Search Results (442)

Polymer films and polymer blend films are widely used as functional materials; however, their photophysical behavior cannot be fully explained solely by bulk properties such as relative permittivity or glass transition temperature. In this study, we investigate how local polymer microenvironments regulate fluorescence responses by employing two strongly emissive solvatochromic dyes—FπPCM, a D–π–A-type π-conjugation-extended fluorene dye, and PK, a D–π–A-type pyrene dye—as molecular probes. The photophysical properties of these dyes were systematically examined in a series of transparent polymer matrices, including polystyrene, polycarbonate, poly(methyl methacrylate), poly(vinyl chloride), triacetylcellulose, poly(butyl methacrylate), and poly(2-ethyl-2-oxazoline). Polymer films containing the dyes were prepared by solution casting from homogeneous polymer–dye solutions onto quartz substrates followed by solvent evaporation. Both dyes exhibited polymer-dependent variations in fluorescence wavelength, quantum yield, and lifetime, reflecting not only differences in polymer polarity but also local chain packing and specific dye–polymer interactions. Fluorescence lifetime analysis of PS/POz blend films revealed microscopic heterogeneity even in miscible systems, quantitatively captured using averaged lifetime parameters. Temperature-dependent fluorescence measurements further demonstrated that thermal history and structural relaxation significantly influence local polymer environments. In particular, ratiometric fluorescence analysis of PMMA/PBMA blend films enabled reproducible temperature sensing over a wide range from 30 to 120 °C, despite an overall negative temperature response. These results establish solvatochromic dyes as versatile optical probes for evaluating local polymer microenvironments and highlight their potential for polymer-state monitoring and fluorescence-based temperature-sensing applications. Full article

A novel membrane was synthesized in this work by grafting 1-vinyl-3-ethylimidazolium tetrafluoroborate ([C₂VIm][BF₄]) onto a polyvinylidene fluoride (PVDF) backbone, followed by the introduction of a sulfonated graphene oxide (SGO) dispersion into the polymer solution. This composite was transformed into a composite proton-conducting membrane via a solution casting process and subsequently underwent protonation. Successful grafting was confirmed using analytical techniques including Fourier Transform Infrared Spectroscopy (FTIR), ¹H Nuclear Magnetic Resonance (NMR) and X-ray Photoelectron Spectroscopy (XPS). Scanning Electron Microscopy with Energy Dispersive X-ray Spectroscopy (SEM-EDS) analysis verified the homogeneous distribution of the SGO filler. Analysis reveals that incorporating SGO as a filler substantially augments the performance of anion exchange membranes. Key enhancements include a tensile strength increase to 37.97 MPa, water uptake of 10.34%, an ion exchange capacity of 1.68 mmol/g, and the through-plane proton conductivity of 15.47 mS/cm. While vanadium permeability rose marginally to 2.02 × 10⁻⁷ cm²/min, it remains drastically lower than that of Nafion 115. The composite proton-conducting membrane also displayed robust chemical stability. The membrane was finally integrated into a vanadium redox flow battery (VRFB) for performance evaluation. At a current density of 100 mA/cm², it exhibits a satisfactory coulombic efficiency (CE) of 97.84%, excellent capacity retention, and superior cycling stability. These results demonstrate that the PVDF-g-IL/SGO-based composite proton-conducting membrane is an ideal candidate material for vanadium flow battery applications. Full article

This work presents the fabrication and a systematic evaluation of an ionic polymer-metal composite (IPMC) sensor, focusing on its potential for human motion monitoring and human–computer interaction. The sensor was fabricated via a solution casting and electroless plating process, and its morphology characterized using scanning electron microscopy. The sensing performance was comprehensively assessed, revealing high sensitivity (1.059 mV/N) in the low-pressure region, a fast response time (~50 ms), and reliable stability over prolonged cyclic testing. Furthermore, the sensor can respond to both the magnitude and rate of applied mechanical stimuli. To explore its application potential, the IPMC was tested in scenarios ranging from input pattern recognition—including distinguishing mouse-click patterns, handwritten letters, and binary-encoded presses—to human motion monitoring, where it effectively captured and differentiated signals from facial expressions, swallowing, breathing, and joint movements. The results suggest that the developed IPMC sensor is a promising candidate for applications in wearable health monitoring and flexible interactive systems. Full article

