Search Results (423)

Flexible piezoelectric sensors based on electrospun poly(vinylidene fluoride) (PVDF)/polyacrylonitrile (PAN)/graphene nanofibers were fabricated and evaluated for passive human body motion detection. Optimized electrospinning yielded smooth, continuous fibers with diameters of 200–250 nm and uniform films with thicknesses of 20–25 µm. Fourier transform infrared (FTIR) spectroscopy confirmed a high fraction of the piezoelectrically active β-phase in PVDF, which was further enhanced by post-deposition thermal treatment. Graphene and lithium phosphate were incorporated to improve electrical conductivity, β-phase nucleation, and piezoelectric response, while PAN provided mechanical reinforcement and flexibility. Custom test platforms were developed to simulate low-amplitude mechanical stimuli, including finger bending and pulsatile pressure. Under applied pressures of 40, 80, and 120 mmHg, the sensors generated stable millivolt-level outputs with average peak voltages of 25–30 mV, 53–60 mV, and 80–90 mV, respectively, with good repeatability and an adequate signal-to-noise ratio. These results demonstrate that PVDF/PAN/graphene nanofiber films are promising candidates for flexible, wearable piezoelectric sensors capable of detecting subtle physiological signals, and highlight the critical roles of electrospinning conditions, functional additives, and post-processing treatments in tuning their electromechanical performance. Full article

Poly(vinylidene fluoride) (PVDF) nanofibers have emerged as promising materials for flexible piezoelectric sensors, yet their performance is fundamentally constrained by the limited formation and alignment of the electroactive β-phase. In this study, we report a phase-engineering strategy that integrates ionic functionalization, inorganic nanofiller incorporation, and post-fabrication corona poling to achieve enhanced crystalline ordering and electromechanical coupling in electrospun PVDF nanofibers. Tetrabutylammonium perchlorate increases solution conductivity, enabling uniform, bead-free fiber formation, while barium titanate nanoparticles act as nucleation centers that promote β-phase crystallization at the expense of the non-polar α-phase. Subsequent corona poling further aligns molecular dipoles and strengthens remnant polarization within both the PVDF matrix and embedded nanoparticles. Structural analyses confirm the synergistic evolution of crystalline phases, and piezoelectric measurements demonstrate a substantial increase in peak-to-peak output voltage under dynamic loading conditions. This combined phase-engineering approach provides a simple and scalable route to high-performance PVDF-based piezoelectric sensors and highlights the importance of coupling crystallization control with dipole alignment in designing next-generation wearable electromechanical materials. Full article

High-performance piezoelectric poly(vinylidene fluoride) (PVDF) has great application potential in the field of microsensors, but achieving efficient polarization remains a challenge. Here, the in situ doping electrospinning technique is employed to enhance the piezoelectric properties by introducing a single dose of zinc oxide (ZnO) or barium titanate (BaTiO₃,BTO) dopants. The effects of key processing parameters on the morphology of nanofiber membranes were systematically investigated. In addition, the influence of zinc oxide (ZnO) or barium titanate (BTO) dopant concentrations on the piezoelectric properties of PVDF was examined. The microstructure, electrical performance, and β-phase content of the composite membranes were characterized. Results indicate that the composite film with a doping formulation of 16 wt% PVDF and 10 wt% ZnO exhibits optimal overall performance: the β-phase content of PVDF reaches 52.8%, and the output voltage reaches 1.5 V, which is 2.5 times higher than that of the undoped PVDF nanofiber membranes. This study provides an effective doping strategy for the fabrication of high-performance piezoelectric nanofiber membranes. Full article

