Hybridized exciton-polariton resonances in core-shell nanoparticles
arXiv:1609.04932 · doi:10.1088/2040-8986/aa5517
Abstract
The goal of nanophotonics is to control and manipulate light at length scales below the diffraction limit. Typically nanostructured metals are used for this purpose, light being confined by exploiting the surface plasmon-polaritons such structures support. Recently excitonic (molecular) materials have been identified as an alternative candidate material for nanophotonics. Here we use theoretical modelling to explore how hybridisation of surface exciton-polaritons can be achieved through appropriate nanostructuring. We focus on the extent to which the frequency of the hybridised modes can be shifted with respect to the underlying material resonances.
arXiv comment16 pages, 9 figures
References in corpus (7)
- Strong coupling between surface plasmon polaritons and emitters
- Realizing strong light-matter interactions between single nanoparticle plasmons and molecular excitons at ambient conditions
- Strong coupling between a metallic nanoparticle and a single molecule
- Constraints on relaxation rates for N-level quantum systems
- Particle plasmons: Why shape matters
- Evidence of Excitonic Optical Tamm States using Molecular Materials
- Localized exciton-polariton modes in dye-doped nanospheres: a quantum approach
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- Coupled electric dipole model for a Su-Schrieffer-Heeger chain of optically resonant coreshell nanoparticles