JP4512944B2 - Solid oxide fuel cell separator - Google Patents
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Description
この発明は、電気伝導性に優れかつ使用寿命の長い固体電解質型燃料電池用セパレータに関するものである。 The present invention relates to a separator for a solid oxide fuel cell having excellent electrical conductivity and a long service life.
一般に、固体電解質型燃料電池は、固体電解質の片面に空気極を積層させ、固体電解質の他方の片面に燃料極を積層させてセルを構成し、このセルの空気極に接して空気極集電体を積層させ、このセルの燃料極に接して燃料極集電体を積層させ、さらに空気極集電体の外側に空気が通る溝を有するセパレータを積層させ、さらに燃料極集電体の外側に水素が通る溝を有するセパレータを積層させた構造を有しており、かかる構造を有する積層体をさらに複数積層させて起電力を高めることにより実用に供している。 In general, a solid oxide fuel cell has a cell formed by laminating an air electrode on one side of a solid electrolyte and laminating a fuel electrode on the other side of the solid electrolyte, and is in contact with the air electrode of this cell. And a separator having a groove through which air passes on the outside of the air electrode current collector, and further on the outside of the fuel electrode current collector. A separator having a groove through which hydrogen passes is laminated, and a plurality of laminates having such a structure are further laminated to increase the electromotive force for practical use.
前記固体電解質は一般にイットリアで安定化したジルコニア（以下、ＹＳＺという）で構成されているが、近年、Ｌｎ1-xＡxＧａ1-y-zＢ1Ｂ2Ｏ3（但し、Ｌｎ＝Ｌａ、Ｃｅ、Ｐｒ、Ｎｄ、Ｓｍの１種または２種以上、Ａ＝Ｓｒ、Ｃａ、Ｂａの１種または２種以上、Ｂ1＝Ｍｇ、Ａｌ、Ｉｎの１種または２種以上、Ｂ2＝Ｃｏ、Ｆｅ、Ｎｉ、Ｃｕの１種または２種以上、ｘ＝０．０５〜０．３、ｙ＝０〜０．２９、ｚ＝０．０１〜０．３、ｙ＋ｚ＝０．０２５〜０．３）で示される酸化物なども使用されている。
空気極は（Ｓｍ、Ｓｒ）ＣｏＯ3、（Ｌａ、Ｓｒ）ＭｎＯ3などのセラミックスで構成されており、燃料極はＮｉ／ＹＳＺサーメット、Ｎｉ／（Ｃｅ、Ｓｍ）Ｏ2サーメットなどで構成されている。そして空気極集電体は白金メッシュで構成されており、燃料極集電体はＮｉメッシュまたは発泡Ｎｉで構成されている。
さらにセパレータには、一般に、ステンレス鋼、Ｎｉ基耐熱合金、Ｃｏ基耐熱合金が使用されるが、コスト的に見てステンレス鋼が広く使用されている。ステンレス鋼として、ＳＵＳ４３０（成分組成：Ｃｒ：１６〜１８％、Ｍｎ：１％以下、残部：Ｆｅおよび不可避不純物）で代表されるフェライト系ステンレス鋼、ＳＵＳ３０３（成分組成：Ｃｒ：１７〜１９％、Ｎｉ：８〜１０％、Ｍｎ：２％以下、Ｓｉ：１％以下、残部：Ｆｅおよび不可避不純物）で代表されるオーステナイト系ステンレス鋼、ＳＵＳ４０３（成分組成：Ｃｒ：１１．５〜１３％、Ｍｎ：１％以下、残部：Ｆｅおよび不可避不純物）で代表されるマルテンサイト系ステンレス鋼があることが知られており、これらステンレス鋼の表面には極めて薄いＣｒ系酸化物（例えば、Ｃｒ2Ｏ3）からなる受動態被膜が形成されており、このＣｒ系酸化物が高温耐食性に寄与している。
The solid electrolyte is generally composed of yttria-stabilized zirconia (hereinafter referred to as YSZ). Recently, Ln 1-x A x Ga 1-yz B 1 B 2 O 3 (where Ln = La, Ce , Pr, Nd, or Sm, one or more of A = Sr, Ca, or Ba, B 1 = Mg, Al, or one or more of In, B 2 = Co, One or more of Fe, Ni and Cu, x = 0.05 to 0.3, y = 0 to 0.29, z = 0.01 to 0.3, y + z = 0.025 to 0.3 ) And the like are also used.
