Studies on the electrostatic effects of stretched PVDF films and nanofibers.
Ontology highlight
ABSTRACT:
SUBMITTER: Lin Y
PROVIDER: S-EPMC8093351 | biostudies-literature |
REPOSITORIES: biostudies-literature
Similar Datasets
Project description:Polyvinylidene fluoride (PVDF) and poly(methyl methacrylate) (PMMA) blend films were prepared using biaxial stretching. The effects of PMMA content and stretching ratio on the crystallinity and β phase fraction of PVDF in blend films were investigated. The distributions of crystallinity and β phase fraction on variable locations were also studied. The results of FTIR and XRD showed that β phase appeared in PVDF/PMMA blends after extrusion and casting procedures. Although β phase fraction decreased after preheating, there was still an increasing trend during following biaxial stretching. More importantly, the increase in PMMA content improved β phase fraction, and the highest β phase fraction of 93% was achieved at PMMA content of 30 wt% and stretching ratio of 2×2. Besides, the reduction in PMMA content and the increase in stretching ratio improved the crystallinity of PVDF. The mechanical properties of the stretched films were significantly improved by increasing the stretching ratio as well. The uniform stress distribution on different regions of biaxial stretching films contributed to the uniform distribution of β phase fraction and crystallinity of PVDF with the aid of simulation. This work confirmed that biaxial stretching can be a candidate method to prepare PVDF/PMMA blend films with uniform distributions of comparable β phase and crystallinity of PVDF.
| S-EPMC8037939 | biostudies-literature
Project description:Energy harvested from human body movement can produce continuous, stable energy to portable electronics and implanted medical devices. The energy harvesters need to be light, small, inexpensive, and highly portable. Here we report a novel biocompatible device made of poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) nanofibers on flexible substrates. The nanofibers are prepared with electrospinning followed by a stretching process. This results in aligned nanofibers with diameter control. The assembled device demonstrates high mechanical-to-electrical conversion performance, with stretched PVDF-HFP nanofibers outperforming regular electrospun samples by more than 10 times. Fourier transform infrared spectroscopy (FTIR) reveals that the stretched nanofibers have a higher β phase content, which is the critical polymorph that enables piezoelectricity in polyvinylidene fluoride (PVDF). Polydimethylsiloxane (PDMS) is initially selected as the substrate material for its low cost, high flexibility, and rapid prototyping capability. Bombyx Mori silkworm silk fibroin (SF) and its composites are investigated as promising alternatives due to their high strength, toughness, and biocompatibility. A composite of silk with 20% glycerol demonstrates higher strength and larger ultimate strain than PDMS. With the integration of stretched electrospun PVDF-HFP nanofibers and flexible substrates, this pilot study shows a new pathway for the fabrication of biocompatible, skin-mountable energy devices.
| S-EPMC6418575 | biostudies-literature
Project description:This paper describes a simple electrospinning approach for fabricating poly(3-hexylthiophene) (P3HT)/poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) semiconductive nanofiber mat triboelectric nanogenerators (TENGs). Measurements of the electrical properties of the P3HT/PVDF-HFP semiconductive nanofiber TENGs revealed that the output voltage could be enhanced up to 78 V with an output current of 7 μA. The output power of the device reached 0.55 mW, sufficient to power 500 red light-emitting diodes instantaneously, as well as a digital watch. The P3HT/PVDF-HFP semiconductive nanofiber TENG could be used not only as a self-powered device but also as a sensor for monitoring human action. Furthermore, it displayed good durability when subjected to 20,000 cycles of an external force test.
| S-EPMC9437044 | biostudies-literature
Project description:Herein, we investigate the morphology, structure and piezoelectric performances of neat polyvinylidene fluoride hexafluoropropylene (PVDF-HFP) and PVDF-HFP/Co-ZnO nanofibers, fabricated by electrospinning. An increase in the amount of crystalline ?-phase of PVDF-HFP has been observed with the increase in Co-doped ZnO nanofiller concentration in the PVDF-HFP matrix. The dielectric constants of the neat PVDF-HFP and PVDF-HFP/2 wt.% Co-ZnO nanofibers are derived as 8 and 38 respectively. The flexible nanogenerator manipulated from the polymer nanocomposite (PVDF-HFP/Co-ZnO) exhibits an output voltage as high as 2.8?V compared with the neat PVDF-HFP sample (~120?mV). These results indicate that the investigated nanocomposite is appropriate for fabricating various flexible and wearable self-powered electrical devices and systems.
| S-EPMC5768784 | biostudies-literature
Project description:In recent years, several studies have validated the use of piezoelectric materials for in situ biological stimulation, opening new interesting insights for bio-electric therapies. In this work, we investigate the morphological properties of polyvinylidene fluoride (PVDF) in the form of microstructured films after temperature-driven phase transition. The work aims to investigate the correlations between morphology at micrometric (i.e., spherulite size) and sub-micrometric (i.e., phase crystallinity) scale and in vitro cell response to validate their use as bio-functional interfaces for cellular studies. Morphological analyses (SEM, AFM) enabled evidence of the peculiar spherulite-like structure and the dependence of surface properties (i.e., intra-/interdomain roughness) upon process conditions (i.e., temperature). Meanwhile, chemical (i.e., FTIR) and thermal (i.e., DSC) analyses highlighted an influence of casting temperature and polymer solution on apolar to polar phases transition, thus affecting in vitro cell response. Accordingly, in vitro tests confirmed the relationship between micro/sub-microstructural properties and hMSC response in terms of adhesion and viability, thus suggesting a promising use of PVDF films to model, in perspective, in vitro functionalities of cells under electrical stimuli upon mechanical solicitation.
