中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Tracking the Fate of Surface Plasmon Resonance-Generated Hot Electrons by In Situ SERS Surveying of Catalyzed Reaction

文献类型:期刊论文

作者Liu, Rui; He, Zuoliang; Sun, Jiefang; Liu, Jingfu; Jiang, Guibin
刊名SMALL
出版日期2016-12-14
卷号12期号:46页码:6378-6387
英文摘要Plasmonic catalysis is an emerging process that utilizes surface plasmon resonance (SPR) process to harnesses solar energy for the promotion of catalyzed reactions. In most cases, SPR generated hot electrons (HEs) play an indispensable role in this solar-chemical energy shift process. Therefore, understanding the effectiveness of the HEs in promoting chemical reactions, and identifying the key factors that contribute to this utilization efficiency is of profound importance. Herein, the authors outline an in situ surface enhanced Raman spectroscopy protocol to track the fate of HEs. This is based on the unheeded HEs-acceleration nature of the p-nitirothiophenol hydrogenation reaction. By this way, the authors discover that unlike Au@Pd nanostructures which experience a 20-fold increase in rate constant, HEs primary leak to surrounding H+/O species through Ag pinholes in Ag@Pd. This work sheds light on why Ag is seldom employed as a plasmonic cocatalyst, and provides a new viewpoint to design plasmonic nanocatalysts with efficient light utilization.
收录类别SCI
源URL[http://ir.rcees.ac.cn/handle/311016/35971]  
专题生态环境研究中心_环境化学与生态毒理学国家重点实验室
推荐引用方式
GB/T 7714
Liu, Rui,He, Zuoliang,Sun, Jiefang,et al. Tracking the Fate of Surface Plasmon Resonance-Generated Hot Electrons by In Situ SERS Surveying of Catalyzed Reaction[J]. SMALL,2016,12(46):6378-6387.
APA Liu, Rui,He, Zuoliang,Sun, Jiefang,Liu, Jingfu,&Jiang, Guibin.(2016).Tracking the Fate of Surface Plasmon Resonance-Generated Hot Electrons by In Situ SERS Surveying of Catalyzed Reaction.SMALL,12(46),6378-6387.
MLA Liu, Rui,et al."Tracking the Fate of Surface Plasmon Resonance-Generated Hot Electrons by In Situ SERS Surveying of Catalyzed Reaction".SMALL 12.46(2016):6378-6387.

入库方式: OAI收割

来源:生态环境研究中心

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