The air electrode is composed of ceramics such as (Sm, Sr) CoO 3 , (La, Sr) MnO 3 , and the fuel electrode is composed of Ni / YSZ cermet, Ni / (Ce, Sm) O 2 cermet, etc. Yes. The air electrode current collector is made of platinum mesh, and the fuel electrode current collector is made of Ni mesh or foamed Ni.
Further, stainless steel, Ni-base heat-resistant alloy, and Co-base heat-resistant alloy are generally used for the separator, but stainless steel is widely used in terms of cost. As stainless steel, ferritic stainless steel represented by SUS430 (component composition: Cr: 16 to 18%, Mn: 1% or less, balance: Fe and inevitable impurities), SUS303 (component composition: Cr: 17 to 19%, Austenitic stainless steel represented by Ni: 8 to 10%, Mn: 2% or less, Si: 1% or less, balance: Fe and inevitable impurities), SUS403 (component composition: Cr: 11.5 to 13%, Mn It is known that there is a martensitic stainless steel represented by 1% or less, the balance: Fe and inevitable impurities), and the surface of these stainless steels has an extremely thin Cr-based oxide (for example, Cr 2 O 3 ) Is formed, and this Cr-based oxide contributes to high-temperature corrosion resistance.
しかし、このセパレータを構成するステンレス鋼の表面に形成されているＣｒ2Ｏ3膜は絶縁膜であるところから電気伝導性が極めて悪く、そのためにセパレータが相互に接触する部分における抵抗が大きくなり、セパレータ相互の接触部分における抵抗により起電力が大きく消耗し、それによって発電効率が大幅に低下する。 However, since the Cr 2 O 3 film formed on the surface of the stainless steel constituting this separator is an insulating film, the electrical conductivity is extremely poor, and therefore the resistance at the part where the separators contact each other increases. The electromotive force is greatly consumed due to the resistance at the contact portion between the separators, thereby greatly reducing the power generation efficiency.
これを改善するために、ステンレス鋼からなるセパレータの表面にＣｒ2Ｏ3膜よりも酸素の少ない電気伝導性が格段に優れているＣｒ2Ｏ3-x（ただし、ｘ＝０．０５〜１）からなる組成のクロム酸化物層を形成し、このＣｒ2Ｏ3-x（ただし、ｘ＝０．０５〜１）からなる組成のクロム酸化物層の上に銀メッキ層を形成してなる電気伝導性に優れかつ使用寿命の長い固体電解質型燃料電池用セパレータが提供されている（特許文献１参照）。
しかし、従来のステンレス鋼からなる母材の表面にＣｒ2Ｏ3-x（ただし、ｘ＝０．０５〜１）からなる組成のクロム酸化物層を介して銀メッキ層が形成されている固体電解質型燃料電池用セパレータは、１０００時間程度使用しても電気抵抗は大幅に加熱することは無いが、さらに一層長期間使用すると、セパレータの電気抵抗が上昇し、そのために従来のセパレータが相互に接触する部分における抵抗が大きくなり、セパレータ相互の接触部分における抵抗により起電力が大きく消耗し、それによって発電効率が大幅に低下するようになって交換を余儀なくされる。したがって、一層長期間使用しても電気抵抗の上昇することが少ないセパレータが求められていた。 However, a solid is formed by forming a silver plating layer on the surface of a base material made of conventional stainless steel with a chromium oxide layer having a composition made of Cr 2 O 3-x (where x = 0.05 to 1). The separator for an electrolyte fuel cell does not heat up significantly even after being used for about 1000 hours. However, if it is used for a longer period of time, the electrical resistance of the separator increases. The resistance at the contact portion is increased, and the electromotive force is greatly consumed due to the resistance at the contact portion between the separators, so that the power generation efficiency is greatly reduced and the replacement is unavoidable. Therefore, there has been a demand for a separator that does not increase in electrical resistance even when used for a longer period of time.
