Journal of Energy Storage
·
2026
·
IF 10.7
Xinze Wu,Hu Wang,Jiangchao Chen,Pengfei Pang,Haiping Li,Kunpeng Jiang,Yunyun Zhao,Wenping Liu,Guisheng Zhu,Huarui Xu
Dendrite growth and interfacial instability in conventional liquid electrolytes limit the practical application of lithium metal batteries (LMBs). Composite solid electrolytes (CSEs) offer a promising alternative, yet challenges remain in achieving high ionic conductivity and low interfacial resistance. In this study, a series of sponge-like porous Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 @PMMA/PVDF-HFP CSE membranes (LPPH1:x) were fabricated via phase separation-solution casting. A multistage ion transport channel was constructed through the synergistic combination of the polymer matrix, inorganic fillers, and liquid electrolytes. The incorporation of PMMA suppressed the crystallization of PVDF-HFP, while the ester groups in PMMA facilitated Li salt dissociation through coordination with Li + . LPPH1:3 exhibited optimal comprehensive performance: a high ionic conductivity of 2.75 × 10 −3 S·cm −1 at room temperature, a Li + transference number of 0.62, and an electrochemical stability window of 4.9 V. Moreover, the symmetric cell demonstrated stable cycling for over 2000 h at 0.2 mA·cm −2 . The LiFePO 4 full cell retained 96.4% capacity after 200 cycles at 0.5C. Post-cycling characterization confirmed that LPPH1:3 suppressed lithium dendrite growth and maintained a stable interfacial structure. This work provides an innovative material design strategy and theoretical foundation for developing high-performance solid-state LMBs.
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高影响因子
JOURNAL OF POLYMER SCIENCE
·
2025
·
IF 3.6
Jian-Wu Xiao,Dong-Dong Mai,Dong-Liang Shi,Guo-Cui Bao,Yin-Qian Lu,Li-Bao Chen,Xiao-Ying Pei,Jing-Shui Xu,Fu-An He,Kwok-Ho Lam
The CoFe 2 O 4 @reduced graphite oxide (rGO) was prepared by a one-step solvothermal reaction, and then the Ag nanoparticles were deposited on the CoFe 2 O 4 @rGO by a green mild reduction reaction to form the novel Ag-CoFe 2 O 4 @rGO filler, followed by the modification of Ag-CoFe 2 O 4 @rGO using hexadecyltrimethoxysilane to form the novel H-Ag-CoFe 2 O 4 @rGO filler. The homogeneous distribution of the Ag-CoFe 2 O 4 @rGO and H-Ag-CoFe 2 O 4 @rGO fillers in the polar PVDF plastic polymer and nonpolar SBS elastomer copolymer, respectively, to form the corresponding composites was proved by SEM. The polar crystal content of the PVDF matrix in the Ag-CoFe 2 O 4 @rGO(10 wt.%)/PVDF composite was 36.13%, while the corresponding value for pure PVDF was 29.38%. The dielectric constant at 1000 Hz of Ag-CoFe 2 O 4 @rGO(10 wt.%)/PVDF and H-Ag-CoFe 2 O 4 @rGO(10 wt.%)/SBS composites was 15.54 and 2.78, respectively, while the corresponding values for pure PVDF and pure SBS were 8.39 and 2.05, respectively. Additionally, although both pure PVDF and pure SBS were non-magnetic, the magnetization values of Ag-CoFe 2 O 4 @rGO(10 wt.%)/PVDF and H-Ag-CoFe 2 O 4 @rGO(10 wt.%)/SBS composites were 0.83 emu/g and 0.47 emu/g, respectively, at 50,000 Oe. The as-prepared Ag-CoFe 2 O 4 @rGO/PVDF and H-Ag-CoFe 2 O 4 @rGO/SBS composites should have the potential for different applications including dielectric capacitors, dielectric elastomers, sensors, EMI shielding, and so on. Graphical Preparation process of CoFe 2 O 4 @rGO and Ag-CoFe 2 O 4 @rGO hybrid filler.
