Composite Films Research Articles

Sandwich-structured SrTiO3/PEI composite films with high-temperature energy storage performance

Dielectric capacitors are widely used in aerospace and power systems due to their non-polluting, high power density and fast charge/discharge rates. Polyetherimide (PEI) exhibits excellent temperature tolerance, high withstand voltage and low dielectric loss. However, its relatively low dielectric constant restricts its energy storage density. In this paper, a sandwich-structured composite film with the outer layer of pure PEI and the middle layer of strontium titanate (SrTiO3)/PEI is prepared by the solution casting method. At room temperature, the composite film with 5 vol% two-dimensional (2D) SrTiO3 plates achieves an outstanding energy storage density of 19.46 J cm−3 and an ultra-high energy storage efficiency of 97.05% under an electric field of 630 MV m−1. Furthermore, this composite film exhibits a maximum energy storage density of 10.34 J cm−3 and an energy storage efficiency of 88.13% at 150 °C. Combined with finite element simulation results, it confirms that the synergistic effect of 2D SrTiO3 plates and sandwich-structured can effectively hinder the development of electric trees. This work presents a sophisticated approach to design and preparation of dielectric composites suitable for the applications of high-temperature energy storage.

Quantum‐Dots Matrix Encapsulated CsPbI3 Polycrystal Composite Films for Efficient and Bright Deep‐Red Light‐Emitting Diodes

AbstractAll‐inorganic CsPbI3 perovskite is a promising emitter for deep‐red light‐emitting diodes (LEDs). However, presently fabricated CsPbI3 polycrystalline films are composed of island‐like polycrystals, encountering the problems of serious interface current leakage and low‐efficiency carrier radiative recombination. Here, a CsPbI3‐xBrx quantum dots (QDs) matrix encapsulated CsPbI3 polycrystal film is reported to address the low‐efficiency issue of island‐like CsPbI3 polycrystalline film applied in deep‐red LEDs. The developed QDs matrix encapsulation strategy has two benefits. One is the filling of void space in the island‐like CsPbI3 polycrystal film to suppress the interface current leakage. The other more important benefit is utilizing the strong carrier confinement effect of QDs to strengthen the formation of excitons in the composite film and thus improve the electroluminescence efficiency. Moreover, interesting grain growth is found between CsPbI3‐xBrx QDs and CsPbI3 polycrystals, which further enhances the exciton transfer effect brought by the QDs matrix and optoelectronic properties of the fabricated composite films. Based on the obtained high‐quality QDs/polycrystal composite films, efficient and bright deep‐red LEDs are achieved with a peak external quantum efficiency of 15.24% and a maximum luminance of 3691 cd m−2.

Thermal conductivity of epoxy resin films doped with a polythiophene/graphene complex or aluminum nitride

AbstractPolymer composites with thermal conductivity are attractive for heat dissipation in electronic devices. We prepared epoxy resin‐based composite films filled with polythiophene [poly(3‐hexylthiophene‐2,5‐diyl)] (P3HT)/graphene complex or aluminum nitride (AlN). The composite films were characterized by electron microscopic observation, thermogravimetric analysis, and thermal conductivity measurements. The addition of a small content of P3HT/graphene complex (<1 wt%) increased both the out‐of‐plane and in‐plane thermal conductivities of the epoxy resin. The addition of AlN also increased thermal conductivity, but ≥40 wt% was required to obtain thermal conductivity comparable with that of an epoxy resin film doped with 0.9 wt% P3HT/graphene complex. The present results illustrate the potential of P3HT/graphene complexes as fillers for improving the thermal conductivity of epoxy resins without affecting their insulating properties.Highlights Polythiophene/graphene fillers increased epoxy resin films' thermal conductivity. To raise the thermal conductivity of epoxy resin films high AlN content was needed. In‐plane/out‐of‐plane epoxy resin films' thermal conductivities were evaluated.