そこで、本発明者等は、上述のような観点から、電気伝導性に優れかつ一層使用寿命の長い高温耐食性に優れたセパレータを得るべく研究を行った。その結果、ＦｅおよびＦｅ以外の金属成分（以下、この金属成分をＭという。但し、Ｍは、ＣｒおよびＭｎ、あるいは、Ｃｒ、ＭｎおよびＮｉである。）からなるステンレス鋼を水蒸気中、温度：４５０〜７００℃、１〜５０時間保持するとステンレス鋼母材の表面にＦｅＯＦｅ2Ｏ３およびＭＯＦｅ2Ｏ３からなるスピネル型構造を有する酸化物層が形成され、このスピネル型構造を有する酸化物層の上に銀メッキ層が形成したのち熱処理して得られた固体電解質型燃料電池用セパレータは、（ｉ）ステンレス鋼の表面にＣｒ２Ｏ３−ｘ（ただし、ｘ＝０．０５〜１）からなる組成のクロム酸化物層を形成し、その上に銀メッキ層を形成したのち熱処理して得られた従来の固体電解質型燃料電池用セパレータに比べて電気抵抗値が低い、
(ii)前記従来の固体電解質型燃料電池用セパレータに比べて一層長期間使用しても電気抵抗の上昇が少なく、したがって、使用寿命が一層向上する、という研究結果が得られたのである。
In view of the above, the present inventors have studied to obtain a separator having excellent electrical conductivity and a long service life and excellent high-temperature corrosion resistance. As a result, stainless steel made of metal components other than Fe and Fe (hereinafter, this metal component is referred to as M, where M is Cr and Mn, or Cr, Mn and Ni ) in water vapor, temperature: When held at 450 to 700 ° C. for 1 to 50 hours, an oxide layer having a spinel structure composed of FeOFe 2 O 3 and MOFe 2 O 3 is formed on the surface of the stainless steel base material, and the oxide layer having this spinel structure The solid oxide fuel cell separator obtained by heat treatment after the silver plating layer was formed on (i) Cr 2 O 3-x (where x = 0.05 to 1) on the surface of stainless steel An electric resistance value is lower than that of a conventional solid oxide fuel cell separator obtained by forming a chromium oxide layer having a composition of ,
(ii) As a result of the research, it has been found that the electrical resistance does not increase much even when used for a longer period of time than the conventional solid oxide fuel cell separator, and therefore the service life is further improved.
この発明は、かかる研究結果に基づいてなされたものであって、
（１）ＦｅおよびＦｅ以外の金属成分（以下、Ｍという。但し、Ｍは、ＣｒおよびＭｎ、あるいは、Ｃｒ、ＭｎおよびＮｉである。）からなる鉄基耐熱合金の母材の表面に形成された酸化物層の上に銀メッキ層が形成されてなる固体電解質型燃料電池用セパレータにおいて、
前記酸化物層は、ＦｅＯＦｅ2Ｏ３およびＭＯＦｅ2Ｏ３からなるスピネル型構造を有する酸化物層である固体電解質型燃料電池用セパレータ、に特徴を有するものである。
The present invention has been made based on the results of such research,
(1) Fe and metal components other than Fe (hereinafter referred to as M, where M is Cr and Mn or Cr, Mn and Ni ) . In a solid oxide fuel cell separator in which a silver plating layer is formed on the oxide layer,
The oxide layer has a characteristic FeOFe 2 O 3 and MOFe oxide layer der Ru solid body electrolyte fuel cell separator having a spinel structure consisting of 2 O 3, the.
この発明は、安価なステンレス鋼などの鉄基耐熱合金をセパレータの母材とする電気伝導性に優れかつ使用寿命の一層長いセパレータを提供することができるので、複数の積層体からなる固体電解質型燃料電池の発電効率を高めて一層長期間稼動させることができ、実用化のために優れた効果を発揮するものである。 The present invention can provide a separator having an excellent electrical conductivity and a longer service life using an iron-based heat-resistant alloy such as inexpensive stainless steel as a base material of the separator, and therefore, a solid electrolyte type comprising a plurality of laminates The power generation efficiency of the fuel cell can be increased and the fuel cell can be operated for a longer period of time, and exhibits excellent effects for practical use.
