Search Results (363)

The growing demand for sustainable, flexible, and high-performance electrode materials for energy storage has motivated the development of polymer-based composite electrodes with enhanced electrochemical properties. In this study, flexible cobalt oxide (Co₃O₄)-iron oxide (Fe₂O₃) nanoparticle-impregnated sodium alginate (NaAlg) as the polymer matrix composite membranes were developed via a simple solution-casting method to exploit the synergistic pseudocapacitive behaviour of mixed metal oxides together with the excellent film-forming ability, flexibility, and eco-friendly nature of NaAlg. The prepared membranes’ structural features, morphology, and electrochemical properties were examined through a set of techniques, such as Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Universal Testing Machine (UTM), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), potentiodynamic polarisation (PDP), and galvanostatic charge–discharge (GCD). Characterisation techniques validated the effective loading of Co₃O₄ and Fe₂O₃ nanoparticles within the NaAlg matrix, and revealed the efficient interfacial interactions, structural integrity, and electrochemical properties of the composites. GCD tests showed a very high specific capacitance of 571.43 F g⁻¹ at 1.2 A g⁻¹. The best-performing electrode produced a top energy density of 155.56 Wh kg⁻¹ at a power density of 2800 W kg⁻¹ and still showed around 91% capacitance retention after 2500 charging–discharging cycles with coulombic efficiency close to 100%. Boosted electrochemical performance is due to the synergistic effect of Co₃O₄-Fe₂O₃ nanoparticles that not only offer plenty of electroactive sites but also help in effective electron and ion transport within the polymer matrix. The results obtained here confirmed the capabilities of Co₃O₄-Fe₂O₃@NaAlg composite membranes as green and potent electrode materials for future supercapacitor devices. Full article

Hemoglobin (Hb) and its glycated variant (HbA1c) are essential clinical biomarkers for diagnosing anemia, acute hemorrhage, and long-term glycemic control. The growing demand for decentralized point-of-care (POC) testing has accelerated the development of rapid, inexpensive, and portable electrochemical sensing platforms. These technologies exploit the intrinsic redox activity of the heme prosthetic group, yet achieving efficient direct electron transfer (DET) remains a fundamental challenge because the electroactive iron center is deeply embedded within the globin structure. This review critically examines recent advances in electrochemical Hb sensing, tracing the evolution of electrode architectures from conventional carbon substrates to nanostructured materials, including graphene, MXenes, metal–organic frameworks (MOFs), and molecularly imprinted polymers (MIPs). We compare the advantages and limitations of non-enzymatic biomimetic platforms and affinity-based sensing strategies, including aptamer- and antibody-based biosensors, with emphasis on electron-transfer efficiency, molecular selectivity, analytical performance, and suitability for POC implementation. Beyond analytical performance, we evaluate the principal barriers to clinical translation, including biofouling, whole-blood matrix effects, viscosity-dependent mass transport, manufacturing scalability, and the persistent gap between validation in synthetic media and performance in clinical samples. Finally, we discuss emerging applications in wearable menstrual health monitoring and ingestible gastrointestinal bleeding sensors, highlighting the integration of advanced electrochemical materials with miniaturized electronics as a pathway toward practical, consumer-oriented diagnostics. Full article

Glow-discharge plasma (GDP) poling is revisited as an electrode-free method for activating piezoelectricity in poly(vinylidene fluoride) (PVDF) films. Although this method was proposed several decades ago, its effect on the properties of PVDF films has remained poorly understood. In this work, we demonstrate that GDP enables efficient poling of oriented PVDF films without pre-deposited electrodes and investigate the relationship between plasma treatment time, structural evolution, and piezoelectric response. Commercially available 25 μm-thick oriented PVDF films (PolyK) were treated in a DC glow discharge for 15 s to 15 min and characterized using FTIR, DSC, piezoresponse force microscopy, UV–Vis–NIR spectrophotometry, quasi-static d₃₃ measurements and water contact-angle measurements. GDP poling produced a side-averaged piezoelectric coefficient d₃₃ of up to ~25 pC/N within 1–5 min, with local maxima at approximately 1, 2.5, and 5 min. This behavior was accompanied by pronounced changes in the domain structure, including an increase in the ferroelectric domain size from 86 to 552 nm, while the crystallinity and electroactive phase fraction changed only moderately. Plasma treatment also increased the wettability of the plasma-facing surface, reducing the water contact angle from about 85° to 42° within 3 min. At longer treatment times (>5 min), however, the piezoelectric response decreased and the optical transparency deteriorated because of increased haze and turbidity, most likely associated with plasma-induced chemical modification of the surface layers. These results indicate that GDP poling has an effective processing window of 1–5 min. The proposed approach provides a vacuum-compatible and electrode-free route for preparing PVDF films with increased surface wettability for flexible piezoelectric sensors, wearable electronics, and integrated polymer-based devices, because it is compatible with electrode deposition on an already activated polymer surface within a single vacuum cycle. Full article

