Composite Films Research Articles

Influence of carbon content and irradiation modes on the antibiotic removal from water using VIS-activated TiO2/expanded graphite composite photocatalysts

TiO2/expanded graphite (TiO2/EG) composite films were applied to water treatment for sulfadiazine (SDZ) degradation in a continuous flat plate photochemical reactor. The films were synthesized by sol-gel method and deposited on borosilicate glass by airbrush spray coating technique, forming a TiO2/C heterojunction. Increasing the amount of carbon promoted more efficient photocatalytic removal of SDZ under simulated sunlight, which increased from 9.1% in the absence of carbon to 49.8% for the material containing 7.5% C. From the formation of the TiO2/C heterojunction, morphological modifications, changes in the electronic structure and reduction of the band gap energy were observed. Type-II heterojunction formation was observed. Foreground and background irradiation modes were investigated, and a possible photocatalytic mechanism was proposed. TiO2/7.5 %-EG exhibited the best photocatalytic performance, with the possibility of reuse. The films showed good reusability in the SDZ degradation over 4 photocatalytic cycles. The influence of irradiation modes and the role of oxidizing species were discussed. The results showed that TiO2/EG hybrid films are a promising alternative for practical photocatalytic applications under sunlight.

Room temperature self-healing and high gas barrier properties of elastomer composites incorporated with liquid metal

Flexible electronic devices require stretchable packaging materials that provide a hermetic seal. However, conventional soft materials often exhibit strong gas permeability, making it difficult to achieve stable operation, which requires films with high deformability, self-healing capability, and gas barrier functionality. In this study, a layer by layer (LBL) method was employed to uniformly coat a controllable thickness of liquid metal (LM) onto a designed and synthesized self-healing thermoplastic polyurethane (TPU) film, successfully developing a stretchable gas barrier film (TPU/LM) with high gas barrier properties. The designed polyurethane film significantly enhanced the adhesion of the liquid metal, effectively preventing leakage. The experimental results show that the water vapor transmission rate (WVTR) of the TPU/LM composite film with a thickness of 40 μm is 4.04g/(m2·day). Compared to the film without LM, the gas barrier performance has been improved by approximately 16 times. Additionally, there is a significant enhancement in nitrogen (N2) barrier, with a permeation rate reaching 4.0*10−17 cm3 cm/(cm2·s·Pa), effectively blocking the N2 permeation. This demonstrates the universality of the TPU/LM in gas barrier applications. Furthermore, the TPU/LM film also demonstrated excellent electromagnetic shielding effectiveness. The self-healing capability of the stretchable gas barrier film allows it to recover its initial gas barrier performance after mechanical damage. Humidity-sensitive resistors encapsulated with TPU/LM exhibited stable operation in both air and 90 % humidity environments, confirming the superior barrier properties of the TPU/LM. Generally, the developed TPU/LM is suitable for packaging applications in the next generation of flexible electronic devices.

Photodimerization-Triggered Photopolymerization of Triene Coordination Polymers Enables Macroscopic Photomechanical Movements.

Controlling the packing of olefinic molecules in crystals is essential for triggering solid-state [2 + 2] photocycloaddition reactions and the synthesis of photocontrolled smart materials. Herein, we report the stepwise photodimerization-triggered photopolymerization of two triene coordination polymers (CPs), {[Zn(2-BBA)2(tpeb)]·0.5CH3CN}n (1, 2-HBBA = 2-bromobenzoic acid, tpeb = 1,3,5-tri-4-pyridyl-1,2-ethenylbenzene) and {[Zn(3-BBA)2(tpeb)]·CH3CN)}n (2, 3-HBBA = 3-bromobenzoic acid). Upon irradiation with 420 nm light, each pair of closely packed and parallel olefinic bonds in 1 undergoes a [2 + 2] cycloaddition reaction, which connects two adjacent Z-shaped chains into a ladder-like coordination chain [Zn(2-BBA)2(bpbdpvpcb)0.5]n (1a, bpbdpvpcb = 1,3-bis(4-pyridyl)-2,4-bis(3,5-di(2-(4-pyridyl)vinyl)phenyl]cyclobutene) through single-crystal to single-crystal (SCSC) transformation. After photodimerization from 1 to 1a has occurred, the olefinic bonds that were initially distant are brought in close enough proximity to meet the requirements for a subsequent [2 + 2] cycloaddition reaction. Upon further light irradiation, the neighboring bpbdpvpcb ligands in 1a experience a SCSC photopolymerization based on [2 + 2] photocycloaddition and transform into poly-3b,4,5,5a,8b,9,10a-octahydro-4,5,9,10-tetrapyridyl-2,7-di(2-(4-pyridyl)vinyl)dicyclobuta[e,l]-pyren (poly-otpdpvdcbp). 2 showed similar structural changes under UV light illumination. Under light exposure, single crystals of 1 and 2 with different morphologies exhibit bending, cracking, and jumping photomechanical motions. The composite film (1-PVA) engineered by dispersing crystalline particles of 1 in poly(vinyl alcohol) (PVA) displays interesting light-wavelength-dependent photomechanical motions and can perform photodriven swimming on a liquid surface. This work provides a useful and promising approach to enable photodimerization of those photoinactive olefin pairs embedded in CPs and opens a new route to synthesize organic polymers by using olefinic CP platforms.

