Abstract
We consider fluid adsorption near a rectangular edge of a solid substrate that interacts with the fluid atoms via long range (dispersion) forces. The curved geometry of the liquid-vapour interface dictates that the local height of the interface above the edge must remain finite at any subcritical temperature, even when a macroscopically thick film is formed far from the edge. Using an interfacial Hamiltonian theory and a more microscopic fundamental measure density functional theory (DFT), we study the complete wetting near a single edge and show that , as the chemical potential departure from the bulk coexistence tends to zero. The exponent depends on the range of the molecular forces and in particular for three-dimensional systems with van der Waals forces. We further show that for a substrate model that is characterised by a finite linear dimension , the height of the interface deviates from the one at the infinite substrate as in the limit of large . Both predictions are supported by numerical solutions of the DFT.
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