Liquid Crystal Materials Research Articles

Solution-processed planarly oriented thin films of cholesteric liquid-crystalline semiconductors

We have successfully fabricated cholesteric liquid-crystalline (CLC) semiconductor thin films from the mixture of dimeric and monomeric compounds based on oligo(p-phenylenevinylene) units by spin-coating method. This is the first example of solution-processed planarly orientated thin film in CLC semiconductors. The mixture exhibited a CLC phase at lower temperatures than the compound alone, allowing the fabrication of spin-coated CLC thin films at room temperature. Furthermore, the dimeric compound has trifluoromethyl groups that exhibited high solubility in organic solvents such as chloroform due to its improved hydrophobicity. In addition, the high hydrophobicity of the trifluoromethyl groups lowers the surface tension of the liquid–crystal material, resulting in planar orientation.

Excitation-Dependent Circularly Polarized Luminescence Inversion Driven by Dichroic Competition of Achiral Dyes in Cholesteric Liquid Crystals.

The development of stimuli-responsive chiral cholesteric liquid crystals (CLCs) materials holds significant potential for achieving three-dimensional (3D) anti-counterfeiting and multi-level information encryption. However, constructing phototunable CLCs systems with easy fabrication and fast response remains a great challenge. Herein, we exploit an excitation-dependent CLCs (ExD-CLCs) material by establishing dynamically photoresponsive dichroic competition between two achiral dyes: a negative dichroic dye (SP-COOH) and a positive dichroic dye (Nile Red, NR) within a CLCs medium. The ExD-CLCs exhibits a negative CPL signal (glum = -0.16) at 650 nm when excited at 365 nm. Remarkably, under excitation at 430 nm, the CPL signal is inverted, and the glum value increases to +0.26. Notably, the helical superstructure and handedness of the ExD-CLCs remain unchanged during this reversal process. The CPL signal reversal is driven by the dichroic competition between the SP-COOH dimer, which displays strong negative dichroism in its open-ring isomer form and silent negative dichroism in its closed-ring isomer form, and the NR dye, which exhibits static positive dichroism. Leveraging these excitation-dependent CPL properties, the quadruplex numerical anti-counterfeiting using ExD-CLCs is achieved.

Influence of side-methyl substitution position on the phase state and microwave dielectric properties of triphenylacetylene-based liquid crystals.

Liquid crystal materials are well known in display applications, and their unique birefringence and electrical tunability can be utilised in microwave devices. This innovative technology modulates and filters microwave signals, replacing conventional semiconductors for a broad operational frequency band and tunable phase shift. Although isothiocyanatobiphenylacetylene-based liquid crystals exhibit low viscosity and large dielectric anisotropy, their applications in microwave communication are hampered by their broad near-crystalline phase temperature ranges. To address this limitation, this study designed and synthesized six fluorinated biphenylacetylene liquid crystal compounds with various benzene ring side-methyl substitutions (n = 3-5). The molecular structures, liquid crystal phases, and microwave dielectric properties were evaluated. Our findings indicate that compounds with methyl substitution at the Y2 position exhibited reduced melting points, an expanded nematic phase temperature range (ΔT n ≈ 92.3 °C), and an absence of near-crystalline phases. These compounds still maintain high microwave dielectric constants within the 9-30 GHz frequency band (Δε r = 0.9-1.3) and reduced maximum permittivity losses compared to their non-methyl-substituted counterparts, thereby improving the efficiency in the microwave frequency band. In contrast, the Y1 position substitution results in a significantly narrower nematic phase temperature range (approximately 2.6 °C on average) and a substantial decrease in the dielectric constant, with a Δε r reduction of about 0.3 compared to the Y2 substitution. This work shows that the side-methyl substitution can improve the performance of triphenylacetylene-based liquid crystals in microwave communication, providing valuable insight to aid the discovery of novel microwave liquid crystals.

