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JOURNAL OF APPLIED POLYMER SCIENCE · 2026 ·Vol. 143 ·期 43 ·e71497 · IF 3.1

Functional Cellulose Acetate/PVDF Binary Piezoelectric Membranes Toward Reducing Self-Discharge in Solid-State Supercapacitors

Qijie Wu,Wenjuan Li,Kewei Shu

Supercapacitors are high-power-density energy storage devices essential for applications requiring rapid energy delivery. However, their practical implementation is often hindered by significant self-discharge. Functional separators capable of regulating ion transport offer an effective strategy to mitigate self-discharge without compromising electrochemical performance. In this work, a functional binary piezoelectric membrane based on cellulose acetate (CA) and poly(vinylidene fluoride) (PVDF) is fabricated via electrospinning and employed as a high-performance separator. The electrospun PVDF matrix provides intrinsic piezoelectricity, enabling the modulation of ion flux via a built-in electric field. Meanwhile the incorporation of CA significantly enhances electrolyte affinity, liquid uptake, and mechanical integrity. Benefiting from high porosity, and strong polarity, the separator delivers outstanding electrochemical performance in solid-state supercapacitors, achieving a high specific capacitance of 194.5 F g −1 at 0.5 A g −1 with over 10,000 stable cycles. Crucially, the functional separator effectively suppresses the self-discharge rate to ~18.7 mV h −1 and retains 44% of the initial voltage after 24 h, which is an approximately 28% improvement in charge retention over the commercial separator. This work demonstrates that electrospun piezoelectric CA/PVDF composite membranes are promising functional separators for next-generation supercapacitors with low self-discharge.

✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING RESEARCH & DESIGN · 2026 · IF 4

Superhydrophobic MXene/PVDF composite membrane with in-situ Joule heating for ultra-high water production

Hangyang Chen,Shuya Lou,Jun Yuan,Jing Huang,Weiquan Lin,Jiqing Wan,Bing Zhu,Chuanshuai Dong

Conventional Seawater desalination membrane distillation technology suffers from reduced efficiency due to temperature polarisation, severely limiting its practical application. To address this challenge, this study employs surface grafting modification of MXene with HTEOS to fabricate MXene-based composite membranes with hydrophobic properties. The composite membrane exhibits outstanding Joule heating response under DC voltage, demonstrating excellent cycling stability with the cycle-to-cycle peak-temperature fluctuation remained below 2.6% over 20 on/off cycles. Building upon this, a novel in-situ heating-enhanced sweep gas membrane distillation (SGMD) system was established to investigate the influence of operating parameters—including gas flow rate—and in-situ heating on transmembrane permeation flux. Experimental results indicate that the optimum MXene-to-HTEOS hydrolysate volume ratio was 10:2, yielding a water contact angle of 145.0 °. Compared with the PVDF membrane without Joule heating, the maximum flux enhancement of MXene-P@PVDF membrane reached 134.4% at a gas flow rate of 0.1 m 3 ·h −1 under 10 V. At a feed temperature of 40℃, a gas flow rate of 0.3 m 3 ·h −1 , and a liquid flow rate of 10 mL·min −1 , the permeation flux increased from 0.793 to 1.827 kg·m −2 ·h −1 . This substantially improves MD efficiency while mitigating temperature polarisation effects.

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FirePhysChem · 2026 · IF 5.1

Rational Design of Al@PVDF@HMX Composite Energetic Material Exhibits Ultra-high Heat of Explosion

Ying-Nan Dong,Yi-Fan Jiang,Wei-Qiang Pang,Feng-Qi Zhao,Ding Liu,Jing-Ni Wang,Chang Nie,Wen-Gang Qu

