Transparent Poly Research Articles

TwinDemic detection: A non-enzymatic signal amplification system for on-site detection of multiple respiratory viruses

The simultaneous occurrence of multiple respiratory viruses, such as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2 [CoV]) and influenza A virus (IAV), presents a challenge for accurate diagnosis and treatment. To address this, we developed the TwinDemic Detection (TDD) system—an integrated point-of-care diagnostic platform that can simultaneously detect CoV and IAV using a multi-respiratory virus identification approach. The TDD system contains a transparent poly(methyl methacrylate) microfluidic chip with a hydrogel-based gene detection sensor and a handheld fluorescence reader. This system uses a fuel-stimulated DNA probe to detect viral RNA and amplify the fluorescence signal without the need for enzymatic or thermal controls. The system’s performance was tested using 45 human nasopharyngeal samples; results revealed positive and negative predictive values of 93.3 % and 96.7 % for CoV, and 100 % and 96.7 % for IAV, respectively. This system enables the accurate and simultaneous detection of multiple respiratory viruses for public health surveillance and shows potential for use as a point-of-care molecular test to monitor a wider range of viruses in the future.

Flexible and Transparent Electrovibration-Based Haptic Display with Low Driving Voltage.

Electrovibration haptic technology, which provides tactile feedback to users by swiping the surface with a finger via electroadhesion, shows promise as a haptic feedback platform for displays owing to its simple structure, ease of integration with existing displays, and simple driving mechanism. However, without electrical grounding on a user's body, the frequent requirement of a high driving voltage near 50 V limits the use of electrovibration haptic technology in practical display applications. This study introduces materials and fabrication strategies that considerably reduce the driving voltage. We used a transparent poly(vinylidene fluoride) (PVDF) thin film deposited on transparent conductive polymers through a simple spin-coating process, thereby enabling easy integration with existing display technologies. The high dielectric constant characteristics of PVDF enabled the production of tactile cues at low voltages (approximately 15 V), which are within the safety limits of common electronics. We verified the feasibility of our electrovibration haptic feedback system on the basis of the absolute threshold voltage through two-alternative forced choice psychological tests. The results revealed that the PVDF dielectric layer exhibited a relatively lower absolute threshold than commonly used polymer films, which possess a relatively lower dielectric constant. To validate the tactile attributes, a Likert five-point scale survey was conducted, considering flat, concave, and convex curvatures. The results indicated that our haptic device can render diverse surface textures, such as "hairy" and "groovy", on the fingertips through the control of applied pulse width modulated voltage signals.

Burning and flame extinction patterns of PMMA under external heating and oxygen deficiency

The paper presents an experimental study investigating the impact of under-oxygenated conditions on the burning characteristics and flame extinction of horizontal transparent poly(methyl-methacrylate) (PMMA) slabs subjected to external heating. Small-sized solids are exposed to various constant levels of radiant heat flux in a nitrogen-diluted environment at ambient pressure. The study aims to understand the multivariable dependence of PMMA combustion on oxygen and heating levels. The analysis goes beyond the study of global and local variables to provide an understanding of the mechanisms involved, revealing a notable effect on burning characteristics and flame extinction mechanisms by blow-off. The results provide a detailed assessment of the surface energy balance and flame bulk properties. The results demonstrate good repeatability up to a certain oxygen limit, beyond which the flame combustion regime exhibits stochastic behaviour. The study of heat transfer mechanisms has revealed that flame radiation and external heating play a predominant role in the heating of horizontal solid fuels, In contrast, within the flame, convection is the main contributor to solid heating, rather than flame radiation. Solid characteristics show linear trends proportional to oxygen depletion, while gas phase characteristics show monotonic trends strongly influenced by the changing combustion regime. The surface temperature of the solid is highly sensitive to the test conditions that affect the energy balance. Dimensionless parameters are developed and data are correlated with existing literature. The analysis demonstrates that the linear or monotonic trends are maintained regardless of external heating. Finally, models are proposed and validated to predict both the extinction limit and the burning rate independently of irradiance and oxygen levels.