Salisbury screen-type radar absorption structures (RASs) consisting of a resistance sheet, a spacer, and a conductive base provide an efficient method for microwave absorption. An impedance-matched resistance sheet allows microwaves to enter, whereas superior microwave absorbers enhance their performance further. In the present work, an impedance matching composite film was prepared by using polymer/iron/iron nanowires. By varying the polymer, poly (methyl methacrylate) (PMMA), poly (vinylidene fluoride) (PVDF), and poly (vinyl alcohol) (PVA), to iron powder ratios (1:1, 2:1, and 4:1), composite films were synthesized and examined by scanning electron microscopy, X-ray diffraction, and the four-point probe method to determine the materials’ characteristics. An impedance-matched composite film was prepared based on the selected composition with 1–10 wt.% iron nanowire additions. Experimental results showed that the polymeric composite film prepared by a ratio of iron-PVA of 4:1 exhibited a sheet resistance of 49 ± 9.7 Ω/sq due to well dispersion of iron powder in PVA. With 1 wt.% Fe nanowire addition, the optimal composite sheet resistance was 329.7 ± 45.3 Ω/sq, which corresponded to an impedance matching degree (i.e., |Z_in/Z₀| value) of 0.88 ± 0.12 and can be used as a resistance sheet for a Salisbury screen-type absorber in RAS applications. Full article

Solid polymer and composite polymer electrolytes have been investigated as a replacement for liquid electrolytes in lithium batteries and have shown promising conductivities at room temperature. However, the literature reports often do not fully investigate the effects of residual solvent or testing apparatus conditions, leading to discrepancies in reported performance and possible conflation of conductivity values. Using combinations of poly (vinylidene fluoride-co-hexafluoropropylene), succinonitrile, and lithium lanthanum zirconium tantalum oxide, this work aims to develop an understanding of how polymer electrolyte composition, including solvent retention, affects conductivity. A custom-designed controllable pressure test fixture was utilized to determine ionic conductivity of the composite polymer electrolyte films at a wide range of pressures (1.5–18.7 psi) and temperatures 10–90 °C. Applied pressure during testing greatly influences apparent conductivities, with optimal composite film conductivity values ranging from 1.2 × 10⁻⁵ to 4.1 × 10⁻⁵ S cm⁻¹ at room temperature. At elevated temperatures, the composite films achieved greater than 1 mS cm⁻¹. The ideal pressure was found to be dependent on the polymer electrolyte additives. Symmetric cell testing showed over 99% Coulombic efficiency for over one hundred cycles at 0.1 mA cm⁻². The results of this work highlight the importance of careful characterization of electrolyte films and controlled test fixture pressure when developing polymer electrolytes. Full article

Calcium (Ca²⁺ ions) is one of the dominant elements that contribute to water hardness, scaling in pipes, bathroom faucets, and kitchen utensils. Herein, we report on the development of poly(vinylidene fluoride-co-hexafluoropropylene) cellulose acetate (PVDF-HFP/CA) films for the treatment of Ca²⁺ ions as one of the constituents that causes water hardness. CA and PVDF-HFP polymers, and their blend consisting of 3 wt.% PVDF-HFP/CA, were effectively synthesised through the phase inversion technique. Analysis using thermogravimetric analysis (TGA), Fourier transform infrared (FTIR) spectroscopy, and scanning electron microscopy (SEM) confirmed the effective incorporation of 3 wt.% PVDF-HFP into the cellulose acetate film. Parameters such as temperature, initial concentration, pH, adsorbent dosage and contact time were investigated in batch studies during the removal of Ca²⁺ ions in synthetic water samples. Under optimal conditions (pH 7, adsorbent dosage of 0.5 mg/L, and concentration of 120 mg/L), the 3 wt.% PVDF-HFP/CA film achieved a 99% adsorption efficiency for Ca²⁺ ions in 90 min. The adsorption process adhered to pseudo-second-order and Freundlich isotherm models, which suggest that the adsorption of Ca²⁺ ions is heterogeneous. The maximum adsorption efficiency achieved was 56 mg/g, indicating an endothermic physisorption process. The 3 wt.% PVDF-HFP/CA film maintained higher adsorption in the presence of counter ions and in a binary system, and it could be recycled at least three times. Thus, the findings demonstrated that the 3 wt.% PVDF-HFP/CA film could be a valuable material for Ca²⁺ ions removal to acceptable drinking water levels. Full article

