Vinylidene Fluoride Research Articles

Agricultural waste rice husk/poly(vinylidene fluoride) composite: a wearable triboelectric energy harvester for real-time smart IoT applications

Agricultural waste rice husk/poly(vinylidene fluoride) composite: a wearable triboelectric energy harvester for real-time smart IoT applications

Enhanced Electroactive Phases of Poly(vinylidene Fluoride) Fibers for Tissue Engineering Applications

Nanofibrous materials generated through electrospinning have gained significant attention in tissue regeneration, particularly in the domain of bone reconstruction. There is high interest in designing a material resembling bone tissue, and many scientists are trying to create materials applicable to bone tissue engineering with piezoelectricity similar to bone. One of the prospective candidates is highly piezoelectric poly(vinylidene fluoride) (PVDF), which was used for fibrous scaffold formation by electrospinning. In this study, we focused on the effect of PVDF molecular weight (180,000 g/mol and 530,000 g/mol) and process parameters, such as the rotational speed of the collector, applied voltage, and solution flow rate on the properties of the final scaffold. Fourier Transform Infrared Spectroscopy allows for determining the effect of molecular weight and processing parameters on the content of the electroactive phases. It can be concluded that the higher molecular weight of the PVDF and higher collector rotational speed increase nanofibers’ diameter, electroactive phase content, and piezoelectric coefficient. Various electrospinning parameters showed changes in electroactive phase content with the maximum at the applied voltage of 22 kV and flow rate of 0.8 mL/h. Moreover, the cytocompatibility of the scaffolds was confirmed in the culture of human adipose-derived stromal cells with known potential for osteogenic differentiation. Based on the results obtained, it can be concluded that PVDF scaffolds may be taken into account as a tool in bone tissue engineering and are worth further investigation.

Improved properties of CoFe2O4@rGO/PVDF composites prepared through a solution-mixing approach

In this work, a hybrid material based on CoFe2O4 nanoparticles immobilized on reduced graphene oxide (CoFe2O4@rGO) was successfully synthesized through a one-step green solvothermal method. Subsequently, the resultant CoFe2O4@rGO was further modified by aminopropyltriethoxysilane to form the A-CoFe2O4@rGO hybrid, serving as the filler of poly(vinylidene fluoride) (PVDF). The facile preparation of A-CoFe2O4@rGO was confirmed through various microstructural characterization techniques. PVDF-based composites with varying contents of A-CoFe2O4@rGO (1 wt%, 3 wt%, 5 wt%, 7 wt%, and 10 wt%) were prepared using a solution-mixing approach. SEM results revealed uniform distribution of the A-CoFe2O4@rGO filler within the PVDF matrix. The XPS results indicated an obvious interfacial interaction between the A-CoFe2O4@rGO filler and PVDF matrix. Consequently, the crystallization degree and β crystalline content of PVDF matrix in the A-CoFe2O4@rGO(7 wt%)/PVDF composite were enhanced to 52.3 % and 32.1 %, respectively, compared to 42.2 % and 26.0 %, respectively, in pure PVDF. The A-CoFe2O4@rGO(10 wt%)/PVDF composite enhanced electrical conductivity and dielectric constant at 100 Hz, with values of 1.33 × 10−7 S/m and 22.1, respectively, compared to 1.86 × 10−9 S/m and 8.6, respectively, in pure PVDF. In addition, despite the non-magnetic nature of pure PVDF, the A-CoFe2O4@rGO(10 wt%)/PVDF composite possessed a magnetization value of 1.64 emu/g at 60,000 Oe. The comprehensive enhancement in crystallization behavior, electrical, dielectric, and magnetic properties demonstrates the potential of the A-CoFe2O4@rGO/PVDF composite for various applications.

Highly effective ultrafiltration membranes based on plastic waste for dye removal from water.

