铜
催化作用
吸附
电化学
化学
无机化学
电解质
过渡金属
材料科学
电极
物理化学
冶金
生物化学
作者
Hefei Li,Tianfu Liu,Pengfei Wei,Long Lin,Dunfeng Gao,Guoxiong Wang,Xinhe Bao
标识
DOI:10.1002/anie.202102657
摘要
Electrochemical CO2 reduction reaction (CO2 RR) to multicarbon hydrocarbon and oxygenate (C2+ ) products with high energy density and wide availability is of great importance, as it provides a promising way to achieve the renewable energy storage and close the carbon cycle. Herein we design a Cu-CuI composite catalyst with abundant Cu0 /Cu+ interfaces by physically mixing Cu nanoparticles and CuI powders. The composite catalyst achieves a remarkable C2+ partial current density of 591 mA cm-2 at -1.0 V vs. reversible hydrogen electrode in a flow cell, substantially higher than Cu (329 mA cm-2 ) and CuI (96 mA cm-2 ) counterparts. Induced by alkaline electrolyte and applied potential, the Cu-CuI composite catalyst undergoes significant reconstruction under CO2 RR conditions. The high-rate C2+ production over Cu-CuI is ascribed to the presence of residual Cu+ and adsorbed iodine species which improve CO adsorption and facilitate C-C coupling.
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