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We designed an external stimulus-responsive anti-Stokes emission switching using dual-annihilator-based triplet–triplet annihilation upconversion systems. This system, which was constructed by incorporating a palladium porphyrin derivative as a sensitizer and 9,10-diphenylanthracene (DPA) and 9,10-bis(triisopropylsilyl)ethynylanthracene (TIPS) as annihilators into polymer thin films, produced TIPS- and DPA-based anti-Stokes emission under low and high excitation powers, respectively. The mechanism involves the following: under low excitation power, triplet energy transfer from triplet-excited PdOEP to DPA is induced, followed by relay to TIPS. This results in the generation of triplet-excited TIPS, and the subsequent triplet–triplet annihilation between them produces TIPS-based anti-Stokes emission. Conversely, under high excitation power, the high-density triplet-excited DPA, generated through triplet energy transfer from PdOEP, undergoes triplet–triplet annihilation among themselves, resulting in the generation of DPA-based anti-Stokes emission. Additionally, we achieved energy savings by reducing the required excitation power for switching through the utilization of plasmonic metal nanoparticles. The strong local electromagnetic fields associated with the localized surface plasmon resonance of metal nanoparticles enhance the photoexcitation efficiency of PdOEP, subsequently increasing the density of triplet-excited DPA. As a result, anti-Stokes emission switching becomes feasible at lower excitation powers. [ABSTRACT FROM AUTHOR]

Penetrant-induced plasticization has prevented the industrial deployment of many polymers for membrane-based gas separations. With the advent of microporous polymers, new structural design features and unprecedented property sets are now accessible under controlled laboratory conditions, but property sets can often deteriorate due to plasticization. Therefore, a critical understanding of the origins of plasticization in microporous polymers and the development of strategies to mitigate this effect are needed to advance this area of research. Herein, an integrative discussion is provided on seminal plasticization theory and gas transport models, and these theories and models are compared to an exhaustive database of plasticization characteristics of microporous polymers. Correlations between specific polymer properties and plasticization behavior are presented, including analyses of plasticization pressures from pure-gas permeation tests and mixed-gas permeation tests for pure polymers and composite films. Finally, an evaluation of common and current state-of-the-art strategies to mitigate plasticization is provided along with suggestions for future directions of fundamental and applied research on the topic. [ABSTRACT FROM AUTHOR]

Oxygen diffusion properties in thin polymer films are key parameters in industrial applications from food packaging, over medical encapsulation to organic semiconductor devices and have been continuously investigated in recent decades. The established methods have in common that they require complex pressure-sensitive setups or vacuum technology and usually do not come without surface effects. In contrast, this work provides a low-cost, precise and reliable method to determine the oxygen diffusion coefficient D in bulk polymer films based on tracking the phosphorescent pattern of a programmable luminescent tag over time. Our method exploits two-dimensional image analysis of oxygen-quenched organic room-temperature phosphors in a host polymer with high spatial accuracy. It avoids interface effects and accounts for the photoconsumption of oxygen. As a role model, the diffusion coefficients of polystyrene glasses with molecular weights between 13k and 350k g/mol are determined to be in the range of (0.8–1.5) × 10–7 cm2/s, which is in good agreement with previously reported values. We finally demonstrate the reduction of the oxygen diffusion coefficient in polystyrene by one quarter upon annealing above its glass transition temperature. [ABSTRACT FROM AUTHOR]

Boosting the circularly polarized luminescence of small organic molecules has been a stubborn challenge because of weak structure rigidity and dynamic molecular motions. To investigate and eliminate these factors, here, we carried out the structure‐property relationship studies on a newly‐developed axial chiral scaffold of bidibenzo[b,d]furan. The molecular rigidity was finely tuned by gradually reducing the alkyl‐chain length. The environmental factors were considered in solution, crystal, and polymer matrix at different temperatures. As a result, a significant amplification of the dissymmetry factor glum from 10−4 to 10−1 was achieved, corresponding to the situation from (R)‐4C in solution to (R)‐1C in polymer film at room temperature. A synergistic strategy of increasing the intramolecular rigidity and enhancing the intermolecular interaction to restrict the molecular motions was thus proposed to improve circularly polarized luminescence. The though‐out demonstrated relationship will be of great importance for the development of high‐performance small organic chiroptical systems in the future. [ABSTRACT FROM AUTHOR]

In this work, full‐color and stable white organic afterglow materials with outstanding water, organic solvents, and temperature resistances have been developed for the first time by embedding the selected polycyclic aromatic hydrocarbons into melamine‐formaldehyde polymer via solution polymerization. The afterglow quantum yields and lifetimes of the resulting polymer films were up to 22.7 % and 4.83 s, respectively, under ambient conditions. For the coronene‐doped sample, its afterglow color could be linearly tuned between yellow and blue by adjusting the temperature, and it could still emit an intense blue afterglow with a lifetime of 0.68 s at 440 K. Moreover, the films showed a bright and stable white afterglow at 370 K with a lifetime of 2.80 s and maintained an excellent afterglow performance after soaking in water and organic solvents for more than 150 days. In addition, the application potential of the polymer films in information encryption and anti‐counterfeiting was also demonstrated. [ABSTRACT FROM AUTHOR]

The effect of plasmonic nanoparticles (NPs) on the fluorescence and phosphorescence intensity of organic dye molecules was studied theoretically and experimentally. A theoretical model that takes into account nonradiative transfer of excitation energy from a molecule to an NP and the changes in the rates of spontaneous emission and light absorption by a molecule near an NP was proposed to calculate the luminescence intensity of a molecule in the presence of a plasmonic NP. Numerical estimates for an erythrosine molecule and a silver NP showed that the greatest increase in luminescence was observed at distances of 4–8 nm between the molecule and the NP surface. Experimentally observed changes in luminescence spectra and shortening of the erythrosine triplet state lifetime in poly(vinyl alcohol) films doped with silver NPs were explained using the proposed model. [ABSTRACT FROM AUTHOR]

