Vibrational damping effects on electronic energy relaxation in molecular aggregates

Abstract

Representation of molecular vibrational degrees of freedom by independent harmonic oscillators, when describing electronic spectra or electronic excitation energy transport, raises unfavourable effects as vibrational energy relaxation becomes inaccessible. A standard theoretical description is extended in this paper by including both electronic-phonon and vibrational-phonon couplings. Using this approach we have simulated a model pigment-protein system and have shown that intermode coupling leads to the quenching of pigment vibrational modes, and to the redistribution of fluctuation spectral density with respect to the electronic excitations. Moreover, new energy relaxation pathways, opened by the vibrational-phonon interaction, allow to reach the electronic excited state equilibrium quicker in the naturally occurring water soluble chlorophyll binding protein (WSCP) aggregate, demonstrating the significance that the damping of molecular vibrations has for the intrarmolecular energy relaxation process rate.