Direct Photocatalysis by Plasmonic Nanostructures

被引:810
作者
Kale, Matthew J. [1 ]
Avanesian, Talin [1 ]
Christopher, Phillip [1 ,2 ]
机构
[1] Univ Calif Riverside, Dept Chem & Environm Engn, Riverside, CA 92521 USA
[2] Univ Calif Riverside, Program Mat Sci & Engn, Riverside, CA 92521 USA
关键词
photocatalysis; surface plasmons; selectivity; nanoparticles; solar energy; ENHANCED RAMAN-SCATTERING; ELECTRON-STIMULATED-DESORPTION; SUPPORTED GOLD NANOPARTICLES; VISIBLE-LIGHT; METAL NANOPARTICLES; OPTICAL-PROPERTIES; HIGHLY EFFICIENT; CHARGE-CARRIERS; CARBON-DIOXIDE; PHOTOCHEMISTRY;
D O I
10.1021/cs400993w
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
Recent reports have shown that plasmonic nanostructures can be used to drive direct photocatalysis with visible photons, where nanostructures act as the light absorber and the catalytic active site. These reports have showcased direct plasmon driven photocatalysis as a route to concentrate and channel the energy of low intensity visible light into adsorbed molecules, enhancing the rates of chemical transformations, and offering pathways to control reaction selectivity. In this perspective, we will discuss the fundamental photophysics of localized surface plasmon resonance (LSPR) excitation in the context of driving chemical transformations. The various demonstrated chemical conversions executed using direct plasmonic photocatalysis will be reviewed. Experimental observations, such as the dependence of photocatalytic rate on illumination intensity and photon energy, will be related to microscopic mechanisms of photocatalysis. In addition, theoretical treatments of various mechanisms within the process of direct plasmonic photocatalysis will be discussed and related to experimental studies. Throughout the Perspective, the possibility of activating targeted adsorbate bonds to allow rational manipulation of reaction selectivity in direct plasmonic photocatalysis will be discussed.
引用
收藏
页码:116 / 128
页数:13
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