催化作用
镍
电化学
选择性
二氧化碳电化学还原
过渡金属
一氧化碳
化学
星团(航天器)
电催化剂
无机化学
电解
材料科学
电极
有机化学
物理化学
计算机科学
程序设计语言
电解质
作者
Qi Hao,Dongxue Liu,Ruiping Deng,Haixia Zhong
标识
DOI:10.3389/fchem.2021.837580
摘要
Single-atom catalysts (SACs) with metal–nitrogen (M–N) sites are one of the most promising electrocatalysts for electrochemical carbon dioxide reduction (ECO 2 R). However, challenges in simultaneously enhancing the activity and selectivity greatly limit the efficiency of ECO 2 R due to the improper interaction of reactants/intermediates on these catalytic sites. Herein, we report a carbon-based nickel (Ni) cluster catalyst containing both single-atom and cluster sites (NiNx-T, T = 500–800) through a ligand-mediated method and realize a highly active and selective electrocatalytic CO 2 R process. The catalytic performance can be regulated by the dispersion of Ni–N species via controlling the pyrolysis condition. Benefitting from the synergistic effect of pyrrolic-nitrogen coordinated Ni single-atom and cluster sites, NiNx-600 exhibits a satisfying catalytic performance, including a high partial current density of 61.85 mA cm −2 and a high turnover frequency (TOF) of 7,291 h −1 at −1.2 V vs. RHE, and almost 100% selectivity toward carbon monoxide (CO) production, as well as good stability under 10 h of continuous electrolysis. This work discloses the significant role of regulating the coordination environment of the transition metal sites and the synergistic effect between the isolated single-site and cluster site in enhancing the ECO 2 R performance.
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