PVDF Research Articles

Enhancing the combustion of silicon nanoparticles via plasma-assisted fluorocarbon surface modification

Nanostructured silicon has great potential as an energetic material due to its high energy density, close to that of aluminum; however, its combustion kinetics are strongly affected by the presence of a native oxide layer. As the particle size is reduced, the material behavior is dominated by surface effects, highlighting the need for new approaches to fabricate silicon nanoparticles and precisely control their surface chemistry. Here, we describe the use of low-temperature plasma to nucleate and grow < 10 nm silicon particles. The resulting aerosol is passed through a second plasma reactor, to which a fluorocarbon monomer is supplied. The second plasma initiates the growth of a polymeric shell onto the silicon particles, resulting in a highly conformal coating. Chemical analysis confirms that the polymer shell is compositionally similar to polyvinylidene fluoride (PVDF). We find that the fluorocarbon shell acts as an artificial passivation layer that significantly delays the onset of oxidation in air. In addition, the direct contact between the fluorocarbon shell and silicon core lowers the ignition temperature compared to the physical mixtures of silicon nanoparticles and PVDF. It leads to a higher pressurization rate and a lower combustion time when tested in a combustion cell. This is consistent with the combustion process being initiated by the exothermic interfacial reactions between the silicon core and the fluorocarbon shell. Mass spectroscopy confirms this hypothesis because silicon fluoride is produced only for the core–shell structure, and not for a physical mixture of silicon and PVDF. This study provides an example of a new processing technique capable of controlling the interfacial chemistry of small nanoparticles with beneficial effects on their combustion.

Flexible and ferroelectric electrospun PVDF- non-stoichiometric PZT nanogenerators (PENGs) membranes for low-frequency acoustic energy harvesting

Acoustic energy harvesting (AEH) at low-frequency has been exposed to serious problems such as low energy of input sound and lack of efficient materials to absorb the sound and convert it to electrical power. This study focused on the enhancement of the AEH performance of polyvinylidene fluoride (PVDF) membrane via the incorporation of non-stoichiometric PZT (nsPZT) nanoneedles as piezoelectric nanogenerators (PENG). The nanofibrous membranes with different amounts of PENG (x = 0, 2.5, 5, and 10 wt %) were synthesized by the electrospinning method. The nsPZT was provided via Nd3+ and Nb5+ co-doping as a novel approach. The microstructures revealed that the PENG was embedded well inside the fibers (x = 2.5), while the agglomerates were formed at higher amounts (x = 10). Also, the fiber diameters and porosity of membranes were changed. It was found that the maximum crystallization of the β-phase of PVDF has occurred at x = 2.5 (71 %). The dielectric of the PVDF membrane decreased with increasing the x factor due to the formation of further pores. In contrast, the ferromagnetic properties, piezoelectric sensitivity, and electrical conductivity were improved by adding the PENG. The maximum coercivity of 750 Oe, piezoelectric sensitivity of 1.959 V N−1, and minimum sheet resistance of 1.2 kΩ.sq−1 were achieved by x = 2.5. The noise reduction coefficient (NRC) of the PVDF membrane was enhanced drastically (53–163 %) by adding the PENG. The AEH performance was also enhanced by adding the PENG. The highest power density was achieved 0.0822 W g−1 (56.23 W m−2) by the PVDF-PENG membrane (x = 2.5) under 90 dB sound pressure at 2000 Hz frequency. These findings suggest the high potential of nanofibrous PVDF-PENG membrane for use in low-frequency AEH systems.

Effect of drying temperature on binder/current collector interfacial adhesion in electrode manufacturing of Li-ion batteries

Li-ion battery manufacturing process parameters are critical to the electrode properties and the final cell electrochemical performance. During the electrode drying process, the drying temperature plays a critical role on the binder migration, which affects the interfacial adhesion between the electrode and the current collector. However, the influence of the temperature on the properties of the binder material and the binder/current collector interface is yet unknown. In this work, we studied the effect of drying temperature on the interfacial adhesion between the binder and the current collector by direct coating of polyvinylidene fluoride (PVDF) solution on Al foil and then drying at various temperatures. The interfacial adhesion strength between the PVDF and the Al foil was significantly increased, from 9.72 N/m (dried at room temperature) to > 665.80 N/m (dried at 200 ℃) with increased temperature. DSC and XRD analyses showed the changes in the crystalline forms of PVDF under different drying temperature. This work revealed that the drying temperature during electrode manufacturing should be considered from the aspects of both binder migration in mid-stage and PVDF crystalline properties in late-stage solvent drying.