Additive manufacturing (AM) has expanded the design space for actuator systems by enabling complex internal geometries, multimaterial architectures, functional gradients, embedded channels, and application-specific components that are difficult to realize using conventional fabrication alone. These capabilities are particularly relevant when actuator performance is governed by the coupling between material selection, printed architecture, stimulus response, and system-level integration. This review examines additively manufactured actuators and actuator components using a material-architecture-function-integration framework. The actuator classes considered include soft pneumatic and fluidic actuators, electroactive and piezoelectric polymer actuators, shape-memory and 4D-printed actuators, magnetic and magnetoactive actuators, and printed pneumatic, hydraulic, mechanical, and aerospace-grade actuator components. Representative applications are discussed across biomedical and rehabilitation systems, aerospace and deployable mechanisms, soft robotics, and industrial automation. Beyond summarizing printed actuator demonstrations, the review analyzes the integration barriers that determine whether AM actuators can transition from laboratory prototypes to functional systems. These barriers include material durability, leakage, fatigue, dielectric breakdown, filler dispersion, interfacial failure, dimensional variability, environmental sensitivity, auxiliary hardware requirements, sensing, control, and benchmarking. By organizing recent developments across actuator classes, application domains, and integration strategies, this review clarifies where AM provides a functional advantage over conventional fabrication and where further validation is required for reliable deployment. Full article

The chemically modified ammonium lignosulfonate (ALS) powders with carboxylic acids such as, oleic (OA) and lactic acid (LA) and γ-butyrolactone (BL) under dielectric barrier plasma discharge (DBD) have been characterized by average molecular weight and particle size determinations, morphology examination by optical and electronic microscopy (SEM), the study of the thermal properties by thermogravimetry (TG/DTG), differential scanning calorimetry (DSC), differential thermal analysis (DTA) and antioxidant activity tests by DPPH method. The thermal characterization of the modified lignosulfonates reveals their improved thermal stability comparatively with ALS. It has been established that the obtained microparticles are aggregates of particles, covered by modified polymer and exhibit a particular behavior depending on the chemical structure of the used modifier, leading to multifunctional active lignin-based products with better homogeneity. By surface modification, the antioxidant capacity of modified lignosulfonate powders has been maintained. Full article

Corrosion-protective coatings have progressed from passive barrier systems and chromate-based technologies toward multifunctional materials that integrate barrier durability, interfacial adhesion, active inhibition, electrochemical response, and self-healing capabilities. However, the intellectual framework connecting these technological developments remains fragmented, as most reviews focus on specific material families rather than on the broader evolution of the field. This study examines technological paradigms in corrosion-protective coatings through a citation network analysis of highly cited publications retrieved from Web of Science and processed with CitNetExplorer. The most influential publications were thematically reviewed to identify dominant materials, coating architectures, protection mechanisms, seminal contributions, and bridge articles. Four principal paradigms were identified: smart and self-healing coatings based on nanocontainers, layered double hydroxides, mesoporous silica, halloysite, zeolites, hydroxyapatite reservoirs, and microcapsules; chromate-free sol–gel and silane pretreatments based on organic–inorganic hybrid matrices, organosilanes, rare-earth inhibitors, and oxide nanoparticles; graphene and graphene oxide-based nanocomposite coatings in which two-dimensional fillers enhance tortuosity, reduce water uptake, and reinforce polymer matrices and coating–substrate interfaces; and electroactive coatings based mainly on polyaniline and polypyrrole, where protection is associated with passivation, redox mediation, and dopant-controlled inhibition. The findings indicate that corrosion-protective coatings have evolved through partially overlapping and increasingly integrated paradigms rather than through a single technological trajectory. This citation network analysis clarifies the transition from chromate replacement toward active, nanostructured, electroactive, and self-healing corrosion-protective systems. Full article

