Fast Electro-optic Response Research Articles

Microsecond electro-optic switching in the nematic phase of a ferroelectric nematic liquid crystal.

Nematic liquid crystals exhibit nanosecond electro-optic response to an applied electric field which modifies the degree of orientational order without realigning the molecular orientation. However, this nanosecond electrically modified order parameter (NEMOP) effect requires high driving fields, on the order of 108 V/m for a modest birefringence change of 0.01. In this work, we demonstrate that a nematic phase of the recently discovered ferroelectric nematic materials exhibits a robust and fast electro-optic response. Namely, a relatively weak field of 2 × 107 V/m changes the birefringence by ≈ 0.04 with field-on and-off times around 1 μs. This microsecond electrically modified order parameter (MEMOP) effect shows a greatly improved figure of merit when compared to other electro-optical switching modes in liquid crystals, including the conventional Frederiks effect, and has a potential for applications in fast electro-optical devices such as phase modulators, optical shutters, displays, and beam steerers.

Chiral liquid crystal dimers with smectic phases for stabilization of anticlinic state in surface-stabilised geometry

The growing demand for enhanced optical quality and faster electro-optical response in liquid crystal (LC) photonic devices has expanded the search for advanced materials capable of improving the properties of LCs beyond conventional ones. Among these compounds are LC dimers with ferroelectric and antiferroelectric properties which can be incorporated into LC mixtures to enhance performance. However, existing dimers often feature high melting temperatures, enthalpies, and other physicochemical characteristics that render them unsuitable as dopants in antiferroelectric liquid crystal (AFLC) mixtures targeted to modern photonic devices. Here, we show the design and physicochemical properties of novel dimers which are characterized by low melting points, high tilt angles and spontaneous polarizations, temperature-stable helical structures, and reasonably broad temperature ranges of ferroelectric or antiferroelectric phases. These features have facilitated the effective use of one dimer as a dopant in AFLCs. This eliminates the primary drawback of the electro-optical effect based on the surface-stabilised geometry of AFLCs by strongly promoting the anticlinic state in this effect. Importantly, for the first time, the above can be achieved without affecting any other physicochemical or optical properties of AFLCs. Thus, the obtained results represent a pivotal link between the longstanding concept of developing AFLCs that meet the stringent requirements for electro-optical effects based on surface-stabilised geometry and the realization of novel photonic devices demonstrating all the benefits of this effect.

A New Class of Chiral Nematic Phase with Helical Polar Order (Adv. Mater. 35/2021)

Liquid Crystals A new class of cholesteric phase with local polar order is realized by Fumito Araoka and Hiroya Nishikawa in article number 2101305. In general, the periodicity of the conventional cholesteric liquid crystal corresponds to the half-pitch of the helix, having head-and-tail symmetry in the local nematic director. On the other hand, the newly found polar cholesteric liquid crystal is characterized with a full-pitch periodicity of the helix due to the polar degeneracy in the local nematic director. This delivers some unprecedented properties, such as fast electro-optic response based on the photonic band modulated with polar helix deformation.

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 microscopy.

Orientational order induced by a polymer network in the isotropic phase of liquid crystal.

