A highly active perovskite anode with an in situ exsolved nanoalloy catalyst for direct carbon solid oxide fuel cells

被引:7
|
作者
Ma, Minjian [1 ]
Yang, Xiaoxia [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 Catalys, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
PERFORMANCE DIRECT CARBON; ELECTROCHEMICAL PERFORMANCE; SOFC ANODES; HIGH-POWER; TEMPERATURE; REDUCTION; COMPOSITE; ELECTRODE; CHALLENGES; CONVERSION;
D O I
10.1039/d1ta04044h
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
Effective utilization of carbonaceous fuels is essential to address the economic and environmental challenges in the future. Direct carbon solid oxide fuel cells (DCSOFCs) offer a promising solution, but their performance is hindered by the sluggish anode processes and poor stability. Herein, a novel layered perovskite, (PrBa)(0.95)Fe1.6Ni0.2Nb0.2O5+delta (PBFNN), is developed as a highly effective anode material for DCSOFCs. FeNi3 nanoparticles on the perovskite substrate are in situ exsolved under the reduction of carbon, and the resulting alloy-perovskite interfaces can promote efficient reverse Boudouard reaction (RBR) by the optimized CO2 capture and RBR activation. Therefore, the carbon fuel can be efficiently converted into CO because of the highly active RBR on the surface of the PBFNN anode, which further promotes the electrochemical oxidation of CO, leading to enhanced electrochemical performance of the anode. An electrolyte-supported DCSOFC employing the PBFNN anode yields superior performances but using additive-free carbon fuels, and delivers a peak power density of 605.1 mW cm(-2) at 800 degrees C and superior stability over 120 h at 750 degrees C. Our work highlights that PBFNN is a high-performance and robust alternative perovskite anode for DCSOFCs.
引用
收藏
页码:17327 / 17335
页数:9
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