过电位
镍
电化学
材料科学
碳纳米管
催化作用
铜
合金
电极
化学工程
氢
无机化学
纳米技术
化学
冶金
物理化学
有机化学
工程类
作者
Tianyu Zhang,Han Xu,Hongbin Yang,Aijuan Han,Enyuan Hu,Yaping Li,Xiao‐Qing Yang,Lei Wang,Junfeng Liu,Bin Liu
标识
DOI:10.1002/anie.202002984
摘要
Abstract Single‐atom catalysts (SACs) show great promise for electrochemical CO 2 reduction reaction (CRR), but the low density of active sites and the poor electrical conduction and mass transport of the single‐atom electrode greatly limit their performance. Herein, we prepared a nickel single‐atom electrode consisting of isolated, high‐density and low‐valent nickel(I) sites anchored on a self‐standing N‐doped carbon nanotube array with nickel–copper alloy encapsulation on a carbon‐fiber paper. The combination of single‐atom nickel(I) sites and self‐standing array structure gives rise to an excellent electrocatalytic CO 2 reduction performance. The introduction of copper tunes the d‐band electron configuration and enhances the adsorption of hydrogen, which impedes the hydrogen evolution reaction. The single‐nickel‐atom electrode exhibits a specific current density of −32.87 mA cm −2 and turnover frequency of 1962 h −1 at a mild overpotential of 620 mV for CO formation with 97 % Faradic efficiency.
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