実施例１
ＳＵＳ４３０（成分組成：Ｍｎ：０．５％、Ｃｒ：１７％、残部：Ｆｅおよび不可避不純物）からなり縦：７０ｍｍ、横：２５ｍｍ、厚さ：５ｍｍ（面積；１７．５ｃｍ２）の寸法を有するフェライト系ステンレス鋼板を水蒸気中、温度：５００℃、３０時間保持することにより、表面にＦｅＯＦｅ2Ｏ３、ＣｒＯＦｅ2Ｏ３、ＭｎＯＦｅ2Ｏ３からなるスピネル型構造を有する酸化物層を形成し、このスピネル型構造を有する酸化物層の上に厚さ：５μｍの電気Ａｇメッキ層を形成し、次いで、これらＡｇメッキを施したＳＵＳ４３０板を温度：７００℃、１時間保持することにより熱処理を施し、本発明セパレータ１を作製した。
さらに、比較のために、先に用意した厚さ：５ｍｍを有するＳＵＳ４３０板を母材とし、その表面に厚さ：２μｍの無電解Ｎｉメッキ層を形成し、さらにその上に厚さ：５μｍの電気Ａｇメッキ層を形成し、次いで、これらメッキを施したＳＵＳ４３０フェライト系ステンレス鋼板を大気中、温度：７５０℃、２０時間保持の熱処理を施すことにより、Ｃｒ２Ｏ２．５３のＣｒ酸化物層を介してＡｇメッキ層を形成した従来セパレータ１を作製した。
このようにして得られた本発明セパレータ１および従来セパレータ１における表裏両面に抵抗測定用電極を接触させ、厚さ方向に５００ｍＡ／ｃｍ２、すなわち、８．７５Ａを流した時の抵抗値Ｒを△Ｅ＝２ＩＲ（ただし、△Ｅはセパレータの電圧降下、係数：２はセパレータの両面を考慮した係数）の式より求め、本発明セパレータ１および従来セパレータ１における表裏両面被膜の抵抗値の合計を「全抵抗」として表１に示した。この場合、セパレータ母材の厚さ方向の抵抗値は、十分小さいので無視して算出した。
さらに前記本発明セパレータ１および従来セパレータ１の全抵抗を２で割って片面の被膜の抵抗値とし、この値にセパレータ片面の測定面積（面積；１７．５ｃｍ２）を乗じた値を「単位面積当りの表面抵抗」として求め、その結果を表１に示した。
Example 1
It consists of SUS430 (component composition: Mn: 0.5%, Cr: 17%, balance: Fe and inevitable impurities) and has dimensions of length: 70 mm, width: 25 mm, thickness: 5 mm (area: 17.5 cm 2 ). By holding the ferritic stainless steel plate in water vapor at a temperature of 500 ° C. for 30 hours, an oxide layer having a spinel structure composed of FeOFe 2 O 3 , CrOFe 2 O 3 , MnOFe 2 O 3 is formed on the surface, An electric Ag plating layer having a thickness of 5 μm is formed on the oxide layer having the spinel structure, and then a heat treatment is performed by holding the Ag-plated SUS430 plate at a temperature of 700 ° C. for 1 hour. The separator 1 of the present invention was produced.
Further, for comparison, a SUS430 plate having a thickness of 5 mm prepared in advance is used as a base material, an electroless Ni plating layer having a thickness of 2 μm is formed on the surface, and a thickness of 5 μm is further formed thereon. A Cr 2 O 2.53 Cr oxide layer is formed by forming an electric Ag plating layer and then subjecting the plated SUS430 ferritic stainless steel sheet to a heat treatment in the atmosphere at a temperature of 750 ° C. for 20 hours. A conventional separator 1 in which an Ag plating layer was formed via a was prepared.
The resistance measurement electrode R is obtained when 500 mA / cm 2 , that is, 8.75 A is flowed in the thickness direction by bringing resistance measuring electrodes into contact with both front and back surfaces of the separator 1 of the present invention and the conventional separator 1 thus obtained. ΔE = 2IR (where ΔE is the voltage drop of the separator, coefficient: 2 is a coefficient considering both sides of the separator), and the sum of the resistance values of the front and back double-sided coatings in the separator 1 of the present invention and the conventional separator 1 is obtained. The total resistance is shown in Table 1. In this case, the resistance value in the thickness direction of the separator base material was sufficiently small and thus ignored.
Further, the total resistance of the separator 1 of the present invention and the conventional separator 1 is divided by 2 to obtain the resistance value of the coating on one side, and this value is multiplied by the measured area (area: 17.5 cm 2 ) on one side of the separator. The surface resistance per hit ”is shown in Table 1.