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高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2021
·
IF 7.312
Zhiqiang Sun,Panpan Wang,Dongwei Lu,Caihong Liu,Jun Ma
Three dimensional (3D) poly(N-vinylpyrrolidone)-grafted-mesoporous silica (MS-g-PVP) was first synthesized, and explored as a filler for enhancing filtration performance of poly(vinylidene fluoride) (PVDF) composite membrane in this study. Membrane structure, interfacial property and filtration performance of the composite membranes were studied in detail. The relationships of mesoporous silica properties with membrane performance was systemically revealed. The 3D morphology of MS-g-PVP, that stably anchored in PVDF, endowed the membrane with defects-free, uniform and straight finger-like pores structure, and thus greatly enhanced water flux (maximized to 80.7 L m -2 h −1 , over 5.7 times than that of pristine PVDF membrane), without BSA rejection efficiency changing (98.6%). Three reasons can be accounted for the membrane performance improvement: i. The hydrophilic MS-g-PVP well dispersed in PVDF membrane matrix, and facilitated the formation of the evenly porous structure for the composite membrane; ii. Surface segregation of MS-g-PVP with the amount and diversity of oxygen-/nitrogen-containing groups on membrane surface, thus improving membrane surface hydrophilicity with contact angle decreasing from 89.0 ° to 70.6 ° ; iii. Numerous mesopores inside of MS-g-PVP provided additional water pathways. In addition, these synergistic effects also enhanced the fouling-resistance of PVDF/MS-g-PVP membrane, whose flux recovery ratio maintained at 85.8% even after three “fouling-cleaning” dynamic BSA solution (0.2 g L -1 ) filtration cycles.
研究领域:
材料科学
·
环境工程
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高影响因子
COMPOSITES SCIENCE AND TECHNOLOGY
·
2018
·
IF 5.16
Min Sang,Sheng Wang,Mei Liu,Linfeng Bai,Wanquan Jiang,Shouhu Xuan,Xinglong Gong
In this paper, a versatile polyvinylidene fluoride/carbonyl iron (PVDF/CI) composite film was prepared by doping magnetic carbonyl iron (CI) particles into piezoelectric polyvinylidene fluoride (PVDF) matrix. Without influencing the piezoelectric structure of PVDF, CI particles enhanced the Young's modulus and maximum tensile strength of composite films. Due to the magnetic driven characteristic, PVDF/CI composite films exhibited distinct magnetic-mechanic-electric coupling properties. The piezoelectric charge signals could be generated by applying the bending deformation or magnetic field . Taking PVDF/CI-10% (CI content was 10 wt%) film as an example, the piezoelectric charges under 2, 4, 6, 8, and 10 mm bending displacement were 3.0, 9.6, 14.9, 18.6, and 24.6 pC respectively. Moreover, when the magnetic field varied from 0 to 600 mT, the generated magneto-electric charges of PVDF/CI-10% film increased from 0 to 676 pC. The quantitative relationship between magnetic field and magneto-electric charges was obtained by the polynomial fitting method and the correlation coefficient was up to 0.97. Owing to the ideal piezoelectricity, excellent stability, light weight and desirable flexibility, PVDF/CI composite films showed promising applications in deformation sensor and magnetic field sensor.
研究领域:
材料科学
·
传感器技术
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高影响因子
Surfaces and Interfaces
·
2024
·
IF 5.7
Siyuan Xu,Hongtao Chi,Chuanguo Ma,Xiaolei Li,Ping Zhang,Peibang Dai
In this paper, a multi-filler synergistic strategy combined with multi-layer hot pressing technology was developed to optimize the thermal conductivity and insulation properties of composite materials. Boron nitride nanosheets (BNNS), aluminium oxide (Al 2 O 3 ) microspheres and silver (Ag) nanoparticles were incorporated to construct a three-dimensional thermal conduction network within a polyvinylidene fluoride (PVDF) thermally conductive composite film . An electrospun PVDF fiber film was first prepared to be used as a template. BNNS and Al 2 O 3 were then electrostatically assembled on the surface of the PVDF fiber and in the film to obtain continuous BNNS/PVDF fiber film and Al 2 O 3 /PVDF fiber film, respectively. Ag nanoparticles were then prepared in situ on the Al 2 O 3 /PVDF fiber film to obtain an Ag-enhanced Al 2 O 3 /PVDF fiber film. A sandwich structured PVDF composite film (B-A@Ag-B/PVDF) was finally prepared by hot pressing, using the BNNS/PVDF fiber films as the top and bottom layers and the Ag-enhanced Al 2 O 3 /PVDF fiber film as the middle layer. The resulting B-A@Ag-B/PVDF composite film, with a total filler mass fraction of 32.1 %, had in-plane and through-plane thermal conductivities of 4.13 W m – ¹ K – ¹ and 1.05 W m – ¹ K – ¹, respectively, improvements of 1620 % and 452 % compared to those of pure PVDF. In addition, the through-plane electrical conductivity was as low as 5.38 × 10 – ¹¹ S/cm, matching the standards for insulating materials . The B-A@Ag-B/PVDF composite film demonstrates significant potential for advanced thermally conductive polymer composites .