Current methods to develop surfactant phase diagrams are time-intensive and fail to capture the kinetics of phase evolution. Here, the design and performance of a quantitative swelling technique to study the dynamic phase behavior of surfactants are described. The instrument combines cross-polarized optical and short-wave infrared imaging to enable high-resolution, high-throughput, and in situ identification of phases and water compositions. Data across the entire composition spectrum for the dynamics and phase evolution of a binary aqueous non-ionic surfactant solution at two isotherms are presented. This instrument provides pathways to develop non-equilibrium phase diagrams of surfactant systems—critical to predicting the outcomes of formulation and processing. It can be applied to study time-dependent material relationships across a diverse range of materials and processes, including the dissolution of surfactant droplets and the drying of aqueous polymer films. [ABSTRACT FROM AUTHOR]

The abuse of doxycycline (DC) can lead to residues in animals and water environments, which severely threaten human health; however, currently accepted detection methods are generally complicated and cannot be used for real-time detection. Therefore, developing a method for rapid real-time detection of DC microcontent residues is highly important. Herein, based on the Mach–Zehnder interference, we propose a simple tapered droplet structure fiber sensor with a high detection sensitivity. By modifying the sensing region with a molecularly imprinted polymer film of DC, this sensor realizes the specific detection of DC and has a detection sensitivity of 58.81 pm/ppm for DC in a large concentration range of 0–300 ppm. This sensor can be used to detect DC microcontent in aqueous solutions in real time. [ABSTRACT FROM AUTHOR]

Extended π-conjugation with backbone-planarity-driven π-π stacking dominates charge transport in semiconducting polymers (SCPs). The roles of SCP film morphology and macromolecular conformation concerning the substrate in influencing charge transport and its impact on device performance have been a subject of extensive debate. Face-on SCPs promote out-of-plane charge transport primarily through π-π stacking, with conjugated polymeric chains assisting transport in connecting crystalline domains, whereas edge-on SCPs promote in-plane charge transport primarily through conjugation and π-π stacking. In this work, we fabricated three different types of devices, namely, organic field effect transistors, organic Schottky diodes, and organic bistable memristors, as representatives of planar and vertical devices. We demonstrate that a planar device, i.e., an organic field effect transistor, performs well in an edge-on conformation exhibiting a field-effect mobility of 0.12 cm2V−1s−1 and on/off ratio >104, whereas vertical devices, i.e., organic Schottky diodes and organic memristors, perform well in a face-on conformation, exhibiting exceptionally high on/off ratios of ~107 and 106, respectively. [ABSTRACT FROM AUTHOR]

In this study, various diamine monomers were used to synthesize aramid polymer films via a low-temperature solution condensation reaction with diacid chloride. For diamines with relatively high basicity, the reaction system became opaque because amine salt formation inhibited polymer synthesis. Meanwhile, low-basicity diamines with strong electron-withdrawing groups, such as CF3 and sulfone, were smoothly polymerized without amine salt formation to provide highly viscous solutions. The acid byproduct HCl generated during polymerization was removed by adding propylene oxide to the reaction vessel and converting the acid into highly volatile inert substances. The resulting solutions were used as varnishes without any additional purification, and polymer films with an excellent appearance were easily obtained through a conventional casting and convection drying process. The films neither tore nor broke when pulled or bent by hand; furthermore, even when heated up to 400 °C, they did not decompose or melt. Moreover, polymers prepared from 2,2-bis(trifluoromethyl)benzidine (TFMB) and bis(4-aminophenyl)sulfone (pAPS) did not exhibit glass transition until decomposition. The prepared polymer films showed a high elastic modulus of more than 4.1 GPa and a high tensile strength of more than 52 MPa. In particular, TFMB-, pAPS-, and 2,2-bis(4-aminophenyl)hexafluoropropane-based polymer films were colorless and transparent, with very high light transmittances of 95%, 96%, and 91%, respectively, at 420 nm and low yellow indexes of 2.4, 1.9, and 4.3, respectively. [ABSTRACT FROM AUTHOR]

To analyze X-ray diffraction patterns obtained from polyimide films subjected to external influence (uniaxial tension and exposure at liquid helium temperature), radial distribution function (RDF) curves were constructed and the geometry of the 4,4′-oxydiphenylene-pyromellitimide monomer (PM) was calculated. From the RDF analysis, it follows that uniaxial tension of PM polymer films leads to a change in the geometry of the monomer, and exposure at low temperatures leads to mutual ordering of the polymer chains. [ABSTRACT FROM AUTHOR]

This article is devoted to the study of various dielectric and optoelectrical parameters nonlinear optic behaviors, thermal lens and self-diffraction parameters of Fluorescein (FLs) doped polymethyl methacrylate (PMMA) films. The films were prepared with 60 mM. These studies are based on the calculated values of refractive, absorption coefficient, energy gap, extinction coefficient and nonlinear Refraction index (n 2) . The polymer films were prepared using the casting technique. All samples were previously investigated by UV–Vis–NIR spectrophotometric measurements and Optical microscopy SEM and ATM. Utilizing thermal lens spectrometry, an investigation of the thermo-optical characteristics as well as the nonlinear refractive index was carried out. In this method, a pump beam and a probe beam were brought into collinear alignment with one another. To determination the nonlinear Refraction index (n 2) . High values of nonlinear refractive index predict a bright future for materials in optical applications. These results indicate that the new dye is a promising candidate for applications in nonlinear optical devices. Investigations were carried out on organic photovoltaic devices in addition to devices consisting of active layers with conducting polymer of PHPP:P3HT film and PHPP:P3HT/Fls. The methods of polymer and dyes synthesis are presented and their physical properties are given. [ABSTRACT FROM AUTHOR]

