Perturbation theory is used to study the solvation of nonpolar molecules in water, supported by extensive computer simulations. Two contributions to the solvent-mediated solute-water interactions are identified: a cavity potential of mean force that transforms by a simple translation when the solute size changes, and a solute-size-independent cavity-expulsion potential. The latter results in weak dewetting of the solute-water interface that can explain the approximate area dependence of solvation free energies with apparent surface tensions similar to macroscopic values.
Reference
Hummer G and Garde S (). "Cavity Expulsion and Weak Dewetting of Hydrophobic Solutes in Water
," Phys. Rev. Lett., 80 (19), 4193-4196
Bibtex
@article{hummer1998cavity, title = {Cavity expulsion and weak dewetting of hydrophobic solutes in water}, author = {Hummer, Gerhard and Garde, Shekhar}, journal = {Phys. Rev. Lett.}, volume = {80}, number = {19}, pages = {4193--4196}, year = {1998}, doi = {10.1103/PhysRevLett.80.4193} }