High performance and stability of double perovskite-type oxide NdBa0.5Ca0.5Co1.5Fe0.5O5+δ as an oxygen electrode for reversible solid oxide electrochemical cell

被引:58
|
作者
Tian, Yunfeng [1 ]
Liu, Yun [2 ]
Wang, Wenjie [1 ]
Jia, Lichao [1 ]
Pu, Jian [1 ]
Chi, Bo [1 ]
Li, Jian [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Mat Sci & Engn, Ctr Fuel Cell Innovat, State Key Lab Mat Proc & Die & Mould Technol, Wuhan 430074, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, China EU Inst Clean & Renewable Energy, Wuhan 430074, Hubei, Peoples R China
来源
JOURNAL OF ENERGY CHEMISTRY | 2020年 / 43卷 / 43期
基金
英国工程与自然科学研究理事会; 中国国家自然科学基金;
关键词
Reversible solid oxide electrochemical cell; Double perovskite; Composite electrode; Stability; Reversibility; COMPOSITE CATHODES; LAYERED PEROVSKITE; EVOLUTION REACTION; CO2; ELECTROLYSIS; POWER-GENERATION; REDUCTION; NANOPARTICLES; ELECTROCATALYST; OPTIMIZATION; CATALYST;
D O I
10.1016/j.jechem.2019.08.010
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In this study, we successfully synthesized double perovskite-type oxide NdBa0.5Ca0.5Co1.5Fe0.5O5+delta (NBCCF) using a conventional wet chemical method as the oxygen electrode for reversible solid oxide electrochemical cells (RSOCs). The polarization resistance (R-p) of the composite electrode NBCCF-Gd0.1Ce0.9O2 (GDC) is only 0.079 Omega cm(2) at 800 degrees C under air. The single cell based on NBCCF-GDC electrode displays a peak power density of 0.941 W/cm(2) in fuel cell mode and a low R-p value of 0.134 Omega cm(2). In electrolysis cell mode, the cell displays an outstanding oxygen evolution reaction (OER) activity and shows current density as high as 0.92 A/cm(2) with 50 vol% AH (Absolute Humidity) at 800 degrees C and applied voltage of 1.3 V. Most importantly, the cell exhibits admirable durability of 60 h both in electrolysis mode and fuel cell mode with distinguished reversibility. All these results suggest that NBCCF is a promising candidate electrode for RSOC. (C) 2019 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.
引用
收藏
页码:108 / 115
页数:8
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