Waste cigarette filters-based polymer blends membrane for filtration of high loaded natural organic matter river water

Waste cigarette filter (WCF) is one of the most common wastes found in the environment. Cigarette filters contain up to 96% cellulose acetate (CA), which can be used as a material for membrane fabrication. However, the CA-based membrane from WCF posed a weak mechanical property (brittle). Therefore, the objective of this work is to improve mechanical property of CA-based membrane from WCF by preparing blend membranes with polyvinylidene fluoride (PVDF) polymer and evaluate their performance for filtration of real river water containing high natural organic matter (NOM) concentrations. The variations of WCF and PVDF used were 100:0, 75:25, 50:50, 25:75, and 0:100. The membranes were then characterized to determine the morphology, pore size and pore size distribution, hydrophilicity, mechanical properties, and filtration performance of the membrane using clean water and river water. The SEM test results showed the presence of spherulites on the surface of the blend membrane, indicating that crystallization occurred during membrane formation. The spherulites resulted in smaller pore size, narrower pore size distribution, higher hydrophilicity, and mechanical properties. Meanwhile, the filtration test results showed that blend membranes produced higher permeability compared to pristine WCF, PVDF, and commercial-based CA membranes, where the result of river water permeability was in the range of 875–1062.5 L/m2.h.bar. The membrane fouling formation was aligned well with the result of permeability and is dominated by irreversible fouling formation from the dynamic cake layer built on the membrane surface, with NOM rejections of 26.6–33.8%, suggesting the need for further developments.

Dielectric and photocatalytic characteristics of novel CaCu3Ti4O12 modified Ba0.5Sr0.5TiO3-based heterojunction synthesized by wet-chemistry method

The study presents a comprehensive investigation into the synthesis, characterization, and application of barium strontium titanate-calcium copper titanate (BST-CCTO) heterojunction, offering insights into their potential for high-energy-density capacitors and photocatalytic applications. It discusses the synthesis methods for BST, CCTO nanoparticles and their heterojunction. It delves into the structural analysis of prepared heterojunctions using techniques like X-ray diffraction (XRD), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The photocatalytic performance of heterojunctions, particularly in the degradation of organic dyes and pharmaceutical waste under visible light, is explored. Results demonstrate the superior photocatalytic efficiency of BST-CCTO heterojunction, i.e., B2 (99.5 % for RhB) compared to individual BST (78.4 %), suggesting potential applications in environmental remediation. This study also explores the development and properties of dielectric materials, particularly focusing on polyvinylidene fluoride (PVDF) and its composites with high-dielectric ceramics such as BST and CCTO. Various aspects of dielectric behavior, including polarization mechanisms and frequency dependence, are also discussed. Dielectric studies reveal the enhanced dielectric constant (50.93 at 1 kHz for 3 wt% loading of B3) of PBCT-3 composite as compared to pure PVDF composite (10 at 1 kHz), attributed to factors such as interface engineering, complementary electrical properties, and grain boundary effects. The mechanisms underlying the interaction between fillers and PVDF matrix are elucidated, highlighting the role of interface engineering and polarization enhancement in optimizing dielectric performance.

