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论文类型：期刊论文

发表时间：2009-07-15

发表刊物：SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY

收录刊物：SCIE、PubMed

卷号：73

期号：2

页面范围：382-387

ISSN号：1386-1425

关键字：Surface-enhanced Raman scattering spectrum; Adsorption site effect; Charge-transfer excited state; DFT; Pyridine-silver complexes

摘要：Density functional theory (DFT) and time-dependent DFT (TDDFT) methods have been used to investigate the adsorption site effect of Raman scattering for neutral and charged pyridine-Ag-4 complexes. The Calculated results show that the SERS spectra are strongly dependent on adsorption site and the configuration of new complexes. The normal Raman spectra of neutral and charged pyridine-Ag-4 complexes are similar with that of isolated pyridine but with an enhancement factor below 10 times. This enhancement is ascribed to ground state chemical enhancement. The pre-surface-enhanced Raman scattering (SERS) spectra were calculated at 1256 rim, 769 nm and 744.3 nm, which are nearly resonant with the charge transfer excited states S-2 for neutral and charged pyridine-Ag-4 complexes, respectively. We obtain the enhancement factor about 104 to 105 in pre-SERS spectra which is mainly Caused by charge transfer resonance Raman enhancement. The three-dimensional cube representation is also applied to describe the photoinduced CT, which are considered as direct evidence of chemical enhancement, between pyridine and two isomers of Ag-4 clusters. (C) 2009 Elsevier B.V. All rights reserved.