Highly Efficient Electrocatalytic CO2 Reduction to C2+ Products on a Poly(ionic liquid)-Based Cu0-CuI Tandem Catalyst

被引:124
作者
Duan, Guo-Yi [1 ]
Li, Xiao-Qiang [1 ,2 ]
Ding, Guang-Rong [1 ,2 ]
Han, Li-Jun [1 ]
Xu, Bao-Hua [1 ,2 ]
Zhang, Suo-Jiang [1 ,2 ]
机构
[1] Chinese Acad Sci, Beijing Key Lab Ion Liquids Clean Proc, CAS Key Lab Green Proc & Engn, Inst Proc Engn,State Key Lab Multiphase Complex S, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Engn, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; conversion; Electrochemistry; Ionic liquids; Polymer modification; Tandem catalyst; ELECTROCHEMICAL REDUCTION; CARBON-MONOXIDE; COPPER; ELECTROREDUCTION; PHOTOELECTRON; ELECTRON; ETHYLENE; SPECTRA; METHANE; XPS;
D O I
10.1002/anie.202110657
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electroreduction of CO2 on a polymer-modified Cu-based catalyst has shown high multi-electron reduction (>2 e(-)) selectivity, however, most of the corresponding current densities are still too small to support industrial applications. In this work, we designed a poly(ionic liquid) (PIL)-based Cu-0-Cu-I tandem catalyst for the production of C2+ products with both high reaction rate and high selectivity. Remarkably, a high C2+ faradaic efficiency (FEC2+) of 76.1 % with a high partial current density of 304.2 mA cm(-2) is obtained. Mechanistic studies reveal the numbers and highly dispersed Cu-0-PIL-Cu-I interfaces are vital for such reactivity. Specifically, Cu nanoparticles derived Cu-0-PIL interfaces account for high current density and a moderate C(2+ )selectivity, whereas Cu-I species derived PIL-Cu-I interfaces exhibit high activity for C-C coupling with the local enriched *CO intermediate. Furthermore, the presence of the PIL layer promotes the C2+ selectivity by lowering the barrier of C-C coupling.
引用
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页数:10
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