Surface-enhanced Raman spectroscopy toward application in plasmonic photocatalysis on metal nanostructures

被引:92
|
作者
Chen, Xue-Jiao
Cabello, Gema
Wu, De-Yin
Tian, Zhong-Qun [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
关键词
Surface-enhanced Raman spectroscopy; Metal nanostructures; Photochemistry; Plasmonic photocatalysis; SUPPORTED GOLD NANOPARTICLES; CATALYTIC COUPLING REACTIONS; VISIBLE-LIGHT IRRADIATION; P-AMINOTHIOPHENOL; SILVER NANOPARTICLES; PHOTOCYCLOREVERSION REACTION; ARTIFICIAL PHOTOSYNTHESIS; NITROAROMATIC COMPOUNDS; ADSORBED MOLECULES; AG-NANOPARTICLES;
D O I
10.1016/j.jphotochemrev.2014.10.003
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Among photothermal, photovoltaic and photochemical techniques, photochemistry is superior in energy storage and transportation by converting photons into chemical fuels. Recently plasmonic photocatalysis, based on localized surface plasmon resonance (LSPR) generated from noble metal nanostructures, has attracted much attention. It promotes photochemical reaction efficiency by optimizing the solar spectrum absorption and the surface reaction kinetics. The deeper understanding is in urgent need for the development of novel plasmonic photocatalysts. Surface-enhanced Raman spectroscopy (SERS), which is also originated from the LSPR effect, provides an excellent opportunity to probe and monitor plasmonic photoreactions in situ and in real-time, with a very high surface sensitivity and energy resolution. Here, fundamentals of plasmonic photocatalysis and SEAS are first presented based on their connections to the LSPR effect. Following by a validity analysis, latest studies of SERS applied for the plasmon mediated photochemical reaction are reviewed, focusing on the reaction kinetics and mechanism exploration. Finally, limitations of the present study, as well as the future research directions, are briefly analyzed and discussed. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:54 / 80
页数:27
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