Ion-sensitive phase transitions driven by Debye-H\"uckel non-ideality
Kyle J. Welch, Fred Gittes

TL;DR
This paper demonstrates that Debye-Hückel non-ideality alone can induce volume phase transitions and criticality in dilute electrolytes, without the need for elastic networks, using a mean-field theoretical approach.
Contribution
It introduces a Landau mean-field model showing ion non-ideality drives phase transitions, revealing tunable critical points based on ion valence ratios.
Findings
Debye-Hückel non-ideality causes phase transitions in dilute electrolytes.
Critical points are tunable by ion valence ratios.
Model aligns with existing theories on volume-temperature phase transitions.
Abstract
We find that the Debye-H\"uckel nonideality of dilute aqueous electrolytes is sufficient to drive volume phase transitions and criticality, even in the absence of a self-attracting or elastic network. Our result follows from a Landau mean-field theory for a system of confined ions in an external solution of mixed-valence counterions, where the ratio of squared monovalent to divalent ion concentration provides a temperature-like variable for the phase transition. Our analysis was motivated by long-studied volume phase transitions via ion exchange in ionic gels, but our findings agree with existing theory for volume-temperature phase transitions in charged hard-sphere models and other systems by Fisher and Levin, and McGahay and Tomozawa. Our mean-field model predicts a continuous line of gas-liquid-type critical points connecting a purely monovalent, divalent-sensitive critical point at…
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Taxonomy
TopicsSpectroscopy and Quantum Chemical Studies · Material Dynamics and Properties · Electrostatics and Colloid Interactions