Tailoring the PVDF membrane surface with polyoxypropylene-polyoxyethylene brush via in-situ grafting for enhanced oil/water emulsion separation

Membrane technology has been widely applied in oil-water separation owing to low energy consumption and high separation efficiency, but membrane fouling is a fatal factor affecting membrane performance and service life. Inspired by polyether nonionic detergents, a liquid surfactant polymer with polyoxypropylene-polyoxyethylene (PPO-PEO) segments was tailored to the surface of polyvinylidene fluoride (PVDF) membrane via in-situ grafting to improve its antifouling and oil-water separation properties. Firstly, in order to activate the inert surface of the PVDF membrane, poly(styrene-co-maleic anhydride) (SMA) was blended with PVDF to prepare the MA@PVDF as membrane substrate. Then, PPO-PEO brushes were grafted onto the surface of the substrate by an alcoholysis reaction to fabricate the PPO-PEO@PVDF membrane. The chemical structure and the surface morphology of the PPO-PEO tailored PVDF membrane surface were characterized, and the separation performance for oil/water emulsion was explored. The results show that the optimized grafting amount of PPO-PEO on the PVDF membrane is up to 476.2±3.0mg·g-1, and the pure water flux of the corresponding PPO-PEO@PVDF membrane is 191.3±4.0L·m-2·h-1, which is more than 20 times higher than that of the control PVDF membrane (around 7L·m-2·h-1). The water wetted PPO-PEO brushes on the surface of the PVDF membrane can hinder the adhesion of oily substances, and the separation efficiency of the PPO-PEO@PVDF membrane for kerosene/water emulsion reaches 91.7±0.6%, which is much higher than that of the MA@PVDF membrane without PPO-PEO brushes. The PPO-PEO tailored PVDF membrane provides useful strategies for the surface modification of membranes with enhanced performances of antifouling and oil-water separation.

Architecting side chain grafted poly (vinylidene fluoride) based graphene oxide composite polyelectrolyte membranes for hydrogen and direct methanol fuel cells

Chemically modified poly (vinylidene fluoride) (PVDF) as polyelectrolyte has generated immense interest due to its high efficiency in electrochemical energy devices. Herein, the design of a polymer electrolyte membrane (PEM) is formulated by the synergistic fusion of graphene oxide (GO) into chemically grafted PVDF with 2-acrylamido-2-methylpropane sulfonic acid (AMPS) by solution phase intercalation producing GO@PVDF-g-PAMPS composite membranes. Ozone-induced graft copolymerization technique is employed to prepare PVDF-g-PAMPS with 18.3% (w/w) degree of grafting. Incorporation of GO into the polymeric membrane generates appropriate hydrophilic-hydrophobic phase separation and constructs well-organized sub-nano slit-like pathways that elevate the proton conduction. PAG-0 membrane without any filler shows a proton conductivity (κ) of 15.1 mS/cm at 80°C whereas PAG-2 membrane (with 2% w/w GO loading) shows a κ of 25.9 mS/cm under similar conditions. The presence of a perfluorinated backbone furnishes excellent oxidative stability to the PEMs by retaining 95% of total mass and 97.3% of κ after dipping in harsh Fenton's reagent at 60°C for 6 h. Representative PAG-2 shows a peak power density of 152.9 mW/cm2 with a maximum current density of 480.6 mA/cm2 (fuel cell operating conditions: 75°C at 100% RH) in hydrogen fuel cell and a peak power density of 37.7 mW/cm2 in methanol fuel cell. Moreover, PAG-2 retains 91% of its initial OCV after 50 h of the durability test.

Simple fabrication of breathable poly (vinylidene fluoride) fibrous membranes decorated by silica nanoparticles with enhanced waterproof property

In recent years, scientists have undertaken various preparation approaches to improve the waterproof and moisture permeability of fiber membranes, among which electrospinning has emerged as the simplest and most effective one. In this paper, poly (vinylidene fluoride) /silica (PVDF/SiO2) fibrous membranes were prepared by one-step electrospinning combined with heat treatment. The morphology, surface wettability, water resistance and moisture permeability of the fibrous membranes were also characterized. When the concentration of PVDF was 12 wt.%, the nanofiber membranes exhibited the most uniform and optimal morphology. In addition, the fiber membranes not only exhibited a high water contact angle (WCA) (135.56 °) and a small maximum pore size (dmax) (1.77 μm), but also demonstrated a large hydrostatic pressure (116.86 kPa) and a moderate water vapor transmission rate (WVTR) (3.53 kg m-2 d-1). The PVDF/SiO2 fibrous membranes with good waterproof and moisture permeability obtained in this work are expected to improve the comfort of protective textiles and expand the application range.

