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Cellulose has advantages of easy availability, low price, renewability and biodegradability, making it a very promising substitute for fossil-based materials. A safe composite cellulose membrane for quasi-solid-state lithium ion batteries has been developed by coating cellulose separators with poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and lithium aluminum titanium phosphate (LATP). This membrane exhibits excellent electrochemical performance, with an ionic conductivity as high as 2.1 mS cm−1, and a lithium-ion transference number of 0.57. The membrane shows good electrolyte wetting properties, with porosity and liquid electrolyte uptake of 47.2 % and 401.7 %, respectively. It has good thermal stability and can maintain its dimensional stability even at 200 ℃. The capacity retention of the quasi-solid-state LiFePO4/Li battery assembled with this membrane after 200 cycles at 0.2 C is about 86.7 %. The quasi-solid-state battery has good thermal stability and is not prone to thermal runaway.

Abstract This study is the first application of a PVDF-HFP-based polymer inclusion membrane incorporating the poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and di(2-ethylhexyl)phosphoric acid (D2EHPA) as the base polymer and extractant for the extraction of bismuth(III), respectively. It is demonstrated that the PIM comprised of 60 wt% PVDF-HFP and 40 wt% D2EHPA is the most effective in the extraction of bismuth(III) from feed solution containing 20 mg L−1 bismuth(III) and 0.2 mol L−1 sulfate adjusted to pH 1.4. The extracted bismuth(III) ions are back-extracted quantitatively to the receiving solution containing 1 mol L−1 sulfuric acid. The stoichiometry experiments reveal that the Bi: D2EHPA ratio in the bismuth(III) extracted complex is 1:6, and D2EHPA is dimer. Moreover, it is shown that the studied PIM has high selectivity in the extraction of bismuth(III) over other interfering ions such as Mo(VI), Cr(III), Al(III), Fe(III), Ni(II), Zn(II), Cd(II), Co(II), Cu(II), and Mn(II). The interference of Fe(III) is also eliminated by masking with fluoride, leading finally to a nearly pure extraction of bismuth(III).

High piezoelectric composite films composed of poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and ferromagnetic cobalt ferrite (CoFe2O4) (0.00 ​wt% to 0.2 ​wt%) are prepared by a solution casting method accompanied by uniaxial stretching and high electric field poling. The decisive effect of the poling electric field on the power generating capability was confirmed by the experiments. For pure PVDF-HFP films, when the maximum electric field Emax is 120 ​MV/m, the calibrated open circuit voltage reaches 2.93 ​V, which is much higher than those poled at lower electric fields (70 ​MV/m: 1.41 ​V; 90 ​MV/m: 2.11 ​V). Furthermore, the addition of CoFe2O4 also influences the piezoelectricity dramatically. In the samples containing 0.15 ​wt% CoFe2O4, the calibrated open circuit voltage increases to the maximum value of 3.57 ​V. Meanwhile, the relative fraction of the β-phase and the crystallinity degree are 99% and 48%, respectively. The effects of CoFe2O4 nanoparticles on initial crystallization, uniaxial stretching and high electric field poling are investigated by XRD, FTIR and DSC.

Abstract In today's technological landscape, advancing methods for producing conductive membranes that simplify and streamline the development of advanced interface materials is crucial. This study introduces a versatile and innovative method for fabricating superhydrophilic, conductive nanofibrous membranes based on the in situ synthesis of polypyrrole nanoparticles on poly(vinylidene fluoride‐co‐hexafluoropropylene) (PVDF‐HFP) electrospun fibers. The composite membranes morphologically exhibit a particle‐decorated nanofibrous configuration, with polypyrrole nanoparticles distributed along the individual fibers' surface. The nanoparticle‐nanofiber configuration shows distinctive properties; electrochemically, the electrospun mats demonstrate excellent inherent electrical conductivity, good cyclic and high electrochemical stability, and low resistance. Furthermore, the amphiphilic and superhydrophilic behavior, achieved through nanotopography, porosity and interactions between the intrinsically conductive polymer and the PVDF‐HFP fibers, enables efficient uptake of polar and nonpolar analytes. The membranes also demonstrate good in vitro cell viability of both murine and human fibroblasts. Given its efficient interaction with liquids and omnidirectional 360‐degree conductivity, this material emerges as an excellent candidate for use as a biocompatible, multifunctional interface layer. The produced nanoparticle‐nanofibrous membrane materials offer a promising platform for interface applications, featuring enhanced spatiotemporal configurations and wide‐ranging applicability.

