材料科学
阴极
电极
化学工程
涂层
极化(电化学)
拉曼光谱
钙钛矿(结构)
陶瓷
降级(电信)
催化作用
功率密度
氧气
分析化学(期刊)
复合材料
纳米技术
化学
物理化学
电信
生物化学
物理
功率(物理)
光学
有机化学
量子力学
计算机科学
工程类
色谱法
作者
Hua Zhang,Kang Xu,Fan He,Yucun Zhou,Kotaro Sasaki,Bote Zhao,YongMan Choi,Meilin Liu,Yu Chen
标识
DOI:10.1002/aenm.202200761
摘要
Abstract Protonic ceramic fuel cells (PCFCs) are one of the most efficient energy conversion devices. However, the performance of current PCFCs is greatly limited by the sluggish oxygen reduction reaction (ORR) kinetics and the fast degradation of the cathode due to contaminants poisoning (such as Cr species and steam). Here, a surface regulation of a double perovskite PrBa 0.5 Sr 0.5 Co 1.5 Fe 0.5 O 5+ δ (PBSCF) cathode by a Pr 0.9 Fe 0.7 Co 0.3 O 3 (PFC) catalyst coating to enhance the ORR activity and stability is reported. When tested in direct contact with Cr in the air with 3% H 2 O at 650 °C, the polarization resistance ( R p ) of the PFC coated PBSCF (PFC‐PBSCF) electrode increases from ≈0.39 to 0.45 Ω cm 2 after 100 h operation; in contrast, the R p of a PBSCF electrode increases from 0.63 to 0.82 Ω cm 2 . Further, a PCFC with the PFC‐PBSCF cathode demonstrates an excellent peak power density (≈1.08 W cm –2 at 650 °C) and significantly enhanced durability (degradation rate of 0.03% h −1 ), much better than those of the cells with a PBSCF cathode (≈0.75 W cm –2 and degradation rate of 0.12% h −1 ). Raman spectroscopy and density functional theory calculations indicate that the PFC catalyst coating diminishes the formation of Cr species, such as (Ba 1‐ x Sr x )CrO 4 , on the cathode surface.
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