Search Results (478)

This study presents a full polymer piezoelectric flextensional energy harvester (FPPFEH) comprising a single-layer poly(vinylidene fluoride) (PVDF) film bonded to a 3D-printed polylactic acid (PLA) flextensional frame. For an arm inclination angle of $\theta =10°$, the free-body model gives a theoretical geometric force-amplification factor of $M_{\mathrm{F}}=\cot \theta \approx 5.67$; this value represents an ideal upper bound and was not independently validated by local force or strain measurements. During assembly, the film was tensioned only to remove visible slack and maintain a flat configuration. No intentional pretension was applied, and any residual tension was not measured. Off-resonance force-controlled tests showed that the generated voltage was approximately proportional to the dynamic input force and nearly independent of frequency after accounting for attenuation caused by the finite measurement-input impedance. The ideal quasi-static model overpredicted the absolute voltage by a nearly constant factor across the tested force range. This offset is consistent with a lumped reduction associated with frame compliance and the in-plane anisotropy of the PVDF film, neither of which was independently measured. At $30\mathrm{Hz}$ and $12.32{\mathrm{N}}_{\mathrm{rms}}$, the rectified output charged a $6600\mathsf{\mu }\mathrm{F}$ supercapacitor to $2.10\mathrm{V}$ in $14\min$, corresponding to $14.55\mathrm{mJ}$ of stored energy. Under base-acceleration excitation from $0.05$ g to 1 g, the voltage peak occurred between $112.88$ and $116.49\mathrm{Hz}$, close to the electrical anti-resonance near $114\mathrm{Hz}$, and reached $12.11{\mathrm{V}}_{\mathrm{peak}}$ at 1 g. Near resonance, the highest measured power among the tested resistive loads occurred between 150 and $200\mathrm{k}\Omega$; however, the exact optimal resistance could not be resolved from the four tested loads. These results demonstrate off-resonance force-driven energy storage and resonance-mode vibration energy harvesting within the tested conditions. 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

Poly(vinylidene fluoride) (PVDF) exhibits excellent piezoelectric properties governed by the content and orientation of its polar phases. Herein, a synergistic regulation strategy integrating a flow field induced by a designed solid-phase extrusion die and ion–dipole interactions introduced by CTAB is established to achieve highly oriented β phase in PVDF. The incorporation of CTAB promotes the formation of the γ phase before extrusion, providing a structurally favorable precursor for the subsequent flow-induced γ-β phase transformation. During solid-phase extrusion, the converging flow field drives extensive molecular chain alignment, promoting the γ-β phase transformation and substantially enhancing both β phase content and orientation. The synergistic effects of CTAB-induced ion–dipole interactions and the converging flow field further regulate the melting behavior and crystal perfection of PVDF, driving the transformation of the lamellar structure into highly oriented lamellar bundles along the extrusion direction. Among all compositions studied, the blends containing 5 wt% CTAB exhibit the optimal polar phase content and orientation characteristics, along with the highest dielectric constant. This work elucidates the synergistic regulation of PVDF hierarchical structures by ion–dipole interactions and flow fields, offering an effective strategy for fabricating high-performance piezoelectric PVDF materials. Full article

The transport of metal ions from highly saline matrices remains challenging due to the elevated ionic strength and complex chemical speciation that characterize seawater and desalination brines. In this work, the influence of membrane composition on Cd(II) transport through polymer inclusion membranes (PIMs) was evaluated using cellulose triacetate (CTA), poly(vinyl chloride) (PVC), and poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) membranes containing Aliquat 336. Membranes were tested using model NaCl solutions, seawater, and desalination brine, and the effects of membrane mass, polymer matrix, carrier/plasticizer composition, and receiving phase were investigated. Reducing the CTA membrane mass by 50% did not significantly affect transport efficiency, indicating that membrane composition had a greater influence on Cd(II) transport than membrane mass under the conditions evaluated. Among the evaluated formulations, the optimum PVDF-HFP membrane contained 60 wt.% PVDF-HFP, 30 wt.% Aliquat 336, and 10 wt.% butyl stearate (BTS), achieving a transport efficiency of 95.5% and an initial flux of 2.7 × 10⁻⁶ mol m⁻² s⁻¹ in desalination brine. The use of 0.5 M HNO₃ as the receiving phase markedly improved Cd(II) transport in both synthetic saline solutions and real seawater and desalination brine compared with ultrapure water. These results highlight the importance of polymer–plasticizer interactions in controlling Cd(II) transport and demonstrate the potential of PVDF-HFP/Aliquat 336/BTS membranes for metal recovery from complex saline media. Full article