Design of a double-layered material as a long-acting moisturizing hydrogel-elastomer and its application in the field protection of elephant ivories excavated from the Sanxingdui Ruins.

The sudden change in the environment from a dark, low-oxygen, low-temperature, high-humidity underground stable environment to an environment with much-improved temperature and humidity, a high oxygen content, enhanced light exposure, and increased harmful organisms has greatly affected the stability of the ivory unearthed from the Sanxingdui site. Therefore, the implementation of an effective emergency protection strategy for ivory excavated at Sanxingdui is imperative and urgently needed. However, the current gauze technique used at many archaeological sites suffers from short timescales, poor transparency of the material, and susceptibility to reverse osmosis of the ivory. Therefore, in this study, a transparent poly(acrylamide-acrylic acid) (P(AM-AA)) hydrogel-poly(dimethylsiloxane) (PDMS) elastomer bilayer was designed for the effective protection of excavated ivory. In this system, a hydrophobic PDMS elastomer was constructed on the surface of the hydrogel by the introduction of a silane coupling agent to inhibit the loss of water from the hydrogel to the external environment, thus prolonging the preservation of ivory by the protective material. The covalent interface between the hydrogel and the elastomer allowed the double-layer composite to exhibit excellent interfacial bonding. In addition, the double-layer material demonstrated a high mechanical strength of 1.2 MPa and a water binding ratio of ∼31%, which allowed it to form strong hydrogen bonds with the silanol structure. When the hydrogel was placed in an air environment (temperature: 25 °C; relative humidity: 65% RH), the water-retention rate of the double-layer material was still more than 60% after 5 days, thus the double-layer material showed excellent performance. Meanwhile, the double-layer material had a transmittance of more than 90% and exhibited a high degree of transparency, which makes it possible to promptly observe the changes occurring on the surface of the ivory. The combination of the aforementioned properties makes the bilayer a promising material for moisturizing and protecting excavated ivory in situ. Based on these properties, we used the prepared P(AM-AA)/PDMS double-layer material directly for wrapping the K8 ivory with the highest water content at Sanxingdui. The weight retention rate of the ivory was around 70% after 50 days of placement (temperature: 25 °C; relative humidity: 60% RH), the macroscopic morphology did not change significantly and the mechanical properties of the wrapped ivory were basically unchanged, which indicated that the double-layer material has an excellent on-site protection effect on the ivory excavated from Sanxingdui. This work provides new ideas and methods for the temporary conservation of wet heritage.

Synthesis of Highly Transparent Semi-aromatic Poly(amide–imide)s from Alicyclic Diamines and Dicarboxylic Acids Derived from 2,2'-Di(trifluoromethyl)benzidine with Trimellitic Anhydride

Synthesis of Highly Transparent Semi-aromatic Poly(amide–imide)s from Alicyclic Diamines and Dicarboxylic Acids Derived from 2,2'-Di(trifluoromethyl)benzidine with Trimellitic Anhydride

Synthesis and properties of transparent PMMA/cellulose nanocomposites prepared by in situ polymerization in green solvent

