个人信息Personal Information
教授
博士生导师
硕士生导师
性别:男
毕业院校:中科院大连化学物理研究所
学位:博士
所在单位:物理学院
学科:原子与分子物理. 光学
电子邮箱:mdchen@dlut.edu.cn
Direct visual evidence for the chemical mechanism of surface-enhanced resonance Raman scattering via charge transfer: (II) Binding-site and quantum-size effects
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论文类型:期刊论文
发表时间:2009-09-01
发表刊物:JOURNAL OF RAMAN SPECTROSCOPY
收录刊物:SCIE、Scopus
卷号:40
期号:9
页面范围:1172-1177
ISSN号:0377-0486
关键字:chemical enhancement; charge transfer; SERRS; binding site; quantum size
摘要:We describe quantum-size and binding-site effects on the chemical and local field enhancement mechanisms of surface-enhanced resonance Raman scattering (SERRS), in which the pyridine molecule is adsorbed on one of the vertices of the Ag(20) tetrahedron. We first investigated the influence of the binding site on normal Raman scattering (NRS) and excited state properties of optical absorption spectroscopy. Second, we investigated the quantum-size effect on the electromagnetic (EM) and chemical mechanism from 300 to 1000 nm with charge difference density. It is found that the strong absorption at around 350 nm is mainly the charge transfer (CT) excitation (CT between the molecule and the silver cluster) for large clusters, which is the direct evidence for the chemical enhancement mechanism for SERRS; for a small cluster the strong absorption around 350 nm is mainly intracluster excitation, which is the direct evidence for the EM enhancement mechanism. This conclusion is further confirmed with the general Mie theory. The plasmon peak in EM enhancement will be red-shifted with the increase of cluster size. The influence of the binding site and quantum-size effects on NRS, as well as chemical and EM enhancement mechanisms on SERRS, is significant. Copyright (C) 2009 John Wiley & Sons, Ltd.