Synergistically electronic tuning of metalloid CdSe nanorods for enhanced electrochemical CO2 reduction

被引:22
作者
Chen, Tao [1 ,2 ]
Liu, Tianyang [3 ]
Shen, Xinyi [1 ]
Zhang, Wei [1 ]
Ding, Tao [1 ]
Wang, Lan [1 ,2 ]
Liu, Xiaokang [1 ]
Cao, Linlin [1 ]
Zhu, Wenkun [2 ]
Li, Yafei [3 ]
Yao, Tao [1 ]
机构
[1] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Peoples R China
[2] Southwest Univ Sci & Technol, Sch Natl Def Sci & Technol, State Key Lab Environm Friendly Energy Mat, Mianyang 621010, Sichuan, Peoples R China
[3] Nanjing Normal Univ, Jiangsu Collaborat Innovat Ctr Biomed Funct Mat, Sch Chem & Mat Sci, Jiangsu Key Lab New Power Batteries, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
cadmium selenium; Ag doping; Se vacancies; CO2; electroreduction; ELECTROCATALYTIC ACTIVITY; CARBON-DIOXIDE; ELECTROREDUCTION; CATALYST; SELENIDE; FORMATE; COPPER; SITES;
D O I
10.1007/s40843-021-1696-x
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Engineering the electronic properties of catalysts to target intermediate adsorption energy as well as harvest high selectivity represents a promising strategy to design advanced electrocatalysts for efficient CO2 electroreduction. Herein, a synergistically tuning on the electronic structure of the CdSe nanorods is proposed for boosting electrochemical reduction of CO2. The synergy of Ag doping coupled with Se vacancies tuned the electronic structure of the CdSe nanorods, which shows the metalloid characterization and thereby the accelerated electron transfer of CO2 electroreduction. Operando synchrotron radiation Fourier transform infrared spectroscopy and theoretical simulation revealed that the Ag doping and Se vacancies accelerated the CO2 activation process and lowered the energy barrier for the conversion from CO2 to *COOH; as a result, the performance of CO2 electroreduction was enhanced. The as-obtained metalloid Ag-doped CdSe nanorods exhibited a 2.7-fold increment in current density and 1.9-fold Faradaic efficiency of CO than pristine CdSe nanorod.
引用
收藏
页码:2997 / 3006
页数:10
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