Exploration of blend polymer membrane with desire performances is a highly essential research topic because it makes them as key component of the battery technologies. However, the blend membrane cannot simultaneously meet out the high electrical insulation and ion conductivity. Here, we report porous PVdF-HFP based polymer membrane blended with P123 polymer which is prepared by phase inversion technique and along with solution casting technique for comparison. Especially, the major improvements can be claimed with porous PVdF-HFP blend with P123 matrix by phase inversion process that could be mainly due to increasing the disorganize crystallinity of the PVdF-HFP, thereby enhancing the ionic conductivity of PVdF-HFP/P123 than the same prepared by traditional solution casting. More importantly, our studies reveals that, besides having an effect of crystallinity and high ionic conduction PVdF-HFP/P123 blend matrix yield homogeneous pores with higher pore density when prepared by phase inversion approach. We attribute this to remarkable enhancement in higher electrolyte uptake and higher cation transport in the blend membrane. This facilitates high ionic conductivity of 7.06 × 10−5 S/cm and electrochemical stability of 2.8 V,while the solution casting approach display low ionic conductivity of 1.63 × 10−6 S/cm and electrochemical stability of 2.2 V, respectively. A symmetric supercapacitor device is fabricated with the membrane prepared by phase inversion process, resulting in a high specific capacitance of 80 F/g at the current density of 0.25 A/g with 90.51% specific capacitance retention at 0.5 A/g. The energy density of 90.9 W/kg can be achieved at the power density of 0.375 W/kg.

The present study investigates the influence of photosensitizer selection and the polymer electrolyte composition on the performance of quasi-solid-state dye-sensitized solar cells (QsDSSCs). Two benchmark ruthenium dyes, N719 and Z907, alongside a novel photoactive phenothiazine dye were used. Each dye was incorporated into a QsDSSC architecture employing poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) as the gel electrolyte matrix, with varying molecular weights, to investigate their impacts on the overall device performance and long-term stability. Our results demonstrated that the N719 dye exhibited the highest power conversion efficiency (PCE), attributed to its strong absorption in the visible spectrum and efficient electron injection into the TiO2 photoanode. Z907, on the other hand, showed moderate PCE due to its broader absorption profile but slower electron injection kinetics. The phenothiazine dye revealed promising PCE, with tunable absorption properties and efficient charge transfer. Furthermore, the impact of PVDF-HFP polymer gel electrolytes with varying molecular weights on cell stability was explored. The QsDSSC incorporating the PVH80 polymer with the phenothiazine dye exhibited reduced dye desorption, due to the effective dye molecules’ immobilization by the gel matrix, and consequently enhanced long-term stability over 600 h. This comparative study sheds light on the interplay between dye selection, the polymer gel’s properties, and QsDSSCs’ performance. These insights are crucial in designing robust and efficient QsDSSCs for practical applications.

As a representative flexible piezoelectric polymer, polyvinylidene fluoride (PVDF) and its copolymers have been widely used in energy harvesters and piezoelectric sensors. In this work, hybrid nanocomposite films were prepared by adding a small amount of carbon black (CB) and Ni nanoparticles to the poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) matrix using the solution casting method, followed by stretching and poling to increase the electroactive β-phase content. The results show that the hybrid fillers consisting of 0.3 wt% CB and 0.1 wt% Ni nanoparticles exhibit the best piezoelectric performance. The maximum output voltage of the PVDF-HFP/CB/Ni films reaches 3.5 V under 1 mm micro-vibration, which is 75% higher than that of pure PVDF-HFP films. Characterization results by X-ray diffraction analysis, Fourier-transform infrared spectrometry, and differential scanning calorimeter analysis show that the hybrid fillers are more effective in promoting the phase transformation from the α-phase to the β-phase in the matrix due to synergistic effect.

