SENSORS AND ACTUATORS A-PHYSICAL
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2024
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IF 4.1
Ding Zhang,Renkun Zhang,Jiatai Sun,Jingxiang Zhang,Qiuying Zhao,Haiyan He,Huajie Huang,Lu Yang,Yuanping Xu
Recently, flexible pressure sensors rooting in piezoresistive mechanism have gained immense popularity due to their excellent application potential in the fields of software robotics, electronic skins and human health monitoring, etc. However, the trade-off between sensitivity and pressure range still remains challenging for the wide application of piezoresistive sensors . Herein, a novel flexible pressure sensor constructing from electrospun ionic liquids/Multi-walled carbon nanotubes/poly(vinylidene fluoride) (ILs/MWCNTs/PVDF) ternary composite that permits high-sensitivity detection over broad pressure range is implemented. Benefitting from the filamentous porous network coupled with urchin-shaped beads, the newly developed active ternary composite showed excellent compressibility and high sensitivity to pressure, endowing the resultant piezoresistive sensor with broad-pressure detection ranging from 1.0 Pa to 307 kPa with a maximum sensitivity of 0.075 kPa −1 . Simultaneously, the proposed sensor present fast response/recovery time of 120/80 ms and high operation stability over 14000 cyclic pressings. Also, the feasibility of sensor in effectively monitoring various physiological signals, recognizing keyboards and expressing spatial pressure distribution is demonstrated, implying their great potential as viable high-performance pressure sensor.
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高影响因子
ACS Applied Nano Materials
·
2024
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IF 5.3
Wenbin Sun,Huazhen Liu,Zilong Guo,Anqi Li,Chuang Gao,Chunxiang Lu,Wenjing Zhou,Jiantao Zhang,Yuanyuan Liu
Piezoelectric materials can actively provide a bioelectric microenvironment by converting mechanical stimulations into electrical signals. Combining the excellent flexibility of piezoelectric polymers and the outstanding piezoelectric properties of piezoelectric ceramics, piezoelectric composites are attractive in tissue repair due to their high response to micromechanical stimulations. However, issues such as agglomeration, dielectric differences, and poor interfacial contact with polymers have limited the role of ceramics in improving the overall properties of the composites. In this work, functionalized multiwalled carbon nanotubes (F-MWCNTs) are applied to disperse zinc oxide (ZnO) in the PVDF–TrFE matrix to prepare electrospun composite fiber films. Through the assistance of hydrogen bonding, F-MWCNTs act as bridges connecting ZnO nanoparticles with PVDF–TrFE, which improves the content and crystallinity of the β phase. Furthermore, this strategy enhances the local electric field and reduces dielectric differences, resulting in improved polarization and piezoelectric properties. Results show that the composite fiber film with 0.35 wt % F-MWCNTs could obtain an open-circuit voltage of up to 8.2 V, a β phase content of 83.36%, and a crystallinity of 57.63%. Meanwhile, due to the synergistic effect of F-MWCNTs and ZnO, the tensile strength and Young’s modulus are increased from 3.5 and 11.0 to 6.6 and 19.49 MPa, respectively. Additionally, cellular experiments show that composite fiber films have good bioactivity and promote cell proliferation and adhesion, especially with 0.35 wt % F-MWCNTs. In conclusion, the composite fiber film possesses good piezoelectric and mechanical properties and enhances the cellular activity, making it a good tissue engineering scaffold.