表１に示される結果から、加熱試験前と加熱試験後の全抵抗および単位面積当りの表面抵抗を比較すると、本発明セパレータ１は、従来セパレータ１に比べて加熱試験前の全抵抗および単位面積当りの表面抵抗の値が小さく、さらに加熱試験後の全抵抗および単位面積当りの表面抵抗の上昇が小さいところから、本発明セパレータ１は、従来セパレータ１に比べて電気伝導性に優れかつ本発明セパレータ１は従来セパレータ１に比べて一層長期間使用することができることが分かる。 From the results shown in Table 1, when comparing the total resistance and the surface resistance per unit area before and after the heating test, the separator 1 of the present invention compared to the conventional separator 1 with the total resistance and unit area before the heating test. Since the value of the surface resistance per unit is small, and the increase in the total resistance after the heating test and the surface resistance per unit area is small, the separator 1 of the present invention is superior in electrical conductivity and has a higher electrical conductivity than the conventional separator 1. It can be seen that the separator 1 can be used for a longer period of time than the conventional separator 1.
実施例２
ＳＵＳ４０３（成分組成：Ｍｎ：０．５％、Ｃｒ：１３％、残部：Ｆｅおよび不可避不純物）からなる厚さ：５ｍｍのマルテンサイト系ステンレス鋼板を水蒸気中、温度：５００℃、３０時間保持することにより、表面にＦｅＯＦｅ2Ｏ３、ＣｒＯＦｅ2Ｏ３、ＭｎＯＦｅ2Ｏ３からなるスピネル型構造を有する酸化物層を形成し、このスピネル型構造を有する酸化物層の上に厚さ：５μｍの電気Ａｇメッキ層を形成し、次いで、これらＡｇメッキを施したＳＵＳ４０３板を温度：７００℃、１時間保持することにより熱処理を施すことにより本発明セパレータ２を作製した。
さらに、比較のために、先に用意した厚さ：５ｍｍを有するＳＵＳ４０３板を母材とし、その表面に厚さ：２μｍの無電解Ｎｉメッキ層を形成し、さらにその上に厚さ：５μｍの電気Ａｇメッキ層を形成し、次いで、これらメッキを施したＳＵＳ４０３マルテンサイト系ステンレス鋼板を大気中、温度：７５０℃、２０時間保持の熱処理を施すことにより、Ｃｒ２Ｏ２．５３のＣｒ酸化物層を介してＡｇメッキ層を形成した従来セパレータ２を作製した。
このようにして得られた本発明セパレータ２および従来セパレータ２の加熱試験前後の「全抵抗」および「単位面積当りの表面抵抗」を実施例１と同様にして測定し、その結果を表２に示した。
Example 2
Maintaining a martensitic stainless steel plate having a thickness of 5 mm made of SUS403 (component composition: Mn: 0.5%, Cr: 13%, balance: Fe and inevitable impurities) in steam at a temperature of 500 ° C. for 30 hours. Then, an oxide layer having a spinel structure composed of FeOFe 2 O 3 , CrOFe 2 O 3 , and MnOFe 2 O 3 is formed on the surface, and an electric layer having a thickness of 5 μm is formed on the oxide layer having the spinel structure. The present invention separator 2 was produced by forming an Ag plating layer and then subjecting the Ag-plated SUS403 plate to a heat treatment by maintaining the temperature at 700 ° C. for 1 hour.
Furthermore, for comparison, a SUS403 plate having a thickness of 5 mm prepared in advance is used as a base material, an electroless Ni plating layer having a thickness of 2 μm is formed on the surface, and a thickness of 5 μm is further formed thereon. By forming an electric Ag plating layer and then subjecting these plated SUS403 martensitic stainless steel plates to heat treatment in the atmosphere at a temperature of 750 ° C. for 20 hours, Cr 2 O 2.53 Cr oxide A conventional separator 2 in which an Ag plating layer was formed through the layers was produced.
The “total resistance” and “surface resistance per unit area” before and after the heating test of the separator 2 of the present invention and the conventional separator 2 thus obtained were measured in the same manner as in Example 1, and the results are shown in Table 2. Indicated.
