燃料电池
阴极
氧气
氧化物
材料科学
氧还原
氧还原反应
化学工程
化学
冶金
有机化学
工程类
电极
物理化学
电化学
作者
Fan He,Feng Zhu,Kang Xu,Yangsen Xu,Dongliang Liu,Guangming Yang,Kotaro Sasaki,YongMan Choi,Yu Chen
标识
DOI:10.1016/j.apcatb.2024.124175
摘要
One big obstacle for the oxygen reduction reaction (ORR) electrode in solid oxide fuel cells (SOFCs) is the poor reaction activity and fast degradations caused by CO2 poisoning. Here we report our design of an active A-site Ca-rich high-entropy Pr0.1875Ba0.1875Sr0.1875La0.1875Ca0.25CoO3-δ (PBSLC25C) electrode, guided by the O p-band theory. When applied as a cathode in solid oxide fuel cells (SOFCs), it demonstrates high ORR activity and excellent CO2 tolerance under realistic operating conditions. Ni-YSZ-based anode-supported cells with PBSLC25C cathodes demonstrate excellent peak power densities of 1.14 W cm-2, 1.04 W cm-2, and 0.77 W cm-2 in the air with 1%, 5%, and 10% CO2, respectively, at 750 oC. The engineered high-entropy PBSLC25C effectively diminishes the CO2 poisoning effect and maintains active surfaces for fast oxygen exchange, as confirmed by the cell durability test in air containing CO2 (5 and 10 vol%), Raman spectroscopy, and density functional theory calculations.
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