AbstractIn order to contribute to the demanded sustainability transparent poly(methyl methacrylate) (PMMA) composites with cellulose nanocrystals (CNC) up to high shares of 50 wt% were prepared by in situ radical polymerization in green solvent Cyrene. The weight average molecular weights of PMMA were in the range from 144,000 to 160,000 g mol−1 and the dispersity was in the range of 1.49 to 1.89 with high conversion of monomer to polymer. The DSC thermal analysis showed that the glass transition temperature of pure PMMA was at 99°C while in composites increased from 103°C up to 129°C with the increase of CNC from 1 wt% to 50 wt%. TGA shows that the addition of CNC does not have a significant effect on the thermal stability of PMMA. In composites Young's modulus increases with the increasing CNC ratio and composites with 50 wt% of CNC showed more than twice the modulus of the PMMA matrix. The SEM images indicate uniform distribution of CNC in polymer matrix. The transparent and semitransparent PMMA/cellulose composites of improved sustainability with higher modulus of elasticity and glass transition temperature can be used as lightweight materials for a wide range of technical and everyday applications as well as optical lenses or acoustic lenses for ultrasound transducers and other devices.Highlights Cellulose nanocrystals/PMMA composites fabricated by a green in situ process. Synthesized PMMA matrices have high molecular weights. Improved elastic modulus and glass transition temperature were achieved. Prioritizing eco‐friendly chemicals for a greener production approach.

Minimizing the polymer content of compressed transparent synthetic wood from renewable biomass sources: A comparative life cycle assessment

Transparent wood derived from renewable biomass resources has an enormous potential for utilizing in constructions, electrons devices, energy storage, etc. However, due to its high polymer content, the currently described transparent wood could not be developed in a sustainable manner. Herein, a feasible strategy for synthesizing compressed transparent wood was proposed to minimize the content of polymerized poly(methyl methacrylate) in composites, involving the poly(methyl methacrylate) partial-filling into the delignified wood and densification. This synthesis method prompted a substantial reduction of poly(methyl methacrylate) content (58.8%) in the obtained compressed transparent wood contrasted with the typical transparent wood (91.8% poly(methyl methacrylate) content). Besides, an ideal optical transmittance of 77.9% with 0.4 mm thickness and an optical haze of 49.2% with 0.7 mm thickness at 800 nm wavelength were achieved. Also, the improved tensile strength and flexural strength of compressed transparent wood were up to 85.0 MPa and 145.3 MPa, respectively. Additionally, a comparative life cycle assessment was conducted to assess the environmental impacts. The total environmental impact score was separately reduced by 23%, and 28% compared to the typical transparent wood and poly(methyl methacrylate) polymer, suggesting the feasibility of sustainable manufacture of transparent wood materials by decreasing polymer content. The compressed transparent wood also showed much lower thermal conductivities (0.28–0.31 W/mk) than glass and contributed to offering uniform illumination.

Self-Healing Transparent Poly(dimethyl)siloxane with Tunable Mechanical Properties: Toward Enhanced Aging Materials for Space Applications.

When exposed to the geostationary orbit, polymeric materials tend to degrade on their surface due to the appearance of cracks. Implementing the self-healing concept in polymers going to space is a new approach to enhancing the lifespan of materials that cannot be replaced once launched. In this study, the elaboration of autonomous self-healing transparent poly(dimethylsiloxane) (PDMS) materials resistant to proton particles is presented. The PDMS materials are functionalized with various compositions of urea and imine moieties, forming dynamic covalent and/or supramolecular networks. The hydrogen bonds induced by the urea ensure the formation of a supramolecular network, while the dynamic covalent imine bonds are capable of undergoing exchange reactions. Materials with a broad range of mechanical properties were obtained depending on the composition and structure of the PDMS networks. As coating applications in a spatial environment were mainly targeted, the surface properties of the polymer are essential. Thus, percentages of scratch recovery were determined by AFM. From these data, self-healing kinetics were extracted and rationalized based on the polymer structures. The obtained data were in good agreement with the relaxation times determined by rheology in stress relaxation experiments. Moreover, the accelerated aging of materials under proton irradiation, simulating a major part of the geostationary environment, revealed a strong limitation or disappearance of cracks while keeping the transparency of the PDMS. These promising results open routes to prepare new flexible autonomous polymeric materials for space applications.

