化学
电合成
电化学
杂原子
亚硫酸盐
电解质
分子
法拉第效率
无机化学
支撑电解质
组合化学
碳纳米管
质子化
阴极
反应机理
密度泛函理论
电催化剂
偶联反应
三键
单一债券
电极
钴
催化作用
计算化学
有机化学
反应中间体
联轴节(管道)
作者
Aimin Li,Mengjie Liu,Hsiwen Wu,Haoming Yu,Ke Luo,Y Zhang,Qing He,Jie Zhang
摘要
Carbon–heteroatom (C–X, X = N, S, P, etc.) coupling represents a promising strategy to diversify the product scope of the electrocatalytic CO2 reduction reaction (eCO2RR). To date, most studies have focused on single C–X bond formation between CO2 and one heteroatom source in one electrochemical reaction. The formation of multiple C–X bonds in eCO2RR remains largely unexplored due to the inherent complexity of multicomponent and multistep reaction pathways. Herein, we report, for the first time, the formation of multiple C–X bonds in eCO2RR, where (hydroxyamino)methanesulfonate (HAMS), a compound containing both C–N and C–S bonds, is synthesized via electroreduction of CO2 in an electrolyte solution containing nitrate/nitrite (NO3–/NO2–) and sulfite (SO32–) using a cobalt phthalocyanine supported on the carbon nanotube (CoPc/CNT) catalyst. Mechanistic studies and theoretical calculations reveal that the formation of HAMS proceeds via C–N coupling followed by C–S bond formation. By adjusting the electrolyte composition, the maximum faradaic efficiency of 5.8% and the highest partial current density of −2.4 mA cm–2 were achieved for HAMS. This work demonstrates a rare one-pot electrosynthesis of products with multiple C–X bonds (i.e., involving both C–N and C–S coupling) and provides a new route toward constructing functionally complex molecules from simple, abundant precursors.
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