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Circularly polarized luminescence (CPL) materials have shown great application potential in the fields of three-dimensional displays, bioimaging, and information encryption and decryption. The chirality enhancement of CPL by a physical chiral environment, involving the delivery of structural asymmetry from helical architectures to luminescent molecules through electromagnetic field resonance, represents an innovative approach for constructing high-performance CPL materials. Liquid crystal polymers (LCPs), possessing helical superstructures, show great potential in constructing CPL systems. By modulating the chirality transfer from the helical structural environment of LCPs to luminescent sources via distinct strategies, the CPL properties of LCP-based composites are readily generated and tailored. This review summarizes the newest construction strategies of LCP-based CPL materials and provides a perspective on their emerging applications and future opportunities. This review can deepen our understanding of the fundamentals of chirality transfer and shed light on the development of functional chiral luminescent materials.

A 2 × 2 ultra-wideband MIMO flexible antenna with a low profile and good isolation was designed for Internet of Things (IoT) realms and wearable devices. The antenna elements were placed on a novel flexible substrate of liquid crystal polymer (LCP) with compact dimensions fed by a coplanar waveguide (CPW). In order to ameliorate isolation, the cross-shaped decoupling branches were placed among the antenna elements. The proposed UWB antenna can operate from 2.9 GHz to 10.86 GHz with a good reflection coefficient of S11 < −10 dB as well as a high isolation better than 22 dB. Its operating bands include 5G, WiFi, X-band, etc. Moreover, the parameters of diversity performance were also tested. These parameters included an average gain of approximately 4 dB, a low ECC of less than 0.01, and good diversity gain of 9.999. The flexible MIMO antenna performs well in bending and on-body conditions. To sum up, the antenna has good prospects in IoT applications and wearable fields.

An aromatic copolyester liquid crystal polymer (LCP) was introduced into carbon-fiber-reinforced polyamide–polyurethane (CF/PA-PU) composites through melt blending to improve the tribological properties of the composites. The effects of LCP on the mechanical, processing, and thermal properties of CF/PA-PU composites were compared to those of commonly-used graphite (Gr). The results showed that at 5 wt.% LCP content, the coefficient of friction (COF) was decreased by 16.06%, and the wear rate by 32.22% in the LCP/CF/PA-PU composite compared to the CF/PA-PU composite. Furthermore, using LCP instead of Gr showed significantly improved mechanical properties and reduced processing viscosity. The tensile strength of 5%LCP/CF/PA-PU composite could reach 99.08 MPa, while the equilibrium torque was reduced, being 26.85% higher and 18.37% lower than those of CF/PA-PU composite, respectively. The thermal stability of LCP/CF/PA-PU composites was also enhanced. The addition of 5 wt.% LCP to CF/PA-PU composite increased the initial decomposition temperature by 14.19% compared to CF/PA-PU. In sharp contrast, the addition of Gr increased equilibrium torque and actual processing temperature leading to processing difficulties and instability. This approach offers a novel strategy for tribological applications and tackles the problem of high viscosity in CF/PA-PU composites.

Fiber-shaped electrical heaters with high flexibility and excellent adaptability make an ideal candidate for the application of wearable electronics but still suffer from low strength and poor durability. Herein, an all-in-one Joule-heating fiber capable of outstanding mechanical properties, good heating efficiency, and long-term stability is reported by using polymer-assisted metal deposition to firmly coat Cu nanoparticles on high-performance liquid crystal polymer (LCP) fibers. Taking advantage of LCP, the resultant fibers exhibit a satisfying temperature threshold (up to 200 °C) and immense strength (2.94 GPa). By virtue of dense and continuous Cu film, these fibers show low electrical resistance (5.51 Ω/cm) and an ultrafast response rate (12.6 °C·s−1) at low supplied voltages (0.5–3.5 V). Benefiting from the levodopa/polyethyleneimine interface design, such fibers maintain nearly constant resistance after repeatable bending, folding, and even washing (50 cycles). Based on the above-mentioned merits, a wearable patch with a Joule-heating function is knitted by using as-made fibers to offer therapeutic benefits for human body joints. This work demonstrates prospective potential for enriching the challenging applications of fiber-shaped electrical heating systems.

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.

Electromagnetically induced transparency (EIT) metamaterials (MTMs) based on the bright-dark mode theory have gained great interest in slow light, sensing, and energy storage in recent years. Typically, various split ring resonators with magnetic response have been proposed as dark resonators in EIT MTMs. Here, we have employed a cut-wire (CW) and two electric-field-coupled inductor-capacitor (ELC) resonators with a pure electrical response on a liquid crystal polymer (LCP) substrate with a low loss tangent to fulfill the EIT effect in the terahertz (THz) region. The former works as the bright mode, and the latter functions as the dark mode. The EIT phenomenon results from the destructive interference between these two modes, which can be verified by numerical simulation and near field distribution. In addition, a Lorentz oscillator model was studied to quantitatively analyze the relationship between the coupling strength and the coupling distance. As a demonstration, an EIT MTM device with 5000 units was fabricated and characterized, which showed a transmission window with a peak value of 0.75 at 0.414 THz. This work may inspire new multifunctional EIT MTMs, especially the flexible applications at THz frequencies.