Molecularly imprinted polymers (MIPs) offer robust, cost-effective, and highly selective alternatives to fragile biological receptors. Specifically, electropolymerization has emerged as a versatile strategy that enables the precise, in situ formation of uniform MIP films directly on electrode surfaces. This review provides a comprehensive overview of electropolymerized MIPs (eMIPs) supported on advanced carbon-based materials for electrochemical (bio)sensing. We emphasize how the synergistic integration of eMIPs with carbonaceous architectures significantly enhances electron transfer, active surface area, and overall analytical sensitivity. Key fabrication aspects are systematically discussed, including monomer selection, electropolymerization parameters, and efficient template removal. A central aspect of this work is the critical categorization of sensing mechanisms into direct and indirect detection strategies. This distinction elucidates how eMIPs can quantify a broad spectrum of electroactive and non-electroactive targets in complex matrices, while strategically avoiding excessively high applied potentials. Finally, alongside outlining the transition of these systems into portable technologies, we address a critical shortcoming in the current literature: the urgent need for analytical standardization through the rigorous reporting of Imprinting and Selectivity Factors using Non-Imprinted Polymer (NIP) controls. Full article

Artificial muscles are an emerging class of actuators designed to mimic the compliant, efficient, and versatile behavior of biological muscles for fields including the following: soft robotics, prosthetics, wearable enhancements, haptic interfaces, and biomedical devices. These systems encompass various actuation mechanisms, including pneumatic, hydraulic, thermal, ionic, electrochemical, and electrostatic. Each with distinct tradeoffs in voltage, strain, output force, bandwidth, efficiency, and manufacturability. Among them, electrostatic actuators have attracted increased attention due to their fast response times, high energy densities, strong compatibility with soft materials, and scalability from microscale devices to large-area and stacked actuators. However, challenges such as dielectric breakdown, material fatigue, and fabrication complexity continue to limit widespread deployment. This review presents a structured classification of various artificial muscle technologies and an in-depth examination of electrostatic actuators including dielectric elastomers, electrostrictive and ferroelectric polymers, liquid crystal elastomers, electrostatic film motors, stacked architectures, and microscale/milliscale devices. In this review the operating principles, materials, architectures, performance characteristics, and failure modes of electrostatic actuators will be discussed. Additionally, a comparison will highlight tradeoffs across actuator families based on metrics such as voltage, force, strain, bandwidth, and manufacturability. Lastly, we outline future research directions in materials, physics-informed modeling, system integration, and scalable fabrication necessary to advance electrostatic artificial muscles toward practical, real-world deployment. Full article

Polymeric fibers represent a vital class of functional materials due to their versatile properties, such as wide availability, low cost, recyclability, biodegradability, and excellent mechanical and chemical stability. Polymer fibers can be fabricated at both micro- and nanoscale dimensions using a variety of processing techniques. This review provides a comprehensive overview of the principal methods employed for polymer fiber preparation, including electrospinning, melt and solution blowing, dry and wet spinning, template synthesis, phase separation, and self-assembly. The technical principles, as well as the advantages and limitations, of each technique are systematically discussed. The review also explores polymeric fibers as smart materials for actuation applications. Particular focus is given to stimulus-responsive fiber systems such as shape memory fibers, hydrogel fibers, liquid crystal fibers, and electroactive polymers. Overall, this review establishes a coherent framework linking polymer fiber fabrication strategies with structure–property–function relationships, offering practical guidance for material selection and accelerating the development of next-generation smart polymer fibers for advanced actuation and multifunctional applications. Full article