Developing sustainable lithium-ion batteries (LIBs) requires binder–carbon interfaces that combine mechanical compatibility, interfacial cohesion, and reduced environmental impact. In this work, density functional theory calculations were used to evaluate the interactions of representative binder monomers acrylonitrile (AN), pyrrole (PY), vinylidene fluoride (VDF), and tetrafluoroethylene (TFE) with pristine graphene and chitosan-functionalized graphene oxide (GO/chitosan). Structural, energetic, electronic, and topological features were analyzed using counterpoise-corrected interaction energies, frontier-orbital descriptors, molecular electrostatic potential maps, projected density of states, noncovalent interaction analysis, and quantum theory of atoms in molecules topology. Final interaction energies were obtained at the M06-2X/def2-TZVP level with Boys–Bernardi counterpoise correction to provide a more robust description of weak noncovalent adsorption. Most binder–surface interactions fall within a weak, near-thermoneutral adsorption regime. On pristine graphene, AN and PY exhibit weakly favorable adsorption, with minimum counterpoise-corrected interaction energies of −3.13 and −2.10 kcal mol⁻¹, respectively, whereas TFE and VDF show orientation-dependent, near-neutral behavior. GO/chitosan introduces oxygen-containing and amino functionalities that modify the adsorption balance, particularly for selected perpendicular configurations of fluorinated monomers, although the net stabilization remains modest. NCI, QTAIM, MEP, and PDOS analyses indicate that surface functionalization increases the chemical heterogeneity and directionality of local contacts; however, these local descriptors do not necessarily translate into strong global adsorption energies. Overall, the results identify GO/chitosan as a chemically tunable interface for binder–carbon compatibility in LIB electrodes and demonstrate the importance of triple-ζ, counterpoise-corrected calculations for evaluating weak binder–surface interactions. Full article

Polymers, including poly(vinylidene fluoride) (PVDF), have been widely used in daily life and industries, such as in membrane filtration, food packing and heat exchanging. However, pristine polymers suffer from inherently low thermal conductivity. Herein, thermally conductive poly(vinylidene fluoride) (PVDF) composites were prepared by incorporating eutectic gallium–indium (EGaIn) liquid metals (LMs) and carbon fibers (CFs) as dual fillers. The effects of the LMs and the CFs on the thermal and mechanical properties of the PVDF composites were characterized via thermal conductivity, morphology, crystallinity, and mechanical testing. The CFs improved the dispersion of the LM droplets within the PVDF matrix, forming continuous thermally conductive pathways, thereby enhancing the composite thermal conductivity. A maximum thermal conductivity of 0.40 W/(m·K), an increase of 154% over the pure PVDF, was achieved when 1 wt% CF was added to the PVDF composites containing 5 wt% LMs. Mechanical testing showed that the CFs compensated for the slight reduction in tensile strength due to the LM addition, yielding a tensile strength of 30 ± 3 MPa, slightly higher than that of the pure PVDF. Characterization analyses confirmed that the crystalline and chemical structure of the PVDF matrix were preserved after the filler addition, indicating minimal alteration of the PVDF matrix. These results suggest that the PVDF/LM/CF composites exhibit a balanced enhancement of the thermal conductivity and mechanical strength, making them potential candidates for thermal management applications. This study provides insights into designing high-performance polymer composites with dual functionality for advanced engineering applications. Full article

Poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) polymer electrolytes suffer from low ionic strength and poor mechanical performance. Meanwhile, lithium lanthanum titanate (LLTO) fillers exhibit severe agglomeration and weak interfacial compatibility with the polymer matrix. To solve these problems, 3-glycidoxypropyltrimethoxysilane (KH560) at four different concentrations (1 wt%, 2 wt%, 3 wt%, 4 wt%) was loaded onto polydopamine-modified LLTO (PDA@LLTO). The modified materials were mixed with PVDF-HFP, and composite solid electrolytes were fabricated by the solution casting method. The epoxy groups in KH560 undergo ring-opening reactions with amino and hydroxyl moieties on PDA, while its trimethoxysilane groups crosslink with the polymer matrix, forming a robust “LLTO-PDA-KH560-polymer” interfacial structure. This dual modification markedly improves the dispersion of PDA@LLTO, strengthens interfacial adhesion, and enhances the mechanical and electrochemical properties of the composite electrolyte. All KH560 loadings suppress LLTO agglomeration, and the 3 wt% grafting ratio yields the optimal performance: a uniform and dense microstructure, a room-temperature ionic conductivity of 5.92 × 10⁻⁴ S cm⁻¹, an electrochemical stability window extended to 4.88 V, and a tensile strength over 50% higher than the ungrafted sample. The modified electrolyte effectively inhibits lithium dendrite growth and enhances the cycling stability of solid-state batteries. This work demonstrates that KH560-PDA synergistic modification enables comprehensive performance optimization of composite electrolytes, offering a viable strategy for designing high-performance electrolytes for solid-state lithium-metal batteries. Full article

