Electrochemical reduction of CO2 in a symmetrical solid oxide electrolysis cell with La0.4Sr0.6Co0.2Fe0.7Nb0.1O3-δ electrode

被引:59
|
作者
Yang, Zhibin [1 ]
Ma, Chaoyang [1 ]
Wang, Ning [1 ]
Jin, Xinfang [2 ]
Jin, Chao [3 ]
Peng, Suping [1 ]
机构
[1] China Univ Min & Technol, Sch Chem & Environm Engn, Res Ctr Fuel Cell, Beijing 100083, Peoples R China
[2] Univ Massachusetts, Dept Mech Engn, Lowell, MA 01854 USA
[3] Soochow Univ, Soochow Inst Energy & Mat Innovat, Coll Energy, Suzhou 215006, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; electrolysis; Solid oxide electrolysis cell; Perovskite oxides; Electrode materials; La0.4Sr0.6Co0.2Fe0.7Nb0.1O3-delta; CATHODE MATERIAL; ANODE MATERIAL; FUEL-CELL; CATALYST; FABRICATION; H2O;
D O I
10.1016/j.jcou.2019.07.021
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
La0.4Sr0.6Co0.2Fe0.7Nb0.1O3-delta (LSCFN) perovskite oxide is investigated as electrode materials of a symmetrical solid oxide electrolysis cell (SOEC) for CO2 reduction reaction. A high current density of 0.442 A cm(-2) and a low polarization resistance are obtained @1.5 V with pure CO2 at 800 degrees C because of excellent CO2 adsorbability of LSCFN. When reducing carrier gas, such as CO and/or H-2 is flowed, the polarization resistance decreases further. Interesting, when H-2/CO contents increase, the current density firstly increases and then reaches a plateau, the behavior is different from the conventional Ni-cermet based SOEC. Due to the reverse water gas shift reaction when H-2 exists, the cell performance of CO2 electrolysis with H-2 as carrier gas is better than that with CO as carrier gas. The SOEC can be continuously operated for 150 h without any attenuation when H-2/CO2 = 3/7 mixture gas is filled @ 0.24 A cm(-2) at 800 degrees C. The study indicates that LSCFN is a promising electrode material for CO2 electrolysis.
引用
收藏
页码:445 / 451
页数:7
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