Excellent Transparency Research Articles

Fabrication and characterization of UV-curable thiol-functionalized siloxane elastomers with enhanced adhesion for flexible substrates

The rapid advancement of flexible and wearable devices has increased the demand for substrate materials with excellent elasticity, biocompatibility, and transparency. Polydimethylsiloxane (PDMS) is widely used in these applications due to its advantageous properties. However, its inherently low surface energy limits its adhesion in high-stretchability contexts. To address this issue, various surface modification techniques have been developed, but these methods often alter the intrinsic properties of PDMS or introduce complexities in the manufacturing process. This study proposes elastomers based on ultraviolet (UV)-curable siloxane resins, which retain outstanding flexibility and transparency while significantly enhancing adhesion properties. UV-curable siloxanes were synthesized to prepare elastomers that were evaluated for their mechanical, thermal, and surface properties in comparison with PDMS. Results indicate that the prepared elastomers can be rapidly cured under UV exposure, achieving storage moduli 6 and 37 times higher than those of PDMS at 25°C and 100°C, respectively. Furthermore, thermal conductivity improved by 60%, and the coefficient of thermal expansion was reduced by 26%, demonstrating superior mechanical stability across diverse conditions. Adhesion properties were also markedly enhanced, as shown by peel-test adhesion strength that was 7 times greater than that of conventional PDMS.

Construction of epoxy resin with enhanced flame retardancy, mechanical properties, and satisfactory transparency based on a novel bi‐DOPO and hydrogen‐bonding network

AbstractEstablishment of high‐performance epoxy resin with satisfactory fire safety, mechanical properties, and excellent transparency is urgently desirable, but still remains significant challenges. Herein, a super‐tough yet high flame retardant epoxy resin (EP/BTD) was designed and prepared by incorporating bi‐DOPO structure and hydrogen‐bonding networks. Although the phosphorus content was only 0.69 wt% (10 wt% of bi‐DOPO flame retardant [BTD]), EP/BTD‐10 showed a high limiting oxygen index value (33.4%), satisfactory UL‐94 rating (V‐0), and good heat suppression ability (total heat release [THR] and peak heat release rate [PHRR] reduced to 29.0% and 42.2%, respectively). Furthermore, the flame retardant mechanism of EP/BTD was illustrated and attributed to dual‐phase fire‐retardant effect. Additionally, EP/BTD‐7.5 featured notably mechanical properties, of which the tensile strength, elongation at break and impact strength increased by 44.6%, 40.0%, and 232.6%, respectively, due to hydrogen‐bonding network and π–π interaction. More importantly, EP/BTD maintained high visible light transmittance and excellent UV‐blocking properties. In summary, this work provided a guidance for the development of high‐performance epoxy resin and was expected to expand the practical applications.

Aluminum-Doped Indium Oxide Electron Transport Layer Grown by Atomic Layer Deposition: Highly Efficient and Damage-Resistant Interconnection Solution for All-Perovskite Tandem Solar Cells with 25.46% Efficiency.

In fabricating high-efficiency all-perovskite tandem solar cells (APTSCs) with a p-i-n configuration, the electron transport layer (ETL) plays a critical role in facilitating the transport of photogenerated electrons from the front cell to the recombination layer and protecting the front cell from damage during rear cell fabrication. This study introduces aluminum-doped In2O3 (AIO) films grown by atomic layer deposition (ALD) as a promising ETL for high-efficiency APTSCs. ALD-grown AIO films with an optimized Al concentration exhibit superior charge transport characteristics, excellent transparency, and damage-resistant barrier properties against solution infiltration compared with conventional SnO2 ETLs and undoped ALD In2O3. Using an ALD SnO2/3 at.% AIO bilayer as the electron transport layer, an efficiency of 18.33% is achieved from single-junction wide bandgap perovskite solar cells. Furthermore, the use of ALD SnO2/3 at.% AIO ETL enables the reliable fabrication of APTSCs with negligible solution damage to the front cell and minimized power loss. Consequently, APTSC employing the ALD AIO-based ETL exhibit an excellent photoconversion efficiency of 25.46%, outperforming APTSCs with the ALD SnO2 ETL.

