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Scientific Reports · 2016 ·Vol. 6 ·期 1 ·1-8 · IF 5.228

Polarization of an electroactive functional film on titanium for inducing osteogenic differentiation

Zhou Zhengnan,Li Weiping,He Tianrui,Qian Lei,Tan Guoxin,Ning Chengyun

To enhance the surface bioactivity of titanium (Ti) prostheses, an electroactive polyvinylidene fluoride (PVDF) film was prepared on a Ti substrate to provide a mimetic of the electrical microenvironment, which facilitated the performance of cell functions. The results of cell proliferation and differentiation assays indicated that polarization of the PVDF-Ti (PTi) altered its surface charge, thus inducing adhesion, proliferation and osteogenic differentiation of cells. The polarized PVDF-Ti (PPTi) may therefore find applications in bone regeneration.

研究领域: 生物材料 · 组织工程 · 生物医学工程
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APPLIED SURFACE SCIENCE · 2018 · IF 4.439

Engineering a self-driven PVDF/PDA hybrid membranes based on membrane micro-reactor effect to achieve super-hydrophilicity, excellent antifouling properties and hemocompatibility

Jian-Hua Li,Xing-Xing Ni,De-Bin Zhang,Hui Zheng,Jia-Bin Wang,Qi-Qing Zhang

A facile and versatile approach for the preparation of super-hydrophilic, excellent antifouling and hemocompatibility membranes had been developed through the generation in situ of bio-inspired polydopamine (PDA) microspheres on PVDF membranes. SEM images showed that the PDA microspheres were uniformly dispersed on the upper surface and the lower surface of the modified membranes. And there were a great number of PDA microspheres immobilized on the cross-section, but the interconnected pores structure was not destroyed. These facts indicated the existence of membrane micro-reactor effect for the whole membrane structure. Considering the remarkable improvement of hydrophilicity, antifouling properties, and permeation fluxes, we also proposed the cluster phenolic hydroxyl effect for the PVDF/PDA hybrid membranes. And the cluster phenolic hydroxyl effect can be ascribed to the all directions distributed phenolic hydroxyl groups on the whole membrane structure. Besides, the self-driven filtration experiments showed the great wetting ability and permeability of the PVDF/PDA hybrid membranes in filtration process without any external pressure. This implied the existence of accelerating self-driven force after the water flow flowed into the internal of membranes, which contributed to the increase of water flow velocity. All the three aspects were in favor of the enhancement of hydrophilicity, antifouling properties and permeability of the modified membranes. Moreover, the conventional filtration tests, oil/water emulsion filtration tests and protein adsorption tests were also carried out to discuss the practical applications of PVDF/PDA hybrid membranes. And the hemocompatibility of the modified membranes was also proved to enhance greatly through the hemolysis tests and platelet adhesion tests, indicating that the membranes were greatly promising in biomedical applications. The strategy of material modification reported here is substrate-independent and can be extended to other substrate materials, and allows the development of novel functional membranes through secondary treatments.

CAS / MDL: 9048-46-8 85-83-6
研究领域: 材料科学 · 生物医学工程
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DALTON TRANSACTIONS · 2021 ·Vol. 50 ·期 25 ·8927-8937 · IF 4.39

Selective adsorption of malachite green (MG) and fuchsin acid (FA) by ZIF-67 hybridized polyvinylidene fluoride (PVDF) membranes

Ying Liu,Na Wang,Zhongqiao Sun,Yide Han,Junli Xu,Yan Xu,Junbiao Wu,Hao Meng,Xia Zhang

MOF/polymer hybrid membranes integrate the surface activity of MOFs and the advantages of PVDF membranes, and can be used as adsorption membranes in the efficient removal of target organics. In this work, a new hybrid membrane of ZIF-67/PVDF with varying ZIF-67 dosages has been fabricated through a facile mechanical blending followed by a lyotropic phase transition. Methods including field-emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), FT-IR analyses and surface hydrophobicity/hydrophilicity measurements are applied to characterize the structure, physicochemical properties and membrane performances. Two synthetic triarylmethane dyes, cationic malachite green (MG) and anionic fuchsin acid (FA), are chosen as the main adsorption targets to evaluate the adsorption capacities of the resulting ZIF-67/PVDF hybrid membranes. Interestingly, all of the ZIF-67/PVDF hybrid membranes exhibit distinctly favorable efficiencies and selectivities toward MG and FA compared to pristine PVDF, which proves the positive roles of ZIF-67 in the adsorption ability of the hybrid membranes. The adsorption conditions are optimized and the adsorption kinetics and thermodynamics are analysed to study the adsorption mechanism. The reusability and the structural stability of the hybrid membranes undergoing cyclic adsorption processes are also discussed. To the best of our knowledge, this is the first time that good adsorption capacities for MG and FA for these MOF/PVDF membranes have been reported. This work highlights the prospective applications of MOF/PVDF hybrid membranes in the rapid and effective removal of target organics in the treatment of waste water.

