一步电还原法制备Cu-Sn合金催化剂实现高效电还原CO2制备甲酸盐OA
Fabrication of Cu-Sn alloy catalysts via one-step electrodeposition for efficient electroreduction of CO2 to formate
电催化 CO2 还原(CO2 Reduction Reaction,CO2RR)被视为降低CO2排放和生产多种高价值化合物的有效途径.本工作采用一步电沉积法制备了类麦穗状枝晶结构的Cu-Sn合金催化剂用于CO2选择性电还原为甲酸盐.实验结果表明,与Cu和Sn电极相比,因其独特的类麦穗状结构可为反应过程提供大量的活性位点,Cu-Sn合金催化剂对甲酸盐展现出较高的催化活性和选择性,甲酸盐的法拉第效率最高可达80%,并且在-1.7--2.0 V的电位窗口下均可以达到70%以上的法拉第效率.结合电化学数据及XPS分析表明,Cu原子和Sn原子共同调节了电还原过程中CO2*-中间体的吸附.该制备方法可为CO2RR设计双金属催化剂提供新的途径.
Electrocatalytic CO2 reduction reaction(CO2RR)is regarded as an effective approach to reduce CO2 emissions and produce various high-value compounds.In this study,a Cu-Sn alloy catalyst with a wheat-ear-like dendritic structure was prepared via a simple one-step electrodeposition method and used for the selective electro-reducing CO2 to formate.Experimental results demonstrate that,compared to Cu and Sn electrodes,the Cu-Sn alloy catalyst exhibits higher catalytic activity and selectivity toward formate due to its unique wheat-ear-like structure,which could provide abundant active sites for the reaction process.The Faradaic efficiency for formate reaches up to 80%,and remains above 70%within the potential range from-1.7--2.0 V.Combined electrochemical data and XPS analysis revealed that Cu and Sn atoms collectively modulate the adsorption of the CO2*-intermediate during the electroreduction process.Therefore,this simple preparation method offers a new pathway for the design of bimetallic catalysts for CO2RR.
苗家赫;杨颂;胡昊;白亚东;杨言言;余钟亮
太原理工大学化学与化工学院,山西太原 030024||上饶师范学院化学与环境科学学院,江西上饶 334001||江西省教育厅黑滑石功能材料制备与应用重点实验室,江西上饶 334001太原理工大学化学与化工学院,山西太原 030024上饶师范学院化学与环境科学学院,江西上饶 334001||江西省教育厅黑滑石功能材料制备与应用重点实验室,江西上饶 334001太原理工大学化学与化工学院,山西太原 030024上饶师范学院化学与环境科学学院,江西上饶 334001||江西省教育厅黑滑石功能材料制备与应用重点实验室,江西上饶 334001上饶师范学院化学与环境科学学院,江西上饶 334001||江西省教育厅黑滑石功能材料制备与应用重点实验室,江西上饶 334001
资源环境
CO2电还原甲酸盐合金电沉积
CO2 electroreductionformatealloyelectrodeposition
《燃料化学学报(中英文)》 2026 (3)
114-123,10
Supported by the Natural Science Foundation of Jiangxi Province(20242BAB25167)and the National Natural Science Foundation of China(22169017).江西省自然科学基金(20242BAB25167)和国家自然科学基金(22169017)资助
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