Sr2Fe1.5Mo0.4Ti0.1O6-? perovskite anode for high-efficiency coal utilization in direct carbon solid oxide fuel cells

被引:11
作者
Cui, Wencan [1 ]
Ma, Minjian [1 ]
Sun, Jiaxiang [1 ]
Ren, Rongzheng [1 ]
Xu, Chunming [1 ]
Qiao, Jinshuo [1 ]
Sun, Wang [1 ]
Sun, Kening [1 ]
Wang, Zhenhua [1 ]
机构
[1] Beijing Inst Technol, Sch Chem & Chem Engn, Beijing Key Lab Chem Power Source & Green Catalysi, Beijing 100081, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Direct carbon fuel cells; Anode; Coal utilization; Perovskite; Stability; HIGH-PERFORMANCE; ELECTROCHEMICAL PERFORMANCE; SULFUR; TEMPERATURE; ELECTRODE; SR2FE1.5MO0.5O6-DELTA; PYROLYSIS; BIOCHAR; GAS; PROGRESS;
D O I
10.1016/j.jpowsour.2022.232562
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
Efficient and direct utilization of coal-based fuels is the developmental direction of direct carbon solid oxide fuel cells (DCSOFCs), but their performance is hindered by poor catalytic activity and contaminant poisoning of anode materials. Herein, a Ti-doped double perovskite oxide Sr2Fe1.5Mo0.4Ti0.1O6-delta(SFMT) was developed as the coal-based DCSOFC anode to improve its catalytic activity and resistance to sulfur poisoning. X-ray photoelectron spectroscopy confirms that SFMT shows abundant oxygen vacancy concentration under reducing atmosphere. The as-fabricated DCSOFC with the SFMT anode delivers a maximum power density of 506.5 mW cm-2 at 800 degrees C when using bituminous coal as the fuel. Electrochemical impedance spectroscopy reveals that Ti doping can effectively promote electrochemical processes on the anode side. Both thermogravimetric analysis and CO temperature-programmed desorption demonstrate that the performance improvement of SFMT is ascribed to its promoted catalytic activity in coal gasification and its increased CO adsorption capacity. The operational period of this coal-based DCSOFC increases from 2 to 10 h after Ti doping, which can be explained by the enhanced structural stability of SFMT under a sulfur-containing environment. Our work may provide some new insight on the design of high-activity anode materials and the understanding of anode reaction mechanisms for coal-based DCSOFCs.
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页数:9
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