Highly active and stable (La0.24Sr0.16Ba0.6)(Co0.5Fe0.44Nb0.06)O3-δ (LSBCFN) cathodes for solid oxide fuel cells prepared by a novel mixing synthesis method

被引:64
作者
Chen, Xinbing [1 ,2 ]
Jiang, San Ping [1 ]
机构
[1] Curtin Univ Technol, Dept Chem Engn, Fuels & Energy Technol Inst, Perth, WA 6102, Australia
[2] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China
基金
中国国家自然科学基金;
关键词
CHROMIUM DEPOSITION; BA0.5SR0.5CO0.8FE0.2O3-DELTA CATHODE; METALLIC INTERCONNECT; ELECTRICAL-PROPERTIES; OXYGEN STOICHIOMETRY; CR ALLOY; TEMPERATURE; PERFORMANCE; ELECTROLYTES; DEGRADATION;
D O I
10.1039/c3ta10230k
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
Lanthanum and/or barium strontium cobalt ferrite perovskite oxide materials are highly active cathodes for solid oxide fuel cells (SOFCs) operated at intermediate temperatures of 600-900 degrees C. However, they are vulnerable to degradation by chromium deposition and poisoning by volatile Cr species from chromia-forming metallic interconnects. Here we report the development of a new mixed ionic and electronic conductor, lanthanum strontium barium cobalt ferrite niobium perovskite, (La0.24Sr0.16Ba0.6)(Co0.5Fe0.44Nb0.06)O3-delta (LSBCFN), prepared by a novel direct mixing synthesis of (La0.6Sr0.4)(Co0.2Fe0.8)O3-delta (LSCF) and Ba(Co0.7Fe0.2Nb0.1)O3-delta (BSCN). The electrical conductivity of LSBCFN is 124 S cm(-1) at 600 degrees C, which is significantly higher than 11 S cm(-1) measured on BSCN at the same temperature. The new LSBCFN cathode which combines the structural stability and activity of BCFN and the high conductivity of LSCF not only exhibits better electrochemical activity for the O-2 reduction reaction than either LSCF or BCFN in the temperature range of 600-900 degrees C, but most importantly, it shows excellent stability and tolerance toward chromium deposition and poisoning under SOFC operation conditions. A semi-quantitative analysis indicates that the Cr deposition at the electrode is closely related to the surface segregation of Sr and Ba.
引用
收藏
页码:4871 / 4878
页数:8
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