Effect of CsPbBr3 perovskite quantum dots on molecular alignment, dielectric and memory effect of a cyanobiphenyl based liquid crystal

We demonstrate here the impact of doping of CsPbBr3 perovskite quantum dots (CsPbBr3 PQDs, diameter ∼ 7–9 nm) on the molecular alignment, dielectric and memory effect of nematic (N) and smectic A (SmA) phases of a thermotropic liquid crystal material, namely 4-octyl-4′-cyanobiphenyl (8CB) using polarising optical microscope and dielectric spectroscopy. There is no significant change in the alignment of N and SmA phases of 8CB by the doping of CsPbBr3 PQDs, except the color change attributed to the tuned birefringence of 8CB by PQDs. The slight aggregation of PQDs is observed in both LC phases of 1.0 wt% CsPbBr3 PQDs-8CB composite and which could be due to the higher dopant concentration in 8CB matrix. The dielectric parameters (permittivity, loss and anisotropy) of N and SmA phases of 8CB are found to be strongly dependent on the dopant concentration. The dielectric anisotropy (Δε′) of 8CB is observed to decrease with increase in the dopant concentration except 0.5 wt% composite. The temperature dependent Δε′ further confirms that there is no significant change in the clearing temperature of composites as compared to pure 8CB. The short axis molecular relaxation observed in both N and SmA phases of pure 8CB and its composites on the application of 40 V bias. The slight spectral shift of this relaxation towards lower frequency side and decrease in the amplitude of ɛ″ in both SmA and N phases of 1.0 wt% composite as compared to the pure 8CB and composites with concentration lower than 1.0 wt%. The partial memory effect is observed in SmA phase of pure 8CB through voltage-dependent dielectric permittivity and cross-polarised optical textures. The observed memory effect in SmA phase is found to improve with increase in the concentration of PQDs. Most importantly, the complete memory effect is observed in SmA phase of 1.0 wt% CsPbBr3 PQDs-8CB composite. This could be attributed to the holding of smectic layers reorientation achieved at 40 V bias for longer duration after the removal of 40 V bias voltage. A point to be noted here is that no memory effect is observed in the N phase of pure 8CB and its composites with CsPbBr3 PQDs. Our results on CsPbBr3 PQDs-8CB composites are clearly indicative towards their potential applications in next generation tunable electro-optical and long-lasting soft memory devices. Moreover, results on these composites would also serve as the testbeds for theoretical and computational studies to explore the mechanism responsible for tunable optical, dielectric and electro-optical properties of 8CB by the dopant CsPbBr3 PQDs.

Carbon dots induced homeotropic alignment in a negative dielectric nematic liquid crystal material

Abstract Recently, doping guest materials such as quantum dots (QDs) into liquid crystals (LCs) has been of great interest since their addition substantially enhances the properties of LC and opens new avenues for scientific advancement. Here, we report the induction of homeotropic alignment in cells without alignment layers of the negative dielectric nematic liquid crystal, N-(4-Methoxybenzylidene)-4-butylaniline (MBBA) by doping with carbon dots (CDs ∼2.8 ± 0.72 nm). The CDs-MBBA composites (CDs concentration: 0.002, 0.01, 0.03, 0.1 and 0.3 wt%) were investigated using optical polarising microscopy, electro-optical and dielectric techniques. Polarizing optical micrographs and voltage dependent optical transmission revealed the induced homeotropic alignment for all the composites under investigation. Interestingly, the least concentrated sample, 0.002 wt% exhibited partial homeotropic alignment. However, due to light leakage, the optical transmission value below threshold voltage was relatively higher than the rest of the composites. MBBA is a negative dielectric material, hence the application of a voltage across the cell was able to switch the alignment from a dark to a bright state for all composites. However, above a certain voltage (>threshold voltage), the bright state produced some instabilities. The value of dielectric permittivity was observed to decrease with increasing concentration, confirming the effect of CDs in producing homeotropic alignment in MBBA. Measurements as a function of temperature were conducted to examine the thermal stability of the induced alignment. The alignment was found to be stable throughout the nematic phase of MBBA. The induction of such alignment without conventional alignment (i.e., rubbing of polyimides) technique can be helpful in addressing the evolving display demands by making liquid crystal displays (LCDs) and other display devices cost effective.