In this study, flexible nanocomposites made from PVDF-HFP reinforced with carbon nanotubes (CNTs) and graphene nanoplatelets (GNPs) are manufactured using a sonication and solvent casting method for monitoring purposes. More specifically, the effect of the volume batch under the sonication process is explored. For CNT-based composites, the electrical conductivity decreases as the batch volume increases due to less effective dispersion of the CNTs during the 30-min sonication. The maximum electrical conductivity achieved in this type of sensor is 1.44 ± 0.17 S/m. For the GNP-based nanocomposites, the lower the batch volume is, the more breakage of nanoplatelets is induced by sonication, and the electrical response decreases. This is also validated by AC analysis, where the characteristic frequencies are extracted. Here, the maximum electrical conductivity measured is 8.66 ± 1.76 S/m. The electromechanical results also show dependency on the batch volume. In the CNT-based nanocomposites, the higher gauge factor achieved corresponds to the batch size, where the sonication may be more effective because it leads to a dispersed pathway formed by aggregates connected by tunneling mechanisms. In contrast, in the CNT-based nanocomposites, the GF depends on the lateral size of the GNPs. The biggest GF of all sensors is achieved with the PVDF-HFP/GNP sensors, having a value of 69.36 × 104 at 35% of strain, while the highest GF achieved with a PVDF-HFP/CNT sensor is 79.70 × 103 at 70%. In addition, cycling tests show robust electromechanical response with cycling for two different strain percentages for each type of nanocomposite. The sensor with the highest sensitivity is selected for monitoring two joint movements as proof of the applicability of the sensors manufactured.

This study is concerned with the nonlinear creep characteristics of extruded Poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) dominated by β-phase polymorphs over the temperature range 40 °C − 80 °C and tensile stress levels between 5 MPa and 12.5 MPa. The measured data using the developed experimental setup as well as the dynamic mechanical analyzer invariably suggested a nonlinearity taking place at temperatures near to 60 °C, where αc-relaxation began corresponding to 100 °C above the measured glass transition temperature of PVDF-HFP. The results from accelerated testing conditions indicated the transition to tertiary creep stage at 24% to 28% strain, irrespective of test condition, referred to as critical strain range. Following the identification of Findley power law model constant at different test conditions, a generalized temperature- and stress-dependent model was developed with only 7 constants. The comparisons between the measured and modeled data conveyed the model effectiveness in describing the nonlinear creep characteristics of the polymer over the measured temperature and stress levels. Time-temperature-compliance master curves were consequently constructed using the developed generalized model, which in combination with the critical strain failure criterion, provided the essential design data including the maximum allowable ranges of stress and temperature for achievement of 20 years creep life.

This study presents the potential of sulfonated poly (ether-ether-ketone)/ poly (vinylidene fluorideco-hexafluoro propylene)/SiO2 (SPEEK/PVdF-HFP/SiO2) composite proton exchange membrane for the use of microbial fuel cell. Silica particles (SiO2) were admixed with SPEEK/PVdF-HFP with various ratios. Scanning electron microscope (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Thermal Gravimetric Analysis (TGA) and Differential Scanning Calorimetric (DSC) were examined for characterizing the PEM membrane. Proton conductivity, oxygen diffusivity, ion exchange capacity (IEC), water uptake and performance for polymer composites using MFCs were analysed. The highest proton conductivity value of 8 × 10−2 S cm−1 was obtained for the SiO2–7.5 wt.% incorporated polymer membrane of SPEEK (80 wt.%) / PVdF-HFP (20 wt.%). The maximum voltage generation and power density of 998.5 ± 2 mV and 1.5 mW/m2 were noticed, respectively. This study suggests that the incorporation of SiO2 in polymer composite membrane has potential for an alternative PEM.

