Dielectric ordering of water molecules arranged in a dipolar lattice

  • Intermolecular hydrogen bonds impede long-range (anti-)ferroelectric order of water. We confine H2O molecules in nanosized cages formed by ions of a dielectric crystal. Arranging them in channels at a distance of ~5 Å with an interchannel separation of ~10 Å prevents the formation of hydrogen networks while electric dipole-dipole interactions remain effective. Here, we present measurements of the temperature-dependent dielectric permittivity, pyrocurrent, electric polarization and specific heat that indicate an order-disorder ferroelectric phase transition at T0 ≈ 3 K in the water dipolar lattice. Ab initio molecular dynamics and classical Monte Carlo simulations reveal that at low temperatures the water molecules form ferroelectric domains in the ab-plane that order antiferroelectrically along the channel direction. This way we achieve the long-standing goal of arranging water molecules in polar order. This is not only of high relevance in various natural systems but might open anIntermolecular hydrogen bonds impede long-range (anti-)ferroelectric order of water. We confine H2O molecules in nanosized cages formed by ions of a dielectric crystal. Arranging them in channels at a distance of ~5 Å with an interchannel separation of ~10 Å prevents the formation of hydrogen networks while electric dipole-dipole interactions remain effective. Here, we present measurements of the temperature-dependent dielectric permittivity, pyrocurrent, electric polarization and specific heat that indicate an order-disorder ferroelectric phase transition at T0 ≈ 3 K in the water dipolar lattice. Ab initio molecular dynamics and classical Monte Carlo simulations reveal that at low temperatures the water molecules form ferroelectric domains in the ab-plane that order antiferroelectrically along the channel direction. This way we achieve the long-standing goal of arranging water molecules in polar order. This is not only of high relevance in various natural systems but might open an avenue towards future applications in biocompatible nanoelectronics.show moreshow less

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Metadaten
Author:M. A. Belyanchikov, M. Savinov, Z. V. Bedran, P. Bednyakov, P. Proschek, J. Prokleska, V. A. Abalmasov, J. Petzelt, E. S. Zhukova, V. G. Thomas, A. Dudka, A. Zhugayevych, A. S. Prokhorov, V. B. Anzin, R. K. Kremer, J. K. H. Fischer, Peter LunkenheimerORCiDGND, Alois LoidlORCiDGND, E. Uykur, M. Dressel, B. Gorshunov
URN:urn:nbn:de:bvb:384-opus4-795097
Frontdoor URLhttps://opus.bibliothek.uni-augsburg.de/opus4/79509
ISSN:2041-1723OPAC
Parent Title (English):Nature Communications
Publisher:Springer Science and Business Media LLC
Type:Article
Language:English
Year of first Publication:2020
Publishing Institution:Universität Augsburg
Release Date:2020/09/17
Tag:General Biochemistry, Genetics and Molecular Biology; General Physics and Astronomy; General Chemistry
Volume:11
Issue:1
First Page:3927
DOI:https://doi.org/10.1038/s41467-020-17832-y
Institutes:Mathematisch-Naturwissenschaftlich-Technische Fakultät
Mathematisch-Naturwissenschaftlich-Technische Fakultät / Institut für Physik
Mathematisch-Naturwissenschaftlich-Technische Fakultät / Institut für Physik / Lehrstuhl für Experimentalphysik V
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 53 Physik / 530 Physik
Licence (German):CC-BY 4.0: Creative Commons: Namensnennung (mit Print on Demand)