Low-Temperature Metallomesogen Model Structures and Mixtures as Potential Materials for Application in Commercial Liquid Crystal Devices

The present work was the preliminary study of phase diagrams and miscibilities of low-temperature metallomesogen (MOM) model structures based on rod-like palladium (Pd) alkyl/alkoxy-azobenzene metal complexes and their mixtures with commercial liquid crystal materials for potential application. The initial results indicated the accessible temperature range and mesgenic miscibility between parent ligand, MOMs and commercial liquid crystal mixtures. The eutectic ligand/MOM composition with other MOMs and commercial nematic liquid crystal materials exhibited complete mesogenic miscibility and wide low-temperature mesogenic stability for eventual utilization in commercial liquid crystal devices.

Controlling the dielectric constant values of nematic liquid crystals using ferroelectric and multiferroic nanoparticles

Notably, the simultaneous manifestation of ferromagnetic and ferroelectric properties at ambient temperature has spurred significant interest in incorporating multiferroic bismuth ferrite nanoparticles (BiFeO3) into liquid crystal matrices. In this study, the parallel and perpendicular dielectric components (ε∥ and ε⊥) and dielectric anisotropy (△ε=ε∥−ε⊥) of two different nanoparticles, barium titanate (BaTiO3) and BiFeO3, doped into E7, were measured at various temperatures and frequencies. Nematic mixture E7, a widely utilized nematic liquid crystal in research and display technologies, is a eutectic mixture composed of four cyanobiphenyl derivatives i.e. 5CB, 7CB, 8OCB, and 5CT. The findings indicate a substantial reduction in dielectric anisotropy upon introducing nanoparticles into the nematic liquid crystal environment. This research highlights the significant influence of barium titanate nanoparticles, which are smaller (approximately 12 nm), on the dielectric constant. This effect was analyzed based on varying concentrations and compared to a nanoparticle with ferroic properties. Moreover, the dielectric constant can be modulated through an alternative approach. Specifically, applying an electric field during the filling process of liquid crystal cells leads to changes in the dielectric constant. These changes, observed for both nanoparticles, were particularly evident at a precise concentration of 0.1 wt%, resulting in a decreased dielectric constant.

Bioinspired Mechanochromic Liquid Crystal Materials: From Fundamentals to Functionalities and Applications.

Inspired by intriguing color changeable ability of natural animals, the design and fabrication of artificial mechanochromic materials capable of changing colors upon stretching or pressing have attracted intense scientific interest. Liquid crystal (LC) is a self-organized soft matter with anisotropic molecular alignment. Due to the sensitivity to various external stimulations, LC has been considered as an emerging and appealing responsive building block to construct intelligent materials and advanced devices. Recently, mechanochromic LC materials have becoming a hot topic in multifields from flexible artificial skins to visualized sensors and smart biomimetic devices. In this review, the recent progress of mechanochromic LCs is comprehensively summarized. Firstly, the mechanism and functionalities of mechanochromic LC is introduced, followed by preparation of various functional materials based on mechanochromic LCs. Then the applications of mechanochromic LCs are provided. Finally, the conclusion and outlooks of this field is given. This overview is hoped to provide inspiration in fabrication of advanced functional soft materials for scientists and engineers from multidisciplines including materials science, elastomers, chemistry, and physical science.

A new homologous series of semi-conducting liquid crystals based on phenyl-anthracene: synthesis and effect of the alkyloxy terminal chain on charge transport and photoconductive properties.