Bioinspired fabrication of transparent poly(vinyl alcohol)-based films with excellent strength, ultraviolet blocking performance, and water vapor barrier properties

The development of biodegradable plastics with advanced mechanical performance and multifunctionality using renewable materials is highly important for their industrial applications. In this work, a novel eco-friendly and high-performance film was constructed by incorporating lignin–Cu nanoparticles (LNP@Cu) to poly(vinyl alcohol) (PVA) to mimic the granular nanostructure in mussel byssus cuticle. LNP@Cu with abundant o-quinone and o-phenol groups was prepared by the reduction of Cu(NO3)2 using alkaline lignin. The nanoparticles were found to have a spherical morphology with a diameter of approximately 500 nm and the LNP@Cu formed dense hydrogen bonds with the PVA matrix. The mechanical properties of the bioinspired films were dramatically improved and far superior to previously reported PVA films and the majority of engineering plastics. With 5 wt% of LNP@Cu loading, the films showed the optimal tensile strength of 106.9 MPa and toughness of 76.6 MJ m−3, which are 2.27 and 4.04 times as high as those of the neat PVA film, respectively. In addition, the fabricated PVA films exhibited excellent ultraviolet (UV)-shielding property and high transparency. Compared with the pristine PVA film, reinforced films showed decreased hydrophilicity and water vapor transmission rates. Overall, these excellent properties make the fabricated films a great potential for applications in packaging and UV shielding fields, giving inspirations for the design of robust green polymeric materials that meet industrial requirements.

Superlubricity Achieved by a Transparent Poly(vinylpyrrolidone) Composite Hydrogel with Glycerol Ethoxylate in Ocular Conditions.

Efficient and stable ocular lubrication is pivotal in safeguarding eye tissues from wear, especially under repetitive strain due to frequent blinking. Hydrogels have been reported to possess adjustable mechanical properties, biocompatibility, durability, and elevated water content and extensive utilization in medical fields. In this work, a kind of visible photo-cross-linking poly(vinylpyrrolidone) (PVP) hydrogel was designed and synthesized using 1-vinyl-2-pyrrolidone (NVP) and poly(ethylene glycol) diacrylate (PEGDA). To optimize the structure and improve the lubrication performance of hydrogels, we prepared and investigated glycerol ethoxylate (GE)-introduced composite hydrogels (GE/PVP). The results show that the addition of 3 wt % GE helped the hydrogel to form a uniform and dense porous matrix and reduce the frictional coefficient (COF) by over 50%, achieving superlubricity (COF ≈ 0.005). However, with the excessive increase of GE (6 wt %), the structure of the hydrogel is destroyed, inducing pore walls to thin and expand. After that, a lubrication mechanism of the GE/PVP composite hydrogel was proposed, in which the addition of GE reduced the surface tension of the hydrogel, enhanced the hydration ability of the hydrogel, and thus decreased the friction between sliding surfaces. Besides, the cytotoxicity tests show that the composite hydrogels possess good biocompatibility. Overall, the as-synthesized hydrogels hold great potential as lubricating medium for use in ocular applications.

Unusual flexibility of transparent poly(methylsilsesquioxane) aerogels by surfactant-induced mesoscopic fiber-like assembly

High-performance thermal insulators represented by aerogels are regarded as one of the most promising materials for energy savings. However, significantly low mechanical strength has been a barrier for aerogels to be utilized in various social domains such as houses, buildings, and industrial plants. Here, we report a synthetic strategy to realize highly transparent aerogels with unusually high bending flexibility based on poly(methylsilsesquioxane) (PMSQ) network. We have constructed mesoscopic fine fiber-like structures of various sizes in PMSQ gels by the combination of phase separation suppression by tetramethylammonium hydroxide (TMAOH) and mesoscopic fiber-like assembly by nonionic poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) (PEO-b-PPO-b-PEO) type surfactant. The optimized mesoscale structures of PMSQ gels have realized highly transparent and resilient monolithic aerogels with much high bendability compared to those reported in previous works. This work will provide a way to highly insulating materials with glasslike transparency and high mechanical flexibility.

