Cu(II)/Cu(0) electrocatalyzed CO2 and H2O splitting

被引:72
作者
Chen, Zuofeng [1 ]
Kang, Peng [1 ]
Zhang, Ming-Tian [1 ]
Stoner, Brian R. [2 ]
Meyer, Thomas J. [1 ]
机构
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[2] RTI Int, Res Triangle Pk, NC 27709 USA
基金
美国国家科学基金会;
关键词
CARBON-DIOXIDE; ELECTROCHEMICAL REDUCTION; WATER; HYDROCARBONS; COPPER(II); ELECTRODES;
D O I
10.1039/c3ee24487c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In an earlier report we showed that in concentrated carbonate/bicarbonate solutions, simple Cu(II) salts are highly reactive as water oxidation electro-catalysts. We report here, based on earlier results in the literature, that Cu(0) films on a boron-doped diamond substrate are active toward CO2 reduction to CO and formate. The current densities are higher by similar to 2.8 fold than a bulk polycrystalline copper electrode due to the enhanced surface area of the electroplated Cu(0) films. When combined, the two half reactions, catalyzed by Cu(II) and Cu(0), provide a basis for the net electrochemical splitting of CO2 into CO/HCOO- and O-2 in CO2/HCO3- buffered aqueous solutions. The resulting electrochemical cell is remarkable for the simple nature of the catalysts, solution conditions, and cell configuration.
引用
收藏
页码:813 / 817
页数:5
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