π-Conjugated systems are the key to the charge transport properties of organic semiconductors. Four multifunctional mesogenic materials were designed and synthesised from 2-amino anthracene and para-hydroxybenzaldehyde. Each material contains a central, rigid phenyl-anthracene core and one flexible alkyloxy chain with different lengths based on the concept of combining liquid crystal (LC) materials featuring facile processability, highly ordered alignment, and effective charge transport. (E)-N-(Anthracen-2-yl)-1-(4-(alkyloxy)phenyl) methanimine (n-OPIA) with n = 8, 10, 12, and 16 was chemically characterized by nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry. Their thermal behaviours were performed by means of differential scanning calorimetry and polarised optical microscopy and showed differences in mesomorphic behaviours with respect to the alkyloxy chain length. Concerning their frontier molecular energy levels, they were studied by optical spectroscopy and cyclic voltammetry and compared to values obtained via ab initio density-functional theory (DFT) calculations. LC field-effect transistors (LC-FETs) using a solvent vapour enhanced drop casting based n-OPIA material showed efficient electrical parameters and interesting photoconductive properties, indicating their potential applications in multifunctional integrated devices. As the alkyloxy chain length of the n-OPIA compounds increased, the hole mobility, on/off current ratio, and responsivity decreased. The 8-OPIA homologue exhibits a mobility one order of magnitude larger than the previously studied homologue, namely 10-OPIA.

Dispersion and self-assembly of 2,5-dimercapto-1,3,4-thiadiazole (DMTD) functionalized silver QDs in 6 CHBT liquid crystal

ABSTRACT Silver nanoparticles were synthesised using silver nitrate and tri-sodium citrate and were functionalized with 2,5-Dimercapto-1,3,4-thiadiazole (DMTD) linking molecules. Functionalized silver nanoparticles dispersed within 4-(trans-4-n hexylcyclohexyl) isothiocyanatobenzoate (6CHBT) liquid crystal (LC) matrices have attracted significant attention because of their potential for tailoring tuneable surface plasmonic, optical, and electronic properties by controlling the self-assembly of silver dots. The unique combination of functionalized nanoparticles and 6CHBT LCs offers a versatile platform for manipulating interactions at the nanoscale. The dispersion of functionalized Ag nanoparticles within the LCs appears to substantially modify the plasmonic and opto-electronic properties of the Ag QDs. The formation and morphology of the self-assembled structures of silver nanoparticles were confirmed by Optical and Scanning Electron Microscopy. Optical microscopy (OM) and Scanning Electron Microscopy (SEM) images of Ag-doped 6CHBT confirmed the formation of nano-micro spheres, as well as ring and rod-like structures in LC media. We have used High-Resolution X-ray diffraction (HR-XRD), Fourier-Transform Infrared Spectroscopy (FTIR), Surface-Enhanced Raman Spectroscopy (SERS), Optical Microscopy (OM), Scanning Electron Microscopy (SEM), Ultraviolet-visible-near-infrared Spectroscopy (UV-Vis-NIR), and Fluorescence (FL) Spectroscopy. We calculated the electronic properties such as the bandgap of the synthesised Ag QDs and functionalized Ag QDs using UV-Vis-NIR and Tauc’s plot curves. Surface-enhanced Raman spectroscopy, Optical microscopy, SEM, and UV-Vis-NIR spectral data were used to correlate the properties of the LC and QDs hybrid systems.

Dielectric analysis of unpolymerized and photopolymerized NOA65 in a parallel-plate cell

The flourishing development of liquid crystal research in recent decades has highlighted the importance of polymer materials in enhancing liquid–crystal material and device properties, demonstrating tremendous potential in a wide range of industries. One of the polymer materials widely used in polymer-dispersed liquid crystal is Norland UV-curable optical adhesive (NOA65). This study focuses on the dielectric behavior of the optical adhesive in a parallel-plate cell. Given the broadness and asymmetry of the dielectric dispersion curve, the two-relaxation Havriliak–Negami model was employed to analyze the complex dielectric spectra of NOA65 before and after photocuring. Experimental results indicate that as temperature rises, the dielectric relaxation of NOA65 undergoes a blue shift, leading to an eventual overlap with pseudo-dielectric relaxation at a higher frequency. This brings about an increase in the obtained signal in the dielectric loss spectrum, implying that the observed feature of pseudo-dielectric relaxation is actually superposed or contributed by the intrinsic relaxation signal. Furthermore, as temperature continues to rise, the intrinsic dielectric loss signal of NOA65 becomes untraceable beyond the frequency span within which the pseudo-dielectric relaxation signal lies.

