Search Results (1,436)

This study investigates the enhancement of electrical conductivity in poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) thin films through the incorporation of few-layer graphene (mG). Nanocomposite films were prepared by spin coating from liquid dispersions containing approximately 10 wt% mG. The resulting films exhibited high optical transmittance (~80%) and significantly reduced sheet resistance, reaching values as low as 1.8 kΩ/□. These improvements in electrical and optical performance are attributed to enhanced charge transport arising from π–π interactions between graphene and PEDOT:PSS, as well as conformational changes in the polymer chains. The PEDOT:PSS/mG composites were successfully applied both as conductive inks, forming conductive trails capable of powering a light-emitting diode (LED), and as hole transport layers in organic light-emitting diodes (OLEDs). Comprehensive optical and electrical characterization of the composite films and the corresponding OLED devices demonstrates the strong potential of PEDOT:PSS/mG nanocomposites for use in flexible and printed electronic applications. Full article

ZnS is one of the most promising wide-bandgap semiconductors for optoelectronic and sensing applications owing to its efficient ultraviolet–blue emission, high exciton binding energy, and chemical stability. However, the synthesis of ZnS nanocrystals in silicon-compatible porous matrices remains largely unexplored. In this work, ordered arrays of ZnS nanocrystals were synthesized for the first time in SiO₂/Si track templates fabricated by swift heavy ion irradiation followed by selective chemical etching. ZnS nanocrystals were deposited by electrochemical deposition from aqueous solutions containing ZnCl₂ and thiourea precursors. The structural, optical, and electrical properties of the resulting ZnS/SiO₂/Si nanocomposites were investigated using scanning electron microscopy, X-ray diffraction, Raman spectroscopy, photoluminescence spectroscopy, and electrical measurements. The fabricated templates contained vertically aligned pores with a density of approximately 10⁸ cm⁻² and an average diameter of about 500 nm. Electrochemical deposition resulted in a pore filling efficiency of approximately 88%. X-ray diffraction analysis confirmed the formation of crystalline ZnS with a cubic zinc blende structure. The nanocomposites exhibit intense ultraviolet–blue photoluminescence in the 335–477 nm range, with pronounced emission peaks at 372 and 400 nm characteristic of ZnS nanocrystals. Current–voltage measurements indicate predominantly electronic conductivity, with a conductivity of 1.54 × 10⁻⁶ Ohm⁻¹·cm⁻¹, comparable to values reported for polycrystalline ZnS films. To support the experimental observations, the electronic structure of ZnS was analyzed using density functional theory within the LCAO framework. The calculated bandgap of 3.4 eV is consistent with previously reported theoretical and experimental data. The obtained results demonstrate that SiO₂/Si track templates provide a promising platform for the fabrication of ordered ZnS nanoarrays with potential applications in silicon-compatible optoelectronic and sensing devices. Full article

Although chitosan (CS)- and essential oil (EO)-based packaging systems have been widely reviewed, a focused synthesis connecting nano-delivery design with interfacial regulation, film-network evolution, release behavior, and preservation performance in real food systems remains lacking. This review addresses that gap by examining CS-based nano-delivery systems for EOs in active food packaging, with an emphasis on how carrier design and multiscale organization govern functional performance. Major delivery strategies, including nanoemulsions, nanoparticles, nanogels, Pickering emulsions, nanofibrous systems, and nanocomposites, are discussed in relation to EO stabilization, dispersion uniformity, and controlled release. Their effects on film microstructure, mechanical and barrier properties, thermal stability, optical behavior, and antimicrobial and antioxidant activities are further evaluated alongside preservation outcomes in fruits, vegetables, dairy products, meat, and aquatic products. Particular attention is given to structure-function relationships across the carrier, interface, and film-network levels, and to the distinction between established active-packaging functions and emerging smart-packaging applications. Current challenges include EO compositional variability, limited cross-study comparability, sensory constraints, migration and regulatory concerns, and insufficiently scalable fabrication routes. Future work should prioritize mechanism-informed interfacial design, standardized evaluation frameworks, food-specific release-preservation correlations, and scalable green manufacturing. Full article