This feature article presents insights concerning the correlation of plasma‐enhanced chemical vapor deposition and plasma‐enhanced atomic layer deposition thin film structures with their barrier or membrane properties. While in principle similar precursor gases and processes can be applied, the adjustment of deposition parameters for different polymer substrates can lead to either an effective diffusion barrier or selective permeabilities. In both cases, the understanding of the film growth and the analysis of the pore size distribution and the pore surface chemistry is of utmost importance for the understanding of the related transport properties of small molecules. In this regard, the article presents both concepts of thin film engineering and analytical as well as theoretical approaches leading to a comprehensive description of the state of the art in this field. Perspectives of future relevant research in this area, exploiting the presented correlation of film structure and molecular transport properties, are presented. [ABSTRACT FROM AUTHOR]

This work aims to provide new insights into the link between the growth mechanisms of functionalized plasma polymer films (PPFs) and the substrate temperature (TS). By means of AFM‐based techniques, it has been demonstrated that the mechanical behavior of the coatings is dramatically affected by TS and the precursor employed (i.e., 1‐propanethiol or 1‐propylamine). While propylamine‐based PPFs behave as hard elastic materials regardless of TS, propanethiol‐based PPFs evolve from viscous liquids to elastic solids with increasing TS. This behavior can be understood considering the glass transition temperature of PPF. For both precursors, the latter is correlated to the cross‐linking density controlled through the energy density brought by positive ions to the growing film. [ABSTRACT FROM AUTHOR]

The cardiovascular diseases (CVD) continue to be the major threat to global public health over the years, while one of the effective methods to treat CVD is stent intervention. Biomedical magnesium (Mg) alloys have great potential applications in cardiovascular stents benefit from their excellent biodegradability and absorbability. However, excessive degradation rate and the delayed surface endothelialization still limit their further application. In this study, we modified a Mg-Zn-Y-Nd alloy (ZE21B) by preparing MgF 2 as the corrosion resistance layer, the dopamine polymer film (PDA) as the bonding layer, and hyaluronic acid (HA) loaded astaxanthin (ASTA) as an important layer to directing the cardiovascular cells fate. The electrochemical test results showed that the MgF 2 /PDA/HA-ASTA coating improved the corrosion resistance of ZE21B. The cytocompatibility experiments also demonstrated that this novel composite coating also selectively promoted endothelial cells proliferation, inhibited hyperproliferation of smooth muscle cells and adhesion of macrophages. Compared with the HA-loaded rapamycin (RAPA) coating, our MgF 2 /PDA/HA-ASTA coating showed better blood compatibility and cytocompatibility, indicating stronger multi-functions for the ZE21B alloy on cardiovascular application. [ABSTRACT FROM AUTHOR]

Cellulose derivatives are promising raw material as emulsifier, thickening or suspending agent, excipient, drug release agent, adhesive or water-based coating for food, building or pharmaceutical industries. Additives such as plasticizers or surfactants are frequently incorporated into such biopolymers to improve their properties. The aim of this work is to formulate, by introducing dedicated additives, biopolymer films based on cellulose derivatives and to explore their surface properties. The study investigates the influence of hydrophilic and hydrophobic additives on the surface properties of hypromellose films. The surface structure and morphology of hypromellose films shows the presence of nano-clusters, the which disappear as surfactant content increases. So does the surface average roughness and the surface free energy of the formulated films, suggesting the formation of a weak boundary layer at the film surface. As a consequence, a sharp decrease of nano-adhesion and nanofriction forces is observed. Hydrophilic additive induces the swelling of hypromellose clusters and an increase of the film surface free energy as well as nano-friction and nano-adhesion forces. The present study clearly underlines the strong dependence of the surface properties of the formulated films on additive nature and concentration as well as the interplay with additive-biopolymer matrix compatibility. Formulation appears then as an original and simple way to tune and target surface morphology and surface properties of biobased polymer films. [ABSTRACT FROM AUTHOR]

Biaxially oriented polypropylene (BOPP) is one of the most commonly used commercial capacitor films, but its upper operating temperature is below 105 °C due to the sharply increased electrical conduction loss at high temperature. In this study, growing an inorganic nanoscale coating layer onto the BOPP film's surface is proposed to suppress electrical conduction loss at high temperature, as well as increase its upper operating temperature. Four kinds of inorganic coating layers that have different energy band structure and dielectric property are grown onto the both surface of BOPP films, respectively. The effect of inorganic coating layer on the high‐temperature energy storage performance has been systematically investigated. The favorable coating layer materials and appropriate thickness enable the BOPP films to have a significant improvement in high‐temperature energy storage performance. Specifically, when the aluminum nitride (AlN) acts as a coating layer, the AlN‐BOPP‐AlN sandwich‐structured films possess a discharged energy density of 1.5 J cm−3 with an efficiency of 90% at 125 °C, accompanying an outstandingly cyclic property. Both the discharged energy density and operation temperature are significantly enhanced, indicating that this efficient and facile method provides an important reference to improve the high‐temperature energy storage performance of polymer‐based dielectric films. [ABSTRACT FROM AUTHOR]

Aluminum-doped zinc oxide (AZO) films have emerged as promising transparent electrodes for various optoelectronic applications due to their superior transparency, electrical conductivity, and cost-effectiveness compared to indium tin oxide (ITO). Despite their widespread use, investigations into the electromechanical properties of AZO films, especially under various mechanical deformations, remain limited. This study employs RF magnetron sputtering to deposit AZO films on polyethylene naphthalate (PEN) substrates and explores their mechanical behavior through uniaxial tensile fragmentation and bending tests, coupled with in-situ optical microscopy. Changes in electrical resistance of AZO films were monitored in situ during deformation. Fatigue behavior was examined to further understand mechanical failure, and SEM was used for surface characterization. A critical strain of about 3.1 percent was detected during uniaxial tensile testing, marking the onset of cracks in AZO-coated PEN. In contrast to thicker films, thinner films demonstrated improved stretchability beyond the initiation of crack onset strain. Tension and compression bending tests revealed that the material has excellent bendability, as shown by its critical radii of 5.4 mm and 3.9 mm, respectively. The bending reliability of AZO films under compression was found to be superior than that under tension. Bending fatigue experiments demonstrated that AZO films could withstand cyclic stress without experiencing no ticeable cracks after 100 cycles and with very minor resistance change. This study contributes to the creation of more reliable and optimized flexible optoelectronic devices by giving substantial quantitative data on the performance of AZO films when exposed to mechanical stress. [ABSTRACT FROM AUTHOR]

