文献类型：期刊文献

英文题名：The effect of the alkyl chain length of the tetraalkylammoniumcation on CO2 electroreduction in an aprotic medium

作者：Niu, Dongfang[1];Wang, Haiyang[1];Li, Huicheng[1];Zhang, Xinsheng[1]

机构：[1]E China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China

年份：2015

卷号：52

起止页码：58

外文期刊名：ELECTROCHEMISTRY COMMUNICATIONS

收录：;EI(收录号：20150700515751);WOS:【SCI-EXPANDED(收录号:WOS:000352850700016)】；

基金：The present work was financially supported by the National Natural Science Foundation of China (No. 21303053), the Fundamental Research Funds for the Central Universities (WA1314058) and the Open Project of State Key Laboratory of Chemical Engineering (SKL-ChE-14C02).

语种：英文

外文关键词：CO2 electroreduction; Tetraalkylammonium salts; Ion pairing; Cation adsorption

摘要：The effect of tetraalkylammonium cation (TAA(+)) chain length on CO2 electroreduction is investigated on an Ag electrode in a DMF solution. Linear sweep voltammetric (LSV) studies show that the onset potentials of CO2 reduction move to increasingly negative potentials upon increasing the alkyl chain length of the tetraalkylammoniumcation of the supporting electrolyte. Density functional theory (DFT) computations indicate that the onset potential of CO2 reduction is dependent on the strength of ion pairing between TAA(+) cation and the electrogenerated CO2 center dot-center dot CO2 disturbance experiments reveal that the peak current of CO2 reduction is determined by the quantity of TAA(+) cation adsorbed on the Ag surface. (C) 2015 Elsevier B.V. All rights reserved.