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      Nematic twist-bend phase with nanoscale modulation of molecular orientation

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          Abstract

          A state of matter in which molecules show a long-range orientational order and no positional order is called a nematic liquid crystal. The best known and most widely used (for example, in modern displays) is the uniaxial nematic, with the rod-like molecules aligned along a single axis, called the director. When the molecules are chiral, the director twists in space, drawing a right-angle helicoid and remaining perpendicular to the helix axis; the structure is called a chiral nematic. Here using transmission electron and optical microscopy, we experimentally demonstrate a new nematic order, formed by achiral molecules, in which the director follows an oblique helicoid, maintaining a constant oblique angle with the helix axis and experiencing twist and bend. The oblique helicoids have a nanoscale pitch. The new twist-bend nematic represents a structural link between the uniaxial nematic (no tilt) and a chiral nematic (helicoids with right-angle tilt).

          Abstract

          Theories predict the existence of a nematic liquid crystal phase with a local twist-bend structure, but no experimental proof is available over the past 40 years. Borshch et al. identify this phase for the first time in two different materials containing dimeric molecules.

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          Most cited references33

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          Les états mésomorphes de la matière

          G. Friedel (1922)
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            Liquid crystal 'blue phases' with a wide temperature range.

            Liquid crystal 'blue phases' are highly fluid self-assembled three-dimensional cubic defect structures that exist over narrow temperature ranges in highly chiral liquid crystals. The characteristic period of these defects is of the order of the wavelength of visible light, and they give rise to vivid specular reflections that are controllable with external fields. Blue phases may be considered as examples of tuneable photonic crystals with many potential applications. The disadvantage of these materials, as predicted theoretically and proved experimentally, is that they have limited thermal stability: they exist over a small temperature range (0.5-2 degrees C) between isotropic and chiral nematic (N*) thermotropic phases, which limits their practical applicability. Here we report a generic family of liquid crystals that demonstrate an unusually broad body-centred cubic phase (BP I*) from 60 degrees C down to 16 degrees C. We prove this with optical texture analysis, selective reflection spectroscopy, Kössel diagrams and differential scanning calorimetry, and show, using a simple polarizer-free electro-optic cell, that the reflected colour is switched reversibly in applied electric fields over a wide colour range in typically 10 ms. We propose that the unusual behaviour of these blue phase materials is due to their dimeric molecular structure and their very high flexoelectric coefficients. This in turn sets out new theoretical challenges and potentially opens up new photonic applications.
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              On the spontaneous symmetry breaking in the mesophases of achiral banana-shaped molecules

              I Dozov (2001)
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                Author and article information

                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Pub. Group
                2041-1723
                05 November 2013
                : 4
                : 2635
                Affiliations
                [1 ]Liquid Crystal Institute and Chemical Physics Interdisciplinary Program, Kent State University , Kent, Ohio 44242, USA
                [2 ]Department of Electronic and Electrical Engineering, Trinity College, University of Dublin , Dublin 2, Ireland
                [3 ]Department of Chemistry, School of Natural and Computing Sciences, University of Aberdeen , AB24 3UE Scotland, UK
                [4 ]Department of Chemistry, University of Hull , Hull HU6 7RX, UK
                Author notes
                Article
                ncomms3635
                10.1038/ncomms3635
                3831290
                24189583
                29f53ef6-c632-4303-9b39-7ecc049eced1
                Copyright © 2013, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.

                This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

                History
                : 11 July 2013
                : 18 September 2013
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