CAS / MDL: 10026-22-9
研究领域: 环境科学 · 材料科学 · 化学工程
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JOURNAL OF ELECTROCERAMICS · 2024 · IF 1.7

Ionic-conductive poly (vinylidene fluoride) polymer as a versatile binder to stabilize high-voltage LiCoO2 cathode materials

Wang Yikui,Tao Jianming,Wang Jiangjie,Chen Shaoyang,Yang Yanmin,Lin Yingbin

Serious structural irreversibility and interfacial side reactions pose major challenges for the stable operation of LiCoO 2 cathodes at high voltages. Herein, we report a polymer-based solid electrolyte (SLP) composed succinonitrile, LiTFSI and PVDF as a binder to address these issues. The SLP binder exhibits superior performance compared to traditional PVDF and PVDF binders with LiTFSI, with higher ionic conductivity (8.46 × 10 − 5 S cm − 1 at 30 ℃), lower activation energy of 0.38 eV and excellent adhesion. Even with just 3% SLP binder, LiCoO 2 cathode operating at a cutoff voltage of 4.6 V and loaded with ~ 6.0 mg cm − 2 active material demonstrates improved rate capability at higher compaction densities, delivering a discharge specific capacity of 146.5 mAh g − 1 after 100 cycles at 0.5 C-rate. The SLP binder not only enhances Li + conduction but also facilitates the formation of a stable cathode-electrolyte interphase, thus reducing the Li + diffusion barrier and interface polarization, and enhancing battery’s performance at low temperature. Furthermore, the SPL binder’s high compatibility and elasticity with the electrolyte mitigate irreversible structural changes and volume expansion in LiCoO 2 during cycling, leading to better preservation of the layered structure and lower internal stress for stable cycling under high temperatures. This strategy provides a novel interface protection idea for electroceramic cathode materials and may facilitate commercial development.

研究领域: 材料科学 · 电化学 · 电池技术
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Nano Energy · 2024 · IF 16.8

Biomimetic fiber of PVDF@Ag enabling the multimodal sensing for biomechanics and biomolecules integrated by textile carrier

Dongzhen Chen,Yang Li,Jianzhao Gao,Meng Zhang,Junhao Liang,Tao Fu,Xiaoming Wu,Xinhai He,Liangjun Xia,Weilin Xu

Intelligent wearables with integrated biomechanics and biomolecule multimodal sensing systems are crucial for personalized healthcare. However, the modes of action of biomechanics and biomolecule sensing work in different ways. Hence, a method for manufacturing biomimetic fibers made of polyvinylidene fluoride (PVDF)@silver (Ag) is initially devised, and a textile carrier serves as a link for multimodal sensing of biomechanics and biomolecules. PVDF nanofiber membranes are created using a one-step electrospinning process . Next, by lowering the silver ion’s reduction potential, compact and homogenous Ag nanoparticles (NPs) are formed in-situ on the high-curvature PVDF fibers. Consequently, a PVDF@Ag fiber membrane with a piezoelectric response and a localized surface plasmon resonance (LSPR) effect is created, making it suitable for wearable sensors that can detect secreta molecules as well as muscle movements. PVDF@Ag fiber is twisted, taking inspiration from the spiral structure of butterfly antennae. Compared to untwisted, twisted PVDF@Ag fiber, this produces a surface-enhanced Raman scattering (SERS) output signal that is more stable and can resist for signal attenuation caused by tensile deformation during wearable sensing. The “fingerprint” spectra of SERS enable noninvasive extraction and detection of secretion signals at sweat and respiration. Additionally, a plausible correlation between the range of secretions produced and health-related data is examined. Additionally, the integrated PVDF@Ag by polyester fabric exhibits superior air permeability , moisture absorption , and antimicrobial properties. And, this multimodal sensing mechanism has an algorithm implanted with deep learning support. All things considered, the PVDF@Ag fiber functions as a bridge between biomolecules and biomechanics, which is essential for applications involving wearable healthcare management.