Enhancing the combustion efficiency of aluminum (Al) is a crucial research direction for solid propellants. Constructing an efficient fuel-oxidizer interaction environment through interfacial regulation is an effective approach. In this work, a synergistic strategy integrating polyvinylidene fluoride (PVDF)-mediated interface regulation with core-shell structuring was adopted to fabricate a dual-layer core-shell Al@PVDF@HMX composite energetic materials (EMs). This composite exhibits an ultra-high heat of explosion (8416.8 J·g⁻¹), which is over 52.8% higher than that of the Al+HMX physical mixture. Explosion residue measurements show that the primary combustion products were AlN and Al₂O₃, and no large Al agglomerations were detected, meaning that the inhibition of Al particle agglomeration by the dual-layer core-shell structure and the shell-breaking combustion effect induced by PVDF should be the key factors for the heat of explosion enhancement. Simultaneously, it was demonstrated that the composite is superior safety to HMX, as its impact sensitivity (8%) and friction sensitivity (36%) are decreased by 91% and 64%, respectively. This work indicates that the dual-layer core-shell structured Al@PVDF@HMX can synergistically improve the reaction between Al and HMX, providing a new approach to improve the energy efficiency and safety of EMs.

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Nanomaterials · 2026 ·Vol. 16 ·期 11 ·664 · IF 4.8

Processing-Enhanced β-Phase Formation in BaTiO3/PVDF Composite Fibers with High Electroactive Phase Content

Marouene Ben Ouali,Anik Das,Chayma Ben Harrath,Xu Lei,Rony Mia

Flexible piezoelectric fibers are promising materials for next-generation wearable and flexible electronic devices due to their lightweight structure, mechanical flexibility, and electromechanical response. In this study, BaTiO3/PVDF composite fibers were prepared by melt spinning under an electrostatic field, followed by thermal drawing to enhance the electroactive phase content. The effects of BaTiO3loading, draw ratio, thermal stretching ratio, stretching rate, and electric field strength on the crystalline structure of the fibers were systematically investigated. Fourier transform infrared spectroscopy, X-ray diffraction, differential scanning calorimetry, and electron microscopy were used to evaluate phase evolution, crystallinity, and filler distribution. The results showed that the processing conditions significantly influenced the transformation of PVDF from the α-phase to the electroactive β-phase. The optimized fibers were obtained at 1 wt.% BaTiO3, a thermal stretching ratio of 5, a stretching rate of 40 mm/min, and an electric field strength of 18 kV, resulting in a crystallinity of 61.3% and a β-phase content of 95.5%. The enhanced structural characteristics indicate the strong potential of the developed composite fibers for flexible electroactive applications, though direct electromechanical characterization is required for device integration.

✓ 已验证 DOI PubMed 高影响因子
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COMBUSTION SCIENCE AND TECHNOLOGY · 2025 · IF 1.5

Study on AP and PVDF for Improving the Ignition and Combustion Performance of Boron Particles

Haitian Gong,Daolun Liang,Mengxia Sun,Jianzhong Liu

Boron (B) particles offer the advantage of high energy density for ramjet applications but suffer from challenges including difficult ignition, low combustion efficiency, and agglomeration. This study employed ammonium perchlorate (AP), a common propellant oxidizer, and polyvinylidene fluoride (PVDF), a fluorine-containing compound, to improve the ignition and combustion characteristics of boron particles. Two types of samples were prepared: boron particles coated with AP, and boron particles mechanically mixed with PVDF. Thermal analysis indicated that both AP coating and PVDF addition facilitated the thermal decomposition of boron, significantly lowering its decomposition temperature. Laser ignition experiments under two different atmospheres revealed that AP coating consistently intensified boron combustion. The ignition delay time was reduced and the combustion temperature was increased. However, the effectiveness of PVDF addition may be influenced by the ambient oxygen concentration. Consequently, both AP coating and PVDF addition are advantageous for enhancing boron combustion.