Applicable and low-cost ultrafiltration membranes based on waste polystyrene (WPS) blend and poly vinylidene fluoride (PVDF) were effectively cast on nonwoven support using phase inversion method. Analysis was done into how the WPS ratio affected the morphology and antifouling performance of the fabricated membranes. Cross flow filtration of pure water and various types of polluted aqueous solutions as the feed was used to assess the performance of the membranes. The morphology analysis shows that the WPS/PVDF membrane layer has completely changed from a spongy structure to a finger-like structure. In addition, the modified membrane with 50% WPS demonstrated that the trade-off between selectivity and permeability is met by a significant improvement in the rejection of the membrane with a reduction in permeate flux due to the addition of PVDF. With a water permeability of 50 LMH and 44 LMH, respectively, the optimized WPS-PVDF membrane with 50% WPS could reject 81% and 74% of Congo red dye (CR) and methylene blue dye (MB), respectively. The flux recovery ratio (FRR) reached to 88.2% by increasing PVDF concentration with 50% wt. Also, this membrane has the lowest irreversible fouling (Rir) value of 11.7% and lowest reversible fouling (Rr) value of 27.9%. The percent of cleaning efficiency reach to 71%, 90%, and 85% after eight cycles of humic acid (HA), CR, and MB filtration, respectively, for the modified PS-PVDF (50%-50%). However, higher PVDF values cause the membrane's pores to become clogged, increase the irreversible fouling, and decrease the cleaning efficiency. In addition to providing promising filtration results, the modified membrane is inexpensive because it was made from waste polystyrene, and as a result, it could be scaled up to treat colored wastewater produced by textile industries. PRACTITIONER POINTS: Recycling of plastic waste as an UF membrane for water/wastewater treatment was successfully prepared and investigated. Mechanical properties showed reasonable response with adding PVDF. The modified membrane with 50% PS demonstrated that the trade-off between selectivity and permeability is met by a significant improvement in the rejection.

Augmenting Piezoelectric Performance of Poly (vinylidene fluoride) Nanogenerator with Zinc Oxide Nanorods Decorated Reduced Graphene Oxide Nanosheets

Augmenting Piezoelectric Performance of Poly (vinylidene fluoride) Nanogenerator with Zinc Oxide Nanorods Decorated Reduced Graphene Oxide Nanosheets

Contribution of graphene oxide (GO)-containing polydimethylsiloxane (PDMS) binder to the surface modification of electrospun PVDF membrane towards development of photothermal vacuum membrane distillation (PVMD)

Given the scarcity of water and energy resources and their potential to escalate into future crises, water and energy have emerged as the paramount challenges of the present century. To address these challenges, simultaneously, a novel membrane distillation (MD) technique named photothermal MD (PMD) has come to the forefront in recent years. The PMD is rapidly advancing, particularly in the field of desalination, towards increasing the use of sustainable solar energy. In this work, the surface of poly(vinylidene fluoride) (PVDF) electrospun membrane was turned into a photothermal surface by binding graphene oxide (GO) nanosheets using a binder solution made of polydimethylsiloxane (PDMS) with different concentrations (0.1, 0.5, 1, 2, 3 wt%). Subsequently, the environmentally-friendly low-pressure plasma polymerization method was employed to polymerize perfluorodecyl acrylate (PFDA) monomers on the surface of coated electrospun membrane to achieve an omniphobic surface. In this regard, the contact angles of water, oil, and ethanol/water (70/30 v/v) solution on the surface of the coated membranes were measured to be 144°, 124.4°, and 120.8°, respectively. Compared to the uncoated electrospun membrane, the one coated with GO-containing binder solution with optimum PDMS concentration of 0.1 wt%, showed a significant increase in flux by 41 % at 1 sun irradiation during photothermal vacuum MD (PVMD). In the PVMD process, the conventional method of feed heating was substituted with membrane surface heating utilizing solar energy. Additionally, vacuum was employed to facilitate the passage of water vapor through the membrane pores. This increment was further highlighted by salt rejection remained constant at 99.9 %. It was also found that PDMS concentration in the GO-containing binder solution adversely affects the membrane efficiency, exhibiting a decreasing trend from 54.1 % to 17.5 % when PDMS concentration increases from 0.1 to 3 wt%. Additionally, the long-term performance assessment of the prepared membrane coated with the binder solution with optimum PDMS concentration of 0.1 wt% demonstrated its acceptable resistance against wetting by the NaCl aqueous solution (35 g/L) containing 0.3 mM sodium dodecyl sulfate (SDS).

