La0.5Sr0.5Fe0.9Mo0.1O3-8-CeO2 anode catalyst for Co-Producing electricity and ethylene from ethane in proton-conducting solid oxide fuel cells

被引:40
|
作者
Wang, Lijuan [1 ]
Fan, Yun [1 ]
Li, Jun [2 ]
Shao, Lin [1 ]
Xi, Xiuan [1 ]
Fu, Xian-Zhu [1 ]
Luo, Jing-Li [1 ]
机构
[1] Shenzhen Univ, Coll Mat Sci & Engn, Shenzhen 518055, Peoples R China
[2] Foshan Univ, Sch Mat Sci & Hydrogen Energy, Foshan 528000, Peoples R China
基金
中国国家自然科学基金;
关键词
SOFC; Anode; Perovskite; Co-producing electricity and ethylene; CeO2; COBALT-FREE CATHODE; PERFORMANCE; COGENERATION; TEMPERATURE; PEROVSKITE; REDUCTION; ELECTROLYTE; HYDROGEN; METHANE; POWER;
D O I
10.1016/j.ceramint.2021.05.121
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A La0.5Sr0.5Fe0.9Mo0.1O3-8-CeO2 (LSFM-CeO2) composite was prepared by impregnating CeO2 into porous La0.5Sr0.5Fe0.9Mo0.1O3-8 perovskite and was used as an anode material for proton-conducting solid oxide fuel cells (SOFCs). The maximum power densities of the BaZr0.1Ce0.7Y0.2O3-8 (BZCY) electrolyte-supported single cell with LSFM-CeO2 as the anode reached 291 mW cm-2 and 190 mW cm-2 in hydrogen and ethane fuel at 750 degrees C, respectively, which are significantly higher than those of a single cell with only LSFM as the anode. Additionally, the ethylene selectivity and ethylene yield from ethane for the fuel cell at 750 degrees C were as high as 93.4% and 37.1%, respectively. The single cell also showed negligible degradation in performance and no carbon deposition during continuous operation for 22 h under an ethane fuel atmosphere. The improved electrochemical performance due to the impregnation of CeO2 can be a result of enhanced electronic and ionic conductivity, abundant active sites, and a broad three-phase interface in the resultant composite anode. The LSFM-CeO2 composite is believed to be a promising anode material for proton-conducting SOFCs for co-producing electricity and highvalue chemicals from hydrocarbon fuels.
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页码:24106 / 24114
页数:9
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