Transparent, Flexible, Responsive Switching "Delayed" Amphiphilic Coatings Designed on the Basis of the Full-Cycle Antifouling Strategy.

Marine fouling on the surface of ships and equipment not only creates problems of enhanced resistance to navigation and increased energy consumption but also leads to unclear vision and inaccurate data collection. Antifouling coatings to resist fouling are effective, but it is difficult to achieve long-lasting fouling protection with a single interface state. Switching the status of the interface by intelligent response is a reasonable way to achieve full-cycle efficient antifouling. In this study, the hydrophobic and active antifouling interface in the initial state was achieved by adopting the fluorine-containing group and the natural extract (citronellol) as the antifouling active site. The switching of the interface relies on silanes, which respond to the generation of zwitterions in a seawater environment. Eventually, the interface switched from the hydrophobic state to the amphiphilic state with delayed formation, which achieved continued antifouling. Based on the full-cycle antifouling concept, the combination of low surface energy and antifouling active ingredients in the initial state sustainably switched surfaces in the midterm (free radicals generated during the hydrolysis process), and amphiphilic interfaces formed by "delays" produced an antifouling effect from the initial stage to the subsequent stage. The excellent antifouling activity (bacterial and diatom attachment inhibition by over 90% and significantly reduced mussel adhesion force), optical transparency, and flexibility of these coatings indicate the potential for the application of antifouling coatings prepared from hyperbranched silicone-based resins; they can also be used for data extraction sensors, underwater probes, marine photovoltaics, and other areas where transparency is required.

Overcoming the Tradeoff of Visible Transparency and Electrical Conductance via Dual Smoothing of Dielectric/Metal Interfaces in Cu-Thin-Layer-Based Transparent Electrodes.

The rapid advancement of flexible optoelectronic devices, such as light-emitting diodes, solar cells, and electrochromic devices, necessitates the development of high-performance flexible transparent electrodes (TEs). Dielectric/metal/dielectric (DMD)-type TEs are promising alternatives to conventional indium tin oxide (ITO) due to the high electrical conductance, excellent visible transparency, and sufficient mechanical flexibility. However, the tradeoff between electrical conductance and visible transparency poses a challenge to performance enhancement. This study introduces an Ar-ion-mediated interface modification method to address this tradeoff by dual smoothing of dielectric/metal interfaces in TiOx/Cu/ZnO TEs. Implementing this dual smoothing methodology significantly enhances both electrical conductance and visible light transmittance, achieving a Haacke figure of merit 200% higher than that of an unmodified otherwise identical structure. The highest figure of merit is 0.113 Ω-1, a record high for Cu-thin-layer-based DMD TEs, far surpassing ITO electrode values. Further, the enhanced optoelectronic performance remains highly durable under severe and simultaneous electrical, thermal, and mechanical stresses, showcasing the potential for significant advances in flexible optoelectronics.

Physical Properties of HfO2 Nano Structures Deposited using PLD

On Quartz substrates, high purity transparent conductive the Di-Oxide of the (HfO2) Nano and micro-structure films were successfully coated. The method of (PLD) Deposition using Pulsed Laser, and the influence of laser energy was investigated. The XRD results revealed two distinct phases, cubic and monoclinic crystal shapes. Peaks in the Fourier-transform infrared (FTIR) spectra showed that HfO2 nanofilm was forming.The findings of the optical characteristics reveal an excellent transparency of nearly 80% (89 percent). As the laser wavelength decreases, the optical energy band gap values for Nanostructure of HfO2 were prepared, with values ranging from 5.24 to 5.53 eV. Also, the EDX results showed the appearance of hafnium peaks and oxygen peaks in varying proportions, which confirms that hafnium oxide is definitely obtained The results of the AFM reveal that when the pulsed laser intensity increases, the average grain diameter values increase from 52.96 to 74.54 nm. With regard to optimum pulsed laser energy, the based on I-V characterization, the generated factor ideality for created diodes was discovered to be decreasing, and the corresponding values of the barrier height grew. The ideality factor of the diode made the optimum pulsed laser energy (1800 mJ) was greater (n=3.1).

