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首页> 外文期刊>Applied Surface Science >Coupling plasmonic noble metal with TiO_2 for efficient photocatalytic transfer hydrogenation: M/TiO_2 (M = Au and Pt) for chemoselective transformation of cinnamaldehyde to cinnamyl alcohol under visible and 365 nm UV light
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Coupling plasmonic noble metal with TiO_2 for efficient photocatalytic transfer hydrogenation: M/TiO_2 (M = Au and Pt) for chemoselective transformation of cinnamaldehyde to cinnamyl alcohol under visible and 365 nm UV light

机译:将等离激元贵金属与TiO_2偶联以进行有效的光催化转移加氢:M / TiO_2(M = Au和Pt)用于在可见光和365 nm紫外光下将肉桂醛化学选择性转化为肉桂醇

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摘要

M/TiO2 (M = Au and Pt) were prepared by a solvothermal method combined with an in situ photoreduction process and their photocatalytic performance for transfer hydrogenation of cinnamaldehyde (CAL) to form cinnamyl alcohol (COL) in the presence of isopropanol was investigated under visible light and 365 nm UV light. Although the photocatalytic transformation of CAL to COL can be realized over both Au/TiO2 and Pt/TiO2, they show different activity order under visible light and 365 nm UV light, ie, Au/TiO2 show superior activity than Pt/TiO2 under visible light, while an opposite activity order was observed under 365 nm UV light. The hydrogenation to form COL over Pt/TiO2 reached a turnover frequency (TOF) of 197 h(-1) under 365 nm UV light, which is among the highest in all the already reported systems for hydrogenation and transfer hydrogenation of CAL to form COL. The superior performance observed over Pt/TiO2 at 365 nm can be ascribed to a synergistic effect of plasmonic Pt and the direct excitation of TiO2. This study not only provides a green method for the transfer hydrogenation of CAL to form COL, but also highlights the great potential of coupling of plasmonic noble metal nanoparticles with semiconductor photocatalysts for light-induced organic transformations. (C) 2018 Elsevier B.V. All rights reserved.
机译:溶剂热法结合原位光还原法制备了M / TiO2(M = Au和Pt),并研究了在异丙醇存在下它们对肉桂醛(CAL)加氢生成肉桂醇(COL)的光催化性能。可见光和365 nm紫外线。尽管可以在Au / TiO2和Pt / TiO2上实现CAL到COL的光催化转化,但是它们在可见光和365 nm紫外光下显示出不同的活性顺序,即Au / TiO2在可见光下显示出比Pt / TiO2更好的活性。 ,而在365 nm紫外线下观察到相反的活性顺序。在365 nm紫外线下,在Pt / TiO2上加氢形成COL的周转频率(TOF)达到197 h(-1),在所有已报道的CAL加氢和转移加氢形成COL的系统中是最高的。在365 nm处观察到的优于Pt / TiO2的性能归因于等离子体Pt的协同效应和TiO2的直接激发。这项研究不仅为转移CAL氢化形成COL提供了一种绿色方法,而且还强调了等离激元贵金属纳米粒子与半导体光催化剂偶联的巨大潜力,可用于光诱导的有机转化。 (C)2018 Elsevier B.V.保留所有权利。

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