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A highly active perovskite anode with an in situ exsolved nanoalloy catalyst for direct carbon solid oxide fuel cells.

Authors :
Ma, Minjian
Yang, Xiaoxia
Ren, Rongzheng
Xu, Chunming
Qiao, Jinshuo
Sun, Wang
Sun, Kening
Wang, Zhenhua
Source :
Journal of Materials Chemistry A; 8/28/2021, Vol. 9 Issue 32, p17327-17335, 9p
Publication Year :
2021

Abstract

Effective utilization of carbonaceous fuels is essential to address the economic and environmental challenges in the future. Direct carbon solid oxide fuel cells (DCSOFCs) offer a promising solution, but their performance is hindered by the sluggish anode processes and poor stability. Herein, a novel layered perovskite, (PrBa)<subscript>0.95</subscript>Fe<subscript>1.6</subscript>Ni<subscript>0.2</subscript>Nb<subscript>0.2</subscript>O<subscript>5+δ</subscript> (PBFNN), is developed as a highly effective anode material for DCSOFCs. FeNi<subscript>3</subscript> nanoparticles on the perovskite substrate are in situ exsolved under the reduction of carbon, and the resulting alloy–perovskite interfaces can promote efficient reverse Boudouard reaction (RBR) by the optimized CO<subscript>2</subscript> capture and RBR activation. Therefore, the carbon fuel can be efficiently converted into CO because of the highly active RBR on the surface of the PBFNN anode, which further promotes the electrochemical oxidation of CO, leading to enhanced electrochemical performance of the anode. An electrolyte-supported DCSOFC employing the PBFNN anode yields superior performances but using additive-free carbon fuels, and delivers a peak power density of 605.1 mW cm<superscript>−2</superscript> at 800 °C and superior stability over 120 h at 750 °C. Our work highlights that PBFNN is a high-performance and robust alternative perovskite anode for DCSOFCs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20507488
Volume :
9
Issue :
32
Database :
Complementary Index
Journal :
Journal of Materials Chemistry A
Publication Type :
Academic Journal
Accession number :
151959258
Full Text :
https://doi.org/10.1039/d1ta04044h