This review analyzes electrochemically deposited polyaniline (PANI) nanocomposite thin films containing metallic, semiconducting, and dielectric fillers, including Ag/PANI, Mo/MoO_x/PANI, CeO₂/PANI, Fe₂O₃/PANI, Al₂O₃/PANI, CuO/PANI, Co₃O₄/PANI, and CoFe₂O₄/PANI. The work examines how filler chemistry and loading influence optical-gap evolution, Urbach disorder, dielectric dispersion, nonlinear optical response, structural coherence, and dc conductivity under comparable electrochemical growth conditions. The comparative analysis shows that optical-gap narrowing and conductivity enhancement are not necessarily coupled. Ag/PANI exhibits simultaneous optical softening and improved conductivity, consistent with metallic bridging, dielectric screening, and enhanced charge connectivity. In contrast, Mo/MoO_x/PANI shows strong optical-gap reduction but reduced conductivity, indicating that optically active interfacial states may remain localized or mobility-limiting. Oxide fillers produce additional regimes: CeO₂/PANI can suppress Urbach disorder and microstrain through order stabilization, whereas Al₂O₃/PANI may widen higher-energy transitions and reduce transport through wide-gap barrier effects. Based on these contrasts, a unified framework is proposed that separates the interfacial electronic function from the transport-connectivity function. This approach classifies PANI nanocomposites into transport-assisted metallic, mobility-limiting interfacial, order-stabilized oxide, and barrier-dominated dielectric regimes, providing practical criteria for selecting filler type and loading windows in optoelectronic, sensing, and photonic applications. Full article

This study focuses on sustainable atmospheric water harvesting (AWH) using film-containing green nanomaterials. Particular emphasis is given to chitosan as a sustainable biopolymer matrix due to its intrinsic hydrophilicity, biodegradability, film-forming ability and abundance of amino and hydroxyl functional groups that favor water adsorption and nanoparticle interaction. ZnO, SiO₂ and Fe-Zn-SiO₂ nanoparticles with abundant hydroxyl groups were synthesized from plant-based materials such as biomass from peanut and banana wastes, as well as plant extracts. Nanocomposite membranes containing nanoparticles with a high specific surface area and moisture-sensitive behavior were successfully developed. Results showed that bilayer films outperformed monolayer systems in water harvesting performance. In particular, the bilayer film composed of Chitosan/G-ZnO (10 wt.%) on the top layer and Chitosan/G-SiO₂ (10 wt.%) in the bottom layer displayed outstanding hydrophilic properties with water contact angles reduced to 42–43°. The material demonstrated an equilibrium adsorption capacity for water at 0.90 g/g and a passive yield of 1.5–2.2 mL/g per day. The improved adsorption behavior was attributed to the synergistic effect between the hydroxyl-rich oxide nanoparticles, the intrinsic water affinity of chitosan, and the layered porous structure. Moreover, the samples showed good thermal and mechanical stability and retained their structure after several uses. These findings highlight the potential of chitosan-centered green nanocomposites as sustainable materials for passive AWH applications. Full article

Edible and medicinal mushrooms, including cultivated and wild species, are increasingly recognized as valuable functional foods and nutraceutical resources due to their high nutritional value, abundance of bioactive compounds, and documented health-promoting properties. However, their high perishability results in substantial postharvest quality losses and limits commercial shelf life. This review provides a comprehensive overview of recent advances in mushroom preservation technologies, with particular emphasis on emerging non-thermal approaches such as cold plasma treatment, active packaging systems, and electrostatic field technologies. Conventional and advanced drying methods, edible coatings, biopreservation, fermentation and irradiation are also critically evaluated. Cold plasma treatment effectively reduces microbial contamination and enzymatic browning while maintaining firmness and nutritional quality, whereas active packaging systems based on chitosan films, nanocomposites, and modified atmospheres help reduce moisture loss, delay senescence, and preserve physicochemical properties during storage. Electrostatic field treatment combined with modified atmosphere packaging has shown additional potential for extending refrigerated shelf life. Among drying technologies, freeze-drying generally provides the highest retention of colour, texture and bioactive compounds, although its industrial application remains constrained by high energy consumption and operational costs. Overall, current evidence suggests that integrated preservation approaches offer the greatest potential for improving shelf-life extension and quality retention. Nevertheless, further research is required to address challenges related to industrial scalability, process standardization, economic feasibility and long-term quality assessment. Full article