This work is devoted to the study of nanosized polymer polyvinylidene fluoride (PVDF) thin ferroelectric films (two-dimensional ferroelectrics) and their composites with graphene layers, using molecular dynamics methods to (1) study and calculate the polarization switching time depending on the electric field and film thickness, (2) study and calculate the polarization switching time depending on changes of the PVDF in PVDF-TrFE film, and (3) study the polarization switching time in PVDF under the influence of graphene layers. All calculations at each MD run step were carried out using the semi-empirical quantum method PM3. A comparison and analysis of the results of these calculations and the kinetics of polarization switching within the framework of the Landau–Ginzburg–Devonshire theory for homogeneous switching in ferroelectric polymer films is carried out. The study of the composite heterostructures of the "graphene-PVDF" type, and calculations of their polarization switching times, are presented. It is shown that replacing PVDF with PVDF-TrFE significantly changes the polarization switching times in these thin polymer films, and that introducing various graphene layers into the PVDF layered structure leads to both an increase and a decrease in the polarization switching time. It is shown that everything here depends on the position and displacement of the coercive field depending on the damping parameters of the system. These phenomena are very important for various ferroelectric coatings. [ABSTRACT FROM AUTHOR]

The deterioration of fruits during production, transportation, and storage has become one of the main challenges in supplying fruits based on consumer requirements. Therefore, the application of suitable packaging containing effective additives to improve the properties of the used film, is very important. In this article, the studies were conducted on the use of Zeolite as an effective additive to improve the properties of polymer packaging films owing to its high porosity and low toxicity. The results showed that the presence of zeolite in a packaging film can lead to the improvement of visual observation and firmness, reduction of weight loss and total soluble solids (TSS), and increase in the pH of the packed fruits. The results obtained from reviewing the literature show that the use of zeolite has different effects on the gas permeation or adsorption through the packaging films which can control the degradative parameters of fruits and vegetables. Surface modifiers can increase the efficiency of zeolites in packaging films which are also evaluated in this article. Highlights: Packaging of fruits with the use of polymer films and zeolite as an additive increases their shelf life.Ethylene is a flammable gas with the formula C2H4 that accelerates the fruit ripening.Zeolites are hydrated aluminosilicates of alkali or alkaline earth cations that are crystalline and microporous.Zeolites are widely used in the packaging of polymeric composites, due to their chemical structure and unique characteristics.The visual features, firmness, pH, TSS, TA, and weight loss are factors to be investigated for each fruit. [ABSTRACT FROM AUTHOR]

The mucilage that accumulated in the Sea of Marmara in 2021 turned into an environmental disaster that threatened not only marine life but also the shipping and tourism industries. However, because of the partially organic structure of marine mucilage, it has the potential to be used as an additive for polymer films. In this study, bioplastic films were prepared from PVA with a series of mucilage content from 0% to 50% by mass, and their properties were investigated. The FT‐IR spectra revealed a shift in hydroxyl peaks, suggesting an interaction between the mucilage and PVA. SEM images showed the formation of crystal forms at the higher mucilage content of 20%, indicating ionic saturation of the PVA matrix. EDX and XRD analyses revealed that the crystal was NaCl coming from the mucilage composition. The tensile strength of the neat PVA film was measured as 9.86 MPa and improved to 14.56 MPa with 5% mucilage content, which is attributed to the ionic cross‐linking. The tensile properties were preserved up to 20% of the mucilage content, and then sudden decrements were observed. The transmittance percentage (T%) of the neat PVA film in UV–Vis spectra (800–200 nm) was detected as 75% at 500 nm and decreased down to 39% with increased mucilage content up to 50%. Furthermore, a rising limit of linearity (LOL) of the spectrums was observed from 350 to 580 nm, with increasing mucilage content from 5% to 50%. The biofilms showed antibacterial activity against Escherichia coli and Staphylococcus aureus bacteria. Hence, a robust and biodegradable film having UV protection and antibacterial activity was developed from the marine mucilage bio‐waste. Highlights: Poly(vinyl alcohol)/marine mucilage biocomposite films were prepared.Biocomposite films showed increased UV‐A, UV‐B, and UV‐C protection with increased mucilage content.Enhanced tensile strength of biocomposite films up to 20 wt% mucilage content was determined due to ionic crosslink formed by NaCl salt ions.Biocomposite exhibited antibacterial activity against Escherichia coli and Staphylococcus aureus. [ABSTRACT FROM AUTHOR]

Due to their functional and processing versatility, organic semiconductors have gained much interest in recent years. Tailoring the charge transport in a polymeric semiconductor system is imperative for developing optimized devices. Factors such as selection of solvent species and annealing temperature play a significant role in deciding the morphology of the polymer semiconductor and hence the device performance. Bottom-gate bottom-contact organic field-effect transistors were fabricated with regioregular poly(3-hexylthiophene) (P3HT) as the active material. The effects of using chlorobenzene and o-dichlorobenzene as the solvents for P3HT and annealing temperatures on the device performance were evaluated. The devices made using chlorobenzene showed greater field-effect mobility compared to those fabricated with o-dichlorobenzene. This behavior can be attributed to the disentanglement of polymer chains in a solvent with better matching solubility parameters and subsequent ease of arranging in ordered structures during processing. Furthermore, annealing the o-dichlorobenzene devices at temperatures closer to the crystallization temperature of P3HT showed an increase in field-effect mobility. At temperatures closer to the crystallization temperature, a polymer film in a semidry state can allow increased ordering of the chains leading to enhanced charge transportation. [ABSTRACT FROM AUTHOR]

