电解
氧化还原
阳极
材料科学
阴极
极化(电化学)
氢
兴奋剂
化学工程
氧化物
热膨胀
无机化学
化学
电极
电化学
催化作用
电解质
物理化学
复合材料
光电子学
冶金
工程类
生物化学
有机化学
作者
Yunfeng Tian,Caichen Yang,Yitong Li,Shuai He,Xinxin Wang,Yihan Ling,Wenlu Li,Bo Chi,Jian Pu
出处
期刊:Journal of The Electrochemical Society
[The Electrochemical Society]
日期:2021-10-01
卷期号:168 (10): 104515-104515
被引量:9
标识
DOI:10.1149/1945-7111/ac2e1e
摘要
The main barrier to symmetrical solid oxide cells (SSOCs), where the same catalytic materials are used simultaneously as the anodes and the cathodes, is to find a redox-stable catalyst that exhibits superior catalytic activities for both fuel oxidation/reduction and oxygen reduction/evolution reactions. Here, we report a simple strategy by Sc doping La0.6Ca0.4Fe0.8Ni0.2O3−δ (LCFN) with enhanced electrocatalytic activity and stability in SSOCs. La0.6Ca0.4Fe0.7Sc0.1Ni0.2O3−δ (LCFSN) oxide has better crystal structural stability, lower coefficient of thermal expansion (TEC) and good conductivity. In addition, LCFSN has lower polarization resistance both in air, CO2 or H2 compared with LCFN. Moreover, the SSOCs with LCFSN showed the maximum power densities of 0.332 and 0.234 W cm−2 when operating in humidified hydrogen at 850 °C and 800 °C, respectively, and the cell shows maximum current densities of 1.093 A cm−2 for CO2 electrolysis at 850 °C and 1.8 V. In addition, the cell also has good stability toward both fuel cell and electrolysis cell. Therefore, this work suggests that B site Sc doping is a promising approach to the redox-stable catalyst for SSOCs.
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