Vinylidene Fluoride-hexafluoropropylene Research Articles

Modified Si3N4 filler enhancing the energy storage performance and thermal stability of a P(VDF‐HFP) based composite

AbstractTo improve the high‐temperature stability of poly(vinylidene fluoride hexafluoropropylene) P(VDF‐HFP)‐based composite film for its potential application in energy storage, the modified silicon nitride (mSi3N4) nanoparticles are fabricated using silane coupling agent (KH‐570) and introduced into P(VDF‐HFP). When the mass fraction of mSi3N4 is 7.5 wt%, the recoverable energy density (Wrec) of the mSi3N4/ P(VDF‐HFP) composite film reaches to 1.79 J/cm3 under a 125 MV/m electric field, which is 82.7% higher than pure P(VDF‐HFP). Interestingly, the dielectric properties of mSi3N4/P(VDF‐HFP) show a considerable thermal stability at a high‐frequency ranging from −20 to 160°C, providing an effective approach for preparing energy storage composites working for high‐temperature environments.

Development of Turbocharging-Ability Hybrid Nanogenerators Comprising Bipolar PVDF-HFP/MXene Electrospun Composites.

Coupling piezo-active and triboelectric materials has recently emerged as an effective technique for developing high-performance hybrid nanogenerators (HNGs). This is the first paper to report the fabrication of piezo-active poly(vinylidene fluoride-hexafluoropropylene)(PVDF-HFP)/MXene-based hybrid composite fibers through conventional electrospinning. Here, the effect of MXene content (1-5%) on the surface potential and electrical performance of the as-synthesized composites is investigated and optimized. PVDF-HFP/3% MXene (PHM3)/Nylon 12+A-rGo (NY2)-HNG, which contains the best-performing composite (PMH3; containing 3% of MXene), exhibits turbocharging properties (charging a 10 µF capacitor with 16V within 100 s) and can continuously operate low-power electronics. Interestingly, PHM3 (with a negative surface potential) is transformed into PPHM3 (with a positive surface potential of +2190V) via corona poling. This study proposes a new class of HNGs containing frictional layers comprising bipolar PVDF-HFP/3% MXene composites (PHM3/PPHM3-HNG) with an excellent output performance of 297V and 5.1µA that exhibit broad application prospects in energy harvesting.

Na3Zr2Si2PO12-Polymer Composite Electrolyte for Solid State Sodium Batteries.

The integration of the flexibility of organic polymer electrolyte and high ionic conductivity of the ceramic electrolyte is attempted in search of efficient and safer battery. Composite solid polymer electrolyte (CSPE) provides high ionic conductivity with a sustainable thin film of electrolyte having the synergistic effect of ionic liquid and active inorganic filler. The CSPE is synthesized by the solution cast technique using Na3Zr2Si2PO12 (NZSP) as ceramic and poly(vinylidene fluoride-hexafluoropropylene) with Salt-Ionic liquid as polymer electrolyte. X-ray diffraction (XRD) of CSPE includes amorphous nature due to the polymer part as well as crystalline peaks of ceramic NZSP, simultaneously. The prepared CSPE sample shows homogeneous and interconnected surface morphology is observed by Scanning electron microscopy (SEM) image. Thermogravimetric analysis (TGA) shows electrolyte is thermally stable up to 200 °C and differential scanning calorimetry (DSC) reveals decrease in degree of crystallinity due to NZSP addition in the CSPE. By complex impedance spectroscopy (CIS), room temperature ionic conductivity of the prepared CSPE is found ~1.03 mS/cm. The dielectric behaviour of the prepared electrolyte is also studied to investigate the ion dynamics within the sample. The cationic transference number is 0.53 and the electrochemical stability window (ESW) of the CSPE is 4.9 V which is suitable for sodium solid-state batteries applications.

In Situ Fabrication of Solvent-Free Solid Polymer Electrolytes for Wide-Temperature All-Solid-State Lithium Metal Batteries.

