Composite Films Research Articles

Robust Superhydrophobic Films Based on an Eco-Friendly Poly(l-lactic acid)/Cellulose Composite with Controllable Water Adhesion.

Poly(l-lactic acid) (PLLA) featuring desirable biodegradability and biocompatibility has been recognized as one of the promising eco-friendly biomaterials. However, low crystallization and poor mechanical and chemical performances dramatically hamper its practical application. In this work, we report that functionalized cellulose/PLLA composite superhydrophobic stereocomplex films with controllable water adhesion and protein adsorption can be fabricated by a facile approach for the first time. First, cellulose is surface-modified by means of two silanization modification methods. Then, superhydrophobic cellulose/PLLA composite films are prepared through a solvent-evaporation-induced phase separation method. The two cellulose/PLLA composite films exhibit extreme water repellency but tunable water adhesion from sticky to slippery. The protein adsorption capacity of the cellulose/PLLA composite films can also be regulated. In addition, the stereocomplexation of the composite film provides excellent mechanical properties with an elongation at break of 22.36%, which is 237.8% higher than that of a pure PLLA film, which is more suitable for biomaterials. Furthermore, good biodegradability of the PLLA composite films in nature enables the bio-based composites as alternative materials to replace conventional petroleum-based polymers. The superhydrophobic films have also been demonstrated for many applications, including slippery surfaces, liquid transportation without loss, and antifouling.

Active Passivation of Anion Vacancies in Antimony Selenide Film for Efficient Solar Cells.

Binary antimony selenide (Sb2Se3) is a promising inorganic light-harvesting material with high stability, non-toxicity and wide light harvesting capability. In this photovoltaic material, it has been recognized that deep energy level defects with large carrier capture cross section, such as VSe (selenium vacancy), lead to serious open-circuit voltage (VOC) deficit and in turn limit the achievable power conversion efficiency (PCE) of Sb2Se3 solar cells. Understanding the nature of deep-level defects and establishing effective method to eliminate the defects are vital to improving VOC. In this study, we propose a novel directed defect passivation strategy to suppress the formation of VSe and maintaining the composition and morphology of Sb2Se3 film. In particularly, through systematic study on the evolution of defect properties, we reveal the pathway of defect passivation reaction. Owing to the inhibition of defect-assisted recombination, the VOC increases, resulting in an improvement of PCE from 7.69% to 8.90%, where is the highest efficiency of Sb2Se3 solar cells prepared by thermal evaporation method with superstrate device configuration. This study proposes a new understanding of the nature of deep-level defects and enlightens the fabrication of high quality Sb2Se3 thin film for solar cell applications. This article is protected by copyright. All rights reserved.

Effect of copper in the stabilization of Al/CuO energetic semiconductor bridge

The long-term storage performance of energetic multilayer nanofilms is of great significance for their applications. In this paper, it is proposed to add a 10 nm Cu barrier layer between Al/CuO composite films to increase their storage stability. The Al/CuO composite film and Al/Cu/CuO composite film were aged for 14 days in an environment with a relative humidity of 40% and a temperature of 71 °C. Scanning electron microscopy and differential scanning calorimetry were used to analyze the microstructure and thermodynamic properties of the energetic films before and after aging, and the electrical detonation performance and ignition ability of energy-containing semiconductor bridges were studied. The results indicate that after aging for 14 days in an environment with a relative humidity of 40% and a temperature of 71 °C, the Al layer of the Al/CuO composite film becomes thinner, the Al2O3 interface layer increases, and the heat release decreases. The interlayer microstructure of the Al/Cu/CuO energetic multilayer nanofilms did not change significantly, and the addition of a 10 nm Cu layer formed a low-temperature Al–Cu alloy, reducing the reaction initiation temperature from 626 to 570 °C. The critical ignition time and critical ignition energy of the Al/CuO-energetic semiconductor bridge (ESCB) increased, the flame duration shortened from 440 to 300 μs, the flame size decreased by 50%, the plasma temperature decreased, and aging had no significant effect on the electrical explosion performance of Al/Cu/CuO-ESCB. After aging for 14 days in an environment with a relative humidity of 40% and a temperature of 71 °C, the maximum ignition gap of B/KNO3 for Al/CuO-ESCB decreased from 1.4 to 1.2 mm, while the maximum ignition gap for Al/Cu/CuO-ESCB remained at 1.6 mm, which significantly improved the ignition performance and long storage performance of the energetic semiconductor bridge.

