Statistical methods and library search approaches for fast and reliable identification of dyes using surface-enhanced Raman spectroscopy (SERS)

• NCJ Number: 304230
• Journal: Analytical Methods Issue: 5 Dated: 2013 Pages: 4205-4212
• Author(s): Federica Pozzi ; Simone Porcinai ; John R. Lombardi; Marco Leona
• Date Published: 2013
• Length: 13 pages
• Grant Number(s): 2006-DN-BX-K034
• Agencies: NIJ-Sponsored

Annotation

This article reports on a project that assembled the core of a comprehensive library which contains 100 Raman and surface-enhanced Raman spectroscopy (SERS) reference spectra of natural and synthetic organic colorants.

Abstract

The identification of organic colorants is of high importance in the cultural heritage field, where they are found as paint components and textile dyes, and in forensic science, because of their use in inks and paints, food colorants and textile dyes. Surface-enhanced Raman spectroscopy (SERS) has emerged as a promising technique for the detection of these materials, yet concerns over the sensitivity of SERS spectra of dyes to chemical and instrumental variables (such as pH, choice of SERS substrates and/or aggregants, and excitation wavelength) have prevented its widespread use in analytical applications. Over the last few years, the development of several microanalytical approaches has considerably increased the chances of success in the identification of minute amounts of dyes by SERS. However, the need for searchable databases is still largely to be fulfilled. In the current project, experiments to classify 20 query SERS spectra of dyes from a variety of museum objects were conducted using principal component analysis (PCA) and the correlation coefficient (CC) algorithm. The effect of spectral transformations such as baseline correction, selecting a standard frequency range, normalization, smoothing, as well as carrying out the search on the second derivative of the spectra, was systematically evaluated. This study demonstrates that SERS spectra of organic colorants can be reliably matched against a well-constructed spectral library regardless of the instrumentation and the colloids used, as well as of the pH conditions at which the measurements were conducted. (publisher abstract modified)