All-solid-state lithium metal batteries (ASSLMBs) have been regarded as promising candidates to settle the safety issues of liquid electrolytes for rechargeable lithium batteries. However, the currently reported gel polymer electrolytes still have flammable liquid solvents, thus leading to the potential safety hazard. Here, solvent-free deep eutectic solid polymer electrolytes (SPEs) are designed and fabricated via an in situ polymerization, which are composed of a poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) electrospun membrane, succinonitrile (SN), poly(ethylene glycol) diacrylate (PEGDA200, Mn = 200 g mol-1), lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), and lithium difluoro(oxalato)borate (LiDFOB). The deep eutectic solvent (DES) with SN/LiTFSI provides a superior room-temperature ionic conductivity, while the PEGDA200 precursor acts as cross-linking network to form SPEs under thermal initiation for free radical polymerization, and LiDFOB can form a stable solid electrolyte interface (SEI) layer. The PVDF-HFP electrospun membrane with a three-dimensional nanofibrous network structure for SN/PEGDA200/LiTFSI/LiDFOB SPEs exhibits a wide electrochemical stability window, high lithium-ion transference number, and good compatibility with the lithium metal anode. Furthermore, the obtained SPEs assembled with Li//LiMn0.6Fe0.4PO4, Li//LiFePO4, and Li//LiNi0.8Co0.1Mn0.1O2 asymmetric cells show excellent cycling performance and rate capability at a wide temperature. This strategy provides a promising path in designing high-energy-density ASSLMBs for practical application.

Optimizing the polar phase transformation in PVDF-HFP/BaTiO3-activated carbon composite films with the mixture design of experiments

ABSTRACT A salient bottleneck to driving the wider use of polyvinylidene fluoride (PVDF) and its copolymers in smart applications is the requirement for a high-voltage poling process required to activate their β -phase crystal structure before the realisation of the piezoelectricity response. In pursuit of enhancing the β-phase content of PVDF-based films, various approaches have been employed in recent years. Yet, a perfect solution to the challenge remains elusive. Here, we report a preliminary investigation into the production of unpoled poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) films reinforced with barium titanate (BaTiO3) and activated carbon (AC) to improve the piezoelectric property. Employing the mixture design of experiments (MDOE) method, various formulations of the composite’s constituents weight fractions were determined. Afterwards, series of composite films were produced via a toxic-free solution casting method and characterised by Fourier Transform Infrared Spectrum (FTIR) to determine the β-phase content. A non-linear polynomial regression model was established from the experimental FTIR data, and the adequacy of the model was confirmed using ANOVA. Subsequently, an MDOE-enabled optimisation was undertaken, generating a formulation of the composite to obtain the highest β-phase content to be 15 wt.% BaTiO3 and 0.74 wt.% AC. This combination produces a theoretically predicted β-phase content of 72.7 %. A further experimental test employing the optimal formulation produced a β-phase content of 71.90 %, achieved with neither mechanical stretching, thermal annealing, nor electrical poling.

Lithium-Rich Porous Aromatic Framework Doped Quasi-Solid Polymer Electrolyte for Lithium Battery with High Cycling Stability.

Lithium-ion batteries (LIBs) have revolutionized the energy storage landscape and are the preferred power source for various applications, ranging from portable electronics to electric vehicles. The constant drive and growth in battery research and development aim to enhance their performance, energy density, and safety. Advanced lithium batteries (LIBs) are considered to be the most promising electrochemical storage devices, which can provide high specific energy, volumetric energy density, and power density. However, the trade-off between ionic conductivity and cycling stability is still a major contradiction for SPEs. In this work, a novel hydroxylated PAF-1 was designed and synthesized through post-modification, and the lithium-rich single-ion porous aromatic framework PAF-1-OLi was thereafter prepared by lithiation, achieved with a specific surface area to be 155 m2 g-1 and a lithium content of 2.01 mmol g-1. PAF-1-OLi, lithium bis(trifluoromethanesulfony)limine (LiTFSI), and poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) were compounded to obtain PAF-1-OLi/PVDF by solution casting, which had good mechanical, thermodynamic, and electrochemical properties. The ion conductivity of PAF-1-OLi/PVDF infiltrated with plasticizer was 2.93 × 10-4 S cm-1 at 25 °C. The tLi+ was 0.77, which was much higher than that of the traditional dual-ion polymer electrolytes. The electrochemical window of PAF-1-OLi/PVDF can reach 4.9 V. The Li//PAF-1-OLi/PVDF//LiFePO4 battery initial discharge specific capacity was 147 mAh g-1 and reached 134.9 mAh g-1 after 600 cycles with a capacity retention rate of 91.2%, demonstrating its good cycling stability. The anionic part of lithium salt was fixed on the framework of PAF-1 to increase the Li+ transfer number of PAF-1-OLi/PVDF. The lithium-rich PAF-1-OLi and the LiTFSI provided abundant Li+ sources to transfer, while PAF-1-OLi helped to form a continuous Li+ transport channel, effectively promoting the migration of Li+ in the PAF-1-OLi/PVDF and effectively improving the Li+ conductivity. This study afforded a novel polymer electrolyte based on lithium-rich PAF-1-OLi, which has excellent electrochemical performance, providing a new choice for the polymer electrolyte of lithium batteries.

