Poly(ionic liquid)-based bimetallic tandem catalysts for highly efficient carbon dioxide electroreduction

被引:12
|
作者
Li, Xiao-Qiang [1 ,2 ]
Duan, Guo-Yi [1 ]
Wang, Rui [1 ,3 ]
Han, Li-Jun [1 ]
Wang, Yao-Feng [1 ,2 ]
Xu, Bao-Hua [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Proc Engn, Beijing Key Lab Ion Liquids Clean Proc, CAS Key Lab Green Proc & Engn,State Key Lab Multip, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Engn, Beijing 100049, Peoples R China
[3] East China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
CO; 2; conversion; Electrocatalysis; Organic-inorganic hybrids; Ionic liquids; Electrolysis; SPECTRA; CU; COPPER;
D O I
10.1016/j.apcatb.2022.121459
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
Poly(ionic liquid)-metal (PIL-metal) hybrids were developed as a platform for facilely constructing tandem catalysts to reach highly efficient electrocatalytic reduction of CO2 (CO2RR). By introducing extra metal with distinct CO2RR response to Cu-PIL hybrids, Cu@PIL@Ag and Cu@PIL@Bi were obtained. Remarkably, Cu@PIL@Ag exhibits an excellent C2+ Faradaic efficiency (FEC2+) of 83.2% with a high partial current density (jC(2+)) of 416.1 mA cm(-2) in 3 M KOH and an even higher jC2+ (708.9 mA cm(-2)) in 1 M KOH, while Cu@PIL@Bi possesses high FEC1 (> 60%) and low FEC2+ (< 5%) in a wide potential range. Mechanistic studies demonstrate the output of such a tandem system, either synergistic or maladjusted, depends on not only CO2RR response of Ag and Bi but also specific Cu-Ag and Cu-Bi interactions. Besides, the PIL layer could adjust the reactivity by promoting the dispersion and availability of active sites and enriching the local key intermediates.
引用
收藏
页数:13
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