CAS / MDL: 50-81-7
研究领域: 材料科学 · 生物医学工程 · 传感技术
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JOURNAL OF POLYMER SCIENCE · 2021 ·Vol. 59 ·期 5 ·412-427 · IF 0

Facile way of dynamically tailoring microporous structures in polyvinylidene fluoride films prepared by thermally induced phase separation

Bin Yang,Qinting Chen,Mengya Ding,Yang Pan,Peng Zhang,Shuqing Wang,Jiasheng Qian,Jibin Miao,Ru Xia,Peng Chen,You Shi,Youlei Tu

Polyvinylidene fluoride (PVDF) films were prepared via thermally induced phase separation (TIPS) using diphenyl carbonate as the diluter in an attempt to disclose the competitive relationship between crystal growth and droplet growth during phase separation process. By varying the quenching temperature different temperature gradient fields were established, which were theoretically evaluated via enthalpy transformation method. The effects of polymer concentration and quenching temperature on evolution of hierarchical morphologies in TIPS films were systematically investigated. According to the morphological characteristics, the cross-sectional morphology of the films with lower polymer concentration ( Φ P = 25%) could be divided into three layers; while that of higher polymer concentration counterpart ( Φ P = 55%) only presented a bi-layered structure. The reason for this could be ascribed to the effect of cooling rate on both crystal growth and droplet growth during TIPS process, which further determined the formation of the hierarchical structure in microporous films. With an increasing quenching temperature, both pore size and porosity of PVDF films increased, accompanied by an improvement on both thermal stability and dynamic mechanical thermal property. The present study could insightfully supply a facile route to fabricate structure-controllable microporous films of crystalline polymers via an appropriate regulation of the TIPS quenching parameters. Graphical Based upon the phase diagram of polyvinylidene fluoride (PVDF)/diphenyl carbonate (DPC) system, the effects of polymer concentration and quenching temperature on the morphologies in thermally induced phase separation (TIPS) films are quantitatively established. TIPS films with lower (below monotectic point) and higher (above monotectic point) polymer concentrations present three-layered and bi-layered hierarchical structures, respectively, primarily originating from the competition between crystal growth and droplet growth during the phase separation.

CAS / MDL: 102-09-0
研究领域: 材料科学 · 高分子工程 · 化学工程
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CERAMICS INTERNATIONAL · 2018 · IF 3.057

Enhanced dielectric properties and discharged energy density of composite films using submicron PZT particles

Guanliang Chen,Xiujuan Lin,Jianan Li,John G. Fisher,Yan Zhang,Shifeng Huang,Xin Cheng

Flexible dielectric composite films are highly desirable materials with potential application in capacitors due to their high energy density and discharged efficiency. However, agglomeration induced by the large surface energy of nanoparticles and their large dielectric losses are unfavorable to the improvement of energy density. Submicron lead zirconate titanate (PZT) particles have shown great potential as filler in achieving a high energy storage capacity because of their excellent dielectric properties and good dispersion. In this work, calcined PZT particles were used to prepare PZT/polyvinylidene fluoride (PVDF) composite films. The results showed that composite films of high quality could be obtained even with high contents of submicron PZT particles. The introduction of PZT particles significantly improved the dielectric performance of composite films compared with that of the pristine PVDF film. The discharged energy density of composite films with 10 vol% PZT particles achieved 6.41 J/cm 3 at 250 kV/mm. A high efficiency of 87.25% was obtained at 50 kV/mm. These findings confirm the feasibility of PZT particles as inorganic filler in composite films for energy storage applications.