Two amide-preformed aromatic diamine monomers, N,N-bis(4-(3-aminobenzamido)phenyl)-N’,N’-bis(4-methoxyphenyl)-1,4-phenylenediamine (m-6) and N,N-bis(4-(4-aminobenzamido)phenyl)-N’,N’-bis(4-methoxyphenyl)-1,4-phenylenediamine (p-6), were synthesized and utilized to prepare two series of electroactive poly(amide-imide)s (PAIs) through a two-step polycondensation reaction with commercially available aromatic tetracarboxylic dianhydrides. The obtained polymers exhibited solubility in various polar organic solvents, and most of them could form transparent, flexible films via solution casting. Thermal analysis indicated glass transition temperatures (T_g) ranging from 250 °C to 277 °C, as measured by DSC, with no significant weight loss observed before 400 °C in TGA tests. Cyclic voltammograms (CV) of the polymer films on ITO-coated glass substrates revealed two reversible oxidation redox pairs between 0.67 and 1.04 V vs. Ag/AgCl in an electrolyte-containing acetonitrile solution. The PAI films showed stable redox activity with high optical contrast both in the visible and near-infrared regions, transitioning from colorless in the neutral state to green and blue in the oxidized states. Furthermore, the polymer films retained good electrochemical and electrochromic stability even after more than 100 cyclic switching operations. The PAIs displayed outstanding electrochromic performance, including high optical contrast (up to 95%), rapid response times (below 4.6 s for coloring and 5.7 s for bleaching), high coloration efficiency (up to 240 cm²/C), and low decay in optical contrast (less than 5% after 100 switching cycles for most PAIs). Full article

Thick (900–1500 µm), crack-free lithium manganese oxide (LMO) electrodes with a polyvinylidene fluoride (PVDF)-based polymer electrolyte were prepared using an innovated slurry casting method. The selectivity and intercalation capacity of the thick electrodes of 900–1500 μm were evaluated in aqueous chloride solutions containing main cations in synthetic Salar de Atacama brine using cyclic voltammetry (CV) measurements. The CV data indicated that a high Li⁺ selectivity of Li/Na = 152.7 could be achieved under potentiostatic conditions. With the thickest electrode, while the mass specific intercalation capacity was 6.234 mg per gram of LMO, the area specific capacity was increased by 3–11 folds compared to that for conventional thin electrodes to 0.282 mg per square centimeter. In addition, 82% of capacity was retained over 30 intercalation/dis-intercalation cycles. XRD and electrochemical analyses revealed that both Faradaic diffusion-controlled or battery-like intercalation and Faradaic non-diffusion controlled or pseudocapacitive intercalation contributed to the capacity and selectivity. This work demonstrates a practical technology for thick electrode fabrication that promises to result in a significant reduction in manufacturing and operational costs for lithium extraction from brines. Full article

