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Preparation and Electrochemical Performance of Cobalt-free Cathode Material Ba0.5Sr0.5Fe0.9Nb0.1O3-δ for Intermediate-temperature Solid Oxide Fuel Cells

Preparation and Electrochemical Performance of Cobalt-free Cathode Material Ba0.5Sr0.5Fe0.9Nb0.1O3-δ for Intermediate-temperature Solid Oxide Fuel Cells

作     者:LONG Wen XU Huawei HE Tianmin 

作者机构:Key Laboratory of Physics and Technology for Advanced Batteries Ministry of Education College of Physics Jilin University Changchun 130012 P. R. China 

出 版 物:《Chemical Research in Chinese Universities》 (高等学校化学研究(英文版))

年 卷 期:2014年第30卷第5期

页      面:806-810页

核心收录:

学科分类:0808[工学-电气工程] 08[工学] 080502[工学-材料学] 0805[工学-材料科学与工程(可授工学、理学学位)] 

基  金:Supported by the National Natural Science Foundation of China(No. 10974065) and the Applied Basic Research Programs of Science and Technology Development of Jilin Province  China(No.20130102011JC) 

主  题:Solid oxide fuel cell Cathode Phase formation Chemical stability Electrochemical performance 

摘      要:Perovskite oxide Ba0.5Sr0.5Fe0.9Nb0.1O3-δ(BSFN) as a cobalt-free cathode for intermediate-temperature solid oxide fuel cells(IT-SOFCs) on the Ce0.5Sm0.2O1.9(SDC) and La0.9Sr0.1Ga0.8Mg0.23O3-δ(LSGM) electrolytes was prepared and investigated. The single phase BSFN oxide with a cubic perovskite structure and relatively high elec- trical conductivities was obtained after sintering at 1250℃ for 10 h in air. The BSFN cathode exhibited excellent chemical stability on the SDC and LSGM electrolytes at temperatures below 950 ℃. The area specific resistance of the BSFN cathode on the SDC and LSGM electrolytes were 0.024 and 0.021 Ω·cm2 at 800℃, respectively. The maximum power densities of the single cell with BSFN cathode in 300 μm-thick SDC and LSGM electrolytes achieved 414 and 516 mW/cm2 at 800℃, respectively. These results show that the BSFN material is a promising co- bait-free cathode candidate to be used in IT-SOFCs. A combination of the BSFN cathode and LSGM electrolyte is preferred owing to its excellent electrochemical performance.

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