CAS / MDL: 68-12-2
研究领域: 材料科学 · 电气工程 · 能量存储
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JOURNAL OF POWER SOURCES · 2022 · IF 9.794

PVDF-based electrolyte decorated by Li29Zr9Nb3O40 Li-ion conductor and electrochemical performance of related solid-state batteries

Jiahao Chen,Hong Zhang,Hongzhu Chen,Enjie Xia,Yanmei Wu,Zhicheng Li

Solid-state Li-ion batteries (LIBs) have recently attracted much attention for their high safety and energy density . Polyvinylidene fluoride (PVDF) is as a potential electrolyte for solid-state LIBs due to its high permittivity, wide voltage window and excellent thermal stability. Here, Y 3+ -doped Li 29 Zr 9 Nb 3 O 40 (LZNO) Li-ionic conductor with room temperature conductivity (σ 25 ) of 1.26 × 10 −4  S cm −1 is prepared. LZNO decorated PVDF-based composite solid electrolytes (CSEs) are fabricated. The PVDF-based CSE with 10% (mass ratio) of LZNO shows σ 25 of 2.34 × 10 −4  S cm −1 , and has thermal stability with melting temperature up to 332 °C and voltage window of 4.8 V. The assembled Li ( Ni 0.8 Co 0.1 Mn 0.1 ) O 2 |CSE|Li cells show initial specific discharge capacity of 216.7 mAh g −1 at 0.1 C, and exhibit high capacity and cycle performance. LiFePO 4 |CSE|Li cells display initial specific discharge capacity of 137.4 mAh g −1 at 0.5 C and high cycle performance. Addition of LZNO powder in CSEs can inhibit the dehydrofluorination of PVDF during the charge-discharge of cells, alleviate the deterioration of interface resistance, and greatly improve the specific discharge capacity of cells at high rates.

CAS / MDL: 90076-65-6 7585-20-8
研究领域: 材料科学 · 电化学 · 能源存储
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Journal of Environmental Chemical Engineering · 2025 · IF 7.2

Electrospun Mn-doped ZIF-67 composite nanofibers with high water stability for efficient adsorption of antibiotics in aqueous systems

Xiaolin Yue,Can Cui,Shaolin Deng,Lan Wang,Ping Li,Anhong Li,Yizhong Zhang,Rui Hao,Wenyuan Tan

Currently, Zeolitic imidazolate frameworks (ZIFs) face challenges in antibiotic adsorption due to their inherent difficulty in recovery and susceptibility to hydrolysis. To overcome these limitations, herein, Mn-doped ZIF-67 was synthesized via coordination modification and then electrospun with high-mechanical-strength polyvinylidene fluoride (PVDF) to produce Mn-ZIF-67@PVP/PVDF composite nanofiber membranes. Characterization results based on SEM, XRD, and FT-IR analyses demonstrate that the layered nanofiber membrane provides abundant attachment sites for Mn-ZIF-67. Antibiotic adsorption experiments further reveal that the composite membrane exhibits facile recyclability, with Mn-ZIF-67 retaining 80 % of its initial adsorption capacity after five consecutive cycles, while maintaining its crystalline structure and remarkable aqueous stability throughout repeated utilization. The composite membrane achieved maximum adsorption capacities of 583.43 mg/g for tetracycline (TC) and 122.42 mg/g for ciprofloxacin (CIP). The adsorption process followed pseudo-first-order kinetics and Langmuir isotherm models, while thermodynamic analysis revealed a spontaneous and endothermic nature. The adsorption performance showed minimal impact from coexisting ions and pH variations. These superior characteristics of enhanced adsorption performance, exceptional water stability, and convenient recoverability endow the Mn-ZIF-67@PVP/PVDF composite membrane with significant practical advantages over conventional ZIF materials for antibiotic removal applications.

研究领域: 环境科学 · 材料科学 · 纳米技术 · 化学工程 · 水处理
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Small Science · 2024 ·Vol. 4 ·期 7 ·2400046 · IF 11.1

Long-Lasting Hydrogen Evolution and Efficient Dew Harvest Realized via Electrospinning Polyvinylidene Fluoride Membrane on Hybrid Hydrogels

Jie Yu,Mengmeng Chen,Neng Hu,Weijia Wang,Lin Lei,Huiqing Fan,Peter Müller-Buschbaum,Qi Zhong

Long-lasting hydrogen evolution and efficient dew harvest is realized via electrospinning a polyvinylidene fluoride (PVDF) membrane on hybrid hydrogels embedded with photocatalytic g-C 3 N 4 /Pt nanosheets. Due to the hindrance of water evaporation by the hydrophobic PVDF membrane, the drying process of the hybrid hydrogels significantly slows down. Hence, the g-C 3 N 4 /Pt nanosheets can continue working on photocatalytic splitting of the water molecules in the hydrogels. When the thickness of the PVDF membrane is 48 μm, the hydrogen evolution rate can reach 2,543 μmol h −1 g −1 , which is 38% more than that of the hybrid hydrogel without covering. Therefore, the hybrid hydrogels covered with PVDF membrane are able to work with high efficiency for 12 h, sufficient for hydrogen evolution during the daytime. In addition, the hydrophobic PVDF membrane and hydrophilic hydrogels construct a Janus structure and induce a fast transport of water molecules from the hydrophobic to hydrophilic side. It is beneficial for the rapid collection of dew in the morning. Based on the long-lasting hydrogen evolution and efficient dew harvest, the present hybrid hydrogels covered with PVDF membrane are very suitable for the environment rich in solar resource and lack of water supply, such as desert or prairie.