Synthesis, Optical, Electrical, Fluorescence, Dielectric, Thermal, and Mechanical Characterization of 3-Aminopyridine (Scaffold in Drugs) Single Crystal

Objectives: To screen the optical, electrical, fluorescence, dielectric, thermal, and mechanical behavior of the 3-aminopyridine single crystal for its suitability in optoelectronic applications. Methods: A good single crystal of 3-aminopyridine (3-AP) was grown by the slow evaporation method. Findings: The lattice parameters of the grown crystal were determined using a single crystal X-ray diffractometer as, a = 6.184 (4) Å, b = 15.350 (6) Å, c = 5.361 (7) Å and the required functional groups C-N, NH2 bonds of 3-AP were recognized by the FTIR studies. The grown crystal was screened using the UV-Vis-NIR spectrum to understand the transmission and absorption character of the crystal. The various optical constants such as absorption coefficient, optical conductivity, and electrical conductivity of the crystal have been determined from the UV-Vis transmission plot. The lower cut-off wavelength of the 3-AP crystal was observed at 250 nm. The band gap of the grown crystal is found to be 4.5 eV. The emission property of the crystal was studied using fluorescence spectra. Violet, blue, and red emissions are observed from the fluorescence spectra. Thermal screening of the 3-AP crystal was performed using TGA and DTA. The 3-AP crystal remains stable up to 220 ºC and then the crystal begins to decompose up to 260 ºC due to the loss of the -NH2 group of the 3-aminopyridine. The Vickers hardness test revealed the nature of the material as soft type with Meyer’s index (n) of 2. The electronic polarization behavior of the crystal was examined using the dielectric study. Novelty: The lower cut-off wavelength of 250 nm, wide band gap of 4.5 eV, excellent transparency in the entire visible and near-infrared region, violet, blue, and red emission by the material are the distinguishing and mandatory features for optoelectronic applications. These features are good as compared to the 3-AP derivatives reported earlier. Keywords: Unit cell, Absorption, Emission, Conductivity, Strength, Loss

Easy fabrication of PVA-CaO-CuO composite films for efficient photocatalyst: Towards distinct luminescence property, morphology and thermal stability

PVA-CuO-CaO composites in the film form were synthesized by loading the different compositions of metal oxides (CuO and CaO) ranging from 5 to 25 wt% via solvent casting approach. The applications of the prepared composites as photocatalysts were assessed together with the findings of photoluminescence (PL) characteristics, optical clarity, morphological features, and thermal properties. Fourier-transformed infrared (FTIR), ultraviolet–visible (UV–vis), and photoluminescence (PL) spectra exposed the systematic and viableintegration of metal oxides (CuO-CaO) into the PVA matrix in PVA-CuO-CaO composites. The modifications of PL property of PVA-CuO-CaO composites were recognized rather than bare PVA. The prepared composite films exhibited excellent optical transparency irrespective of the addition of metal oxides. Both TGA and DSC data showed that the thermal properties of the composites could be significantly enhanced by incorporating CuO and CaO. DSC measurements demonstrated that the Tm of PVA-CuO-CaO composites is improved substantially (∼7 to 38 °C) than PVA. The distinct morphological structures of the obtained composites were identified with variations in CuO and CaO addition remaining diameter in the 30–200 nm range. The photocatalytic assessments revealed the better photocatalytic performance of PVA-CuO-CaO composites for removing methylene blue (MB) than bare PVA. By eliminating organic pollutants, the current study may provide a new perspective on the preparation of water-processable PVA-CuO-CaO photocatalysts for wastewater management.

