Influence of photothermal nanomaterials localization within the electrospun membrane structure on purification of saline oily wastewater based on photothermal vacuum membrane distillation.

Today, synergistic combination of special nanomaterials (NMs) and electrospinning technique has emerged as a promising strategy to address both water scarcity and energy concerns through the development of photothermal membranes for wastewater purification and desalination. This work was organized to provide a new perspective on membrane design for photothermal vacuum membrane distillation (PVMD) through optimizing membrane performance by varying the localization of photothermal NMs. Poly(vinylidene fluoride) omniphobic photothermal membranes were prepared by localizing graphene oxide nanosheets (GO NSh) (1) on the surface (0.2 wt%), (2) within the nanofibers structure (10 wt%) or (3) in both positions. Considering the case 1, after 7 min exposure to the 1 sun intensity light, the highest temperature (∼93.5 °C) was recorded, which is assigned to the accessibility of GO NSh upon light exposure. The case 3 yielded to a small reduction in surface temperature (∼90.4 °C) compared to the case 1, indicating no need to localize NMs within the nanofibers structure when they are localized on the surface. The other extreme belonged to the case 2 with the lowest temperature of ∼71.3 °C, which is consistent with the less accessibility of GO NSh during irradiation. It was demonstrated that the accessibility of photothermal NMs plays more pronounced role in the membrane surface temperature compared to the light trapping. However, benefiting from higher surface temperature during PVMD due to enhanced accessibility of photothermal NMs is balanced out by decrease in the permeate flux (case 1: 1.51 kg/m2 h and case 2: 1.83 kg/m2 h) due to blocking some membrane surface pores by the binder. A trend similar to that for flux was also followed by the efficiency. Additionally, no change in rejection was observed for different GO NSh localizations.

The Role of Phase Migration of Carbon Nanotubes in Melt-Mixed PVDF/PE Polymer Blends for High Conductivity and EMI Shielding Applications.

In this work, the effects of blend ratio and mixing time on the migration of multi-walled carbon nanotubes (MWCNTs) within poly(vinylidene fluoride) (PVDF)/polyethylene (PE) blends are studied. A novel two-step mixing approach was used to pre-localize MWCNTs within the PE phase, and subsequently allow them to migrate into the thermodynamically favored PVDF phase. Light microscopy images confirm that MWCNTs migrate from PE to PVDF, and transmission electron microscopy (TEM) images show individual MWCNTs migrating fully into PVDF, while agglomerates remained trapped at the PVDF/PE interface. PVDF:PE 50:50 and 20:80 polymer blend nanocomposites with 2 vol% MWCNTs exhibit exceptional electromagnetic interference shielding effectiveness (EMI SE) at 10 min of mixing (13 and 16 dB, respectively-at a thickness of 0.45 mm), when compared to 30 s of mixing (11 and 12 dB, respectively), suggesting the formation of more interconnected MWCNT networks over time. TEM images show that these improved microstructures are concentrated on the PE side of the PVDF/PE interface. A modified version of the "Slim-Fast-Mechanism" is proposed to explain the migration behavior of MWCNTs within the PVDF/PE blend. In this theory, MWCNTs approaching perpendicular to the interface penetrate the PVDF/PE interface, while those approaching in parallel or as MWCNT agglomerates remain trapped. Trapped MWCNTs act as barriers to additional MWCNTs, regardless of geometry. This mechanism is verified via TEM and scanning electron microscopy and suggests the feasibility of localizing MWCNTs at the interface of PVDF/PE blends.

Copper(0) Mediated Single Electron Transfer Controlled Radical Polymerization toward CF Bonds on Poly(vinylidene fluoride).

