-sectional area film resistance were measured by an AC impedance method. As the measuring device, FRA 5080 manufactured by NF circuit design block was used. The measurement frequency was 10 Hz to 2 MHz. The AC applied voltage was 100 mV, and the DC applied voltage was 0 V. Moreover, the measurement environment at that time was measured under the conditions of 80, 50 ° C., 30, 50, 70, and 95% RH.

表2にナフィオン(Nafion(登録商標)、Dupont社製)、尿素を混合、酸処理除去したナフィオン(Nafion(登録商標)、Dupont社製)、およびモノエチレングリコールを混合、酸処理したナフィオン(Nafion(登録商標)、Dupont社製)の相対湿度とプロトン伝導度の関係を示す。
Table 2 shows Nafion (Nafion (registered trademark), manufactured by Dupont), Nafion mixed with urea and removed by acid treatment (Nafion (registered trademark), manufactured by Dupont), and Nafion (Nafion mixed with acid and treated with monoethylene glycol). (Registered trademark) manufactured by Dupont) shows the relationship between the relative humidity and proton conductivity.

表2より、実施例と比較例とを比較すると、実施例1及び2によれば、モノエチレングリコールまたは尿素を添加した高分子電解質は、低加湿、または高加湿下においても、ともにプロトン伝導性が高いことを確認できた。   From Table 2, when Examples and Comparative Examples are compared, according to Examples 1 and 2, the polymer electrolyte to which monoethylene glycol or urea is added is proton conductive even under low or high humidification. Was confirmed to be high.

以上より、実施例と比較例との比較から、本発明によれば、双極子モーメントが2.0D(デバイ)以上であるモノエチレングリコールまたは尿素を添加した高分子電解質は、低加湿、または高加湿下においてもともにプロトン伝導性が高く、ガス透過性も高くなることが確認できた。このことから、本発明に係る高分子電解質は、高分子電解質膜だけでなく、電極触媒層の高分子電解質としてもより有用であることが確認できた。 As described above, according to the comparison between the example and the comparative example, according to the present invention, the polymer electrolyte added with monoethylene glycol or urea having a dipole moment of 2.0 D (Debye) or higher has a low humidification or high It was confirmed that both proton conductivity and gas permeability were high even under humidification. From this, it was confirmed that the polymer electrolyte according to the present invention is more useful not only as a polymer electrolyte membrane but also as a polymer electrolyte of an electrode catalyst layer.

本発明は、電気自動車、携帯電話、自動販売機、水中ロボット、潜水艦、宇宙船、水中航走体、水中基地用電源等に用いる固体高分子形燃料電池に利用することができる。   INDUSTRIAL APPLICABILITY The present invention can be used for a polymer electrolyte fuel cell used for an electric vehicle, a mobile phone, a vending machine, an underwater robot, a submarine, a spacecraft, an underwater vehicle, a power source for an underwater base, and the like.

1 固体高分子電解質膜
2 電極触媒層
3 電極触媒層
12 膜電極接合体
4 ガス拡散層
5 ガス拡散層
6 空気極(カソード)
7 燃料極(アノード)
8 ガス流路
9 冷却水流路
10 セパレータ


DESCRIPTION OF SYMBOLS 1 Solid polymer electrolyte membrane 2 Electrode catalyst layer 3 Electrode catalyst layer 12 Membrane electrode assembly 4 Gas diffusion layer 5 Gas diffusion layer 6 Air electrode (cathode)
7 Fuel electrode (anode)
8 Gas flow path 9 Cooling water flow path 10 Separator


Claims (8)