Abstract Recently, demands for high‐performance polymer film capacitors at elevated temperatures have become more urgent. High dielectric constant is essential for dielectric materials to achieve substantial energy density at relatively low electric fields, which is of great significance to practical applications, while improving the permittivity of high‐temperature polymer dielectrics without a remarkable deterioration in other electrical properties still remains a challenge. Here, a polymer nanocomposite containing z‐aligned high‐k nanowires sandwiched by e‐beam evaporation deposited Al2O3 films was developed based on the optimal structure proposed by the phase‐field simulation. It is found that z‐aligned nanowires are more effective in promoting the dielectric constant than random‐aligned ones, and a large increase in dielectric constant is observed at relatively low content of nanofillers. Outer insulating layers effectively suppress the electric conduction and improve the breakdown strength. Consequently, the nanocomposite with only 1 volume fraction of z‐aligned nanowires exhibits a breakdown strength, electrical resistance, and charge–discharge efficiency as high as neat PEI, but more than twice the discharged energy density than it at 150 °C. This study realises the optimal structure predicted by simulation in experiment, obtaining high‐permittivity, high‐temperature nanocomposites at no expense of other electrical properties, and making it possible to achieve high discharged energy density at relatively low electric fields.

Abstract The authors report a novel electret‐based miniature electrostatic motor with an electret film as the stator and a metal electrode as the rotor. A particular commutator is used to transform the polarity of the metal electrode. When the size of the electret‐based electrostatic motor (EEM) is 42 × 44 × 15 mm3, the maximum power consumption is only 5.4 mW. The rotation speed of the EEM increases with the increase of the supply voltage, and the maximum rotation speed can reach up to 2864 rpm. Powered by two nickel‐hydride batteries with a rated capacity of 1700 mAh, the EEM can drive a fan with a diameter of 40 mm to rotate continuously for 18 h. The EEM has the characteristics of low power consumption and convenient fabrication. Experimental results show that the EEM demonstrates high reliability and has potential applications in micro‐electromechanical systems.

Abstract Piezoelectrets, also called ferroelectrets, can exhibit promising piezoelectric properties and have plenty of applications in wearable health monitoring. Usually, the cellular structure of piezoelectrets is of outstanding importance for their sensing properties, and structure improvement and optimisation would be a possible way to realise high‐performance piezoelectrets. The authors proposed a compound‐structured piezoelectret system, where a layer of polypropylene foam was sandwiched between two layers of solid polytetrafluoroethylene, resulting in a combination of a foam‐structured and a layer‐structured piezoelectrets. The compound systems are thin and flexible, they can exhibit stable electrical outputs, they have relatively broader linear working range under pressure, and promising mechanical sustainability for multiple testing. The results reveal that the compound system can be considered as a simple addition of both components, and each component contributes linearly and independently to the whole system. The application potential of this proposed compound system has been demonstrated by sleep monitoring together with carotid and radial pulse recordings, where many useful physiological information including breath, heartbeat, and pulse details can be extracted from the signals acquired by the compound system. A type of flexible sensor system that is very competitive for future portable and wearable applications may be provided.

Abstract Bacterial biofilm is an important factor in bacterial drug resistance. Recently, it has been proved that electret films can inhibit the bacterial biofilm, while its mechanism of action on biofilms is under further investigation. In this work, taking Staphylococcus aureus as an example, the inhibition of positive electret on bacterial biofilm was verified and its mechanism was explained. Two factors have been found to explain the inhibition mechanism of electret on bacterial biofilms. One is probably due to its inhibition of the expression of key genes related to bacterial biofilms induced by the electric field of positive electret, and the other is to prevent the aggregation of bacteria rather than the direct bactericidal effect. The conclusions are expected to be extended to other types of bacteria and expand the application of electrostatic materials in the field of biomedicine.

We investigate the local viscosity of a polymer glass around its glass transition temperature by using environment-sensitive fluorescent molecular rotors embedded in the polymer matrix. The fluorescence of the rotors depends on the local viscosity, and measuring the fluorescence intensity and lifetime of the probe therefore allows us to measure the local free volume in the polymer glass when going through the glass transition. This also allows us to study the local viscosity and free volume when the polymer film is put under an external stress. We find that the film does not flow homogeneously but undergoes shear banding that is visible as a spatially varying free volume and viscosity. [ABSTRACT FROM AUTHOR]

The activation, by residual stress, of the fast portion of rotational motion of single fluorescent probe molecules inside a polymer thin film near its glass transition temperature is studied at a single molecular level. Spin-casted poly n-butyl methacrylate thin films without thermal annealing are chosen as the model system and single molecule fluorescence defocused microscopy is adopted as the method. The rotational motion of the probes under residual stress is found to be more activated than that under mere thermal activation, and the kinetic energy exhibits a monotonic increase with the stress strength. A rough linear dependence of rotational kinetic energy at low stress is found, yielding the value of characteristic volume for the residual stress to activate the motion of the probes. The values of the volume are close to the van der Waals volume of the probes, indicating that the activation of the fast dynamics by residual stress is localized. The activation effect is weakened and vanishes at or above the glass transition temperature due to stress relaxation. The effect is also absent at temperatures far below Tg due to the frozen molecular motion with a much higher activation energy. [ABSTRACT FROM AUTHOR]

Generating strong rapid adhesion between hydrogels has the potential to advance the capabilities of modern medicine and surgery. Current hydrogel adhesion technologies rely primarily on liquid-based diffusion mechanisms and the formation of covalent bonds, requiring prolonged time to generate adhesion. Here, we present a simple and versatile strategy using dry chitosan polymer films to generate instant adhesion between hydrogel-hydrogel and hydrogel-elastomer surfaces. Using this approach we can achieve extremely high adhesive energies (>3,000 J/m²), which are governed by pH change and non-covalent interactions including H-bonding, Van der Waals forces, and bridging polymer entanglement. Potential examples of biomedical applications are presented, including local tissue cooling, vascular sealing, prevention of surgical adhesions, and prevention of hydrogel dehydration. We expect these findings and the simplicity of this approach to have broad implications for adhesion strategies and hydrogel design. [ABSTRACT FROM AUTHOR]

