Bismuth doped Sr2Fe1.5Mo0.5O6-3 double perovskite as a robust fuel electrode in ceramic oxide cells for direct CO2 electrolysis

JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY(2023)

引用 0|浏览27
暂无评分
摘要
Electrochemical conversion of CO 2 to CO is an economically feasible method for mitigating greenhouse gas emissions. Among various electrochemical approaches, solid oxide electrolysis cells (SOECs) show high potential for CO 2 reduction reaction (CO 2 -RR) due to their ability to operate at high temperatures, resulting in fast reaction kinetics and increased efficiency. Considering their main energy loss is still associated with the large overpotential at the fuel electrode, the development of the highly efficient and durable cathode for SOECs has been extensively searched after. Here, we propose an A-site doping strategy to enhance the properties of Sr 2 Fe 1.5 Mo 0.5 O 6 -3 (SFM), which improve its performance as a cathode in SOECs for CO 2 -RR, demonstrating favorable activity and durability. The structural and physiochemical characterizations, together with DFT calculations, show that the partial replacement of Sr by Bi in the SFM double perovskite not only improves CO 2 adsorption capability at the catalyst surface but also enhances oxygen ionic conduction inside the bulk oxide, resulting in enhanced CO 2 electrocatalysis performance in SOECs. Specifically, a La 0.8 Sr 0.2 Ga 0.8 Mg 0.2 O 3 -3 (LSGM) electrolyte-supported single cell with the new Bi-doped SFM cathode demonstrates a large current density of 1620 mA cm -2 at a cell potential of 1.6 V at 850 & DEG;C with good operational stability up to 200 h. Bi-doped SFM thus represents a highly promising cathode for ceramic CO 2 electrolyzers and could accelerate our transition towards a carbon-neutral society. & COPY; 2023 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.
更多
查看译文
关键词
Bismuth doped perovskite, Sr 2 Fe 1, 5Mo 0, 5 O 6-3, CO 2 electrocatalysis, Fuel electrode, Solid oxide cells
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要