The effect of clay modification on the structure, dielectric behaviour and mechanical properties of PVDF/PMMA/CTAMag polymer nanocomposites as potential flexible performance materials

Abstract In this approach, nanocomposites of PVDF/PMMA/CTAMag films have been successfully synthesized. Modified Maghnite was used as inorganic reinforcement. In this study, nanocomposite polymers were developed based on a mixed matrix of poly(vinylidene fluoride) (PVDF) and poly(methyl methacrylate) (PMMA) of composition (80/20 w/w) in dispersion containing 0, 1, 3, 5 and 7 wt % fillers of organomodified montmorillonite nanoclay (CTAMag) in the melt state. The results obtained by scanning electron microscopy (SEM), XRD traces and FTIR spectra highlighted the homogeneous flexible character of the PVDF/PMMA/CTAMag films and their intercalated and intercalated/exfoliated surface morphology, in addition to the presence of PVDF α, β and γ phase crystallites in these complex films. The increased presence of the modified clay in the host matrix of the PVDF/PMMA blend significantly influenced the melting temperature and the degree of crystallinity of the PVDF crystallites. The scattering of the dielectric spectra, which covers a wide range of frequencies from 20 Hz to 1 GHz, indicates the presence of the phenomenon of interfacial polarization associated with the dielectric capacitance complex at lower frequencies in these composites at 27 °C. The mechanical properties of these composites were evaluated as a function of the load and the mixed matrix of these composites.

A BaTiO3@polyacrylonitrile/poly(vinylidene fluoride) nanofibrous composite membrane with high piezoelectricity based on the central combination design method and cross-electrospinning technology

The rapid development of piezoelectric sensors has been studied extensively, owing to their good flexibility, wearability, high sensitivity and low cost. However, some inorganic materials with good piezoelectricity cannot make sensors flexible, and the organic materials with good flexibility have a weak output electrical signal and low strength. In order to explore and optimize the preparation technology of piezoelectric sensors, a BaTiO3@polyacrylonitrile (PAN)/poly(vinylidene fluoride) (PVDF) nanofibrous composite membrane (NCM) was prepared by cross-electrospinning technology and the central combination design (CCD) method. The morphology, structure, hydrophobicity, mechanical properties and piezoelectricity of the BaTiO3@PAN/PVDF NCMs were investigated. The BaTiO3@PAN/PVDF NCMs had the better hydrophobicity and mechanical properties compared with the pure PAN/PVDF NCM. The 5BaTiO3@PAN/PVDF NCM designed by CCD had a more uniform fiber diameter, and a more stable output voltage with a 46% improvement. With the help of cross-electrospinning technology and the CCD method, the NCM will be outstanding for the development of fabricating flexible wearable piezoelectric sensors.

Solid polymer electrolytes with LiClO4 – Theoretical study of polyvinylidene halides

The potential of polyvinylidene halides PVDX (X = F, Cl, Br, I), as a materials for energy had been examined by computational chemistry. The reaction of polymer chains with lithium perchlorate was analyzed and we focused on the stability and reactivity of PVDX composites including their different crystalline α- or β-crystal forms. The characterization of cluster models in PVDX-α and PVDX-β, encompassing their geometry, electrostatic potentials, electron density, Gibbs-free energy difference, and HOMO-LUMO gap were examined. Further, an analysis of the crystal structure has unveiled modifications in the HOMO-LUMO gap, geometric distortions, and alterations in the models' reactivity.The results of theoretical study were compared to the results obtained experimentally. Structural information from FTIR spectra showed that PVDF crystalline form affects the ionic conductivity of the polymer composite and thereby its functionality as a solid polymer electrolyte. Significantly, insights into the reactivity and then the functionality of the poly(vinylidene fluoride) have been acquired, serving as a valuable supplement to the existing experimental data.