Fabrication of Single-Ion Conductors Based on Liquid Crystal Polymer Network for Quasi-Solid-State Lithium Ion Batteries.

Single-ion conductive polymer electrolytes can improve the safety of lithium ion batteries (LIBs) by increasing the lithium transference number (tLi+) and avoiding the growth of lithium dendrites. Meanwhile, the self-assembled ordered structure of liquid crystal polymer networks (LCNs) can provide specific channels for the ordered transport of Li ions. Herein, single-ion conductive nematic and cholesteric LCN electrolyte membranes (denoted as NLCN-Li and CLCN-Li) were successfully prepared. NLCN-Li was then coated on commercial Celgard 2325 while CLCN-Li was coated on poly(vinylidene fluoride-hexafluoropropylene) film, coupled with plasticizer, to make NLCN-Li/Cel and CLCN-Li/Pv quasi-solid-state electrolyte membranes, respectively. Their electrochemical properties were evaluated, and it was found that they possessed benign thermal stability and electrolyte/electrode compatibility, high tLi+ up to 0.98 and high electrochemical stability window up to 5.2 V. A small amount (0.5M) of extra Li salt added to the plasticizer could improve the ion conductivity from 1.79 × 10-5 to 5.04 × 10-4 S cm-1, while the tLi+ remained 0.85. The assembled LFP|Li batteries also exhibited excellent cycling and rate performances. The orderliness of the LCN layer played an important role in the distribution and movement of Li ions, thereby affecting the Li deposition and growth of Li dendrites. As the first report of nematic and cholesteric LCN single-ion conductors, this work sheds light on the design and fabrication of ordered quasi-solid-state electrolytes for high-performance and safe LIBs.

Molecular Dynamics Study of Adhesion-Related Structural Properties for PVDF-HFP Polymer Binders

The current lithium-ion battery (LIB) market is expanding rapidly. Binders are essential to maintaining the high capacity and longevity of batteries. These binders can be classified into organic binders used for cathodes and aqueous binders used for anodes. Among them, Poly(vinylidene fluoride) (PVDF) binder is a representative organic binder that offers excellent electrochemical stability. To solve low adhesive force and weak mechanical strength of conventional PVDF binders, hexafluoropropylene (HFP) is added to improve these properties. However, the present poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) binders still show lower adhesive force than other polymeric binders, and therefore further research works are necessary.In this study, we employ classical molecular dynamics (MD) simulations to investigate the structural properties of the PVDF-HFP copolymers. To create realistic disordered PVDF-HFP polymers, we develop a computational scheme that can randomly arrange the angles and sequences of the constituent polymer chains. By varying the ratio of randomly arranged PVDF-HFP copolymers to 0/100, 5/95, 10/90, 15/85, and 20/80, we build a solution model that mimics the HFP concentration of PVDF-HFP (0–20%, Sigma Aldrich) used in the actual experiments. N-methyl-2-pyrrolidone (NMP) used as solvents. To create a large-scale model, we utilize the Large-scale Atomic/Molecular Massively Parallel Simulator (LAMMPS) and set parameters by using OPLS force field. This allows us to build a simulation model containing approximately 40,000 atoms consisting of 10 PVDF-HFP polymers and 1500 NMP monomers.After creating the simulation model, approximately eight steps of molecular dynamics simulation are performed by referring to the process of making the actual polymer film. In this process, NMP molecules are evaporated to produce a polymer film consisting only of PVDF-HFP polymers. Then we perform the adhesion analysis by applying forces to five polymer film models with different composition ratios in various conditions. Throughout these processes, we find the characteristic changes depending on the composition ratio. Finally, we will present the possible routes that can lead to the enhanced adhesive properties of PVDF-HFP, which is a key requirement to the development of high performance binders.