Enhancing the mechanical properties of polylactic acid (PLA) composite films using Pueraria lobata root microcrystalline cellulose

To enhance the mechanical properties of polylactic acid (PLA) material, the PLA-based composite films are prepared by using Pueraria lobata (Willd.) Ohwi root microcrystalline cellulose (PRMCC) treated with 3-aminopropyl triethoxysilane (KH550) silane coupling agent as the dispersed phase through solvent casting method. The effects of the concentrations of PRMCC and KH550 as well as the KH550 pretreating condition (ethanol concentration) on the tensile properties of PLA-based composite films are investigated. The PLA-based composite film treated with 5 wt% PRMCC and 18 wt% KH550 (pretreated by 90 % EtOH) exhibits the greatest performance. Its elongation at break value is detected to be 4.0 %, 1.6 times as large as that of pure PLA film. The water absorption of the as-prepared PLA-based composite film is reduced from 0.49 % of the unmodified PLA/PRMCC film to 0.12 %. Moreover, the modified PLA-based composite film has a hydrophobic surface and exhibits good thermal stability. Compared with pure PLA film, the modified PLA-based composite film exhibits improved UV shielding performance with acceptable transparency. Furthermore, after adding poly(butylene adipate-co-terephthalate) (PBAT) to the composite system, the elongation at break of the PLA-based composite film is up to 7.2 %. This research can provide theoretical guidance for enhancing the performance of PLA products.

Modified Chitosan-Based Coating/Packaging Composites with Enhanced Antibacterial, Antioxidant, and UV-Resistant Properties for Fresh Food Preservation.

Chitosan-based biomass packaging materials are a promising material for food preservation, but their limited solubility, antioxidant capacity, UV resistance, and mechanical properties severely restrict their application. In this study, we developed a novel chitosan-based coating/packaging composite (QCTO) using quaternary ammonium salt and tannic acid (TA)-modified chitosan (QCS-TA) and oxidized chitosan (OCS). The introduction of quaternary ammonium salt and TA effectively improves the water solubility and antibacterial, antioxidant, and UV-resistant properties of chitosan. The Schiff-base bond formed between OCS and QCS-TA, along with the TA-mediated multiple interactions, conferred the prepared composite film with good mechanical properties (69.9 MPa tensile strength) and gas barrier performance to water (14.3 g·h-1·m-2) and oxygen (3.5 g·mm·m-2·h-1). Meanwhile, the prepared QCTO composites demonstrate excellent biocompatibility and safety and are applied as coatings for strawberries and bananas as well as packaging films for mushrooms. These preservation experiments demonstrated that the prepared composites are able to effectively reduce weight loss, prevent microbial growth, maintain color, and significantly prolong the shelf life of fresh products (bananas, strawberries, and mushrooms extended shelf life by 6, 5, and 6 days, respectively). Therefore, the developed QCTO coating/packaging film shows great potential for applications in the field of food preservation and packaging.

