共 40 条
Fast oxygen exchange kinetics of pore-free Bi1-xSrxFeO3-δ thin films
被引:64
作者:

Wedig, Anja
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机构:
Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany

Merkle, Rotraut
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h-index: 0
机构:
Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany

Stuhlhofer, Benjamin
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机构:
Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany

Habermeier, Hanns-Ulrich
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Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany

Maier, Joachim
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Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany

Heifets, Eugene
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Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany
机构:
[1] Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany
关键词:
SURFACE EXCHANGE;
ELECTROCHEMICAL CHARACTERIZATION;
IONIC-CONDUCTIVITY;
MODEL ELECTRODES;
PEROVSKITE;
CATHODE;
SOFC;
DIFFUSION;
TRANSPORT;
ZIRCONIA;
D O I:
10.1039/c1cp21684h
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 oxygen incorporation/extraction kinetics of the potential solid oxide fuel cell (SOFC) cathode material Bi1-xSrxFeO3-delta with x = 0.5 and 0.8 was studied by electrochemical impedance spectroscopy on geometrically well-defined pore-free thin film electrodes. The oxygen exchange rate was found to be higher than that of La1-xSrxFeO3-delta and-among cobalt-free perovskites-only surpassed by Ba1-xSrxFeO3-delta which is however known to be unstable in a SOFC environment.
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收藏
页码:16530 / 16533
页数:4
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