Twist-bend nematic phase in cyanobiphenyls and difluoroterphenyls bimesogens

The paper reviews assignment of the low-temperature nematic phase observed in simple bimesogenic or dimeric systems based on cyanobiphenyls and difluoroterphenyls to the twist-bend nematic phase, NTB, using a range of experimental techniques. These include DSC, X-rays, Polarising Microscopy, electro-optics, birefringence and measurements of the electroclinic effect arising from flexoelectricity. An emphasis is laid on the observations of the chiral domains of opposite handedness at zero field in an otherwise achiral liquid crystalline system in this phase. These observations are a direct consequence of the structure of the twist-bend phase predicted by Ivan Dozov for achiral bent core molecules. The paper reviews the electro-optic phenomena and the observed electroclinic effect and how these observations assign it as the NTB phase. Results of the nanoscale helical pitch measurements using freeze-fracture microscopy are reviewed and discussed briefly. Results of the measurements of elastic constants especially close to the N–NTB transition are also reviewed

Characterization of the Submicrometer Hierarchy Levels in the Twist-Bend Nematic Phase with Nanometric Helices via Photopolymerization. Explanation for the Sign Reversal in the Polar Response

Photopolymerization of a reactive mesogen mixed with a mesogenic dimer, shown to exhibit the twist-bend nematic phase (NTB), reveals the complex structure of the self-deformation patterns observed in planar cells. The polymerized reactive mesogen retains the structure formed by liquid crystalline molecules in the twist bend phase, thus enabling its observation by scanning electron microscopy (SEM). Hierarchical ordering scales ranging from tens of nanometers to micrometers are imaged in detail. Submicron features, anticipated from earlier X-ray experiments, are visualized directly. In the self-deformation stripes formed in the NTB phase, the average director field is found tilted in the cell plane by an angle of up to 45° from the cell rubbing direction. This tilt explains the sign inversion being observed inthe electro-optical studie

Orientational order of a ferroelectric liquid crystal with small layer contraction

We present spectroscopic and optical studies of a non-layer-shrinkage ferroelectric liquid crystal DSiKN65. The orientational order parameters S, measured with respect to the smectic layer normal using IR spectroscopy on a sample aligned homeotropically, does not exhibit any significant variation between the smectic-A* and smectic-C* phases. In contrast the birefringence of a planar homogenous sample abruptly increases at the smectic-A* to smectic-C* transition. This suggests a general increase in the orientational order, which can be described by the orientational order parameters S\u27 defined with respect to the director. Simultaneous increase of S\u27 and the director tilt θ may explain the low shrinkage of smectic layers, which is consistent with recent theoretical models describing the smectic-A* to smectic-C* transition for such materials

Spontaneous Helix Formation in Non-Chiral Bent-Core Liquid Crystals with Fast Linear Electro-Optic Effect

Liquid crystals (LCs) represent one of the foundations of modern communication and photonic technologies. Present display technologies are based mainly on nematic LCs, which suffer from limited response time for use in active colour sequential displays and limited image grey scale. Herein we report the first observation of a spontaneously formed helix in a polar tilted smectic LC phase (SmC phase) of achiral bent-core (BC) molecules with the axis of helix lying parallel to the layer normal and a pitch much shorter than the optical wavelength. This new phase shows fast (∼30 μs) grey-scale switching due to the deformation of the helix by the electric field. Even more importantly, defect-free alignment is easily achieved for the first time for a BC mesogen, thus providing potential use in large-scale devices with fast linear and thresholdless electro-optical response. les

Nematic twist-bend phase with nanoscale modulation of molecular orientation

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)

Chiral light in twisted Fabry-P\'erot cavities

Fundamental studies of the interaction of chiral light with chiral matter are important for the development of techniques that allow handedness-selective optical detection of chiral organic molecules. One approach to achieve this goal is the creation of a Fabry-P\'erot cavity that supports eigenmodes with a desired electromagnetic handedness, which interacts differently with left and right molecular enantiomers. In this paper, we theoretically study chiral Fabry-P\'erot cavities with mirrors comprising one-dimensional photonic crystal slabs made of van der Waals As$_2$S$_3$, a material with one of the highest known in-plane anisotropy. By utilizing the anisotropy degree of freedom provided by As$_2$S$_3$, we design Fabry-P\'erot cavities with constitutional and configurational geometrical chiralities. We demonstrate that in cavities with constitutional chirality, electromagnetic modes of left or right handedness exist due to the chirality of both mirrors, often referred to as handedness preserving mirrors in the literature. At the same time, cavities with configurational chirality support modes of both handednesses due to chiral morphology of the entire structure, set by the twist angle between the optical axes of the upper and lower non-chiral anisotropic mirrors. The developed chiral Fabry-P\'erot cavities can be tuned to the technologically available distance between the mirrors by properly twisting them, making such systems a prospective platform for the coupling of chiral light with chiral matter.Comment: 33 pages, 9 figure

The beauty of twist-bend nematic phase: Fast switching domains, first order fréedericksz transition and a hierarchy of structures

The twist-bend nematic phase (NTB) exhibits a complicated hierarchy of structures responsible for several intriguing properties presented here. These are: the observation of a fast electrooptic response, the exhibition of a large electroclinic effect, and the observation of an unusual pattern of the temperature dependence of birefringence of bent-shaped bimesogens in parallel-rubbed planar-aligned cells. These unusual effects inspired the use of highly sophisticated techniques that led to the discovery of the twist-bend nematic phase. Results of the optical retardation of a parallel-rubbed planar-aligned cell show that the ‘heliconical angle’ (the angle the local director makes with the optical axis) starts increasing in the high temperature N phase, it exhibits a jump at the N–NTB transition temperature and continues to increase in magnitude with a further reduction in temperature. The liquid crystalline parallel-rubbed planar-aligned and twist-aligned cells in this phase exhibit fascinating phenomena such as a demonstration of the beautiful stripes and dependence of their periodicity on temperature. The Fréedericksz transition in the NTB phase is found to be of the first order both in rubbed planar and homeotropic-aligned cells, in contrast to the second order transition exhibited by a conventional nematic phase. This transition shows a significant hysteresis as well as an abrupt change in the orientation of the director as a function of the applied electric field. Hierarchical structures are revealed using the technique of polymer templating the structure of the liquid crystalline phase of interest, and imaging of the resulting structure by scanning electron microscop