Equilibrium structure of a dense trimesic acid monolayer on a homogeneous solid surface: from atomistic simulation to thermodynamics

Abstract

A general methodology for determining the thermodynamic characteristics of rigid organic crystals on the atomistic level is presented. The proposed approach is based on a combination of grid interpolation of the precalculated intermolecular potential and kinetic Monte Carlo simulation of the gas-crystal system with an explicit interphase. The two-phase system is stabilized in a wide range of external parameters with an imposed external potential and damping field. The damping field reduces the intermolecular potential at the edges of the crystals and turns it off in the gas phase. To determine the thermodynamic characteristics of a crystal the conditions of equality of chemical potentials in coexisting phases are used. The intermolecular pairwise potential can be calculated on the atomistic or quantum level. In the kinetic Monte Carlo simulations, a grid interpolation of the precalculated potential is performed on each iteration of the algorithm. We have applied the approach to the thermodynamic analysis of a dense monolayer of trimesic acid on a homogeneous surface. The calculated free energy and entropy for the dense “superflower” and filled chicken-wire phases obey the Gibbs–Duhem equation, which confirms the thermodynamic consistency of our approach. Using the proposed approach, we have revealed that the dense “superflower” phase becomes metastable at zero pressure and 470–500 K. Under these conditions, the filled chicken-wire structure with partially released hexagonal cages is thermodynamically favourable. The proposed approach is a potentially universal tool for the thermodynamic analysis of crystals formed by “rigid” organic molecules of any complexity on the atomistic level.