Pineapple waste is an underexplored source for producing nanocomposites, from which nanocellulose, namely cellulose nanocrystals (CNCs) or cellulose nanofibers (CNFs), can be produced. This review summarizes extraction methods from different pineapple residues (leaves, crown leaves, stem, peel, pulp, and pomace), covering top-down processes (hydrolysis, oxidation, carboxymethylation, and mechanical fibrillation) and bottom-up strategies (ionic liquids and deep eutectic solvents). The review examines the influence of the morphology and crystallinity of nanocellulose on the functional performance of the nanocomposites. Strategies for processing pineapple-derived nanocellulose composites are analyzed by technique (solution casting, film stacking, and melt blending/extrusion) and polymer matrices (starch, PVA, chitosan, PLA, PHBV, PBAT, proteins, and polysaccharides), including typical loading levels for most polymer-reinforced systems (0.5–5 wt.%), while higher levels (15–50 wt.%) are used in particular cases such as PVA, CMC, and cellulosic matrices. The impact on mechanical strength, barrier behavior, UV shielding, and optical properties is summarized, along with reports of self-reinforced and hybrid cellulose-derived matrices. A benchmarking section was prepared to show nanocellulose loading ranges, trends in properties, and processing-relevant information categorized by type of matrix. Finally, the review describes the potential roles of pineapple waste within a bioeconomy context and identifies some extraction by-products that could be incorporated into diverse value chains. Full article

Polysulfone (PSF), despite its excellent thermal and mechanical stability, exhibits moderate gas separation performance and poor compatibility with inorganic fillers, resulting in interfacial voids and structural defects. This study addressed these limitations by incorporating vinyltrimethoxysilane (VTMS)-functionalized TiO₂ nanoparticles into PSF matrix to develop mixed matrix membranes (MMMs) for selective CO₂/N₂ separation. Membranes with 1–5 wt.% VTMS@TiO₂ loadings were fabricated via solution casting, and their gas separation performance was systematically evaluated. VTMS modification enhanced the dispersion and interfacial adhesion of TiO₂ within the PSF matrix, as confirmed by SEM, FTIR, XRD, and TGA analyses. The 4 wt.% VTMS@TiO₂ loaded membrane showed optimal performance, with a CO₂ permeability of 8.48 barrer and a CO₂/N₂ selectivity of 26.50 due to stronger polymer–filler interactions and enhanced CO₂ affinity by VTMS functional groups. This membrane has shown stable transport behavior and favorable CO₂ selectivity as confirmed by pressure- and temperature-dependent permeation studies. Robeson plot analysis showed that the optimized membrane approached the upper bound, demonstrating a significant improvement over pure PSF. The study confirmed that VTMS-functionalized TiO₂ enhanced both permeability and selectivity through improved filler dispersion, interfacial integrity, and CO₂ affinity. Full article

MXene–polymer hybrids combine the high in-plane conductivity and rich surface chemistry of MXenes with the processability and mechanical tunability of polymers for lithium-metal and lithium–sulfur batteries. Most reported systems still rely on HF-etched MXenes, introducing F-rich terminations, safety and waste issues, and poorly controlled surfaces. This review instead centers on fluoride-free synthesis routes, benchmarks them against HF methods, and translates route–termination relationships into practical rules for choosing polymer backbones. We track the evolution from early linear hosts such as PEO- and PVDF-type polymers to polar nitrile or carbonyl matrices, crosslinked and ionogel networks, and emerging biopolymers and COF-type porous frameworks that are co-designed with MXene terminations to regulate ion transport, interfacial chemistry, and mechanical robustness. These chemistry–backbone pairings are linked to five scalable fabrication modes, including solution blending and film casting, in situ polymerization, surface grafting, layer-by-layer assembly, and electrospinning, and to roles as solid or quasi-solid electrolytes, artificial interphases, separator-like coatings, and electrode-facing architectures. Finally, we highlight key evidence gaps and reporting standards needed to de-risk scale-up of green MXene–polymer batteries. Full article