Natural lacquer, a bio-based polymer derived from Toxicodendron vernicifluum, has attracted renewed scientific interest as a sustainable coating material with exceptional mechanical durability, chemical resistance, and aesthetic qualities. This review synthesizes current knowledge on the chemical composition, enzymatic curing mechanisms, and structure–property relationships of lacquer-based polymer systems, with particular focus on recent advances in functional modification and processing technology. Key findings indicate that laccase-catalyzed oxidative polymerization, operating optimally at pH 6.0–7.5 and 20–30 °C, governs the formation of a highly cross-linked urushiol network whose properties are fundamentally determined by side-chain unsaturation and emulsion stability. Mechanistic analysis reveals that polyurethane hybridization improves weathering resistance by introducing flexible aliphatic segments and additional hydrogen-bonding cross-links, while graphene oxide incorporation enhances anticorrosion performance through a physical barrier mechanism that prolongs ionic diffusion pathways. UV-curable LPEA derivatives achieve an 83% reduction in curing time relative to ambient-cured lacquer, enabling integration with industrial spray-coating lines. Despite these advances, several critical limitations remain inadequately resolved. Allergen reduction strategies have not yet achieved sufficient quantitative efficiency for large-scale commercial deployment, and the long-term stability of nanocomposite lacquer films under sustained UV exposure and hydrothermal conditions is not well established. Furthermore, most high-performance modification systems reported in the literature are demonstrated only on laboratory scale, with scalability, substrate compatibility, and lifecycle performance remaining largely unvalidated. The review identifies the absence of standardized performance evaluation protocols and the fragmentation of structure–property data across studies as key barriers to systematic progress, and proposes that future work prioritize the development of integrated processing–modification–performance frameworks to guide the rational design of next-generation lacquer-based functional materials. Full article

Impaired wound healing arises from interacting biological and material challenges, including persistent infection, biofilm formation, oxidative stress, unresolved inflammation, impaired angiogenesis, defective epithelialization, hemorrhage, and insufficient real-time assessment of wound status. Quantum dot (QD) and nanodot nanosystems have emerged as a versatile class of bioactive wound interfaces capable of addressing these barriers through functions that extend beyond passive coverage. This review synthesizes the design rationale, material composition, validation strategies, functional outcomes, mechanistic interpretation, and translational relevance of QD-enabled platforms for precision wound repair. Across the reviewed literature, carbon dots, graphene QDs, black phosphorus QDs, metal and metal oxide QDs, transition-metal nanodots, and hybrid nanocomposites were incorporated into hydrogels, films, sponges, nanofibers, microneedles, scaffolds, membranes, sprays, and injectable matrices. Their major precision-enabling attributes include localized antimicrobial and antibiofilm activity, redox-adaptive behavior, photothermal and photodynamic activation, inflammatory and macrophage modulation, hemostasis, controlled therapeutic delivery, angiogenic and epithelial support, and fluorescence-based monitoring. The strongest conceptual advance is the transition from static wound dressings toward adaptive biointerfaces that can sense, respond to, or compensate for local wound state abnormalities. Nevertheless, the field remains largely preclinical, with important gaps in long-term safety, standardized characterization, clinically predictive models, manufacturing reproducibility, regulatory alignment, and human validation. Future progress will depend on rationally simplified multifunctional platforms, rigorous comparative testing, wound state-specific evaluation frameworks, and translation-oriented safety and usability studies. QD nanosystems therefore represent a promising foundation for precision wound repair, provided that their multifunctionality is matched by equally rigorous evidence of safety, reproducibility, and clinical relevance. Full article

