Photocatalytic activation of CO2 under visible light by Rhenium complex encapsulated in molecular sieves

被引:0
|
作者
Jin-Soo Hwang
Dae Sung Kim
Chul Wee Lee
Sang-Eon Park
机构
[1] Korea Research Institute of Chemical Technology (KRICT),Catalysis Center for Molecular Engineering (CCME)
来源
Korean Journal of Chemical Engineering | 2001年 / 18卷
关键词
Cationic Rhenium Complex; FT-IR Mass Spectroscopy; Molecular Sieve; Photocatalytic Activation of CO; UV-DRS; Visible Light;
D O I
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中图分类号
学科分类号
摘要
The photocatalytic activation of CO2 over molecular sieve-encapsulated cationic rhenium complex has been investigated under visible light (λ>350 nm). The cationic rhenium complex, [Re(I)(CO)3(bpy)(py)]+(bpy=2,2′bipyridine, py=pyridine), has been encapsulated by ion-exchange method using the aqueous solution of [Re(I)(CO)3 (bpy)(py)]+PF6- into the microporous NaY and the mesoporous A1MCM-41 molecular sieve acting as supramolecular heterogeneous host. To confirm the encapsulation of [Re(IXCO)3(bpy)(py)]+ into the pores of molecular sieve, XeNMR and FT-IR spectroscopies have been applied before and after the [Re(I)(CO)3(bpy)(py)]+ encapsulation. To investigate the photophysical and photochemical properties, molecular sieve-encapsulated cationic rhenium complex has been studied by UV-Visible diffuse reflectance spectroscopy (UV-DRS) with photoirradiation (λ>350 nm) at room temperature. By monitoring the photoreaction of CO2 over the photocatalysts, the conversion of CO2 into CO and carbonate species has been observed by usingin-situ FT-IR and time-resolved mass spectroscopy. From the experimental results, the photocatalytic activation mechanism of CO2 on the catalyst under visible light (λ>350 nm) could be proposed via the photo-induced reaction of two electrons and two protons, resulting from water decomposition.
引用
收藏
页码:919 / 923
页数:4
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