Modeling the Influence of Solvation on the Electrochemical Double Layer of Salt / Solvent Mixtures

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Auteurs principaux: Schwetlick, Constantin, Schammer, Max, Latz, Arnulf, Horstmann, Birger
Format: Preprint
Publié: 2024
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author Schwetlick, Constantin
Schammer, Max
Latz, Arnulf
Horstmann, Birger
author_facet Schwetlick, Constantin
Schammer, Max
Latz, Arnulf
Horstmann, Birger
contents Modelling electrolytes accurately on both a nanoscale and cell level can contribute to improving battery chemistries.[Armand and Tarascon, Nature, 2008, 451, 652-657] We previously presented a thermodynamic continuum model for electrolytes.[arXiv:2010.14915] In this paper we include solvation interactions between the ions and solvent, which alter the structure of the electochemical double layer (EDL). We are able to combine a local solvation model -- permitting examination of the interplay between electric forces and the ion-solvent binding -- with a full electrolyte model. Using this, we can investigate double layer structures for a wide range of electrolytes, especially including highly concentrated solutions. We find that some of the parameters of our model significantly affect the solvent concentration at the electrode surface, and thereby the rate of solvent decomposition. Firstly, an increased salt concentration weakens the solvation shells, making it possible to strip the solvent in the EDL before the ions reach the surface. The strength of the ion-solvent interaction also affects at which potential difference the solvation shells removed. We are therefore able to qualitatively predict EDL structures for different electrolytes based on parameters like molecule size, solvent binding energy and salt concentration.
format Preprint
id arxiv_https___arxiv_org_abs_2408_04314
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle Modeling the Influence of Solvation on the Electrochemical Double Layer of Salt / Solvent Mixtures
Schwetlick, Constantin
Schammer, Max
Latz, Arnulf
Horstmann, Birger
Chemical Physics
Soft Condensed Matter
Modelling electrolytes accurately on both a nanoscale and cell level can contribute to improving battery chemistries.[Armand and Tarascon, Nature, 2008, 451, 652-657] We previously presented a thermodynamic continuum model for electrolytes.[arXiv:2010.14915] In this paper we include solvation interactions between the ions and solvent, which alter the structure of the electochemical double layer (EDL). We are able to combine a local solvation model -- permitting examination of the interplay between electric forces and the ion-solvent binding -- with a full electrolyte model. Using this, we can investigate double layer structures for a wide range of electrolytes, especially including highly concentrated solutions. We find that some of the parameters of our model significantly affect the solvent concentration at the electrode surface, and thereby the rate of solvent decomposition. Firstly, an increased salt concentration weakens the solvation shells, making it possible to strip the solvent in the EDL before the ions reach the surface. The strength of the ion-solvent interaction also affects at which potential difference the solvation shells removed. We are therefore able to qualitatively predict EDL structures for different electrolytes based on parameters like molecule size, solvent binding energy and salt concentration.
title Modeling the Influence of Solvation on the Electrochemical Double Layer of Salt / Solvent Mixtures
topic Chemical Physics
Soft Condensed Matter
url https://arxiv.org/abs/2408.04314