Oxygen ionization and diffusion at SOFC cathode/electrolyte interface under cathodic polarization

被引:8
|
作者
Horita, Teruhisa [1 ]
Shimonosono, Taro [1 ]
Kishimoto, Haruo [1 ]
Yamaji, Katsuhiko [1 ]
Brito, Manuel E. [1 ]
Yokokawa, Harumi [1 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Tsukuba, Ibaraki, Japan
关键词
SOFC; Isotope oxygen; Cathode; Electrolyte; Diffusion; LA0.9SR0.1MNO3-X/YTTRIA-STABILIZED ZIRCONIA INTERFACE; YTTRIA-STABILIZED ZIRCONIA; SURFACE EXCHANGE KINETICS; OXIDE FUEL-CELLS; ELECTRODE; REDUCTION; SITES;
D O I
10.1016/j.ssi.2012.04.026
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
Oxygen ionization and diffusion were visualized at cathode/interlayer/electrolyte interfaces by isotopic oxygen labeling (O-16/O-18 exchange) in real flatten tube solid oxide fuel cells. Three-flatten tube cell-stacks were exposed to O-18(2) under fuel cell operation conditions at different current densities (J = 0, 0.10, and 0.25 A/cm(2) at a temperature of 650 degrees C), and the distribution of O-18 was observed at the quenched samples by secondary ion mass spectrometry (SIMS). An increase of O-18 concentration at LaFeO3 based cathode and a peak O-18 concentration formation around the CeO2-based interlayer were observed. The increase of O-18 concentration at the LaFeO3 based cathode is attributed to an increase of oxygen surface exchange rates under polarization. The peak O-18 concentration increased with current densities through the interlayer/electrolyte interfaces. The formation of O-18 peak can be related to the formation of a slow O-18-diffusion layer at the interlayer/electrolyte interfaces. Possible mechanism for formation of the O-18 peak around the interlayer/electrolyte interfaces was considered. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:141 / 145
页数:5
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