Issue 34, 2009

SERS enhancement by aggregated Au colloids: effect of particle size

Abstract

Aggregated Au colloids have been widely used as SERS enhancing media for many years but to date there has been no systematic investigation of the effect of the particle size on the enhancements given by simple aggregated Au colloid solutions. Previous systematic studies on isolated particles in solution or multiple particles deposited onto surfaces reported widely different optimum particle sizes for the same excitation wavelength and also disagreed on the extent to which surface plasmon absorption spectra were a good predictor of enhancement factors. In this work the spectroscopic properties of a range of samples of monodisperse Au colloids with diameters ranging from 21 to 146 nm have been investigated in solution. The UV/visible absorption spectra of the colloids show complex changes as a function of aggregating salt (MgSO4) concentration which diminish when the colloid is fully aggregated. Under these conditions, the relative SERS enhancements provided by the variously sized colloids vary very significantly across the size range. The largest signals in the raw data are observed for 46 nm colloids but correction for the total surface area available to generate enhancement shows that particles with 74 nm diameter give the largest enhancement per unit surface area. The observed enhancements do not correlate with absorbance at the excitation wavelength but the large differences between differently sized colloids demonstrate that even in the randomly aggregated particle assemblies studied here, inhomogeneous broadening does not mask the underlying changes due to differences in particle diameter.

Graphical abstract: SERS enhancement by aggregated Au colloids: effect of particle size

Supplementary files

Article information

Article type
Paper
Submitted
26 Mar 2009
Accepted
11 Jun 2009
First published
30 Jun 2009

Phys. Chem. Chem. Phys., 2009,11, 7455-7462

SERS enhancement by aggregated Au colloids: effect of particle size

S. E. J. Bell and M. R. McCourt, Phys. Chem. Chem. Phys., 2009, 11, 7455 DOI: 10.1039/B906049A

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