The first copper(0) mediated controlled radical polymerization (CRP) of methyl methacrylate (MMA) toward CF bonds onto poly(vinylidene fluoride) (PVDF) is reported with rather high activity. By avoiding the halogen exchange, Cu0 instead of CuI complexes utilized as catalyst is responsible for the significantly improved polymerization activity. Using FH decoupled nuclear magnetic resonance technique, the grafting sites onto PVDF are finely located. From this, detailed topologic information including the grafting density, average length of each side chain, along with the overall grafted content of PMMA, is detected by tracking the polymerization as a function of time. This work offers not only a facile CRP strategy based on inactive CF bonds but also a deep insight into the cleavage of F-bearing compounds in organic chemistry.

The Structure Design of Piezoelectric Poly(vinylidene Fluoride) (PVDF) Polymer-Based Sensor Patch for the Respiration Monitoring under Dynamic Walking Conditions.

This study reports a piezoelectric poly(vinylidene fluoride) (PVDF) polymer-based sensor patch for respiration detections in dynamic walking condition. The working mechanism of respiration signal generation is based on the periodical deformations on a human chest wall during the respiratory movements, which in turn mechanically stretch the piezoelectric PVDF film to generate the corresponding electrical signals. In this study, the PVDF sensing film was completely encapsulated within the sensor patch forming a mass-spring-damper mechanical system to prevent the noises generated in a dynamic condition. To verify the design of sensor patch to prevent dynamic noises, experimental investigations were carried out. Results demonstrated the respiration signals generated and the respiratory rates measured by the proposed sensor patch were in line with the same measurements based on a commercial respiratory effort transducer both in a static (e.g., sitting) or dynamic (e.g., walking) condition. As a whole, this study has developed a PVDF-based sensor patch which is capable of monitoring respirations in a dynamic walking condition with high fidelity. Other distinctive features include its small size, light weight, ease of use, low cost, and portability. All these make it a promising sensing device to monitor respirations particularly in home care units.

Improvement of the Piezoresistive Behavior of Poly (vinylidene fluoride)/Carbon Nanotube Composites by the Addition of Inorganic Semiconductor Nanoparticles.

Conductive polymer composites (CPCs), obtained by incorporating conductive fillers into a polymer matrix, are suitable for producing strain sensors for structural health monitoring (SHM) in infrastructure. Here, the effect of the addition of inorganic semiconductor nanoparticles (INPs) to a poly (vinylidene fluoride) (PVDF) composite filled with multi-walled carbon nanotubes (MWCNTs) on the piezoresistive behavior is investigated. INPs with different morphologies and sizes are synthesized by a hydrothermal method. The added inorganic oxide semiconductors showed two distinct morphologies, including different phases. While particles with flower-like plate morphology contain phases of orth-ZnSnO3 and SnO, the cauliflower-like nanoparticles contain these metal oxides and ZnO. The nanoparticles are characterized by field-emission scanning electron microscopy (FE-SEM) and X-ray diffraction (XRD), and the nanocomposites by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). Cyclic tensile testing is applied to determine the strain-sensing behavior of PVDF/1 wt% MWCNT nanocomposites with 0-10 wt% inorganic nanoparticles. Compared to the PVDF/1 wt% MWCNT nanocomposite, the piezoresistive sensitivity is higher after the addition of both types of nanoparticles and increases with their amount. Thereby, nanoparticles with flower-like plate structures improve strain sensing behavior slightly more than nanoparticles with cauliflower-like structures. The thermogravimetric analysis results showed that the morphology of the semiconductor nanoparticles added to the PVDF/MWCNT matrix influences the changes in thermal properties.

Highly Sensitive Interdigitated Capacitive Humidity Sensors Based on Sponge-Like Nanoporous PVDF/LiCl Composite for Real-Time Monitoring.