Fabrication of passive cooling fabric as thermal management curtain for building energy-saving

In the past years, a great deal of attention has been paid to passive cooling envelope materials or smart windows to cope with the increase in building energy consumption due to global warming. However, combining curtains with passive cooling could enable on-demand thermal management based on its dynamically adjustable characteristics. Herein, a superhydrophobic passive cooling cotton fabric with low thermal conductivity (0.0342 W/mK), high solar reflectivity (0.9280) and high infrared emissivity (0.9698) was obtained by wrapping the cotton fabric with a porous SiO2/poly(vinylidene fluoride-hexafluoropropylene) composite coating via solvent exchange phase separation and sanding. The superhydrophobic passive cooling fabrics realized an average of 10.3 °C cooling during the daytime and showed impressive passive cooling performance relative to the pristine cotton. Notably, the superhydrophobic passive cooling fabric demonstrated superior daytime cooling and nighttime insulation performance during outdoor testing and energy consumption simulations compared to commercial curtains. Therefore, superhydrophobic passive cooling cotton fabrics as curtains allow for reducing the energy consumption in building thermal management and broadening the practical application of radiative cooling materials.

Vanadium-doped Li6.7La3Zr1.7V0.3O12 and PVDF-HFP enhanced the ionic conductivity and cycling stability of composite solid electrolytes for All-Solid-State lithium batteries

Solid electrolytes receive widespread attention due to their high safety, high energy density and simplicity of processing. However, the poor interface stability between the solid electrolyte and the electrode leads to a significant increase in interface resistance, greatly reducing the electrochemical performance of lithium-ion batteries (LIBs). Here we designed and prepared a new type of solid composite electrolytes (SCEs), which were composed of poly (ethylene oxide) (PEO) blended with poly (vinylidene fluoride-hexafluoro propylene) (PVDF-HFP) and doped with cubic phase Li6.7La3Zr1.7V0.3O12 (LLZVO) particles. Compared with our previous work, the addition of PVDF-HFP can further reduce the crystallinity of PEO, limit the formation of lithium dendrites, and make the electrolyte/electrode interface more stable. The SCEs had better ionic conductivity of 2.04 × 10-4 S cm−1 and 2.03 × 10-3 S cm−1 at 30 ℃ and 80 ℃, respectively, and the Li/SCEs/Li symmetrical battery cycled for 1800 h without short circuit. Moreover, the coulombic efficiency of LiFePO4/SCEs/Li battery remained at 98 % after 300 cycles. This opens up a new direction for the research of garnet-type composite solid electrolytes with lower interface resistance.

Hydrogen-bond-driven high ionic conductivity, Li+ transfer number, and lithium-interface stability of poly(vinylidene fluoride-hexafluoropropylene)-based solid-state electrolytes

Poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP)-based solid electrolytes with wide electrochemical windows and high thermal stabilities are promising candidates for use in solid-state lithium batteries. However, the practical applications of these electrolytes are currently hindered by their low room-temperature ionic conductivity, limited Li+ transfer number, and the poor stability of the lithium/electrolyte interface. This study proposes a ‘one stone, three birds’ modification method, wherein a small amount of lithium carboxymethylcellulose (CMC-Li) containing rich hydroxyl groups is added to form abundant hydrogen bonds with numerous electronegative C–F groups in the PVDF-HFP molecular chain and lithium bistrifluoromethane sulfonimide (LiTFSI). The strong connections formed between CMC-Li and PVDF-HFP or TFSI− significantly reduced the crystallinity of PVDF-HFP, promoted the dissociation of LiTFSI, and anchored TFSI−, achieving a synchronous improvement in the ionic conductivity and Li+ transfer number. The hydrogen bonds drove the densification of the membrane surface, improving the lithium/electrolyte compatibility at the interface. The ionic conductivity of the modified electrolytes was 5.1 × 10−4 S cm−1 and the Li + transfer number was 0.72 at room temperature. A Li||Li symmetric cell demonstrated stable cycling over 1000 h at 0.2 mA cm−2, where the initial discharge capacity of an all-solid-state cell was enhanced to 165.1 mAh g−1, with steady cycling for 400 runs. Thus, this study provides a novel and effective method for promoting the practical application of solid-state electrolytes.

PIEZORESISTIVE SENSORS BASED ON PVDF-HFP REINFORCED WITH GNPs FOR HEALTH MONITORING APPLICATIONS

Wearable technology has become increasingly popular in recent years. Wearable sensors are systems made of flexible substrates which good adaptability to human motion monitoring. In parituclar, they allow doctors to obtain real-time data from patients by detecting small changes in baseline values over time, such as the movement of various joints or muscles, heart activity, breathing, and even sweat. In this regard, polymers can offer good flexibility, stretchability, and long-term reliability, which, together with the possibility of modifying their electrical response with conductive nanofillers, makes them promising for the fabrication of this kind of sensors, as their electrical conductivity changes with applied strain. In this work, piezoresistive sensors based on poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) reinforced with graphene nanoplatelets via solvent casting are presented. Here, both the electrical and electromechanical responses are evaluated as a function of different processing conditions, more specifically, sonication time and evaporation temperature. Then, several successful proof-of-concept tests have been carried out from human motion monitoting to pressure sensing applications, with very high sensitivities, being very promising for this kind of applications.

