离子液体
催化作用
法拉第效率
四氟硼酸盐
电化学
电解
化学
电解质
无机化学
营业额
化学工程
电极
物理化学
有机化学
工程类
作者
Jaecheol Choi,Tânia M. Benedetti,Rouhollah Jalili,Ashley Walker,Gordon G. Wallace,David L. Officer
标识
DOI:10.1002/chem.201603359
摘要
The efficient and selective catalytic reduction of CO2 is a highly promising process for both of the storage of renewable energy as well as the production of valuable chemical feedstocks. In this work, we show that the addition of an ionic liquid, 1-butyl-3-methylimidazolium tetrafluoroborate, in an aprotic electrolyte containing a proton source and FeTPP, promotes the in situ formation of the [Fe(0) TPP](2-) homogeneous catalyst at a less negative potential, resulting in lower overpotentials for the CO2 reduction (670 mV) and increased kinetics of electron transfer. This co-catalysis exhibits high Faradaic efficiency for CO production (93 %) and turnover number (2 740 000 after 4 hour electrolysis), with a four-fold increase in turnover frequency (TOF) when compared with the standard system without the ionic liquid.
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