Performance Properties and Finite Element Modelling of Forest-Based Bionanomaterials/Activated Carbon Composite Film for Sustainable Future

Thanks to its highly crystalline structure and excellent thermal, optical, electrical and mechanical properties, carbon and its derivatives are considered the preferred reinforcement material in composites used in many industrial applications, especially in the forest and forest products sector, including oil, gas and aviation. Since hydroxyethyl cellulose (HEC) is a biopolymer, it has poor mechanical and thermal properties. These properties need to be strengthened with various additives. This study aims to improve the thermal and mechanical properties of hydroxyethyl cellulose by preparing hydroxyethyl cellulose/activated carbon (HEC/AC) composite materials. With this study, composites were obtained for the first time and their mechanical properties were examined using a 3D numerical modeling technique. The thermal stability of the prepared composite materials was investigated via thermal gravimetric analysis (TGA). The samples were heated from 30 °C to 750 °C with a heating rate of 10 °C/min under a nitrogen atmosphere and their masses were measured subsequently. The mechanical properties of the composites were investigated via the tensile test. The viscoelastic properties of the composite films were determined with dynamic mechanical thermal analyses (DMTA) and their morphologies were examined with scanning electron microscopy (SEM) images. According to the results, the best F3 sample (films containing 3 wt.% activated carbon) had an elastic modulus of 168.3 MPa, a thermal conductivity value of 0.068 W/mK, the maximum mass loss was at 328.20 °C and the initial storage modulus at 30 °C was 206.13 MPa. It was determined that the hydroxyethyl cellulose composite films containing 3 wt.% activated carbon revealed the optimum results in terms of both thermal conductivity and viscoelastic response and showed that the obtained composite films could be used in industrial applications where thermal conductivity was required.

Development of multilayer composite film based on protein‐polysaccharides with the addition of onion waste extracts and their impact on the shallot quality

AbstractAt present, multilayer composite film is attractive in the production of biodegradable films due to its essential film properties. The current study mainly focused on overcoming the problems of poor water barrier and mechanical strength observed in monolayer films (SA‐CMC and G/SA‐CMC) made from gluten (G), sodium alginate (SA), and carboxymethylcellulose (CMC). The film was developed with the addition of onion waste extracts (OWEs), primarily from peel and stalk, to enhance functional properties. The multilayer composite film consists of three layers: an outer layer made of G, an inner layer made of SA, CMC, and a middle layer made of G/SA‐CMC. The developed composite film exhibited improved physical properties (thickness: 0.348–0.629 mm and moisture: 20.889%–21.403%), mechanical properties (tensile strength: 21.943–20.640 MPa), and barrier properties (WVP: 0.212–0.516 g/m.s.Pa × 10−14) compared to monolayer films (SA‐CMC and G/SA‐CMC). The addition of OWEs enhanced the multilayer film's phenolic (20.076 and 36.175 mgGAE/g) and antioxidant activity (73.850% and 42.667%). The study found that the multilayer control film had minimal changes in weight loss (9.75% ± 0.18%) and firmness (6.68 ± 0.64 N) compared to OWEs‐added films (9.93% ± 0.49–10.02% ± 0.14% and 6.61 ± 0.37 to 6.64 ± 0.18 N). However, fresh‐peeled shallot onion packed with control film exhibited higher bacterial counts (6.70 ± 0.42 CFU/g) and yeast and mold counts (5.08 ± 0.20 CFU/g) than those packed with the OWEs‐added film (6.49 ± 0.28–6.56 ± 0.27 CFU/g and 4.75 ± 0.18–4.89 ± 0.21 CFU/g), indicating that OWEs protect the onions from microbial degradation. Overall, the multilayer control film (without OWEs) showed better results for storing the fresh‐peeled shallot onion at 4°C for 21 days.Highlights Onion waste extracts have potent high antioxidant and antimicrobial properties Multilayer film's physical, mechanical, barrier, and functional properties improved Addition of onion waste extracts increased the film's antimicrobial activity Control film showed a better effect for storing fresh‐peeled shallot onion Developed film can store fresh‐peeled shallot onion for 21 days at 4°C.

Structural, morphological, and chemical composition of ternary ZrHfN thin films deposited by reactive co-magnetron sputtering