Bivalent metal ion co-doped methylammonium lead tribromide perovskite nanocrystal scintillator for X-ray imaging

Perovskite scintillators with low cost, easy preparation, environmental stability, and high-resolution have become candidates for X-ray imaging applications. Here, based on the calculation results of surface formation energy (Ef) and vacancy defect energy (Evac), a series of co-doped perovskite nanocrystals (NCs) with photoluminescence high quantum yield (PLQY) and fast luminescence decay time had been prepared by doping several bivalent metal ions into the B-site of methylammonium lead tribromide (MAPbBr3). In addition, the scintillator with flexibility was prepared using poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) as the carrier, showing excellent stability and scintillation performance, with a light yield of 21,200 photons/MeV, imaging resolution reached 11.7 lp/mm, and low detection limits of 462 nGyair s−1. Finally, we demonstrated the scintillator characteristic with high-quality imaging results and excellent tolerance under high dose rate X-ray (25 mGy s−1). Therefore, the combination of co-doped nanocrystals with excellent optical properties and PVDF-HFP further paves the way for the development of a scintillator.

Composite polymer electrolyte facilitated by enhanced amorphousity and Li+ conduction using LaFeO3-embedded PVDF-HFP for solid-state lithium metal battery

Composite polymer electrolytes (CPEs) are a promising alternative to flammable conventional liquid electrolytes for high-safety lithium-ion batteries. Establishing low-cost filler that enhances the amorphous nature of polymer in the CPEs and exhibits efficient Lewis acid-base interaction between fillers and anions of lithium salt, leading to improved dissociation of salts for enhanced conduction, is indispensable. In this work, for the first time, we construct a solid composite polymer electrolyte of poly(vinylidene fluoride hexafluoropropylene) embedded LaFeO3 (LFO) particles prepared by solution casting and electrospinning methods and study their performances. The 5 wt% LFO filler embedded CPE made by means of solution casting and electrospinning methods exhibited the highest ionic conductivity of 5.9 × 10-4 and 1.49 × 10-3 S cm−1 at room temperature and electrochemical stability window up to 4.6 and 4.45 V, respectively. Further, as-assembled solid-state lithium-ion batteries using electrospun CPE showed an initial discharge capacity of 166 mAh/g at 0.1C-rate and solution-casted CPE showed excellent cycling stability with 98.6 % capacity retention at 0.3C-rate even at 50th cycle. Such excellent performance originated from the introduction of the LFO particles as filler into the polymer matrix to enhance the ionic conductivity, mechanical strength and lithium metal compatibility of the resulting CPEs.

Innovative low-energy enrichment of sulfuric acid using PVDF-HFP anion exchange membranes with acid-blocking properties

In recent years, the electrodialysis (ED) technology has gained substantial attention for its role in recovering sulfuric acid from industrial wastewater. However, the typical anion exchange membranes (AEMs) have been known to exhibit notable proton leakage during ED, which can severely hinder the efficiency of acid concentration. To overcome this issue, we utilized a substrate made of poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP). This choice capitalizes on the presence of fluorine-containing groups for enhanced acid stability and tertiary amine groups to minimize water content, resulting in a significant improvement in proton-blocking capabilities of the AEMs. It is worth noting that, through a combination of partial cross-linking and quaternization, these AEMs not only maintain their acid concentration performance but also substantially reduce energy consumption. Additionally, we conducted a thorough analysis of the delicate balance between current efficiency and energy consumption in acid recovery systems. In contrast to conventional AEMs and commercially available proton-blocking membranes such as ACM, we highlight the exceptional acid concentration capability (CH+ = 1.28 M) and the low energy consumption (3.3 kWh/kg) of AEM-1.2. This research breakthrough marks a significant advancement in the development of acid-blocking AEMs and strongly advocates for more efficient sulfuric acid recovery from industrial wastewater.

Natural Clay-Modified Piezocatalytic Membrane for Efficient Removal of Coliform Bacteria from Wastewater.