This research aims to fabricate hydrophobic electrospun air filters with ultra-high performance against virions. In order to achieve this goal, constant basis weight electrospun poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) with low-bead, high-bead, and ultra-high-bead fibre structures were used to fabricate single and multilayer filters by controlling the Dimethylformamide (DMF)-to-acetone ratio of the solvent. The water contact angle of the fabricated layers ranged from 131° for low-bead structures to 135° for ultra-high-bead structures, indicating their overall high hydrophobicity. The size-resolved filtering efficiency and pressure drop tests on the fabricated filters showed that low-bead structure for both single and multilayer filters and high-bead structure for single-layer filters enhance the quality factor remarkably. The results showed that the single-layer ultra-high-bead structure air filters had a filtering efficiency of 99.33%, superior to N95 air filters (96.54%) and comparable to double N95 filters (99.86%). However, the electrospun air filter showed a pressure drop of 169.3 Pa and a quality factor of 27.6×10−3 Pa−1compared to a pressure drop of 388 Pa and quality factor of 16.9×10−3 Pa−1 for double N95 air filters. Therefore, it has a high potential to be used as the filtration media in hospitals, long-term care centers, and masks to provide superior protection against virions for healthcare providers and patients.

Nowadays, bacterial infection is regarded as a serious threat to humankind, which needs to be taken care of. The emergence of antibiotic resistance and multidrug resistance (MDR) is rendering this situation more troublesome. However, several alternative treatment regimens have aided such diseases quite well in the recent past, among which dynamic antibacterial therapies combat this situation quite well. Among various dynamic therapies, piezodynamic therapy is a very recent avenue, in which mechanical stimuli have been exploited to treat bacterial infections. Herein, piezo-active bismuth ferrite-loaded poly(vinylidene fluoride-co-hexafluoropropylene) polymer has been utilized to eradicate gram-positive bacteria (E. faecalis) and gram-negative bacteria (E. coli). The sample has been designed in a free-standing membrane form, which, under soft ultrasound (~10 kHz), generates reactive radicals to ablate bacteria. Initially, the structure and morphology of the membrane have been substantiated by using X-ray diffraction and scanning electron microscopy methods; besides, Fourier transform infrared spectrum of the sample depicts a tremendously high value of polarizability and further confirms the piezo-activity of the membrane. More than 99% of E. coli and E. faecalis have been successfully eradicated within 30 min of ultrasound. Moreover, the solid-state structure and hydrophobic nature of the membrane help us to reuse it in a cyclic manner, which is possibly reported herein for the very first time. This novel membrane could be deployed in healthcare systems and pigment industries and could be exploited as a self-cleaning material.

Poly(vinylidene fluoride) (PVDF) and its copolymers exhibit excellent piezoelectric properties and are potential materials for high efficiency energy harvesting devices. In this study, poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) films are prepared by the solution casting method. The prepared film is then subjected to mechanical stretching and poling process. By adjusting the temperature of the poling process and the elongation ratio of the mechanical stretching process, the relative content of β-phase F(β) increases significantly, leading to high piezoelectric performance. The maximum output voltage of the PVDF-HFP films poled at 40°C reaches 3.67 V, 71% higher than that of the films poled at room temperature. Fourier transform infrared spectroscopy analysis (FTIR), XRD (X-ray diffraction), and differential scanning calorimetry are used to investigate the influences of mechanical stretching and poling process on the crystal structure to discover the enhancement mechanism. This work provides a straightforward and low-cost route to prepare high piezoelectric PVDF-HFP-based materials.

Abstract Lithium metal batteries (LMBs) show several limitations, such as high flammability and Li dendrite growth. All‐solid‐state LMBs (ASSLMBs) are promising alternatives to conventional liquid electrolyte (LE)‐based LMBs. However, it is challenging to prepare a solid electrolyte with both high ionic conductivity and low electrode–electrolyte interfacial resistance. In this study, to overcome these problems, a solid composite electrolyte (SCE) consisting of Li6.25La3Zr2Al0.25O12 and polyvinylidene fluoride‐co‐hexafluoropropylene is used, which has attracted considerable attention in recent years as a solid‐state electrolyte. To operate LMBs without an LE, optimization of the electrode–solid‐electrolyte interface is crucial. To achieve this, physical and chemical treatments are performed, i.e., direct growth of each layer by drop casting and thermal evaporation, and plasma treatment before the Li evaporation process, respectively. The optimized ASSLMB (amorphous V2O5−x (1 µm)/SCE (30 µm)/Li film (10 µm)) has a high discharge capacity of 136.13 mAh g−1 (at 50 °C and 5 C), which is 90% of that of an LMB with an LE. It also shows good cycling performance (>99%) over 1000 cycles. Thus, the proposed design minimizes the electrode–solid‐electrolyte interfacial resistance, and is expected to be suitable for integration with existing commercial processes.