Vividly colored cholesteric liquid crystal polymer network (CLCN) patterns based on epoxy resin are used in decorative and anti-counterfeiting applications. These films are typically prepared via cationic photopolymerization and post-polymerization to achieve a high cross-linking degree. In this work, the cross-linking degree is controlled by varying the UV irradiation dosage during photopolymerization. Following this, the reflection band of the CLCN film changes after removing non-cross-linked compounds with acetone. Leveraging the low cationic polymerization rate and the chain termination capability of methanol, a structurally colored CLCN film with regionally tailored cross-linking was fabricated. With the treatment of acetone, a colorful pattern was observed. Moreover, upon immersion in methanol, the film swelled, revealing a colorful pattern. After the evaporation of methanol, the pattern disappeared. Consequently, this CLCN film holds significant potential for information encryption applications.

Crosslinked liquid crystal polymers (CLCPs) are a promising type of smart polymer material with excellent two‐way shape memory behavior under the stimulation of various external conditions. Among the various external stimuli, light with the advantages of instantaneity, high accuracy, remote controllability, pollution‐free, etc., has been widely used in the control of CLCPs. Traditional photoresponsive CLCP systems based on photoisomerization are limited by the penetration depth of ultraviolet light, the number of useful photochemical reactions, and long‐term stability. Recently, a strategy for designing photoresponsive CLCPs based on the photothermal effect has attracted scientific attention. Photothermal materials in the CLCP matrix can convert light into heat through plasma resonance or energy transition under the light irradiation of a certain wavelength, and locally heat the CLCP matrix to beyond the liquid crystal‐to‐isotropic phase transition temperature, thus achieving reversible macroscopic deformation. Combining photothermal materials and CLCPs can decrease the dependence on specific photosensitive groups such as azobenzene mesogens and endow photoresponsive CLCPs with design flexibility. Herein, the photothermal‐responsive CLCPs under the stimulations of different light wavelengths and their application fields are reviewed. In addition, the current challenges in the field of photothermal‐responsive CLCPs are summarized, and a brief outlook on future development is proposed.

In recent years, π-conjugated liquid crystalline molecules with optoelectronic functionalities have garnered considerable attention, and integrating these molecules into side-chain liquid crystalline polymers (SCLCPs) holds potential for developing devices that are operational near room temperature. However, it is difficult to design SCLCPs with excellent processability because liquid crystalline mesogens are rigid rods, have low solubility in organic solvents, and have a high isotropization temperature. Recently, we developed near-room-temperature π-conjugated nematic liquid crystals based on “bridged stilbene”. In this work, we synthesized a polyacrylate SCLCP incorporating a bridged stilbene that exhibited a nematic phase near room temperature and could maintain liquid crystallinity for more than three months. We conducted a thorough phase structure analysis and evaluated the optical properties. The birefringence values of the resulting polymers were higher than those of the corresponding monomers because of the enhanced order parameters due to the polymer effect. In addition, the synthesized polymers inherited mesogen-derived AIE properties, with high quantum yields (Φfl = 0.14–0.35) in the solid state. It is noteworthy that the maximum fluorescence wavelength exhibited a redshift of greater than 27 nm as a consequence of film formation. Thus, several unique characteristics of the SCLCPs are unattainable with small molecular systems.

Optically responsive materials are applied in sensing, actuators, and optical devices. One such class of material is dye-doped liquid crystal polymers that self-assemble into cholesteric mesophases that reflect visible light. We report here the synthesis and characterization of a family of linear and mildly crosslinked terpolymers prepared by the ROMP of norbornene-based monomers. The three monomers were composed of (i) rhodamine dye through one or two norbornene end groups utilizing flexible C10-alkane spacers, (ii) a cholesteryl liquid crystal (LC) using C9-alkane spacers, and (iii) PEG side chains. We investigated how these architectural variations in these terpolymers impacted their hierarchically self-assembled mesophase properties. We probed their composition, morphology, thermal, mechanic, photochromic, and mechanochromic properties using, inter alia, 1H NMR spectroscopy, DSC, temperature-dependent SAXS, diffuse reflectance UV-vis spectroscopy, and optical polarization microscopy. The new terpolymers exhibited architecture-dependent thermochromic, mechanochromic, and piezochromic properties arising from LC–rhodamine dye interactions. We found that a compromise between the rigidity and flexibility of the terpolymer architectures needed to be stricken to fully express stimuli-responsive properties. These terpolymers also showed distinctly different properties compared to those of a previously reported structurally related liquid crystalline copolymer made from two monomers. These findings help to define the design principles for optimally stimuli-responsive liquid crystalline polymers.