| Literature DB >> 29522686 |
Tomáš Neuman1, Ruben Esteban1,2, David Casanova1,2, Francisco J García-Vidal1,3, Javier Aizpurua1.
Abstract
As the size of a molecular emitter becomes comparable to the dimensions of a nearby optical resonator, the standard approach that considers the emitter to be a point-like dipole breaks down. By adoption of a quantum description of the electronic transitions of organic molecular emitters, coupled to a plasmonic electromagnetic field, we are able to accurately calculate the position-dependent coupling strength between a plasmon and an emitter. The spatial distribution of excitonic and photonic quantum states is found to be a key aspect in determining the dynamics of molecular emission in ultrasmall cavities both in the weak and strong coupling regimes. Moreover, we show that the extreme localization of plasmonic fields leads to the selection rule breaking of molecular excitations.Entities:
Keywords: Plasmon−exciton coupling; nanoplasmonics; point-dipole approximation; quantum chemistry; quantum nano-optics; single-molecule spectroscopy
Year: 2018 PMID: 29522686 DOI: 10.1021/acs.nanolett.7b05297
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189