Abstract
We present a direct observation of an ultrafast time-resolved emission spectrum of a dye molecule in solution, the time resolution of the system being 2 \ifmmode\times\else\texttimes\fi{} ${10}^{\ensuremath{-}12}$ sec. Vibrational relaxation within the vibrational manifold of the excited electronic state of rhodamine 6G occurs within 6 \ifmmode\times\else\texttimes\fi{} ${10}^{\ensuremath{-}12}$ sec. We discuss the implications of these results for the understanding of homogeneous broadening of excited electronic states of large molecules.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