Per- and polyfluoroalkyl substances (PFAS) such as perfluorooctanoic acid (PFOA) persist in aquatic environments due to their extremely strong C–F bonds and high environmental stability/poor biodegradability, creating an urgent demand for high-performance and scalable adsorption treatment technologies. This study reports the synthesis, characterization, and fixed-bed column adsorption performance of a dual-polymer-modified activated carbon adsorbent engineered for enhanced PFAS capture. Activated carbon (AC) was sequentially functionalized with polyethyleneimine (PEI) and poly(chlorotrifluoroethylene–co-vinylidene fluoride) (Kel–F) to form the fluorine-rich, amine-grafted composites AC–PEI–KelF and AC–PEI–KelF–PEI. Surface-area studies of the modified AC adsorbents showed a reduction in surface area of about a factor of two, possibly due to pore blockage by the polymers. Continuous-flow column breakthrough studies demonstrated dramatic improvements in perfluorooctanoic acid (PFOA) removal efficiency, with 50% maximum breakthrough time increasing from 80 min for AC to 540 min for AC–PEI–KelF and 1500 min for the AC–PEI–KelF–PEI formulation. Thomas model adsorption capacities for AC, AC–PEI–KelF and AC–PEI–KelF–PEI were, respectively, 65, 490, and 1130 mg/g. The adsorption mechanism, using selective mobile phases, was shown to be due to a combination of electrostatic and hydrophobic/fluorophilic interactions. Kinetic analysis showed that adsorption exhibited pseudo-second-order behavior, with multi-stage intraparticle diffusion. The optimized composite also exhibited strong regeneration stability, retaining 79% performance after six adsorption–desorption cycles, and displayed high selectivity for PFOA, even in the presence of structurally related competitors such as octanoic acid. The adsorption of perfluoropentanoic acid and undecafluoro-2-methyl-3-oxahexanoic acid (GenX) was also significant, and some interaction with trifluoroacetic acid was noted. Full article

The remediation of contaminants of emerging concern (CECs) requires innovative, high-efficiency, and sustainable technologies. Here, we investigate active polymeric membranes incorporating TiO₂/ZnO heterojunctions for synergistic sono-enhanced photocatalytic water treatment under both UV and visible-light irradiation. TiO₂/ZnO composites were synthesized and characterized, confirming the formation of type II heterojunctions with tailored optical properties for sunlight-driven photocatalysis. The catalysts were integrated into poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and poly(vinylidene fluoride-co-trifluoroethylene) (PVDF-TrFE) matrixes using electrospinning (ES) and thermally induced phase separation (TIPS). ES membranes, specifically the ZnO-rich heterojunction within a PVDF-TrFE matrix (3T-7Z@TrFE ES), achieved the highest performance toward ciprofloxacin (CIP) degradation, reaching 71 and 57% under UV and visible light, respectively. The hybridization of the method by coupling ultrasound induced significant synergistic effects, with relative enhancement factors up to 1.38. Furthermore, the sono-enhanced photocatalytic pathway shifted the degradation mechanism towards the early fragmentation of the harmful piperazine ring, yielding a more sustainable degradation process. In addition, the composite membranes showed selective antibacterial activity against S. aureus, making this a multifunctional platform able not only to degrade CECs but also to mitigate membrane fouling. Overall, this work demonstrates the potential of tailored heterojunctions and composite membranes as sustainable platforms for the remediation of recalcitrant CECs in water, highlighting the synergy between photoactivity, piezoelectricity, and mechanistic control. Full article

Icing phenomena on wind turbine blades and components are a major problem, causing downtimes that increase maintenance costs, reducing the blade’s lifespan, or in severe cases, even leading to component damage. A nanofiber-based bi-layer liquid-infused surface (BLIS) coating was prepared and characterized, combining good adhesion to wind turbine blades with low ice adhesion. The BLIS coating was produced by a new method combining electrospinning and a heat treatment step, containing a poly ethyl-2-cyanoacrylate (PECA)-based adhesive layer, a slippery layer of poly vinylidene fluoride-co-hexafluoropropylene (PVDF-HFP) copolymer, and an infiltrated perfluoropolyether lubricant. Thermogravimetric analysis (TGA) was used to ensure the thermal stability of the polymers in the nanofiber coating layers and to optimize the heat treatment process of the layers. Microstructural changes were studied by scanning electron microscopy (SEM) and surface roughness measurements. Contact angle measurements and sliding velocity tests on wind turbine blade segments at icing conditions of 0 °C and +5 °C indicate that the water sliding properties of the BLIS coating were improved compared to uncoated blades. In addition, coated blade segments showed a 50% lower ice adhesion strength than uncoated blades. Full article