High-performance and ultra-robust triboelectric nanogenerator based on hBN nanosheets/PVDF composite membranes for wind energy harvesting

Triboelectric nanogenerator (TENG) is a novel energy technology that converts high-entropy mechanical energy from the environment into electrical energy using triboelectrification and electrostatic induction effects. However, the low surface charge density and easy wear of traditional triboelectric materials are bottlenecks for their practical applications. Here, a remarkable triboelectric properties, superior mechanical properties, exceptional wear resistance, and high thermal conductivity hexagonal boron nitride nanosheets (hBNNS)/ polyvinylidene difluoride (PVDF) composite negative triboelectric material is developed. The inclusion of hBNNS as an electron acceptor and nucleating agent not only effectively boosted the surface charge density (711 μC/m2) and mechanical characteristics of the composite membrane, but also the friction coefficient (COF) and thermal conductivity of the 2 wt% hBNNS/PVDF composite membrane decreased by 28.6 % and increased by 22.2 % compared to the PVDF matrix, respectively. The optimized TENG delivers a peak voltage of 434 V, a current of 53 μA, and a power of 4.84 mW. Furthermore, it exhibits exceptional ultra-robust, enabling continuous operation for 72 h at a wind speed of 17.5 m/s while maintaining performance above 90.6 %. Additionally, the TENG is capable of effectively powering a smart hygrothermograph and realizing wireless real-time monitoring, or directly lit up 102 white LEDs in a serial connection. This work addresses the challenges of low output performance and limited lifespan in TENG from a material perspective, providing a valuable reference method for the design of negative triboelectric materials with high surface charge density, good mechanical properties, low COF, and high thermal conductivity.

MOF-based photothermal Janus membrane with robust anti-fouling performance for enhanced membrane distillation

As a promising desalination technology, photothermal membrane distillation (PMD) is confronted with challenges such as low freshwater yield and membrane fouling. Herein, we have introduced a copper-based metal-organic framework (Cu-CAT) into a hydrophilic/superhydrophobic polyvinylidene fluoride (PVDF) Janus tree-like nanofiber membrane (TLNMs) to construct photothermal Janus TLNMs (P-Janus TLNMs) for enhanced PMD. Given the exceptional photothermal properties of the hydrophilic Cu-CAT layer, coupled with the fine pore structure and elevated porosity characteristics of the superhydrophobic PVDF TLNMs, P-Janus TLNMs have demonstrated outstanding performance when integrated into a PMD system. Upon exposure to solar illumination of 1 kW·m−2, the P-Janus TLNMs achieved a remarkable surface temperature of 88 °C, yielding a permeation flux of 1.46 L m−2 h−1, a salt rejection rate exceeding 99.99 %, and an energy utilization rate of 81 %. Furthermore, after 20 days of continuous operation with simulated seawater containing oil and surfactant, the P-Janus TLNMs presented a salt rejection of 99.9 % and a stable permeation flux of 1.71 L m−2 h−1 at the feed/permeate temperatures of 24/20 °C. This work introduces a novel membrane with immense potential for boosting permeation flux and enhancing anti-fouling properties in PMD, thereby advancing the frontier of sustainable seawater desalination.

Slurry Casted Ultrathin Li3Zr2Si2PO12 Electrolyte Film for Solid-State Lithium Metal Batteries.

Thin and flexible solid-state electrolyte (SSE) films with high ionic conductivity and low interfacial resistance are urgently required for lithium metal batteries (LMBs). However, it's still challenging to reduce the film thickness to <20µm, especially for those with high ceramic contents. Herein, a facile slurry casting method is developed to prepare the ultra-thin (14µm) Li3Zr2Si2PO12 (LZSP) films with ceramic content up to 91% using a composite polymer binder, polyvinylidene fluoride (PVDF), and polyethylene oxide (PEO). It shows that PEO not only enhanced the film flexibility but also makes it be easily peeled off to form a freestanding membrane, PLN. To promote the interfacial ion transport, PEO/lithium bis(trifluoromethylsulfonyl)imide (LiTFSI) is introduced to the film surface, and the resultant tri-layer film, PPLN, shows a satisfying room temperature ionic conductivity of 0.116mScm-1, high Li+ transference number of 0.79, and good compatibility with metal lithium. As a result, LMBs using LiFePO4 cathode and PPLN electrolyte exhibit excellent safety as well as electrochemical performances in the wide temperature range between room temperature (RT) and 100°C.