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高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2024
·Vol. 31
·期 19
·28695-28705
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IF 0
Liu Hongyu,Ye Wei,Zhang Huan,Wang Huicai,Wei Junfu
Here, polyaniline/polyvinylidene fluoride (PANI/PVDF) nanofiber composite membrane was fabricated using electrostatic spinning technology to remove hexavalent chromium Cr(VI). The employment of PANI not only extremely enhanced the hydrophilic property of the nanofiber membrane, but also facilitated the transfer of Cr 2 O 7 2− from water to the membrane. The PANI/PVDF membrane had an extremely excellent performance in getting rid of Cr(VI) and a quite large flux (250 L/m 2 h). The maximum adsorption quantity of the membrane could reach 334.5 mg/g in which adsorption played 52.12% part and reduction played 47.87% part. The removal rate could reach nearly 100% immediately in the permeate solution under filtration while it needed 240 min to reach 100% only by static adsorption. Therefore, the interception of the membrane and the adsorption reduction of PANI had synergistic effect on removal of Cr(VI). Furthermore, the removal rate of Cr(VI) could still reach 95.97% after reused 8 times. The membrane showed a very good reusability and application prospect. Graphical Abstract
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PubMed
Desalination and Water Treatment
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2024
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IF 1
Yiqiao Xie,Ling Yu,Yang Yu
The high-performance hydrophobic membranes are crucial for the practical application of membrane distillation (MD). The fluorination treatment or inorganic particle incorporation has been widely applied for improving the hydrophobicity of membrane surface. However, the economic and facile method for the fabrication of hydrophobic membranes is still urgently needed. In this study, the fluorinated graphene oxide (FGO) nanosheets were synthesized and used as hydrophobic additives for the polyvinylidenefluoride (PVDF) electrospun nanofiber membrane. The membrane hydrophobicity was greatly improved after the addition of FGO nanosheets due to their inherent strong hydrophobicity and the induced formation of finer nanofibers. In comparison to the control membrane (pristine PVDF membrane), the water flux of the proposed composite membrane with superior salt rejection efficiency of 99.9% was increased by 41.5% (22.2 L/m 2 .h) when treating 3.5 wt% NaCl solution at the temperature difference of 40 °C. The excellent stability of the prepared membrane was verified by a 120-h continuous AGMD operation. The findings from this study demonstrates the FGO nanosheets could be considered as promising materials for the fabrication of high-performance AGMD membranes to promote the application of large-scale AGMD in the desalination and water treatment.
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高影响因子
DESALINATION
·
2024
·
IF 8.3
Shuaijun Yu,Yazhen Jiang,Geting Xu,Edison Huixiang Ang,Zhipeng Xu,Junbin Liao,Jiangnan Shen
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 ( C H + = 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.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2025
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IF 13.2
Fei Bi,Zhemei Zheng,Rongrong Li,Ruiying Du,Li Zhao,Shanshan Xiao,Liyan Wang,Xiangting Dong
Photocatalytic composite membranes (BPMs) are preferred materials for wastewater treatment due to their high photocatalytic activity and ease of recovery. However, conventional blending modification methods for preparing BPMs often lead to drawbacks such as uneven distribution of photocatalysts, low loading efficiency, facile detachment of photocatalysts, poor reusability, and a limited specific surface area of the membranes. These issues significantly diminish their photocatalytic activity and restrict their practical applications. To address these challenges, this thesis introduces a novel preparation method for PVP-modified PVDF/BiOBr photocatalytic membranes, using a combination of electrospinning and solvothermal techniques. This approach enhances the stability of BiOBr microspheres on the PVDF nanofiber membranes, effectively tackling the issue of loading powder photocatalysts. These membranes, composed of PVDF nanofibers and uniformly sized BiOBr microspheres, exhibit a significant specific surface area of 15.69 m 2 /g. The modified PVDF/BiOBr photocatalytic membranes demonstrate remarkable degradation efficiencies: 100 % degradation of Rhodamine B (RhB) in 25 min, 93.8 % degradation of tetracycline (TC) in 30 min, and 74.6 % degradation of hexavalent chromium ions (Cr 6+ ) in 60 min. Moreover, after five cyclic experiments, the photocatalytic degradation rate of sample M 3 remains above 99 % with a minimal loss rate of only 0.5 %. The method developed for preparing PVDF/BiOBr photocatalytic membranes represents a universally applicable and straightforward strategy for fabricating advanced membrane materials. This preparation technique not only provides innovative design ideas and fabrication methods for new photocatalytic materials but also extends to other functional materials. The PVDF/BiOBr photocatalytic membrane materials hold great promise in offering technical and theoretical support for photocatalytic wastewater treatment.