Polymer–ceramic piezoelectric composites are widely investigated to combine the high piezoelectric performance of ferroelectric ceramics with the flexibility and processability of electroactive polymers. However, achieving enhanced dielectric properties while preserving the intrinsic piezoelectric response of the polymer matrix remains challenging, particularly due to dielectric mismatch between the constituent phases and interfacial effects. In this work, barium titanate (BaTiO₃) loaded poly(vinylidene fluoride-trifluoroethylene) (PVDF-TrFE) nanocomposites were fabricated by solvent casting using polyvinylpyrrolidone (PVP) and polysorbate 80 (PS80) as dispersing agents, aiming to obtain polarizable materials capable of retaining high piezoelectric strain coefficient (d₃₃) values and potentially exploiting the opposite polarity of matrix and filler through tailored poling strategies. Morphological, crystallographic, structural, thermal, thermomechanical, dielectric, and piezoelectric characterizations were performed by SEM/EDXS, XRD, FTIR, DSC, TGA, DMTA, dielectric spectroscopy, and d₃₃ measurements. Both dispersants improved filler dispersion and film densification, increasing the crystalline fraction of the matrix, without altering the relative fraction of β-phase (up to 93%). PVP enabled moderate and stable permittivity enhancement with weak frequency dependence, whereas PS80 introduced an electrically active interfacial contribution that amplified low-frequency permittivity at high filler loadings but made the permittivity more frequency-dependent. The piezoelectric response (between −20 pC/N and −25 pC/N) remained predominantly governed by the polymer phase, suggesting limited polarization played by BaTiO₃. These results underlined the critical role of interfacial electrical properties in designing stable high-performance flexible PVDF-TrFE/BaTiO₃ composites. Full article

Multifunctional polymer–ferrite composites based on poly(vinylidene fluoride) (PVDF) and magnetic fillers are of increasing interest for applications requiring coupled electrical, dielectric, and magnetic responses. However, the relationship between magnetic filler concentration, PVDF phase composition, and the resulting multifunctional properties remains insufficiently understood. In this work, PVDF/BaFe₁₂O₁₉ (PVDF/BaF) composite membranes containing 2–20 wt.% BaF were fabricated using a combined non-solvent and thermally induced phase-inversion (NIPS–TIPS) method. Structural evolution was analyzed by X-ray diffraction and quantitative FTIR spectroscopy, thermal behavior by differential scanning calorimetry, optical properties by diffuse reflectance spectroscopy, dielectric response in the frequency range 10³–10⁶ Hz, and magnetic characteristics by vibrating sample magnetometry. At moderate filler concentrations (2–10 wt.%), BaFe₁₂O₁₉ nanoparticles acted as effective β-phase nucleating centers, leading to electroactive phase fractions of 97.7–99.9% and a maximum β-phase content of 86.7% for PVDF/BaF10. At higher loadings (15–20 wt.%), particle agglomeration and restricted chain mobility promoted a transition toward α-phase-dominated crystallization. Thermal analysis indicated competing nucleation and confined crystallization processes, while optical and dielectric measurements revealed nonmonotonic changes associated with interfacial interactions and Maxwell–Wagner–Sillars polarization. Magnetic measurements showed a linear increase in saturation magnetization with filler concentration and a nonmonotonic coercivity dependence with a pronounced change near the critical agglomeration concentration. These results demonstrate that the multifunctional response of PVDF/BaFe₁₂O₁₉ membranes is governed by the interplay between β-phase nucleation, interfacial polarization, and magnetic particle interactions, with approximately 10 wt.% ferrite providing the most balanced electrical, dielectric, and magnetic characteristics. Full article

Laser-induced graphene (LIG) enables rapid conversion of polymer substrates into conductive carbon materials. In this study, nitrogen-containing carbon nanomaterials were fabricated on polyetherimide (PEI) substrates using empirical screening of two specific process points. The resulting materials were characterized using scanning electron microscopy, Raman spectroscopy, X-ray photoelectron spectroscopy, cyclic voltammetry, and electrochemical impedance spectroscopy to correlate structural features with electron-transfer behavior. Raman and XPS analyses showed different structure and morphology depending on irradiation regime. The carbon materials with a higher sp³ fraction (≈55–59%), larger in-plane crystallite size (L_a up to 8.0 nm), and pronounced π–π* shake-up satellites indicated enhanced graphitic ordering when a shorter nanosecond laser was used. These structural differences resulted in substantially lower charge-transfer resistance (0.53–0.79 kΩ·cm³) and larger electroactive surface areas for the porous electrodes compared with foam structured carbon nanomaterials. The results show that, under the selected fabrication conditions, variations in laser processing parameters correspond to differences in graphitic ordering and electron-transfer properties in PEI-derived laser-induced carbon materials. Full article

