Design of a perovskite oxide cathode for a protonic ceramic fuel cell

被引:6
|
作者
Yao, Penghui [1 ]
Zhang, Jian [2 ]
Qiu, Qianyuan [1 ]
Li, Gen [1 ]
Zhao, Yicheng [2 ]
Yu, Fangyong [3 ]
Li, Yongdan [1 ]
机构
[1] Aalto Univ, Dept Chem & Met Engn, Kemistintie 1, FI-00076 Aalto, Finland
[2] Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin Key Lab Appl Catalysis Sci & Technol, Sch Chem Engn & Techno,State Key Lab Chem Engn, Tianjin 300072, Peoples R China
[3] Shandong Univ Technol, Sch Chem & Chem Engn, Zibo 255049, Peoples R China
关键词
Protonic ceramic fuel cells (PCFC); Oxygen reduction reaction (ORR); Proton transfer; OXYGEN REDUCTION REACTION; HIGH-PERFORMANCE; ELECTROCHEMICAL PROPERTIES; DEFECT CHEMISTRY; ELECTROLYTES; GENERATION; ZIRCONATE; STACK;
D O I
10.1016/j.ceramint.2023.11.015
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
High catalytic activity, low-cost and stable cathode in a temperature range 550-700 degrees C is essential for the development of protonic ceramic fuel cells (PCFCs). Doping nickel into perovskite La0.5Sr0.5MnO3-delta(LSM) is designed as a cobalt-free cathode based on theoretical calculations and experiments. La0.5Sr0.5Mn0.9Ni0.1O3-delta (LSMNi) as cathode shows higher proton conductivity and ORR activity than the undoped LSM. The PCFCs with LSMNi exhibit low polarization resistance and high peak power density 1.1 W cm-2 at 700 degrees C. The density functional theory simulations indicate that doping with nickel decreases the oxygen vacancy formation energy and promotes the formation of hydroxide defects. The decrease in proton transfer energy barriers and hydration energy improves the proton conductivity. The improved performance is attributed to fast proton transfer and rapid kinetics of oxygen reduction on the surface of LSMNi. This work provides a novel approach to design cobalt-free cathode for a protonic ceramic fuel cell.
引用
收藏
页码:2373 / 2382
页数:10
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