Binder-Free Three-Dimensional Porous Graphene Cathodes via Self-Assembly for High-Capacity Lithium–Oxygen Batteries

The porous architectures of oxygen cathodes are highly desired for high-capacity lithium–oxygen batteries (LOBs) to support cathodic catalysts and provide accommodation for discharge products. However, controllable porosity is still a challenge for laminated cathodes with cathode materials and binders, since polymer binders usually shield the active sites of catalysts and block the pores of cathodes. In addition, polymer binders such as poly(vinylidene fluoride) (PVDF) are not stable under the nucleophilic attack of intermediate product superoxide radicals in the oxygen electrochemical environment. The parasitic reactions and blocking effect of binders deteriorate and then quickly shut down the operation of LOBs. Herein, the present work proposes a binder-free three-dimensional (3D) porous graphene (PG) cathode for LOBs, which is prepared by the self-assembly and the chemical reduction of GO with triblock copolymer soft templates (Pluronic F127). The interconnected mesoporous architecture of resultant 3D PG cathodes achieved an ultrahigh capacity of 10,300 mAh g−1 for LOBs. Further, the cathodic catalysts ruthenium (Ru) and manganese dioxide (MnO2) were, respectively, loaded onto the inner surface of PG cathodes to lower the polarization and enhance the cycling performance of LOBs. This work provides an effective way to fabricate free-standing 3D porous oxygen cathodes for high-performance LOBs.

A flexible self-cleaning/antibacterial PVDF/T-ZnO fabric based on piezo-photocatalytic coupling effect for smart mask

Abstract A novel flexible composite fabric has been engineered by combining piezoelectric poly (vinylidene fluoride) (PVDF) and tetrapod zinc oxide (T-ZnO) nanostructures, which are integrated onto a nonwoven fabric substrate. This fabric exhibits a wide array of functionalities, notably self-cleaning and antibacterial properties, facilitated by the synergistic piezo-photocatalytic coupling effect. Through the utilization of the piezoelectric effect inherent in PVDF/T-ZnO in tandem with the photocatalytic attributes of T-ZnO nanostructures, the fabric achieves concurrent degradation of organic pollutants and antibacterial efficacy when exposed to mechanical vibration and solar irradiation. The piezo-photocatalytic coupling effect engenders an internal electric field that aids in the effective separation of photo-generated carriers (electrons and holes), thereby diminishing recombination rates and augmenting the efficiency of the photocatalytic degradation process. Notably, organic pollutants such as methylene blue and azithromycin exhibit degradation levels of 96.0% and 92.6%, respectively, within a timeframe of 25 and 60 minutes. The incorporation of PVDF/T-ZnO results in an approximate 40% enhancement in the degradation rate of organic substances compared to the use of T-ZnO in isolation. Furthermore, the composite fabric showcases exceptional antibacterial efficacy, effectively inhibiting the proliferation of Staphylococcus aureus. Experimental findings reveal that the average antibacterial zone diameter of the PVDF/T-ZnO fabric measures at 7.68 mm, significantly surpassing that of the T-ZnO fabric and nonwoven fabric. Given its remarkable self-cleaning and antibacterial attributes, the PVDF/T-ZnO fabric exhibits substantial potential for diverse applications, including the development of intelligent masks tailored for deployment in healthcare settings and polluted environments.

A Microporous Gel Polymer Electrolyte with High Mg2+ Ionic Conductivity at Room Temperature

Rechargeable magnesium batteries have attracted much attention due to the high theoretical volumetric capacity, abundance, and safety. However, solid‐state Mg batteries have been rarely studied because of limited choices of solid‐state electrolyte materials. In this research, poly(vinylidene fluoride)/poly(propylene carbonate) (PVDF/PPC) as matrix were prepared using a simple solution casting method. Ethylene carbonate (EC), diethyl carbonate (DEC), and magnesium(II) bis(trifluoromethanesulfonyl) imide [Mg(TFSI)2] were selected to prepare liquid electrolyte. A classification of novel gel polymer electrolytes (GPEs), PVDF/PPC/Mg(TFSI)2, was synthesized and investigated. The electrochemical measurements show that PVDF/PPC/Mg(TFSI)2 polymer electrolytes exhibit a high ionic conductivity, close to 10‐2 S cm‐1, at room temperature. The electrochemical stability window of PVDF/PPC‐based GPE was up to 3 V (versus Mg2+/Mg). Materials characterization shows that these GPEs have a porous structure, providing a pathway for magnesium ion transport. Thermal analysis and crystal structure results indicate that PVDF crystallinity was affected by the addition of PPC. Additionally, the ion transport mechanism in the gel polymer electrolyte has been discussed.