Advances in and Future Perspectives on High-Power Ceramic Lasers

Advancements in laser glass compositions and manufacturing techniques has allowed the development of a new category of high-energy and high-power laser systems which are being used in various applications, such as for fundamental research, material processing and inertial confinement fusion (ICF) technologies research. A ceramic laser is a remarkable revolution in solid state lasers. It exhibits crystalline properties, high yields, better thermal conductivity, a uniformly broadened emission cross-section, and a higher mechanical constant. Polycrystalline ceramic lasers combine the properties of glasses and crystals, which offer the unique advantages of high thermal stability, excellent optical transparency, and the ability to incorporate active laser ions homogeneously. They are less expensive and have a similar fabrication process to glass lasers. Recent developments in these classes of lasers have led to improvements in their efficiency, beam quality, and wavelength versatility, making them suitable for a broad range of applications, such as scientific research requiring ultra-fast laser pulses, medical procedures like laser surgery and high-precision cutting and welding in industrial manufacturing. The future of ceramic lasers looks promising, with ongoing research focused on enhancing their performance, developing new doping materials and expanding their functional wavelengths. The ongoing progress in high-power ceramic lasers is continuously expanding the limits of laser technology, therefore allowing the development of more powerful and efficient systems for a wide range of advanced and complex applications. In this paper, we review the advances, limitations and future perspectives of ceramic lasers.

Efficient synthesis of cellulose acetate through one-step homogeneous acetylation of cotton cellulose in binary ionic liquids

Cellulose acetate (CA) is an important cellulose derivative with a wide range of applications. To adopt a more efficient and environmentally friendly method to synthesize cellulose acetate, a binary ionic liquid mixture of 1-butyl-3-methylimidazole chloride salt (BmimCl) and 1-butyl-3-methyldihydroimidazole phosphate (BmimH2PO4) was used. Compared to the conventional methods, this approach didn't require pre-activation of cellulose and the process of homogeneous acetylation proceeded without a catalyst. By simply adjusting the reaction conditions, cellulose acetate with a degree of substitution (DS) in the range of 0.83–3.0 was produced by one-step homogeneous acetylation without hydrolysis. Furthermore, the cellulose acetate film produced by solvent casting exhibited smooth surface characteristics, 95 % transparency, and 57.9 MPa tensile strength. Therefore, this study highlights the importance of using binary ionic liquid mixtures for facile synthesis of cellulose acetate. Due to their excellent transparency and mechanical properties, newly synthesized cellulose acetate films could replace commercial films.

Hierarchy-constructed superhydrophobic and transparent coating modified intraocular lens by layer-by-layer self-assembly for glistening reduction and antiadhesion

Intraocular lens (IOL) implantation surgery is the most effective treatment for cataract. However, glistening formed by the incoming liquid microvacuoles can significantly damage postoperative visual quality after prolonged implantation, for which there is still lack of effective clinical treatment. In this study, inspired by the amazing water-repellency of natural superhydrophobic surface, a functionalized IOL material modified with the superhydrophobic and transparent coating was prepared using layer-by-layer electrostatic self-assembly technique combined with fluorination. After the alternate deposition of multiple cationic/anionic polyelectrolytes and silica nanoparticles of varying sizes on IOL materials, the constructed multilayered films with special surface roughness were further fluorinated to reduce surface energy. In addition to its excellent superhydrophobicity and transparency, this multilayered coating could efficiently eliminate the glistening formation of IOL under accelerated condition in vitro. Furthermore, the in vitro experiments with water droplets, cells, and bacteria suggested the superior antiadhesion property of such coating modified materials. The biocompatibility evaluation, both in vitro and in vivo, demonstrated the great biocompatibility of the materials modified with superhydrophobic and transparent coating. Therefore, this multilayered coating with excellent superhydrophobic and transparent characteristics can provide an available approach aiming at anti-glistening and antiadhesion of IOL materials. Advances in the fabrication process of surface coating with specific functions will enhance the practical application and clinical success of modified IOLs.

Polyimide Aerogel Fiber Bundles for Extreme Thermal Management Systems in Aerospace Applications.