With the rapid development of communication, electronics, medical, and energy industries in modern society, film capacitors have garnered widespread attention and undergone significant growth. However, the low energy density (U_e) resulting from low breakdown strength (E_b) significantly limits the application of thin-film capacitors. In this work, we use a low-cost and effective dip-coating method to apply boron nitride (BN) layers onto the outer layers of poly(vinylidene fluoride-co-hexafluoropropylene)/barium titanate (P(VDF-HFP)/BT) composite films to prepare boron nitride-poly(vinylidene fluoride-co-hexafluoropropylene/barium titanate-boron nitride (BN-P(VDF-HFP)/BT-BN) composite films with a sandwich structure that exhibits extremely high E_b and U_e. The experimental results show that the sandwich-structured BN-P(VDF-HFP)/BT-BN films containing 7.5 wt% BT nanoparticles obtained 530 MV/m E_b and 18.12 J/cm³ U_e, both of which are much higher than those of the corresponding monolayer films. In addition, the finite element simulation results show that the designed sandwich-structured films can reduce local field strength distortion, decrease leakage current, and suppress the development of breakdown channels, thereby significantly improving E_b and U_e. In summary, this study presents a low-cost and effective method for enhancing the breakdown strength and energy density of thin-film capacitors. Full article

Leaching of the extractant from polymer inclusion membranes (PIMs) into the feed and receiving aqueous solutions shortens their life. Therefore, when a particular PIM extractant has been selected, it is important to choose a base polymer that will minimize to the greatest extent extractant leaching compared to other base polymers, thus providing the best stability of the PIM. However, comparisons of the stability of PIMs composed of the same extractant and different base polymers is usually conducted by multiple cycles of extraction and back-extraction steps, which are time-consuming and labor-intensive. An alternative approach based on thermal analysis (thermogravimetric analysis (TGA) and differential thermal analysis (DTA)) was developed and applied to PIMs containing 40 wt.% Aliquat 336, one of the most frequently used PIM extractants, and the three most frequently used PIM base polymers, i.e., poly(vinyl chloride) (PVC), cellulose triacetate (CTA), and poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP). The temperatures and enthalpies associated with Aliquat 336 release were compared, with PVDF-HFP exhibiting the highest values, indicating the strongest interaction between the extractant and the polymer matrix and, thus, the highest stability. The PVC-based PIM was predicted to be the most prone to extractant leaching among the PIMs studied. This stability ranking was confirmed theoretically by quantum chemistry (DFT) calculations, which provided molecular-level insights into the likely interaction sites between Aliquat 336 and the polymer chains. An experimental validation of the above leaching order was also provided by PIM leaching experiments in aqueous 0.1 M and 0.05 M NaCl solutions, where membrane mass losses over a 24 h period were determined. The results of the current study demonstrated thermal analysis to be a fast and viable approach in comparing the stability of PIMs with the same extractant but different base polymers. Full article

The inherent hydrophobicity of poly(vinylidene fluoride) (PVDF) ultrafiltration membranes leads to severe membrane fouling when processing proteinaceous solutions and organic contaminants, significantly limiting their practical applications. This study presents a novel metal-ion mediated co-deposition strategy for fabricating high-performance antifouling poly(vinylidene fluoride) (PVDF) hollow fiber ultrafiltration membranes. Through Zn²⁺ coordination-driven self-assembly, a uniform and stable composite coating of dopamine (DA), tannic acid (TA), and ZIF-8 nanoparticles was successfully constructed on the membrane surface under mild conditions. The modified membrane exhibited significantly enhanced hydrophilicity, with a water contact angle of 21° and zeta potential of −29.68 mV, facilitating the formation of a dense hydration layer that effectively prevented protein adhesion. The membrane demonstrated exceptional separation performance, achieving a pure water permeability of 771 L/(m²∙h∙bar) and bovine serum albumin (BSA) rejection of 97.7%. Furthermore, it showed outstanding antifouling capability with flux recovery rates exceeding 83.6%, 74.7%, and 71.5% after fouling by BSA, lysozyme, and ovalbumin, respectively. xDLVO analysis revealed substantially increased interfacial free energy and stronger repulsive interactions between the modified surface and protein foulants. The antifouling mechanism was attributed to the synergistic effects of hydration layer formation, optimized pore structure, additional water transport pathways from ZIF-8 incorporation, and electrostatic repulsion from negatively charged surface groups. This work provides valuable insights into the rational design of high-performance antifouling membranes for sustainable water treatment and protein separation applications. Full article

