Types Of Liquid Crystals Research Articles

Unlocking the potential of liquid crystals as phase change materials for thermal energy storage

This review paper examines the innovative use of liquid crystals (LCs) as phase change materials in thermal energy storage systems. With the rising demand for efficient energy storage, LCs offer unique opportunities owing to their tunable phase transitions, high latent heat, and favorable thermal conductivity. This paper covers various types of LCs, such as nematic, smectic, and cholesteric phases, and their roles in enhancing thermal energy storage. It discusses the mechanisms of LC phase transitions and their impact on energy storage efficiency. Strategies to improve the thermal conductivities of LCs and LC polymers have also been explored. One method involves embedding LC units within the molecular structure to promote orderly arrangement, facilitate heat flow, and reduce phonon scattering. Aligning polymer chains through external fields or mechanical processes significantly improves intrinsic thermal conductivity. The inclusion of thermally conductive fillers and optimization of filler-matrix interactions further boost thermal performance. Challenges related to the scalability, cost-effectiveness, and long-term stability of LC-based phase change materials are addressed, along with future research directions. This review synthesizes the current knowledge and identifies gaps in the literature, providing a valuable resource for researchers and engineers to develop advanced thermal energy storage technologies, contributing to sustainable energy solutions.

Polar Order in a Fluid Like Ferroelectric with a Tilted Lamellar Structure – Observation of a Polar Smectic C (SmCP) Phase

AbstractThe discovery of fluid states of matter with spontaneous bulk polar order is appreciated as a major discovery in the fields of soft matter and liquid crystals. Typically, this manifests as polar order superimposed atop conventional phase structures and is thus far limited to orthogonal phase types. Here we report a family of materials which exhibit a previously unseen state of matter which we conclude is a polar smectic C phase, and so we term it SmCP. The spontaneous polarisation of the SmCP phase is over two orders of magnitude larger than that found in conventional ferroelectric SmC phase of chiral materials used in some LCD devices. Fully atomistic molecular dynamics simulations faithfully and spontaneously reproduce the proposed structure and associated bulk properties; comparison of experimental and simulated X‐ray scattering patterns shows excellent agreement. The materials disclosed here have significantly smaller dipole moments than typical polar liquid crystals such as RM734 which suggests the role of molecular electrical polarity in generating polar order is perhaps overstated, a view supported by consideration of other molecular systems.

Polar Order in a Fluid Like Ferroelectric with a Tilted Lamellar Structure - Observation of a Polar Smectic C (SmCP) Phase.

The discovery of fluid states of matter with spontaneous bulk polar order is appreciated as a major discovery in the fields of soft matter and liquid crystals. Typically, this manifests as polar order superimposed atop conventional phase structures and is thus far limited to orthogonal phase types. Here we report a family of materials which exhibit a previously unseen state of matter which we conclude is a polar smectic C phase, and so we term it SmCP. The spontaneous polarisation of the SmCP phase is over two orders of magnitude larger than that found in conventional ferroelectric SmC phase of chiral materials used in some LCD devices. Fully atomistic molecular dynamics simulations faithfully and spontaneously reproduce the proposed structure and associated bulk properties; comparison of experimental and simulated X-ray scattering patterns shows excellent agreement. The materials disclosed here have significantly smaller dipole moments than typical polar liquid crystals such as RM734 which suggests the role of molecular electrical polarity in generating polar order is perhaps overstated, a view supported by consideration of other molecular systems.

Investigation of liquid crystal epoxy resin composites for application in cryogenic environments

AbstractIt is well accepted that the intrinsic thermal conductivity is extremely important in achieving excellent thermal conductivity composite and can be improved via incorporation of mesogens. In this work, an azomethine type liquid crystal epoxy (LCE) with aliphatic ether was designed and synthesized with expected structure, and the liquid crystal epoxy resin (LCER), together with KH‐550‐modified boron nitride (K‐BN)/LCER composites, has been obtained. Results show an increase of 31.6% in the thermal conductivity of the matrix, which could result in an enhancement of 57.7% for the composites when compared with E‐51. Additionally, the coefficient of thermal expansion (CTE), dielectric properties, and shear strength of LCER and K‐BN/LCER composites were assessed across a broad temperature range. Remarkably, the 30 wt% K‐BN/LCER composites showed a maximum decrease of 37.8% in CTE, while maintaining adequate shear strength to fulfill the bonding requirement and high thermal conductivity at both RT and −196°C.