Liquid electrolytes in conventional lithium-ion batteries pose safety risks associated with flammability, leakage, and explosion, whereas solid polymer electrolytes are generally limited by insufficient ionic conductivity at ambient temperature, restricting the development of high-energy lithium batteries. To address these issues, flexible poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)-based gel polymer electrolyte membranes (GPEs) were prepared via a slit-coating process combined with UV curing. NASICON-type lithium aluminum titanium phosphate (Li_1.3Al_0.3Ti_1.7P₃O₁₂, LATP) and garnet-type tantalum-doped lithium lanthanum zirconate (Li_6.4La₃Zr_1.4Ta_0.6O₁₂, LLZTO) were introduced as inorganic ceramic fillers to improve the ion-transport and interfacial properties of the GPE. Among the investigated samples, the PVDF-HFP-based GPE containing 10 wt% LLZTO exhibited the best overall performance, with an ionic conductivity of 3.40 × 10⁻⁴ S·cm⁻¹ at ambient temperature and a Li⁺ transference number of 0.77. Cyclic voltammetry results showed that the LLZTO-modified electrolyte membrane exhibited sharper and more symmetric redox peaks, higher peak current response, and better curve overlap during repeated cycles, indicating improved electrochemical reversibility and interfacial stability. In addition, LLZTO incorporation enhanced the mechanical strength, broadened the electrochemical stability window, and improved the flame-retardant behavior of the membrane. The LiFePO₄/GPE/Li cell assembled with the optimized membrane delivered an initial discharge capacity of 160 mAh·g⁻¹ at 0.1 C and maintained 80 mAh·g⁻¹ at 1 C, demonstrating good rate capability. Moreover, a capacity retention of 96% was maintained after 100 cycles at 0.1 C, confirming excellent cycling stability. Therefore, this work provides an effective strategy for the structural optimization and scalable preparation of high-performance gel polymer electrolyte membranes for lithium battery 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

The development of durable and practical polymer-supported photocatalytic materials that are suitable for use in continuous-flow systems has become an increasingly pressing issue in the field of water treatment. In this study, FeTiO₃/BiOCl heterojunction structures were synthesized at different ratios and integrated into a poly(vinylidene fluoride) (PVDF) matrix to develop photocatalytic thin-film systems. The resulting materials were characterized by Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and UV–visible diffuse reflectance spectroscopy (UV-DRS) analyses. In photocatalytic experiments conducted under visible light, a 66.3% removal of doxycycline was achieved for pristine FeTiO₃ within 180 min, whilst the FTO@BiOCl(III) composite reached 74.4%. In the PVDF-based thin-film system, the film catalyst demonstrated a removal efficiency of 68.9%. When the pH effect was investigated, the highest total removal of 90.3% was achieved under pH 6.0 conditions. Radical scavenging experiments revealed that superoxide radicals were the predominant active species (a decrease to 30.5% in the presence of benzoquinone (BQ). In experiments conducted in the air-lift reactor system, the P-FTO@BiOCl(III) film achieved approximately 65% removal after 9 h and maintained its structural stability. The PVDF-supported FeTiO₃/BiOCl heterojunction thin-film system offers a noteworthy alternative for environmental applications due to its suitability for continuous systems, structural stability and effective photocatalytic performance. 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

In this study, poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) films embedded with silver nanoparticles were fabricated to investigate their antibacterial performance against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). Inspired by the nanoscale topographies of natural antibacterial surfaces, such as dragonfly and cicada wings, microstructured pillars were introduced onto the polymer surface to enhance its bactericidal activity by increasing the effective contact area. Surface morphology was characterised using scanning electron microscopy (SEM), including higher-magnification imaging of micropillar surfaces, while energy-dispersive X-ray spectroscopy confirmed the presence of silver. Higher-magnification SEM revealed nanoscale surface features on the micropillars, attributed to embedded or surface-associated silver nanoparticles. Antibacterial performance was evaluated using confocal laser scanning microscopy with live/dead staining. The PVDF-HFP/Ag films exhibited a significant reduction in bacterial viability, particularly against S. aureus (reducing viability to 0.6% ± 1.1%), while showing moderate activity against E. coli (41.0% ± 3.7% viability). While the fabricated micropillars (~5 µm) are larger than bacterial cells and unlikely to induce direct mechanical rupture, they increase surface interaction. To further investigate the theoretical antibacterial mechanism of scaled-down features, finite element analysis (FEA) was performed to model the mechanical interaction between bacterial cells and nanostructured pillars. The simulation results indicated localised stress concentrations that could compromise bacterial membrane integrity, suggesting a possible mechanobactericidal contribution if the microstructures are further reduced to the nanoscale, in addition to the primary biochemical effects of silver nanoparticles. FEA results do not aim to explain the experimentally observed antibacterial performance and should be interpreted only as a conceptual investigation. These findings demonstrate the potential of bio-inspired PVDF-HFP/Ag films as antibacterial materials for food packaging and related applications, subject to future comprehensive toxicity and quantitative microbiological evaluations. Full article