Over the last 40 years, applied mathematicians and physicists have proposed a number of mathematical models that produce structures exhibiting a fractal dimension. This work has coincided with the discovery that objects with fractal dimension are relatively common in the natural and human-produced worlds. One particularly successful model of fractal growth is the diffusion limited aggregation (DLA) model, a model as notable for its simplicity as for its complex and varied behavior. It has been modified and used to simulate fractal growth processes in numerous experimental and empirical contexts. In this work, we present an alternative fractal growth model that is based on a growing mass that bonds to particles in a surrounding medium and then exerts a force on them in an iterative process of growth and contraction. The resulting structure is a spreading triangular network rather than an aggregate of spheres, and the model is conceptually straightforward. To the best of our knowledge, this model is unique and differs in its dynamics and behavior from the DLA model and related particle aggregation models. We explore the behavior of the model, demonstrate the range of model output, and show that model output can have a variable fractal dimension between 1.5 and 1.83 that depends on model parameters. We also apply the model to simulating the development of polymer thin films prepared using spin-coating which also exhibit variable fractal dimensions. We demonstrate how the model can be adjusted to different dewetting conditions as well as how it can be used to simulate the modification of the polymer morphology under solvent annealing. [ABSTRACT FROM AUTHOR]

Conductive polymers have attracted attention for wearable and implantable thermoelectric devices due to their lightweight, flexibility, and solubility. With the development of microsystems, thermoelectric power generation devices are trending toward miniaturization, flexibility, high integration, and lightweight thin films. Therefore, the study of the thickness of thermoelectric materials has become increasingly important. In this study, we prepared ultrathin polymer thermoelectric (TE) films with different thicknesses (14–52 nm) by modifying the substrate with self-assembled monolayers (SAMs). The thickness-dependent thermoelectric performances on SAMs are investigated. It is found that SAMs regulate the carrier concentration in polymer ultrathin TE films, and a smoother surface contributes to the improvement of carrier mobility, thus optimizing the thermoelectric performance. The maximum modulation of thermoelectric performance is observed at a film thickness of approximately 35 nm, which contains nine molecular layers. [ABSTRACT FROM AUTHOR]

A new method for synthesizing cross‐linked 4,4‐difluoro‐4‐bora‐3a,4a‐diaza‐s‐indacenes (BODIPYs) using a radical‐based thiol‐ene click reaction is developed. This method is simple, efficient, and cost‐effective, and it produces polymers with unique optical, electrochemical, and surface morphology properties. Significant blue shifts in absorption and photoinduced electron transfer in emissions are observed in the cross‐linked BODIPY thin films. Cross‐linking also leads to the restriction of conjugation, which results in the breakage of the terminal vinyl group, an increase in the oxidation potential, and a slight upshift in the HOMO position. As a result, the electrochemical band gap is widened from 1.88 to 1.94 eV for polymer bearing N,N‐dimethylamino‐BODIPY and from 1.97 to 2.02 eV for polymer bearing N,N‐diphenylamino‐BODIPY moieties. Monomer thin films form planar surfaces due to crystallinity, while amorphous cross‐linked BODIPY polymers form more rough surfaces. Additionally, photopatterning on the film surface is successfully performed using different patterned masks. This new method for synthesizing cross‐linked BODIPYs has the potential to be used in a variety of applications, including organic electronics, bioimaging, and photocatalysis. [ABSTRACT FROM AUTHOR]

Development of biobased aliphatic polyesters with better mechanical (tensile) properties in film has attracted considerable attention. This report presents the synthesis of soluble network biobased aliphatic polyesters by acyclic diene metathesis (ADMET) polymerization of bis(undec-10-enyl)isosorbide diester [M1, dianhydro-D-glucityl bis(undec-10-enoate)] in the presence of a tri-arm crosslinker [CL, glycerol tris(undec-10-enoate)] using a ruthenium–carbene catalyst, and subsequent olefin hydrogenation using RhCl(PPh3)3. The resultant polymers, after hydrogenation (expressed as HCP1) and prepared in the presence of 1.0 mol% CL, showed better tensile properties than the linear polymer (HP1) with similar molecular weight [tensile strength (elongation at break): 20.8 MPa (282%) in HP1 vs. 35.4 MPa (572%) in HCP1]. It turned out that the polymer films prepared by the addition of CL during the polymerization (expressed as a 2-step approach) showed better tensile properties. The resultant polymer film also shows better tensile properties than the conventional polyolefins such as linear high density polyethylene, polypropylene, and low density polyethylene. [ABSTRACT FROM AUTHOR]

There have been many studies on surface acoustic wave (SAW) sensors for detecting sulfur-containing toxic or harmful gases. This paper aims to give an overview of the current state of polymer films used in SAW sensors for detecting deleterious gases. By covering most of the important polymer materials, the structures and types of polymers are summarized, and a variety of devices with different frequencies, such as delay lines and array sensors for detecting mustard gas, hydrogen sulfide, and sulfur dioxide, are introduced. The preparation method of polymer films, the sensitivity of the SAW gas sensor, the limit of detection, the influence of temperature and humidity, and the anti-interference ability are discussed in detail. The advantages and disadvantages of the films are analyzed, and the potential application of polymer films in the future is also forecasted. [ABSTRACT FROM AUTHOR]

