Impact of dynamic electrostatic disorder on hole mobility in rubrene: a nonadiabatic molecular dynamics investigation.

Abstract

High-mobility organic molecular crystals such as rubrene are important materials for organic electronics, yet a quantitatively predictive description of their charge transport properties remains challenging. Direct mixed quantum-classical nonadiabatic molecular dynamics simulations provide a promising route by explicitly propagating the charge carrier wavefunction, without assuming a specific transport mechanism. However, previous large-scale simulations of apolar molecular crystals have commonly neglected dynamic electrostatic disorder, since evaluation of electrostatic interactions is computationally demanding and the approximation appears plausible for apolar systems. Here, we use the damped shifted-force (DSF) real-space electrostatic summation method, combined with an efficient addition-subtraction scheme, to include dynamic electrostatic disorder in fragment orbital-based surface hopping (FOB-SH) simulations of room-temperature hole transport in rubrene. We find that electrostatic interactions increase the reorganization energy for (hypothetical) nearest neighbour hopping by 29 and 39 meV along the a and b-directions, respectively, relative to a baseline value of 152 meV obtained without electrostatics. In FOB-SH simulations, electrostatic interactions lead to increased site energy disorder, reducing the spatial extent of the hole wavefunction, as measured by a decrease in the inverse participation ratio from 13 to 9, and lowering the predicted mobility along the high-mobility direction from 35 to 21 cm² V^-1 s^-1, in close agreement with experiment.