Ternary Phase-Field Simulation of Poly(vinylidene fluoride) Microporous Membrane Structures Prepared by Nonsolvent-Induced Phase Separation with Different Additives and Solvent Treatments

Ternary Phase-Field Simulation of Poly(vinylidene fluoride) Microporous Membrane Structures Prepared by Nonsolvent-Induced Phase Separation with Different Additives and Solvent Treatments

Selective and Controlled Grafting from PVDF-Based Materials by Oxygen-Tolerant Green-Light-Mediated ATRP.

Poly(vinylidene fluoride) (PVDF) shows excellent chemical and thermal resistance and displays high dielectric strength and unique piezoelectricity, which are enabling for applications in membranes, electric insulators, sensors, or power generators. However, its low polarity and lack of functional groups limit wider applications. While inert, PVDF has been modified by grafting polymer chains by atom transfer radical polymerization (ATRP), albeit via an unclear mechanism, given the strong C-F bonds. Herein, we applied eosin Y and green-light-mediated ATRP to modify PVDF-based materials. The method gave nearly quantitative (meth)acrylate monomer conversions within 2 h without deoxygenation and without the formation of unattached homopolymers, as confirmed by control experiments and DOSY NMR measurements. The gamma distribution model that accounts for broadly dispersed polymers in DOSY experiments was essential and serves as a powerful tool for the analysis of PVDF. The NMR analysis of poly(methyl acrylate) graft chain-ends on PVDF-CTFE (statistical copolymer with chlorotrifluoroethylene) was carried out successfully for the first time and showed up to 23 grafts per PVDF-CTFE chain. The grafting density was tunable depending on the solvent composition and light intensity during the grafting. The initiation proceeded either from the C-Cl sites of PVDF-CTFE or via unsaturations in the PVDF backbones. The dehydrofluorinated PVDF was 20 times more active than saturated PVDF during the grafting. The method was successfully applied to modify PVDF, PVDF-HFP, and Viton A401C. The obtained PVDF-CTFE-g-PnBMA materials were investigated in more detail. They featured slightly lower crystallinity than PVDF-CTFE (12-18 vs 24.3%) and had greatly improved mechanical performance: Young's moduli of up to 488 MPa, ductility of 316%, and toughness of 46 × 106 J/m3.

Large electrocaloric effect near room temperature induced by domain switching in ferroelectric nanocomposites

The solid-state refrigeration technique based on the electrocaloric effect (ECE) of ferroelectric materials has been regarded as a promising alternative to vapor compression systems due to its advantages of high efficiency and easy miniaturization. However, the small adiabatic temperature change (ATC) and narrow operating temperature range of ferroelectric materials are key obstacles for their practical applications of ECE refrigeration. To improve the ECE performance of ferroelectric polymer poly(vinylidene fluoride) [P(VDF-TrFE)], PbZr1−xTixO3 (PZT) nanoparticles with larger polarization is herein introduced to form ferroelectric nanocomposites. The phase-field simulation is employed to investigate the dynamic hysteresis loops and corresponding domain evolution of the ferroelectric nanocomposites. The temperature-dependent ATC values are calculated using the indirect method based on the Maxwell relation. The appearance of the double hysteresis loop is observed in P(VDF-TrFE) nanocomposite filled with PbZr0.1Ti0.9O3 nanoparticles [P(VDF-TrFE)–PZT0.9], which is mainly caused by a microscopic domain transition from single domain to polar vortex. Compared to the P(VDF-TrFE), enhanced ATC values associated with the domain transition are unveiled in P(VDF-TrFE)–PZT0.9, and the temperature range of excellent ECE is also effectively broadened. In addition, as the component x of filled PZT nanoparticles increases to cross the morphotropic phase boundary (MPB), the maximum ATC value shows a significant increase. The results presented in this work not only explain the mechanism of domain transition induced excellent ECE in the P(VDF-TrFE)–PZT nanocomposite, but also stimulate future studies on enhancing ECE of P(VDF-TrFE) by introducing ferroelectric nanofillers.

