Eine Substanz, zwei Flüssigkeiten

The pressure dependence of the crystallization temperature of different forms of expanded high-density amorphous ice (eHDA) was scrutinized. Crystallization at pressures 0.05-0.30 GPa was followed using volumetry and powder x-ray diffraction. eHDA samples were prepared via isothermal decompression of very high-density amorphous ice at 140 K to different end pressures between 0.07-0.30 GPa (eHDA). At 0.05-0.17 GPa the crystallization line T (p) of all eHDA variants is the same. At pressures>0.17 GPa, all eHDA samples decompressed to pressures <0.20 GPa exhibit significantly lower T values than eHDA and eHDA. We rationalize our findings with the presence of nanoscaled low-density amorphous ice (LDA) seeds that nucleate in eHDA when it is decompressed to pressures <0.20 GPa at 140 K. Below ~0.17 GPa, these nanosized LDA domains are latent within the HDA matrix, exhibiting no effect on T of eHDA. Upon heating at pressures ⩾0.17 GPa, these nanosized LDA nuclei transform to ice IX nuclei. They are favored sites for crystallization and, hence, lower T . By comparing crystallization experiments of bulk LDA with the ones involving nanosized LDA we are able to estimate the Laplace pressure and radius of ~0.3-0.8 nm for the nanodomains of LDA. The nucleation of LDA in eHDA revealed here is evidence for the first-order-like nature of the HDA → LDA transition, supporting water's liquid-liquid transition scenarios.

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“…Control of piston displacement and pressure was accomplished using the commercial software TESTXPERT 7.1 (Zwick). For further details see [45].…”

Section: Apparatusmentioning

confidence: 99%