Preparation and study of polyvinylidene fluoride film with high UV aging resistance

Abstract Polyvinylidene fluoride materials were widely used in the preparation of solar panel films due to their excellent weather resistance and heat resistance. In this work, Polyvinylidene fluoride films with UV absorbers (PF/UV films) were prepared by customized extrusion equipment. The properties of these films were demonstrated with a scanning electron microscope (SEM), water contact angle (WCA), thermogravimetric analyzer (TGA), differential scanning calorimetry (DSC), and tensile strength tester. Furthermore, the SEM observation suggested that PF/UV films had smooth surfaces without significant defects. The WCA results illustrated that PF/UV films had better hydrophobicity than polyvinylidene fluoride films. The TGA and DSC curves indicated that the initial decomposition temperature and the melting temperature of the PF/UV film were 365.1°C and 169.2°C, respectively. Furthermore, the results of UV transmittance indicated that the UV aging resistances of PF/UV film were higher than that of polyvinylidene fluoride film.

Biostability assessment of ultrapure water piping materials in the semiconductor industry and their susceptibility to Ralstonia growth

The pipes used for ultrapure water (UPW) distribution are constructed using high-quality materials to ensure purity. However, there remains a risk of contamination based on the pipe type. This study is the first to comprehensively evaluate the biological implications of various UPW pipe materials used in the semiconductor industry. The results showed that Polyvinylidene fluoride (PVDF) exhibited lower organic carbon leaching (0.08 mg/L) and a reduced biomass formation potential (BFP) (approximately 5 × 105 cells/cm2) compared to chlorinated polyvinyl chloride (CPVC) pipes. In particular, Ralstonia, an oligotrophic bacterium commonly found in UPW systems, formed a significant biofilm on pipe surfaces, notably in stainless steel (SUS) and CPVC pipes. Furthermore, particle contamination, a critical concern in semiconductor manufacturing, was investigated, focusing on potential contamination sources generated by pipe leaching and the presence of bacteria. The bacterial composition of the selected UPW was investigated, revealing Herbaspirillum, a nitrogen-fixing bacterium, as the dominant species, account for 66.15 %. Notably, the composition of the feedwater was different from that of the UPW. This study also highlights the limitations of culture-based methods, particularly in detecting bacteria under oligotrophic conditions, which are often unculturable. Flow cytometry (FCM) shows promise for the quick detection of bacterial contamination by providing total cell counts. Moreover, cytometric fingerprinting analysis revealed phenotypic differences between the communities. Nevertheless, further development of a simplified and widely applicable cell counting protocol is required for its effective integration into UPW production.

Preparation of polyelectrolyte based on bottle brush Polyethylene glycol‐Poly(N‐isopropylacrylamide) copolymers

AbstractThe increased demand for high energy‐density batteries led to using lithium metal (Li) anode. However, safety issues associated with Li anode encouraged the researchers to use less reactive and safer electrolytes with higher electrochemical stability. High ionic conductivity (σ), wider electrochemical stability window, and higher mechanical strength alongside the ability to self‐heal possible structural damages were at the center of focus for developing efficient solid electrolytes. In this regard, we developed a group of solid polymer electrolytes (SPEs) with high σ and electrochemical stability. In this regard, bottle brush polyethylene glycol (bbPEG) was synthesized using a chain transfer reaction. Polynipaam (PNIPAAM) blocks were also incorporated into the structure to prepare a block copolymer based on PNIPAM‐bbPEG‐PNIMAM represented by the ABA structure. The block copolymer was then blended with polyvinylidene fluoride (PVDF) with the block copolymer to PVDF weight ratio of 7:2% and 25% bis(trifluoromethane) sulfonamide (TFSI) salt was added and the final mixture was UV‐cured. The results indicated that the final SPE possessed high ionic conductivity with a relatively high lithium‐ion transference number () of 0.416 and the σ of 1.265 × 10−5 S/cm at 25°C.