Production of Stable Electrically Conductive PVDF Membranes Based on Polydopamine-Polyethyleneimine-Assisted Deposition of Carbon Nanotubes.

Electrically conductive membranes (ECMs) have emerged as a multifunctional separation technology that integrates membrane filtration with electrochemical reactions. Physical stability remains a critical challenge for ECMs synthesized by coating polymer membranes with conductive materials. In this article, polydopamine (PDA) and polyethyleneimine (PEI) were used to facilitate the synthesis of significantly more stable ECMs using poly(vinylidene fluoride) (PVDF) ultrafiltration membranes and carbon nanotubes (CNTs). Four different synthesis methods were compared in terms of the final surface stability and separation properties: (1) CNTs deposited on PEI-crosslinked PDA-coated PVDF membranes, (2) PEI-crosslinked CNTs deposited on PDA-coated PVDF, (3) PDA, PEI and CNTs sequentially deposited layer-by-layer on PVDF, and (4) PEI-crosslinked PDA deposited on CNT-coated PVDF. The results revealed that method 1 generated ECMs with the greatest physical stability, highest electrical conductivity (18,518 S/m), and sufficient permeability (395.2 L/(m2·h·bar). In comparison, method 2 resulted in membranes with the highest permeability (2128.5 L/(m2·h·bar), but with low surface conductivity (502 S/m) and poor physical stability (i.e., 53-75% lower peel-off forces compared to other methods). Overall, methods 1, 3, and 4 can be used to make highly conductive membranes with a 97-99% removal of methyl orange by electrochemical degradation at -3 V.

Processing and characterisation of hot rolling pressed PVDF films with enhanced field-induced polarisation

Poly (vinylidene fluoride) (PVDF) based polymers are good candidates for high-power energy storage in dielectric capacitors. So far, most studies reporting PVDF with high energy density are based on solution casting, a method ill-suited for large-scale production. In this work, we develop PVDF films with high crystallinity (47%) and ultrahigh β-phase (∼97%) using Hot Rolling Press (HRP). During HRP, the crystallinity, fraction of β-phase, internal stress, and the piezoelectric coefficient d33 increased with rolling temperature. The anisotropic stress imposed by two rollers led to a highly preferred orientation of the HRP film along the rolling direction. Notably, the HRP film exhibits an enhanced field-induced polarisation Pin-max value (0.16 C m−2) compared to conventional PVDF films (0.10 C m−2), with an energy density of 32.6 J cm−3 at 871 kV mm-1. The good low field dielectric (εr ∼19 @ 1 kHz) and piezoelectric (d33 ∼30 pC N-1) properties with high-temperature stability (up to 100 °C), and its suitability for in-line continuous production, make HRP PVDF films promising for low field dielectric and piezoelectric applications.

Zeolite-Based Poly(vinylidene fluoride) Ultrafiltration Membrane: Characterization and Molecular Weight Cut-Off Estimation with Support Vector Regression Modelling.