Rapid ion conduction enabled by synergism of oriented liquid crystals and Electron-Deficient boron atoms in multiblock copolymer electrolyte for advanced Solid-State Lithium-Ion battery

Rapid ion conduction enabled by synergism of oriented liquid crystals and Electron-Deficient boron atoms in multiblock copolymer electrolyte for advanced Solid-State Lithium-Ion battery

Development of a high-frequency dielectric spectrometer using a portable vector network analyzer

A simple and novel setup for high-frequency dielectric spectroscopy of materials has been developed using a portable vector network analyzer. The measurement principle is based on radio frequency reflectometry, and both its capabilities and limitations are discussed. The results obtained on a typical liquid crystal prove that the device can provide reliable spectra between 107 and 109 Hz, thus extending the capabilities of conventional impedance analyzers.

Quantum optical control experiment using Mach–Zehnder interferometer and twisted nematic liquid crystals

A Mach–Zehnder interferometer with an optical phase control by a twisted nematic (TN) liquid crystal (LC) device was studied. In a typical TN LC device, a change in the optical rotation state of π/2 can be obtained by applying a voltage of about 5 V with a cell thickness of several-micron. The TN cell is inserted into one optical path in the Mach–Zehnder interferometer. We obtained a pattern change when voltage was applied to the LC cell due to the change of the optical interference state. As a result, a change in the number of photons under weak light conditions is observed.

Impact of Molecular-level Structural Disruption on Relaxation Dynamics of Polymers with End-on and Side-on Liquid Crystal Moieties.

In side-chain liquid crystal polymers (SCLCPs), short side chains are attached on a flexible polymer backbone, and each side chain can have a liquid crystal (LC) group attached at the final bead in either an end-on or a side-on configuration. SCLCPs with random sequences of end-on and side-on LC moieties exhibit nonmonotonic thermal behavior as a function of composition, with some mixed sequences having a lower isotropic to LC phase transition than either purely end-on or side-on configurations. The origin of this nonmonotonic thermal trend lies in the disruption of molecular-level positional ordering and alignment due to the different preferred types of ordering of the different LC attachment types. We compare coarse-grained molecular dynamics (MD) simulations and experiments on SCLCP systems with only one type of LC moiety and demonstrate qualitative agreement in the observed mesophases of end-on and side-on SCLCP systems. Specifically, end-on SCLCPs display a smectic B-like mesophase, with layers of polymer between LC layers, while side-on SCLCPs exhibit a quasi-hexagonal columnar structure of polymer and a nematic surrounding the LC mesophase. Detailed analysis of SCLCP systems with various compositions of these types of LC attachments via MD reveals structural disruption in systems with intermediate compositions. Simulation snapshots and anisotropy ratio measurements show how random SCLCP systems deviate from the expected behavior of prolate or oblate systems in terms of their conformation. This molecular disruption in random SCLCP systems, particularly with a high composition of side-on LC moieties, also significantly impacts the relaxation dynamics. Modifying the composition of the LC type of attachment (molecular structure) is a possible route to tuning both the phase behavior and mechanical response of these systems.

