Collective vibrational strong coupling effects on molecular vibrational relaxation and energy transfer: Numerical insights via cavity molecular dynamics simulations

TL;DR

This study uses cavity molecular dynamics simulations to show that collective vibrational strong coupling accelerates molecular vibrational relaxation and energy transfer, with effects depending on cavity parameters and scaling with the number of molecules.

Contribution

It provides numerical insights into how vibrational strong coupling influences relaxation dynamics, highlighting collective effects and parameter dependencies.

Findings

VSC accelerates vibrational relaxation via polariton excitation.

Relaxation rates depend on cavity detuning and molecular concentration.

The VSC effect scales with the number of molecules, similar to superradiance.

Abstract

For a small fraction of hot CO2 molecules immersed in a liquid-phase CO2 thermal bath, classical cavity molecular dynamics simulations show that forming collective vibrational strong coupling (VSC) between the C=O asymmetric stretch of CO2 molecules and a cavity mode accelerates hot-molecule relaxation. The physical mechanism underlying this acceleration is the fact that polaritons, especially the lower polariton, can be transiently excited during the nonequilibrium process, which facilitates intermolecular vibrational energy transfer. The VSC effects on these rates (i) resonantly depend on the cavity mode detuning, (ii) cooperatively depend on molecular concentration or Rabi splitting, and (iii) collectively scale with the number of hot molecules, which is similar to Dicke's superradiance. For larger cavity volumes, due to a balance between this superradiant-like behavior and a smaller light-matter coupling, the total VSC effect on relaxation rates can scale slower than $1/N$, and the average VSC effect per molecule can remain meaningful for up to $N \sim10^4$ molecules forming VSC. Moreover, we find that the transiently excited lower polariton prefers to relax by transferring its energy to the tail of the molecular energy distribution rather than equally distributing it to all thermal molecules. Finally, we highlight the similarities of parameter dependence between the current finding with VSC catalysis observed in Fabry-Perot microcavities.