Origin of vibrational features in the excitation energy transfer dynamics of perylene bisimide J-aggregates Available to Purchase

We investigate the role of intramolecular normal mode vibrations in the excitation energy transfer (EET) dynamics of perylene bisimide J-aggregates composed of 2 or 25 units using numerically exact methods. The calculations employ a Frenkel exciton Hamiltonian where the ground and excited electronic states of each molecular unit are coupled to 28 intramolecular normal mode vibrations at various temperatures. The electronic populations exhibit strong damping effects, a lengthening of the EET time scale, and complex dynamical patterns, which depend on aggregate length, temperature, as well as electronic and vibrational initial conditions and which are not additive. The early evolution is dominated by high-frequency vibrational modes, but all modes are responsible for the observed dynamics after the initial 25 fs. Overall, we observe significant changes in the electronic populations upon varying the temperature between 0 and 600 K. With a Franck–Condon (FC) initial excitation, a strongly coupled vibrational mode introduces new peaks to the dimer populations, which show very weak temperature sensitivity. The first of these peaks is also seen in the long aggregate, but subsequent recurrences appear strongly quenched and merged. These structures are drastically altered if a non-FC initial condition is assumed. Additional insights are obtained from the diagonal elements of the dimer electronic-vibrational reduced density matrix. We find that the vibronic peaks result from depletion of the crossing region during the early coherent evolution of the vibrational density away from the crossing point, which allows the premature back-transfer of excitation to the initially excited unit.