We studied the paranematic ordering induced by a polymer network in the isotropic phase of a liquid crystal (LC) that occurs in polymer-stabilized cells with bend configuration of the LC director (π cells) fabricated via photopolymerization of photoreactive monomer RM 82 added in small concentrations (3-5 wt %) to a nematic LC [4-cyano-4'-pentylbiphenyl (5CB)] when low voltage was applied across the cell. The polymer network formed in the nematic phase of the LC consists of fine fibrils that are aligned along the LC director and thus mirror the bend deformation of the LC at the time of polymerization. When heated to temperatures above the nematic-to-isotropic (N-I) phase transition such highly ordered polymer network anchors LC molecules providing ordering of the LC around the fibrils which results in unusually high optical retardation of the cell, R_{cell}. We present a theoretical model that relates R_{cell} to the degree of order of the fibrils, the anchoring energy of the LC molecules on the surface of the polymer fibrils, and the fibril radius r_{0}. Fitting of the experimental R_{cell}(T) curves with the developed model reveals correlation of r_{0} with the nematic correlation length ξ_{0} which characterizes penetration of the nematic order in the isotropic phase of the LC. Accepting ξ_{0} as a material constant of about 1 nm leads to a very small radius of the fibrils, r_{0}∼1nm, which is also supported by other reported experimental data. High optical retardation and fast electro-optical response of the cells at the temperatures deep into the isotropic phase point toward the enhancement of the polymer-induced paranematic order by a well-oriented layer of LC molecules that are absorbed on the surface of fibrils. Application of high voltage at the isotropic phase temperatures results in high variations of the optical retardation of the cells. Characteristic on and off response times were about 10-100 μs, independent of the cell gap. Combination of large voltage-driven changes of the optical retardation occurring in the low-viscosity isotropic state with switching times that are at least two orders of magnitude shorter than the typical relaxation times of the cells operating in the nematic phase make such polymer-stabilized π cells very promising for application in fast electro-optical switches and light modulators.

All-inorganic perovskite quantum dots stabilized blue phase liquid crystals.

All-inorganic perovskite quantum dots (PQDs) have been effectively incorporated in the three-dimensional ordered structure of blue phase liquid crystals (BPLCs) to stabilize the BPLCs. Uniform dispersion, reduced phase transition temperature, widened BP temperature range, dynamic and fast electro-optical response and static optical display of selective reflection mode and photoluminescence mode have been confirmed with a given concentration of PQDs. Such a novel strategy of assembling all-inorganic PQDs in BPLCs shows favorable prospects for wide-range and near room temperature BPLCs, responsive BPLCs, multifunctional display materials and tunable bandgap lasers.

Photomodulated Electro-optical Response in Self-Supporting Liquid Crystalline Physical Gels.

Photoresponsive liquid crystal (LC) physical gels have attracted more and more attention because of the nature of strong response via light stimulus. Although many efforts on the breaking and recovering of physical gels through photoisomerization have been focused, fast electro-optical response and high mechanical properties even upon light irradiations are difficult to achieve at the same time. In this work, two kinds of azobenzene-containing gelators (AG1 and AG2) with different terminal groups were designed and synthesized. Both gelators could induce the nematic LC P0616A self-assemble into anisotropic phase-separated LC physical gels at low contents. Their phase-transition behavior, thermal stability, microstructure, and mechanical strength were systematically studied. Compared with AG2 in P0616A, the P0616A/AG1 gels showed better mechanical property. When the gelator content was above 3 wt %, the P0616A/AG1 gels possessed good self-supporting ability with a storage modulus more than 104 Pa. Thus, the photoresponsive electro-optical properties and structures of P0616A/AG1 gels were focused in detail. It was surprising that the electro-optical response speed of the P0616A/AG1 gels could be promoted upon UV irradiation. In particular, the decay time (τoff) was only about half when compared with the initial state, whereas the gels still exhibited good self-supporting ability; also the network of the LC physical gels had no change at macro- and microstructural levels. These exciting results would open a door for the application of this material in electro-optical devices.

High performance liquid crystalline physical gels prepared by side chain liquid crystalline polymers

