Ln1-xSrxMnO3 (Ln = Pr, Nd, Sm and Gd) as the cathode material for solid oxide fuel cells

被引:116
作者
Sakaki, Y
Takeda, Y [1 ]
Kato, A
Imanishi, N
Yamamoto, O
Hattori, M
Iio, M
Esaki, Y
机构
[1] Mie Univ, Fac Engn, Dept Chem, Tsu, Mie 5148507, Japan
[2] Chubu Elect Power Co, Elect Power R&D Ctr, Nagoya, Aichi 4598522, Japan
关键词
solid oxide fuel cell; thermal expansion; cathode material; Pr1-xSrxMnO3; Nd1-xSrxMnO3; Sm1-xSrxMnO3; Gd1-xSrxMnO3;
D O I
10.1016/S0167-2738(98)00440-8
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The perovskite type manganite systems, Ln(1-x)Sr(x)MnO(3) (Ln = La, Pr, Nd, Sm, and Gd; 0 less than or equal to x less than or equal to 0.5) were studied as the electrode materials for solid oxide fuel cells (SOFC) from the view point of applications to the co-firing process of the electrolyte and electrode at a higher temperature. The reactivity tests with yttria-stabilized zirconia (YSZ) showed that the formation of the pyrochlore Ln(2)Zr(2)O(7) was suppressed for the perovskites having smaller lanthanoids than La, especially for the Pr1-xSrxMnO3 and Nd1-xSrxMnO3 systems. No reaction product appeared between the Ln(1-x)Sr(x)MnO(3) perovskite and YSZ even at a high annealing temperature of 1400 degrees C when the lanthanoid elements were Pr, Nd and Sm and the Sr content was around 30% (x = 0.3). The adjustment of the thermal expansion rate of Ln(1-x)Sr(x)MnO(3) to YSZ needed more Sr substitution with an increase of the atomic number of lanthanoids. The Sr contents, x, showing comparable values with 8m/o YSZ were around x = 0.1-0.2 in La1-xSrxMnO3, 0.3 in Pr1-xSrxMnO3 and Nd1-xSrxMnO3 and more than 0.4 in Sm1-xSrxMnO3 and Gd1-xSrxMnO3. The electrical conductivity, which may strongly relate with the polarization of electrode reaction, showed about 200 S/cm at 1000 degrees C for all Ln(0.7)Sr(0.3)MnO(3) systems. The polarization measurements as an air electrode showed no significant dependence on the kind of lanthanoid elements. From the viewpoint of the electrode activity, high electrical conductivity, low reactivity and good compatibility with YSZ, Pr0.7Sr0.3MnO3 and Nd0.7Sr0.3MnO3 are considered to be the most suitable electrode materials for the co-firing process. (C) 1999 Elsevier Science BN. All rights reserved.
引用
收藏
页码:187 / 194
页数:8
相关论文
共 8 条
[1]   DOPED PRMNO3 PEROVSKITE OXIDE AS A NEW CATHODE OF SOLID OXIDE FUEL-CELLS FOR LOW-TEMPERATURE OPERATION [J].
ISHIHARA, T ;
KUDO, T ;
MATSUDA, H ;
TAKITA, Y .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1995, 142 (05) :1519-1524
[2]   STUDY OF ORDER-DISORDER TRANSFORMATION OF FLUORITE STRUCTURE WITH PYROCHLORE TYPE PHASES OF FORMULA (1-X) ZRO2-XLN2O3 [J].
MICHEL, D ;
PEREZYJO.M ;
COLLONGUES, R .
MATERIALS RESEARCH BULLETIN, 1974, 9 (11) :1457-1468
[3]  
SINGHAL SC, 1997, SOLID OXIDE FUEL CEL, V5, P37
[4]   OXIDE PYROCHLORES - A REVIEW [J].
SUBRAMANIAN, MA ;
ARAVAMUDAN, G ;
RAO, GVS .
PROGRESS IN SOLID STATE CHEMISTRY, 1983, 15 (02) :55-143
[5]   Gd(1-x)A(x)MnO(3) (A=Ca and Sr) for the electrode of solid oxide fuel cells [J].
Takeda, Y ;
Tu, HY ;
Sakaki, H ;
Watanabe, S ;
Imanishi, N ;
Yamamoto, O ;
Phillipps, MB ;
Sammes, NM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1997, 144 (08) :2810-2816
[6]   STABILITY OF LA(1-X)A(X)MNO(3-Z) (A=CA, SR) AS CATHODE MATERIALS FOR SOLID OXIDE FUEL-CELLS [J].
TAKEDA, Y ;
SAKAKI, Y ;
ICHIKAWA, T ;
IMANISHI, N ;
YAMAMOTO, O ;
MORI, M ;
MORI, N ;
ABE, T .
SOLID STATE IONICS, 1994, 72 :257-264
[7]   STABILITY AND ANTIPHASE DOMAIN-STRUCTURE OF THE PYROCHLORE SOLID-SOLUTION IN THE ZRO2-GD2O3 SYSTEM [J].
UEHARA, T ;
KOTO, K ;
KANAMARU, F ;
HORIUCHI, H .
SOLID STATE IONICS, 1987, 23 (1-2) :137-143
[8]   PEROVSKITE-TYPE OXIDES AS OXYGEN ELECTRODES FOR HIGH-TEMPERATURE OXIDE FUEL-CELLS [J].
YAMAMOTO, O ;
TAKEDA, Y ;
KANNO, R ;
NODA, M .
SOLID STATE IONICS, 1987, 22 (2-3) :241-246