Reinforced chemical adsorption ability for efficient CO2 electrolysis in solid oxide electrolysis cell via a dual-exsolution strategy

被引:5
作者
Wang, Enli [1 ]
Jin, Chao [1 ]
Zhao, Liang [1 ]
Yang, Zhibin [2 ]
Liu, Changfei [1 ]
Wang, Sailong [1 ]
Lei, Xueling [3 ]
Chao, Ming [1 ]
Xu, Hanyu [1 ]
Yang, Ruizhi [1 ]
机构
[1] Soochow Univ, Soochow Inst Energy & Mat Innovat, Coll Energy, Suzhou 215006, Peoples R China
[2] China Univ Min & Technol Beijing, Res Ctr Solid Oxide Fuel Cell, Beijing 100083, Peoples R China
[3] Jiangxi Normal Univ, Dept Phys, Nanchang 330022, Jiangxi, Peoples R China
关键词
Solid oxide electrolysis cells; Perovskite materials; Exsolution; Heterointerface; CO2; electrolysis; IN-SITU CONSTRUCTION; CARBON-DIOXIDE; PEROVSKITE CATHODE; NANOPARTICLES; REDUCTION; TITANATE; PERFORMANCE; PARTICLES; CATALYST; SURFACE;
D O I
10.1016/j.cej.2024.153129
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Accelerating sluggish kinetics of CO2 2 reduction reaction (CO2RR) is of great importance for efficiently converting CO2 2 into valuable chemical products in solid oxide electrolysis cells (SOECs). Here, a novel dual-exsolution strategy is proposed to enhance CO2 2 electrolysis properties of La 0.4 Sr 0.6 Co 0.2 Fe 0.7 Nb 0.1 O 3-s (LSCFN) cathode. With simultaneously exsolved CoFe alloy and Bi nanoparticles on LSCFN cathodic matrix, the as-prepared SOEC delivers a high current density of 539 mA cm-- 2 for CO2 2 electrolysis at 800 degrees C and 1.5 V, and successfully runs over 170 h without any attenuation. The introduction of Bi exsolution not only promotes CoFe exsolution, provides additional oxygen vacancies, but also greatly boost the kinetics of CO2 2 adsorption/dissociation/activation. This work offers new insights into tailoring perovskite electrocatalysts for the CO2 2 electrolysis via dualexsolution strategy.
引用
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页数:9
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