Zeolite serves as a promising additive for enhancing the hydrophilicity of polymeric membranes, yet its utilization for bolstering the mechanical strength of the membrane remains limited. In this study, poly(vinylidene fluoride) (PVDF) membranes were modified by incorporating various concentrations of zeolite (0.5-2 wt%) to improve not only their mechanical properties, but also other features for water filtration. Membranes with and without zeolite incorporation were fabricated via a dry-wet phase inversion technique, followed by the application of a series of characterization techniques in order to study their morphological structure, mechanical strength, and hydrophilicity. The membrane filtration performance for each membrane was evaluated based on pure water flux and Bovine Serum Albumin (BSA) rejection. Field-Emission Scanning Electron Microscopy (FESEM) images revealed a dense, microvoid-free structure across all of the PVDF membranes, contributing to a high pristine PVDF membrane tensile strength of 14 MPa. The addition of 0.5 wt% zeolite significantly improved the tensile strength up to 19.4 MPa. Additionally, the incorporation of 1 wt% zeolite into PVDF membrane yielded improvements in membrane hydrophilicity (contact angle of 67.84°), pure water flux (63.49% increase), and high BSA rejection (95.76%) compared to pristine PVDF membranes. To further improve the characterization of the zeolite-modified PVDF membranes, the Support Vector Regression (SVR) model was adopted to estimate the molecular weight cut off (MWCO) of the membranes. A coefficient of determination (R2) value of 0.855 was obtained, suggesting that the SVR model predicted the MWCO accurately. The findings of this study showed that the utilization of zeolite is promising in enhancing both the mechanical properties and separation performance of PVDF membranes for application in ultrafiltration processes.

On-Demand MXene-Coupled Pyroelectricity for Advanced Breathing Sensors and IR Data Receivers.

MXene-inspired two-dimensional (2D) materials like Ti3C2Tx are widely known for their versatile properties, including surface plasmon, higher electrical conductivity, exceptional in-plane tensile strength, EMI shielding, and IR thermal properties. The MXene nanosheets coupled poly(vinylidene fluoride) (PVDF) nanofibers with d33 ∼-26 pm V-1 are able to capture the smaller thermal fluctuation due to a superior pyroelectric coefficient of ∼130 nC m-2 K-1 with an improved (∼7 times with respect to neat PVDF nanofibers) pyroelectric current figure of merit (FOMi). The significant enhancement of the pyroelectric response is attributed to the confinement effect of 2D MXene (Ti3C2Tx) nanosheets within PVDF nanofibers, as evidenced from polarized Fourier transform infrared (FTIR) spectroscopy and scanning probe microscopy (SPM). In subsequent studies, the practical applications of self-powered pyroelectric sensors of MXene-PVDF have been demonstrated. The fabricated flexible, hydrophobic pyroelectric sensor could be utilized as an excellent pyroelectric breathing sensor, a proximity sensor, and an IR data transmission receiver. Further, supervised machine learning algorithms are proposed to distinguish different types of breathing signals with ∼98% accuracy for healthcare monitoring purposes.

Facile design of amphiphobic PVDF membranes utilizing synergy of pore structure and surface fluorination: A demonstration in membrane distillation

Amphiphobic membranes have attracted much attention in membrane distillation (MD) applications, due to its potential in simultaneously resisting membrane wetting and fouling when treating complex wastewater. The current amphiphobic membranes often require non-trivial design of multilevel re-entrant structure. Here we proposed a new class of amphiphobic membranes without multilevel re-entrant surface, by creating a composite poly(vinylidene fluoride)/polyvinyl alcohol/SiO2 membrane with asymmetric structure and well-controlled small surface pores via the NTIPS method, followed by direct fluorination via chemically binding the –OH of polyvinyl alcohol and low surface energy moieties 1H,1H,2H,2H-perfluorodecyl-triethoxysilane, assisted by 3-aminopropyltriethoxysilane and trimesoyl chloride. The amphiphobic membrane showed superior liquid entry pressure above 5 bar with various simulated saline feeds containing surfactants and organic pollutants. The amphiphobic membrane demonstrated robust anti-wetting and anti-fouling performance through a series of 24-h direct contact MD experiments using the above feeds, presenting stable water flux and high rejection, e.g., flux of 50.6 kg/(m2·h) and rejection >99.9 % with feed containing 3.5 wt% NaCl, 1 mM FA, and 2 mM SDS. The results demonstrated the fabrication of robust amphiphobic membrane through simple procedure utilizing the synergy between pore structure and surface chemistry, inspiring more efforts to design adequate membranes for treating complex wastewater.