Next-generation wastewater treatment and recycling rely on membrane-based processes, but they face a trade-off among permeability, selectivity, and fouling resistance. In the present study, thin-film nanocomposite (TFN) membranes were fabricated by incorporating a ternary TiO₂-SiO₂-biochar nanofiller into a polysulfone (PSf) support using nonsolvent-induced phase separation, after which m-phenylenediamine and trimesoyl chloride were used via interfacial polymerization to produce a selective polyamide layer. The membrane compositions were M1 (22 wt.% PSf), M2 (22 wt.% PSf/0.5 wt.% TiO₂/0.5 wt.% SiO₂/0.5 wt.% biochar), and M3 (polyamide-coated M2). FTIR, XRD, SEM, contact-angle, porosity, and mechanical analyses supported successful membrane formation and changes in morphology, wettability, and structural strength after nanofiller incorporation and TFC coating. The addition of a nanofiller increased the hydrophilicity of the membranes by decreasing the water contact angle from 98.6 ± 0.8° for pristine PSf to 35.6 ± 1.5° for the nanocomposite membrane. Consequently, the pure-water permeability increased from 21 to 37 L m⁻² h⁻¹ bar⁻¹. After polyamide layer formation, the optimized TFN membrane maintained a contact angle of 55.4 ± 3.8° and achieved a high Congo red rejection of 98% with permeate flux of 7–9 L m⁻² h⁻¹ bar⁻¹. The membrane also showed good antifouling performance, with flux recovery ratios exceeding 90%. For heavy-metal-containing solutions, the optimized membrane showed apparent removal efficiencies of 78–98% for multivalent heavy metals (Pb²⁺, Hg²⁺, Cd²⁺, Mn²⁺, Zn²⁺, Cu²⁺, Ni²⁺, Fe³⁺, As³⁺, and Cr⁶⁺). Static adsorption tests showed the order M2 > M3 > M1, confirming that exposed TiO₂-SiO₂-biochar sites contribute to pollutant uptake, while the superior filtration performance of M3 is attributed to the combined effect of the polyamide selective layer and adsorption-assisted interactions. Overall, the TiO₂-SiO₂-biochar-based TFN membrane provides a promising platform for dye removal and preliminary heavy-metal attenuation from contaminated water. Full article

Machine learning (ML)-assisted design of epsilon-negative polymer nanocomposites requires a clear connection between experimentally controllable synthesis parameters, core–shell nanoparticle geometry, and the resulting effective optical response. The targeted optical response is unusual because the polymer film is predicted to exhibit near-zero or negative real effective permittivity in selected visible spectrum regions, arising from Ag core plasmonic polarizability, SiO₂-mediated dielectric spacing, nanoparticle filling factor, and effective medium coupling rather than from the intrinsic polymer matrix. In this study, a two-stage ML-assisted synthesis-to-optics framework is developed for Ag@SiO₂ core–shell nanoparticle/polymer composite films intended for visible spectrum effective permittivity screening. In the first stage, Stöber synthesis parameters, including water volume, ethanol volume, TEOS content, catalyst volume, reaction time, Ag nanoparticle size, and Ag nanoparticle concentration, were used to predict SiO₂ shell thickness. In the second stage, Ag core size, SiO₂ shell thickness, wavelength, and nanoparticle filling factor were used to screen the real effective permittivity of Ag@SiO₂/polymer nanocomposites within an effective medium design space. Using a duplicate-aware validation workflow, Gradient Boosting provided the strongest held-out test performance for shell thickness prediction, with a test R² of 0.8997, MAE of 7.1822 nm, RMSE of 8.8344 nm, and cross-validation R² of 0.5371 ± 0.4648. The relatively large cross-validation variability indicates that the model is useful for interpolation-based synthesis screening but should not be interpreted as fully robust across heterogeneous literature-derived data. For the optical response task, the highest held-out test performance was obtained by a Decision Tree model (test R² = 0.7586), but cross-validation results were unstable, indicating that the epsilon model should be interpreted as a design space screening tool rather than a generalizable predictor. Design window analysis identified candidate negative effective permittivity regions primarily at 400 nm and high nanoparticle filling factor, with predicted $\mathrm{R}\mathrm{e}\left({\epsilon }_{\mathrm{e}\mathrm{f}\mathrm{f}}\right)$ values ranging from −5.4229 to −0.2086 across selected windows. The main contribution of this work is the treatment of SiO₂ shell thickness as a bridge variable between Stöber-derived synthesis control and effective permittivity screening. Experimental validation remains necessary to confirm the predicted design windows, particularly because shell uniformity, Ag core polydispersity, nanoparticle aggregation, polymer dispersion, high-filling-factor feasibility, and effective medium validity can strongly influence the measured optical response. Full article

