Abstract
The evidence for the existence of a chemical mechanism in surface-enhanced resonance Raman scattering (SERRS) of rhodamine 6G (R6G) adsorbed on colloidal silver excited at 1064 nm is reported on the basis of experimental and theoretical analyses. A weak absorption peak at around 1060 nm for R6G-functionalized silver nanoparticles was observed, which is not present in the individual spectra of R6G or silver nanoparticles. Theoretically, the charge difference density reveals that this weak absorption is a metal-to-molecule charge transfer excited state. Copyright (C) 2010 John Wiley & Sons, Ltd.
Original language | English |
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Pages (from-to) | 719-720 |
Journal | Journal of Raman Spectroscopy |
Volume | 41 |
Issue number | 7 |
DOIs | |
Publication status | Published - 2010 |
Subject classification (UKÄ)
- Condensed Matter Physics
Free keywords
- charge transfer excited state
- 1064 nm
- SERS
- chemical mechanism