表２に示される結果から、加熱試験前と加熱試験後の全抵抗および単位面積当りの表面抵抗を比較すると、本発明セパレータ２は、従来セパレータ２に比べて加熱試験前の全抵抗および単位面積当りの表面抵抗の値が小さく、さらに加熱試験後の全抵抗および単位面積当りの表面抵抗の上昇が小さいところから、本発明セパレータ２は、従来セパレータ２に比べて電気伝導性に優れかつ本発明セパレータ２は従来セパレータ２に比べて一層長期間使用することができることが分かる。 From the results shown in Table 2, when comparing the total resistance before and after the heating test and the surface resistance per unit area, the separator 2 of the present invention compared to the conventional separator 2 with the total resistance and unit area before the heating test. Since the value of the surface resistance per contact is small, and the increase in the total resistance after the heating test and the surface resistance per unit area is small, the separator 2 of the present invention is superior in electrical conductivity compared to the conventional separator 2 and the present invention. It can be seen that the separator 2 can be used for a longer period of time than the conventional separator 2.
実施例３
ＳＵＳ３０３（成分組成：Ｓｉ：０．５％、Ｍｎ：１％、Ｎｉ：９％、Ｃｒ：１８％、残部：Ｆｅおよび不可避不純物）からなる厚さ：５ｍｍのオーステナイト系ステンレス鋼板を水蒸気中、温度：５００℃、３０時間保持することにより、表面にＦｅＯＦｅ2Ｏ３、ＣｒＯＦｅ2Ｏ３、ＮｉＯＦｅ2Ｏ３、ＳｉＯＦｅ2Ｏ３、ＭｎＯＦｅ2Ｏ３からなるスピネル型構造を有する酸化物層を形成し、このスピネル型構造を有する酸化物層の上に厚さ：５μｍの電気Ａｇメッキ層を形成し、次いで、これらＡｇメッキを施したＳＵＳ３０３板を温度：７００℃、１時間保持することにより熱処理を施すことにより本発明セパレータ材３を作製した。
さらに、比較のために、先に用意した厚さ：５ｍｍを有するＳＵＳ３０３板を母材とし、その表面に厚さ：２μｍの無電解Ｎｉメッキ層を形成し、さらにその上に厚さ：５μｍの電気Ａｇメッキ層を形成し、次いで、これらメッキを施したＳＵＳ３０３マルテンサイト系ステンレス鋼板を大気中、温度：７５０℃、２０時間保持の熱処理を施すことにより、Ｃｒ２Ｏ２．５３のＣｒ酸化物層を介してＡｇメッキ層を形成した従来セパレータ材３を作製した。
このようにして得られた本発明セパレータ３および従来セパレータ３の加熱試験前後の「全抵抗」および「単位面積当りの表面抵抗」を実施例１と同様にして測定し、その結果を表３に示した。
Example 3
Thickness: 5 mm austenitic stainless steel plate made of SUS303 (component composition: Si: 0.5%, Mn: 1%, Ni: 9%, Cr: 18%, balance: Fe and inevitable impurities) in steam at a temperature : An oxide layer having a spinel structure composed of FeOFe 2 O 3 , CrOFe 2 O 3 , NiOFe 2 O 3 , SiOFe 2 O 3 , and MnOFe 2 O 3 is formed on the surface by holding at 500 ° C. for 30 hours. Then, an electric Ag plating layer having a thickness of 5 μm is formed on the oxide layer having the spinel structure, and then the SUS303 plate subjected to the Ag plating is kept at a temperature of 700 ° C. for 1 hour to perform heat treatment. The separator material 3 of the present invention was produced by applying.
Further, for comparison, a SUS303 plate having a thickness of 5 mm prepared in advance is used as a base material, an electroless Ni plating layer having a thickness of 2 μm is formed on the surface, and a thickness of 5 μm is further formed thereon. By forming an electric Ag plating layer and then subjecting these plated SUS303 martensitic stainless steel plates to heat treatment in the atmosphere at a temperature of 750 ° C. for 20 hours, Cr 2 O 2.53 Cr oxide A conventional separator material 3 in which an Ag plating layer was formed through the layers was produced.
The “total resistance” and “surface resistance per unit area” before and after the heating test of the separator 3 of the present invention and the conventional separator 3 thus obtained were measured in the same manner as in Example 1, and the results are shown in Table 3. Indicated.
