Electrically enhanced hot hole driven oxidation catalysis at the interface of a plasmon-exciton hybrid

被引:105
|
作者
Lin, Weihua [1 ,2 ]
Cao, En [1 ,2 ,3 ]
Zhang, Liqiang [4 ]
Xu, Xuefeng [1 ]
Song, Yuzhi [3 ]
Liang, Wenjie [2 ]
Sun, Mengtao [1 ,2 ]
机构
[1] Univ Sci & Technol Beijing, Sch Math & Phys, Ctr Green Innovat, Beijing Key Lab Magnetophotoelect Composite & Int, Beijing 100083, Peoples R China
[2] Chinese Acad Sci, Inst Phys, Beijing Key Lab Nanomat & Nanodevices, Beijing Natl Lab Condensed Matter Phys, Beijing 100190, Peoples R China
[3] Shandong Normal Univ, Sch Phys & Elect, Jinan 250014, Shandong, Peoples R China
[4] China Univ Petr, State Key Lab Heavy Oil Proc, Changping 102249, Peoples R China
基金
中国国家自然科学基金;
关键词
RAMAN-SPECTROSCOPY; P-AMINOTHIOPHENOL; SURFACE; NANOPARTICLES; SERS; GRAPHENE; PHOTOCATALYSIS; ULTRAFAST; ELECTRONS; GOLD;
D O I
10.1039/c7nr08878g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work, an electro-optical device based on a graphene-Ag nanoparticle hybrid is fabricated as the substrate of graphene mediated surface enhanced Raman scattering (G-SERS) manipulated by the gate and bias voltages. Plasmon-exciton coupling promotes co-driven surface catalytic reactions, where the density of states (DOS) of holes and electrons on graphene is well controlled by the gate voltage, and the kinetic energy of holes and electrons is driven by the bias voltage (or current). Our experimental results reveal that the hot holes on graphene mainly contribute to plasmon-exciton co-driven oxidation reactions. The contribution of hot electrons to oxidation reactions is less important. Our novel electro-optical device can be potentially applied in controlling plasmon-exciton co-driven oxidation or reduction reactions by tuning the gate and bias voltages.
引用
收藏
页码:5482 / 5488
页数:7
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