In this study, a sponge-like poly(vinylidene fluoride) (PVDF)/lithium chloride (LiCl) nanocomposite-entrenched interdigitated capacitive (IDC) sensor was developed for real-time humidity-sensing applications. Here, we demonstrated a sponge-like nanoporous structure ranging from 200 nm to 2 µm size holes, the PVDF/LiCl structure fabricated on an interdigitated capacitor (IDC) electrode functioning as a high-performance sensor because of the presence of ionized LiCl. The nanoporous PVDF/LiCl composite-based humidity sensor exhibited a high sensitivity of 12.6 nF/% relative humidity (RH), a linearity of 0.990, and a low hysteresis of 2.6% in the range of 25-95% RH. The composite film exhibited a response time of 17.7 s, a recovery time of 21 s, and an intensified increase of 8.02 nF/s (a decrease of 6.7 nF/s). The sensor designed demonstrates ultra-high sensing characteristics with 10 times higher sensitivity, i.e., 12.678.96 pF/%RH as compared to other polymer-based composite humidity sensors. Owing to the sensing performance and portability, the proposed nanoporous PVDF/LiCl composite-based IDC sensor is expected to be a promising platform for a wide range of humidity-sensing applications, including real-time breath monitoring and non-contact sensing.

3D Printing-Enabled In-Situ Orientation of BaTi2O5 Nanorods in ß-PVDF for High-Efficiency Piezoelectric Energy Harvesters.

Piezoelectric energy harvesters (PEHs) with a three-dimensional (3D) structure are arousing increasing interest because of the ability to efficiently convert mechanical energy into electricity catering for self-powered systems. Among them, 3D PEHs composed of 1-3-type piezoelectric composites which exploit one-dimensional (1D) piezoceramic fillers rather than conventional powders are particularly attractive. However, an issue involving the orientation of the 1D fillers to utilize the piezoelectric effect renders the 3D structural design for high-efficiency energy conversion more challenging. Herein, for the first time, we introduce the fused deposition modeling (FDM) 3D printing to the flexible construction of poly(vinylidene fluoride) (PVDF)-based 3D PEHs by incorporating 1D BaTi2O5 (BT2) nanorods as piezoelectric fillers. The shearing force generated by FDM successfully realizes the in situ uniform orientation of BT2 nanorods in the PVDF (98% ß crystals) matrix along the nozzle extrusion direction. Besides, by coupling 3D printing with the appealing piezoelectric anisotropy feature of BT2 nanorods, the 3D PEH is able to generate different piezoelectric responses to the same applied external force from X, Y, and Z directions. Furthermore, an optimized 3D conical array structure is constructed to amplify the effective deformation of the PEH to enhance its piezoelectric output. As expected, customized PEH can continuously power commercial electronic devices and monitor various human motions, indicating 3D printing as a multifunctional strategy to fabricate 3D PEHs with 1-3-type piezoelectric composite materials for self-powering microelectronic applications.

Poly(vinylidene fluoride) Intestinal Sleeve Implants for the Treatment of Obesity and Type 2 Diabetes.

Currently, treatment of diabetes and associated obesity involves Roux-en-Y gastric bypass or sleeve gastrectomy to reduce the absorption of nutrients from the intestine to achieve blood glucose control. However, the surgical procedure and subsequent recovery are physically and psychologically burdensome for patients, with possible side effects, so alternative treatments are being developed. In this study, two methods, solution casting and machine direction orientation (MDO), were used to prepare intestinal implants made of poly(vinylidene fluoride) (PVDF) film and implant them into the duodenum of type 2 diabetic rats for the treatment of obesity and blood glucose control. The PVDF film obtained by the MDO process was characterized by FT-IR, Raman spectroscopy, XRD and piezoelectricity tests, which showed higher composition of ß crystalline phase and better elongation and mechanical strength in specific directions. Therefore, the material was finally tested on rats after it was proven to be non-toxic by biological toxicity tests. The PVDF was implanted into alloxan-induced diabetic rats, which were used as a model of impaired insulin secretion due to pancreatic beta cell destruction rather than obesity-induced diabetes, and rats were tracked for 24 days, showing significantly improved body weight and blood glucose levels. As an alternative therapeutic option, intestinal sleeve implant showed future potential for application.

Highly Tunable Piezoresistive Behavior of Carbon Nanotube-Containing Conductive Polymer Blend Composites Prepared from Two Polymers Exhibiting Crystallization-Induced Phase Separation.