Investigating the in-vitro bioactivity, biodegradability and drug release behavior of the newly developed PES/HA/WS biocompatible nanocomposites as bone graft substitute

The nucleation of carbonate-containing apatite on the biomaterials surface is regarded as a significant stage in bone healing process. In this regard, composites contained hydroxyapatite (Ca10(PO4)6(OH)2, HA), wollastonite (CaSiO3, WS) and polyethersulfone (PES) were synthesized via a simple solvent casting technique. The in-vitro bioactivity of the prepared composite films with different weight ratios of HA and WS was studied by placing the samples in the simulated body fluid (SBF) for 21 days. The results indicated that the the surface of composites containing 2 wt% HA and 4 wt% WS was completely covered by a thick bone-like apatite layer, which was characterized by Grazing incidence X-ray diffraction, attenuated total reflectance–Fourier transform infrared spectrometer, field emission electron microscopy and energy dispersive X-ray analyzer (EDX). The degradation study of the samples showed that the concentration of inorganic particles could not influence the degradability of the polymeric matrix, where all samples expressed similar dexamethasone (DEX) release behavior. Moreover, the in-vitro cytotoxicity results indicated the significant cyto-compatibility of all specimens. Therefore, these findings revealed that the prepared composite films composed of PES, HA, WS and DEX could be regarded as promising bioactive candidates with low degradation rate for bone tissue engineering applications.

Synergetic Improvement of Flexoelectric Coefficient in liquid Crystal Embedded Flexible PVDF Polymer Composite for Energy Harvesting Applications.

Flexoelectricity is the universal electric polarization of dielectrics upon exertion of a non-uniform strain gradient. With the advancement of nano-technology and miniaturization of electronic devices, flexoelectricity holds the promise to address the power requirements for such device operation. The direct flexoelectric effect in liquid crystal (LC) embedded Poly(vinylidene fluoride) (PVDF) polymer films is examined for the first time by the application of external strain on the films. Physical characterizations such as DSC, dielectric spectroscopy, XRD and FESEM are carried out to study the composite films' intrinsic and extrinsic properties like dielectric, crystallinity and morphologies. The value of the flexoelectric coefficient (μ12) increases with the concentration of LC incorporation. At 3wt%, μ12 attains a maximum value of 68 nC/m, which is more than a three-fold increase compared to that of the pure PVDF film. The role of Maxwell Wagner Sillars (MWS) polarization in determining flexoelectric polarization in polymer composites is also discussed. Moreover, the influence of the microstructure and domain size formation in determining the flexoelectric response are discussed in detail to infer the behaviour of the flexoelectric coefficients of the films. Potential device applications based on this phenomenon have been proposed for future research in sensing and actuation. This article is protected by copyright. All rights reserved.

Synergistic Effect of PBz/Epoxy/PCLA Composite Films with Improved Thermal Properties

Polybenzoxazines (PBzs) are advanced forms of phenolic resins that possess many attractive properties, including thermally induced self-curing polymerization, which produces void-free polymer products without any by-product formation. They also possess a high Tg (glass transition temperature) and thermal stability, but the produced materials are brittle in nature, due to which the final form of their application is very difficult. Hence, in this paper, an attempt has been made to overcome the brittleness of PBz by blending it with epoxy and ε-caprolactam (CPLA) to produce free-standing PBz/Epoxy/PCLA (polycaprolactam) films. The curing process between the three components (i.e., Bzo, epoxy, and caprolactam) was monitored using differential scanning calorimetric (DSC) analysis. The results show that there is no appreciable shift in curing the exotherm observed, except a slight shift in the curing process. However, the heat liberated during the exotherm (ΔH) decreases drastically from 121 to 84 J/g, indicating that the content of benzoxazine is very important as it is involved in the polymerization process through oxazine ring-opening. The morphological studies analyzed using SEM and AFM analyses indicate that there was no observable phase separation up to 30 wt.% of CPLA loading, whereas a higher CPLA content of 50 wt.% causes agglomeration and leads to distinctive phase separation. Moreover, the thermal stability of the composite film, PBz/Epoxy/PCLA30, is also increased with a 10% degradation temperature, T10, of 438 °C, when compared with an PBz/Epoxy film. From the obtained results, it is evident that the formation of a composite film through the melt blending process could produce a tough and thermally stable film without sacrificing individual properties.

