Electrocatalysis of CO2 Reduction in Brush Polymer Ion Gels

被引:24
|
作者
McNicholas, Brendon J.
Blakemore, James D.
Chang, Alice B.
Bates, Christopher M.
Kramer, Wesley W.
Grubbs, Robert H. [1 ]
Gray, Harry B. [1 ]
机构
[1] CALTECH, Beckman Inst, 1200 East Calif Blvd,Mail Code 139-74, Pasadena, CA 91125 USA
关键词
CARBON-DIOXIDE; ELECTROCHEMICAL REDUCTION; TRIBLOCK COPOLYMER; CATALYTIC-ACTIVITY; LIQUIDS; ELECTROLYTES; CONDUCTIVITY; CONVERSION; COMPLEXES; MONOXIDE;
D O I
10.1021/jacs.6b08795
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The electrochemical characterization of brush polymer ion gels containing embedded small molecule redox-active species is reported. Gels comprising PS-PEO-PS triblock brush polymer, 1-butyl-3-methyl-imidazolium bis(trifluoromethylsulfonyl)imide (BMIm-TFSI), and some combination of ferrocene (Fc), cobaltocenium (CoCp2+), and Re(bpy)(CO)(3)Cl (1) exhibit diffusion-controlled redox processes with diffusion coefficients approximately one-fifth of those observed in neat BMIm-TFSI. Notably, 1 dissolves homogeneously in the interpenetrating matrix domain of the ion gel and displays electrocatalytic CO, reduction to CO in the gel. The catalytic wave exhibits a positive shift versus Fels compared with analogous nonaqueous solvents with a reduction potential 450 mV positive of onset and 90% Faradaic efficiency for CO production. These materials provide a promising and alternative approach to immobilized electrocatalysis, creating numerous opportunities for application in solid-state devices.
引用
收藏
页码:11160 / 11163
页数:4
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