X-ray studies of the transformation from high- to low-density amorphous water
Author(s) -
Daniel Mariedahl,
Fivos Perakis,
Alexander Späh,
Harshad Pathak,
Kyung Hwan Kim,
Chris J. Benmore,
Anders Nilsson,
Katrin AmannWinkel
Publication year - 2019
Publication title -
philosophical transactions of the royal society a mathematical physical and engineering sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.074
H-Index - 169
eISSN - 1471-2962
pISSN - 1364-503X
DOI - 10.1098/rsta.2018.0164
Subject(s) - amorphous solid , amorphous ice , crystallization , pair distribution function , tetrahedron , reciprocal lattice , polyamorphism , diffraction , chemical physics , materials science , crystallography , physics , chemistry , thermodynamics , optics , quantum mechanics
Here we report about the structural evolution during the conversion from high-density amorphous ices at ambient pressure to the low-density state. Using high-energy X-ray diffraction, we have monitored the transformation by following in reciprocal space the structure factor S OO ( Q ) and derived in real space the pair distribution function g OO ( r ). Heating equilibrated high-density amorphous ice (eHDA) at a fast rate (4 K min –1 ), the transition to the low-density form occurs very rapidly, while domains of both high- and low-density coexist. On the other hand, the transition in the case of unannealed HDA (uHDA) and very-high-density amorphous ice is more complex and of continuous nature. The direct comparison of eHDA and uHDA indicates that the molecular structure of uHDA contains a larger amount of tetrahedral motives. The different crystallization behaviour of the derived low-density amorphous states is interpreted as emanating from increased tetrahedral coordination present in uHDA. This article is part of the theme issue ‘The physics and chemistry of ice: scaffolding across scales, from the viability of life to the formation of planets'.
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