High performance La0.3Ca0.7Cr0.3Fe0.7O3-δ air electrode for reversible solid oxide fuel cell applications

被引:40
作者
Molero-Sanchez, Beatriz [1 ]
Prado-Gonjal, Jesus [2 ]
Avila-Brande, David [2 ]
Chen, Min [1 ]
Moran, Emilio [2 ]
Birss, Viola [1 ]
机构
[1] Univ Calgary, Dept Chem, Calgary, AB T2N 1N4, Canada
[2] Univ Complutense Madrid, Fac Ciencias Quim, Dept Quim Inorgan, E-28040 Madrid, Spain
基金
加拿大自然科学与工程研究理事会;
关键词
Reversible solid oxide fuel cells; Air electrode; Mixed conducting oxides; Oxygen reduction; Oxygen evolution; Electrocatalysis; THERMAL-EXPANSION; DOPED CERIA; ELECTROCHEMICAL PROPERTIES; ELECTRICAL-PROPERTIES; MIXED CONDUCTIVITY; TEMPERATURE; CATHODE; PR; ND; LA;
D O I
10.1016/j.ijhydene.2014.11.127
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A novel mixed-conducting perovskite oxide (La0.3Ca0.7Fe0.7Cr0.3O3-delta, LCFCr), prepared using the combustion method, has been developed as a new air electrode material for reversible solid oxide fuel cells (RSOFCs) applications. XRD analysis showed that the LCFCr powder is a pure crystalline phase with an orthorhombic perovskite structure and that its thermal expansion coefficient matches closely with several commonly used solid electrolytes, while TEM analysis confirmed the high purity of the LCFCr powders. The electrochemical activity of LCFCr, screen-printed on a gadolinium doped ceria electrolyte, towards both the oxygen reduction (ORR) and oxygen evolution (OER) reactions, was examined at 600-800 degrees C in stagnant air using a symmetrical RSOFC configuration. Under open circuit conditions, LCFCr showed a very low polarization resistance (R-p) of only 0.07 Omega cm(2) at 800 degrees C, comparable to some of the best-performing oxide materials reported by others. The LCFCr air electrode was also found to be very stable, with very little loss in performance and no interfacial damage observed, even after 100 h at a 0.4 V (OER) and -0.4 V (ORR) overpotentials. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1902 / 1910
页数:9
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