Rationale for $10^{14}$ enhancement factor in single molecule Raman spectroscopy
| dc.creator | Gaponenko, S. V. | |
| dc.creator | Guzatov, D. V. | |
| dc.date | 2008-11-11 | |
| dc.date.accessioned | 2026-07-07T10:17:27Z | |
| dc.date.available | 2026-07-07T10:17:27Z | |
| dc.description | We extend the Purcell's original idea [Phys. Rev. \textbf{69}, 682 (1946)] on modification of photon spontaneous \textit{emission} rate to modification of photon spontaneous \textit{scattering} rate. We find the interplay of local incident field enhancement and local density of photon states enhancement in close proximity to a silver nanoparticle may result in up to $10^{14}$-fold rise of Raman scattering cross-section. Thus single molecule Raman detection is found to be explained by consistent quantum electrodynamic description without any chemical mechanism involved. A model of the so-called "hot points" in surface enhanced spectroscopy has been elaborated as local areas with high Q-factor at incident and scattered (emitted) light frequencies. For verification of the model we consider further experiments including transient Raman experiments to clarify incident field enhancement and scanning near-field optical mapping of local density of photon states. | |
| dc.description | 5 pages, 2 figures | |
| dc.identifier | https://arxiv.org/abs/0811.1673 | |
| dc.identifier | http://arxiv.org/abs/0811.1673 | |
| dc.identifier.uri | http://salesiana.dossiersoluciones.com/handle/123456789/173855 | |
| dc.subject | Optics | |
| dc.subject | Chemical Physics | |
| dc.title | Rationale for $10^{14}$ enhancement factor in single molecule Raman spectroscopy | |
| dc.type | text |