Liquid crystalline physical gels (LCPGs) with stable mechanical properties and fast electro-optical response properties were prepared through the self-assembly of side chain liquid crystalline polymers (SCLCPs) with different spacer length poly [ω-4′-cyano-(1, 1′-biphenyl)] acrylate (PmACB, m is the spacer length of SCLCP, m = 0, 2, 4) as gelators in a nematic liquid crystal, 4-pentyl-4′-cyanobiphenyl (5CB). The gel-sol phase transition temperature (TGS), micro morphology, mechanical properties and electro-optical properties of LCPGs (SCLCPs/5CB) were systematically studied. The results show that only P0ACB can form stable liquid crystalline physical gels in 5CB and show excellent thermal stability, good self-supporting ability and fast electro-optical response properties. The TGS of 6 wt% P0ACB/5CB gel is 192 °C, and it also showed stable mechanical properties, its storage modulus is about 1.0 × 104 Pa. The threshold voltage (Vth) and saturation voltage (Vsat) of P0ACB/5CB gel with 3 wt% concentration are 0.29 V μm−1and 3.906 V μm−1 respectively, and the off state response time is only 6.748 ms. Moreover, the addition of the polymer does not affect the electro-optical response of the LCPGs.

CuInS2/ZnS QD-ferroelectric liquid crystal mixtures for faster electro-optical devices and their energy storage aspects

CuInS2/ZnS core/shell quantum dots (CIS/ZnS QDs) dispersed ferroelectric liquid crystal (FLC) mixtures have been characterized for their application in electro-optical devices, energy storage, and solar cells. Physical properties of the CIS/ZnS QD-FLC (ferroelectric liquid crystal) mixtures have also been investigated with varying QD concentrations in order to optimize the critical concentration of QDs in mixtures. The presence of QDs breaks the geometrical symmetry in the FLC matrix, which results in a change in the physical properties of the mixtures. We observed the reduced values of primary and secondary order parameters (tilt angle and spontaneous polarization, respectively) for mixtures, which also depend on the concentration of QDs. The reduction of spontaneous polarization in QDs-FLC mixtures is attributed to the adverse role of flexoelectric contribution in the mixtures. The 92% faster electro-optic response and enhanced capacitance indicate the possible application of these mixtures in electro-optical devices and solar cells. Photoluminescence emission of pure FLC and QDs-FLC mixtures has been thermally tailored, which is explained by suitable models.

Dual-Band Modulation of Visible and Near-Infrared Light Transmittance in an All-Solution-Processed Hybrid Micro-Nano Composite Film.

Smart windows with controllable visible and near-infrared light transmittance can significantly improve the building's energy efficiency and inhabitant comfort. However, most of the current smart window technology cannot achieve the target of ideal solar control. Herein, we present a novel all-solution-processed hybrid micronano composite smart material that have four optical states to separately modulate the visible and NIR light transmittance through voltage and temperature, respectively. This dual-band optical modulation was achieved by constructing a phase-separated polymer framework, which contains the microsized liquid crystals domains with a negative dielectric constant and tungsten-doped vanadium dioxide (W-VO2) nanocrystals (NCs). The film with 2.5 wt % W-VO2 NCs exhibits transparency at normal condition, and the passage of visible light can be reversibly and actively regulated between 60.8% and 1.3% by external applied voltage. Also, the transmittance of NIR light can be reversibly and passively modulated between 59.4% and 41.2% by temperature. Besides, the film also features easy all-solution processability, fast electro-optical (E-O) response time, high mechanical strength, and long-term stability. The as-prepared film provides new opportunities for next-generation smart window technology, and the proposed strategy is conductive to engineering novel hybrid inorganic-organic functional matters.

Manifestation of strong magneto-electric dipolar coupling in ferromagnetic nanoparticles−FLC composite: evaluation of time-dependent memory effect

ABSTRACTRod-shaped 5 wt.% copper-doped ZnO (ZnO:Cu2+) ferromagnetic nanoparticles (NPs), prepared by hydrothermal method, were dispersed in ferroelectric liquid crystal (FLC) named Felix 17/100. The effect of ferromagnetic NPs on the physical properties of FLC material (Felix 17/100) has been investigated by dielectric, electro-optical and polarising optical microscopic methods. A noteworthy time-dependent memory has been observed in the NPs-dispersed FLC composite attributed to the coupling of magnetic field associated to NPs with the director orientation of FLC. Improvement in spontaneous polarisation and dielectric susceptibility of FLC material has been ensued with the addition of ferromagnetic NPs. Faster electro-optic response, at lower applied voltage, has also been observed in NPs-dispersed FLC composite. These changes are accredited to the magneto-electric dipolar coupling existing due to the interactions between magnetic-dipole and electric-dipole moments of magnetic NPs and FLC material, respectively. The formation of periodic domains capable to show memory effect has been observed in composite. The observed time-dependent memory was confirmed by dielectric and electro-optical methods. FLC material enriched with the properties of ferromagnetic NPs can be utilised in advanced multifunctional optical devices, time-dependent memory-based security devices and computational purposes.

