Supercooled Liquid Water Diffusivity at Temperatures near the Glass Transition Temperature
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arXiv
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| Autores principales: | , , , |
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| Formato: | Preprint |
| Publicado: |
2025
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| _version_ | 1866912220933259264 |
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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 |