Comparison of (Pr, Ba, Sr)FeO3-δ-SDC composite cathodes in proton-conducting solid oxide fuel cells

被引:15
|
作者
Cai, Bin [1 ]
Song, Teng-Fei [1 ]
Su, Jin-Rui [1 ]
He, Hao [1 ]
Liu, Yang [1 ]
机构
[1] Zhengzhou Univ, Minist Educ, Key Lab Mat Phys, Sch Phys & Microelect, Zhengzhou 450052, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
(Pr; Ba; Sr)FeO3-delta; Cubic perovskite structure; Electrochemical performance; Co-free composite cathodes; H-SOFCs; OXYGEN REDUCTION REACTION; ELECTROCHEMICAL PROPERTIES; THERMAL-EXPANSION; HIGH-PERFORMANCE; CARBONATE COPRECIPITATION; PEROVSKITE; PR; ELECTRODE; PHASE; ND;
D O I
10.1016/j.ssi.2020.115379
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
Three kinds of Co-free Ba0.5Sr0.5FeO3-delta (BSF), Pr0.5Ba0.5FeO3-delta (PBF), and Pr0.5Ba0.25Sr0.25FeO3-delta (PBSF) cathode materials (CMs) with cubic perovskite structure were prepared by combining EDTA-citrate process and solid state reaction. The lattice constant is the largest for BSF, and the smallest for PBSF due to the difference of Ba2+, Sr2+, and Pr3+ ionic radii. A good chemical compatibility was observed among BSF (PBF or PBSF), Sm0.2Ce0.8OFeO2-delta (SDC) and BaZr0.1Ce0.7Y0.2O3-delta (BZCY) even their mixture was co-fired at 1000 degrees C for 6 h. For single cells with NiO-BZCYIBZCY1CM-SDC (CM = BSF, PBF, or PBSF) configuration, the best electrochemical performance was obtained for PBSF at 650 degrees C and higher working temperatures while it was achieved for BSF at 600 degrees C. Analyses on the electrochemical impedance spectra show that the polarization process of H-SOFCs with PBSF-SDC composite cathode should be mainly controlled by the charge transfer and diffusion of the oxygen ions while that for both BSF-SDC and PBF-SDC might be dominated by proton behavior.
引用
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页数:10
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