CAS / MDL: 24937-79-9
研究领域: 含能材料 · 燃烧科学 · 推进剂技术 · 材料工程
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JOURNAL OF APPLIED POLYMER SCIENCE · 2025 · IF 2.8

Asymmetric Bilayer PA6@Co/AgNWs/PVDF Composite Enabling Absorption-Dominant High-Efficiency Electromagnetic Interference Shielding

Bozhen Wu,Xuejiao Song,Yongkang Meng,Yanghua Song,Zhongpu Shi,Yan Liu

Advances in electronic device miniaturization and system integration, alongside rapid progress in wireless communication technologies, have significantly amplified electromagnetic interference problems. This development necessitates the creation of high-performance electromagnetic shielding materials. This study presents a new design for electromagnetic shielding composites comprising an asymmetric structure of cobalt-coated nylon 6 microspheres (PA6@Co), silver nanowires (AgNWs) and poly(vinylidene fluoride) (PVDF). Specifically, PA6 microspheres were prepared using anionic reaction-induced phase separation, and cobalt was plated on their surfaces, thereby forming magnetic PA6@Co microspheres. The magnetic saturation intensity of these microspheres can reach 80 emu/g. The asymmetric PA6@Co/AgNWs/PVDF electromagnetic shielding composites with absorption-dominant characteristics were constructed using AgNWs as the conductive filler and PVDF as the matrix. The results show that within the X-band (8.2–12.4 GHz) range, the PA6@Co/AgNWs/PVDF composite material exhibits excellent electromagnetic shielding performance. Its maximum electromagnetic shielding efficiency (SET) reaches 48.1 dB, and the absorption coefficient (A) is 0.8, demonstrating a distinct absorption-dominant shielding characteristic. This asymmetric structural design strategy solves the limitations of traditional shielding materials and provides a new approach to developing environmentally friendly, efficient electromagnetic shielding materials.

研究领域: 材料科学 · 电磁功能材料 · 纳米复合材料 · 聚合物复合材料
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Membranes · 2025 ·Vol. 15 ·期 7 ·216 · IF 3.6

High-Performance Thin Film Composite Nanofiltration (NF) Membrane Constructed on Modified Polyvinylidene Fluoride (PVDF) Substrate

Junliang Dong,Qianzhi Sun,Xiaolin Feng,Ruijun Zhang

The inherent hydrophobic nature of PVDF material renders it challenging to establish a stable aqueous hydration layer, thereby limiting its suitability as a substrate for the preparation of nanofiltration (NF) membranes. In this study, we developed a novel modification approach that effectively enhances the hydrophilicity of PVDF substrates through the incorporation of sulfonic acid-doped polyaniline (SPANI) and hyperbranched polyester (HPE) into the PVDF casting solution, followed by cross-linking with trimesoyl chloride (TMC). The introduction of SPANI and HPE, which contain reactive polar amino and hydroxyl groups, improved the hydrophilicity of the substrate, while the subsequent cross-linking with TMC effectively anchored these components within the substrate through the covalent linking between TMC and the reactive sites. Additionally, the hydrolysis of TMC yielded non-reactive carboxyl groups, which further enhanced the hydrophilicity of the substrate. As a result, the modified PVDF substrate exhibited improved hydrophilicity, facilitating the construction of an intact polyamide layer. In addition, the fabricated TFC NF membrane demonstrated excellent performance in the advanced treatment of tap water, achieving a total dissolved solid removal rate of 57.9% and a total organic carbon removal rate of 85.3%. This work provides a facile and effective route to modify PVDF substrates for NF membrane fabrication.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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JOURNAL OF ELECTRONIC MATERIALS · 2025 · IF 2.5

Fabrication of Humidity Sensors Based on Nitrogen-Doped Graphene Quantum Dot-Embedded PVDF/TPU Membrane

