Abstract
A mean-field statistical thermodynamic analysis of monolayer adsorption of rigid square and rectangular plate-like molecules on a homogeneous planar surface is developed. The analysis is simplified by only considering facewise and edgewise modes of adsorption in restricted orthogonal orientations parallel to the surface. The free energy density, adsorbate population distribution and surface spreading pressure are obtained as a function of adsorbate density and compared for square plate molecules using three different sequences of adsorbate molecule placement on the surface to evaluate the configurational degeneracy. It is found that edgewise adsorbed molecules can be anisotropically ordered if the edge length of square and rectangular plate-like molecules exceeds three length units in the absence of anisotropic dispersion interactions. If intermolecular dispersion interactions are present and of sufficient strength, the spreading pressure-density isotherms can exhibit one or two van der Waals loops for square plate molecules with three van der Waals loops possible for rectangular plate adsorbate molecules. The phase transitions for the adsorbed monolayer corresponding to the appearance of these van der Waals loops are discussed.