表３に示される結果から、加熱試験前と加熱試験後の全抵抗および単位面積当りの表面抵抗を比較すると、本発明セパレータ３は、従来セパレータ３に比べて加熱試験前の全抵抗および単位面積当りの表面抵抗の値が小さく、さらに加熱試験後の全抵抗および単位面積当りの表面抵抗の上昇が小さいところから、本発明セパレータ３は、従来セパレータ３に比べて電気伝導性に優れかつ本発明セパレータ３は従来セパレータ３に比べて一層長期間使用することができることが分かる。 From the results shown in Table 3, when comparing the total resistance before and after the heating test and the surface resistance per unit area, the separator 3 of the present invention has a total resistance and unit area before the heating test as compared with the conventional separator 3. Since the value of the surface resistance per unit is small, and the increase in the total resistance after the heating test and the surface resistance per unit area is small, the separator 3 of the present invention is superior in electrical conductivity and has a higher electrical conductivity than the conventional separator 3. It can be seen that the separator 3 can be used for a longer period of time than the conventional separator 3.
Claims (2)
前記酸化物層は、ＦｅＯＦｅ2Ｏ３およびＭＯＦｅ2Ｏ３からなるスピネル型構造を有する酸化物層であることを特徴とする固体電解質型燃料電池用セパレータ。 An oxide formed on the surface of a base material of an iron-based heat-resistant alloy made of Fe and a metal component other than Fe (hereinafter referred to as M, where M is Cr and Mn, or Cr, Mn and Ni ) In the solid oxide fuel cell separator in which a silver plating layer is formed on the layer,
The oxide layer, FeOFe 2 O 3 and MOFe solid body electrolyte fuel cell separator you characterized in that an oxide layer having a spinel structure consisting of 2 O 3.
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| JP5170815B2 (en) * | 2006-07-04 | 2013-03-27 | 日産自動車株式会社 | Solid oxide fuel cell unit and stack |
| JP5283323B2 (en) * | 2006-09-20 | 2013-09-04 | 住友精密工業株式会社 | Fuel cell interconnector and cell stack |
| US8507145B2 (en) | 2007-08-13 | 2013-08-13 | Honda Motor Co., Ltd. | Fuel cell and method of producing the fuel cell |
| JP2010238517A (en) * | 2009-03-31 | 2010-10-21 | Mitsubishi Materials Corp | Solid polymer fuel cell using porous metal gas diffusion sheet performing outstanding contact surface conductivity for long period of time as structural member |
| JP2013054954A (en) * | 2011-09-05 | 2013-03-21 | Nippon Telegr & Teleph Corp <Ntt> | Solid oxide fuel cell stack and interconnector |
| JP2013118178A (en) * | 2011-10-31 | 2013-06-13 | Osaka Gas Co Ltd | Solid oxide fuel cell |
| JP2013118177A (en) * | 2011-10-31 | 2013-06-13 | Osaka Gas Co Ltd | Solid oxide fuel cell |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JPH11501764A (en) * | 1995-03-15 | 1999-02-09 | セラミック・フューエル・セルズ・リミテッド | Fuel cell interconnect device |
| JP2001196077A (en) * | 2000-01-13 | 2001-07-19 | Tokyo Gas Co Ltd | Separator for solid electrolyte fuel cell |
| JP2002289215A (en) * | 2001-03-23 | 2002-10-04 | Mitsubishi Materials Corp | Separator for solid electrolyte fuel cell with excellent conductivity |
| WO2003026052A1 (en) * | 2001-09-18 | 2003-03-27 | Furuya Metal Co., Ltd. | Bipolar plate for fuel cell and method for production thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPH11501764A (en) * | 1995-03-15 | 1999-02-09 | セラミック・フューエル・セルズ・リミテッド | Fuel cell interconnect device |
| JP2001196077A (en) * | 2000-01-13 | 2001-07-19 | Tokyo Gas Co Ltd | Separator for solid electrolyte fuel cell |
| JP2002289215A (en) * | 2001-03-23 | 2002-10-04 | Mitsubishi Materials Corp | Separator for solid electrolyte fuel cell with excellent conductivity |
| WO2003026052A1 (en) * | 2001-09-18 | 2003-03-27 | Furuya Metal Co., Ltd. | Bipolar plate for fuel cell and method for production thereof |
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