In the modern era, water pollution, especially from industries, agricultural farms, and residential areas, is caused by the release of a large scale of heavy metals, organic pollutants, chemicals, etc., into the environment, posing a serious threat to aquatic ecosystems and nature. Moreover, untreated sewage waste discharged directly into nearby water bodies can cause various diseases to mankind due to the high load of fecal coliform bacteria. This work demonstrates the development of a biocompatible, cost-effective, highly robust, efficient, flexible, freestanding, and reusable membrane using naturally formed biocompatible kaolinite clay-doped poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) for effective piezodynamic destruction of coliform bacteria. In this study, Escherichia coli (E. coli) and Enterococcus faecalis (E. faecalis) have been used to evaluate the mechanical stimulus-responsive antibacterial efficacy of the nanocomposite membrane. The membrane can effectively eradicate nearly 99% viable E. coli and 97% E. faecalis within a span of 40 min under mechanical stimulation (soft ultrasound ∼15 kHz). To further understand the mechanism, an evaluation of reactive oxygen species and bacterial FESEM was performed. These studies revealed that bacterial cells suffered severe visible cell damage after 40 min of piezocatalysis, elucidating the fact that the synthesized membrane is capable of producing a superior piezodynamic antibacterial effect.

Poly (Vinylidene Fluoride-Hexafluoropropylene)-Lithium Titanium Aluminum Phosphate-Based Gel Polymer Electrolytes Synthesized by Immersion Precipitation for High-Performance Lithium Metal Batteries.

Gel polymer electrolytes (GPEs) have high safety and excellent electrochemical performance, so applying GPEs in lithium batteries has received much attention. However, their poor lithium ion transfer number, cycling stability, and low room temperature ionic conductivity seriously affect the utilization of gel polymer electrolytes. This paper successfully synthesized flexible poly (vinylidene fluoride-hexafluoropropylene)-lithium titanium aluminum phosphate (PVDF-HFP-LATP) gel polymer electrolytes using the immersion precipitation method. The resulting GPE has a porous honeycomb structure, which ensures that the GPE has sufficient space to store the liquid electrolyte. The GPE has a high ionic conductivity of 1.03 ×10-3 S cm-1 at room temperature (25 °C). The GPE was applied to LiFePO4/GPE/Li batteries with good rate performance at room temperature. The discharge specific capacity of 1C was as high as 121.5 mAh/g, and the capacity retention rate was 94.0% after 300 cycles. These results indicate that PVDF-HFP-LATP-based GPEs have the advantage of simplifying the production process and can improve the utility of gel polymer lithium metal batteries.

Composite polymer electrolyte based on poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) for solid-state batteries

Using solid-state electrolytes (SSEs) with excellent thermal and electrical stability to replace liquid electrolytes, and assembling solid-state lithium-ion batteries (SSLIBs) is considered the best solution to these safety issues. However, it is difficult for a single electrolyte to have the characteristics of high ionic conductivity, low interface resistance, and high stability of the counter electrode at the same time. In this work, the composite polymer electrolyte membrane (CPE) of inorganic Li1.3Al0.3Ti1.7(PO4)3 (LATP) and organic poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) polymer was successfully prepared by traditional casting method. The addition of LATP (10 wt %) ceramic powder makes CPE membrane (CPE-10) exhibit excellent electrochemical performance: the lithium-ion transference number and electrochemical window are as high as 0.60 and 4.94 V, respectively. Moreover, the CPE-10 showed excellent Li-metal stability, thereby enabling the Li–Li symmetric cells to stably run for over 300 h at 0.1 mA/cm2 with effective lithium dendrite inhibition. When paired with a high-voltage LiNi0.6Co0.2Mn0.2O2 (NCM622) cathode, the Li/CPE-10/NCM622 cell exhibited excellent electrochemical performance: the highest specific discharge capacity of 152 mAh/g could be conducted at 0.2C after 50 cycles corresponding to 100% Coulombic efficiencies. The prepared CPE-10 demonstrates excellent electrochemical performance, providing an effective design strategy for SSLMBs.

Studies on potassium-ion conducting gel polymer electrolytes containing poly(vinylidene fluoride-hexafluoropropylene) polymer, potassium permanganate salt added with different plasticizers

Studies on potassium-ion conducting gel polymer electrolytes containing poly(vinylidene fluoride-hexafluoropropylene) polymer, potassium permanganate salt added with different plasticizers

Hydrophilic Carbon Quantum Dots Assisting Porous P(VDF-HFP) film for Self-powered Humidity Sensing with High Sensitivity and Low Hysteresis

The self-powered has become the development trend of electronic devices in the "double carbon" era. However, environmental humidity has a significant impact on the piezoelectric properties of poly(vinylidene fluoride-hexafluoropropylene) (P(VDF-HFP))...