Sulfonated poly(ether ether ketone) (SPEEK) is one of the most studied ionic polymers for polymer electrolyte membranes (PEMs) in fuel cells (PEMFCs). To improve its proton conductivity, novel SPEEK/praseodymium-doped zinc spinel ferrite composite membranes of 130–170 μm thickness were prepared via ultrasound-assisted dispersion of various proportions of synthesized doped ferrite nanoparticles into the polymer solution, followed by a simple solution-casting method. The morphology (as observed by SEM and confirmed by DMA) and the conducted physical and chemical tests typical for PEMs, such as water uptake (32–44% at 80 °C), ionic exchange capacity (1.67–1.80 mEq/g), chemical (around 1% loss in Fenton reagent after 24 h), thermal stability (up to 190 °C) and tensile strength (39–50 MPa), were proven to depend on the content of inorganic filler in the composite (up to 5%). The proton conductivity of composite membranes (0.21–2.82 × 10⁻² S/cm at 80 °C) was assessed by broadband dielectric spectroscopy. The membrane with a content of 0.25 wt.% ZnFe_1.96Pr_0.04O₄ showed the best proton conductivity (3.41 × 10⁻² S/cm at 60 °C), as compared to 1.60 × 10⁻² S/cm for Nafion117 measured under the same conditions, demonstrating its suitability as a PEM for fuel cell applications. Full article

A comprehensive investigation was conducted focusing on two series of poly(lactic acid) (PLA)-based nanocomposites filled with small amounts (0.5 and 1.0%) of metal (Ag/Cu) nanoparticles (NPs). Our work aimed to synthesize PLA/Ag nanocomposites via in situ ring-opening polymerization (ROP), and for comparison purposes, the same materials were also prepared via solution casting followed by melt mixing. PLA/Cu nanocomposites were also prepared via melt extrusion. Gel permeation chromatography (GPC) and intrinsic viscosity measurements [η] showed that the incorporation of Ag nanoparticles (AgNPs) resulted in a decrease in the molecular weight of the PLA matrix, indicating a direct effect of the AgNPs on its macromolecular structure. Fourier-transform infrared spectroscopy (FTIR) revealed no significant changes in the characteristic peaks of the nanocomposites, except for an in situ sample containing 1.0 wt% of AgNPs, where slight interactions in the C=O region were detected. Differential scanning calorimetry (DSC) analysis confirmed the semi-crystalline nature of the materials. Glass transition temperature was strongly affected by the presence of NPs in the case of the in situ-based samples. Melt crystallized studies suggested potential indirect polymer–NP interactions, while isothermal melt crystallization experiments confirmed the nucleation ability of the NPs. The mechanical performance was assessed via tensile and flexural measurements, revealing that the in situ-based samples exhibited remarkable flexibility. Moreover, during the three-point bending tests, none of the in situ nanocomposite samples broke. In this context, next-generation PLA-based nanocomposites have been proposed for advanced applications, including flexible printed electronics. Full article

The shift towards renewable resources has positioned agar, a natural seaweed polysaccharide, as a pivotal and sustainable material for developing next-generation energy storage technologies. This review highlights the transformative role of agar-based composites as a game-changing and eco-friendly platform for supercapacitors, batteries, and fuel cells. Moving beyond the traditional synthetic polymers, agar introduces a novel paradigm by leveraging its natural gelation, superior film-forming ability, and inherent ionic conductivity to create advanced electrolytes, binders, and matrices. The novelty of this field lies in the strategic fabrication of synergistic composites with polymers, metal oxides, and carbon materials, engineered through innovative techniques like electrospinning, solvent casting, crosslinking, 3D printing, and freeze-drying. We critically examine how these innovative composites are breaking new ground in enhancing device efficacy, flexibility, and thermal stability. Ultimately, this analysis not only consolidates the current landscape but also charts future pathways, positioning agar-based materials as a pivotal and sustainable solution for powering the future. Full article

Liquid Crystalline Elastomers (LCEs) are a class of shape-changing polymers with exceptional mechanical properties and potential as artificial muscles/polymer actuators. Much work has been dedicated to expanding the methods available for processing LCEs into various forms using different manufacturing techniques such as 3D printing, film casting, and microfluidic processing. Recently, several works have reported processing LCEs into long fibres and have highlighted the advantages that fibrous LCEs boast over LCE films. However, the development of alternative methods to produce fibrous LCEs is warranted to fully expedite this field of research. In this study, a method for continuous production of disulphide crosslinked LCE fibres via the technique of wet spinning is explored and reported on. Furthermore, the results show that the mechanical properties, actuation force, and actuation strain can be tuned by adjusting how much crosslinker is incorporated into the wet-spinning dope solution. Depending on the given formulation, the reported fibres could repeatedly actuate in response to thermal energy with actuation forces ranging from 0.002 to 0.02 N per fibre and actuation strains ranging from 9.7 to 33%. Full article

