On the growth rate of ices: Effect of pressure and ice phase

Ice, the solid phase of water, can adopt a wide range of structures, making it of interest from both fundamental and applied perspectives. In this study, we used molecular dynamics simulations to compute the growth rates of four ice phases: Ih, III, V, and VI. To enable comparisons at the same temperature, different pressures were applied to each phase. Our analysis of pressure effects on the growth rate of ice Ih revealed only a minor influence, allowing us to attribute variations in growth rates primarily to structural differences among ice phases. We observed that ices Ih and VI exhibit similar growth rates, whereas ices III and V grow significantly faster. Rapidly growing ice phases exhibit a high growth efficiency, meaning that less molecular motion is needed to form the solid. We hypothesize that proton ordering may influence ice growth, as partially ordered ice phases (III and V) exhibit faster growth rates than fully disordered phases (Ih and VI). Alternative explanations for ice growth rate trends, such as unit cell complexity or melting entropy, are ruled out. Finally, we assessed the predictive capability of the Wilson-Frenkel theory. While the theory does not inherently account for structural complexity-resulting in similar growth rates across all phases-we found that introducing a phase-specific characteristic length enables it to accurately reproduce our simulation results.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2025-05-15
DOI
https://doi.org/10.1063/5.0265605
Citations
1
Primary Topic
nanoparticles nucleation surface interactions
Type
article
Field-Weighted Citation Impact
1.30

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article

On the growth rate of ices: Effect of pressure and ice phase

Eduardo Sanz, S. Blazquez
1 citations
The Journal of Chemical Physics
nanoparticles nucleation surface interactions
1.30
article

On the growth rate of ices: Effect of pressure and ice phase

Eduardo Sanz, S. Blazquez
article en
1 citations

Abstract

Ice, the solid phase of water, can adopt a wide range of structures, making it of interest from both fundamental and applied perspectives. In this study, we used molecular dynamics simulations to compute the growth rates of four ice phases: Ih, III, V, and VI. To enable comparisons at the same temperature, different pressures were applied to each phase. Our analysis of pressure effects on the growth rate of ice Ih revealed only a minor influence, allowing us to attribute variations in growth rates primarily to structural differences among ice phases. We observed that ices Ih and VI exhibit similar growth rates, whereas ices III and V grow significantly faster. Rapidly growing ice phases exhibit a high growth efficiency, meaning that less molecular motion is needed to form the solid. We hypothesize that proton ordering may influence ice growth, as partially ordered ice phases (III and V) exhibit faster growth rates than fully disordered phases (Ih and VI). Alternative explanations for ice growth rate trends, such as unit cell complexity or melting entropy, are ruled out. Finally, we assessed the predictive capability of the Wilson-Frenkel theory. While the theory does not inherently account for structural complexity-resulting in similar growth rates across all phases-we found that introducing a phase-specific characteristic length enables it to accurately reproduce our simulation results.

The Journal of Chemical PhysicsVol. 162(19)
Universidad Complutense de Madrid (ES)
Ministerio de Ciencia e Innovación
Clean water and sanitation
Openalex Percentile: Top 23%
nanoparticles nucleation surface interactions
1.30
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