Synthesis of colorless transparent poly(amide-imide) with high modulus and low thermal expansion coefficient and its performance study

To meet the needs of high dimensional stability and high transparency of colorless polyimide (CPI) films, a series of poly(amide-imide) (PAI) films were synthesized by copolymerization of 4,4′-(hexafluoroisopropylidene)diphthalic anhydride (6FDA), terephthaloyl chloride (TPC) and 2,2′-bis(trifluoromethyl)benzidine (TFDB). By adjusting the ratio of 6FDA and TPC, the resulting PAI films exhibited high glass transition temperature (Tg) ranging from 347 to 366 °C, low coefficient of thermal expansion (CTE) values of 4–48 ppm/K, excellent optical performance with transmittances at 400 nm (T400) of 79–83 %, and sufficient mechanical performance. The rigid rod-like amide bonds in the molecular chains increased with the introduction of TPC, which increased the hydrogen bonding between the molecular chains, significantly reduced the CTE and improved the tensile strength and modulus. In particular, PAI-7 exhibited excellent comprehensive performance with a high Tg of 366 °C, a relatively low CTE value of 13 ppm/K, excellent transmittance of 81 % at 400 nm and high tensile modulus of 6.5 GPa, which was expected to be used in the field of flexible displays.

Flexible and transparent humidity sensors based on hyperbranched poly(ionic liquid)s for wearable sensing

The rapid development of wearable electronics is driving the exploration of flexible and transparent humidity sensors. However, the limited humidity response and mechanical flexibility of sensitive materials hinder the normal operation of the device. In this research, flexible humidity sensors with a fast response time (1 s) were prepared using transparent imidazolium-based hyperbranched poly(ionic liquid)s (HPIL). The sensor performance was improved by regulating the counter anions with different hydrophobicity, such as trifluoromethanesulfonimide ion (TFSI-). The HPIL-TFSI sensor featured an improved response under low humidity condition (6%∼33% RH) with good linearity, excellent bending humidity response, mechanical stability, and long-term stability over a wide humidity range from 6% to 98% RH. Moreover, accurate sensing was achieved for respiratory monitoring, non-contact sensing, and detecting moisture on patched skin. The HPIL-TFSI sensor paves the way for the production of high-performance wearable sensor platforms.

Photoluminescence of Argan-Waste-Derived Carbon Nanodots Embedded in Polymer Matrices.

In this work, photoluminescent (PL) carbon nano dots (CNDs) prepared from argan waste were embedded in highly optical transparent poly(styrene-co-acrylonitrile) (PSA) and cyclo-olefin copolymer (COC) matrices, which were further processed into thin films. In the first step, the luminescent CNDs were prepared through thermal processing of fine-groundargan waste, followed, in the second step, by direct dispersion in the polymer solutions, obtained by solving PSA and COC in selected solvents. These two polymer matrices were selected due to their high optical transparency, resilience to various environmental factors, and ability to be processed as quality thin films. The structural configuration of the CNDs was investigated through EDX, XPS, and FTIR, while DLS, HR-SEM, and STEM were used for their morphology investigation. The luminescence of the prepared CNDs and resulted polymer nanocomposites was thoroughly investigated through steady-state, absolute PLQY, and lifetime fluorescence. The quality of the resulted CND-polymer nanocomposite thin films was evaluated through AFM. The prepared highly luminescent thin films with a PL conversion efficiency of 30% are intended to be applied as outer photonic conversion layers on solar PV cells for increasing their conversion efficiency through valorization of the UV component of the solar radiation.