Multilayer packaging—engineered by integrating complementary materials such as plastics, paper, and aluminum—has become a cornerstone technology for enhancing shelf life, minimizing spoilage, and reinforcing the mechanical integrity of packaging formats including films, pouches, and bottles. In this study, a laminate was developed by thermally bonding polylactic acid (PLA) with a poly(butylene adipate-co-terephthalate) (PBAT)/thermoplastic starch (TPS) matrix embedded with silver nanoparticles (Ag-NPs) at 0–3 wt.%. The resulting structures were systematically evaluated for their barrier performance, physicochemical characteristics, and antimicrobial functionality. Fourier-transform infrared (FTIR) spectroscopy confirmed the absence of chemical interactions between Ag-NPs and the polymer matrix, indicating physical dispersion rather than chemical bonding. However, at higher loading (3 wt.%), scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX) revealed notable nanoparticle aggregation. Functionally, the multilayer films demonstrated markedly improved water vapor barrier properties compared to single-layer PBAT/TPS films. Migration studies showed that silver release increased with nanoparticle concentration and was significantly enhanced under acidic conditions relative to distilled water. Importantly, Ag-NP-incorporated laminates exhibited pronounced antibacterial activity against Staphylococcus aureus. Collectively, these findings highlight the potential of Ag-NP-enriched, starch-based multilayer laminates as next-generation active packaging systems that combine with effective microbial control. Full article

Raw lacquer, a natural polymer derived from the bast of lacquer trees (Toxicodendron vernicifluum), is renowned as the “King of Coatings” due to its exceptional film-forming properties, abrasion resistance, corrosion resistance, and biocompatibility. However, its inherent limitations—including stringent drying conditions, slow curing rates, deep coloration, and difficult application—have severely restricted its modernization and widespread adoption. This review systematically summarizes recent research advances in the modification and application of raw lacquer, focusing on four major modification strategies: (1) Nanocomposite modification—incorporating functional nanofillers such as Al₂O₃, cellulose nanofibrils (CNF), polydopamine (PDA) melanin-like nanoparticles, and SiO₂ to significantly enhance film hardness, compactness, UV-aging resistance, and drying kinetics. (2) Chemical structure modification—employing molecular design strategies including aminoanthraquinone grafting, tung oil blending, water-based emulsification, and terpene/allyl group functionalization to improve hydrophobicity, flexibility, fast-drying properties, and achieve dual photo/oxygen curing. (3) Biomass synergistic composites—utilizing natural polymers such as chitosan and lignin, along with bio-inspired adhesion mechanisms (e.g., PDA), to confer advanced functionalities including antibacterial and antifouling properties. (4) Curing behavior regulation—precisely controlling drying kinetics through inorganic salt ion microenvironment engineering, nonionic surfactants, and salicylaldehyde Schiff base-based driers. Building upon these foundations, this review further expands on the emerging high-value applications of modified lacquer in preventive conservation of cultural heritage, advanced functional coatings (anti-corrosion, super-hydrophobicity, flame retardancy), biomedical materials (hemostasis, antibacterial activity, drug-controlled release, water treatment adsorption), and intelligent responsive flexible electronics. Finally, addressing challenges including weak fundamental research, bottlenecks in green industrialization, and lack of standardization, future development directions are proposed encompassing interdisciplinary innovation, sustainable modification strategies, integration of multifunctional intelligent systems, and big data-driven research paradigms, aiming to provide theoretical guidance and technical references for the high-value utilization and modernization of lacquer resources. Full article

