La0.4Sr0.6Co0.7Fe0.2Nb0.1O3-δ -Gd0.2Ce0.8O2-δ as Symmetrical Electrode Material for Reversible Solid Oxide Cells

被引:0
作者
Xu, Na [1 ]
Sun, Mengzhen [1 ]
Geng, Duo [1 ]
Yu, Longjiao [1 ]
Xu, Zhanlin [1 ]
机构
[1] Key Laboratory of Preparation and Application of Environmental Friendly Materials, Ministry of Education, Jilin Normal University, Changchun,130103, China
来源
Xiyou Jinshu Cailiao Yu Gongcheng/Rare Metal Materials and Engineering | 2021年 / 50卷 / 11期
关键词
Solid electrolytes - Sulfur - Niobium compounds - Electrodes - Gallium compounds - Electrolysis - Magnesium compounds - Cerium compounds - Iron compounds - Gadolinium compounds - Screen printing - Solid oxide fuel cells (SOFC) - Strontium compounds;
D O I
暂无
中图分类号
学科分类号
摘要
La0.4Sr0.6Co0.7Fe0.2Nb0.1O3-δ-Gd0.2Ce0.8O2-δ (LSCFN-GDC) with high catalytic performance was synthesized by one-step co-synthesis method for developing a symmetrical reversible solid oxide cell (SOC) electrode. Electrolyte-supported symmetrical SOCs were fabricated by tape-casting and screen-printing methods with La0.8Sr0.2Ga0.83Mg0.17O3-δ (LSGM) as the electrolyte and LSCFN-GDC as both anode and cathode. The configuration of SOC is LSCFN-GDC||LSGM||LSCFN-GDC. Solid oxide fuel cell (SOFC) and solid oxide electrolysis cell (SOEC) modes were used to test the performance of SOCs. The results show that the maximum power densities are 1.036, 0.996, 0.479, and 0.952 W/cm2 under the atmosphere of fuel gas of H2 (3% H2O), H2 (0.01% H2S), CH4, and C3H8 at 850℃, respectively. The current density at the electrolytic voltage of 1.3 V is 0.943 A/cm2 during the electrolysis of H2 (50% H2O). LSCFN-GDC has good coking-resistance, sulfur-tolerance, and redox stability, and its stable performance can be sustained for 700 h under the atmosphere of H2 (0.01% H2S), CH4, H2 (3% H2O), and H2 (50% H2O). The results indicate that the one-step method is a facile and optimized fabrication procedure of electrode and LSCFN-GDC||LSGM||LSCFN-GDC SOCs have great potential in further application. Copyright © 2021, Northwest Institute for Nonferrous Metal Research. Published by Science Press. All rights reserved.
引用
收藏
页码:3885 / 3889
相关论文
empty
未找到相关数据