Radiative and non-radiative photokinetics alteration inside a single metallic nanometric aperture
Jerome Wenger, Benoit Cluzel, Jose Dintinger, Nicolas Bonod,, Anne-Laure Fehrembach, Evgeny Popov, Pierre-Francois Lenne, Thomas W., Ebbesen, and Herve Rigneault

TL;DR
This study investigates how a nanometric aperture in aluminum influences the fluorescence rates of Rhodamine 6G molecules, revealing detailed insights into radiative and non-radiative decay processes that enhance fluorescence.
Contribution
It provides a detailed analysis of photokinetic rate enhancements inside a single nanometric aperture, combining fluorescence correlation spectroscopy and lifetime measurements.
Findings
15-fold increase in fluorescence rate per molecule
Detailed influence of excitation, radiative, and non-radiative decay processes
Broad applicability to various nanostructures
Abstract
We resolve the photokinetic rates enhancement of Rhodamine 6G molecules diffusing in a water-glycerol mixture within a single nanometric aperture milled in an opaque aluminium film. Combining fluorescence correlation spectroscopy and lifetime measurements, we report the relative influence of excitation, radiative and non-radiative decay in the fluorescence process, giving a detailed description of the physics behind the overall 15 fold enhancement of the average fluorescence rate per molecule. This procedure is broadly adaptable to a wide range of nanostructures.
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Taxonomy
TopicsGold and Silver Nanoparticles Synthesis and Applications · Plasmonic and Surface Plasmon Research · Photochemistry and Electron Transfer Studies