Aerogel fibers are an emerging class of ultralightweight materials, which, compared to conventional bulk monolithic and aerogel films, provide better flexibility and extensibility. Despite the recent advancements in this field, due to their highly porous structure, their mechanical properties can be deteriorated. Inspired by the textile industry, we report the development of aerogel fiber bundles with twisted structures as a promising strategy to enhance the mechanical performance and practicality of aerogel fibers. Polyimide (PI) aerogel fibers were prepared via the sol-gel confined transition method. The fibers showed a unique nanostructured assembly with high specific surface area, excellent optical transparency, outstanding flexibility at diverse extreme conditions, self-extinguishing behavior, and superior thermal insulation performance. Using PI aerogel fibers as the backbone, aerogel fiber bundles in various configurations were designed and fabricated. A systematic study was performed to analyze the effect of design parameters on the mechanical performance of the bundles. Results revealed an optimal twist level for bundles, leading to a peak in mechanical properties across various bundle configurations. The observed improvement in mechanical properties was attributed to increased fiber-to-fiber binding strength, enhanced friction, and interlocking mechanism of fibers, underscoring the potential of the optimized twist level for enhancing the performance of aerogel fiber bundles. Overall, the development of aerogel fiber bundles holds great promise in revolutionizing the production of high-performance ultralightweight materials for thermal management applications.

Starch-calcium inclusion complexes: Optimizing transparency, anti-fogging, and fluorescence in thermoplastic starch

With the increasing demand for anti-fogging transparent material and environmental concern, developing sustainable intrinsically hydrophilic and anti-fogging thermoplastic material is important. In this work, thermoplastic starch (TPS) films with good anti-fogging and optical properties were prepared via coordinative interactions with calcium chloride (CaCl2), zinc chloride (ZnCl2) and magnesium chloride (MgCl2). Among them, TPS with the incorporation of CaCl2 exhibited excellent anti-fogging and high optical transparency. Notably, the haze of TPS-0.2Ca just increased from 2.5 % to 3.8 %, with transparency remaining robust at 80 %. FTIR, XPS and 2D-WAXD results demonstrated the formation of inclusion complexes between Ca2+ and hydroxyl groups, which could modulate the hydrophobicity and hydrophilicity of TPS. Moreover, DMA, POM, and AFM results revealed that the formation of starch-calcium inclusion complex was crucial for achieving uniform intensity distribution, reduced crystalline areas, minimized light scattering, and decreased surface roughness, thereby contributing to the high transparency and low haze of TPS-Ca. Furthermore, TPS-Ca samples exhibited inherent fluorescent properties under UV light, showing the potential as disposable and eco-friendly fluorescence materials. This work provides new insights into design of sustainable TPS-based materials that combine robust antifogging performance with advanced optical property.

Micro-injection molding applied to production of optical products-example of lens

Abstract Injection moulding is essential for the mass production of plastic products. This study focuses on the application of micro-injection moulding to produce optical products using self-designed moulds and core structure processing techniques. The chosen material for injection is acrylic PMMA, renowned for its excellent finish, weather resistance, heat resistance, transparency, and gloss. Post-injection, the products were evaluated for their optical properties. The TRIZ analysis provided insights into problem-solving directions and cost reduction strategies. The implementation of a one-mould, four-cavity design enabled mass production, significantly enhancing production efficiency.

Highly Transparent, Mechanically Robust, and Conductive Eutectogel Based on Oligoethylene Glycol and Deep Eutectic Solvent for Reliable Human Motions Sensing.

Recently, eutectogels have emerged as ideal candidates for flexible wearable strain sensors. However, the development of eutectogels with robust mechanical strength, high stretchability, excellent transparency, and desirable conductivity remains a challenge. Herein, a covalently cross-linked eutectogel was prepared by exploiting the high solubility of oligoethylene glycol in a polymerizable deep eutectic solvent (DES) form of acrylic acid (AA) and choline chloride (ChCl). The resulting eutectogel exhibited high transparency (90%), robust mechanical strength (up to 1.5 MPa), high stretchability (up to 962%), and desirable ionic conductivity (up to 1.22 mS cm-1). The resistive strain sensor fabricated from the eutectogel exhibits desirable linear sensitivity (GF: 1.66), wide response range (1-200%), and reliable stability (over 1000 cycles), enabling accurate monitoring of human motions (fingers, wrists, and footsteps). We believe that our DES-based eutectogel has great potential for applications in wearable strain sensors with high sensitivity and reliability.

