Plasmon-driven reaction controlled by the number of graphene layers and localized surface plasmon distribution during optical excitation
Original Articles|Updated:2024-09-25
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Plasmon-driven reaction controlled by the number of graphene layers and localized surface plasmon distribution during optical excitation
Plasmon-driven reaction controlled by the number of graphene layers and localized surface plasmon distribution during optical excitation
LSA2015年4卷第4期
Affiliations:
1.Department of Physics and Key Laboratory of Artificial Micro- and Nano-structures of the Ministry of Education, Hubei Nuclear Solid Physics Key Laboratory, Wuhan University, Wuhan 430072, China
2.Laboratory of Functional Nanomaterials and Printed Electronics, School of Printing and Packaging, Wuhan University, Wuhan 430072, China
3.State Key Laboratory of Luminescence and Applications, Changchun Institute of Optics,Fine Mechanics and Physics, Chinese Academy of Sciences, Changchun 130033, China
4.School of Physical Engineering, Zhengzhou University, Zhengzhou 450052, China
5.Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China
Plasmon-driven reaction controlled by the number of graphene layers and localized surface plasmon distribution during optical excitation[J]. LSA, 2015,4(4).
Dai, Z. G. et al. Plasmon-driven reaction controlled by the number of graphene layers and localized surface plasmon distribution during optical excitation. Light: Science & Applications, 4, e342 (2015).
Plasmon-driven reaction controlled by the number of graphene layers and localized surface plasmon distribution during optical excitation[J]. LSA, 2015,4(4). DOI: 10.1038/lsa.2015.115.
Dai, Z. G. et al. Plasmon-driven reaction controlled by the number of graphene layers and localized surface plasmon distribution during optical excitation. Light: Science & Applications, 4, e342 (2015). DOI: 10.1038/lsa.2015.115.
Plasmon-driven reaction controlled by the number of graphene layers and localized surface plasmon distribution during optical excitation
Graphene-plasmonic hybrid platforms have attracted an enormous amount of interest in surface-enhanced Raman scattering (SERS); however
the mechanism of employing graphene is still ambiguous
so clarification about the complex interaction among molecules
graphene
and plasmon processes is urgently needed. We report that the number of graphene layers controlled the plasmon-driven
surface-catalyzed reaction that converts para-aminothiophenol (PATP)-to-
p
p
′-dimercaptoazobenzene (DMAB) on chemically inert
graphene-coated
silver bowtie nanoantenna arrays. The catalytic reaction was monitored by SERS
which revealed that the catalytic reaction occurred on the chemical inertness monolayer graphene (1G)-coated silver nanostructures. The introduction of 1G enhances the plasmon-driven surface-catalyzed reaction of the conversion of PATP-to-
p
p
′-DMAB. The chemical reaction is suppressed by bilayer graphene. In the process of the catalytic reaction
the electron transfer from the PATP molecule to 1G-coated silver nanostructures. Subsequently
the transferred electrons on the graphene recombine with the hot-hole produced by the localized surface plasmon resonance of silver nanostructures. Then
a couple of PATP molecules lost electrons are catalyzed into the
p
p
′-DMAB molecule on the graphene surface. The experimental results were further supported by the finite-difference time-domain method and quantum chemical calculations.
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相关机构
State Key Laboratory of Optoelectronic Materials and Technologies, School of Physics, Sun Yat-sen University
Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences
State Key Laboratory of Optoelectronic Materials and Technologies, Guangdong Province Key Laboratory of Display Material and Technology, School of Electronics and Information Technology
Institute for Microstructure Technology, Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, Eggenstein-Leopoldshafen
Department of Chemistry, University of Cambridge, Lensfield Road