Chitosan films obtained by solution casting were investigated by broadband dielectric spectroscopy (BDS) to explore both their glass transition and the effects of thermal annealing on molecular dynamics, deriving from residual water content as well as from cold crystallization. Glass transition at low temperatures could be evidenced in as-produced as well as thermally annealed films, where non-Arrhenian dielectric relaxation processes, consistent with a structural (α) relaxation, could be detected. The process detected at low temperatures could reflect the dynamics of residual water slaved by the polymer matrix. Secondary (β) relaxations, along with a slow process ascribed to interfacial polarization at the amorphous/crystalline interfaces, were concurrently detected. In most cases, a further Arrhenian process at intermediate temperatures (α_c) was present, also indicative of crystallization. Notably, the α processes, due to the primary relaxation of the polymer matrix plasticized by water, could be discriminated from other processes, present in the same frequency range, thanks to improvements in the dielectric fitting strategy. All relaxation processes showed the expected dependence on T_a. The more accurate exploration of the glass transition for chitosan helps to better rationalize its crystallization behavior, in view of an optimized application of this biopolymer. Full article

This study demonstrates the successful preparation of pristine and modified PVC polymer films with (0.7, 1.0, 2.0, and 3.0 wt%) Cr_1.4Ca_0.6O₄ by the solution casting method. These films were characterized using XRD, FTIR, XPS, SEM, TGA, and a UV–vis spectrophotometer. The XRD confirmed the amorphous nature of PVC films and a tetragonal zircon-type structure of Cr_1.4Ca_0.6O₄ as a dopant in the PVC polymer. The XPS survey spectra of pristine Cr_1.4Ca_0.6O₄ and its composites with PVC reveal essential insights into the materials’ surface composition and chemical states. The spectra clearly show peaks corresponding to O1s, Ca2p, and Cr2p, with the Cr2p signals being notably weaker than the other peaks. SEM images showed a uniform distribution of Cr_1.4Ca_0.6O₄ within the PVC polymer films despite the presence of some minor agglomerations. The TGA analysis revealed that incorporating Cr_1.4Ca_0.6O₄ enhanced the thermal stability of PVC films, particularly at a 0.7 wt% concentration of Cr_1.4Ca_0.6O₄. Moreover, incorporation of Cr_1.4Ca_0.6O₄ improved the optical parameters of PVC films, i.e., linear refractive index, nonlinear refractive index, and optical susceptibility. These findings proposed the modified PVC with Cr_1.4Ca_0.6O₄ for optoelectronic applications. Full article

Multilayer and free-standing films self-assembled from water-soluble anionic azo dye acid yellow 9 (AY9) and both poly(allylamine hydrochloride) (PAH) and chitosan (CS) cationic polyelectrolytes were fabricated from water solution using a layer-by-layer (LbL) technique and characterized by UV–Vis and Raman spectroscopy. Observations were made of a strong, unexpected, and highly unusual colour change from deep red to a distinct dark blue upon exposure of the multilayer films to an acidic environment. The colour change was attributed to the multilayer films only and was not observed either for the polymer or the dye alone, or their mixture in water solution, nor when cast as free-standing films. The significant shift to blue colour of the absorption peaks was quantified with UV–Vis spectroscopy, and a proposed explanation is presented based on density functional theory (DFT) calculations exploring possible and most likely acid-base equilibria configurations of the azo dye that result from being self-assembled. Full article