All-solid-state lithium batteries (ASSLBs) employing Li-rich layered oxide (LLO) cathodes are regarded as promising next-generation energy storage systems owing to their outstanding energy density and intrinsic safety. Polymer-in-salt solid electrolytes (PISSEs) offer advantages such as high room-temperature ionic conductivity, enhanced Li anode interfacial compatibility, and low processing costs; however, their practical deployment is hindered by poor oxidative stability especially under high-voltage conditions. In this study, we report the rational design of a bilayer electrolyte architecture featuring an in situ solidified LiClO₄-doped succinonitrile (LiClO₄–SN) plastic–crystal interlayer between a Li_1.2Mn_0.6Ni_0.2O₂ (LMNO) cathode and a poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)-based PISSE. This PISSE/SN–LiClO₄ configuration exhibits a wide electrochemical stability window up to 4.7 V vs. Li⁺/Li and delivers a high ionic conductivity of 5.68 × 10⁻⁴ S cm⁻¹ at 25 °C. The solidified LiClO₄-SN layer serves as an effective physical barrier, shielding the PVDF-HFP matrix from direct interfacial contact with LMNO and thereby suppressing its oxidative decomposition at elevated potentials. As a result, the bilayer polymer-based cells with the LMNO cathode demonstrate an initial discharge capacity of ∼206 mAh g⁻¹ at 0.05 C and exhibit good cycling stability with 85.7% capacity retention after 100 cycles at 0.5 C under a high cut-off voltage of 4.6 V. This work not only provides a promising strategy to enhance the compatibility of PVDF-HFP-based electrolytes with high-voltage cathodes through the facile in situ solidification of plastic interlayers but also promotes the application of LMNO cathode material in high-energy ASSLBs. Full article

The efficient purification of Pb(II)-containing wastewater is essential for safeguarding public health and maintaining the aquatic environment. In this study, novel hydrous ferric oxide (HFO) nanoparticle-embedded poly(vinylidene fluoride) (PVDF) composite adsorption membranes were developed through a simple blending method for efficient Pb(II) removal. This composite membrane (denoted as HFO-PVDF) combines the excellent selectivity of HFO nanoparticles for Pb(II) with the membrane’s advantage of easy scalability. The optimized HFO-PVDF_(1.5) membrane achieved adsorption equilibrium within 20 h and exhibited excellent adsorption capacity. Moreover, adsorption capacity markedly enhanced with increasing temperature, confirming the endothermic nature of the process. The developed HFO-PVDF membranes demonstrate significant potential for real-world wastewater treatment applications, exhibiting exceptional selectivity for Pb(II) in complex ionic matrices and could be effectively regenerated via a relatively straightforward process. Furthermore, filtration and dynamic regeneration tests demonstrated that at an initial Pb(II) concentration of 5 mg/L, the membrane operated continuously for 10–13 h before regeneration, treating up to 200 L/m² of wastewater before breakthrough, highlighting potential for cost-effective industrial wastewater treatment. This study not only demonstrates the high efficiency of the HFO-PVDF membrane for heavy metal ion removal but also provides a theoretical foundation and technical support for its practical application in water treatment. Full article

A triboelectricity-enhanced piezoelectric nanogenerator (PENG) based on pressure-processed multi-electrospun polymeric layers is herein developed for efficient vibrational energy harvesting. The hybridization of piezoelectric and triboelectric mechanisms through electrospinning has been utilized to enhance electrical output by increasing contact areas and promoting alignment within piezoelectric materials. A multi-layer structure comprising alternating poly (vinylidene fluoride) (PVDF) and poly (hexamethylene adipamide) (PA 6/6) exhibits superior electrical performance. A lateral Janus configuration, providing distinct positive and negative triboelectric polarities, has further optimized device efficiency. This approach introduces a novel operational mechanism, enabling superior performance compared to conventional methods. The fiber-based architecture ensures exceptional flexibility, low weight, and a high surface-to-volume ratio, enabling enhanced energy harvesting. Experimentally, the PENG achieved an open-circuit voltage of 14.59 V, a short-circuit current of 205.7 nA, and a power density of 7.5 mW m⁻² at a resistance of 30 MΩ with a five-layer structure subjected to post-processing under pressure. A theoretical model has mathematically elucidated the output results. Long-term durability (over 345,600 cycles) has confirmed its robustness. Demonstrations of practical applications include monitoring human joint motion and respiratory activity. These results highlight the potential of the proposed triboelectricity-enhanced PENG for vibrational energy harvesting in flexible and wearable electronic systems. Full article