Ultraviolet-cured polyurea-polyurethane acrylate/polysiloxane hybrid anti-fouling coatings with superior mechanical properties, transparency, and durability

The demand for rapidly preparing omniphobic liquid-like anti-fouling coatings has become increasingly important across a wide range of applications. However, achieving a rapid fabrication process that results in coatings with effective anti-fouling properties, alongside the comprehensive performance of the coatings such as hardness, flexibility, transparency, and abrasion resistance, remains a significant challenge. Herein, this paper proposes a synergistic strategy combining ultraviolet (UV) curing and organic/inorganic hybridization, which involves the rapid cross-linking of hyperbranched methacryloxypropyl polysiloxanes (HMO), polyurea-polyurethanes acrylate (SPUA) and bis-vinyl terminated polydimethylsiloxanes (PDMS-bvt) containing multiple double bonds under UV curing for just 60 s. Notably, HMO imparts excellent hardness (7H) and abrasion resistance, while SPUA enhances the coating's flexibility (2 mm bending diameter) and adhesion (5B). The anti-fouling properties of the coating are attributed to PDMS-bvt, which provides self-cleaning, anti-graffiti, and anti-fingerprint capabilities. Additionally, the coating's hydrophobicity and smooth surface significantly reduce ice adhesion strength (21.13 ± 6.9 kPa), offering a passive anti-icing effect. Furthermore, the coating exhibits excellent transparency, with a transmittance of >92 % in the visible region. The coating exhibits remarkable durability, maintaining its anti-fouling performance after exposure to mechanical abrasion (500 abrasion cycles and 1000 bending/release cycles), chemical corrosion (24 h of immersion in organic solutions), and UV aging (168 h). This strategy presents a fast and effective method for preparing multifunctional anti-fouling coatings, with potential applications on foldable screens, high-rise building glazing, and curved surfaces.

Water‐Involved Carbon‐Nitrogen Triple‐Bond Monomer Based Polymerization toward Processable Functional Polyamides under Ambient Conditions

AbstractPolyamide plays a pivotal role in engineering thermoplastics. Constrained by the harsh conditions and arduous procedures for its industrial synthesis, developing facile synthesis of polyamides is still challengeable and holds profound significance. Herein, we successfully utilized water as one of the monomers to synthesize functional polyamides under ambient conditions. A powerful multicomponent polymerization of water, isocyanides, and chlorooximes was established in phosphate‐buffered saline. Soluble and thermally stable polyamides with high weight‐average molecular weights (up to 53 900) were obtained in excellent yields (up to 95 %). The polymerization exhibits unique polymerization‐induced emission characteristics, successfully converting non‐emissive monomers into unconventional emissive polymers. Notably, the resultant polyamides could undergo effective post‐modification via the hydroxyl‐yne click reaction. By incorporating various functional groups into the polyamide, its emission color could be fine‐tuned from blue to green and to red. Remarkably, the refractive index (n) of the polyamide at 589 nm could be increased from 1.6173 to 1.7227 and the Δn could be unprecedentedly as high as 0.1054 for non‐heavy atom‐containing polymers after post‐modification, and its micron‐thick films exhibited excellent transparency in the visible region. Thus, this work not only establishes a powerful polymerization toward novel polyamides but also opens up an avenue for their versatile functionalization.

Water-Involved Carbon-Nitrogen Triple-Bond Monomer Based Polymerization toward Processable Functional Polyamides under Ambient Conditions.

