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Composite electrolyte with Ruddlesden-Popper structure Sm1.2Sr0.8Ni0.6Fe0.4O4+δ for high-performance low temperature solid oxide fuel cells.

Authors :
Ouyang, Yuzhao
Zhu, Decai
Zhu, Chengjun
Zhang, Yingbo
Liu, Jiamei
Jia, Xin
Yu, Jie
Li, Xinfang
Yang, Min
Gao, Xiaowei
Source :
International Journal of Hydrogen Energy. Jan2023, Vol. 48 Issue 1, p268-279. 12p.
Publication Year :
2023

Abstract

Ruddlesden-Popper (R–P) structure oxide has been widely used as the electrode material in low temperature solid oxide fuel cells (LT-SOFCs) because of its high catalytic activity and excellent oxygen transport performance, while the studies on this material served as the electrolyte of LT-SOFCs is rarely reported. Herein, the R–P P-type semiconductor Sm 1.2 Sr 0·8 Ni 0·6 Fe 0·4 O 4+δ (SSNF) oxide material was prepared and then used as electrolyte by constructing P–N heterostructure with the N-type semiconductor Sm 0.075 Nd 0.075 Ce 0·85 O 2-δ (SNDC) oxide material. Experimental results showed that the developed 5SSNF-5SNDC composite electrolyte exhibited a high ionic conductivity of 0.201 S·cm−1 along with remarkable fuel cell power density of 1056 mW·cm−2 at 550·°C. The constructed P–N heterostructure helps to improve the oxygen ion conductivity and thus the electrochemical properties. These results demonstrate that P–N heterojunctions constructed from oxide materials with highly catalytically active R–P structures exhibit excellent electrolyte performance. This work provides a new perspective for developing advanced electrolytes of LT-SOFCs. [Display omitted] • The composite electrolyte has a high oxygen vacancy. • The fuel cell device produces a maximum power density of 1056 mW cm−2 at 550 °C. • The composite electrolyte has a significant ionic conductivity of 0.201 S cm−1. • Ion migration was enhanced by constructing P–N heterojunctions. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03603199
Volume :
48
Issue :
1
Database :
Academic Search Index
Journal :
International Journal of Hydrogen Energy
Publication Type :
Academic Journal
Accession number :
160963086
Full Text :
https://doi.org/10.1016/j.ijhydene.2022.09.204