Charged Microdroplets as Microelectrochemical Cells for CO2 Reduction and C-C Coupling

被引:14
|
作者
Dong, Jianing [1 ]
Chen, Jianxiong [2 ]
Wang, Wenxin [2 ]
Wei, Zhenwei [2 ]
Tian, Zhong-Qun [1 ]
Fan, Feng Ru [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Innovat Lab Sci & Technol Energy Mat Fujian Prov I, State Key Lab Phys Chem Solid Surfaces,IChEM, Xiamen 361005, Peoples R China
[2] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
WATER; ACCELERATION; BICARBONATE; CONVERSION; COMPLEXES; GEOMETRY; KINETICS;
D O I
10.1021/jacs.3c12586
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Charged microdroplets offer novel electrochemical environments, distinct from traditional solid-liquid or solid-liquid-gas interfaces, due to the intense electric fields at liquid-gas interfaces. In this study, we propose that charged microdroplets serve as microelectrochemical cells (MECs), enabling unique electrochemical reactions at the gas-liquid interface. Using electrospray-generated microdroplets, we achieved multielectron CO2 reduction and C-C coupling to synthesize ethanol using molecular catalysts. These catalysts effectively harness and relay electrons, enhancing the longevity of solvated electrons and enabling multielectron reactions. Importantly, we revealed the intrinsic relationship between the size and charge density of a MEC and its reaction selectivity. Employing in situ mass spectrometry, we identified reaction intermediates (molecular catalyst adducts with HCOO) and oxidation products, elucidating the CO2 reduction mechanism and the comprehensive reaction procedure. Our research underscores the promising role of charged microdroplets in pioneering new electrochemical systems.
引用
收藏
页码:2227 / 2236
页数:10
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