An improved method for the treatment of the long range corrections in molecular simulations of inhomogeneous systems with planar interfaces is presented. To evaluate the quality of this approach, Monte Carlo simulations of the Lennard-Jones fluid are performed in the temperature range T* is an element of <0.7, 1.25>. The attention is focused especially on the values of the surface tension, which represents a property significantly sensitive to the truncation of the intermolecular interactions. When the presented approach is employed, the values of coexisting densities and surface tensions obtained with the cutoff distance R(c) = 2.5sigma are within experimental errors identical with those obtained for cutoff distance R(c) = 5.5sigma.

The structure of the water-solid interface for widely varying surface properties is investigated with Monte Carlo simulations using the SPC/E water model. Of particular interest is the relation between the wetting coefficient as a measure of the hydrophobicity of the substrate and the density depletion close to the solid surface. The substrates are modeled as rigid ordered lattices of sites that interact with water molecules through an orientation-independent Lennard-Jones potential of varying strength. Hydrophilic character is obtained by addition of polar hydroxyl groups on the substrate surface, and the influence of density, spatial distribution, and angular orientation of the polar groups on the interfacial water structure is studied.

Neutron reflectivity experiments conducted on self-assembled monolayers (SAMs) against polar (water) and nonpolar (organic) liquid phases reveal further evidence for a density reduction at hydrophobic-hydrophilic interfaces. The density depletion is found at the interface between hydrophobic dodecanethiol (C12) and hexadecanethiol (C16) SAMs and water and also between hydrophilic SAMs (C12/C11OH) and nonpolar fluids. The results show that the density deficit of a fluid in the boundary layer is not unique to aqueous solid-liquid interfaces but is more general and correlated with the affinity of the liquid to the solid surface. In water the variation of pH has only minor influence, while different electrolytes taken from the Hofmeister series seem to increase the depletion. On hydrophobic SAMs an increase in density depletion with temperature was observed, in agreement with Monte Carlo simulations performed on corresponding model systems. The increase in the water density depletion layer is governed by two effects: the surface energy difference between water and the substrate and the chemical potential of the aqueous phase.