Coupling effect on charge-transfer mechanism of surface-enhanced resonance Raman scattering

被引:15
|
作者
Li, Quanjiang [1 ]
Wang, Jingang [2 ,3 ,4 ]
Ding, Qianqian [1 ]
Chen, Maodu [1 ]
Ma, Fengcai [2 ,3 ]
机构
[1] Dalian Univ Technol, Sch Phys & Optoelect Technol, Key Lab Mat Modificat Laser Electron & Ion Beams, Minist Educ, Dalian 116024, Peoples R China
[2] Liaoning Univ, Dept Chem, Shenyang 110036, Peoples R China
[3] Liaoning Univ, Dept Phys, Shenyang 110036, Peoples R China
[4] Shenyang Aerosp Univ, Dept Phys, Shenyang 110036, Peoples R China
关键词
coupling effect; charge transfer; SERRS; DFT; Ac@Au-7 cluster; ELECTRONIC-STRUCTURE; SERS; SILVER; NANOPARTICLES; PYRIDINE; APPROXIMATION; SPECTRA; SHELL; GOLD; AG;
D O I
10.1002/jrs.5077
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
In this work, charge-transfer mechanism of surface-enhanced resonance Raman scattering (SERRS) spectroscopy of pyrazine absorbed on Ac@Au-7 clusters is theoretically investigated, and the coupling effect between the nanoparticles is especially concerned. First, the contributions of coupling effect to surface-enhanced Raman scattering (SERS) are compared between the ground-state nanoparticles. Second, the visualization of charge transfer provides evidence for the coupling effect on the charge-transfer enhancement mechanism of SERRS spectroscopy. The theoretical results show that the coupling effect on charge-transfer mechanism of SERRS can significantly enhance the intensity of SERS spectra up to about 6 x 10(5) times. The different coupling ways not only result in different degree of charge transfer on electronic transitions, but also cause different intensity of charge-transfer absorption peaks. Both of them strongly influence the enhancement of charge-transfer mechanism of SERRS. This study promotes the understanding of charge-transfer enhancement mechanism of SERRS for ultrasensitive Raman spectral analysis at nanoscale. Copyright (c) 2017 John Wiley & Sons, Ltd.
引用
收藏
页码:560 / 569
页数:10
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