Flexible piezoelectric pressure sensor based on BaTiO3-CNT/RTV composite film with filter paper microstructures for monitoring hand motions

Flexible piezoelectric sensors are widely used in various applications such as physiological signal monitoring and human-computer interaction. The present study introduces a BaTiO3-CNT/RTV piezoelectric sensor fabricated using a filter paper template. It incorporates micro-scale fiber stacking and a 1% CNT doping in the microstructure, resulting in a notable enhancement of sensor sensitivity, increasing it from 0.07 V N−1 to 0.69 V N−1, representing an almost tenfold improvement. Furthermore, the study investigates the influence of affecting factors like the flexible substrate of the sensing film, thickness, and mass fractions of various materials on the output voltage. The sensor exhibits superior characteristics such as good repeatability under 5000 cyclic loads, high elongation at break, fast response (80 ms) and recovery times (90 ms), and good linearity. It also demonstrates outstanding sensitivity (12 mV/10°) when monitoring different finger bending states, enabling real-time, sensitive, and reliable hand motion tracking. This sensor holds promising prospects for future developments in the fields of intelligent grasping and sign language translation.

Enhanced Electron Transport and Mitigated Voltage Loss in Perovskite Photovoltaics Using Sb2O5@SnO2 Composite Electron Transport Layer.

The efficacy of electron transport layers (ETLs) is pivotal for optimizing the device performance of perovskite photovoltaic applications. However, colloidal dispersions of SnO2 are prone to aggregation and possess structural defects, such as terminal-hydroxyls (OHT) and oxygen vacancies (VOs), which can degrade the quality of ETLs, impede charge extraction and transport, and affect the nucleation and growth processes of the perovskite layer. In this study, the Sb(OH)4 - ions hydrolyzed from SbCl3 in colloidal dispersion can bind to defect sites and effectively stabilize the SnO2 nanocrystals are demonstrated. Upon oxidative annealing, a Sb2O5@SnO2 composite film is formed, in which the Sb2O5 not only mitigates the aforementioned defects but also broadens the energy range of unoccupied states through its dispersed conduction band. The increased electron affinity (EA) facilitates more efficient capture of photoexcited electrons from the perovskite layer, thus augmenting electron extraction and minimizing electron-hole recombination. As a result, a significant improvement in power conversion efficiency (PCE) from 22.60% to 24.54% is achieved, with an open circuit voltage (VOC) of up to 1.195V, along with excellent stability of unsealed devices under various conditions. This study provides valuable insights for the understanding and design of ETLs in perovskite photovoltaic applications.

Synthesis of Perylene Diimide Modified by POSS and its Assembly Behavior in Solution and SBS Matrix

In this work, Perylene diimide derivatives 1,7- POSS-PDI-C12 (PPC) were synthesized using 1,7-Br-PDI- C12, 18-crown-6 ether as phase transfer agent, K2CO3 as catalyst and THF as solvent in a reaction system. Subsequently, the POSS-SH group was successfully introduced into the perylene imide bay site in high yield. The chemical structure and molecular weight of the products were characterized by 1H-NMR, 13C-NMR, MALDI-TOF MS and FT-IR. The self-assembly behavior in different solvents was studied using the research solution self-assembly method. PPC remained in a single monomolecular state due to the bulky POSS group, which introduced large steric hindrance in the molecular packing, leading to the weakening of the π–π interactions. Then, the Composite thin films containing PPC in SBS was prepared. PPC do not exhibit significant force-chromic behavior owing to the dispersion of single- molecule states. This shows that in the construction of mechanochromic materials, chromophore molecules need to have a certain degree of aggregation in the matrix, but the aggregation degree should not be too high.

