Understanding radiative transitions and relaxation pathways in plexcitons

Molecular aggregates on plasmonic nanoparticles have emerged as attractive systems for the studies of polaritonic light-matter states, called plexcitons. Such systems are tunable, scalable, easy to synthesize, and offer sub-wavelength confinement, all while giving access to the ultrastrong light-matter coupling regime, promising a plethora of applications. However, the complexity of these materials prevented the understanding of their excitation and relaxation phenomena. Here, we follow the relaxation pathways in plexcitons and conclude that while the metal destroys the optical coherence, the molecular aggregate coupled to surface processes significantly contributes to the energy dissipation. We use two-dimensional electronic spectroscopy with theoretical modeling to assign the different relaxation processes to either molecules or metal nanoparticle. We show that the dynamics beyond a few femtoseconds has to be considered in the language of hot electron distributions instead of the accepted lower and upper polariton branches and establish the framework for further understanding.

Automated summary

This study reveals that while the metal destroys optical coherence, the molecular aggregate coupled to surface processes significantly contributes to energy dissipation. Two-dimensional electronic spectroscopy with theoretical modeling is used to assign different relaxation processes to either molecules or metal nanoparticles. The dynamics beyond a few femtoseconds must be considered in the language of hot electron distributions instead of the accepted lower and upper polariton branches, establishing a framework for further understanding.