An acidity-regulated double perovskite cathode for efficient and durable power generation of intermediate-temperature solid oxide fuel cells

被引:3
|
作者
Xu, Aoqin [1 ]
Huan, Daoming [1 ]
Dai, Pengqi [1 ]
Zhang, Lu [1 ]
Xia, Changrong [1 ,2 ]
机构
[1] Univ Sci & Technol China, Dept Mat Sci & Engn, CAS Key Lab Mat Energy Convers, 96 Jinzhai Rd, Hefei 230026, Anhui, Peoples R China
[2] Anhui Estone Mat Technol Co Ltd, Energy Mat Ctr, 2-A1,106 Chuangxin Ave, Hefei 230088, Anhui, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
HIGH-PERFORMANCE; OXYGEN-ELECTRODE; PRBA0.5SR0.5CO1.5FE0.5O5+DELTA; SOFC; CO2; FE;
D O I
10.1039/d4ta02853h
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
As solid oxide fuel cells (SOFCs) move towards commercial viability, it is imperative to reduce operating temperatures to intermediate ranges (500-700 degrees C). Nonetheless, the sluggish kinetics of the oxygen reduction reaction on the cathode remain a significant challenge, dominating the polarization resistance of the full cell as temperature decreases. This study proposes a highly active and durable cathode candidate for intermediate-temperature SOFCs through altering the acidity of double perovskite oxides. Herein, we present a novel A-site Eu-doped double perovskite oxide, EuBa0.5Sr0.5Co2-xFexO5+delta (EBSCFx, x = 0.5, 1.0, and 1.5), demonstrating high efficiency and stability suitable for SOFC deployment. Notably, EBSCF1.0 exhibits remarkable stability and outstanding oxygen reduction reaction activity, boasting a very low interfacial polarization resistance of 0.097 Omega cm2 at 650 degrees C in dry air. Utilizing this cathode, our button cell achieves exceptional electrochemical performance, yielding a peak power density of 1.50 W cm-2 at 650 degrees C accompanied by a 100 h stability test. This work reports a double perovskite oxide EuBa0.5Sr0.5Co2-xFexO5+delta (EBSCFx, x = 0.5, 1, and 1.5) as cathode for IT-SOFC. Specifically, the cell using EBSCF1.0 cathode delivers excellent performance with a PPD of 1.50 W cm-2 at 650 degrees C.
引用
收藏
页码:19392 / 19402
页数:11
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