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Overdoping-induced CeO2-modified PBCF heterostructures for enhanced proton-conducting SOFCs

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成果类型:
期刊论文
作者:
Liu, Kechen;Hou, Zhongyu;Li, Qi;Zhang, Xuan;Zhou, Jing;...
通讯作者:
Fu, Min;Tao, ZT;Zhou, J
作者机构:
[Li, Qi; Zhang, Xuan; Tao, Zetian; Hou, Zhongyu; Fu, Min; Fu, M; Liu, Kechen] Univ South China Hengyang, Sch Resources Environm & Safety Engn, Hengyang 421001, Hunan Province, Peoples R China.
[Zhou, Jing; Zhou, J] Qiannan Normal Univ Nationalities, Sch Chem & Chem Engn, Duyun 558000, Peoples R China.
通讯机构:
[Tao, ZT ; Fu, M] U
[Zhou, J ] Q
Univ South China Hengyang, Sch Resources Environm & Safety Engn, Hengyang 421001, Hunan Province, Peoples R China.
Qiannan Normal Univ Nationalities, Sch Chem & Chem Engn, Duyun 558000, Peoples R China.
语种:
英文
关键词:
In-situ;Exsolution;Heterostructure;Proton conductor;Chemical stability
期刊:
International Journal of Hydrogen Energy
ISSN:
0360-3199
年:
2025
卷:
127
页码:
896-902
基金类别:
National Natural Science Foundation of China [22479072]; Natural Science Foundation of the Higher Education Institutions of Jiangsu Province [18KJA430017]
机构署名:
本校为第一且通讯机构
摘要:
To construct heterostructures with robustly interconnected interfaces, this study employs a co-doping strategy exceeding the stoichiometric ratio. The doping strategy in Pr 0.5 Ba 0.5 Co 0.7 Fe 0.3 Ce x O 3-δ (PBCF) facilitates the exsolution of Ce at the B-site, leading to the formation of a CeO 2 -modified surface layer on PBCF. Structural and morphological analyses confirm the dissolution of CeO 2 particles, with their concentration increasing proportionally to the Ce doping level. Notably, the single cell utilizing the Pr 0.5 Ba 0.5 Co 0.7...

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