Alexander Schubert

Ultrafast Exciton Self-Trapping upon Geometry Deformation in Perylene-Based Molecular Aggregates.

Femtosecond time-resolved experiments demonstrate that the photoexcited state of perylene tetracarboxylic acid bisimide (PBI) aggregates in solution decays nonradiatively on a time-scale of 215 fs. High-level electronic structure calculations on dimers point toward the importance of an excited state intermolecular geometry distortion along a reaction coordinate that induces energy shifts and couplings between various electronic states. Time-dependent wave packet calculations incorporating a simple dissipation mechanism indicate that the fast energy quenching results from a doorway state with a charge-transfer character that is only transiently populated. The identified relaxation mechanism corresponds to a possible exciton trap in molecular materials.

Identification of ultrafast relaxation processes as a major reason for inefficient exciton diffusion in perylene-based organic semiconductors.

The exciton diffusion length (LD) is a key parameter for the efficiency of organic optoelectronic devices. Its limitation to the nm length scale causes the need of complex bulk-heterojunction solar cells incorporating difficulties in long-term stability and reproducibility. A comprehensive model providing an atomistic understanding of processes that limit exciton trasport is therefore highly desirable and will be proposed here for perylene-based materials. Our model is based on simulations with a hybrid approach which combines high-level ab initio computations for the part of the system directly involved in the described processes with a force field to include environmental effects. The adequacy of the model is shown by detailed comparison with available experimental results. The model indicates that the short exciton diffusion lengths of α-perylene tetracarboxylicdianhydride (PTCDA) are due to ultrafast relaxation processes of the optical excitation via intermolecular motions leading to a state from which further exciton diffusion is hampered. As the efficiency of this mechanism depends strongly on molecular arrangement and environment, the model explains the strong dependence of LD on the morphology of the materials, for example, the differences between α-PTCDA and diindenoperylene. Our findings indicate how relaxation processes can be diminished in perylene-based materials. This model can be generalized to other organic compounds.

Theoretical analysis of the relaxation dynamics in perylene bisimide dimers excited by femtosecond laser pulses.

We present a model for the relaxation dynamics in perylene bisimide dimers, which is based on ab initio electronic structure and quantum dynamics calculations including effects of dissipation. The excited-state dynamics proceeds via a mixing of electronic states of local Frenkel and charge-transfer characters, which becomes effective upon a small distortion of the dimer geometry. In this way, it is possible to explain the fast depopulation of the photoexcited state, which we characterize by femtosecond transient absorption measurements. The combined theoretical and experimental analysis hints at a trapping mechanism, which involves nonadiabatic and dissipative dynamics in an excited-state vibronic manifold and provides an atomistic picture that might prove valuable for future design of photovoltaic materials.

Two-dimensional vibronic spectroscopy of coherent wave-packet motion

We theoretically study two-dimensional (2D) spectroscopic signals obtained from femtosecond pulse interactions with diatomic molecules. The vibrational wave-packet dynamics is monitored in the signals. During the motion in anharmonic potentials the wave packets exhibit vibrational revivals and fractional revivals which are associated with particular quantum phases. The time-dependent phase changes are identified by inspection of the complex-valued 2D spectra. We use the Na(2) molecule as a numerical example and discuss various pulse sequences which yield information about vibrational level structure and phase relationships in different electronic states.

Dissipative Wave Packet Dynamics of Hydrophobic → Hydrophilic Site Switching in Phenol-Ar Clusters

We analyze the results of recent pump-probe experiments on the site-switching dynamics of Ar within cationic phenol-Ar(2) clusters. A reaction-path model is employed for the wave packet dynamics. It is shown that the mechanism of energy dissipation is to be included to understand the features of the transient signals. Therefore, a simple recipe to include energy relaxation to the quantum dynamics is introduced. It is then possible to reproduce the measured pump-probe signals by adjustment of only two parameters.

Two-dimensional vibronic spectroscopy of molecular predissociation

We calculate two-dimensional (2D) spectra reflecting the time-dependent electronic predissociation of a diatomic molecule. The laser-excited electronic state is coupled non-adiabatically to a fragment channel, leading to the decay of the prepared quasi-bound states. This decay can be monitored by the three-pulse configuration employed in optical 2D spectroscopy. It is shown that in this way it is possible to state-selectively characterize the time-dependent population of resonance states with different lifetimes. A model of the NaI molecule serves as a numerical example.

A comparative study of different methods for calculating electronic transition rates

We present a comprehensive comparison of the following mixed quantum-classical methods for calculating electronic transition rates: (1) nonequilibrium Fermis golden rule, (2) mixed quantum-classical Liouville method, (3) mean-field (Ehrenfest) mixed quantum-classical method, and (4) fewest switches surface-hopping method (in diabatic and adiabatic representations). The comparison is performed on the Garg-Onuchic-Ambegaokar benchmark charge-transfer model, over a broad range of temperatures and electronic coupling strengths, with different nonequilibrium initial states, in the normal and inverted regimes. Under weak to moderate electronic coupling, the nonequilibrium Fermis golden rule rates are found to be in good agreement with the rates obtained via the mixed quantum-classical Liouville method that coincides with the fully quantum-mechanically exact results for the model system under study. Our results suggest that the nonequilibrium Fermis golden rule can serve as an inexpensive yet accurate alternative to Ehrenfest and the fewest switches surface-hopping methods.

Interference Effects in Vibronic 2D-Spectra of Diatomic Molecules

Abstract We theoretically study interference effects in two-dimensional (2D) vibronic spectra which arise from two electronically excited states taking part in the multi-photon process initiated by femtosecond laser pulses. Therefore, a model is employed which mimiques the situation encountered in many halogen and interhalogen molecules. There, upon excitation from the ground state, an excited bound state and a dissociative state exist which are close in energy. We demonstrate that the different pathways to final states which enter into the third-order polarization result in pronounced interference patterns in the 2D-spectra.