A novel multifunctional naphthalene triazole columnar liquid crystal: synthesis, self-assembly and application in silicon solar cells

Herein, click reaction was used as a crucial step to effectively synthesize a new multifunctional naphthalene triazole columnar liquid crystal ICm/n. The properties of liquid crystal and gel in ICm/n were investigated using POM, DSC, XRD and SEM. ICm/n can self-assemble into square columnar liquid crystals in their pure state and form organogels in N,N-dimethylformamide (DMF). In addition, ICm/n can be used as a Fe3+ chemosensor. Interestingly, the addition of lithium salts has a significant impact on the self-assembly, molecular dynamics and ionic conductivity of the compounds, thus potentially providing nanostructured LC electrolytes with continuous substrate ionic conductivity. Additionally, the use of ICm/n as a dopant in the poly (3,4-ethylenedioxythiophene): polystyrene (PEDOT: PSS) hole injection layer greatly enhanced the photoelectric conversion efficiency (PCE) of Si/PEDOT: PSS heterojunction solar cells, boosting it from 2.08 % to 8.10 %. The current work offers a novel method for creating liquid crystal (LC) materials with several uses for naphthalene triazoles.

Prolonged memory effect in smectic A phase of a thermotropic liquid crystal material

The long-duration memory effect in thermotropic liquid crystal (LC) materials has long been a topic of substantial interest and numerous pioneering works. Although the idea of exploring the memory effect had been started from the nematic (N) phase of LC itself, but due to its very short duration, it was soon shifted to the other LC phases such as ferroelectric LC (FLC) or their derivatives and composites. Therefore, we demonstrate here the prolonged memory effect in a smectic A (SmA) phase of a pristine thermotropic LC material namely 4-octyl-4′-cyanobiphenyl (8CB). The memory effect has also been investigated in the N phase to estimate its duration as compared to the SmA phase. To examine the memory effect, firstly, we measured the dielectric permittivity using the dielectric spectroscopic technique with and without 40 V DC biasing. Furthermore, these results have been confirmed by means of optical textures recorded through a polarizing optical microscope. Moreover, we have also observed the removal and retrieval of two stable states by sequent application of heat and DC biasing to examine the cyclability of the LC compound under testing. We anticipate that our results will definitely bridge the gap that occurred in the advancement of emerging futuristic LC-based memory devices.

Electrically tunable metasurface in TN LC configuration with enhanced quality factor and metaatom-induced alignment.

Dynamic metasurface with subwavelength dimensions has emerged as a key optical technology in recent years. Although various active tuning mechanisms are being proposed, liquid crystal-based dynamic metasurface remains attractive due to its large index variation, electrical tunability, reliability, and mass fabricability. In this work, we report a dynamic metasurface for amplitude modulation in reflection, with twisted nematic liquid crystal configuration to reduce broadband reflection in the off state. The metasurface consists of coupled subwavelength grating fingers, which provide alignment for the liquid crystal without the need for an additional alignment material or process. The alignment of liquid crystal materials was examined between crossed polarizers, and the twist of nematic liquid crystal was confirmed. The coupled grating fingers exhibit a resonance quality factor of 27 at telecommunication wavelength and an amplitude modulation depth of 8 times of the minimum at 1630 nm. This work highlights the potential of liquid crystal-based tunable metasurface, combining polarization control via liquid crystal and spectrum control via metasurface. Furthermore, it also shows a way in which the interaction between liquid crystal and metasurface is used for an alignment layer-free cell assembly process.