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高影响因子
Particuology
·
2024
·
IF 4.1
Sijia Wang,Liang He,Mengting Wang,Xingtong Guo,Xiangyun Qiu,Shoudong Xu,Petr Senin,Ting Bian,Tao Wei
For all-solid-state lithium batteries (ASSLBs), polymer-blended solid composite electrolytes (SCEs) have drawn wide interest owing to their significance in improving the interfacial solid-solid contacts and inhibiting the growth of lithium dendrites . In this work, SCEs based on PVDF-HFP/PMMA matrix containing MOFs (NH 2 -MIL-53(Al)) and LiTFSI were designed and synthesized employing an easy solution casting method. The synthesized samples were examined by XRD , SEM, EDS , and electrochemical tests. It was found that MPP-2 SCE not only has excellent ionic conductivity at 60 °C of 5.54 × 10 −4 S cm −1 , but also exhibits superior interfacial compatibility in Li||Li symmetric batteries , which can constantly cycle for about 800 h at 0.1 mA cm −2 with no short-circuiting. The assembled Li|MPP-2|LiFePO 4 cell exhibited a first discharge specific capacity of up to 157.1 mAh g −1 at 60 °C and 0.2 C. This work may help to further advance the progress of ASSLBs in the future.
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高影响因子
JOURNAL OF MEMBRANE SCIENCE
·
2024
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IF 8.4
Shaojin Jia,Sha Yang,Yu Pan,Salah Ud Din,Yuanjie Cai
As an important part of the fields such as renewable energy and electric vehicles, electrochemical energy storage technology faces significant challenges in improving energy density , extending battery life and improving safety. We successfully prepared a composite battery separator of polyvinylidene fluoride-chlorotrifluorinylene (PVDF-CTFE) and fluorinated polyimide (F-PI) -based materials, mixed it with different contents of boehmite nanoparticles , and then modified it by different doses of electron beam irradiation to improve the performance, especially to overcome the problem of maintaining capacity decline in high-speed charging environment. The results showed that the prepared battery separators exhibited outstanding thermal stability, electrochemical properties and ionic conductivity with 12 % boehmite nanoparticles . After 1000 high-speed charge and discharge cycles in current density of 10C, the battery based on the modified separator still maintained a capacity retention rate of 84.4 %, with the initial discharge specific capacity of 111.9 mAhg −1 . This means that irradiated separators not only maintain a high energy density in a high-speed charging environment, but also overcome the problem of maintaining capacity decline. Electron beam irradiation further improved the comprehensive performance of the separator. After 1000 and 1500 cycles at the current density of 10C and 15C, the specific discharge capacity of the battery can still retain more than 90 % and 80 % of the initial specific discharge capacity, which provides a longer life in practical applications.
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高影响因子
ACS Applied Electronic Materials
·
2024
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IF 4.3
Bin Du,Yinuo An,Xianhua Huan,Liuqing Yang,Yushun Zhao
Polyvinylidene fluoride (PVDF) piezoelectric nanofibers gain significant attention for flexible electronic devices, yet their low piezoelectric conversion efficiency remains a critical barrier to broader application. In this study, multiwalled carbon nanotubes (MWCNTs) are combined with fullerene (C60) to form a distinctive “grape-like” nanostructure (MC), which is then embedded into the PVDF matrix via electrospinning to produce PVDF/MC composite nanofibers. The incorporation of MC increases the β-phase content of the PVDF nanofibers by 11.07%, enhancing their piezoelectric properties, and also acts as localized conductive domains and stress concentration centers, synergistically boosting the output performance of the piezoelectric devices. Consequently, piezoelectric devices based on PVDF/MC-3 wt % composite nanofibers exhibit voltage and current outputs 559.1% and 1382.8% higher than those of pure PVDF, respectively. This innovative strategy of leveraging “grape-like” nanostructures to enhance PVDF’s piezoelectric performance represents a promising pathway toward achieving efficient energy conversion in piezoelectric materials.
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高影响因子
Journal of Environmental Chemical Engineering
·
2025
·
IF 7.2
Tianyi Zhang,Bo Yang,Ming Hao,Xiaodong Hu,Yanbo Liu,Xiaoxiao Wang
Flexible piezoelectric nanogenerators (PENGs) are emerging as sustainable power sources for self-charging wearable electronic devices due to their capability to harvest mechanical energy from the environment. Here, we have developed a high-output flexible PENGs based on electrospun composite nanofibers involving poly(vinylidene fluoride) (PVDF), barium titanate modified by dopamine hydrochloride (PDA@BTO) with an enhanced electroactive phase. On addition of 3 wt % PDA@BTO nanoparticles, the electroactive β-phase of the PVDF is found to be intensified to ∼88.05% as account of the synergistic interfacial interaction between the PDA@BTO nanoparticles and the ferroelectric host polymer substrate on electrospinning. The introduction of carbon black (CB) promotes piezoelectric charge transfer and increases output power. The PBTO/CB/PVDF composite nanofibers delivered the highest V OC of 55 V and the optimal I SC 3.1 μA with 3% PBTO and 1% CB. The fabricated PENG based PBTO/CB/PVDF composite nanofibers successfully charged capacitors with capacities of 0.1 μF, 0.33 μF, and 1 μF to voltages of 1.9 V, 3.2 V, and 10 V within 400 s, respectively. The device has response time of 0.1 s and the d 33 piezoelectric constant of 1.7 pC/N. The piezoelectric devices exhibited minimal variation in voltage and excellent stability over 900 cycles and the prepared piezoelectric device can light up to 20 LEDs. The potential of the piezoelectric composite nanofiber membranes for assembling mechanical energy collectors and piezoelectric sensors was demonstrated.
