In Situ Probing of CO2 Reduction on Cu-Phthalocyanine-Derived CuxO Complex

被引:11
|
作者
Jeong, Yongchan [1 ]
Kim, Yongman [1 ,2 ]
Kim, Young Jae [1 ,2 ]
Park, Jeong Young [1 ,2 ]
机构
[1] Inst Basic Sci IBS, Ctr Nanomat & Chem React, 55 Expo Ro, Daejeon 34126, South Korea
[2] Korea Adv Inst Sci & Technol KAIST, Dept Chem, 291 Daehak Ro, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
CO2; reduction; CuxO complex; Cu phthalocyanine; electrochemical scanning tunneling microscopy; CARBON-DIOXIDE ELECTROREDUCTION; COPPER SINGLE-CRYSTAL; ELECTROCHEMICAL REDUCTION; ELECTROCATALYTIC CONVERSION; HIGHLY EFFICIENT; ACTIVE-SITES; OXIDE; MONOXIDE; CATALYSTS; SURFACE;
D O I
10.1002/advs.202304735
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An in situ measurement of a CO2 reduction reaction (CO2RR) in Cu-phthalocyanine (CuPC) molecules adsorbed on an Au(111) surface is performed using electrochemical scanning tunneling microscopy. One intriguing phenomenon monitored in situ during CO2RR is that a well-ordered CuPC adlayer is formed into an unsuspected nanocluster via molecular restructuring. At an electrode potential of -0.7 V versus Ag/AgCl, the Au surface is covered mainly with the clusters, showing restructuring-induced CO2RR catalytic activity. Using a measurement of X-ray photoelectron spectroscopy, it is revealed that the nanocluster represents a Cu complex with its formation mechanism. This work provides an in situ observation of the restructuring of the electrocatalyst to understand the surface-reactive correlations and suggests the CO2RR catalyst works at a relatively low potential using the CuPC-derived Cu nanoclusters as active species.
引用
收藏
页数:6
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