Self-diffusion coefficients and orientational correlation times in aqueous NaCl solutions: Complementarity with structural investigations

Abstract

The dynamical properties of pure water and aqueous NaCl solutions over a wide range of salt concentrations (0–6 m) at ambient conditions are characterized by molecular dynamics (MD) simulations. MD simulations are performed with a flexible SPC water model as a solvent, while the ions are treated as charged Lennard–Jones particles. In this paper, attention has been focused on the self-diffusion coefficients ( D i ) of ions and water molecules and on orientational correlation time of water molecules. It is found that the self-diffusion coefficients decrease with ion concentration. Moreover, the self diffusion coefficients of sodium and chloride at higher salt concentrations are very comparable which may be due to the formation of clusters of these ions. The deduced rotational dynamics speeds up as the salt concentration increases. Some complementarities between dynamical properties and structural ones, recently obtained, are carried out.