Molecular dynamics simulations of the diffusion of benzene sub-monolayer films on graphite basal plane surfaces

Abstract

A classical molecular dynamics study of the diffusive motion of benzene molecules on graphite basal planes has been performed in the sub-monolayer coverage regime. Atomistic calculations were performed using the second generation forcefield COMPASS as well as the general purpose forcefields Dreiding and Universal. The COMPASS based calculations show evidence for a Brownian nature of the diffusion with a very small diffusion activation barrier of 11 ± 2 meV in agreement with recent helium and neutron spin-echo spectroscopy data [Fouquet P, Hedgeland H, Jardine AP, Alexandrowicz G, Allison W, Ellis J. Measurements of molecule diffusion on surfaces using neutron and helium spin echo. Physica B 2006;385–386:269-71]. Reasonable agreement is also found for the general purpose forcefields if screened charges are used in the description of the Coulombic non-bond interaction. The less computationally intensive Dreiding forcefield was shown to give a good qualitative description of the diffusion validating its applicability for future large scale calculation, i.e., for long times or enlarged systems. A potential energy surface (PES) has been established for the translational and rotational diffusive motion. The PES shows a peculiar dependence of the lateral diffusion barriers on the rotation angle of the benzene molecule which leads to a preferential selection of certain rotational states in the MD trajectories.