Printer toner-assisted immobilization of antibodies on PET for genuinely-2D, flexible ELISA spot arrays

The application of laser printing on a transparent poly(ethylene terephthalate) (PET) foil for toner-assisted immobilization of antibodies is employed for the first time in the preparation of two-dimensional arrays for high throughput ELISA. Two protocols for rapid microfabrication of single- and multi-layer immunoassay substrates with spatially controlled wettability are demonstrated, which include essential steps of laser Printing, UV-ozone Irradiation, and ultrasonically assisted toner Delamination (PID). This study demonstrates the potential of laser toner as an effective and easily removable protectant of PET against permanent hydrophilization by UV irradiation. To prove the feasibility and analytical performance of this novel immunosensing platform, an indirect sandwich immunoassay for human C-reactive protein (hCRP) was selected as a model. Dynamic range, covering CRP levels between 10 ng∙mL−1 and 5.62 µg∙mL−1, with a detection limit of 0.656 ng∙mL−1, as well as excellent signal recovery in human serum (97.3 - 104.5%), confirms clinical suitability of the assay in the analysis of real samples. Thanks to the design and fabrication simplicity, use of commonly available materials and up-scalability, presented methodologies can be successfully applied in the production of substrates for high-throughput immunodiagnostics and flexible microfluidics in Lab-on-a-Foil technology.

Nanodiamond reinforced self-healing and transparent poly(urethane–urea) protective coating for scratch resistance

ABSTRACT With increasing demand for scratch-resistant flexible electronics, the development of transparent coatings with good scratch resistance and self-healing properties has emerged as a key research topic. In this study, a high-strength self-healing poly(urethane – urea) (PUU)-based nanocomposite coating was prepared by introducing functionalized nanodiamond (ND) into a PUU matrix via solution blending. The PUU matrix had hard-segment repeating units and was constructed using isophorone diamine and isophorone isocyanate. The ND particles were modified using a silane coupling agent, 3-aminopropyltriethoxysilane, to obtain well-dispersed KH-ND nanoparticles. KH-ND promoted microphase separation in the PU matrix, inducing the formation of dense and homogeneous hard domains that dissipated stress, prevented further crack development, and improved the mechanical properties and scratch resistance of the coating. In addition, the coating exhibited excellent self-healing properties. Fourier-transform infrared spectroscopy, scanning electron microscopy, and atomic force microscopy were used to characterize the self-healing and hardening mechanisms of the coating. The environmentally friendly PUU/KH-ND coating is easy to prepare and has broad application prospects in transparent and anti-scratch coatings for flexible electronics, automobiles, and home appliances.

Multifunctional visualized electronic skin based on a solvatochromic poly (ionic liquid) ionogel

The biological skins exhibit various fascinating visual functions, such as turning red in response to strain, whitening upon hydrogen peroxide stimulation, and changing color in accordance with the environment (octopus). Inspired by these phenomena, two kinds of multifunctional visualized electronic skin (e-skin) were designed and fabricated based on a novel poly (ionic liquid) ionogel. Herein, we reported a transparent and conductive poly (ionic liquid) ionogel (P(AAm-IL)) by photopolymerizing acrylamide (AAm) with 1-vinyl-3-butylimidazolium tetrafluoroborate (ionic liquid, IL) in ethylene glycol (EG). Interestingly, P(AAm-IL) displays a solvatochromic phenomenon, and typical hydrogen-bonding acceptor solvents like acetone, methanol, and nitromethane induce a whitening effect in it. Based on this ionogel, we fabricated multifunctional strain sensors integrated with the visualized chemical sensing ability. The discoloration mechanism of the chemical sensing was detailed studied. Furthermore, by combining the P(AAm-IL) ionogel with Lithium trifluoroethane sulfonate (LiTf), the blend P(AAm-IL)-Li ionogel exhibits enhanced stretchability (>4300 %), higher conductivity (1.44 × 10−2 S·m−1), good transparency (>80 %) as well as wide operating temperature range (−20 to 80 °C). A sandwich-structured e-skin (Polypyrrole/PAAm-IL-Li/CsPbBr3-TPU) exhibiting both electro-optical dual response to strain was successfully fabricated. The luminescent e-skin not only exhibits highly sensitive electrical responses but also demonstrates visible fluorescence changes in response to external strain variations. These multifunctional visualized e-skins demonstrate great potential for applications in chemical environmental monitoring robotics, wearable electronic devices, and human–computer interaction.

