期刊
ACS CATALYSIS
卷 8, 期 3, 页码 1990-2000出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.7b03274
关键词
CO2 reduction; methanol generation; ionic liquid-modified electrode; imidazole; SEIRAS
资金
- Japan Society for the Promotion of Science (JSPS) [16H04117, 15K05606]
The catalytic conversion of CO2 to useful compounds is of great importance from the viewpoint of global warming and development of alternatives to fossil fuels. Electrochemical reduction of CO2 using aromatic N-heterocylic molecules is a promising research area. We describe a high performance electrochemical system for reducing CO2 to formate, methanol, and CO using imidazole incorporated into a phosphonium-type ionic liquid-modified Au electrode, imidazolepIL/Au, at a low onset-potential of -0.32 V versus Ag/AgCl. This represents a significant improvement relative to the onset-potential obtained using a conventional Au electrode (-0.56 V). In the reduction carried out at -0.4 V, formate is mainly generated and methanol and CO are also generated with high efficiency at -0.6 similar to -0.8 V. The generation of methanol is confirmed by experiments using (CO2)-C-13 to generate (CH3OH)-C-13. To understand the reaction behavior of CO2 reduction, we characterized the reactions by conducting potential- and time-dependent in situ attenuated total reflection surface-enhanced infrared absorption spectroscopy (SEIRAS) measurements in D2O. During electrochemical CO2 reduction at -0.8 V, the C-O stretching band for CDOD (or COD) increases and the C=O stretching band for COOD increases at -0.4 V. These findings indicate that CO2 reduction intermediates, CDOD (or COD) and GOOD, are formed, depending on the reduction potential, to convert CO2 to methanol and formate, respectively.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据