Synthesis and mesomorphic properties of novel multi-arm side-chain liquid crystal polymers with different terminal substituents

ABSTRACT In this study, two novel aromatic ester multi-arm liquid crystal monomers M 1 and M 2 with different terminal substituents centred on 3,4,5-trihydroxybenzoic acid, and a rod-shaped chiral liquid crystal monomer N were designed and synthesised. The synthesised liquid crystal monomers M and N were grafted and copolymerised with polymethylhydrosiloxane (PMHS). The structural characterisation of the synthesised liquid crystal compounds was carried out by FT-IR and 1H-NMR. The mesomorphic properties of the synthesised liquid crystal compounds were characterised by POM and DSC, and the results showed that the multi-arm liquid crystal monomers M 1 and M 2 are typical enantiotropic nematic liquid crystal compounds and N is typical thermotropic enantiotropic cholesteric liquid crystal. Polymers P 1 and P 2 are both cholesteric liquid crystal polymers. The glass transition temperatures and liquid crystal isotropic transition temperatures of polymers P 1 and P 2 series both tend to increase with the increase of multi-arm liquid crystal monomer M.

Synthesis and mesomorphic properties of swallow-tailed liquid crystal monomers and polymers

In this article, we designed and synthesized two novel swallow-tailed liquid crystal monomers (M1 and M2) with different chain lengths and rigidities centered on 3,4,5-trihydroxybenzoic acid and two series of side-chain liquid crystals polymers PN1 and PN2. All liquid crystal monomers and polymers were conformed to the molecular designs by FT-IR and NMR. The liquid crystal properties were tested by DSC and POM, and the results showed that M1 and M2 were thermotropic enantiotropic nematic liquid crystals and the side-chain liquid crystal polymers PN1 and PN2 series were typical amorphous liquid crystal polymers. With the increase of monomer content, the glass transition temperatures and clearing points of PN1 and PN2 series enhanced. With the increase of the number of mesogens in the liquid crystal monomer, the rigidity was enhanced, and the liquid crystal performance of the polymer was better.

Optical and flexoelectric biosensing based on a hybrid-aligned liquid crystal of anomalously small bend elastic constant

Liquid crystal (LC)-based biosensors rely on the response of the LC molecules to perturbation generated by analytes at the interface, leading to the susceptible change in molecular alignment or orientation. The sensitivity of these biosensors is primarily dependent on the LC's material properties and surface anchoring strength. By incorporation of an unconventional mesogenic compound (CB7CB) coupled with the hybrid-alignment cell configuration, this work presents a binary nematic LC for label-free biosensing, manifesting a novel sensing technology that takes advantage of CB7CB-induced flexoelectricity in the transducer. Herein, we prepared LC mixtures by blending a typical rod-like nematic LC (E7) with the bent-core mesogen CB7CB in various weight ratios and studied the effect of the CB7CB content on E7/CB7CB-based biosensing performance in vertically aligned and hybrid-aligned nematic (HAN) cells. Owing to the anomalously small bend elastic constant K33 in CB7CB, the mixture designated CB45 with the highest CB7CB weight percentage (45wt% in this study) was best applicable to biosensing in HAN cells. When observed under a polarizing optical microscope, CB45 in the HAN geometry showed the capability of detection of as low as 10-10g/mL for the protein standard bovine serum albumin (BSA). Moreover, the quantitation of the assay was fulfilled by both dielectric and light transmission measurements of the hybrid-aligned cholesteric CB45/R5011. The limit of detection of 7×10-10g/mL was achieved by spectrometric analysis. To the best of our knowledge, this work is the first to demonstrate flexoelectric biosensing on the basis of flexoelectric polarization associated with giant flexoelectricity in CB7CB partially constituting the LC transducer.

Liquid crystalline matrix-induced viscoelastic mechanical stimulation modulates activation and phenotypes of macrophage.

