Cavity-modified exciton-exciton annihilation in disordered molecular systems

4 May 2026, 14:30
20m
Albano 3: 4205 - SU Conference Room (40 seats) (Albano Building 3)

Albano 3: 4205 - SU Conference Room (40 seats)

Albano Building 3

Albanovägen 20, 114 19 Stockholm
40
Contributed Talk Monday Afternoon

Speaker

Ilia Sokolovskii (University College London)

Description

Recent experiments have shown contradictory effects of strong light-matter coupling on exciton-exciton annihilation (EEA) in organic molecular systems. Here, I will present the results of numerical simulations of polariton dynamics, which reveal the role of strong coupling in changing the EEA rate. These results suggest that in systems with poor exciton mobility, strong coupling allows to partially overcome disorder via delocalisation of excitons owing to the interaction with the common cavity mode. This leads to an enhanced connectivity between excitons and, consequently, to an increase in the EEA rate. Conversely, in systems with high exciton mobility, in which disorder has a much smaller effect on excitation energy transfer, excitons can interact strongly even without coupling to the cavity photons at the exciton densities at which EEA typically occurs. In this case, the EEA rate can be even lower than in bare molecules due to the existence of a competing decay channel associated with photon leakage through the cavity mirrors. We also find that in the weak coupling regime, the EEA rate is always suppressed due to this decay channel regardless of the exciton transport properties. Our simulations resolve the experimental controversy on the effect of strong coupling on EEA and provide guidance for minimising the EEA rate towards a more feasible realisation of Bose-Einstein condensation of polaritons.

Authors

Ilia Sokolovskii (University College London) Dr Ben Humphries (University College London) Prof. Jochen Blumberger (University College London) Prof. Gerrit Groenhof (University of Jyväskylä)

Presentation materials

There are no materials yet.