Silver Supported on Titania as an Active Catalyst for Electrochemical Carbon Dioxide Reduction

被引:201
作者
Ma, Sichao [1 ,3 ]
Lan, Yangchun [2 ,4 ]
Perez, Gaby M. J. [2 ]
Moniri, Saman [2 ]
Kenis, Paul J. A. [2 ,3 ]
机构
[1] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Chem & Biomol Engn, Urbana, IL 61801 USA
[3] Kyushu Univ, Int Inst Carbon Neutral Energy Res WPI I2CNER, Fukuoka 812, Japan
[4] E China Normal Univ, Dept Chem, Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China
关键词
cyclic voltammetry; nanoparticles; silver; supported catalysts; titanium; METAL-ELECTRODES; CO2; REDUCTION; PHOTOCATALYTIC REDUCTION; SURFACE CHARACTERIZATION; TIO2; CONVERSION; CELL; ELECTROCATALYSTS; STABILIZATION; ADSORPTION;
D O I
10.1002/cssc.201300934
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Although significant research efforts have focused on the exploration of catalysts for the electrochemical reduction of CO2, considerably fewer reports have described how support materials for these catalysts affect their performance, which includes their ability to reduce the overpotential, and/or to increase the catalyst utilization and selectivity. Here Ag nanoparticles supported on carbon black (Ag/C) and on titanium dioxide (Ag/TiO2) were synthesized. In a flow reactor, 40wt% Ag/TiO2 exhibited a twofold higher current density for CO production than 40wt% Ag/C. Faradaic efficiencies of the 40wt% Ag/TiO2 catalyst exceeded 90% with a partial current density for CO of 101mAcm(-2); similar to the performance of unsupported Ag nanoparticle catalysts (AgNP) but at a 2.5times lower Ag loading. A mass activity as high as 2700mAmg(Ag)(-1)cm(-2) was achieved. In cyclic voltammetry tests in a three-electrode cell, Ag/TiO2 exhibited a lower overpotential for CO2 reduction than AgNP, which, together with other data, suggests that TiO2 stabilizes the intermediate and serves as redox electron carrier to assist CO2 reduction while Ag assists in the formation of the final product, CO.
引用
收藏
页码:866 / 874
页数:9
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