Accumulating evidence indicates that the mechanical microenvironment exerts profound influences on inflammation and immune modulation, which are likely to be key factors in successful tissue regeneration. The elastic modulus (Em) of the matrix may be a useful adjustable property to control macrophage activation and the overall inflammatory response. This study constituted a series of Em-tunable liquid crystalline cell model (HpCEs) resembling the viscoelastic characteristic of ECM and explored how mechanical microenvironment induced by liquid crystalline soft matter matrix affected macrophage activation and phenotypes. We have shown that HpCEs prepared in this work exhibited typical cholesteric liquid crystal phase and distinct viscoelastic rheological characteristics. All liquid crystalline HpCE matrices facilitated macrophages growth and maintained cell activity. Macrophages in lower-Em HpCE matrices were more likely to polarize toward the pro-inflammatory M1 phenotype. Conversely, the higher-Em HpCEs induced macrophages into an elongated shape and upregulated M2-related markers. Furthermore, the higher-Em HpCEs (HpCE-O1, HpCE-H2, HpCE-H1) could coax sequential polarization states of RAW264.7 from a classically activated "M1" state toward alternatively activated "M2" state in middle and later stage of cell culture (within 3-7 days in this work), suggesting that the HpCE-based strategies could manipulate the local immune microenvironment and promote the dominance of the pro-inflammatory signals in early stages, while M2 macrophages in later stages. The liquid crystalline soft mode fabricated in this work maybe offer a new design guideline for in vitro cell models and applications.

Understanding mesophase pitch from a lyotropic liquid crystalline perspective

This review explores recent research regarding mesophase pitch (MP). Spinnable mesophase pitch (SMP) was used as a model pitch for MP in all experiments. We explain some phenomenological results of the lyotropic liquid crystalline properties of the SMP, which show that the MP behaves as a typical lyotropic liquid crystal. The mesogenic and solvent components of SMP are defined. We define the threshold concentration (TC) as the minimum amount of mesogenic component necessary for SMP to achieve 100 vol% anisotropy. We also report the TCs of various SMPs and discuss the effects of the solvent component. Concerning the identity of the mesogenic component, we discuss quantitative correlations between the size of the layered molecular stacking units and the anisotropic content of the SMP. Research has shown that a layered molecular stacking unit larger than a specific size corresponds to the mesogenic component of the MP. We discuss a novel method for the manufacture of SMPs using our understanding of MP as a lyotropic liquid crystal, which comprises thermal mixing of optimal amounts of the mesogenic and solvent components that were prepared separately under different conditions. This method enables the properties of each component to be optimized without involving a costly hydrogenation process. Finally, we discuss how this approach can be used to increase SMP yield by modifying the contents of the anisotropic mesogenic and solvent components.

Atmospheric fate of typical liquid crystal monomers in the tropospheric gas, liquid, and granular phases

Mineral aerosol particles significantly impact environmental risk prediction of liquid crystal monomers (LCMs). In this work, we investigated the reaction mechanisms and kinetics of three typical LCMs (4-cyano-3,5-difluorophenyl 4-ethylbenzoate (CEB-2F), 4-cyano-3-fluorophenyl 4-ethylbenzoate (CEB-F), and 4-cyanophenyl 4-ethylbenzoate (CEB)) with ozone (O3) in the atmospheric gas, liquid, and particle phases employing density functional theory (DFT). Here, O3 is prone to add to the benzene ring without F atom(s) in the selected LCMs. The ozonolysis products are aldehydes, carboxylic acids, epoxides, and unsaturated hydrocarbons containing aromatic rings. Those products undergo secondary ozonolysis to generate small molecular compounds such as glyoxal, which is beneficial for generating secondary organic aerosol (SOA). Titanium dioxide (TiO2), an essential component of mineral aerosol particles, has good adsorption properties for LCMs; however, it slightly reduces the reactivity with O3. At 298 K, the reaction rate constant of the selected LCMs reacting with O3 in the gas and atmospheric liquid phases is 2.74‒5.53 × 10−24 cm3/(mol·sec) and 5.58 × 10−3‒39.1 L/(mol·sec), while CEB-2F reacting with O3 on (TiO2)6 cluster is 1.84 × 10−24 cm3/(mol·sec). The existence of TiO2 clusters increases the persistence and long-distance transportability of LCMs, which enlarges the contaminated area of LCMs.

Thermoresponsive mobility of liquid crystals and reactive mesogens during photopolymerization-induced phase separation.