Fast electro-optical response of a cell with a homeoplanar layer of a nematic liquid crystal

The refraction of light, i.e., the turn of an extraordinary ray in the liquid crystal layer similar to total internal reflection at an interface between two media, has been studied in a cell with the homeoplanar orientation of the director. The rise, τon, and decay, τoff, times of optical responses have been obtained for various angles of incidence of light on a liquid crystal layer subjected to an electric field. The times τon and τoff of optical responses for the angles of incidence much larger than the angle of total internal reflection are 1–2 ms, which is three orders of magnitude smaller than the relaxation time of an optical response in the case of normal incidence of the ray.

Pico-ampere current sensitivity and CdSe quantum dots assembly assisted charge transport in ferroelectric liquid crystal

Octadecylamine capped CdSe quantum dots (QDs) dispersed 4-(1-methyl-heptyloxy)-benzoic acid 4′-octyloxy-biphenyl-4-yl ester ferroelectric liquid crystal (FLC) were deposited over gold coated quartz substrate using dip-coating. The topographical investigation discloses that the homogeneously dispersed QDs adopt face-on to edge-on assembly in FLC matrix owing to their concentration. Current–voltage (I–V) measurement was performed using conductive atomic force microscopy (CAFM) which yields ohmic to critical diode like I–V curves depending upon the concentration of QDs in FLC. The recorded pico-ampere (pA) current sensitivity in FLC-QDs composites is attributed to micro-second drift time of electron due to weak electronic coupling between the π-electrons on the FLC and s-electrons on the metal surface. The observed pico-ampere sensitivity is the least current sensitivity recorded so far. For FLC-QDs composites, almost 24% faster electro-optic response was observed in comparison to pure FLC. The pico-ampere current sensitivity can be utilized in touch screen displays whereas the change in polarization for low applied electric field ameliorates the increased electrical susceptibility counteracting the internal electric field and its use in electronic data storage and faster electro-optical devices.

Chiral Side Groups Trigger Second Harmonic Generation Activity in 3D Octupolar Bipyrimidine‐Based Organic Liquid Crystals

The design of efficient noncentrosymmetric materials remains the ultimate goal in the field of organic second-order nonlinear optics. Unlike inorganic crystals currently used in second-order nonlinear optical applications, organic materials are an attractive alternative owing to their fast electro-optical response and processability, but their alignment into noncentrosymmetric film remains challenging. Here, symmetry breaking by judicious functionalization of 3D organic octupoles allows the emergence of multifunctional liquid crystalline chromophores which can easily be processed into large, flexible, thin, and self-oriented films with second harmonic generation responses competitive to the prototypical inorganic KH2 PO4 crystals. The liquid-crystalline nature of these chiral organic films also permits the modulation of the nonlinear optical properties owing to the sensitivity of the supramolecular organization to temperature, leading to the development of tunable macroscopic materials.

Thickness-independent dynamics in cholesteric liquid crystals.

We report fast electro-optic response independent of cell thickness in cholesteric liquid crystals (ChLCs). Usually, an electric field normal to the helix axis of ChLCs induces two fast and one slow response components: helical elongation (slow one), helical deformation (fast one), and flexoelectric effect (fast one). In this study, we found that a planarly aligned ChLC applied with an in-plane electric field exhibited only fast response components because the glass substrates suppressed the motion of the helical elongation. Furthermore, we demonstrated complete separation of the remaining fast components by using dielectric measurement system. Consequently, we were able to analyze dynamics of the helical deformation in detail, in which response times exhibited quadratic dependence on the helical pitch and no dependence on the cell thickness.

