Free energy partitioning analysis of the driving forces that determine ion density profiles near the water liquid-vapor interface

Abstract

Free energy partitioning analysis is employed to explore the driving forces for ions interacting with the water liquid-vapor interface using recently optimized point charge models for the ions and SPC/E water. The Na(+) and I(-) ions are examined as an example kosmotrope/chaotrope pair. The absolute hydration free energy is partitioned into cavity formation, attractive van der Waals, local electrostatic, and far-field electrostatic contributions. We first compute the bulk hydration free energy of the ions, followed by the free energy to insert the ions at the center of a water slab. Shifts of the ion free energies occur in the slab geometry consistent with the SPC/E surface potential of the water liquid-vapor interface. Then the free energy profiles are examined for ion passage from the slab center to the dividing surface. The profiles show that, for the large chaotropic I(-) ion, the relatively flat total free energy profile results from the near cancellation of several large contributions. The far-field electrostatic part of the free energy, largely due to the water liquid-vapor interface potential, has an important effect on ion distributions near the surface in the classical model. We conclude, however, that the individual forms of the local and far-field electrostatic contributions are expected to be model dependent when comparing classical and quantum results. The substantial attractive cavity free energy contribution for the larger I(-) ion suggests that there is a hydrophobic component important for chaotropic ion interactions with the interface.