Understanding the degradation mechanisms of Ba-based double perovskite electrodes for solid oxide electrochemical cells

被引:0
作者
Lee, Jinsil [1 ]
Kim, Taeyun [1 ]
Lee, Hyeon Jin [1 ]
Yoon, Kyung Joong [2 ]
Lee, Jong-Ho [2 ]
Joo, Jong Hoon [1 ,3 ]
机构
[1] Gwangju Inst Sci & Technol GIST, Sch Environm & Energy Engn, 123 Cheomdangwagi Ro, Gwangju 61005, South Korea
[2] Korea Inst Sci & Technol KIST, Ctr Energy Mat Res, Seoul 02792, South Korea
[3] Gwangju Inst Sci & Technol, Res Ctr Innovat Energy & Carbon Optimized Synth Ch, 123 Cheomdangwagi Ro, Gwangju 61005, South Korea
基金
新加坡国家研究基金会;
关键词
Double perovskite materials; Surface exchange reactions; Electrode degradation mechanism; Moisture; Carbon dioxide; OXYGEN REDUCTION ACTIVITY; SURFACE MODIFICATION; DOPANT SEGREGATION; PERFORMANCE; CATHODE; CONDUCTIVITY; DEPENDENCE; STABILITY; TRANSPORT; COBALT;
D O I
10.1016/j.cej.2025.159654
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
To shed light on the degradation mechanisms, this study investigated the electrochemical characteristics and phase stability of PrBaFe2O5+omega (PBF) a representative double perovskite material, under atmospheric conditions. A ceramic manufacturing process was applied to fabricate dense bulk electrode for analyzing the surface exchange reaction comprehensively. Furthermore, a defect concentration analysis was performed, which offered insights into the double perovskite material properties and affirmed the accuracy of the analysis system by comparing the surface exchange coefficients utilizing the fabricated dense bulk electrode. When surface exchange reactions were measured in an atmosphere containing CO2 and moisture, significant degradation was observed. Our findings indicated that the deterioration in surface exchange reactions of the double perovskite electrode was primarily due to the hydroxide formation in the atmosphere, leading to phase decomposition.
引用
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页数:9
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