Conductive polymer composites (CPCs) are suitable as piezoresistive-sensing materials. When using CPCs for strain sensing, it is still a big challenge to simultaneously improve the piezoresistive sensitivity and linearity along with the electrical conductivity and mechanical properties. Here, highly tunable piezoresistive behavior is reported for multiwalled carbon nanotube (CNT)-filled CPCs based on blends of two semicrystalline polymers poly(vinylidene fluoride) (PVDF) and poly(butylene succinate) (PBS), which are miscible in the melt. When cooling the homogeneous mixture of the blend components, successive crystallization of PVDF and PBS occurs, creating complex crystalline structures in a mixed amorphous phase. The morphology of the blend matrix, the crystallinity of the blend components, and the dispersion and location of the CNTs in the blend depend on the CNT content and the blend composition. Compared with PVDF/CNT composites, the substitution of 10 to 50 wt % PVDF by PBS in the composites shifts the electrical percolation concentration Φc from 0.79 wt % to filler contents as low as 0.50 wt % while improving the stretchability. The piezoresistive behavior is highly tunable by changing the PVDF/PBS ratio. The ternary composites with matrix compositions of PVDF (90 wt %)/PBS (10 wt %) and PVDF (50 wt %)/PBS (50 wt %) show either higher piezoresistive sensitivity or linearity, respectively, caused by the differences in the microstructure of the CPCs. For example, the crystallinity of PBS in the ternary composites increased from 19.8% to 52.0% as the PBS content increased from 10 wt % to 50 wt %, which is connected with altered CNT distribution and conductive network structure and substantial improvement of the linearity of the electrical response to strains up to >20%. Our findings highly contribute to the understanding of the piezoresistive properties of CPCs based on two semicrystalline polymers and are important for future studies to tune the piezoresistive behavior to achieve simultaneously improved sensitivity and linearity.

Large-area atomic-smooth polyvinylidene fluoride Langmuir-Blodgett film exhibiting significantly improved ferroelectric and piezoelectric responses.

Large roughness and structure disorder in ferroelectric ultrathin Langmuir-Blodgett (LB) film results in severe space scatter in electrical, ferroelectric and piezoelectric characteristics, thus limiting the nanoscale research and reliability of nano-devices. However, no effective method aiming at large-area uniform organic ferroelectric LB film has ever been reported to date. Herein, we present a facile hot-pressing strategy to prepare relatively large-area poly(vinylidene fluoride) (PVDF) LB film with ultra-smooth surface root mean square (RMS) roughness is 0.3 nm in a 30 µm × 30 µm area comparable to that of metal substrate, which maximized the potential of LB technique to control thickness distribution. More importantly, compared with traditionally annealed LB film, the hot-pressed LB film manifests significantly improved structure uniformity, less fluctuation in ferroelectric characteristics and higher dielectric and piezoelectric responses, owing to the uniform dipole orientation and higher crystalline quality. Besides, different surface charge relaxation behaviors are investigated and the underlying mechanisms are explained in the light of the interplay of surface charge and polarization charge in the case of nanoscale non-uniform switching. We believe that our work not only presents a novel strategy to endow PVDF LB film with unprecedented reliability and improved performance as a competitive candidate for future ferroelectric tunnel junctions (FTJs) and nano electro mechanical systems (NEMS), but also reveals an attracting coupling effect between the surface potential distribution and nanoscale non-uniform switching behavior, which is crucial for the understanding of local transport characterization modulated by band structure, bit signal stability for data-storage application and the related surface charge research, such as charge gradient microscopy (CGM) based on the collection of surface charge on the biased ferroelectric domains.

Fabrication of Poly(3,4-ethylenedioxythiophene):Poly(styrenesulfonate)/Poly(vinylidene fluoride) Nanofiber-Web-Based Transparent Conducting Electrodes for Dye-Sensitized Photovoltaic Textiles.

