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arXiv · 1801.07116

Comparison of Single-Ion Molecular Dynamics in Common Solvents

A. Muralidharan·L. R. Pratt·M. I. Chaudhari·S. B. Rempe
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Abstract

Laying a basis for molecularly specific theory for the mobilities of ions in solutions of practical interest, we report a broad survey of velocity autocorrelation functions (VACFs) of Li$^+$ and PF$_6{}^-$ ions in water, ethylene carbonate, propylene carbonate, and acetonitrile solutions. We extract the memory function, $γ(t)$, which characterizes the random forces governing the mobilities of ions. We provide comparisons, controlling for electrolyte concentration and ion-pairing, for van~der~Waals attractive interactions and solvent molecular characteristics. For the heavier ion (PF$_6{}^-$), velocity relaxations are all similar: negative tail relaxations for the VACF and a clear second relaxation for $γ\left(t\right)$, observed previously also for other molecular ions and with \emph{n}-pentanol as solvent. For the light Li$^+$ ion, short time-scale oscillatory behavior masks simple, longer time-scale relaxation of $γ\left(t\right)$. But the corresponding analysis of the \emph{solventberg} Li$^+\left(\mathrm{H}_2\mathrm{O}\right)_4$ does conform to the standard picture set by all the PF$_6{}^-$ results.

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A. Muralidharan, L. R. Pratt, M. I. Chaudhari, S. B. Rempe. 2018-03-15. Comparison of Single-Ion Molecular Dynamics in Common Solvents. https://doi.org/10.1063/1.5023121

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