Multimaterial Printing of Serpentine Microarchitectures with Synergistic Mechanical/Piezoelectric Stimulation for Enhanced Cardiac-Specific Functional Regeneration.

Recreating the natural heart's mechanical and electrical environment is crucial for engineering functional cardiac tissue and repairing infarcted myocardium in vivo. In this study, multimaterial-printed serpentine microarchitectures are presented with synergistic mechanical/piezoelectric stimulation, incorporating polycaprolactone (PCL) microfibers for mechanical support, polyvinylidene fluoride (PVDF) microfibers for piezoelectric stimulation, and magnetic PCL/Fe3O4 for controlled deformation via an external magnet. Rat cardiomyocytes in piezoelectric constructs, subjected to dynamic mechanical stimulation, exhibit advanced maturation, featuring superior sarcomeric structures, improved calcium transients, and upregulated maturation genes compared to non-piezoelectric constructs. Furthermore, these engineered piezoelectric cardiac constructs demonstrate significant structural and functional repair of infarcted myocardium, as evidenced by enhanced ejection and shortening fraction, reduced fibrosis and inflammation, and increased angiogenesis. The findings underscore the therapeutic potential of piezoelectric cardiac constructs for myocardial infarction therapy.

Enhanced energy storage capability of hydroxylated BiFeO3/PVDF composites designed by compositionally gradient multilayer structures

With the development of the microelectronics industry, there is a huge demand for flexible polymer dielectrics with excellent dielectric energy storage capacity, aimed at increasing dielectric constant and enhancing breakdown strength. In this study, the hydroxylated BiFeO3-loaded polyvinylidene fluoride(PVDF) composite films were prepared by electrostatic spinning techniques and the energy storage properties have been investigated. The results show that the dielectric constant and breakdown strength of the composites are effectively influenced by the hydroxylation modification and spatial structure. More interestingly, the seven-grade hydroxylated composite films exhibit a great enhancement of the excellent energy storage performances (Ue, ∼13.21 J/cm3; η, ∼66.2 %). This study demonstrates the immense potential of these composites as highly efficient dielectric materials suitable for use in energy storage capacitors.

Fouling Resistant Liquid-Infused membranes for oil separations

Bioinspired membranes offer an alternative approach to improving the fouling resistance of commercial membranes for oil separations. Here, two perfluoropolyether oils, a lower viscosity Krytox 103 (K103) and a higher viscosity Krytox 107 (K107), were infused into commercial polyvinylidene fluoride (PVDF) ultrafiltration membranes to mimic the Nepenthes pitcher plant. The transmembrane pressure required to perform long-term oil permeance tests was optimized by testing the liquid-infused membranes at different applied pressures. Crystal violet staining and variable pressure scanning electron microscopy qualitatively suggest that the oil layer remained on the membranes after the oil separation experiments were conducted. Over 5 cycles, K103- and K107- liquid-infused membranes exhibited a consistent permeance of ∼ 30000 L m-2h−1 bar−1 at 1.0 bar and ∼ 14500 L m-2h−1 bar−1 at 0.5 bar, respectively. The steady performance further supports a long-lasting oil layer persists on the membrane surface and inside membrane’s pores. Next, experiments were conducted to determine the stability of the Krytox oil post accelerated cleaning tests using bleach. No structural changes to the Krytox oils were detected by thermogravimetric analysis or nuclear magnetic resonance spectroscopy. Dynamic fouling experiments using Escherichia coli K12 revealed that the liquid-infused membranes had higher flux recovery ratios (∼95 %) than the bare PVDF control membranes (∼55 %). Our results demonstrate that liquid-infused membranes exhibit chlorine stability and superior fouling resistance, presenting a promising bioinspired membrane that can be used in pressure-driven oil separation applications.