Human skin comprises multiple hierarchical layers that perform various functions such as protection, sensing, and structural support. Developing electronic skin (E‐skin) with similar properties has broad implications in health monitoring, prosthetics, and soft robotics. While previous efforts have predominantly concentrated on sensory capabilities, this study introduces a hierarchical polymer system that not only structurally resembles the epidermis‐dermis bilayer structure of skin but also encompasses sensing functions. The system comprises a polymeric hydrogel, representing the "dermis", and a superimposed nanoporous polymer film, forming the "epidermis". Within the film, interconnected nanoparticles mimic the arrangement of interlocked corneocytes within the epidermis. The fabrication process employs a robust in situ interfacial precipitation polymerization of specific water‐soluble monomers that become insoluble during polymerization. This process yields a hybrid layer establishing a durable interface between the film and hydrogel. Beyond the structural mimicry, this hierarchical structure offers functionalities resembling human skin, which includes (1) water loss protection of hydrogel by tailoring the hydrophobicity of the upper polymer film; (2) tactile sensing capability via self‐powered triboelectric nanogenerators; (3) built‐in gold nanowire‐based resistive sensor toward temperature and pressure sensing. This hierarchical polymeric approach represents a potent strategy to replicate both the structure and functions of human skin in synthetic designs. [ABSTRACT FROM AUTHOR]

In recent years, the need to use environmentally friendly materials has also triggered increased activity of research and development on water-based formulations for films and coatings. In an effort to meet this goal, waterborne polyurethanes (WBPUs) were developed, which during the coating deposition or the formation of self-standing films release innocuous water to the atmosphere instead of volatile organic compounds (VOCs), as is the case with most traditional solvent-based polymers. One of the most studied applications for this type of materials is water-based paints and coatings. Advances in the development of WBPU have been produced through the careful selection of different sources of hydroxyl group components, as well as different types of chain extenders and emulsifiers. On the other hand, to improve the performance required to the final application composite formulations have been tailored through the addition of organic and inorganic particles/nanoparticles. This review focuses on the relation between formulation-structure and properties of these materials from the initial dispersions to the final coating films. Most commonly used methods of application and their relation to the viscosity of the dispersions have also been briefly considered. [ABSTRACT FROM AUTHOR]

Thin films of conjugated polymer and enzyme can be used to unravel the interaction between components in a biosensor. Using artificial neural networks (ANNs) improves data interpretability and helps construct models with great capacity for classifying and processing information. The present work used kinetic data from the catalytic activity of urease immobilized in different conjugated polymers to create ANN models using time, substrate concentration, and absorbance as input variables since the models had absorbance in a posterior instant as output value to explore the predictivity of the ANNs. The performance of the models was evaluated by Pearson's correlation coefficient (ρ) and mean squared error (MSE) values. After the learning process, a series of new experiments were performed to verify the generality of the models. As the main results, the best ANN model presented 0.9980 and 3.0736 × 10–5 for ρ and MSE, respectively. For the simulation step, intermediary values of substrate concentration were used. The mean absolute percentage error (MAPE) values were 3.34, 3.07, and 3.78 for 12 mM, 22 mM, and 32 mM concentrations, respectively. Overall, with the simulations, it was possible to ascertain the interpolatory capacity of the model, which has a learning mechanism based on absorbance and time as variables. Thus, the potential of ANNs would be in their use in pre-evaluations, helping to determine the substrate concentration at which there is higher catalytic activity or in determining the linear range of the sensor. [ABSTRACT FROM AUTHOR]

The development of soft photoactuators with multifunctionality and improved performance is highly important for their broad applications. Herein, we report on a facile and efficient strategy for fabricating such photoactuators with UV‐NIR dual light‐responsivity, room‐temperature 3D shape reprogrammability and reprocessability, and photothermal healability by doping polydopamine (PDA) nanoparticles into a main‐chain azobenzene semi‐crystalline poly(ester‐amide) (PEA). The PEA/PDA nanoparticle composite was readily processed into free‐standing films with enhanced mechanical and photomechanical properties compared with the blank PEA films. Its physically crosslinked uniaxially oriented films showed rapid and highly reversible photochemically induced bending/unbending under the UV/visible light irradiation at room temperature in both the air atmosphere and water. When exposed to the NIR light, they (and their bilayer films formed with a polyimide film) exhibited photothermally induced bending even at a temperature much lower than their crystalline‐to‐isotropic phase transition temperature based on a unique mechanism (involving photothermally induced polymer chain relaxation due to the disruption of their hydrogen bonds). The room‐temperature 3D shape reprogrammability and reprocessability and photothermal healability of the composite polymer films were also demonstrated. Such multifunctional dual light‐responsive photoactuators with well‐balanced mechanical robustness, actuation stability, 3D shape reprogrammability/reprocessability and photothermal healability hold much promise in various photoactuating applications. [ABSTRACT FROM AUTHOR]

The results of studies of a wavefront sensor based on the Talbot effect, in which a periodic grating made by laser printing is used, are presented. The optical characteristics of periodic gratings printed on polymer films exposed to a continuous radiation density of up to 0.9 W/cm2 have been studied. The possibility of creating efficient configurable wavefront sensors for lasers in the visible and mid-IR spectral ranges is demonstrated. [ABSTRACT FROM AUTHOR]

[Display omitted] • 2D Materials are commonly incinerated which does not increase the recycling quota. • NIR spectroscopy in transflection mode can be used to recycle 2D materials. • Usage of Feature Selection Algorithms to create fast and interpretable classification models. • InLine classification of non-recyclable Film Specimen using proprietary neural networks. Improving the sortability of plastic packaging film waste (PPFW) is crucial for increasing the recycling rate in Austria as they account for 150,000 t of the annually produced 300,000 t of plastic packaging waste. Currently PPFW is thermally recovered, as it is impossible to separate the mechanically recyclable monomaterial films from the non mechanically-recyclable multimaterial films. In this study, machine learning models capable of classifying inline into monolayer and multilayer films of PPFW according to their spectral fingerprint taken in transflection were created. Feature selection methods, like PCA and MRMR F-Tests, identified the most relevant spectral ranges for classification, that show the least redundancy and highest relevance. This effective subset of features decreases the required complexity of the model while reducing prediction time without compromising accuracy. The resulting models achieved a prediction accuracy of 85 % on unseen specimens with minimal prediction latency, effectively showing the inline applicability of these models in sorting aggregates. [ABSTRACT FROM AUTHOR]