This study focuses on a deposited ternary zirconium hafnium nitride (ZrHfN) thin film prepared using the reactive co-magnetron sputtering technique. The effect of the nitrogen (N2) flow rate on the films' structural, morphological, and chemical composition was investigated. The gracing-incidence X-ray diffraction (GIXRD) showed that all ZrHfN thin films exhibited a crystalline face-centered cubic structure with a strong (111) orientation. With increasing the N2 flow rate, the film's crystallography changed based on thermodynamic theory. The films demonstrated uniformity and homogeneity in their ternary nitride composition, as confirmed by transmission electron microscopy-energy dispersive X-ray spectroscopy (TEM-EDS) mapping and electron probe microanalyzer (EPMA). Chemical state analysis using X-ray photoelectron spectroscopy (XPS) indicated the presence of both nitride and oxynitride species in all samples. Notably, the atomic concentration of the main elements (Zr, Hf, and N) remained relatively stable over the controlled N2 flow rate range. However, the N2 flow rate played a crucial role in forming hafnium nitride and oxynitride chemical states, whereas it did not significantly influence the Zr phases, dominated by Zr oxides. Additionally, the hardness of the ternary ZrHfN thin films exhibited enhancement comparable to typical ternary nitrides.

Synergistic effects of starch and carrageenan from Kappaphycus alvarezii in composite film formation: Physicochemical and degradable properties

Rising concerns around plastic pollution from single-use plastic (SUPs), especially food packaging, have driven interest in sustainable alternatives. As such, algae biomass has gained attention for bioplastic production due to algae's rapid growth and abundant polysaccharides. This research focuses on extracting carrageenan from Kappaphycus alvarezii, extensively cultivated in Sabah, Malaysia, and utilizing it in combination with starch and glycerol to develop algae-based films. The physicochemical properties and degradation rate of these films were evaluated, revealing that the addition of carrageenan enhanced overall thermal stability meanwhile increasing water solubility, water content but reducing the degradation rate and swelling degree. This is primarily due to the crystalline structures of carrageenan, which provide a more rigid arrangement compared to the network of starch polymers. However, the incorporation of starch into the blends has enhanced the elongation and surface morphology, resulting in more balanced properties. Overall, these carrageenan films displayed impressive thermal, mechanical, and biodegradability characteristics, establishing their viability as substitutes for conventional plastics.

Preparation & characterization of polyvinyl alcohol/thymol blue composites gel and films for low radiation dosimetry

BackgroundExposure to low radiation has been indispensable due to it is necessity in radiography and it is induced potential effects in patients and radiology staff. Hence the measurement and detection became inevitable for radiation practitioners and the patients. The study aimed to present the synthesis of polyvinyl alcohol gel doped with Thymol Blue dye (PVA/TB) as gel and films for low radiation dosimetry. MethodThe polymer was prepared under controlled parameters (PVA 5%, temperature 80 °C, dopped with 0.01, 0.03, 0.05, 0.07, 0.09 mw of TB). The formed gel and films were irradiated with x-ray as: 0, 2, 4, 6, 8, 10 mGy. ResultsGel and films showed color quenching from yellow to light yellow as the radiation dose increased, as well as gradual significant (R2 = 0.97) reduction in optical density for all concentration (0.01, 0.02–0.09 mw of TB). The UV-spectroscope for (PVA/TB0.01mw) gel showed absorbance peaks at λ = 435, 326 and 279 nm, that decreased significantly (R2 = 0.97) as the radiation dose increases. And XRD for (PVA/TB0.01 mw) reveals the crystallinity of PVA at 2 thetas = 19.5° which increased to 40.5% at 10 mGy. FTIR revealed the chemical bonds with relevant intensities (CH (725.1–781 & 3030 cm−1), C – C (883.2 & 1170.6 cm−1), C – O (1063- 1096 cm−1), CH2 (1357.6 cm−1 wagging, 2879.2 cm−1 alkyl stretch), C = C (1623.8–1651.5 cm−1), C = O (1681.6–1683.6 cm−1), C – OH (3288 cm−1)) that decreased as the radiation dose increased and new radiogenic bonds at vibrational bands 1063–1096 cm−1 referring to C – O – C of Polysaccharide's pyranose and at 2125.1 cm−1 for C ≡ C alkenyl). ConclusionBoth forms of PVA/TB films and gel showed feasibility and applicability for radiation detection and measurement.