Rapid hemostatic covered stent with drug-loaded gelatin-alginate/PVDF Janus composite membrane for coronary artery perforation

The implantation of covered stents has significantly contributed much to the rescue treatment of coronary artery perforation (CAP). The ability to achieve rapid hemostasis in cases of severe coronary artery perforation using covered stents alone has so far been elusive. Here, we investigate a Janus composite covered stent for rapid hemostasis in CAP. The covered stent has the dual functions of sealing perforation and rapid hemostasis, which is suitable for the rescue of CAP. This achievement is realized by assembling the tough polyvinylidene fluoride (PVDF) membrane and the drug-loaded hemostatic coating, thereby amalgamating their distinct functionalities. The PVDF membrane served as a physical shield that prevented blood leakage and blocked procoagulant drugs from forming the thrombus in the vessel. Meanwhile, the drug-loaded hemostatic coating, when in contact with the perforation area, swiftly procoagulant. The in vitro cytocompatibility and coagulation property tests demonstrated excellent biocompatibility and hemostatic performance of the Janus composite covered stent. The approach is applicable across almost all sizes of common bare stents in clinical, which has great potential for the rescue of CAP.

Bio-inspired e-skin with integrated antifouling and comfortable wearing for self-powered motion monitoring and ultra-long-range human-machine interaction

Electronic skin (e-skin) inspired by the sensory function of the skin demonstrates broad application prospects in health, medicine, and human–machine interaction. Herein, we developed a self-powered all-fiber bio-inspired e-skin (AFBI E-skin) that integrated functions of antifouling, antibacterial properties, biocompatibility and breathability. AFBI E-skin was composed of three layers of electrospun nanofibrous films. The superhydrophobic outer layer Poly(vinylidene fluoride)-silica nanofibrous films (PVDF-SiO2 NFs) possessed antifouling properties against common liquids in daily life and resisted bacterial adhesion. The polyaniline nanofibrous films (PANI NFs) were used as the electrode layer, and it had strong “static” antibacterial capability. Meanwhile, the inner layer Polylactic acid nanofibrous films (PLA NFs) served as a biocompatible substrate. Based on the triboelectric nanogenerator principle, AFBI E-skin not only enabled self-powered sensing but also utilized the generated electrical stimulation for “dynamic” antibacterial. The “dynamic-static” synergistic antibacterial strategy greatly enhanced the antibacterial effect. AFBI E-skin could be used for self-powered motion monitoring to obtain a stable signal output even when water was splashed on its surface. Finally, based on AFBI E-skin, we constructed an ultra-long-range human-machine interaction control system, enabling synchronized hand gestures between human hand and robotic hand in any internet-covered area worldwide theoretically. AFBI E-skin exhibited vast application potential in fields like smart wearable electronics and intelligent robotics.

Stimulating the Electrostatic Interactions in Composite Cathodes Using a Slurry-Fabricable Polar Binder for Practical All-Solid-State Batteries

In this work, poly vinylidene fluoride–chlorotrifluoroethylene (PVdF-CTFE) is introduced as a slurry-fabricable polymer binder to fabricate a stable composite cathode using the complex materials of a Li[Ni0.7Co0.1Mn0.2]O2 cathode, Li6PS5Cl electrolyte, and super C carbon, for sulfide-based all-solid-state batteries (ASSBs). The high electronegativity of fluorine in the poly(vinylidene fluoride–chlorotrifluoroethylene (PVdF-CTFE) binder creates a polarized electronic environment in the composite cathode, promoting electrostatic interactions with Li ions. Compared with that of butadiene rubber (BR), the PVdF-CTFE binder has a stronger binding energy to the complex materials in the composite cathode, which enhances the mechanical rigidity of the composite cathode with highly uniform adhesion. In addition, uniform and close contact between the complex materials in the composite cathode reduces the resistance at the interfaces, lowering the energy barrier for Li+ diffusion, and eventually creates a fast Li+ diffusion pathway in the composite cathode. Thus, the pouch-type ASSBs cell, which comprises the composite cathode with the PVdF-CTFE binder, Li6PS5Cl electrolyte sheet, and silver-carbon (Ag/C) Li-free anode delivers a high reversible capacity of 198.5 mAh g–1 at 0.1 C and long-term cycling stability over 300 cycles with a capacity retention of 74.5 % at 0.5 C at 60 °C.