1. Ice VII from aqueous salt solutions: From a glass to a crystal with broken H-bonds
- Author
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Adriaan-Alexander Ludl, Shinichi Machida, Asami Sano-Furukawa, Fabio Pietrucci, Takanori Hattori, Stefan Klotz, Livia E. Bove, Kazuki Komatsu, Hiroyuki Kagi, Institut de minéralogie, de physique des matériaux et de cosmochimie (IMPMC), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de recherche pour le développement [IRD] : UR206-Muséum national d'Histoire naturelle (MNHN)-Centre National de la Recherche Scientifique (CNRS), The University of Tokyo (UTokyo), CROSS-Tokai, Research Centre for Neutron Science and Technology, Japan Atomic Energy Agency, Institute of Condensed Matter Physics [Lausanne], Ecole Polytechnique Fédérale de Lausanne (EPFL), Labex Matisse, ANR-11-IDEX-0004,SUPER,Sorbonne Universités à Paris pour l'Enseignement et la Recherche(2011), and Muséum national d'Histoire naturelle (MNHN)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de recherche pour le développement [IRD] : UR206-Centre National de la Recherche Scientifique (CNRS)
- Subjects
Multidisciplinary ,Aqueous solution ,Materials science ,010304 chemical physics ,Neutron diffraction ,Ionic bonding ,Thermodynamics ,Mineralogy ,02 engineering and technology ,021001 nanoscience & nanotechnology ,01 natural sciences ,Article ,Ice VII ,law.invention ,Crystal ,Molecular dynamics ,law ,0103 physical sciences ,Amorphous ice ,[PHYS.COND]Physics [physics]/Condensed Matter [cond-mat] ,Crystallization ,0210 nano-technology - Abstract
It has been known for decades that certain aqueous salt solutions of LiCl and LiBr readily form glasses when cooled to below ≈160 K. This fact has recently been exploited to produce a « salty » high-pressure ice form: When the glass is compressed at low temperatures to pressures higher than 4 GPa and subsequently warmed, it crystallizes into ice VII with the ionic species trapped inside the ice lattice. Here we report the extreme limit of salt incorporation into ice VII, using high pressure neutron diffraction and molecular dynamics simulations. We show that high-pressure crystallisation of aqueous solutions of LiCl∙RH2O and LiBr∙RH2O with R = 5.6 leads to solids with strongly expanded volume, a destruction of the hydrogen-bond network with an isotropic distribution of water-dipole moments, as well as a crystal-to-amorphous transition on decompression. This highly unusual behaviour constitutes an interesting pathway from a glass to a crystal where translational periodicity is restored but the rotational degrees of freedom remaining completely random.
- Published
- 2016
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