Efficient electrochemical reduction of CO2 into CO promoted by sulfur vacancies

被引:170
作者
Qin, Binhao [1 ,2 ]
Li, Yuhang [1 ]
Wang, Hongjuan [2 ]
Yang, Guangxing [2 ]
Cao, Yonghai [2 ]
Yu, Hao [2 ]
Zhang, Qiao [1 ]
Liang, Hong [1 ]
Peng, Feng [1 ]
机构
[1] Guangzhou Univ, Sch Chem & Chem Engn, Guangzhou 510006, Guangdong, Peoples R China
[2] South China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; electroreduction; Energy conversion; Carbon monoxide; Catalytic mechanism; Sulfur vacancy; OXYGEN VACANCIES; CARBON-DIOXIDE; AQUEOUS CO2; ELECTROREDUCTION; CONVERSION; CATALYSTS; SYNGAS; GAS;
D O I
10.1016/j.nanoen.2019.03.024
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electrochemical conversion of carbon dioxide (CO2) into useful chemicals has attracted a lot of attention to store energy and reduce the greenhouse effect. Herein, a new electrocatalyst of carbon nanotubes coated with cadmium sulfide is reported, the faradaic efficiency (FE) of CO2 reduction reaction (CO2RR) to carbon monoxide (CO) is as high as 95%. We clearly demonstrate that sulfur vacancies (S-vacancies) are in-situ generated on the catalyst surface in CO2RR, which is evidenced by electron paramagnetic resonance spectra (EPR), in-situ differential electrochemical mass spectrometry (DEMS) and inductively-coupled plasma spectrometer (ICP). With the increase of S-vacancies, the catalytic activity of CO2RR to CO improve significantly and the charge-transfer resistance decrease. Combined with in-situ infrared absorption spectroscopy and density functional theory calculations, it can be concluded that the formation of S-vacancies changes the electron density of the catalyst surface and decreases the energy barrier for the conversion of COOH* to CO*. Finally, we tried to power electrochemical reduction of CO2 with solar panel under natural light conditions, the energy conversion efficiency on CdS-CNT catalyst from solar energy to CO has been calculated, predicting a hopeful application prospect in the future.
引用
收藏
页码:43 / 51
页数:9
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