Molecular emission near metal interfaces: the polaritonic regime
Abstract
The strong coupling of a dense layer of molecular excitons with surface-plasmon modes in a metal gives rise to polaritons (hybrid light-matter states) called plexcitons. Surface plasmons cannot directly emit into (or be excited by) free-space photons due to the fact that energy and momentum conservation cannot be simultaneously satisfied in photoluminescence. Most plexcitons are also formally non-emissive, even though they can radiate via molecules upon localization due to disorder and decoherence. However, a fraction of them are bright even in the presence of such deleterious processes. In this letter, we theoretically discuss the superradiant emission properties of these bright plexcitons, which belong to the upper energy branch and reveal huge photoluminescence enhancements compared to bare excitons. Our study generalizes the well-known problem of molecular emission next to a metal interface to collective molecular states and provides new design principles for the control of photophysical properties of molecular aggregates using polaritonic strategies.
Keywords
Cite
@article{arxiv.1711.11213,
title = {Molecular emission near metal interfaces: the polaritonic regime},
author = {Joel Yuen-Zhou and Semion K. Saikin and Vinod M. Menon},
journal= {arXiv preprint arXiv:1711.11213},
year = {2018}
}
Comments
Replaced previous version, noticing that van Hove anomalies are only observed in the direct and reflected contributions of photoluminescence, but they cancel out when added up in the total photoluminescence. The correct phenomenology is that enhancements of photoluminescence are still huge (not infinite) and are near (not exactly at) the critical point