Explicit Solvent Theory of Salt-Induced Dielectric Decrement

TL;DR

This paper develops a field-theoretic model of electrolytes with explicit solvent molecules and salt ions, explaining the linear dielectric decrement with salt concentration and matching various experimental observations.

Contribution

It introduces a virial expansion approach to include many-body salt-solvent interactions beyond weak-coupling approximations, providing a more accurate theoretical framework.

Findings

Reproduces the linear decay of permittivity with salt concentration.

Explains the temperature dependence of dielectric decrement.

Shows valency effects on electrolyte permittivity.

Abstract

We introduce a field-theoretic electrolyte model composed of structured solvent molecules and salt ions coupled by electrostatic and hard-core interactions. Within this explicit solvent theory, we characterize the salt-driven dielectric decrement beyond weak-coupling (WC) electrostatics. The WC approximation of prior formalisms is relaxed by treating the salt charges via a virial expansion. This virial approach enables the explicit inclusion of the many-body salt-solvent interactions, and directly leads to the experimentally observed linear decay of the electrolyte permittivity with added dilute salt. The permittivity formula emerging from our approach indicates that the reduction of the solvent permittivity is induced by the salt screening of the polarization charges suppressing the dielectric response of the solvent. By comparison with experiments, we also show that the salt-dressed permittivity formula can equally reproduce the attenuation of the electrolyte permittivity with rising temperature, the thermal decay of the dielectric decrement, and its intensification with the salt valency. The consistent qualitative agreement of our theory with this wide range of experimental trends points out the electrostatic ion-solvent correlations as the primary mechanism behind the salt-induced dielectric decrement.