Inkjet‐Printed Flexible and Transparent Ti3C2Tx/TiO2 Composite Films: A Strategy for Photoelectrically Controllable Photocatalytic Degradation

The 2D Ti3C2Tx MXene has a large specific surface area, abundant functional groups, and low work function, which has potential in the field of photocatalytic materials. However, the manufacturing of controllable films with high photocatalytic properties and desirable transmittance is a challenging task. Herein, low‐cost, large‐scale, and rapid preparation of Ti3C2Tx/TiO2 flexible composite films have been successfully prepared by inkjet printing technology, which can be applied in complex and special environments, as well as in photoelectrically controllable places for photocatalytic performance. With the increase of the anatase TiO2, the transmittance of Ti3C2Tx/TiO2 films increases from 55.37% to 73.27% at 780 nm, corresponding to the square resistance of 1.112–206.496 kΩ sq−1 and the figure of merit of 0.48–0.005. When the amount of anatase TiO2 is 15%, the film has the best photocatalytic effect on methylene blue (MB) dye, reaching 68.94%. After five cycles of testing, the degradation efficiency of MB dye decreases by only 5.68%, showing that the film has good cycling stability. This work provides a new research direction for photoelectrically controllable photocatalytic degradation in complex and special environments.

Fabrication and Application of Tannin Double Quaternary Ammonium Salt/Polyvinyl Alcohol as Efficient Sterilization and Preservation Material for Food Packaging.

Food packaging films play a vital role in preserving and protecting food. The focus has gradually shifted to safety and sustainability in the preparation of functional food packaging materials. In this study, a bisquaternary ammonium salt of tannic acid (BQTA) was synthesized, and the bioplastics based on BQTA and polyvinyl alcohol (PVA) were created for packaging applications. The impact of BQTA on antibacterial effect, antioxidant capacity, opacity, ultraviolet (UV) protective activity, mechanical strength, thermal stability, and anti-fog of the resultant bioplastics was examined. In vitro antibacterial experiments confirmed that BQTA possesses excellent antimicrobial properties, and only a trace amount addition of BQTA in PVA composite film could inhibit about 100% of Escherichia coli and Staphylococcus aureus. Compared to BQTA/PVA bioplastics with pure PVA, the experiment findings demonstrate that BQTA/PVA bioplastics show strong antioxidant and UV protection action and the performance of fruit preservation. It also revealed a small improvement in thermal stability and tensile strength. The small water contact angle, even at low BQTA concentrations, gave BQTA/PVA bioplastics good anti-fog performance. Based on the findings, bioplastics of BQTA/PVA have the potential to be used to create packaging, and they can be applied as the second (inner) layer of the primary packaging to protect food freshness and nutrition due to their antioxidant activity and biocompatibility.

Amphiphilic colloidal particles/Ca2+ reinforced edible agar nanocomposite film by multiple cross-linking/microphase separation strategies

The agar (AG) film exhibited poor mechanical and water-resistant properties which limited its application for food packaging. The structural modification of AG nanocomposite film greatly impacts their macroscopic properties. In this paper, edible AG nanocomposite films were achieved by incorporating colloidal particles based on conjugates of whey protein isolate (WPI) and alginate oligosaccharides (AOS) as the nanofiller to obtain the micro-phase separation structure and the multiple cross-linking network with the synergistic interactions of the Ca2+ crosslinking. Firstly, WPI-AOS colloidal particles were synthesized through the Wet-heating Maillard reaction. Good compatibility between WPI-AOS colloidal particles and AG was exhibited, resulting in improved mechanical and water-resistant properties of AG composite films. Compared to pure AG film, the tensile strength (TS) of the agar composite film with 10% WPI-AOS colloidal particles increased significantly to 81.87 MPa from 24.02 MPa, and the elongation at break (EAB) also improved to 46.25% from 18.65%. The moisture content (MC), water solubility (WS), and water vapor permeability (WVP) of the AG composite film decreased by 33.1%, 18.0%, and 22.4% respectively. In addition, the multiple cross-linking network hindered the relative sliding between the AG molecular chain, which resulted in improved thermal stability of the composite film. Using soft colloidal particles as nanofillers to fabricate edible films for improving their properties is an effective and promising strategy.

High throughput PTFE@PPS /ACFs porous membrane for continuous highly effective oil-water separation

We proposed a feasible and straightforward approach for fabricating a superhydrophobic polytetrafluoroethylene coated polyphenylene sulfide/aramid composite film (PTFE@PPS/ACFs porous membrane) for oil-water separation. This process involves utilizing a wet paper making process combined with a spray coating technique. The PPS/ACFs composite membrane displays a three-dimensional network structure by the application of wet papermaking approach. The uniformly spray coating of PTFE on its surface results in a superhydrophobic PTFE@PPS/ACFs porous membrane (PPAM). The membrane obtained through this method can effectively separate oil and water. It is remarkable in separating oil-water lotion stabilized by surfactant, achieving a separation efficiency of up to 99.9 % with a high flux of 8000 L/m2·h−1. Additionally, owing to the inherent thermal stability of the membrane, the PPAM is recyclable. In summary, the PTFE@PPS/ACFs porous membrane is a promising for separating various oil-water emulsions. Its outstanding performance, including high separation efficiency, flux, and recyclability, underscores its potential for practical applications for oil-water separation.