Ionogels are emerging hybrid materials and are widely studied due to the combination of thermophysical properties from ionic liquid and mechanical integrity from the polymer matrix. Ionic liquid has received wide attention due to its promising properties, high ionic conductivity, and thermal stability. The liquid nature of ionic liquid has restricted its application. Thus, the confinement of ionic liquid within a polymer matrix has allowed ionogel to be applied in strain sensors and lithium-ion batteries. Nevertheless, the compatibility between the polymer matrix and ionic liquid is crucial for ionogel. Incompatibility between polymer host and ionic liquid results in low ionic conductivity, poor mechanical strength, and undesired for practical application. The interaction between polymer matrix and ionic liquid is studied in this study through optical microscopy. The addition of ionic liquid resulted in the disappearance of the polymer matrix’s highly porous nature, as evidenced by the optical microscopy images. This disappearance of the porous nature suggests the compatibility of the polymer matrix with ionogel. Furthermore, the electrochemical stability of the ionogel is also examined through linear sweep voltammetry technique and achieved 2.3V.

Lithium-ion batteries are popular energy storage devices due to their high energy density. Solid electrolytes appear to be a potential replacement for flammable liquid electrolytes in lithium batteries. This inorganic/hybrid solid electrolyte is a composite of lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) salt, (poly(vinylidene fluoride-hexafluoro propylene) (PVDF-HFP) polymer and sodium superionic conductor (NASICON)-type Li1+xAlxTi2−x(PO4)3 (LATP) ceramic powder. The structure, morphology, mechanical behavior, and electrochemical performance of this composite solid electrolyte, based on various amounts of LiTFSI, were investigated. The lithium-ion transfer and conductivity increased as the LiTFSI lithium salt concentration increased. However, the mechanical strength apparently decreased once the percentage of LITFSI was over 60%. The hybrid electrolyte with 60% LiTFSI content showed high ionic conductivity of 2.14 × 10−4 S cm−1, a wide electrochemical stability window (3–6 V) and good electrochemical stability. The capacity of the Li|60% LiTFSI/PVDF-HFP/LATP| LiFePO4 solid-state lithium-metal battery was 103.8 mA h g−1 at 0.1 C, with a high-capacity retention of 98% after 50 cycles.

A quasi-solid-state polymer electrolyte is prepared by incorporating poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP) in a propylene carbonate (PC) / 1,2-dimethoxyethane (DME) / 1-methyl-3-propylimidazolium iodide (MPII) liquid electrolyte. The amount of PVdF-HFP in the liquid electrolyte is varied from 0.1 to 0.4 g. Incorporation of 0.1 g of PVdF-HFP decreases the conductivity of the DME/PC/MPII liquid electrolyte from 1.3×10-2 to 5.6×10-3 S cm-1. Conductivity decreases gradually with increasing PVdF-HFP. No-flow “jelly-like” electrolyte samples are obtained for PVdF-HFP ? 0.2 g. The decrease in conductivity is the result of the decrease in ion mobility. Ion mobility was calculated by impedance spectroscopy. The PVdF-HFP quasi-solid-state electrolytes were assembled into dye sensitized solar cells (DSSCs). The performance of the DSSCs was measured under illumination of a 100 mW cm-2 Xenon light source. The DSSC without PVdF-HFP polymer shows an efficiency of 4.88% with short-circuit current density, Jsc of 11.24 mA cm-2, fill factor, FF of 70% and open circuit voltage, Voc of 619 mV. The presence of PVdF-HFP deteriorates the performance of DSSCs, but problems such as electrolyte leakage and volatilization are eliminated. The performance of DSSCs was found to be correlated to the conductivity behaviour of the electrolyte.