Effect of doping with carbon dots on the alignment and dielectric properties of nematic liquid crystal 4-cyano-4′-pentylbiphenyl in ITO sample cells without conventional alignment layers for low-cost display applications

The melding of nanomaterials with liquid crystalline materials is at the frontier of scientific research due to the transformative impact of nanoparticles on the functionalities of host liquid crystal materials. Here, we report the effect of doping of carbon dots (CDs) in the nematic liquid crystal (NLC), 5CB (4-cyano-4′-pentylbiphenyl) in indium tin oxide (ITO) sample cells without alignment layers (i.e., unaligned ITO (U-ITO) sample cells) using polarizing optical microscopy and dielectric spectroscopic techniques. Polarizing optical microscopy reveals largely dark optical textures under crossed polarizers confirming vertical alignment of Pure 5CB in U-ITO sample cells. However, defects present in the texture pose severe constraints on the use of induced vertical alignment in U-ITO sample cells for device applications. To improve the quality of vertical alignment, CDs of size 2.8 nm at concentrations of 0.03, 0.05 and 0.1 wt% are doped into 5CB. Optical texture studies show the quality of induced vertical alignment of the 0.03 wt% composite is better than pure 5CB and other composites. Frequency-temperature dependent dielectric studies verify the induced vertical alignment by observation of the short-axis molecular relaxation. The stability of the vertical alignment throughout the nematic phase of 5CB is confirmed through temperature dependent dielectric and optical texture studies. The induced vertical alignment of 5CB in U-ITO sample cells could be attributed to the stronger LC-LC interaction than the ITO-LC interaction. The improvement in the quality of vertical alignment of CDs-5CB composites could be due to the CDs influencing LC-LC and ITO-LC interactions. Finally, the effect of CDs on the increasing dc electrical conductivity of 5CB in U-ITO sample cells is investigated. Our results clearly indicate that CD-5CB composites would be useful in cost-effective display and other photonic devices devoid of alignment layers.

Novel AIE liquid crystals with high CPL-active bearing multiple dodecyl/cholesterol-decorated R-BINOL-cyanostilbene

The well-structured circularly polarized luminescence (CPL) active liquid crystal materials (R-BINC-Al and R-BINC-Ch) were synthesized through Suzuki coupling of the R-binaphthyl-cyanostilbene unit, followed by modification with dodecyl chains or cholesterol groups. The influence of chiral sources on the liquid crystal behavior, optical properties, and chiroptical response of R-BINC-Al and R-BINC-Ch was thoroughly investigated. Such results revealed that both molecules exhibited typical aggregation-induced emission (AIE) properties and strong solid-state fluorescence. Concretely, the quantum efficiency (ΦF) values of samples with multiple chiral sources increased from 46 % to 51 % by forming liquid crystals in the smectic C and cholesteric phases, the chirality can be transferred to the cyanostilbene unit through ordered self-assembly in the mesophase, resulting in a significant CPL signal across the molecules. Rightfully, the dissymmetry factor (glum) was increased from -7.92 × 10–3 to -1.53 × 10–2 with the introduction of chiral cholesteryl groups. our work elucidated the relationship between multiple chiral sources and CPL behavior, offering a systematic approach to designing chiral luminescent materials in the liquid-crystal phase with high ΦF and substantial glum values, providing a theoretical framework for potential applications in optoelectronic devices.

Probing the impact of bent-core mesogen on the dielectric relaxations of ferroelectric liquid crystal

The modulation in dielectric relaxations of a conventional ferroelectric liquid crystal (FLC, SCE9) material by doping the bent-core mesogen (BCM) derived from the oxadiazole bisaniline moiety has been greatly investigated using frequency-temperature dependent dielectric spectroscopy. The application of probing ac voltage (i.e., oscillating voltage, 800 mV) has clearly shown the presence of partially unwound helical mode (p-UHM) along with Goldstone mode (GM). However, the temperature-dependent dielectric studies further demonstrate that p-UHM gets merged with GM at higher temperatures and hence becomes difficult to observe it separately. It appears that doping of BCM into FLC leads to the suppression of p-UHM at lower temperature, but with the increase in the concentration of dopant beyond a certain point, p-UHM mode reappears. Moreover, the significant decrement (∼9 °C) in SmC*-SmA* phase transition temperature of FLC with increase in the dopant BCM concentration up to 3 wt%. We believe that such studies would be certainly useful for the understanding of the plausible interaction between two different shaped mesogens (i.e., rod and bent-core) present in the mixture and could pave the way forward to the use of one type of mesogen in the modulation of the dielectric properties of other mesogen.

