Time-Dependent Electrode Performance Changes in Intermediate Temperature Solid Oxide Fuel Cells

被引:91
作者
Endler, C. [1 ]
Leonide, A. [1 ]
Weber, A. [1 ]
Tietz, F. [2 ]
Ivers-Tiffee, E. [1 ]
机构
[1] Karlsruher Inst Technol, IWE, D-76131 Karlsruhe, Germany
[2] Forschungszentrum Julich, IEF 1, D-52425 Julich, Germany
关键词
cobalt compounds; electrochemical electrodes; ionic conductivity; lanthanum compounds; solid oxide fuel cells; strontium compounds; ANODE-SUPPORTED SOFCS; IMPEDANCE SPECTRA; DECONVOLUTION; RESISTANCE;
D O I
10.1149/1.3270047
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
This study gives evidence that the time-dependent performance changes in anode supported cells for intermediate-temperature solid oxide fuel cells is essentially influenced by the mixed ionic-electronic conducting (MIEC) cathode. The impedance spectra recorded during 700 h of operation at 750 degrees C were interpreted using an appropriate equivalent circuit model by (i) a distribution of relaxation time analysis followed by (ii) a complex nonlinear least squares fit. Four electrode polarization processes were separated by selective experimental parameters. The cathodic part, initially the smallest, is only discovered among the anodic contributions by a change in fuel gas composition from H-2-H2O to CO-CO2 and increases by 310% (15 m cm(2) at 11 h, 62 m cm(2) at 700 h). A Sr (and Co) depletion of the MIEC cathode composition La0.58Sr0.4Co0.2Fe0.8O3-delta possibly caused this degradation. The anodic polarization has a proportion of 92% at the start and decreases to 73% (168 m cm(2) at 11 h, 173 m cm(2) at 700 h). The anode charge-transfer reaction initially causes 60% of the total polarization losses and 50% after 700 h. This is assigned to a change in the triple phase boundary and/or a degradation in ionic conductivity in the anode functional layer. The gas diffusion polarization remains constant at 58 m cm(2).
引用
收藏
页码:B292 / B298
页数:7
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