In this work, poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)/poly(vinylidene fluoride) (PVDF) nanofiber-web-based transparent conducting electrodes (TCEs) were fabricated for use in dye-sensitized photovoltaic textiles. The PEDOT:PSS solution was mixed with dimethyl sulfoxide (DMSO) solvent, and the PEDOT:PSS/DMSO mixture was applied on the PVDF nanofiber web using a simple brush-painting technique to prepare ultrathin and -lightweight, highly transparent TCEs. When the PVDF nanofiber web was treated with a 3:7 PEDOT:PSS and DMSO mixture (P3D7 sample), it exhibited ∼84% transmittance at a wavelength of 550 nm with an average sheet resistance of ∼1.5 kΩ/sq. In addition, it showed a figure of merit (FOM) of 0.104 × 10-3 Ω-1. In the trial test, the P3D7 TCE-based photovoltaic textile exhibited an average voltage of 73.20 mV and an average current of 0.44 mA/cm2.

Chemical and Morphological Transition of Poly(acrylonitrile)/Poly(vinylidene Fluoride) Blend Nanofibers during Oxidative Stabilization and Incipient Carbonization.

Thermally stabilized and subsequently carbonized nanofibers are a promising material for many technical applications in fields such as tissue engineering or energy storage. They can be obtained from a variety of different polymer precursors via electrospinning. While some methods have been tested for post-carbonization doping of nanofibers with the desired ingredients, very little is known about carbonization of blend nanofibers from two or more polymeric precursors. In this paper, we report on the preparation, thermal treatment and resulting properties of poly(acrylonitrile) (PAN)/poly(vinylidene fluoride) (PVDF) blend nanofibers produced by wire-based electrospinning of binary polymer solutions. Using a wide variety of spectroscopic, microscopic and thermal characterization methods, the chemical and morphological transition during oxidative stabilization (280 °C) and incipient carbonization (500 °C) was thoroughly investigated. Both PAN and PVDF precursor polymers were detected and analyzed qualitatively and quantitatively during all stages of thermal treatment. Compared to pure PAN nanofibers, the blend nanofibers showed increased fiber diameters, strong reduction of undesired morphological changes during oxidative stabilization and increased conductivity after carbonization.

Tuning the Piezoresistive Behavior of Poly(Vinylidene Fluoride)/Carbon Nanotube Composites Using Poly(Methyl Methacrylate).

In conductive polymer composites (CPCs), which can be used as both strain sensors and materials with self-diagnosis capabilities for structural health monitoring, the piezoresistive sensitivity can be tuned by changing the electrical filler network structure, mainly influenced by the conductive filler content. Typically, the electrical resistance increases exponentially with strain, and the piezoresistive sensitivity and linearity cannot be improved simultaneously. In this work, we report a facile method to tune the piezoresistive behavior of melt-mixed poly(vinylidene fluoride) (PVDF)/carbon nanotube (CNT, 0.75-2.0 wt %) composites using blending with poly(methyl methacrylate) (PMMA, 5-30 wt %). PVDF and PMMA are completely miscible in the melt state regardless of the proportion. For PVDF-rich blends, the crystallization of PVDF induces separation of the PVDF crystal region from the miscible PVDF/PMMA amorphous blend part during the cooling process. Addition of PMMA tuned the piezoresistive strain behavior and improved the electrical conductivity and toughness at the same time. The PVDF/PMMA/CNT composites show higher sensitivity at low strains than their PVDF/CNT counterparts with comparable initial resistivity. For example, ΔR/R0 at 5% strain is 18.6% for the PVDF(80)/PMMA(20) blend containing 0.75 wt % CNT versus 11.0% for PVDF containing 1 wt % CNT, both having a volume resistivity of around 104 Ω·cm. The PVDF/PMMA/CNT blend composites also show a less steep exponential increase in the sensing response at higher strains, indicating better linearity. These differences are due to the altered microstructure of the composites and the more homogeneous distribution of CNTs between the smaller and less numerous PVDF crystallites when PMMA is added. The concept of modifying the composite microstructure by adding another commercially available miscible polymer offers a simple and effective way to tune the piezoresistive behavior and improve mechanical properties of CPC sensor materials.