Zhu Xingwei,Cheng Yongchao,Gu Xiuquan

A flexible temperature and humidity sensor has been developed based on a composite of polyvinylidene fluoride (PVDF) and thermoplastic polyurethane (TPU). The sensor performance was optimized by introducing graphene quantum dots (NGQDs) and ionic liquids (TFSI) into the polymer composite. This type of humidity sensors has high sensitivity, fast response, and excellent stability, making it suitable for use in wearable health monitoring. The addition of TPU into PVDF facilitates the formation of a porous structure which has both a large specific surface area and high hydrophilicity. After optimizing the PVDF/TPU mass ratio to 5:3, such a humidity sensor displays 1.46 times higher sensitivity than that of pure PVDF film, with a linear response range of 10–90% relative humidity. The response time and recovery time are 7.67 s and 6.37 s, respectively. Owing to the improved hydrophobicity, the sensors also exhibit a good stability in a high humidity environment for > 10 days without significant degradation. Moreover, such a composite also has the capability to distinguish normal breathing from rapid breathing, demonstrating its potential in wearable health monitoring.

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CHINESE JOURNAL OF CHEMICAL ENGINEERING · 2025 · IF 3.7

Efficient leukocyte removal and enhanced biocompatibility using PVDF membranes prepared by vapor-induced phase separation

Ziqi Jin,Shuang Yao,Liang Li,Siyuan Sun,Yue Zhou,Jie Zhou,Zhaohui Wang,Zhaoliang Cui

To develop an efficient filter for removing white blood cells from whole blood, hydrophilic large-pore blended membranes of poly(vinylidene fluoride) (PVDF), polyvinyl pyrrolidone and polyethylene glycol, with good biocompatibility, were prepared using the process of vapor-induced phase separation at various PVDF concentrations. The results demonstrated that at a PVDF mass concentration of 14%, the membrane had increased surface roughness, significantly enhanced hydrophilicity and wettability, and a wetting time of 8 s. The surface roughness of the membrane was also reduced to 31.637 nm. Furthermore, hemolysis rate and protein adsorption tests indicated that the blended membranes possessed excellent biocompatibility. They were reduced to 2.48% and 34.44 μg·cm –2 , respectively. The pore size of the fabricated membrane was relatively large, which reached approximately 8 μm respectively, satisfying the filtration requirements. Lastly, the effects of different temperatures and multi-layered filters on leukocyte removal and the retention of red blood cells and platelets from whole blood were evaluated. The results revealed that the leukocyte removal rate was highest at 4 °C and with three membrane layers, the leukocyte removal rate was highest, reaching 98.36%, while the RBC and platelet content remained nearly unchanged compared with the original blood. This study provides a new approach for blood cell separation that is expected to play a significant role in medical fields such as blood transfusion demonstrating great potential for application and innovation.

CAS / MDL: 111-30-8 127-19-5
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PROGRESS IN ORGANIC COATINGS · 2025 · IF 7.3

Robust, transparent, and superhydrophobic PVDF-TrFE/PDMS nanofiber coatings for anti-fogging and anti-icing

Alix Marcelle Sansi Seukep,Damas Rossel Pandzou,Zhixiang Cui,Dhandapani Kuzhandaivel,Lionel Kinkpe,Xuan Zhou,Zixiang Weng,Longhui Zheng,Jianlei Wang,Xiaohong Ding,Lixin Wu