In this study, we employed one of the green synthesis methods utilizing water extracts prepared from solid industrial wastes of Rosa damascena Mill. (RD) and Oriental variety tobacco (Nicotiana tabacum)-mixed stems and leaves (O) as a natural reducing agent for PdCl₂ to obtain environmentally friendly Pd nanoparticles (PdNPs). Transmission electron microscopy (TEM), selected area electron diffraction (SAED), and energy-dispersive X-ray spectroscopy (EDX) in TEM were applied to determine the morphology, microstructure, phase, and elemental composition of PdNPs synthesized. The concentration of PdNPs in the suspensions was quantified by inductively coupled plasma optical emission spectroscopy (ICP-OES), which is essential for their intended application. Furthermore, the synthesized PdNPs were incorporated as dopant into a polymer matrix (PAZO) developed for optical applications. As will be demonstrated, doping PAZO with specific concentrations (0.1, 0.2, 0.25, 0.3, 0.4, 0.5, and 1 wt. %) of green PdNPs enhances the maximal value of the photoinduced birefringence by more than 50%. This improvement enables more efficient inscription of polarization-selective holographic optical elements in the resulting photoanisotropic nanocomposite materials with nearly 25% higher diffraction efficiency. Using a digital polarization holographic setup, the spatial modulation of polarization was recorded on thin nanocomposite films of the azopolymer PAZO, doped with certain concentrations of the green PdNPs. Full article

Developing a biodegradable film with integrated mechanical robustness and multifunctionality remains a significant challenge for sustainable food packaging. Herein, a pectin/carboxymethyl cellulose composite film (PNZ_xC) incorporated with zinc oxide nanoparticles (ZnO) was fabricated via a solution casting method to achieve the synergistic enhancement of structural and functional properties. ZnO exhibits dual functionality within the polymer matrix, serving both as a reinforcing filler and as a coordination interaction node via interactions with carboxyl groups. At an optimal loading, the PNZ₂C film demonstrates a uniform dispersion of nanoparticles, facilitating the development of a dense network structure and enhancing intermolecular interactions. Consequently, the film showed reduced water vapor and oxygen permeability, attributable to the formation of tortuous diffusion pathways, together with increased surface hydrophobicity and a significantly improved tensile strength of 25.4 MPa. Enhanced thermal stability and excellent UV-blocking performance were also achieved. Notably, the optimized film demonstrated superior preservation performance in blueberry storage, effectively reducing moisture loss and delaying quality deterioration compared with the control. These findings provide new insights into the structure–property relationships of ZnO–polysaccharide nanocomposite systems and highlight a viable strategy for designing high-performance, biodegradable packaging materials with integrated multifunctionality. Full article

This paper presents the results of the preparation and electrical characterization of Ru–Si–O thin-film nanocomposites deposited by magnetron sputtering (pDC) with varying oxygen content ranging from 0% to 50%. Measurements were conducted over a wide frequency range of 50 Hz–5 MHz and temperatures of 20–373 K. Conductivity analysis revealed that DC conduction occurs at low frequencies (≤10³ Hz), while an increase in conductivity associated with electron tunneling mechanisms is observed at higher frequencies. The determined charge transport activation energies range from 3 × 10⁻⁴ eV for the oxygen-free sample to 6 × 10⁻² eV for the high-oxygen samples, indicating a significant effect of composition on the conduction mechanisms. In samples containing 30% and 50% oxygen, two characteristic frequency ranges for the activation of transport processes were observed (e.g., ~10²–10³ Hz and 10⁴–10⁶ Hz), suggesting the coexistence of multiple tunneling mechanisms. Phase angle analysis revealed a transition from values near –90° at 151 K to values near 0° at 333 K, characteristic of parallel RC systems. The minimum dielectric loss tangent occurs in the range of 10³–10⁵ Hz, corresponding to Maxwell–Wagner relaxation. The dispersion coefficient α reaches maximums in two frequency ranges, decreasing with increasing oxygen content. EDS analysis showed a decrease in Ru content from ~24.9 at.% (0% O₂) to ~0.7 at.% (50% O₂) and an increase in oxygen content to ~78 at.% at 10% O₂. The results confirm the transition from metallic conduction to tunneling and hopping mechanisms with increasing oxidation state of the structure. Full article