Measurement and Modeling of the Impedance Characteristics of Porous La1-xSrxCoO3-δ Electrodes

被引:122
作者
Lu, Yunxiang [1 ]
Kreller, Cortney [1 ]
Adler, Stuart B. [1 ]
机构
[1] Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
基金
美国国家科学基金会;
关键词
electrical resistivity; electrochemical impedance spectroscopy; electrolytes; interstitials; lanthanum compounds; porous materials; strontium compounds; surface diffusion; CONDUCTING OXYGEN ELECTRODES; PEROVSKITE-TYPE OXIDES; FUEL-CELL CATHODES; STABILIZED ZIRCONIA; SOLID ELECTROLYTES; INTERFACE REGIONS; POLARIZATION; KINETICS; EXCHANGE; SURFACE;
D O I
10.1149/1.3079337
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Porous La1-xSrxCoO3-delta (LSC) electrodes having Sr composition x=0.4 (LSC-64) and x=0.2 (LSC-82) were fabricated on Sm-doped ceria electrolytes, and studied using electrochemical impedance spectroscopy between T=650-750 degrees C and p(O2)=0.01-1.0 atm. The faradaic portion of the impedance was found to exhibit Gerischer or Gerischer-like characteristics, indicating colimitation by kinetics and transport. The characteristic resistance and frequency response was analyzed using a transport and reaction model that considers parallel bulk and surface diffusion of oxygen, as well as three-dimensional transport effects near the electrode electrolyte interface. In the case of LSC-64, measured characteristics appear to be largely consistent with a bulk transport path, based on independent measurements of the thermodynamic, kinetic, and transport properties of LSC-64. In the case of LSC-82, which has a much lower bulk vacancy concentration under the same conditions, results were inconsistent with an entirely bulk transport path. Results for LSC-82 could be rationalized assuming a parallel surface transport path, where surface mobility is governed by some kind of interstitial or adatom diffusion mechanism.
引用
收藏
页码:B513 / B525
页数:13
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