Polarizable contributions to the surface tension of liquid water

Abstract : Surface tension, gamma, strongly affects interfacial properties in fluids. The degree to which polarizability affects gamma in water is thus far not well established. To address this situation, we carry out molecular dynamics simulations to study the interfacial forces acting on a slab of liquid water surrounded by vacuum using the Gaussian charge polarizable (GCP) model at 298.15 K. The GCP model incorporates both a fixed dipole due to Gaussian distributed charges and a polarizable dipole. We find a well-defined bulklike region forms with a width of approximate to 31 A. The average density of the bulklike region agrees with the experimental value of 0.997 g/cm(3). However, we find that the orientation of the molecules in the bulklike region is strongly influenced by the interfaces, even at a distance five molecular diameters from the interface. Specifically, the orientations of both the permanent and induced dipoles show a preferred orientation parallel to the interface. Near the interface, the preferred orientation of the dipoles becomes more pronounced and the average magnitude of the induced dipoles decreases monotonically. To quantify the degree to which molecular orientation affects gamma, we calculate the contributions to gamma from permanent dipolar interactions, induced dipolar interactions, and dispersion forces. We find that the induced dipole interactions and the permanent dipole interactions, as well as the cross interactions, have positive contributions to gamma, and therefore contribute stability to the interface. The repulsive core interactions result in a negative contribution to gamma, which nearly cancels the positive contributions from the dipoles. The large negative core contributions to gamma are the result of small oxygen-oxygen separation between molecules. These small separations occur due to the strong attractions between hydrogen and oxygen atoms. The final predicted value for gamma (68.65 mN/m) shows a deviation of approximate to 4% of the experimental value of 71.972 mN/m. The inclusion of polarization is critical for this model to produce an accurate value
Type de document :
Article dans une revue
Journal of Chemical Physics, American Institute of Physics, 2006, 125 (9), pp.094712. 〈10.1063/1.2345063〉
Domaine :
Liste complète des métadonnées

https://hal.archives-ouvertes.fr/hal-01153441
Contributeur : Patrice Paricaud <>
Soumis le : mardi 19 mai 2015 - 17:36:33
Dernière modification le : jeudi 16 novembre 2017 - 17:14:19

Lien texte intégral

Identifiants

Collections

Citation

Jose L. Rivera, Francis W. Starr, Patrice Paricaud, Peter T. Cummings. Polarizable contributions to the surface tension of liquid water. Journal of Chemical Physics, American Institute of Physics, 2006, 125 (9), pp.094712. 〈10.1063/1.2345063〉. 〈hal-01153441〉

Partager

Métriques

Consultations de la notice

54