Absorption cross-section spectroscopy of single strong coupling system between plasmon and molecular exciton resonance using single silver nanoparticle dimer generating surface enhanced resonant Raman scattering

Abstract

This study investigated spectral changes in the absorption cross-sections of single strong coupling systems composed of single silver nanoparticle dimers and a few dye molecules during the quenching of surface-enhanced resonant Raman scattering (SERRS). The absorption cross-section was obtained by subtracting the scattering cross-section from an extinction cross-section. The spectral changes in these cross-sections were evaluated using a classical hybridization model composed of a plasmon and a molecular exciton including a molecular multi-level property. The changes in the scattering and extinction cross-sections exhibit blue-shifts in their peak energy and increased peak intensities, respectively, during SERRS quenching. These properties are effectively reproduced in the model by decreasing the coupling energy. In particular, the peaks in the scattering and extinction cross-sections appear as peaks or dips in the absorption cross-sections depending on the degree of scattering loss, which reflects the dimer sizes. These results are useful for optimizing photophysical and photochemical effects mediated by the electronic excited states of strong coupling systems.

30 pages, 6 figures

References in corpus (4)

• Realizing strong light-matter interactions between single nanoparticle plasmons and molecular excitons at ambient conditions
• Observation of intrinsic size effects in the optical response of individual gold nanoparticles
• Surface-enhanced Raman scattering and fluorescence near metal nanoparticles
• Competition between extinction and enhancement in surface enhanced Raman spectroscopy