Comparison between La0.6Sr0.4CoO3-d and LaNi0.6Co0.4O3-d infiltrated oxygen electrodes for long-term durable solid oxide fuel cells

被引:25
|
作者
Ovtar, Simona [1 ]
Hauch, Anne [1 ]
Veltze, Sune [1 ,2 ]
Chen, Ming [1 ]
机构
[1] Tech Univ Denmark, Dept Energy Convers & Storage, Frederiksborgvej 399, DK-4000 Roskilde, Denmark
[2] DFM AS, Kogle Alle 5, DK-2970 Horsholm, Denmark
关键词
Solid oxide fuel cells; Infiltration; Oxygen electrode; Electro-catalyst; Long-term durability; ELECTROLYSIS CELLS; THERMODYNAMIC ANALYSIS; TRANSPORT-PROPERTIES; IONIC-CONDUCTIVITY; IMPEDANCE SPECTRA; DOPED CERIA; PERFORMANCE; CATHODES; STABILITY; YSZ;
D O I
10.1016/j.electacta.2018.02.022
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The degradation of infiltrated oxygen electrodes during long-term operation of solid oxide fuel cells (SOFCs) was studied. The infiltrated oxygen electrodes were prepared by infiltration of the electro-catalysts La0.6Sr0.4CoO3-d (LSC) and LaNi0.6Co0.4O3-d (LCN) into a porous yttria stabilized zirconia (YSZ) backbone that was pre-infiltrated with a gadolinium doped ceria (CGO) barrier layer. The performance of the infiltrated LSC and LCN electro-catalysts were compared for both symmetrical cells and full SOFCs. Galvanostatic long-term performance tests up to 1400 h at 700 degrees C and 0.5 A/cm(2) were conducted and the change of resistance was followed by electrochemical impedance spectroscopy under current load. The cell performance degradation profiles of the LSC and LCN infiltrated cells showed significant differences. The performance of the LSC infiltrated cell stabilized after 700 h of operation and the LCN infiltrated cell degraded throughout the entire testing period. The difference between the intrinsic properties, i.e. its electrochemical activity, ionic conductivity, and reactivity of LSC and LCN materials was hypothesized to be responsible for the observed difference in the degradation profile. (c) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:293 / 304
页数:12
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