离子液体
催化作用
光催化
水溶液
化学
均相催化
均分解
离子键合
键裂
光解
产量(工程)
量子产额
无机化学
光化学
有机化学
激进的
材料科学
离子
物理
荧光
冶金
量子力学
作者
Muhammad I. Qadir,Marcileia Zanatta,Eduarda Sangiogo Gil,Hubert Stassen,Paulo Fernando Bruno Gonçalves,Brenno A. D. Neto,Paulo Eduardo Narcizo de Souza,Jaı̈rton Dupont
出处
期刊:Chemsuschem
[Wiley]
日期:2019-01-21
卷期号:12 (5): 1011-1016
被引量:19
标识
DOI:10.1002/cssc.201802974
摘要
The simple photolysis of CO2 in aqueous solutions to generate CO and/or hydrocarbons and derivatives in the presence of a catalyst is considered to be a clean and efficient approach for utilizing CO2 as a C1 building block. Despite the huge efforts dedicated to this transformation using either semiconductors or homogeneous catalysts, only small improvements of the catalytic activity have been achieved so far. This article reports that simple aqueous solutions of organic salts-denominated as ionic liquids-can efficiently photo-reduce CO2 to CO without using photosensitizers or sacrificial agents. The system relies on the formation of the [CO2 ].- intermediate through homolytic C-C bond cleavage in a cation-CO2 adduct of imidazolium-based ionic liquids (ILs). The system continuously produced CO up to 2.88 mmol g-1 of IL after 40 h of irradiation by using an aqueous solution of 1-n-butyl-3-methylimidazolium-2-carboxylate (BMIm.CO2 ) IL, representing an apparent quantum yield of 3.9 %. The organophotocatalytic principles of our system may help to develop more simple and efficient organic materials for the production of solar fuels from CO2 under mild conditions, which represents a real alternative to those based on semiconductors and homogeneous metal-based catalysts.
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