| S-EPMC8470707 | biostudies-literature
Project description:Piezoelectric nanomaterial-polymer composites represent a unique paradigm for making flexible energy harvesting and sensing devices with enhanced devices' performance. In this work, we studied various metal doped ZnO nanostructures, fabricated and characterized ZnO nanoparticle-PVDF composite thin film, and demonstrated both enhanced energy generation and motion sensing capabilities. Specifically, a series of flexible piezoelectric nanogenerators (PENGs) were designed based on these piezoelectric composite thin films. The voltage output from cobalt (Co), sodium (Na), silver (Ag), and lithium (Li) doped ZnO-PVDF composite as well as pure ZnO-PVDF samples were individually studied and compared. Under the same experimental conditions, the Li-ZnO based device produces the largest peak-to-peak voltage (3.43 Vpp) which is about 9 times of that of the pure ZnO based device, where Co-ZnO, Na-ZnO and Ag-ZnO are 1.2, 4.9 and 5.4 times, respectively. In addition, the effect of doping ratio of Li-ZnO is studied, and we found that 5% is the best doping ratio in terms of output voltage. Finally, we demonstrated that the energy harvested by the device from finger tapping at ~2 Hz can charge a capacitor with a large output power density of 0.45 W/cm3 and light up an ultraviolet (UV) light-emitting diode (LED). We also showed the device as a flexible wearable motion sensor, where different hand gestures were detected by the device with distinctive output voltage amplitudes and patterns.
| S-EPMC7769214 | biostudies-literature
Project description:This paper presents a theory describing the dynamic nuclear polarization (DNP) process associated with an arbitrary frequency swept microwave pulse. The theory is utilized to explain the integrated solid effect (ISE) as well as the newly discovered stretched solid effect (SSE) and adiabatic solid effect (ASE). It is verified with experiments performed at 9.4 GHz (0.34 T) on single crystals of naphthalene doped with pentacene-d14. It is shown that the SSE and ASE can be more efficient than the ISE. Furthermore, the theory predicts that the efficiency of the SSE improves at high magnetic fields, where the EPR line width is small compared to the nuclear Larmor frequency. In addition, we show that the ISE, SSE, and ASE are based on similar physical principles and we suggest definitions to distinguish among them.
| S-EPMC9938721 | biostudies-literature
Project description:This study aimed to develop a novel hybrid piezoelectric structure based on poly(vinylidene difluoride) nanofibers (PVDF NFs) and zinc oxide nanorods (ZnO NRs) which eliminate the need for post poling treatment in such hybrid structures. Mechanism of electrical performance enhancement of the hybrid structure is also discussed in this paper. To study the effect of hybridization on piezoelectric performance, pristine ZnO NRs and pristine PVDF NF nanogenerators were also fabricated. The piezoelectric performance of these three nanogenerators was evaluated under periodic deformation at low frequency. The output power of the hybrid structure was found to be enhanced compared to pristine ZnO NRs and PVDF NFs nanogenerators. Such simple hybrid devices that do not need to complicated post poling treatment are more efficient than previous hybrid PVDF/ZnO nanogenerators for practical application. This improved piezoelectric nanogenerator is expected to enable various applications in the field of self-powered devices and wearable energy harvesting to harvest mechanical energy from the human activities.
| S-EPMC9062380 | biostudies-literature
Project description:Strategies to create thin films using layer-by-layer methods use oppositely charged polymeric polyelectrolytes for both or at least one component to beneficially exploit multitopic electrostatic interactions between the deposited layers with opposite charges. In contrast, the electrostatic deposition of tetracationic 5,10,15,20-tetrakis(1'-methyl-4'-pyridinio)porphyrin tetra(p-toluenesulfonate) (TMPyP(4+)) with tetraanionic polyoxometalates such as EuPW(11)O(39)(4-) or SiW(12)O(40)(4-) onto charged substrates, such as mica, or polar substrates, such as glass and indium-tin oxide (ITO), demonstrates that the use of polymeric components is not a priori necessary. The use of molecules in sequential dipping approaches requires a careful balance in the interaction energies between the oppositely charged molecules, as demonstrated by the observation that a tetraanionic porphyrin such as 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrin does not form layers with TMPyP(4+). In the present case, these systems require several rounds of dipping to obtain films of uniform coverage and durability. The thin films deposited onto glass, quartz, ITO, and mica are surprisingly robust, since they are not removed by sonication in either organic solvents or 100 mM NaCl.
| S-EPMC6257931 | biostudies-literature
Project description:Solid electrolytes are of high interest for the development of advanced electrochemical energy storage devices with all-solid-state architectures. Here, we report the fabrication of the electrolyte membranes based on LiTFSI (LiN(CF3SO2)2) and PEO-PVDF blends with improved properties. We show that addition of PVDF enables preparation of free-standing films of the compositions within the so called "crystallinity gap" of the LiTFSI-PEO system known to provide high ion conductivity. We show that optimal PVDF content enables preparation of the films with reasonable elastic modulus and high ionic conductivity of about 0.3 mS cm-1 at 60 °C and about 0.1 mS cm-1 at room-temperature. Combining FTIR spectroscopy, XRD and DSC measurements we show that a noticeable fraction of PVDF remains crystalline and enhances the mechanical properties of the material, and at the same time it additionally promotes LiTFSI dissociation and disordering. Density functional theory calculations showed that the Li+-PEO-PVDF complexation energy magnitude is almost as high as that of Li-PEO complexes, thus the salt dissociation ability can be retained in spite of the introduction of the substantial amounts of PVDF required for mechanical stability.
| S-EPMC9052884 | biostudies-literature