Nuomici-Inspired Universal Strategy for Boosting Piezoresistive Sensitivity and Elasticity of Polymer Nanocomposite-Based Strain Sensors.

Electrically conductive polymer composites (CPCs) are potential alternatives to conventional strain gauges due to their tunable sensitivity and strain ranges. Currently, to achieve very high piezoresistive sensitivity in thermoplastic-based CPCs with Gauge factors GF above 20 at low tensile strains (ε ≤ 5%) is a big challenge, but critical for structural health monitoring application in infrastructures. Here, inspired by the unique structures of a famous Chinese food, nuomici, we coat carbon nanotubes (CNTs) onto sticky acrylic rubber (AR) granules (ARG) to form nuomici-like CNT@ARG composite granules, which are employed as unique conductive filler to fabricate highly piezoresistive and flexible CPCs based on poly(vinylidene fluoride) (PVDF). This strategy of localizing CNTs densely on the surface of touching rubbery particles resulted in a much more sensitive elastic conductive network built by the CNT@AR composite and showed a big gain effect. The resultant PVDF/CNT@AR nanocomposites (AR content ranging from 0 to 10 wt %) show extremely high piezoresistive sensitivity at low strain, depending on the AR content. In particular, the GF value of PVDF with 1.5 wt % CNT@10 wt % AR is 41 at 5% strain, which is more than one magnitude higher than that (ca. 3) of traditional PVDF/CNT nanocomposite sensors. Moreover, the elongation at break increases by about 60% with the addition of 1.5 wt CNT@10 wt % AR. This study introduces a universal effective strategy for tailoring the mechanical properties and strain sensitivity of conductive network in CPCs, which is critical for the fabrication of high-performance strain sensors.

Hydrophilic Poly(vinylidene Fluoride) Film with Enhanced Inner Channels for Both Water- and Ionic Liquid-Driven Ion-Exchange Polymer Metal Composite Actuators.

This study presents a novel and facile strategy to fabricate a hydrophilic poly(vinylidene fluoride) (PVDF) electrolyte film with enhanced inner channels for a high-performance and cost-effective ion-exchange polymer metal composite (IPMC) actuator. The resultant PVDF composite film is composed of hierarchical micro/nanoscale structures: well-defined polymer grains with a diameter of ∼20 µm and much finer particles with a diameter of ∼390 nm, producing three-dimensional interconnected, hierarchical inner channels to facilitate ion migration of IPMC. Interestingly, the electrolyte matrix film has a high porosity of 15.8% and yields a high water uptake of 44.2% and an ionic liquid (IL, [EMIm]·[BF4]) uptake of 38.1% to make both water-driven and IL-driven IPMC actuators because of the introduction of polar polyvinyl pyrrolidone. Compared to the conventional PVDF/IL-based IPMC, both water-driven and IL-driven PVDF-based IPMCs exhibit high ion migration rates, thus effectively improving the actuation frequency and producing remarkably higher levels of actuation force and displacement. Specifically, the force outputs are increased by 13.4 and 3.0 folds, and the displacement outputs are increased by 2.2 and 1.9 folds. Using an identical electrolyte matrix, water-driven IPMC exhibits stronger electromechanical performance, benefiting to make IPMC actuator with high levels of force and power outputs, whereas IL-driven IPMC exhibits a more stable electromechanical performance, benefiting to make long lifetime IPMC actuator in air. Thus, the resultant IPMCs are promising in the design of artificial muscles with tunable electromechanical performance for flexible actuators or displacement/vibration sensors at low cost.

Ultraviolet- and Microwave-Protecting, Self-Cleaning e-Skin for Efficient Energy Harvesting and Tactile Mechanosensing.