Science and technology of stressed liquid crystals: display and non-display applications

ABSTRACTStressed liquid crystals (SLCs) have emerged as promising tunable electro-optical materials more than a decade ago. They are optically transparent and are characterized by a giant phase modulation of the incident light (Nπ, N >> 1), fast (millisecond and shorter) electro-optical response, and a relatively low driving voltage (∼1 V/μm). Surprisingly, despite their advanced electro-optical performance, these new materials did not receive due attention in the research community. One possible reason of such an inadequate interest in SLCs is the lack of the well-documented procedure describing how to actually produce these materials. This paper is aimed at the development of such a step-by-step practical guide suitable for experimentalist and engineers. The proposed technology is applied to produce and characterize SLCs. In addition, some applications of the materials are briefly discussed and a broader overview of their possible use is outlined.

Slippy interfaceに接触したSmC*相の低電圧・高速駆動

Slippy interfaceに接触したSmC*相の低電圧・高速駆動

Core/shell quantum dots in ferroelectric liquid crystals matrix: effect of spontaneous polarisation coupling with dopant

ABSTRACTIn order to fabricate efficient and superior performance liquid crystal (LC) devices, the physical parameters of the LC mesogens can be duly altered by incorporating non-mesogenic materials like quantum dots (QDs), graphene and polymers. In the present work, the effect of adding core/shell QDs in two ferroelectric liquid crystals (FLCs), along with the change in their physical properties, has been investigated. A small concentration of QDs is dispersed into the two FLCs and temperature variations of vital parameters like spontaneous polarisation (Ps), rotational viscosity, response time, relative permittivity and relaxation strength have been measured for both the FLC materials. The contrast ratio, UV–near visible absorbance as well as photoluminescence (PL) of both the mesogens have also been determined and compared. A faster electro-optical response and the induced phenomenon of PL with a temperature-dependent low-frequency relaxation mode have been observed in Felix 17/100 after the addition of QDs. The present study also provides valuable information about the interaction between QDs and the two FLC systems depending upon polarisation–field (P–E) coupling. The same dopant can interact with FLCs in dissimilar fashion if the intrinsic properties of both the FLCs are different thereby producing different modifications in their respective physical parameters.

Electro-optic switching of dielectrically negative nematic through nanosecond electric modification of order parameter

We present experimental studies of nanosecond electric modification of the order parameter (NEMOP) in a variety of nematic materials with negative dielectric anisotropy. The study demonstrates that NEMOP enables a large amplitude of fast (nanoseconds) electro-optic response with the field-induced birefringence on the order of 0.01 and a figure of merit (FoM) on the order of 104 μm2/s; the latter is orders of magnitude higher than the FoM of the Frederiks effect traditionally used in electro-optic nematic devices. The amplitude of the NEMOP response is generally stronger in nematics with larger dielectric anisotropy and with higher natural (field-free) birefringence.

Electrical addressing of polymer stabilized hyper-twisted chiral nematic liquid crystals with interdigitated electrodes: Experiment and model

Electro-optic switching in short-pitch polymer stabilized chiral nematic liquid crystals was studied and the relative contributions of flexoelectric and dielectric coupling were investigated: polymer stabilization was found to effectively suppress unwanted textural transitions of the chiral nematic liquid crystal and thereby enhance the electro-optical performance (high optical contrast for visible light, a near ideal optical hysteresis, fast electro-optic response). Test cells were studied that possessed interdigitated electrodes to electrically address the liquid crystal. Based on simulations, a well-fitted phenomenological description of the electro-optic response was derived considering both flexoelectro-optic and Kerr-effect based electro-optic response.