Humidity sensors play a critical role in diverse fields such as agricultural production, medical equipment, and weather forecasting. However, the majority of existing humidity sensors rely on batteries or are relatively costly to construct. In this study, a simple, efficient, and battery-free visual humidity sensor was developed by combining cholesteric liquid crystal (CLC) with acrylic acid (AA) and subsequently curing it to form an interpenetrating polymer network (IPN) film. The IPN film changes colour with relative humidity (RH). Moreover, it has been confirmed that the film exhibits excellent repeatability, and its performance remains relatively unaffected by temperature fluctuations. Additionally, the relationship between film thickness and response time is explored in this research. Through orthogonal experiments involving various proportions of CLC, the study also scrutinises the influence of each component on the humidity response performance of the IPN films. During the transition from 40% RH to 90% RH, IPN film sample 3 experienced a remarkable redshift of 123.05 nm in the reflected wavelength. As for sample 9, its humidity response demonstrated an outstanding linearity of 0.9986. Consequently, the experimental outcomes provide strong evidence that this IPN film exhibits superior humidity response capabilities and holds considerable promise for practical applications. [ABSTRACT FROM AUTHOR]

The common approach to creating antimicrobial polymer materials is the distribution of a bactericidal additive in a material by mixing the additive with a solution or a melt of the polymer. This work proposes the method introducing of copper(II) sulfate, which has antimicrobial properties, into a poly(lactic acid) film by forced impregnation of a salt solution via the crazing mechanism. CuSO4 has been found to be uniformly distributed in the bulk of the polymer in the form of particles with sizes of about 100 nm. In the course of the structural modification, the surface of the polymer film becomes rougher and more hydrophobic. The water contact angle increases from 40° to 60°–65°. The incorporation of CuSO4 does not affect the surface properties but has a reinforcing effect on the polymer matrix as is evident from tensile tests (strength and elongation at break increase by 2.5 and 1.4 times, respectively). [ABSTRACT FROM AUTHOR]

Antimicrobial natural polymer film with silver nanoparticles (AgNPs) biosynthesized using aqueous plant root extracts as reducing capping agents and for film formatting show extensive applicability for pathogenic microorganism problems. The formation of AgNPs was confirmed by transmission electron microscopy (TEM) and scanning electron microscopy–energy-dispersive spectroscopy (SEM–EDS) techniques. The antimicrobial activity of biofilm with green AgNPs was analysed by inhibiting the growth of Gram-negative and Gram-positive bacteria culture using the Kirby–Bauer disk diffusion susceptibility test. Total phenolic content and antioxidant activity were slightly higher in aqueous extracts of Sym. Radix than in Sym. Radix/AgNPs. The antimicrobial effect of polymer film/AgNPs against selected test bacteria cultures was substantially more robust than with pure film. Pictures of AgNPs obtained by TEM revealed the presence of spherical-shaped nano-objects with an average size 27.45 nm. SEM–EDS studies confirmed the uniform distribution of metal nanoparticles throughout the biopolymeric matrix. Morphological studies of the surface showed that the obtained surface of the films was even, without holes or other relief irregularities. These apparent Symphyti radix polymer film/AgNPs' biological functions could provide a platform for fighting pathogenic bacteria in the era of multi-drug resistance. [ABSTRACT FROM AUTHOR]

[Display omitted] • Viscoelastic measurements of nanometer-thickness polymer brush films were achieved. • Gap dependence of viscoelasticity was investigated to elucidate the film's lubricity. • Correlation between friction and viscoelasticity was revealed. A hydrated 2-methacryloyloxyethyl phosphorylcholine (MPC) polymer brush exhibits exceptional lubricity. This lubrication mechanism has traditionally been attributed to either the inherent fluidity of the brush or the water film that forms owing to its hydrophilic nature. Given previous findings that the frictional properties of the MPC polymer brush film show load dependence, we hypothesize that the lubrication mechanism can be elucidated by examining the shear gap (varies owing to the load) dependence of the brush's viscoelastic response. MPC polymer brush films with different thicknesses were prepared. Their viscoelastic responses were evaluated across different shear gap widths, and the frictional properties were subsequently compared across states with distinct viscoelastic behaviors. The observed shear viscoelasticity demonstrated a clear gap dependence that correlated with frictional attributes. Our data suggests that the lubrication mechanism shifts based on the shear gap. Specifically, two states exhibited low coefficients of friction: one where the osmotic pressure supports the load while allowing flexible deformation of the brush film, and the other where the brush film undergoes compression and transitions to a fully elastic state. [ABSTRACT FROM AUTHOR]

The potential applications of carbon black are expected to grow as science and technology improve offering up new possibilities for innovation throughout disciplines included in the field of energy storage. The present work shows the influence of carbon black to improve the ionic conductivity of the polymer electrolyte. The synthesis of polyethylene oxide: ammonium iodide based polymer electrolyte incorporated with carbon black varying from 0.01 to 0.06 wt% with respect to PEO: NH4I system by solution casting method. Different characterizations like polarized optical microscopy (POM), impedance spectroscopy, and ionic transference number (tion) are studied in detail. The maximum ionic conductivity is achieved at 0.05 wt% carbon black shows 1.20 × 10−5 S cm−1 at ambient temperature. In accordance with POM data, the amorphous region has increased whereas the crystalline region has shrunk which further indicated the increase in ionic conductivity. The value of (tion) is calculated to be 0.97 which shows the system is ionic in nature. PEO based polymer electrolyte doped carbon black can be used for the fabrication of energy storage devices. [ABSTRACT FROM AUTHOR]