Smart, self-powered, and wearable e-skin that mimics the pressure sensing property of the human skin is indispensable to boost up cutting edge robotics, artificial intelligence, prosthesis, and health-care monitoring technologies. Here, fabrication of a facile and flexible hybrid piezoelectric e-skin (HPES) with multifunctions of tactile mechanosensing, energy harvesting, self-cleaning, ultraviolet (UV)-protecting, and microwave shielding properties is reported. The principal block of the HPES is an SnO2 nanosheets@SiO2 (silica-encapsulated tin oxide nanosheets)/poly(vinylidene fluoride) (PVDF) nanocomposite (SS)-based PES acting as a single unit for simultaneous energy harvesting and tactile mechanosensing. Gentle human finger imparting onto the PES showed outstanding energy conversion efficiency (16.7%) with high power density (550 W·m-3) and current density (0.40 µA·cm-2). This device can generate high enough electrical power to directly drive portable electronics like a light-emitting diode (LED) panel (consisting of 85 commercial LEDs) and to charge up capacitors very rapidly. Thin PES mechanosensors demonstrated promising performance for quantitatively detecting static and dynamic pressure stimuli with a high sensitivity of 0.99 V·kPa-1 and a short response time of 1 ms. PES was also integrated to a health-data glove for precisely monitoring and discriminating fine motions of proximal interphalangeal, metacarpophalangeal, and distal interphalangeal joints of a human finger and bending motion of different human fingers. A (4 × 4) sensing matrix of PES was successfully employed to detect the spatial distribution of static pressure stimuli. The sensing matrix can precisely record the shape and size of an object placed onto it. PES was encapsulated with a nanocomposite film for providing self-cleaning and UV and microwave protection capability to the HPES. The hydrophobic SS film wrapping (water drop contact angle ∼85.6°) of the HPES enables the self-cleaning feature and makes HPES resistive against water and dirt. The HPES was integrated with in-house-made robotic hands, and the responses of the sensors due to grabbing of an object were evaluated. This work explores new prospects for UV- and microwave-protective, self-cleaning e-skin for energy harvesting and mechanosensation, which can eventually boost up the self-powered electronics, robotics, real-time health-care monitoring, and artificial intelligence technologies.

An Ionic Liquid as Interface Linker for Tuning Piezoresistive Sensitivity and Toughness in Poly(vinylidene fluoride)/Carbon Nanotube Composites.

Conductive polymer nanocomposites (CPNCs) have emerged as potential alternatives for metallic foil sensors and semiconductor strain gauges. The simultaneous achievement of high piezoresistive sensitivity and large strain ranges for CPNCs currently presents a great challenge and solving this challenge may extend the applications of CPNCs with self-diagnosis capabilities to many structural health-monitoring (SHM) systems. This paper reports a facile strategy for fabricating highly piezoresistive and tough poly(vinylidene fluoride) (PVDF) based CPNCs by tuning the interactions between the polymer matrix and multiwalled carbon nanotubes (CNT) using an ionic liquid (IL) as an interface linker/modifier. As a result, the presence of IL achieves homogeneous dispersion of CNTs in PVDF but causes a reduced number of CNT-CNT ohmic contacts with higher electrical contact resistance. According to the lower initial resistivity, piezoresistive sensitivity is greatly improved, and the gauge factor (GF) varies from 7 to 60 upon the addition of IL. It is also shown that IL tunes PVDF-CNT interfacial bonding and, as an effective interface linker/modifier, achieves significantly improved sensing strain ranges (increased from ca. 6 to 21%) and toughness (elongation at break increases from 6 to 130%) of CPNCs. These results substantially advance the understanding of the missing relationship between polymer-filler interface interactions and piezoresistive properties and have important implications for future studies of tuning polymer-filler interface bonding properties and piezoresistive sensitivity.

Towards Flexible Dielectric Materials with High Dielectric Constant and Low Loss: PVDF Nanocomposites with both Homogenously Dispersed CNTs and Ionic Liquids Nanodomains.

