Details

Autor(en) / Beteiligte

• Harpham, Michael R
• Ladanyi, Branka M
• Levinger, Nancy E

Titel

The Effect of the Counterion on Water Mobility in Reverse Micelles Studied by Molecular Dynamics Simulations

Ist Teil von

• The journal of physical chemistry. B, 2005-09, Vol.109 (35), p.16891-16900

Ort / Verlag

United States: American Chemical Society

Erscheinungsjahr

2005

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• In this study, mobility and structure of water molecules in Aerosol OT (bis(2-ethylhexyl) sulfosuccinate, AOT) reverse micelles with water content w 0 = 5 and Na+, K+, Cs+ counterions have been explored with molecular dynamics (MD) simulations. Using the Faeder/Ladanyi model (J. Phys. Chem. B, 2000, 104, 1033) of the reverse micelle interior, MD simulations were performed to calculate the self-intermediate scattering function, F S(Q,t), for water hydrogen atoms that could be measured in a quasielastic neutron scattering experiment. Separate intermediate scattering functions (Q,t) and (Q,t) were determined for rotational and translational motion. We find that the decay of (Q,t) is nonexponential and our analysis of the MD data indicates that this behavior arises from decreased water mobility for molecules close to the interface and from confinement-induced restrictions on the range of translational displacements. Rotational relaxation also exhibits nonexponential decay, which is consistent with relatively rapid restricted rotation and slower rotational relaxation over the full angular range. Rotational relaxation is anisotropic, with the O−H bond short-time rotational mobility considerably higher than that of the molecular dipole. This behavior is related to the decreased density of water−water hydrogen bonds in the vicinity of the interface compared to core or bulk water. We find that the interfacial mobility of water molecules is quite different for the three counterion types, but that the core mobility exhibits weak counterion dependence. Differences in interfacial mobility are strongly correlated with structural features, especially ion−water coordination, and the extent of disruption by the counterions of the water hydrogen bond network.