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高影响因子
Surfaces and Interfaces
·
2026
·
IF 6.3
Yue Zhao,Zhaotian Ba,Yu Long,Yuanyi Kang,Tao Zhang,Meng Xin,Guohua Fan,Chuncheng Hao
The performance contradiction between dielectric constant and breakdown strength restricted the significant improvement in energy storage density of common dielectrics. In this work, the ternary BaTiO 3 @Ag/PVDF composites were prepared, in which the fibrous BaTiO 3 fillers were prepared by electrospinning and further modified with silver (Ag) nanoparticles via silver mirror reaction. Dielectric performance of the composites was effectively improved by the hybrid fillers owing to the synergies of the increased polarizations and the Coulomb blockade effect. Dielectric constant and breakdown strength of the composites with only 0.2 wt% filling content reached 14.8 and 421.7 MV/m, which were respectively increased 124.4% and 135.9% compared to that of the pristine PVDF. And the maximum energy storage density was increased to 4.5 J/cm 3 with the ultra-low content of fillers. This work broke the inherent contradictions in single-layer composites and provided novel attempts for dielectric modulation of dielectrics.
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高影响因子
Journal of Energy Storage
·
2026
·
IF 9.8
Hu Wang,Shala Yang,Pengfei Pang,Jiangchao Chen,Yongbo Yan,Mingjie Liao,Dazhi Pang,Zheqi Zhang,Yunyun Zhao,Wenping Liu,Huarui Xu,Guisheng Zhu,Kunpeng Jiang
Poor interfacial stability and dendrite penetration at the lithium metal anode interface are critical bottlenecks hindering the practical application of garnet-type solid electrolytes, despite their high intrinsic ionic conductivity. Herein, we resolve this long-standing trade-off by designing a hierarchical sandwich heterostructure. This architecture comprises a dense Li 6.4 Ga 0.2 La 3 Zr 2 O 12 (C-LGLZO) ceramic scaffold sandwiched between two ZIF-8@SiO 2 /PVDF-HFP (ZSPH) composite interfacial layers. The resulting composite solid electrolyte (CSE) C-LGLZO/ZSPH exhibits exceptional electrochemical properties: a high Li + transference number (t Li+ = 0.77) and an outstanding ionic conductivity of 1.31 × 10 −3 S cm −1 at 30 °C. Mechanistically, while the robust central C-LGLZO scaffold provides a continuous Li + pathway and physically blocks dendrites, the honeycomb-like porous ZSPH interfacial layers homogenize the interfacial electric field and promote a stable solid electrolyte interphase (SEI). This synergistic design endows the CSE with a wide electrochemical stability window (4.8 V vs. Li/Li + ) and enables stable Li plating/stripping for over 1000 h. Furthermore, cells using a LiFePO 4 cathode retain 76.3 % of their capacity after 500 cycles at 0.5C, demonstrating exceptional high-rate cycling stability. This work offers a versatile architectural strategy for engineering robust solid-state batteries (SSBs).
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高影响因子
Journal of Energy Chemistry
·
2022
·
IF 13.599
Qi Ye,Haoyue Liang,Shuhao Wang,Can Cui,Cheng Zeng,Tianyou Zhai,Huiqiao Li
Poly (ethylene oxide) (PEO)-based solid polymer electrolyte is always the most promising candidate for preparing thinner, lighter and safer lithium-ion batteries. However, the lithium dendrites growth of lithium anode and the high-voltage oxidation of cathode are easy to cause the PEO-based battery failure. The way to deal with the different challenges on both sides of the anode and cathode is pursued all the time. In this study, we reported a new strategy to construct the PVDF/PEO/PVDF three-layer structure for solid polymer electrolyte (marked as PVDF@PEO) using PVDF as the functional “skin”. The PVDF@PEO electrolyte can effectively prevent from the lithium dendrites, and shows a stable cycling life over 1000 h in the Li/PVDF@PEO/Li cell. In addition, the PVDF@PEO electrolyte exhibits higher oxidation resistance and can be matched with high-voltage LiCoO 2 cathode. The Li/PVDF@PEO/ LiCoO 2 cell delivered a specific capacity of about 150 mAh g −1 over 150 cycles and maintained good cycling stability. Our research provides insights that the polymer electrolytes constructed with PVDF functional “skin” can simultaneously meet the challenges of both anode and cathode in solid-state lithium-ion batteries (SSLIBs).