The Role of Chemical Composition in Determining the Charge‐Carrier Dynamics in (AgI)x(BiI3)y Rudorffites

AbstractSilver‐bismuth‐based perovskite‐inspired materials (PIMs) are increasingly being explored as non‐toxic materials in photovoltaic applications. However, many of these materials exhibit an ultrafast localization of photogenerated charge carriers that is detrimental for charge‐carrier extraction. In this work, such localization processes are explored for thermally evaporated thin films of compositions lying along the (AgI)x(BiI3)y series, namely BiI3, AgBi2I7, AgBiI4, Ag2BiI5, Ag3BiI6, and AgI, to investigate the impact of changing Ag+/Bi3+ content. A persistent presence of ultrafast charge‐carrier localization in all mixed compositions and BiI3, together with unusually broad photoluminescence spectra, reveal that eliminating silver will not suppress the emergence of a localized state. A weak change in electronic bandgap and charge‐carrier mobility reveals the resilience of the electronic band structure upon modifications in the Ag+/Bi3+ composition of the mixed‐metal rudorffites. Instead, chemical composition impacts the charge‐carrier dynamics indirectly via structural alterations: Ag‐deficient compositions demonstrate stronger charge‐carrier localization most likely because a higher density of vacant sites in the cationic sublattice imparts enhanced lattice softness. Unraveling such delicate interplay between chemical composition, crystal structure, and charge‐carrier dynamics in (AgI)x(BiI3)y rudorffites provides crucial insights for developing a material‐by‐design approach in the quest for highly efficient Bi‐based PIMs.

Green Synthesis and Characterization of Silver Anchored ZnO Nanoparticle as the Antimicrobial Reinforcement for Polylactide (PLA) Films

AbstractThe aqueous extract of endophytic fungi (Periconia sp.) was effectively used as a reducing agent to anchor Ag nanoparticles on the ZnO surface. The XRD, UV‐Vis, SEM‐EDX and TEM analyses were performed to ensure the formation of AgNP@ZnO architecture. TEM analysis confirmed that the 4‐20 nm sized Ag nanoparticles were anchored evenly on the surface of ZnO with 16‐78 nm in size. The antimicrobial study showed the superior performance of AgNP@ZnO functional nanoparticles than the pristine ZnO against pathogenic bacteria Staphylococcus aureus (gram‐positive) and Escherichia coli (gram‐negative). Hence, AgNP@ZnO functional particles were effectively explored as antimicrobial reinforcement for fabricating composite films using polylactic acid (PLA) as a matrix. The obtained nanocomposite films showed excellent antibacterial activity, which increases with increasing AgNP@ZnO loading.This article is protected by copyright. All rights reserved.

Investigation on the Dielectric Properties of PVDF-Matrix Composite Films Containing Functionalized Graphene

Investigation on the Dielectric Properties of PVDF-Matrix Composite Films Containing Functionalized Graphene

Fabrication of sodium lignosulfonate/waterborne polyurethane composites with high biological content to enhance mechanical properties and UV resistance

The conversion of sodium lignosulfonate (SL) into high-value functional materials remains challenging. Hereon, a bio-based waterborne polyurethane (WPU) was synthesized using castor oil and isophorone diisocyanate as the raw materials. SL was used as a functional filler to prepare transparent or translucent composites of sodium lignosulfonate/waterborne polyurethane with good properties through physical blending method. The influence of varying SL contents on the performance of composite emulsions and films were studied. The results indicated that the composite derived from bio-based materials had an occupancy rate of 89.5 %, and all composite emulsions exhibited outstanding storage stability. Interestingly, the addition of sodium lignosulfonate greatly improved the mechanical properties and heat resistance due to the strong interfacial interaction between WPUs and SL molecular chains. Furthermore, the composite film could achieve complete UV shielding performance when the sodium lignosulfonate content reached 9 wt %. This work had significantly expanded the range of high-value-added applications for lignin and potential prospects for its use in the field of sunscreen coatings.