Na0.25K0.25Bi0.5TiO3 (NKBT) perovskite particles are synthesized by solid-state method and used as a filler for polyvinylidene fluoride-co-hexafluoropropylene (PVDF-HFP) co-polymer. X-ray diffraction analysis of NKBT powders shows that the particles have a rhombohedral perovskite crystal structure (R3c symmetry). Raman spectroscopy reveals that the co-polymer crystallizes predominantly into the mixture of polar β- and γ-crystals, while there is also a contribution of the non-polar α-crystal phase. The introduction of the NKBT into the PVDF-HFP results with an increase in effective dielectric permittivity and this effect depends on the inorganic content in the composite. The most interesting result of the present study is that the introduction of NKBT particles induces the appearance of an additional transition peak in the dielectric spectra of the co-polymer matrix. At the fixed frequency of ~2 kHz, the observed process appears at ~10 °C (about 45° above the glass transition temperature) and its magnitude strongly depends on the amount of the NKBT in the composite. Dielectric spectroscopy measurements of the composites are carried out in the wide range of frequencies (from 0.1 Hz to 1 MHz) and temperatures (from −100 to 100 °C). They reveal that the novel process can be clearly distinguished in the frequency range between 160 Hz and ~50 kHz.

Textile-based pressure sensors have garnered considerable interest in electronic textiles due to their diverse applications, including human–machine interface and healthcare monitoring systems. We studied a textile-based capacitive pressure sensor array using a poly(vinylidene fluoride)-co-hexafluoropropylene (PVDF-HFP)/ionic liquid (IL) composite film. By constructing a capacitor structure with Ag-plated conductive fiber electrodes that are embedded in fabrics, a capacitive pressure sensor showing high sensitivity, good operation stability, and a wide sensing range could be created. By optimizing the PVDF-HFP:IL ratio (6.5:3.5), the fabricated textile pressure sensors showed sensitivity of 9.51 kPa−1 and 0.69 kPa−1 in the pressure ranges of 0–20 kPa and 20–100 kPa, respectively. The pressure-dependent capacitance variation in our device was explained based on the change in the contact-area formed between the multi-filament fiber electrodes and the PVDF-HFP/IL film. To demonstrate the applicability and scalability of the sensor device, a 3 × 3 pressure sensor array was fabricated. Due to its matrix-type array structure and capacitive sensing mechanism, multi-point detection was possible, and the different positions and the weights of the objects could be identified.

Composite membranes consisting of N-ethyl-N-methylpyrrolidinium fluoro-hydrogenate (EMPyr(FH)1.7F) ionic liquid and poly(vinylidene fluoride hexafluoro-propylene) (PVdF-HFP) copolymer were successfully prepared in weight ratios of 5:5, 6:4, and 7:3 using a casting method. The prepared membranes possessed rough surfaces, which potentially enlarged the three-phase boundary area. The EMPyr(FH)1.7F/PVdF-HFP (7:3 weight ratio) composite membrane had an ionic conductivity of 41 mS·cm-1 at 120 °C. For a single cell using this membrane, a maximum power density of 103 mW·cm-2 was observed at 50 °C under non-humidified conditions; this is the highest power output that has ever been reported for fluorohydrogenate fuel cells. However, the cell performance decreased at 80 °C, which was explained by penetration of the softened composite membrane into gas diffusion electrodes to partially plug gas channels in the gas diffusion layers; this was verified by in situ a.c. impedance analysis and cross-sectional SEM images of the membrane electrode assembly.

