Electrochemical Impedance Studies of CO2 Reduction in Ionic Liquid/Organic Solvent Electrolyte on Au Electrode

被引:65
|
作者
Yang, Dong-wei [1 ]
Li, Qing-yuan [1 ]
Shen, Feng-xia [1 ]
Wang, Qin [1 ]
Li, Lu [1 ]
Song, Ning [1 ]
Dai, Yong-nian [1 ]
Shi, Jin [1 ]
机构
[1] Kunming Univ Sci & Technol, Coll Met & Energy Engn, State Key Lab Complex Nonferrous Met Resources Cl, 121 St Wenchang Rd 68, Kunming 650093, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon dioxide; Electrochemical reduction; Ionic liquid; Electrochemical impedance spectroscopy (EIS); Catalytic mechanism; CARBON-DIOXIDE; ROOM-TEMPERATURE; FUELS; LIQUIDS; CONVERSION; CATALYSTS; H2O; ELECTROREDUCTION; METHANOL; CELL;
D O I
10.1016/j.electacta.2015.12.025
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electrochemical reduction of CO2 has been studied in 1-butyl-3-methylimidazolium trifluoromethanesulfonate ([Bmim][CF3SO3])/propylene carbonate (PC) solution on Au electrode. The linear sweep voltammetry measurements show that [Bmim][CF3SO3] has significant catalytic effect toward CO2 reduction. In order to study the mechanism of CO2 reduction in [Bmim][CF3SO3]/PC on Au electrode, the electrochemical impedance spectroscopy is employed. The experiment results show that the electrochemical impedance spectroscopy detected in [Bmim][CF3SO3]/PC is different from that detected in tetrabutylammonium trifluoromethanesulfonate ([Bu4N][CF3SO3])/PC solution. The reasonable explanation is that [Bmim](+) is absorbed on the Au electrode, leading to the formation of ionic liquid film. During the CO2 reduction process, absorbed CO2 is reduced to CO2 center dot- radical via single electron transfer. The generated CO2 center dot- radical interacts with [Bmim](+) and inducing the formation of [Bmim-CO2](ad). Thus, the activation energy and overpotential of CO2 reduction are reduced. The electrochemical impedance spectroscopy can be used as a methods to investigate the mechanism of CO2 reduction in nonaqueous solution. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:32 / 37
页数:6
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