Superhydrophobic coatings often present a trade-off between transparency and mechanical robustness for glass substrates. Inspired by the general concept of natural superhydrophobic surfaces, a highly transparent superhydrophobic anti-icing composite coating based on a Polyvinylidene fluoride-trifluoroethylene (PVDF-TrFE)/Polydimethylsiloxane (PDMS) blend polymer via electrospinning technology has been developed. By constructing a PVDF-TrFE/PDMS nanofiber network on a silanized trimethylsilane (TMS-s) /polydimethylsiloxane (PDMS) promoter layer (which acts as an interface-strengthening layer), the gradient structure design of the functional coating on the glass substrate was successfully realized. Experimental results demonstrate that the TMS-s/PDMS promoter layer significantly enhances the interfacial bonding strength between the PVDF-TrFE/PDMS nanofibers and the glass substrate, achieving a water contact angle of 154.1° ± 4°, a sliding angle of 3° ± 1°, and approximately 92.6 % transmittance. The adhesion-enhancing mechanism is further investigated through molecular dynamics simulation analysis. Results reveal that the introduction of TMS-s increases interfacial adhesion, attributed to strong siloxane bonds formed between TMS-s and the glass surface, as well as Si-O-C bonds between TMS-s and PDMS. This combination of interactions significantly improves the coating's mechanical robustness. This study provides a novel strategy for multifunctional protective coatings in applications such as building windows, solar panels, automotive windshields, and aircraft windows.

CAS / MDL: 75-79-6
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Journal of Environmental Chemical Engineering · 2025 · IF 7.2

Mechanism of piezoelectric field-enhanced electron transfer during peroxymonosulfate activation with MoS2/PVDF-HFP films

Tingting Cao,Liping Lin,Yanan Li,Wangshu Tong

Piezoelectric molybdenum disulfide (MoS 2 ) has emerged as a promising candidate for peroxymonosulfate (PMS) activation in advanced oxidation processes (AOPs), yet the mechanistic role of its piezoelectric field, particularly regarding the electron transfer process, is not fully understood. Herein, we construct a MoS 2 /PVDF-HFP (MP) piezoelectric composite film stimulated by ultrasound to elucidate the piezoelectric field's enhancement effect on PMS activation for singlet oxygen ( 1 O 2 ) generation. Notably, the ultrasound-induced piezoelectric field enhanced 1 O 2 production by 26-fold compared to the non-piezoelectric system, leading to significantly improved degradation efficiency (≈94 % within 60 min) of methylene blue (MB). Through a combination of experimental analysis and density functional theory (DFT) calculations, we demonstrate that the piezoelectric field enhances the adsorption of PMS onto the MoS 2 surface (evidenced by a change in adsorption energy from –0.33 eV to –0.42 eV) and facilitates interfacial electron transfer (with an increase of 0.04 e⁻ transferred per PMS molecule), thereby promoting the conversion of PMS to 1 O 2 . This work elucidates the enhancement mechanism of the electron transfer process in the MoS 2 -PMS system and provides a film-based strategy for designing efficient, ultrasound-driven piezoelectric AOPs targeting selective 1 O 2 generation.

研究领域: 环境科学 · 材料科学 · 化学工程 · 物理化学 · 纳米技术
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Nanoscale · 2025 · IF 5.1

Hydrophilicity modification of Nanostructured PVDF based Surface Acoustic Wave Resonators for Ultra-sensitive Humidity Sensing

Yunzheng Zhao,Qianqian Lin

Humidity sensing is of great importance in monitoring moisture levels in the air, which directly impacts health, safety, comfort, and industrial processes. However, current humidity detection technologies still fall short in meeting the requirements of higher-end applications. In this work, high-performance humidity sensors were developed by tuning the hydrophilicity and hydrophobicity of polymer blends composed of PVP, PEG, and PVDF, which were integrated onto the surface of surface acoustic wave (SAW) resonators. By carefully adjusting the blend ratio, a porous and layered nanostructure was achieved, significantly enhancing humidity sensing performance. The optimized sensors exhibited a rapid response time of 2.2 s, a short recovery time of approximately 1.2 s, and a large frequency shift of up to 14 MHz under 15–98% RH. In addition, the devices maintained stable operation for over 2000 seconds with neglegible hysteresis, outperforming commercial counterparts in both sensitivity and response speed. These results demonstrate the great potential of the proposed sensor design for future applications requiring fast, accurate, and reliable humidity sensing.

CAS / MDL: 68-12-2
研究领域: 传感器 · 材料科学 · 纳米技术 · 高分子科学 · 电子学 · 声学
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