High Refractive Index Copolymers from Aromatic Heterocycle‐Based Vinyl Sulfides and Phthalimide/Maleimide Derivatives

AbstractHerein, the rational design and facile synthesis of high‐refractive‐index copolymers with good optical transparency and tunable thermal stability using aromatic heterocycle‐based vinyl sulfides via conventional radical copolymerization is presented. 2‐Thiazolylvinylsulfide (2TVS), 1,3,4‐thiadiazolylvinylsulfide (1,3,4‐TVS), 3‐methylimidazolylvinylsulfide (3MIVS), and 5‐methlthio‐1,3,4‐thiadiazolylvinylsulfide (MeSTVS) are selected to enhance the refractive index, and N‐vinylphthalimide (NVPI) and N‐phenylmaleimide (NPMI) are chosen as comonomers to achieve improved transparency and thermal stability while maintaining the refractive index. The sulfur, ─C═N─, and imide contents in the copolymers are varied by adjusting the monomer structures and their compositions, and their effects on the refractive index, Abbe number, and optical and thermal properties are investigated. The MeTVS monomer in poly(MeSTVS) and poly(MeSTVS‐co‐NVPI) contained three sulfur atoms and two ─C═N─ units; consequently, these polymers exhibit excellent refractive indices in the 1.7139–1.6567 range at 589 nm, Abbe numbers between 19.1–29.1, good transparency (>90% at 400 nm), and tunable thermal properties (Tg = 49–138 °C, Td10 = 244–268 °C). Optically transparent poly(1,3,4‐TVS‐co‐NVPI) films (>95% at 400 nm) with improved thermal stability (Tg = 89–175 °C, Td10 = 251–301 °C) are obtained while maintaining a relatively high refractive index (1.6662–1.6752).

Enhanced water vapor barrier and gas barrier properties of transparent poly(butylene adipate‑co‑terephthalate)/poly(lactic acid)/hexagonal boron nitride nanosheets composite films

The water vapor barrier and gas barrier properties are very important factors for biodegradable packaging films. Herein, nano-sized hexagonal boron nitride nanosheets (hBNNSs) were facilely exfoliated, and novel transparent poly(butylene adipate-co-butylene terephthalate) (PBAT)/poly(lactic acid) (PLA) films incorporated with hBNNS were developed. Compared to those properties of neat PBAT/PLA film, the water vapor barrier of PBAT/PLA/hBNNSs films was greatly enhanced by 67%. Meanwhile, the oxygen permeability (OP) and carbon dioxide permeability (CO2P) of CS/hBNNSs films are significantly lowered by 65% and 93%, respectively. In addition, their thermal stabilities and mechanical property are also enhanced.

A Mechanically Robust, Self‐Healing, and Adhesive Biomimetic Camouflage Ionic Conductor for Aquatic Environments

AbstractFlexible conductive materials capable of simulating transparent ocean organisms have garnered interest in underwater motion monitoring and covert communication applications. However, the creation of underwater flexible conductors that possess mechanical robustness, adhesion, and self‐healing properties remains a challenge. Herein, hydrophobic interaction is combined with electrostatic interaction to obtain a solvent‐free transparent poly(ionic liquid) elastomer (PILE) fabricated using soft acrylate monomers and acrylate ionic liquids. The synergy of hydrophobic and electrostatic interactions can eliminate the hydration of water molecules underwater, giving the PILE adjustable fracture strength, good elasticity, high stretchability, high toughness, fatigue resistance, underwater self‐healing ability, underwater adhesion, and ionic conductivity. As a result, the transparent iontronic sensor generated from the PILE can achieve multifunctional sensing and human motion detection with high sensitivity and stability. In particular, the sensor can also transmit information underwater through stretching, pressing, and non‐contact modes, demonstrating its huge potential in underwater flexible iontronic devices.