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
有机化学
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
Abstract Electrochemical CO 2 reduction reaction (CO 2 RR) to multicarbon hydrocarbon and oxygenate (C 2+ ) 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 Cu 0 /Cu + interfaces by physically mixing Cu nanoparticles and CuI powders. The composite catalyst achieves a remarkable C 2+ 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 CO 2 RR conditions. The high‐rate C 2+ 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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