Power-law analysis of surface-plasmon-enhanced electromagnetic field dependence of blinking SERS of thiacyanine or thiacarbocyanine adsorbed on single silver nanoaggregates

Literature Information

Publication Date 2011-03-17
DOI 10.1039/C0CP02802A
Impact Factor 3.676
Authors

Yasutaka Kitahama, Yuhei Tanaka, Tamitake Itoh, Yukihiro Ozaki


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Abstract

Blinking statistics in surface-enhanced Raman scattering (SERS) of thiacyanine or thiacarbocyanine adsorbed on single Ag nanoaggregates were analyzed by a power law. A power law reproduces the probability distributions of both the bright and dark SERS occurrences against their duration times. As the localized surface plasmon resonance (LSPR) wavelength of a single Ag nanoaggregate approached the excitation wavelength or the excitation laser intensity increases, the power-law exponents were close to −1.5, a value derived from a one-dimensional random walk model. When the LSPR wavelength left the excitation wavelength or the excitation laser intensity decreases, the power-law exponents deviated from −1.5. The decrease in the power-law exponents in the bright SERS, which indicates a decrease in the probabilities of the long-lived bright SERS, and the increase in the power-law exponents in the dark SERS coincide with the increasing shallowness and narrowing of a optical trapping potential well due to a surface-plasmon-enhanced electromagnetic field around a junction of the Ag nanoaggregates excited at a wavelength apart from the LSPR wavelength or under the low laser intensity, i.e., the low original electromagnetic field, respectively.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
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