Reorganization of Interfacial Water by an Amphiphilic Cationic Surfactant Promotes CO2 Reduction

被引:79
作者
Zhang, Zhuo-Qun [1 ]
Banerjee, Soumyodip [2 ]
Thoi, V. Sara [1 ,2 ]
Hall, Anthony Shoji [1 ,2 ]
机构
[1] Johns Hopkins Univ, Dept Mat Sci & Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Chem, Charles & 34Th St, Baltimore, MD 21218 USA
基金
美国国家科学基金会;
关键词
INFRARED-ABSORPTION SPECTROSCOPY; CARBON-DIOXIDE REDUCTION; ELECTROCHEMICAL REDUCTION; COPPER ELECTRODES; POLYCRYSTALLINE COPPER; HYDROGEN EVOLUTION; SELECTIVITY; ELECTROREDUCTION; CU; CONVERSION;
D O I
10.1021/acs.jpclett.0c01334
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
The presence of cetyltrimethylammonium bromide (CTAB) near the surface of a Cu electrode promotes the electrochemical reduction of CO2 to fuels. CTAB increases the CO2 reduction rate by as much as 10x and decreased the HER rate by 4x, leading to similar to 75% selectivity toward the reduction of CO2. Surface enhanced infrared absorption spectroscopy (SEIRAS) was used to probe the effects of CTAB adsorption on the structure of interfacial water and CO2 reduction intermediates. HER suppression was found to arise from the displacement of interfacial water molecules from CTAB adsorption within the double layer. The enhanced CO2 reduction rate can be correlated to an increased population of atop-bound CO and the emergence of a low frequency atop-CO band. These results unravel the role of additives in improving CO2-to-fuels electrocatalysis and establishing this as a powerful methodology for directing product selectivity.
引用
收藏
页码:5457 / 5463
页数:7
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