Shephard Jacob J, Ling Sanliang, Sosso Gabriele C, Michaelides Angelos, Slater Ben, Salzmann Christoph G
Department of Chemistry, University College London , 20 Gordon Street, London WC1H 0AJ, United Kingdom.
Thomas Young Centre, Department of Physics and Astronomy, and London Centre for Nanotechnology, University College London , Gower Street, London WC1E 6BT, United Kingdom.
J Phys Chem Lett. 2017 Apr 6;8(7):1645-1650. doi: 10.1021/acs.jpclett.7b00492. Epub 2017 Mar 27.
The structural nature of high-density amorphous ice (HDA), which forms through low-temperature pressure-induced amorphization of the "ordinary" ice I, is heavily debated. Clarifying this question is important for understanding not only the complex condensed states of HO but also in the wider context of pressure-induced amorphization processes, which are encountered across the entire materials spectrum. We first show that ammonium fluoride (NHF), which has a similar hydrogen-bonded network to ice I, also undergoes a pressure collapse upon compression at 77 K. However, the product material is not amorphous but NHF II, a high-pressure phase isostructural with ice IV. This collapse can be rationalized in terms of a highly effective mechanism. In the case of ice I, the orientational disorder of the water molecules leads to a deviation from this mechanism, and we therefore classify HDA as a "derailed" state along the ice I to ice IV pathway.
通过低温压力诱导“普通”冰I非晶化形成的高密度非晶冰(HDA)的结构性质存在激烈争论。阐明这个问题不仅对于理解HO的复杂凝聚态很重要,而且在更广泛的压力诱导非晶化过程背景下也很重要,这些过程在整个材料范围内都会遇到。我们首先表明,与冰I具有相似氢键网络的氟化铵(NHF)在77 K压缩时也会发生压力崩塌。然而,产物材料不是非晶态,而是NHF II,一种与冰IV同构的高压相。这种崩塌可以用一种高效机制来解释。在冰I的情况下,水分子的取向无序导致偏离这种机制,因此我们将HDA归类为沿冰I到冰IV路径的“脱轨”状态。