Higher oxygen vacancy content and hydration capability enabled by magnesium doping for high-activity protonic ceramic fuel cell cathode

被引:8
|
作者
Zhang, Liming [1 ,2 ]
Pang, Bingjie [1 ]
Hu, Shiqing [1 ]
Cao, Zhongwei [1 ]
Zhang, Peng [1 ]
Zhu, Xuefeng [1 ]
Yang, Weishen [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Liaoning, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
PCFCs; SOFCs; MIEC; Perovskite; Oxygen vacancy; Hydration; COBALT-FREE CATHODE; HIGH-PERFORMANCE; ELECTROCHEMICAL-CELLS; PEROVSKITE CATHODES; GENERATION; STABILITY; OXIDATION; MG;
D O I
10.1016/j.ijhydene.2022.11.268
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
Protonic ceramic fuel cells (PCFCs) are promising power generation equipment because of their high efficiency and low operating temperature. However, the sluggish oxidation-reduction reaction (ORR) kinetics of the cathode seriously limits their further develop-ment. Here, a low-valent alkaline-earth metal Mg-doped BaCo0.4Fe0.4Zr0.2O3-$ (BaCo0.4Fe0.4-Zr0.1Mg0.1O3-$ = BCFZMg0.1) cathode is developed to increase oxygen vacancy concentration and hydration capability of mixed oxygen ion-electron conducting (MIEC) electrode ma-terials. The phase composition, microstructure, and stability in wet air were examined, while the oxygen vacancy, hydration capability, conductivity, and surface species of the materials were investigated. Experimental results demonstrate that the oxygen vacancy concentration, hydration capability, and conductivity are all increased by Mg doping. Consequently, the ORR active sites were expanded to the whole electrode surface, and the electrochemical performance of PCFCs with BCFZMg0.1 cathode was greatly improved (peak power density: >40% increase; polarization resistance: 60-70% decrease). This work provides a new strategy to develop cathodes with high ORR activity for PCFCs by doping Mg into the MIEC perovskite B-site. (c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:10180 / 10190
页数:11
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