Solid electrolytes for Li transport have been prepared by melt-compounding in one single step. Electrolytes are composed of polyvinylidene fluoride–hexafluoropropylene (PVDF–HFP) with PYR13TFSI on its own or with varying concentration of LiTFSI. While the extrusion of PVDF–HFP with PYR13TFSI is possible up to relatively high liquid fractions, the compatibility of PVDF–HFP with LiTFSI/PYR13TFSI solutions is much lower. An organo-modified sepiolite with D-α-tocopherol polyethylene glycol 1000 succinate (TPGS-S) can be used to enhance the compatibility of these blends and allows to prepare homogeneous PYR13TFSI/LiTFSI/PVDF–HFP electrolytes with controlled microphase separations by melt-compounding. The structure and morphology of the electrolytes has been studied by FTIR, differential scanning calorimetry (DSC), SEM, and AFM. Their mechanical properties have been studied by classical strain–stress experiments. Finally, ionic conductivity has been studied in the −50 to 90 °C temperature range and in diffusivity at 25 °C by PFG-NMR. These electrolytes prove to have a microphase-separated morphology and ionic conductivity which depends mainly on their composition, and a mechanical behavior typical of common thermoplastic polymers, which makes them very easy to handle. Then, in this solvent-free and scalable fashion, it is possible to prepare electrolytes like those prepared by solvent casting, but in few minutes instead of several hours or days, without solvent evaporation steps, and with ionic conductivities, which are very similar for the same compositions, above 0.1 mS·cm−1 at 25 °C. In addition, some of the electrolytes have been prepared with high concentration of Li ion, what has allowed the anion exchange Li transport mechanism to contribute significantly to the overall Li diffusivity, making DLi become similar and even clearly greater than DTFSI.

Composite membranes were successfully prepared using a phase-inversion method. The X-ray powder diffraction (XRD) and energy dispersive X-ray (EDX) profiles has confirmed formation of 4.8 wt % Ag/poly(vinylidene fluoride-co-hexafluoropropene) (PVDF-HFP), 3 wt % Ag-MWCNTs/PVDF-HFP (EDX surface composition of Ag nanoparticles) and 1.5 wt % MWCNTs/PVDF-HFP composite membranes. The MWCNTs crystallites are mainly encapsulated by a layer of PVDF-HFP, as evidenced by disappearance of graphitic peak. The scanning electron microscopy (SEM) images have depicted the formation of microporous structure, with few MWCNTs on the surface and strongly interacting with PVDF-HFP as demonstrated by thermogravimetric analysis (TGA), XRD and Fourier transform infrared (FTIR) data. The data indicated an increase in porosity, swellability and water content of the PVDF-HFP membrane with the addition of MWCNTs and/or Ag nanoparticles, showing an improved hydrophilicity. The 1.5 wt % MWCNTs/PVDF-HFP composite membrane showed good desalination and fouling resistance rates, which correlates with a low water contact angle. The combined effects of Ag nanoparticles and MWCNTs do not promote fouling resistance of PVDF-HFP membranes, as shown during NaCl microfiltration (this is linked with high water contact angle as compared to that of MWCNTs/PVDF-HFP composite). Both 1.5 wt % MWCNTs/PVDF-HFP and 3 wt % Ag-MWCNTs/PVDF-HFP composite membranes prevented the bacteria passing through the membrane (100% bacterial load reduction). The surface of 3 wt % Ag-MWCNTs/PVDF-HFP showed good bactericidal and non-leaching properties of the dopant materials (MWCNTs and Ag), as evidenced by bacterial growth on the edges of the membranes.

Electrospun membranes are gaining interest for use in membrane distillation (MD) due to their high porosity and interconnected pore structure; however, they are still susceptible to wetting during MD operation because of their relatively low liquid entry pressure (LEP). In this study, post-treatment had been applied to improve the LEP, as well as its permeation and salt rejection efficiency. The post-treatment included two continuous procedures: heat-pressing and annealing. In this study, annealing was applied on the membranes that had been heat-pressed. It was found that annealing improved the MD performance as the average flux reached 35 L/m2·h or LMH (>10% improvement of the ones without annealing) while still maintaining 99.99% salt rejection. Further tests on LEP, contact angle, and pore size distribution explain the improvement due to annealing well. Fourier transform infrared spectroscopy and X-ray diffraction analyses of the membranes showed that there was an increase in the crystallinity of the polyvinylidene fluoride-co-hexafluoropropylene (PVDF-HFP) membrane; also, peaks indicating the α phase of polyvinylidene fluoride (PVDF) became noticeable after annealing, indicating some β and amorphous states of polymer were converted into the α phase. The changes were favorable for membrane distillation as the non-polar α phase of PVDF reduces the dipolar attraction force between the membrane and water molecules, and the increase in crystallinity would result in higher thermal stability. The present results indicate the positive effect of the heat-press followed by an annealing post-treatment on the membrane characteristics and MD performance.