研究领域:
材料科学
·
电化学
·
能源存储
·
高分子化学
·
固态电池
·
界面工程
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高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2026
·
IF 9.6
Binyi Chen,Shoujing Wei,Yunyun Lei,Xinfan Zhao,Yubin Zhao,Huijie Tian,Ziqian Lu,Liubiao Zhong,Wei Gan,Yejun Qiu,Qunhui Yuan
Poly(vinylidene fluoride) (PVDF) based electrolytes are promising for lithium metal batteries, yet they suffer from low ionic conductivity, severe Li-metal side reactions, and poor dendrite suppression. This study presents a synergistic modification strategy integrating HfO 2 nanoparticles with ionic liquid to develop a high-performance composite electrolyte (PVHE). The incorporated HfO 2 nanoparticles adsorb residual dimethylformamide (DMF) solvent to suppress interfacial side reactions, while simultaneously facilitating the in-situ formation of a Hf-containing stable solid electrolyte interphase (SEI) that improves interfacial stability and inhibits lithium dendrite growth. The ionic liquid enhances the ionic conductivity by reducing the crystallinity of PVDF and regulating the solvation structure, synergistically achieving multiple performance breakthroughs with HfO 2 . The PVHE composite electrolyte exhibits an ionic conductivity of 5.75 × 10 −4 S cm −1 at 30 °C and a critical current density of 2.4 mA cm −2 . The Li|PVHE|Li cell cycles stably for over 1500 h at 0.1 mA cm −2 , and the Li|PVHE|NCM811 cell shows a capacity retention of 80.7% after 500 cycles at 1C. The multicomponent synergistic modification strategy offers a viable pathway toward the practical application of PVDF-based electrolytes and advances the understanding of the interactions among components in composite electrolyte systems.
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PubMed
高影响因子
HIGH ENERGY CHEMISTRY
·
2023
·Vol. 57
·期 1
·28-34
·
IF 0.7
Fan K.,Zhou G. Q.,Gao C. Y.,Li J. H.,Xu F. L.
Abstract This paper reports on the study that gamma-ray irradiation-induced polymerization of N-isopropyl acrylamide (NIPA) to form Poly(N-isopropyl acrylamide) (PNIPA), which was then grafted on the surface of polyvinylidene fluoride (PVDF) membrane to prepare modified PVDF-g-PNIPA membrane. We analyzed the influence of different irradiation doses and dose rates on the grafting rate of modified membranes, and the grafting rate increased with the irradiation dose under a certain irradiation dose. Through analysis of Fourier transform infrared spectroscopy (FTIR) and thermogravimetry (TGA), the efficient progress of the grafting reaction was confirmed. With the increase of the grafting rate, the pore size of the membrane surface decreased gradually, but the surface roughness of the membrane tended to increase through the analyse of scanning electron microscopy (SEM) and atomic force microscopy (AFM). Finally, a mechanistic explanation for the grafting of PNIPA on the surface of PVDF membranes based on these experimental results was proposed.
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高影响因子
Journal of Materials Chemistry C
·
2023
·Vol. 11
·期 18
·6010-6017
·
IF 6.4
Tianran Zhang,Qinzhao Sun,Zepeng Wang,Ruirui Kang,Fang Kang,Rong Xue,Jiping Wang,Lixue Zhang
Electrostatic energy storage dielectric polymers are essential for pulsed power applications due to their high power density. However, it suffers from low energy density and poor efficiency at high temperatures, which seriously hinders its application. Herein, a polyetherimide – MgO/polymethyl methacrylate/poly(vinylidene fluoride) – polyetherimide sandwich-structured composite was prepared by solution casting and hot-pressing. The experimental results show that MgO acted as a nuclear agent to promote the crystallization of PVDF, thereby improving the polarization at high temperatures. At 150 °C, the optimized composite exhibited a high discharge energy density of 3.34 J cm−3 when the charge–discharge efficiency was above 90% at 350 MV m−1. MgO alleviated both the ferroelectric loss and conduction loss at the low electric field as well, resulting in high polarization and high efficiency at the low electric field. Through this work, we made a new attempt to enhance the energy storage performance of high-temperature polymer-based dielectric composites under a low electric field.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Jingxue Wang,Yanting Liang,Zichen Wang,Bingjie Huo,Chao Liu,Xiaxia Chen,Hongwei Xu,Dongmei Li,Zhaoyou Zhu,Yinglong Wang,Fanqing Meng
Using water flow energy in the environment for water treatment is a feasible solution to alleviate energy shortages and environmental pollution. This work prepared a Cu 2 O@MoS 2 /PVDF modified pipeline with superior piezoelectric properties for norfloxacin (NOR) degradation. The piezoelectric coefficient d 33 of Cu 2 O@MoS 2 /PVDF increased by 27.7 % compared with PVDF. The piezoelectric current response test demonstrated that Cu 2 O@MoS 2 /PVDF had a higher current response than PVDF. FTIR showed that the presence of Cu 2 O@MoS 2 significantly increased the piezoelectric β -phase content of PVDF. The Cu 2 O@MoS 2 /PVDF pipeline exhibited the best degradation efficiency of 99.3 % within 40 min when the flow rate reached 1.389 L min −1 . O 2 – and OH have been shown to play an important role in NOR degradation and the possible degradation mechanism and pathways of NOR were proposed. This work provides a promising method for the efficient and green treatment of organic pollutants in water by using water flow energy and has practical application significance.
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