Supercooled Liquid Water Diffusivity at Temperatures near the Glass Transition Temperature

Fuente: arXiv
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Hauptverfasser: Smith, R. Scott, Thornley, Wyatt A., Kimmel, Greg A., Kay, Bruce D.
Format: Preprint
Veröffentlicht: 2025
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author Smith, R. Scott
Thornley, Wyatt A.
Kimmel, Greg A.
Kay, Bruce D.
author_facet Smith, R. Scott
Thornley, Wyatt A.
Kimmel, Greg A.
Kay, Bruce D.
contents Isotopically layered amorphous solid water films were used to measure the diffusivity of deeply supercooled liquid water near the glass transition. The films, composed of separate layers of oxygen 16 and oxygen 18 labeled water, were grown by vapor deposition at low temperature and then heated to observe the intermixing of the isotopic layers. Very slow heating rates (as low as 0.0001 K/s) were used to decouple the diffusion and crystallization processes to ensure that the observed intermixing occurred at temperatures that were well-separated from the onset of crystallization. Numerical simulations of the desorption spectra were used to extract the translational diffusivities. The diffusivities obtained in this paper are consistent with translational liquid-like motion at temperatures near and above the proposed Tg of 136 K. These findings support the idea that the melt of amorphous water, above its glass transition temperature is thermodynamically continuous with normal supercooled liquid.
format Preprint
id arxiv_https___arxiv_org_abs_2502_02876
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Supercooled Liquid Water Diffusivity at Temperatures near the Glass Transition Temperature
Smith, R. Scott
Thornley, Wyatt A.
Kimmel, Greg A.
Kay, Bruce D.
Soft Condensed Matter
Chemical Physics
Isotopically layered amorphous solid water films were used to measure the diffusivity of deeply supercooled liquid water near the glass transition. The films, composed of separate layers of oxygen 16 and oxygen 18 labeled water, were grown by vapor deposition at low temperature and then heated to observe the intermixing of the isotopic layers. Very slow heating rates (as low as 0.0001 K/s) were used to decouple the diffusion and crystallization processes to ensure that the observed intermixing occurred at temperatures that were well-separated from the onset of crystallization. Numerical simulations of the desorption spectra were used to extract the translational diffusivities. The diffusivities obtained in this paper are consistent with translational liquid-like motion at temperatures near and above the proposed Tg of 136 K. These findings support the idea that the melt of amorphous water, above its glass transition temperature is thermodynamically continuous with normal supercooled liquid.
title Supercooled Liquid Water Diffusivity at Temperatures near the Glass Transition Temperature
topic Soft Condensed Matter
Chemical Physics
url https://arxiv.org/abs/2502.02876