Issue 16, 2011

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

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.

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

Supplementary files

Article information

Article type
Paper
Submitted
07 Dec 2010
Accepted
22 Feb 2011
First published
17 Mar 2011

Phys. Chem. Chem. Phys., 2011,13, 7439-7448

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

Y. Kitahama, Y. Tanaka, T. Itoh and Y. Ozaki, Phys. Chem. Chem. Phys., 2011, 13, 7439 DOI: 10.1039/C0CP02802A

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