Solid-fluid Potential Research Articles

Pairwise correlations and wetting transitions at a solid-gas interface

We summarize the main results of our study of the density-density correlation function for Sullivan's model of a gas adsorbed on a solid substrate. In the approach to complete wetting, when a thick film of liquid density is adsorbed at the substrate, long-ranged transverse (parallel to the surface) correlations develop at the edge of the film where the density profile is similar to that of a liquid-gas interface. For a class I wetting situation the range of the transverse correlations increases and ultimately diverges as the bulk gas pressure approaches the saturated vapour pressure. We comment on other situations where long-ranged correlations arise and mention the possibility of observing these in diffraction experiments and in computer simulations. Sullivan's model always predicts a second-order phase transition between class II and class I wetting. By extending his model and allowing the attractive part of the solid-fluid potential to be longer-ranged than the attractive fluid-fluid potential we find that this wetting transition can become a first-order (Cahn) transition.

Long ranged correlations at a solid-fluid interface A signature of the approach to complete wetting

We have investigated the behaviour of the pairwise distribution function for Sullivan's model of a gas adsorbed on a solid substrate. We show that in the approach to complete wetting, when a thick film of liquid density is adsorbed on the substrate, long ranged transverse correlations (parallel to the surface) develop at the edge of the film where the density profile of the fluid resembles that of a liquid-gas interface. The long ranged correlations can be attributed to damped capillary-wave-like fluctuations; for a class I wetting situation the damping decreases and the range of the correlations increases and ultimately diverges as the bulk gas pressure approaches the saturated vapour pressure. Our analysis provides a physical explanation of the long ranged transverse correlations calculated by Foiles and Ashcroft in their recent study of a model of argon at a carbon dioxide substrate. We also predict that long range transverse correlations will occur for the case of adsorption from a dense liquid provided the solid-fluid potential is such that a thick film of gas forms between the substrate and the bulk liquid.