An Up-to-Date Overview of Liquid Crystals and Liquid Crystal Polymers for Different Applications: A Review.

Liquid crystals have been extensively used in various applications, such as optoelectronic devices, biomedical applications, sensors and biosensors, and packaging, among others. Liquid crystal polymers are one type of liquid crystal material, combining their intrinsic properties with polymeric flexibility for advanced applications in displays and smart materials. For instance, liquid crystal polymers can serve as drug nanocarriers, forming cubic or hexagonal mesophases, which can be tailored for controlled drug release. Further applications of liquid crystals and liquid crystal polymers include the preparation of membranes for separation processes, such as wastewater treatment. Furthermore, these materials can be used as ion-conducting membranes for fuel cells or lithium batteries due to their broad types of mesophases. This review aims to provide an overall explanation and classification of liquid crystals and liquid crystal polymers. Furthermore, the great potential of these materials relies on their broad range of applications, which are determined by their unique properties. Moreover, this study provides the latest advances in liquid crystal polymer-based membranes and their applications, focusing especially on fuel cells. Moreover, future directions in the applications of various liquid crystals are highlighted.

Preparation and properties of circularly polarized long-lived fluorescent liquid crystal materials based on TS-FRET mechanism

Circularly polarized long-lived fluorescent materials show unique application values in circularly polarized organic light-emitting diodes, advanced anti-counterfeiting materials, and so forth. However, the circularly polarized long-lived fluorescent materials with large luminescence dissymmetry factor (glum) values and long fluorescence lifetime are rarely reported. In this article, we propose to prepare circularly polarized long-lived fluorescent materials based on triplet-to-singlet Förster-resonance energy transfer (TS-FRET) mechanism. We have prepared circularly polarized long-lived fluorescent luminescent materials with large glum values, long fluorescence lifetime, high luminescent quantum yield and large Stokes shift by blending chiral room temperature phosphorescent liquid crystal Chol-C6-DF with achiral fluorescent component Br–C6-Nap. Attributed to the effective TS-FRET process between Chol-C6-DF and Br–C6-Nap, the obtained doped films show long fluorescence lifetime. When the doping amount of Br–C6-Nap is 2 wt%, the fluorescence lifetime can achieve 103 ms. All obtained doped films exhibit high glum values attributed to selective reflection of chiral liquid crystals. As the doping amount of Br–C6-Nap increases, the |glum| value first increases and then decreases, with a maximum of 1.45. In addition, the doped films also possess high solid-state luminescence quantum yield and large Stokes shift, with a maximum value of 54 % and 284 nm, respectively.

Liquid crystal-based reconfigurable antenna for 5G millimeter-wave

This paper proposed a frequency reconfigurable antenna that utilizes a multilayer structure of liquid crystal (LC) material. This antenna design incorporates a three-layer stacked structure to create an LC-injected cavity. The inverted microstrip line structure is designed to be in contact with the LC, serving as both a radiating element and a bias electrode. A parasitic patch is placed at the top of the antenna to enhance bandwidth. To prevent interference with DC and RF sources, a bias tee is integrated into the microstrip line input. Experimental results demonstrate that the proposed antenna exhibits excellent impedance matching and stable radiation patterns within the operational frequency range. By comparing the simulated performance of the existing LC antenna with our proposed design, the bandwidth is tripled at a center frequency of 30.3 GHz. In addition, the effective area of the proposed reconfigurable antenna (154 mm2) is 24.6% of the area of the previous reconfigurable antenna (625 mm2).