Advancing soy protein isolate-ulvan film physicochemical properties and antioxidant activities through strategic high-pressure homogenization technique

Soy protein-based films often exhibit poor properties, including limited mechanical strength, stability, and bioactivity, which hinder their extensive application in the food industry, particularly in edible packaging. To enhance the properties of soy protein-based films, we employed high-pressure homogenization (HPH) to modify the soybean protein isolate (SPI) molecules and sought to cross-link SPI with ulvan polysaccharide, which possesses distinctive bioactivities. The results confirmed that soluble ulvan polysaccharides were incorporated into the cross-linking system through hydrogen bonding. Results indicated that HPH treatment enhanced SPI's solubility and surface hydrophobicity (H0), promoting hydrogen bonding and hydrophobic interactions between SPI and ulvan, as evidenced by ζ-potential and turbidity measurements. Structural and microstructural analyses of both individual SPI and composite films, using FT-IR, XRD, CD and SEM, demonstrated a high compatibility between HPH-treated SPI and ulvan. The incorporation of ulvan reduced the films' tensile strength (TS), but higher pressure significantly improved it (p < 0.05). Post-HPH modification, the films exhibited increased contact angle and swelling capacity (p < 0.05), indicating enhanced hydrophobicity. Higher pressure treatments resulted in more opaque and yellowish films, thereby diminishing ultraviolet light transmission. Thermal stability analyses, via TGA-DSC, showed that U-HSPI films had improved thermal stability compared to pure SPI films. Moreover, ulvan inclusion boosted the antioxidant capacity of SPI films, especially after HPH treatment. Overall, this study confirms that HPH modification substantially influences the properties and activities of SPI-based films, and the complex films based on SPI and ulvan with improved physicochemical and antioxidant properties exhibit a great potential in the food packaging field.

Robust and Superhydrophobic Polydimethylsiloxane/Ni@Ti3C2Tx Nanocomposite Coatings with Assembled Eyelash-Like Microstructure Array: A New Approach for Effective Passive Anti-Icing and Active Photothermal Deicing.

To solve the problem of ice condensation and adhesion, it is urgent to develop new anti-icing and deicing technologies. This study presented the development of a highly efficient photothermal-enhanced superhydrophobic PDMS/Ni@Ti3C2Tx composite film (m-NMPA) fabricated cost-effectively and straightforwardly. This film was fabricated utilizing PDMS as a hydrophobic agent, adhesive, and surface protector, while Ni@Ti3C2Tx as a magnetic photothermal filler innovatively. Through a simple spraying method, the filler is guided by a strong magnetic field to self-assemble into an eyelash-like microstructure array. The unique structure not only imparts superhydrophobic properties to the surface but also constructs an efficient "light-capturing" architecture. Remarkably, the m-NMPA film demonstrates outstanding superhydrophobic passive anti-icing and efficient photothermal active deicing performance without the use of fluorinated chemicals. The micro-/nanostructure of the film forms a gas layer, significantly delaying the freezing time of water. Particularly under extreme cold conditions (-30 °C), the freezing time is extended by a factor of 7.3 compared to the bare substrate. Furthermore, under sunlight exposure, surface droplets do not freeze. The excellent photothermal performance is attributed to the firm anchoring of nickel particles on the MXene surface, facilitating effective "point-to-face" photothermal synergy. The eyelash-like microarray structure enhances light-capturing capability, resulting in a high light absorption rate of 98%. Furthermore, the microstructure aids in maintaining heat at the uppermost layer of the surface, maximizing the utilization of thermal energy for ice melting and frost thawing. Under solar irradiation, the m-NMPA film can rapidly melt approximately a 4 mm thick ice layer within 558 s and expel the melted water promptly, reducing the risk of secondary icing. Additionally, the ice adhesion force on the surface of the m-NMPA film is remarkably low, with an adhesion strength of approximately 4.7 kPa for a 1 × 1 cm2 ice column. After undergoing rigorous durability tests, including xenon lamp weathering test, pressure resistance test, repeated adhesive tape testing, xenon lamp irradiation, water drop impact testing, and repeated brushing with hydrochloric acid and particles, the film's surface structure and superhydrophobic performance have remained exceptional. The photothermal superhydrophobic passive anti-icing and active deicing technology in this work rely on sustainable solar energy for efficient heat generation. It presents broad prospects for practical applications with advantages such as simple processing method, environmental friendliness, outstanding anti-icing effects, and exceptional durability.

