Self-assembled Gd 0.1 Ce 0.9 O 1.95-BaGd 0.8 La 0.2 Co 2 O 6-δ nanocomposite cathode for efficient protonic ceramic fuel cells

被引:3
作者
Liao, Dan [1 ]
Jia, Lichao [2 ]
Xu, Jianghui [1 ]
Chen, Zhiyi [1 ]
Huang, Jiongyuan [1 ]
Ai, Na [3 ]
Guan, Chengzhi [4 ]
Shao, Yanqun [1 ]
Jiang, San Ping [5 ,6 ]
Chen, Kongfa [1 ]
机构
[1] Fuzhou Univ, Coll Mat Sci & Engn, Fuzhou 350108, Fujian, Peoples R China
[2] Huazhong Univ Sci & Technol, Ctr Fuel Cell Innovat, Sch Mat Sci & Engn, State Key Lab Mat Proc & Die & Mound Technol, Wuhan 430074, Peoples R China
[3] Fuzhou Univ, Fujian Coll Assoc, Instrumental Anal Ctr, Fuzhou 350108, Fujian, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Appl Phys, Key Lab Interfacial Phys & Technol, Shanghai 201800, Peoples R China
[5] Foshan Xianhu Lab, Natl Energy Key Lab New Hydrogen Ammonia Energy T, Foshan 528216, Peoples R China
[6] Curtin Univ, WA Sch Mines Minerals Energy & Chem Engn, Perth, WA 6102, Australia
基金
中国国家自然科学基金;
关键词
Protonic ceramic fuel cells (PCFCs); Nanocomposite cathode; Self; -assembly; Heterointerface; Reaction mechanism; CONDUCTING ELECTROLYTE; LAYERED PEROVSKITES; RELAXATION-TIMES; OXYGEN REDUCTION; DEFECT CHEMISTRY; OXIDE; PERFORMANCE; TEMPERATURE; INTERFACE; PROMOTION;
D O I
10.1016/j.ceramint.2024.03.359
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
Protonic ceramic fuel cells (PCFCs) are characterized by a low activation energy for proton conduction and a high fuel utilization efficiency at low -to -intermediate temperatures. However, the sluggish oxygen reduction reaction kinetics on the cathodes drastically limit the power output performance of PCFCs. Herein, multiphase Gd 0.1 Ce 0.9 O 1.95 - BaGd 0.8 La 0.2 Co 2 O 6- delta (GDC-BGLC) nanocomposite cathodes are prepared by coupling selfassembly and sintering -free electrode construction methods. The nanocomposite cathode comprises mixed H + /e - conducting BGLC and O 2- conducting GDC and BaCoO 3 nanoparticles, and these phases are homogeneously mixed with coherent heterointerfaces. The nanocomposite cathode exhibits a significant increase in surface oxygen vacancies and three-phase boundaries, enhanced catalytic activity, and reduced activation energy for the oxygen reduction and water formation reactions. The results imply that the oxygen reduction and water formation reactions on the multiphase GDC-BGLC nanocomposite electrodes are most likely the dissociation, reduction and diffusion of oxygen species, which in turn is affected by the water vapor formed. An anodesupported single cell with the GDC-BGLC cathode exhibits a peak power density of 810 mW cm -2 at 700 degrees C with excellent operating stability at 650 degrees C for 110 h. This study provides a new strategy for the preparation of a high-performance and durable nanocomposite cathode for PCFCs.
引用
收藏
页码:22574 / 22582
页数:9
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