Ternary Ionic-Liquid-Based Electrolyte Enables Efficient Electro-reduction of CO2 over Bulk Metal Electrodes

被引:30
|
作者
Yang, Jiahao [1 ]
Kang, Xinchen [3 ,4 ]
Jiao, Jiapeng [1 ]
Xing, Xueqing [2 ]
Yin, Yaoyu [3 ,4 ]
Jia, Shuaiqiang [1 ]
Chu, Mengen [1 ]
Han, Shitao [1 ]
Xia, Wei [1 ]
Wu, Haihong [1 ,5 ]
He, Mingyuan [1 ,5 ]
Han, Buxing [1 ,3 ,4 ,5 ]
机构
[1] East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China
[2] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
[3] Univ Chinese Acad Sci, Sch Chem, Beijing 100049, Peoples R China
[4] Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, Key Lab Colloid & Interface & Thermodynam, Beijing 100190, Peoples R China
[5] Inst Ecochongming, Shanghai 202162, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
ELECTROCHEMICAL REDUCTION; CARBON-DIOXIDE; ELECTROREDUCTION;
D O I
10.1021/jacs.3c03259
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Using bulk metals as catalysts to get high efficiencyin electro-reductionof CO2 is ideal but challenging. Here, we report the couplingof bulk metal electrodes and a ternary ionic-liquid-based electrolyte,1-butyl-3-methyl-imidazolium tetrafluoro-borate/ 1-dodecyl-3-methyl-imidazoliumtetrafluoro-borate/ MeCN to realize highly efficient electro-reductionof CO2 to CO. Over various bulk metal electrodes, the ternaryelectrolyte not only increases the current density but also suppressesthe hydrogen evolution reaction to obtain a high Faradaic efficiency(FE) toward CO. FECO could maintain similar to 100% over awide potential range, and metal electrodes showed very high stabilityin the ternary electrolyte. It is demonstrated that the aggregationbehavior of the ternary electrolyte and the arrangement of two kindsof IL cations with different chain lengths in the electrochemicaldouble layer not only increase the wettability to electrode and CO2 adsorption but also extend the diffusion channel of H+, rendering the high current density and FECO.
引用
收藏
页码:11512 / 11517
页数:6
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