Flexibility, dissolvability, heat-sealability, and applicability improvement of pullulan-based composite edible films by blending with soluble soybean polysaccharide

This study aimed to prepare a heat-sealable, water-soluble, edible film based on pullulan (PUL)/soluble soybean polysaccharide (SSPS) for the portable packaging of convenience foods. The effects of the PUL/SSPS ratios on the microstructure, physicochemical properties, barrier properties, and mechanical properties of the PUL/SSPS films were explored. Fourier-transform infrared spectroscopy and X-ray diffraction showed an apparent hydrogen bonding interaction between SSPS and PUL in the PUL/SSPS films. As the SSPS proportion in the PUL/SSPS films increased, the water contact angle, moisture content, water vapor permeability, solubility, oxygen permeability, flexibility, and antioxidant activity increased, whereas light transmittance decreased. The heat-seal strength of the P9S1 film (PUL/SSPS ratio of 9:1) is slightly lower than that of the PUL film (p > 0.05). Furthermore, the application potential of the PUL/SSPS films for packaging peptide powder was evaluated. The P9S1 film exhibited a satisfactory packaging effect and was completely dissolved in water with low turbidity. Therefore, the P9S1 film is a promising packaging material for convenient powdered foods.

Cellulose-based separator woven by double-layer-configuration fibers for high S-load Li-S batteries

Lithium-sulfur (Li-S) battery with high theoretical energy density, has been the most promising next-generation energy storage devices. However, the capacity of the high S-loaded cathode decays rapidly due to the shuttling of soluble polysulfide intermediates between the two electrodes, which seriously inhibits its development. In this work, polyacrylonitrile (PAN) and cellulose composite film (PAN@CE) is designed, which is woven by double-layer configuration fiber. The outer layer of fiber is mainly composed of cellulose, and the inner layer is mainly PAN. From DFT calculations and experiments, the double-layer configuration enriched with nitrogen and oxygen groups can effectively inhibit the shuttle of soluble polysulfides. Meanwhile, the interlaced network structure of PAN@CE improves the electrolyte wettability and provides abundance transport paths for ions. In addition, the film also has good thermal stability. Hence, the cycling stability of Li-S batteries with PAN@CE as separator has been greatly improved. Cellulose-based Li-S battery with 9.1 mg S loading and an E/S ratio of 6.2 μL mg−1 is assembled. Its initial area capacity is 5.67 mAh cm−2. After 200 long cycles, the area capacity keeps above 4.0 mAh cm−2.

A Highly Electrostrictive Salt Cocrystal and the Piezoelectric Nanogenerator Application of Its 3D-Printed Polymer Composite.

Ionic cocrystals with hydrogen bonding can form exciting materials with enhanced optical and electronic properties. We present a highly moisture-stable ammonium salt cocrystal [CH3C6H4CH(CH3)NH2][CH3C6H4CH(CH3)NH3][PF6] ((p-TEA)(p-TEAH)·PF6) crystallizing in the polar monoclinic C2 space group. The asymmetry in (p-TEA)(p-TEAH)·PF6 was induced by its chiral substituents, while the polar order and structural stability were achieved by using the octahedral PF6- anion and the consequent formation of salt cocrystal. The ferroelectric properties of (p-TEA)(p-TEAH)·PF6 were confirmed through P-E loop measurements. Piezoresponse force microscopy (PFM) enabled the visualization of its domain structure with characteristic "butterfly" and hysteresis loops associated with ferro- and piezoelectric properties. Notably, (p-TEA)(p-TEAH)·PF6 exhibits a large electrostrictive coefficient (Q33) value of 2.02 m4 C-2, higher than those found for ceramic-based materials and comparable to that of polyvinylidene difluoride. Furthermore, the composite films of (p-TEA)(p-TEAH)·PF6 with polycaprolactone (PCL) polymer and its gyroid-shaped 3D-printed composite scaled-up device, 3DP-Gy, were prepared and evaluated for piezoelectric energy-harvesting functionality. A high output voltage of 22.8 V and a power density of 118.5 μW cm-3 have been recorded for the 3DP-Gy device. Remarkably, no loss in voltage outputs was observed for the (p-TEA)(p-TEAH)·PF6 devices even after exposure to 99% relative humidity, showcasing their utility under extremely humid conditions.