Flexible dielectric materials with high dielectric constant and low loss have attracted significant attention. In this work, we fabricated novel polymer-based nanocomposites with both homogeneously dispersed conductive nanofillers and ion-conductive nanodomains within a polymer matrix. An unsaturated ionic liquid (IL), 1-vinyl-3-ethylimidazolium tetrafluoroborate ([VEIM][BF4]), was first coated on the surface of multi-walled carbon nanotubes (CNTs) by the mechanical grinding. The ILs coated CNTs were then well dispersed in poly(vinylidene fluoride) (PVDF) matrix by melt-blending. The ILs on the surface of CNTs were subsequently grafted onto the PVDF chains by electron beam irradiation (EBI). The formed ILs grafted PVDF (PVDF-g-IL) finally aggregated into ionic nanodomains with the size of 20⁻30 nm in the melt state. Therefore, novel PVDF nanocomposites with both homogenously dispersed CNTs and ionic nanodomains were achieved. Both carbon nanotubes and ionic nanodomains contributed to the enhancement of the dielectric constant of PVDF significantly. At the same time, such homogeneously dispersed CNTs along with the confined ions in the nandomains decreased current leakage effectively and thus led to the low dielectric loss. The final PVDF nanocomposites exhibited high dielectric constant, low dielectric loss and good flexibility, which may be promising for applications in soft/flexible devices.

[Adsorption Mechanisms Analysis of EfOM on PVDF Ultrafiltration Membranes Modified by SiO2 Using QCM-D and AFM].

To further unravel adsorption mechanisms of effluent organic matter (EfOM) on the PVDF ultrafiltration membranes modified by nano-silica particles from micro perspective during different filtration phases, the membranes were prepared by adjusting the dosage of nano-silicon. The adsorption of EfOM on the surface of the membranes and the interaction between EfOM and the membranes were measured by quartz crystal microbalance with dissipation monitoring (QCM-D) and atomic force microscopy (AFM).The QCM-D results suggested that adsorbing capacity and adsorption rate of EfOM on the hydrophilic surfaces were lower than on the hydrophobic surfaces. Meanwhile, it was found that EfOM underwent adsorption via two steps: In the initial 15 min stage, a rapid adsorption of EfOM accumulated onto the membrane surface; The change in dissipation still occurred when the EfOM adsorption frequency reached balance, which demonstrated that the adsorption of EfOM remained unchanged on the membrane surfaces, and changes in the conformation of adsorption layer still occurred. For the AFM force test, it was found that the EfOM-membranes and EfOM-EfOM interactions declined with the increase of hydrophily, which revealed the essential reason for the decrease of adsorbing capacity and adsorption rate. The combined utilization of QCM-D and AFM effectively explained the effect of modified membranes on adsorption mechanisms of EfOM.

PMN-PT/PVDF Nanocomposite for High Output Nanogenerator Applications.

The 0.7Pb(Mg1/3Nb2/3)O3-0.3PbTiO3(0.7PMN-0.3PT) nanorods were obtained via hydrothermal method with high yield (over 78%). Then, new piezoelectric nanocomposites based on (1-x)Pb(Mg1/3Nb2/3)O3-xPbTiO3 (PMN-PT) nanorods were fabricated by dispersing the 0.7PMN-0.3PT nanorods into piezoelectric poly(vinylidene fluoride) (PVDF) polymer. The mechanical behaviors of the nanocomposites were investigated. The voltage and current generation of PMN-PT/PVDF nanocomposites were also measured. The results showed that the tensile strength, yield strength, and Young's modulus of nanocomposites were enhanced as compared to that of the pure PVDF. The largest Young's modulus of 1.71 GPa was found in the samples with 20 wt % nanorod content. The maximum output voltage of 10.3 V and output current of 46 nA were obtained in the samples with 20 wt % nanorod content, which was able to provide a 13-fold larger output voltage and a 4.5-fold larger output current than that of pure PVDF piezoelectric polymer. The current density of PMN-PT/PVDF nanocomposites is 20 nA/cm². The PMN-PT/PVDF nanocomposites exhibited great potential for flexible self-powered sensing applications.