材料科学
1,2-二氯乙烷
碳纤维
金属
氮气
电极
选择性
电化学
法拉第效率
Atom(片上系统)
无机化学
化学工程
纳米技术
冶金
有机化学
复合材料
物理化学
催化作用
化学
工程类
复合数
计算机科学
嵌入式系统
作者
Guoqiang Gan,Xiaoqing Zhang,Shuyu Bu,Qili Gao,Xin Kong,Yechen Lei,Anquan Zhu,Kai Liu,Chuhao Luan,Tian Zhang,Yang Li,Chun‐Sing Lee,Wenjun Zhang
标识
DOI:10.1002/adfm.202206263
摘要
Abstract Single‐atom catalysts (SACs) have received widespread interest for their high atomic efficiency, enriched active sites, excellent catalytic performance, and low cost. However, the agglomeration of single metal atoms and the use of inactive additives for affixing powdery SACs on planar electrodes may reduce the density of active sites, diminish the charge transport to active sites, and thus suppress their performance. Herein, a series of metal–nitrogen–carbon single‐atom aerogels (M‐SAAs, M: Cu, Ni, Au, Ru) are synthesized via a universal strategy, in which the merits of metal organic frameworks and carbon aerogels are perfectly combined to prevent the agglomeration of single metal atoms and overcome the problem of poor electrical conductivity. The as‐prepared M‐SAAs can be directly employed as self‐supporting electrodes for the electrochemical dechlorination of 1,2‐dichloroethane, and outstanding activity and stability are observed. Significantly, the Cu‐SAA with abundant Cu−N 4 sites shows an extraordinarily high ethylene production rate of 446 µmol h −1 , with a selectivity of 99% and Faradaic efficiency of 64%. Moreover, theoretical calculations are performed to demonstrate the selectivity and activity of different metal active sites. This study provides a new strategy to exploit highly effective SACs and offers an intensive insight into the mechanism of electrochemical dechlorination reactions.
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