Characterization of nanocomposite films based on tomato seed mucilage, gelatin and TiO2 nanoparticles

The aim of the present research was to investigate the interaction effect of incorporating titanium dioxide (TiO2) (0 %, 0.5 %, and 1 %) nanoparticles and manipulating the proportion of tomato seed mucilage (TSM) and gelatin (Ge) (1: 0, 0.33:0.67, 0.67:0.33, and 0:1) on the physical, mechanical, and microbial characteristics of the film. The findings indicated that the incorporation of TiO2 engendered an augmentation in the surface roughness of the film and an elevation in the film's thickness. The mechanical evaluation results revealed that the incorporation of TiO2 into the TSM-Ge films significantly enhanced (p˂0.05) the tensile strength (TS), (up to 300 %), an elevation of Young's modulus, while concurrently leading to a reduction in the elongation at break (EB). The incorporation of TiO2 resulted in a significant enhancement in various properties of the film (p˂0.05), including opacity, contact angle, oxygen permeability (OP), water vapor permeability (WVP), moisture absorption, moisture content, solubility, and swelling. The rise in the proportion of TSM resulted in a concomitant increase in the color differences (ΔE), and yellowness index (YI). Conversely, there was a decrease in the lightness (L*) and the whiteness index (WI). Additionally, an increase was found in opacity, solubility, moisture content, WVP, OP, swelling, and moisture absorption. It was observed that films without TiO2 exhibited no inhibitory effect. However, upon augmenting the concentration of TiO2 to 1 %, notable inhibitory and lethal effects were observed against various microorganisms, including Staphylococcus aureus, Escherichia coli, Aspergillus niger, and Candida glabrata. The results showed that the TSM-Ge composite film containing TiO2, exhibited potential as a viable choice for food packaging susceptible to microbial spoilage.

Anti-Oxidized Self-Assembly of Multilayered F-Mene/MXene/TPU Composite with Improved Environmental Stability and Pressure Sensing Performances

MXenes, as emerging 2D sensing materials for next-generation electronics, have attracted tremendous attention owing to their extraordinary electrical conductivity, mechanical strength, and flexibility. However, challenges remain due to the weak stability in the oxygen environment and nonnegligible aggregation of layered MXenes, which severely affect the durability and sensing performances of the corresponding MXene-based pressure sensors, respectively. Here, in this work, we propose an easy-to-fabricate self-assembly strategy to prepare multilayered MXene composite films, where the first layer MXene is hydrogen-bond self-assembled on the electrospun thermoplastic urethane (TPU) fibers surface and the anti-oxidized functionalized-MXene (f-MXene) is subsequently adhered on the MXene layer by spontaneous electrostatic attraction. Remarkably, the f-MXene surface is functionalized with silanization reagents to form a hydrophobic protective layer, thus preventing the oxidation of the MXene-based pressure sensor during service. Simultaneously, the electrostatic self-assembled MXene and f-MXene successfully avoid the invalid stacking of MXene, leading to an improved pressure sensitivity. Moreover, the adopted electrospinning method can facilitate cyclic self-assembly and the formation of a hierarchical micro-nano porous structure of the multilayered f-MXene/MXene/TPU (M-fM2T) composite. The gradient pores can generate changes in the conductive pathways within a wide loading range, broadening the pressure detection range of the as-proposed multilayered f-MXene/MXene/TPU piezoresistive sensor (M-fM2TPS). Experimentally, these novel features endow our M-fM2TPS with an outstanding maximum sensitivity of 40.31 kPa−1 and an extensive sensing range of up to 120 kPa. Additionally, our M-fM2TPS exhibits excellent anti-oxidized properties for environmental stability and mechanical reliability for long-term use, which shows only ~0.8% fractional resistance changes after being placed in a natural environment for over 30 days and provides a reproducible loading–unloading pressure measurement for more than 1000 cycles. As a proof of concept, the M-fM2TPS is deployed to monitor human movements and radial artery pulse. Our anti-oxidized self-assembly strategy of multilayered MXene is expected to guide the future investigation of MXene-based advanced sensors with commercial values.