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New Sr2FeMo0.5X0.5O6 (X=Ni, Co, Mn, Zn) cathodes for proton-conducting SOFCs.

Authors :
Wang, Lele
Yu, Shoufu
Zhang, Liling
Gu, Yueyuan
Bi, Lei
Source :
International Journal of Hydrogen Energy. Jan2024:Part C, Vol. 50, p887-896. 10p.
Publication Year :
2024

Abstract

Transition metal elements were employed to customize the standard Sr 2 Fe 1.5 Mo 0.5 O 6 (SFM) material, with the goal of improving the performance of the SFM cathode in proton-conducting solid oxide fuel cells (H–SOFCs). Sr 2 FeMo 0.5 X 0.5 O 6 (X = Ni, Co, Mn, Zn) materials were prepared, but it was discovered that only the dopants Ni and Co can form a pure phase, whereas the dopants Mn and Zn produced an obvious secondary phase. When comparing oxygen vacancies and oxygen diffusion kinetics, utilizing the Co-dopant exhibited clear advantages. The Co-doped SFM had a higher oxygen vacancy content and faster oxygen diffusion kinetics than both the standard and Ni-doped SFM cathodes. The energy barrier for the oxygen reduction reaction (ORR) at the Co-doped SFM cathode was 0.76 eV, which was much lower than that for the SFM and Ni-doped SFM, which were 5.52 and 2.28 eV, respectively. As a result, the Co-doped SFM's cathode reaction was greatly accelerated, resulting in a high fuel cell performance of 1306 mW cm−2 at 700 °C. This finding suggests that using the appropriate dopant can alleviate the low-performance problem of the traditional SFM cathode, resulting in a promising cathode option for H–SOFCs. • Sr 2 FeMo 0.5 X 0.5 O 6 (X = Ni, Co, Mn, Zn) cathodes were proposed for H–SOFCs. • The Co dopant showed more advantages compared with other dopants. • The Sr 2 FeMo 0.5 Co 0.5 O 6 cathode delivered high fuel cell performance. • The mechanism for the enhanced cathode performance was revealed. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03603199
Volume :
50
Database :
Academic Search Index
Journal :
International Journal of Hydrogen Energy
Publication Type :
Academic Journal
Accession number :
174184730
Full Text :
https://doi.org/10.1016/j.ijhydene.2023.09.118