Nanostructured aramid fiber/Cu/BN composite Janus films with broadband electromagnetic interference shielding and superior thermally conductive/electrically insulating performance

Modern electronic technology necessitates the development of composite materials with effective electromagnetic protection. This work presents a novel strategy constructing an aramid nanofiber (ANF)-based Janus film (ANF@Cu-ANF/BN) using an electroless plating-vacuum assisted filtration-pressing technique. The film exhibits an unique asymmetric property profile, with one side being electrically conductive and thermally conductive/electrically insulating on the other. Exceptional EMI shielding effectiveness of 105.22 and 106.96 dB is obtained in the 8.2–12.4 GHz and 26.5–40 GHz ranges, respectively. In addition, the film demonstrates an impressive out-of-plane thermal conductivity of 2.703 W/(m·K). suggesting superior thermal management capabilities when integrated into heat sinks for high-power light-emitting diode modules. In terms of mechanical robustness, the film possesses a tensile strength of 14.31 MPa. The ANF@Cu-ANF/BN Janus composite films effectively harmonize electromagnetic shielding, thermal conductivity, and mechanical integrity, offering an innovative pathway of developing advanced materials that fulfill the stringent requirements of modern electronic devices.

Enhanced charge storage in supercapacitors using carbon nanotubes and N-doped graphene quantum dots-modified (NiMn)Co2O4

The integration of ternary metal oxides into carbon materials is anticipated to significantly boost the electrochemical performance of supercapacitor electrodes. This article synthesized carbon nanotubes (CNT)/(NiMn)Co2O4 composite materials using a straightforward hydrothermal method and subsequently prepared composite thin films of CNT/P-(NiMn)Co2O4@NGQD by phosphating and incorporating nitrogen-doped graphene quantum dots (NGQD). These films served as the functional electrode material for supercapacitors, enhancing their performance capabilities. The specific capacity of CNT/P-(NiMn)Co2O4@NGQD was measured at 2172.0 F g−1 at a current density of 1 A g−1, maintaining a capacitance of 1954.0 F g−1 at 10 A g−1, thus demonstrating excellent rate performance. Electrochemical impedance spectroscopy (EIS) further revealed enhancements in electrolyte flow dynamics and capacitance behavior post-NGQD introduction. The energy density of the composite material reached 94.4 Wh kg−1 at power density of 800 W kg−1, demonstrating superior electrochemical performance. The enhancement in these electrochemical properties is attributed to the high specific surface area and active sites of CNT/P-(NiMn)Co2O4@NGQD films, along with the synergistic effects of NGQD and metal ions facilitating rapid electrons and charge transfer. This work provides new insights into developing high-performance supercapacitors.

Enhancing output performance of triboelectric nanogenerators with ZnFe2O4 nanoparticles in biodegradable polylactic acid for sustainable energy harvesting

ABSTRACT The development of triboelectric nanogenerators (TENGs) using sustainable materials addresses the global electronic waste issue. This research focuses on fabricating a TENG device with biodegradable polylactic acid (PLA) as the tribopositive material and polytetrafluoroethylene (PTFE) as the tribonegative material. ZnFe2O4 nanoparticles are incorporated into the PLA matrix to enhance surface charge density and synthesised via a simple combustion method. PLA-ZnFe2O4 composite films were prepared by solvent casting with varying nanofiller content (0.25, 0.45, 0.65, and 0.85 g). Prepared composites were characterised by Powder X-ray Diffraction (PXRD) for crystalline nature and phase purity, Fourier Transform Infrared Spectroscopy (FTIR) for vibrational analysis, and Scanning Electron Microscopy (SEM) for surface morphology. The inclusion of ZnFe2O4 nanoparticles improves TENG output performance, with a maximum output voltage of 18.4 V and a current of 1.57 µA observed for a PLA (poly(lactic acid)) composite with 39.39% nanoparticle content. Electrical studies on the optimised device show successful charging of various capacitors and powering 20 LEDs and a calculator. Body movements like walking and jumping were also tested to measure voltage and current outputs. These findings highlight new possibilities for developing smart, self-powered electronic devices.

