固体氧化物燃料电池
氧化物
钙钛矿(结构)
材料科学
电极
尖晶石
化学工程
降级(电信)
氧气
分解
再分配(选举)
开路电压
无机化学
电压
化学
电子工程
冶金
阳极
物理化学
电气工程
有机化学
法学
工程类
政治
政治学
作者
Jinsil Lee,Yonghun Shin,Taeyun Kim,Wooseon Choi,Min‐Hyoung Jung,Young‐Min Kim,Kyung Joong Yoon,Hu Young Jeong,Donghwa Lee,Jong Hoon Joo
标识
DOI:10.1021/acs.chemmater.3c03283
摘要
Perovskite-based materials are typically used as electrodes in solid oxide cells (SOCs) owing to their high catalytic activity in oxygen exchange reactions. The degradation of typical SOCs is a well-known phenomenon that is primarily attributed to the A-site cation redistribution within perovskite-based electrodes at elevated operating temperatures. To date, investigations of the degradation and stability of perovskite electrodes have predominantly focused on assessing thin-film electrodes under an open-circuit voltage. This study proposes a detailed degradation mechanism of electrodes based on bulk-dense materials under the operating conditions of an actual solid oxide fuel cell. Our findings revealed that La0.6Sr0.4Co0.2Fe0.8O3–δ is decomposed into SrO, spinel phase ((CoFe)3O4), and La-rich perovskite in the subsurface region under cathodic bias conditions. Additionally, the results of this study indicate that the phase decomposition associated with elements in the B-site must be considered to improve the enhancement of the stability and oxygen reduction reaction activity.
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