Molecular interactions between liquid crystals (LCs) and reactive mesogens (RMs) at temperatures across the phase transition regions were comprehensively studied during photopolymerization-induced phase separation (PPIPS) beginning with raw mixtures until the formation of polymer network liquid crystals (PNLCs). Then, the molecules were found to be nonuniformly more and less mobile in response to temperature as PPIPS progressed. Optical birefringence and infrared absorption were carefully measured throughout PPIPS, using 4-cyano-4'-hexylbiphenyl (6CB) and 1,4bis-[4-(3-acryloyloxypropyloxy) benzoyloxy]-2-methylbenzene (RM257) as typical LCs and RMs. Microscopic views of thermoresponsive changes in the molecular orientation order of both LCs and RMs were obtained: LCs and RMs in raw mixtures interacted with one another but uniformly transformed their molecular orientation. Such interactions continuously change to become nonuniform with progress in PPIPS. At the incipient stages of PPIPS, RMs, which are polymerized but not completely networked, inhibit LCs from changing their molecular orientation and vice versa. As PPIPS progresses, some LCs become more mobile and some less mobile owing to RM constraints. The domain configuration of the submicrometer phase separation affects the thermoresponsive mobility of LCs and RMs, that is, LCs become more mobile in LC-richer areas. The quantitative knowledge here provides comprehensive insight that LCs and RMs are mutually constrained and that such interactive behavior varies nonuniformly as PPIPS progresses.

Shear direction switching phenomena in twisted nematic liquid crystal cells for novel differential interference contrast imaging systems

AbstractA lateral shear occurs between ordinary and extraordinary rays in general optical uniaxial crystals, and we can observe a double image through the crystal, indicating a typical birefringence phenomenon. Small lateral shears occur in typical liquid crystal (LC) cells under small voltage applications, where the molecular alignment direction is generally inclined. The small lateral shear is useful for differential interference contrast (DIC) imaging systems, although it must be negligible in a typical LC display panel. In particular, unique lateral shearing properties are exhibited by twisted nematic (TN) LC cells, which are popular and important LC display modes. The 45°‐oblique lateral shear occurs according to the direction of the surface molecular alignment, and the inclination direction (+45° or −45°) depends on the molecular twist direction. If it is possible to switch the twist direction in the TN cell, the lateral shear direction can be switched by 90°, and a full DIC imaging system can be attained because the normal DIC system can obtain one‐directional derivative information along the shear direction. In this work, twist direction switching phenomena in TN cells are investigated by applying a magnetic field in the direction parallel to the cell surface.

Color-selective geometric-phase lenses for focusing and imaging based on liquid crystal polymer films.

The geometric-phase lens (GPLs) with small form factor compared to traditional refractive lenses has been identified as a compelling solution in augmented-/virtual-/mixed-reality (AR/VR/MR) headsets. Formed either with liquid crystals (LCs) or metasurfaces, the GPL is a type of emerging leading technology that implements the arbitrary aspheric phase to realize low loss and minimal ghosting. However, the inherent chromatic abberation (CA) of GPLs can significantly degrade the image quality. A possible solution is the independent spectral phase implementation for RGB. In this work, we propose the design of three types of multi-twist LC based color-selective GPLs (CS-GPLs), exhibiting highly chromatic efficiency spectra with diameter 30 mm, focal length around 41.2~mm, and F -number 1.37. Through theoretical and experimental validation, each type of CS-GPL manifests high diffraction efficiency (>91%) on respective primary color of orthogonal polarization and high transmission on the complementary color of input polarization. The triplet composed by RGB CS-GPLs demonstrates relative contrast ratio and minimal ghosting. The strong color and polarization dependency of CS-GPLs not only provide a novel technique to mitigate CA but also offer more design freedom in the AR/VR/MR polarization and imaging system.