This study explores using polyvinylidene fluoride (PVDF) membranes modified with multi-walled carbon nanotubes (MWCNTs) to treat simulated and industrial brine from coal power stations. The MWCNTs were acid-treated and characterized using Fourier Transform Infrared Spectroscopy (FTIR), Raman, and nitrogen sorption at 77 K, Thermogravimetric analysis (TGA), and Transmission electron microscopy (TEM). The desired membranes were obtained by casting from a solution of N-Methyl-2-pyrrolidone, PVDF, various weight percentages of MWCNTs, and a small amount of polyvinylpyrrolidone. The acid treatment of the MWCNTs introduced oxygen moieties on the surface, and increased pore volume and surface area while maintaining crystallinity and structural integrity remain preserved. The maximum rejection rate achieved was 41.82% with 1 wt.% of acid-treated MWCNTs in the PVDF membrane. Acid-treated MWCNTs loaded membranes had an improved rejection rate, which was 5× higher than membranes without MWCNTs. Full article

Planar heaters are designed to deliver uniform heat across broad surfaces and serve as critical components in applications requiring energy efficiency, safety, and mechanical flexibility, such as wearable electronics and smart textiles. However, conventional metal-based heaters are limited by poor adaptability to curved or complex surfaces, low mechanical compliance, and susceptibility to oxidation-induced degradation. To overcome these challenges, we applied a protein-assisted electroless copper (Cu) plating strategy to electrospun poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) nanofiber substrates to fabricate flexible, conductive planar heating membranes. For interfacial functionalization, a protein-based engineering approach using bovine serum albumin (BSA) was employed to facilitate palladium ion coordination and seed formation. The resulting membrane exhibited a dense, continuous Cu coating, low sheet resistance, excellent durability under mechanical deformation, and stable heating performance at low voltages. These results demonstrate that the BSA-assisted strategy can be effectively extended to complex three-dimensional fibrous membranes, supporting its scalability and practical potential for next-generation conformal and wearable planar heaters. Full article

Background/Objectives: Airborne viral diseases pose a health risk, due to which there is a growing interest in developing filter materials capable of capturing fine particles containing virions from the air and that also have a virucidal effect. Nanofiber membranes made of poly(vinylidene fluoride) dissolved in N,N-dimethylacetamide and functionalized with copper, silver, and zinc nanoclusters were fabricated via electrospinning. This study aims to evaluate and compare the virucidal effects of nanofibers functionalized with metal nanoclusters against the human influenza A virus A/WSN/1933 (H1N1) and SARS-CoV-2. Methods: A comprehensive characterization of materials, including X-ray diffraction, scanning electron microscopy, microwave plasma atomic emission spectroscopy, thermogravimetric analysis, contact angle measurements, nitrogen sorption analysis, mercury intrusion porosimetry, filtration efficiency, and virucidal tests, was used to understand the interdependence of the materials’ physical characteristics and biological effects, as well as to determine their suitability for application as antiviral materials in air filtration systems. Results: All the filter materials tested demonstrated very high particle filtration efficiency (≥98.0%). The material embedded with copper nanoclusters showed strong virucidal efficacy against the SARS-CoV-2 alpha variant, achieving an approximately 1000-fold reduction in infectious virions within 12 h. The fibrous nanowire polymer functionalized with zinc nanoclusters was the most effective material against the human influenza A virus strain A/WSN/1933 (H1N1). Conclusions: The materials with Cu nanoclusters can be used with high efficiency to passivate and kill the SARS-CoV-2 alpha variant virions, and Zn nanoclusters modified activated porous membranes for killing human influenza A virus A7WSN/1933 (H1N1) virions. Full article