材料科学
阴极
氧化物
电化学
钙钛矿(结构)
化学工程
电极
催化作用
兴奋剂
扩散
氧气
介电谱
相(物质)
光电子学
物理化学
生物化学
热力学
物理
工程类
有机化学
化学
冶金
作者
Yunjie Gou,Guangdong Li,Rongzheng Ren,Chunming Xu,Jinshuo Qiao,Wang Sun,Kening Sun,Zhenhua Wang
标识
DOI:10.1021/acsami.1c03514
摘要
Intermediate temperature solid oxide fuel cells (IT-SOFCs) have been extensively studied due to high efficiency, cleanliness, and fuel flexibility. To develop highly active and stable IT-SOFCs for the practical application, preparing an efficient cathode is necessary to address the challenges such as poor catalytic activity and CO2 poisoning. Herein, an efficient optimized strategy for designing a high-performance cathode is demonstrated. By motivating the phase transformation of BaFeO3-δ perovskites, achieved by doping Pr at the B site, remarkably enhanced electrochemical activity and CO2 resistance are thus achieved. The appropriate content of Pr substitution at Fe sites increases the oxygen vacancy concentration of the material, promotes the reaction on the oxygen electrode, and shows excellent electrochemical performance and efficient catalytic activity. The improved reaction kinetics of the BaFe0.95Pr0.05O3-δ (BFP05) cathode is also reflected by a lower electrochemical impedance value (0.061 Ω·cm2 at 750 °C) and activation energy, which is attributed to high surface oxygen exchange and chemical bulk diffusion. The single cells with the BFP05 cathode achieve a peak power density of 798.7 mW·cm–2 at 750 °C and a stability over 50 h with no observed performance degradation in CO2-containing gas. In conclusion, these results represent a promising optimized strategy in developing electrode materials of IT-SOFCs.
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