Catalysis by Dark States in Vibropolaritonic Chemistry

Collective strong coupling between a disordered ensemble of N localized molecular vibrations and a resonant optical cavity mode gives rise to two polariton and N-1≫2 dark modes. Thus, experimental changes in thermally activated reaction kinetics due to polariton formation appear entropically unlikely and remain a puzzle. Here we show that the overlooked dark modes, while parked at the same energy as bare molecular vibrations, are robustly delocalized across ∼2-3 molecules, yielding enhanced channels of vibrational cooling, concomitantly catalyzing a chemical reaction. As an illustration, we theoretically show an ≈50% increase in an electron transfer rate due to enhanced product stabilization. The reported effects can arise when the homogeneous linewidths of the dark modes are smaller than their energy spacings.