Polyamide plays a pivotal role in engineering thermoplastics. Constrained by the harsh conditions and arduous procedures for its industrial synthesis, developing facile synthesis of polyamides is still challengeable and holds profound significance. Herein, we successfully utilized water as one of the monomers to synthesize functional polyamides under ambient conditions. A powerful multicomponent polymerization of water, isocyanides, and chlorooximes was established in phosphate-buffered saline. Soluble and thermally stable polyamides with high weight-average molecular weights (up to 53 900) were obtained in excellent yields (up to 95 %). The polymerization exhibits unique polymerization-induced emission characteristics, successfully converting non-emissive monomers into unconventional emissive polymers. Notably, the resultant polyamides could undergo effective post-modification via the hydroxyl-yne click reaction. By incorporating various functional groups into the polyamide, its emission color could be fine-tuned from blue to green and to red. Remarkably, the refractive index (n) of the polyamide at 589 nm could be increased from 1.6173 to 1.7227 and the Δn could be unprecedentedly as high as 0.1054 for non-heavy atom-containing polymers after post-modification, and its micron-thick films exhibited excellent transparency in the visible region. Thus, this work not only establishes a powerful polymerization toward novel polyamides but also opens up an avenue for their versatile functionalization.

Study on UV-Curable Acrylic Clear Viscoelastic Materials with Grafted Structures

Flexible substrates are crucial for wearable electronic strain sensors, but achieving biocompatibility, low cost, and aesthetic appeal alongside good mechanical performance remains challenging. Acrylic-based clear viscoelastic films (CVFs) are gaining attention due to their excellent transparency and potential for enhanced mechanical properties. This study synthesized copolymers CVF1-4 with varying branch content using soft monomers 2-ethylhexyl acrylate (2-EHA), butyl acrylate (n-BA), and functional monomer acrylic acid (AA). Employing a "grafting-through" strategy, small molecule monomers, ATRP-synthesized oligomer pBA25, and photoinitiator 1,6-hexanediol diacrylate (HDDA) were in-situ polymerized under UV light to form transparent, flexible elastic films CVF1-4. Between -20 to 80 C, CVF1-4 demonstrated excellent mechanical properties such as low modulus (in the kPa range), low glass transition temperature (below -20 C), large deformation (500-600%), and high strain recovery rate (>95%). Among them, CVF3 with 15% branching showed a balanced comprehensive performance, exhibiting primarily elastic behavior at room temperature. Therefore, selecting appropriate molecular composition and grafting structure provides a simple and customizable solution for optimizing CVF properties.

Highly Stable Binary Cross‐Linkable Organic Nonlinear Optical Materials Using Different Acceptors Based on Huisgen Cycloaddition Reaction

Comprehensive SummaryHow to obtain organic electro‐optic materials with large electro‐optic coefficients, high glass transition temperature, and good optical transparency remains a challenge in this field. To solve this problem, we introduce groups that can undergo Huisgen cycloaddition reactions into the donor and electron bridge of chromophores with large hyperpolarizability using tetrahydroquinoline as the donor. Binary cross‐linkable chromophores TLD1‐2 with CF3‐TCF as the acceptor and chromophores TLD3‐4 with 5Fph‐TCF as the acceptor were synthesized. After poling and crosslinking, the Tg of TLD1/TLD2 and TLD3/TLD4 were raised to 152 and 174 °C, respectively. The electro‐optical coefficients of chromophores TLD1/TLD2 and TLD3/TLD4 were as high as 312 pm/V and 287 pm/V, respectively. The long‐term alignment stability test showed that after being left at 85 °C for 500 h, the cross‐linked film TLD3/TLD4 can still maintain more than 98% of the original electro‐optical coefficient value, which is higher than that of TLD1/TLD2 (93%). The chromophore TLD3‐4 exhibited much blue‐shifted maximum absorption wavelengths (~40 nm) compared to TLD1‐2 which was beneficial for reducing optical loss in the device. The combination of high electro‐optic coefficient, strong stability, and excellent optical transparency makes the TLD series of binary cross‐linked materials very promising for practical high‐performance electro‐optic devices.