Abstract
Time resolved fluorescence measurements have become an important tool in applied fluorescence spectroscopy. Recently, it has been pointed out that the controlled manipulation of fluorescence decay rates opens a new dimension in applied fluorescence spectroscopy/ The fluorescence decay rate depends on two independent contributions, the pure radiative rate and the nonradiative rate. The latter one can be influenced by the well known Forster-type resonant energy transfer processes, while the radiative rate can be changed if the molecules are embedded or close to media comprising a dielectric constant markedly different from vacuum. Especially metal nanostructures have been used to alter both decay paths of fluorescent molecules. Apart from a change of those two rates, the absorption cross-section might also be altered.
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Klar, T.A., Dulkeith, E., Feldmann, J. (2005). Time Resolved Fluorescence Measurements of Fluorophores Close to Metal Nanoparticles. In: Geddes, C.D., Lakowicz, J.R. (eds) Radiative Decay Engineering. Topics in Fluorescence Spectroscopy, vol 8. Springer, Boston, MA. https://doi.org/10.1007/0-387-27617-3_8
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