We develop here a mixed quantum mechanical/ molecular dynamics model to investigate charge-transfer dynamics in a set of large organic donor−bridge−acceptor triad molecules. Specifically, we are interested in the differences in electron and nuclear behavior relating to small changes in the molecular makeup of carotenoid−porphyrin−fullerene triads. Our model approximates excitation energies on the order of 1.9 eV which agree with absorption spectra for these triads and isolated porphyrins. Using electron population analysis, we monitor charge migration to the acceptor in time. Approximations of the charge transfer rates reveal ultrafast (picosecond scale) electron dynamics consistent with experimental literature.

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We perform dynamics simulations of donor–bridge–acceptor triads following photoexcitation and correlate nuclear motions with the charge-transfer event using the short-time Fourier transform technique. Broadly, the porphyrin bridges undergo higher energy vibrations, whereas the fullerene acceptors undergo low energy modes. Aryl side groups exhibit torsional motions relative to the porphyrin. Aryl linkers between the bridge and acceptor are restricted from such motions and therefore express ring distortion modes. Finally, we find an amide linker mode that is directionally sensitive to electron motion. This work supports the notion of vibrationally coupled ultrafast charge transfer found in both experimental and theoretical studies and lays a foundational method for identifying key vibrational modes for parametrizing future theoretical models.

We investigate the electronic dynamics of a model organic photovoltaic (OPV) system consisting of polyphenylene vinylene (PPV) oligomers and a [6,6]-phenyl C61-butyric acid methylester (PCBM) blend using a mixed molecular mechanics/quantum mechanics (MM/QM) approach. Using a heuristic model that connects energy gap fluctuations to the average electronic couplings and decoherence times, we provide and estimate of the state-to-state internal conversion rates within the manifold of the lowest few electronic excitations. We show that the electronic dynamics of the OPV are dramatically altered by varying the positions of the molecules simulated at the interface. The lowest few excited states of the model interface rapidly mix allowing low frequency C-C out of plain torsions to modulate the potential energy surface such that the system can sample both intermolecular charge-transfer and charge-separated electronic configurations on sub 100 fs time scales. Our simulations support an emerging picture of carrier generation in OPV systems in which interfacial electronic states can rapidly decay into charge-separated and current producing states via coupling to vibronic degrees of freedom.