Ionization of sodium in water clusters

Abstract

Structures of Na(H2O)n and Na+(H2O)n clusters with n = 1−6, 19, and 28 are determined in the second order of the Moller-Plesset perturbation theory with the use of extended atomic basis set 6–31++G**. It is found that when the number of molecules is sufficient for the formation of two solvation shells around sodium, a continuous hydrogen-bond network is formed in both neutral and charged clusters, and the orientation of each molecule is determined by the balance between interactions with the neighboring water molecules and with the field of the central particle. In the cations, this field is stronger, and up to the third solvation shell, molecules have a predominant orientation with respect to sodium. In the neutral clusters, with an increase in the number of water molecules, the maximum of the electron density distribution of the highest occupied molecular orbital becomes more distant from the sodium nucleus, being shifted toward the cluster surface. The energy of this orbital accordingly decreases in absolute value approaching 22 kcal/mol inmicroparticles. In the charged clusters, the distribution of the positive charge generally correlates with the character of the highest occupied orbital in the neutral systems, so that with an increase in the number of molecules, the atomic charge of sodium decreases and tends to zero as n → ∞. The ionization potential of sodium changes in inverse proportion to the linear size of the cluster, and should not exceed 1.1 eV in watermicroparticles.