The dielectric elastomer is a category of electroactive polymer capable of having large deformation under electric excitation and vice versa. They show great potential for the proper maneuvering of small-scale aerial vehicles due to low density and fast actuation, and the successful design demands a proper prediction of their overall dynamic characteristics. However, these characteristics cannot be accurately predicted from lower-order material approximation and/or one specific elastomer shape under a specific flow velocity, pretension, and relaxation. In this research, a comprehensive modal and aerodynamic analysis for the VHB 4910 dielectric elastomer membrane of three different shapes is computationally investigated under different electric excitations, pretensions, and flow velocities using the higher-order Ogden model. A finite element model and a two-way, fully coupled fluid–structure interaction model are developed to obtain vibration and aerodynamic characteristics, respectively, for different membrane shapes. It is found that the variation in electric excitation, pretension, and air velocity is influential in altering the overall dynamics of the membrane and is unique to specific shapes. The rectangular membrane shows a higher vibration frequency for the fundamental mode, whereas the circular membrane provides higher frequencies in higher modes. Increased relaxation for a membrane prestretch higher than the moderate range of stretch ratio ($\lambda$ = 3) demonstrates a slight increase in lift coefficient within a small range of angle of attack, followed by a decrease after exceeding that range. Both the rectangular and elliptical membranes show more flexibility to delay the stall compared to the circular membrane. The circular membrane is observed to have more potential for enhancing the aerodynamic performance and altering the flow field within a certain range of electric excitation and pretension. Computational results are compared with published experimental results to validate the corresponding models. Full article

The development of high-performance electrochemical sensors requires precise integration of electrode active materials that provide both superior electrocatalytic activity and long-term structural stability. Herein, we report a systematically optimized, one-pot electrochemical deposition approach for the fabrication of nanographenide-based nanoarchitectures, incorporating either a conducting polymer (PEDOT-NG) or Prussian blue (PB-NG). Derived from optimization-driven structural refinement—including applied potential, electrodeposition time, and precursor concentration—the robust nanoarchitecture exhibits a hierarchical morphology that provides an expanded electroactive surface area, accelerating charge transfer and enhancing electrochemical catalytic activity. The optimized PEDOT-NG exhibits exceptional sensitivity for the simultaneous determination of ascorbic acid (AA), dopamine (DA), and uric acid (UA), achieving wide linear ranges with low detection limits of 4.1, 0.12, and 0.18 μM, respectively. The PB-NG achieves a limit of detection of 4.39 μM, driven by highly reversible and stable redox kinetics. This performance is underpinned by narrowed peak-to-peak separations (ΔE) and reduced redox potentials. These results underscore the pivotal role of precise parametric control in developing high-performance electrochemical sensors. Furthermore, this work establishes a comprehensive strategy for designing resilient electrode active materials, thereby paving the way for next-generation electrochemical platforms tailored for diverse and robust sensing environments. Full article

Polymer-based biosensors have evolved from passive supports into active functional elements that dictate analytical performance in complex real-world samples. This critical review with meta-trend analysis examines 96 original research articles published between 2015 and 2025, evaluating how four polymer classes (conductive polymers, redox-mediator polymers, hydrogels, and molecularly imprinted polymers) address matrix effects in food, beverage, environmental and clinical applications. Electrochemical detection dominates (79% of studies), with conductive polymers enabling low-potential operation that excludes electroactive interference. Hydrogels achieve superior precision (RSD below 3%) in protein-rich matrices through biocompatible microenvironments that preserve enzyme kinetics. Molecularly imprinted polymers provide unmatched stability in harsh environments for trace-level detection of heavy metals and toxins, though delayed response times from slow analyte diffusion persist. Critical evaluation exposes validation deficits: 91% of studies omit limits of quantification, while approximately one-third lack reproducibility (33%) and precision (30%). The multi-matrix challenge, maintaining calibration across different hostile environments, remains the primary barrier to commercial deployment. Advanced architectures, including nanocapsulation, hierarchical nanocomposites, and microneedle-integrated systems, offer pathways to overcome limitations in fouling resistance and operational stability. Full article