过电位
催化作用
二氧化碳电化学还原
法拉第效率
循环伏安法
二氧化钛
电化学
二氧化碳
选择性
材料科学
碳纤维
无机化学
炭黑
氧化还原
化学工程
纳米颗粒
电催化剂
电极
化学
纳米技术
一氧化碳
冶金
有机化学
复合材料
天然橡胶
物理化学
工程类
复合数
作者
Sichao Ma,Yangchun Lan,Gaby M. J. Perez,Saman Moniri,Paul J. A. Kenis
出处
期刊:Chemsuschem
[Wiley]
日期:2014-01-28
卷期号:7 (3): 866-874
被引量:185
标识
DOI:10.1002/cssc.201300934
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, 40 wt % Ag/TiO2 exhibited a twofold higher current density for CO production than 40 wt % Ag/C. Faradaic efficiencies of the 40 wt % Ag/TiO2 catalyst exceeded 90 % with a partial current density for CO of 101 mA cm(-2) ; similar to the performance of unsupported Ag nanoparticle catalysts (AgNP) but at a 2.5 times lower Ag loading. A mass activity as high as 2700 mA mgAg (-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.
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