Enhancing self-induced polarization of PVDF-based triboelectric film by P-doped g-C3N4 for ultrasensitive triboelectric pressure sensors

Progress in wearable energy devices has reached the point of popularity over a few decades, as reflected by the rise of numerous sensors and storage devices driven by the urgent need for Internet of Things (IoT) applications. Triboelectric sensor (TES), on the basis of triboelectric nanogenerators (TENGs), exhibits high sensitivity and stability for pressure detection. Maximizing the sensitivity of the TES hinges upon the triboelectric layer selection capable of harnessing triboelectrification and electrostatic induction. Among them, PVDF has gained attention owing to its exceptional flexibility and tribo-negativity. However, the multiphase of pristine PVDF poses challenges, limiting its potential for TES with higher sensitivity. Tackling this issue, herein, we introduced phosphorus-doped graphitic carbon nitride (PCN) into the PVDF films to achieve self-induced polarization to enhance the sensitivity of the triboelectric pressure sensor. Through a controlled annealing temperature, phosphorus atoms are incorporated into the g-C3N4 (CN) matrix, enhancing the electronegativity of PVDF/PCN composite film while inducing a polarized β crystal phase in PVDF, thereby enabling greater attraction of positive charges. Consequently, the triboelectric output with PVDF/PCN composite film exhibited a significant improvement compared to the pristine PVDF film, achieving over a 100 V increment and the ability to power more than 100 LEDs. Furthermore, for the pressure-sensing applications, the TES with flexible PVDF/PCN triboelectric film exhibits a pressure sensitivity of 1.48 V/kPa, which shows a threefold increase in sensitivity compared to the pristine PVDF film (0.51 V/kPa), suggesting their great potential in self-powered wearable pressure sensors.

Fabrication and thermomechanical property investigations of polypropylene/silica and polypropylene/modified silica composite films

In this study, we fabricated polypropylene/silica (PP/S) and polypropylene/modified silica (PP/MS) composite films using the extrusion technique, and characterized, and investigated their thermomechanical behaviors. The characterization of the neat materials and prepared composites was successfully conducted using some advanced spectroscopic techniques. The thermal stability and thermomechanical behaviors of the composites were investigated through thermogravimetry analysis (TGA) and dynamic mechanical analysis (DMA). The tensile tests revealed that the PP/MS composites exhibited the highest strength values, reaching 22.23 MPa with 1.0 % MS. Higher tensile strength was obtained with PP/MS composites compared to PP/S composites, proving the clear effect of the hexadecyltrimethylammonium bromide (HTAB) binder in the composition of the composites. The highest strength values obtained with the PP/S composites were 20.10 MPa at a ratio of 2.5 %.

Silane modified Cr2O3/polyimide nanocomposite films with excellent surface insulation performance for space applications

The exploration of deep space significantly increases the probability of spacecraft failures due to surface electrostatic discharge, which imposes higher vacuum insulation protection requirements on polyimide (PI), the external insulation material of spacecrafts. To address this challenge, this study proposes using silane coupling agent KH550 for organic grafting treatment of Cr2O3nanoparticles, which are then used to dope and modify PI to enhance the vacuum surface insulation of PI films. The KH550 grafting improves the interface strength between the fillers and the matrix, allowing the fillers to be uniformly dispersed in the matrix. Compared to pure PI films, the prepared PI-Cr2O3@KH550 composite films exhibit significantly enhanced vacuum surface flashover voltage, improved surface/volume resistivity, and dielectric properties. The results demonstrate that PI composite films with 0.8% by mass of Cr2O3@KH550 show the most notable performance improvement, with the DC flashover voltage and impulse flashover voltage in vacuum increasing by 20.7% and 27.8%, respectively. The doping of chromium oxide nanoparticles introduces more deep traps into the PI films and reduce the surface resistivity. The higher deep trap density inhibits charge migration, thereby alleviating secondary electron emission and surface electric field distortion. Simultaneously, the lower surface resistivity facilitates dissipating surface charges and improves the surface insulation. These findings are of significant reference value for promoting the enhancement of aerospace insulation performance.