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Optimization of classical nonpolarizable force fields for OH− and H3O+

Douwe Jan BonthuisUniversity of Oxford 1 Rudolf Peierls Centre for Theoretical Physics, , Oxford OX1 3NP, United KingdomShavkat MamatkulovIon-Plasma and Laser Technologies Institute of the Uzbekistan AS 2 , Tashkent, UzbekistanRoland R. NetzFreie Universität Berlin 3 Fachbereich Physik, , 14195 Berlin, Germany
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We optimize force fields for H3O(+) and OH(-) that reproduce the experimental solvation free energies and the activities of H3O(+) Cl(-) and Na(+) OH(-) solutions up to concentrations of 1.5 mol/l. The force fields are optimized with respect to the partial charge on the hydrogen atoms and the Lennard-Jones parameters of the oxygen atoms. Remarkably, the partial charge on the hydrogen atom of the optimized H3O(+) force field is 0.8 ± 0.1|e|--significantly higher than the value typically used for nonpolarizable water models and H3O(+) force fields. In contrast, the optimal partial charge on the hydrogen atom of OH(-) turns out to be zero. Standard combination rules can be used for H3O(+) Cl(-) solutions, while for Na(+) OH(-) solutions, we need to significantly increase the effective anion-cation Lennard-Jones radius. While highlighting the importance of intramolecular electrostatics, our results show that it is possible to generate thermodynamically consistent force fields without using atomic polarizability.

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