Chemical spray deposited SnO2:MoO3 composite thin films for visible light photocatalytic dye degradation application

Chemical spray deposited SnO2:MoO3 composite thin films for visible light photocatalytic dye degradation application

Evaluation of postharvest physiological parameters and shelf life of Agaricus bisporus by addition of anise essential oil Pickering emulsion to corn starch/cassia gum composite film

Evaluation of postharvest physiological parameters and shelf life of Agaricus bisporus by addition of anise essential oil Pickering emulsion to corn starch/cassia gum composite film

Exploring the Interplay between Tribocorrosion and Surface Chemistry of the ASTM F139 Surgical Stainless Steel in Phosphate-Buffered Saline Solution

Surgical ASTM F139 stainless steel is used for temporary fixtures in the biomedical field. Tribocorrosion is a major concern in this application. The aim of the present work was to study the interplay between tribocorrosion behavior and the surface chemistry of the ASTM F139 stainless steel in phosphate-buffered saline solution (PBS). Sliding wear tests were conducted against alumina balls at different electrochemical potentials: open circuit potential (OCP), cathodic potential (−100 mV versus the OCP), and anodic potentials (+200 mVAg/AgCl and +700 mVAg/AgCl). The normal load was 20 N. The wear volume was estimated based on micrographs obtained from the wear tracks using confocal laser scanning microscopy. Moreover, the wear tracks were also examined by scanning electron microscopy (SEM). The surface chemistry of the ASTM F139 specimens was analyzed by X-ray photoelectron spectroscopy (XPS). The wear volume was dependent on the electrochemical potential, being maximized at +700 mVAg/AgCl. Delamination areas and grooves were observed in the wear tracks. Detailed assessment of the surface chemistry inside the wear tracks allowed identification of the main chemical species and their relative quantities, thus enabling correlation of the passive film composition with the observed tribocorrosion behavior.

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.

High performance multifunctional piezoelectric PAN/UiO-66-NO2/MXene composite nanofibers for flexible touch sensor

In this study, a flexible piezoelectric sensor based on polyacrylonitrile (PAN), zirconium-based MOF (UiO-66) with nitro (NO2) and two-dimensional material MXene composite nanofiber film was proposed. When pressure was applied, the three-dimensional structural nanopores were compressed, increasing the intercalation structure between the MXene nanosheets coated in the fibers. The double-packed system produced a higher resistance change under the same pressure load, which can be explained by the fact that the low-conductivity octahedral UiO-66-NO2 particles acted as a similar “buffer” between the highly conductive MXene. At the same time, a large number of hydrogen bonds between the surfaces of the two fillers enhanced the synergistic effect and promoted the interfacial coupling effect, so that more 31-helical conformation in the PAN matrix was converted into a planar zigzag conformation. This improved the piezoelectric performance and enabled the sensor to have a voltage output of about 200 V in the detection range. And because the polyhedral form of UiO-66-NO2 particles provided a rougher surface structure, the piezoelectric sensor can achieve a high sensitivity of 5.62 V/N. The other results showed that the dielectric constant of the designed flexible piezoelectric sensor was increased to 2.67, the dielectric loss was kept at a low level of 0.026, and the maximum elongation was 56.03 %. This multi-functional sensor shows great potential in the fields of health and medical treatment, human-computer interaction, etc.

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

Multifunctional konjac glucomannan/xanthan gum self-healing coating for bananas preservation

Damage to the integrity of the preservation coating on the fruit surface will seriously affect the shelf life of the fruit. In this work, the strong hydrogen bond interaction between xanthan gum (XG) and konjac glucomannan (KGM) could form hydrogel films with self-healing properties. The introduction of gallic acid (GA) was beneficial to further improve the antioxidant activity and UV shielding performance of the composite films. Surprisingly, the mechanical properties and gas (water vapor, O2 and CO2) barrier properties of the KGM film crosslinked by XG were significantly improved. The experiment of banana preservation showed that the composite coating could effectively delay the water loss and browning of bananas, slow down the decomposition of pectin and starch in the flesh, and extend the shelf life of bananas for >6 days. Therefore, this multifunctional coating is an excellent packaging material and has a very broad application prospect in the field of food preservation.