Quantitative evaluation of blinking in surface enhanced resonance Raman scattering and fluorescence by electromagnetic mechanism

被引:71
作者
Itoh, Tamitake [1 ]
Iga, Mitsuhiro [1 ,2 ]
Tamaru, Hiroharu [3 ]
Yoshida, Ken-ichi [1 ]
Biju, Vasudevanpillai [1 ]
Ishikawa, Mitsuru [1 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Hlth Res Inst, Nanobioanal Res Grp, Takamatsu, Kagawa 7610395, Japan
[2] Yokogawa Elect Corp, Tokyo 1800006, Japan
[3] Univ Tokyo, Photon Sci Ctr, Tokyo 1138656, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
SINGLE-MOLECULE; RHODAMINE; 6G; SILVER NANOPARTICLES; ENERGY-TRANSFER; SPECTROSCOPY; SERS; ORIGINS; PLASMON; PROTEIN; FIELDS;
D O I
10.1063/1.3675567
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We analyze blinking in surface enhanced resonance Raman scattering (SERRS) and surface enhanced fluorescence (SEF) of rhodamine 6G molecules as intensity and spectral instability by electromagnetic (EM) mechanism. We find that irradiation of intense NIR laser pulses induces blinking in SERRS and SEF. Thanks to the finding, we systematically analyze SERRS and SEF from stable to unstable using single Ag nanoparticle (NP) dimers. The analysis reveals two physical insights into blinking as follows. (1) The intensity instability is inversely proportional to the enhancement factors of decay rate of molecules. The estimation using the proportionality suggests that separation of the molecules from Ag NP surfaces is several angstroms. (2) The spectral instability is induced by blueshifts in EM enhancement factors, which have spectral shapes similar to the plasmon resonance. This analysis provides us with a quantitative picture for intensity and spectral instability in SERRS and SEF within the framework of EM mechanism. (C) 2012 American Institute of Physics. [doi:10.1063/1.3675567]
引用
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页数:7
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