Fast and Miniaturized Phase Shifter With Excellent Figure of Merit Based on Liquid Crystal and Nanowire-Filled Membrane Technologies

This paper presents a highly miniaturized tuneable microstrip line phase shifter for 5 GHz to 67 GHz. The design takes advantage of the microstrip topology by substituting the ground plane by a metallic-nanowire-filled porous alumina membrane (NaM). This leads to a slow-wave (SW) effect of the transmission line; thus, the transmission line can be physically compact while maintaining its electric length. By applying a liquid crystal (LC) with its anisotropic permittivity as substrate between the transmission line and the NaM, a tuneable microstrip line phase shifter is realized. Three demonstrators are identically fabricated filled with different types of high-performance microwave LCs from three generations (GT3-23001, GT5-26001 and GT7-29001). The measurement results show good matching in a <inline-formula xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><tex-math notation="LaTeX">$50\ \Omega$</tex-math></inline-formula> system with reflection less than −10 dB over a wide frequency range. These demonstrators are able to reach a maximum figure of merit (FoM) of 41 <inline-formula xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><tex-math notation="LaTeX">$^{\circ }$</tex-math></inline-formula> /dB, 48 <inline-formula xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><tex-math notation="LaTeX">$^{\circ }$</tex-math></inline-formula> /dB, and 70 <inline-formula xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><tex-math notation="LaTeX">$^{\circ }$</tex-math></inline-formula> /dB for different LCs (GT3-23001, GT5-26001 and GT7-29001, respectively). In addition, experiments show that all three LCs should be biased with square wave voltage at approximately 1 kHz to achieve maximum tuneability and response speed. The achieved response times with GT3-23001, GT5-26001 and GT7-29001 are 116 ms, 613 ms, and 125 ms, respectively, which are much faster than other reported LC phase shifter implementations. Large-signal analysis shows that these implementations have high linearity with third-order interception (IP3) points of approximately 60 dBm and a power handling capability of 25 dBm.

Analysis of Molecular Disordering Processes in the Phase Transition of Liquid Crystals Observed by Patterned-Illumination Time-Resolved Phase Microscopy.

The initial processes of the phase transition dynamics of liquid crystals (LCs) subject to UV pulse irradiation were clarified using a nanosecond time-resolved imaging technique called pattern-illumination time-resolved phase microscopy (PI-PM). Two types of LCs were studied: a photo-responsive LC and dye-doped LCs. We found two steps of molecular disordering processes in the phase transition, namely local disordering proceeding anisotropically, followed by the spreading of the isotropic phase. These two processes were separated for a photo-responsive LC while being simultaneously observed for the dye-doped LCs. It was found that the photomechanical dyes induced the phase transition process faster than the photothermal dyes.

Rethinking Figure-of-Merits of Liquid Crystals Shielded Coplanar Waveguide Phase Shifters at 60 GHz

The demand for reconfigurable millimetre-wave (mm-Wave) components based on highly anisotropic liquid crystals (LC) is higher than ever before for the UK and worldwide. In this work, 60 GHz investigation on a bespoke shielded coplanar waveguide (SCPW) phase shifter structure filled with 16 types of microwave-enabled nematic LCs respectively indicates that the patterns of the device’s figure-of-merit (FoM, defined as the ratio of maximum differential phase shift to maximum insertion loss) reshuffle from those of the characterised LC materials’ FoM (defined as the ratio of tunability to maximum dissipation factor). To be more specific, GT7-29001- and MDA-03-2838-based phase shifters exhibit the highest FoM for devices, outperforming phase shifters based on GT5-28004 and TUD-566 with the highest FoM for materials. Such a mismatch between the device’s FoM and LC’s FoM implies a nonlinearly perturbed wave-occupied volume ratio effect. Furthermore, the relationship between insertion loss and the effective delay line length is nonlinear, as evidenced by measurement results of two phase shifters (0–π and 0–2π, respectively). Such nonlinearities complicate the established FoM metrics and potentially lead to a renewed interest in the selection and material synthesis of LCs to optimise reconfigurable mmWave devices, and promote their technological exploitation in phased array systems targeting demanding applications such as inter-satellite links and satellite internet.