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高影响因子
POLYMER ENGINEERING AND SCIENCE
·
2024
·
IF 3.2
Wenlong Ma,Tianxu Hao,Xinya Wang,Wei Zhang,Yonggui Li,Mingxing Chen
In this paper, a high-performance composite nanofiber membrane with excellent air filtration and dye degradation properties was prepared by incorporating MIL-53(Fe) nanoparticles into the electrospinning solution. The results showed that the filtration efficiency for PM2.5 of the PP/PVDF-HFP/MIL-53(Fe) composite nanofiber membrane reached up to 99.3% with the addition of 2 wt% MIL-53(Fe). Moreover, the composite nanofiber membrane exhibited steady filtration efficiency across different parameters, including air velocity, PM2.5 concentration, and extended testing time. Furthermore, the incorporation of MIL-53(Fe) significantly enhanced the removal efficiency of the composite nanofiber membrane toward Rh B, resulting in a remarkable 91% removal rate. The polymer/MOF composite nanofiber membranes prepared by simple and cheap electrospinning technology have a wide range of practical applications in the field of environmental protection. Highlights PPM composite nanofiber membrane was prepared via electrospinning method. MIL-53(Fe) nanoparticles were introduced to PPM composite nanofiber membrane. PPM composite nanofiber membrane showed excellent removal efficiency for PM2.5. PPM composite nanofiber showed a good removal performance for RhB in solution.
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高影响因子
Journal of Energy Chemistry
·
2025
·
IF 14.9
Vestince Balidi Mbayachi,Lixin Liang,Bao Zhang,Yaru Zhang,Guiming Zhong,Kuizhi Chen,Guangjin Hou
Composite polymer electrolytes (CPEs) are considered as promising electrolytes for next-generation lithium batteries due to their superior advantages in safety, mechanical stability/flexibility, cathode compatibility, etc. However, achieving high Li + conductivity remains a major challenge, particularly at low temperatures. A key obstacle lies in the limited understanding of the complex interplay among amorphous components, including fillers, plasticizers, and residual solvents, which significantly hampers the rational design of high-performing CPEs. In this contribution, a polyvinylidene fluoride (PVDF)-based composite electrolyte has been developed, exhibiting high room-temperature ionic conductivity/mobility (>1 mS cm −1 /0.95 × 10 −11 m 2 s −1 ), along with excellent electrochemical performances, including a wide stability window (4.8 V vs. Li/Li + ), superior charge/discharge capacity, and reversibility. By performing advanced solid-state nuclear magnetic resonance (ssNMR) techniques, in combination with systematic investigations into solid polymer electrolytes (SPEs), gel polymer electrolytes (GPEs), and CPEs, we establish an efficient NMR-based strategy for deconvoluting the structural and dynamic features of complex electrolyte systems. Notably, the simple 1 H magic-angle spinning (MAS) NMR spectroscopy enables the identification and monitoring of nearly all components in the composite matrix. Motion-Sensitive 1 H- 13 C and 1 H- 7 Li correlation experiments further reveal that the rigidity of PVDF polymer chain segments and the presence of residual solvents are two critical factors governing Li + mobility. Moreover, we demonstrate that the order of the filler and plasticizer addition during the CPE fabrication significantly influences the performance of the electrolyte by regulating the retention of residual solvents. This work not only provides molecular-level insights into the structure-ion mobility relationships in the PVDF-based CPEs but also establishes a general NMR-based characterization approach for investigating other complex composite electrolyte materials.
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高影响因子
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