高分子電解質分散溶液と溶媒と双極子モーメントが、2.0D以上である有機物とを含む高分子電解質インクを作製し、
基材上に前記高分子電解質インクを塗布して塗膜を形成し、前記塗膜を乾燥させることにより得られる膜中の前記有機物を酸処理により除去することを特徴とする高分子電解質の製造方法。
Producing a polymer electrolyte ink comprising a polymer electrolyte dispersion solution, a solvent, and an organic substance having a dipole moment of 2.0D or more;
The polymer electrolyte is formed by applying the polymer electrolyte ink on a substrate to form a coating film, and drying the coating film to remove the organic matter in the film obtained by acid treatment. Method.
前記有機物が、モノエチレングリコールまたは尿素であることを特徴とする請求項1に記載の高分子電解質の製造方法。   The method for producing a polymer electrolyte according to claim 1, wherein the organic substance is monoethylene glycol or urea. 前記高分子電解質インクはスルホン酸を含み、前記有機物が、前記高分子電解質インクのスルホン酸基当量に対して2倍以上であることを特徴とする請求項1または2に記載の高分子電解質の製造方法。   3. The polymer electrolyte according to claim 1, wherein the polyelectrolyte ink contains sulfonic acid, and the organic substance is at least twice the sulfonic acid group equivalent of the polyelectrolyte ink. Production method. 請求項1乃至3のいずれかに記載の製造方法で作製されることを特徴とする高分子電解質。   A polymer electrolyte produced by the production method according to claim 1. 高分子電解質膜と、前記高分子電解質膜を挟持する電極触媒層と、からなる膜電極接合体であって、
請求項4に記載の前記高分子電解質が、前記高分子電解質膜または前記電極触媒層として用いられることを特徴とする膜電極接合体。
A membrane electrode assembly comprising a polymer electrolyte membrane and an electrode catalyst layer sandwiching the polymer electrolyte membrane,
5. The membrane / electrode assembly, wherein the polymer electrolyte according to claim 4 is used as the polymer electrolyte membrane or the electrode catalyst layer.
高分子電解質分散溶液と溶媒と双極子モーメントが、2.0D以上である有機物とを含む高分子電解質インクを作製し、
基材上に前記高分子電解質インクを塗布して塗膜を形成し、前記塗膜を乾燥させることにより得られる膜を電極触媒層で狭持し、
前記膜中の前記有機物を酸処理により除去して高分子電解質膜を形成することを特徴とする膜電極接合体の製造方法。
Producing a polymer electrolyte ink comprising a polymer electrolyte dispersion solution, a solvent, and an organic substance having a dipole moment of 2.0D or more;
Applying the polymer electrolyte ink on a substrate to form a coating film, and sandwiching a film obtained by drying the coating film with an electrode catalyst layer,
A method for producing a membrane / electrode assembly, wherein the organic substance in the membrane is removed by acid treatment to form a polymer electrolyte membrane.
前記有機物が、モノエチレングリコールまたは尿素であることを特徴とする請求項6に記載の膜電極接合体の製造方法。   The method for producing a membrane / electrode assembly according to claim 6, wherein the organic substance is monoethylene glycol or urea. 前記高分子電解質インクはスルホン酸を含み、前記有機物が、前記高分子電解質インクのスルホン酸基当量に対して2倍以上であることを特徴とする請求項6または7に記載の膜電極接合体の製造方法。   The membrane electrode assembly according to claim 6 or 7, wherein the polymer electrolyte ink contains sulfonic acid, and the organic substance is at least twice as much as a sulfonic acid group equivalent of the polymer electrolyte ink. Manufacturing method.
JP2009221843A 2009-09-28 2009-09-28 POLYMER ELECTROLYTE FOR SOLID POLYMER FUEL CELL AND METHOD FOR PRODUCING THE SAME, MEMBRANE ELECTRODE ASSEMBLY CONTAINING THE POLYMER ELECTROLYTE, AND METHOD FOR PRODUCING THE SAME Expired - Fee Related JP5454050B2 (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016207523A (en) * 2015-04-24 2016-12-08 トヨタ自動車株式会社 Inspection method for membrane electrode assembly, and inspection device

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08162123A (en) * 1994-12-05 1996-06-21 Tanaka Kikinzoku Kogyo Kk Polymer electrolyte-type electro-chemical cell and its manufacture
JP2003528438A (en) * 2000-03-20 2003-09-24 シュティヒティン・エネルギーオンデルツォイク・セントラム・ネーデルランド Manufacture of low-temperature fuel cell electrodes
JP2005154710A (en) * 2003-03-10 2005-06-16 Toray Ind Inc Polymer solid electrolyte, method for producing the same, and solid polymer type fuel cell by using the same
JP2005307025A (en) * 2004-04-22 2005-11-04 Kaneka Corp Polyelectrolyte membrane and method for producing the same
JP2008031465A (en) * 2006-07-04 2008-02-14 Sumitomo Chemical Co Ltd Manufacturing method of polyelectrolyte emulsion
JP2011070984A (en) * 2009-09-28 2011-04-07 Toppan Printing Co Ltd Method of manufacturing electrode catalyst layer for fuel cell, and membrane-electrode assembly having the electrode catalyst layer

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08162123A (en) * 1994-12-05 1996-06-21 Tanaka Kikinzoku Kogyo Kk Polymer electrolyte-type electro-chemical cell and its manufacture
JP2003528438A (en) * 2000-03-20 2003-09-24 シュティヒティン・エネルギーオンデルツォイク・セントラム・ネーデルランド Manufacture of low-temperature fuel cell electrodes
JP2005154710A (en) * 2003-03-10 2005-06-16 Toray Ind Inc Polymer solid electrolyte, method for producing the same, and solid polymer type fuel cell by using the same
JP2005307025A (en) * 2004-04-22 2005-11-04 Kaneka Corp Polyelectrolyte membrane and method for producing the same
JP2008031465A (en) * 2006-07-04 2008-02-14 Sumitomo Chemical Co Ltd Manufacturing method of polyelectrolyte emulsion
JP2011070984A (en) * 2009-09-28 2011-04-07 Toppan Printing Co Ltd Method of manufacturing electrode catalyst layer for fuel cell, and membrane-electrode assembly having the electrode catalyst layer

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016207523A (en) * 2015-04-24 2016-12-08 トヨタ自動車株式会社 Inspection method for membrane electrode assembly, and inspection device

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