研究领域: 材料科学 · 环境科学 · 化学 · 能源科学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2019 · IF 6.361

Preparation of mixed-matrix membranes from metal organic framework (MIL-53) and poly (vinylidene fluoride) for use in determination of sulfonylurea herbicides in aqueous environments by high performance liquid chromatography

Jiping Ma,Shuang Li,Gege Wu,Shasha Wang,Xiaotong Guo,Liyan Wang,Xiaoyan Wang,Jinhua Li,Lingxin Chen

Novel mixed-matrix membranes (MMM) were prepared from metal-organic frameworks (MOF) (MIL-53) and poly (vinylidene fluoride) (PVDF), viz MIL-53–PVDF MMM, for the simultaneous dispersion membrane extraction (DME) of seven sulfonylurea herbicides (SUs) in aqueous environments followed by high performance liquid chromatography (HPLC) determination. The MIL-53–PVDF MMM was well characterized and major factors influencing DME performances were systematically investigated including membrane type, MOF dosage, eluent type, solution pH, extraction/elution time and salinity, etc. Under optimal conditions, the MIL-53–PVDF MMM based DME coupled with HPLC exhibited excellent linearity within 0.03–10 μg L −1 for chlorimuronethyl and 0.01–10 μg L −1 for other six SUs individual. High enrichment factor of 250 was obtained, as well as low detection limits and quantification limits ranged from 3.75 to 10.30 ng L −1 and 12.49–34.30 ng L −1 , respectively. Furthermore, the method attained high recoveries of 77.20–111.00% at three spiking levels of SUs, with relative standard deviations of 1.28–14.67% in tap water, seawater and surface water samples. Additionally, the MMM was readily separated from water and well regenerated, and could keep about 80% recovery after 25 cycles. Compared to that reported extraction materials, the MIL-53–PVDF MMM possessed the advantages of high enrichment ability, excellent reusability, good practicality and easy separation, indicating it was a promising alternative for the enrichment of SUs from aqueous environments.

CAS / MDL: 7784-27-2 74222-97-2
研究领域: 环境科学 · 分析化学 · 材料科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Film electrode Li1-xMn2O4/C/PAA-c-CMCLi-b-PVDF by double cross-linking for selective extraction of Li+

Zhihua Zhang,Xiao Du,Zheng Zhang,Qinglong Luo,Zhonglin Zhang,Jun Li,Xiaogang Hao

Because of its excellent stabilities, polyvinylidene fluoride (PVDF) is commonly employed as a binder in electrode fabrication. However, poor adhesion and hydrophilicity limit its applicability. Herein, PVDF as the hydrophobic framework, polyacrylic acid (PAA), and carboxymethylcellulose lithium (CMCLi) composite binders were cross-linked with phytic acid and Li 1-x Mn 2 O 4 /C were used in the formulation. After 100 electrochemical cycles, the film electrode Li 1-x Mn 2 O 4 /C/PAA- c -CMCLi- b -PVDF exhibits excellent adhesion (0.93 N cm −1 ) and a low capacity fading rate (8.2 %). Furthermore, this film electrode demonstrated a high intercalation capacity (32.14 mg g −1 ), a short intercalation equilibrium time (within 2 h), and a fast Li + intercalation rate, which can be attributed to the synergistic effect of electrolyte permeability enhanced by hydrophilic functional groups (–OH and –COOH), dispersibility of electrode material particles improved by high slurry rheology, and the high transport efficiency of –COOH for Li + . These promising results suggest that this double cross-linked Li 1-x Mn 2 O 4 /C/PAA- c -CMCLi- b -PVDF film electrode is suitable for the selective extraction of Li + .

研究领域: 材料科学 · 电化学 · 电池技术
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