Performance of solid oxide fuel cells with LSGM-LSM composite cathodes

被引:38
作者
Armstrong, TJ [1 ]
Virkar, AV [1 ]
机构
[1] Univ Utah, Dept Mat Sci & Engn, Salt Lake City, UT 84112 USA
关键词
D O I
10.1149/1.1517282
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Anode-supported cells comprising Ni + yttria-stabilized zirconia (YSZ) anode, thin (similar to10 mum) YSZ electrolyte, and composite cathodes containing a mixture of La0.8Sr0.2MnO(3-delta) (LSM) and La0.9Sr0.1Ga0.8Mg0.2O(3-lambda) (LSGM) were fabricated. The relative proportions of LSGM and LSM were varied between 30 wt % LSGM + 70 wt % LSM and 70 wt % LSGM + 30 wt % LSM, while the firing temperature was varied between 1000 and 1200degreesC. The cathode interlayer composition had a profound effect on cathode performance at 800degreesC with overpotentials ranging between 60 and 425 mV at 1.0 A/cm(2) and exhibiting a minimum for 50 wt % LSGM + 50 wt % LSM. The cathodic overpotential decreased with increasing firing temperature of the composite interlayer in the range 1000 less than or equal to T less than or equal to 1150degreesC, and then increased dramatically for the interlayer fired at 1200degreesC. The cell with the optimized cathode interlayer of 50 wt % LSM + 50 wt % LSGM fired at 1150degreesC exhibited an area specific cell resistance of 0.18 Ohm cm(2) and a maximum power density of 1.4 W/cm(2) at 800degreesC. Chemical analysis revealed that LSGM reacts with YSZ above 1000degreesC to form the pyrochlore phase, La2Zr2O7. The formation of the pyrochlore phase at the interface between the LSGM/LSM composite cathode and the YSZ electrolyte limits the firing time and temperature of the cathode interlayer. (C) 2002 The Electrochemical Society.
引用
收藏
页码:A1565 / A1571
页数:7
相关论文
共 21 条
[1]   Thin-film solid oxide fuel cell with high performance at low-temperature [J].
deSouza, S ;
Visco, SJ ;
DeJonghe, LC .
SOLID STATE IONICS, 1997, 98 (1-2) :57-61
[2]  
FENG M, 1994, EUR J SOL STATE INOR, V31, P663
[3]   Reactions between a zirconia-based electrolyte and LaCoO3-based electrode materials [J].
Figueiredo, FM ;
Labrincha, JA ;
Frade, JR ;
Marques, FMB .
SOLID STATE IONICS, 1997, 101 :343-349
[4]   Characterization of Sr-doped LaMnO3 and LaCoO3 as cathode materials for a doped LaGaO3 ceramic fuel cell [J].
Huang, KQ ;
Feng, M ;
Goodenough, JB ;
Schmerling, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1996, 143 (11) :3630-3636
[5]  
Huang KQ, 1998, J AM CERAM SOC, V81, P2581, DOI 10.1111/j.1151-2916.1998.tb02664.x
[6]   A solid oxide fuel cell based on Sr- and Mg-doped LaGaO3 electrolyte:: the role of a rare-earth oxide buffer [J].
Huang, KQ ;
Goodenough, JB .
JOURNAL OF ALLOYS AND COMPOUNDS, 2000, 303 :454-464
[7]   DOPED LAGAO3 PEROVSKITE-TYPE OXIDE AS A NEW OXIDE IONIC CONDUCTOR [J].
ISHIHARA, T ;
MATSUDA, H ;
TAKITA, Y .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (09) :3801-3803
[8]   Solid oxide fuel cell using Co doped La(Sr)Ga(Mg)O3 perovskite oxide with notably high power density at intermediate temperature [J].
Ishihara, T ;
Shibayama, T ;
Honda, M ;
Nishiguchi, H ;
Takita, Y .
CHEMICAL COMMUNICATIONS, 1999, (13) :1227-1228
[9]   Effect of sintering temperature on microstructure and performance of LSM-YSZ composite cathodes [J].
Jorgensen, MJ ;
Primdahl, S ;
Bagger, C ;
Mogensen, M .
SOLID STATE IONICS, 2001, 139 (1-2) :1-11
[10]   HIGH-TEMPERATURE AIR CATHODES CONTAINING ION CONDUCTIVE OXIDES [J].
KENJO, T ;
OSAWA, S ;
FUJIKAWA, K .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1991, 138 (02) :349-355