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聚偏氟乙烯基准固态钠离子电池研究进展和改性方法

Research progress and modification methods of PVDF based quasi-solid-state sodium ion batteries

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【作者】 白涵朔董沫含周莉君郭凯赵志奇侯跃辉杨振东张渤海王晓丹吴俊锋唐宾

【Author】 BAI Hanshuo;DONG Mohan;ZHOU Lijun;GUO Kai;ZHAO Zhiqi;HOU Yuehui;YANG Zhendong;ZHANG Bohai;WANG Xiaodan;WU Junfeng;TANG Bin;Interdisciplinary Research Center for Sustainable Energy Science and Engineering, School of Chemical Engineering,Zhengzhou University;Laboratory of Functional Micro-nano Material and Device, School of Physics and Technology, University of Jinan;Henan International Joint Laboratory of Laser Technology in Agriculture Sciences, College of Mechanical & Electrical Engineering, Henan Agricultural University;Mining New Energy Research Institute(MINRI), Core Research Institutes for Coal, China Coal Technology &Engineering Group;Flavors and Fragrance Engineering & Technology Research Center of Henan Province, College of Tobacco Science, Henan Agricultural University;Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Renewable Energy Conversion and Storage Center(ReCast), Nankai University;Tianjin Lishen Battery Joint-Stock Co., Ltd.;

【通讯作者】 王晓丹;唐宾;

【机构】 郑州大学化工学院新能源科学与工程交叉学科研究中心济南大学物理科学与技术学院功能微纳材料与器件实验室河南农业大学机电工程学院河南省农业科学激光技术国际联合实验室中国煤炭科工集团煤炭共性技术研究院矿山新能源研究院河南农业大学烟草学院河南省香料香精工程技术研究中心南开大学可再生能源转换与存储中心先进能源材料化学教育部重点实验室天津力神电池股份有限公司

【摘要】 聚偏氟乙烯(PVDF)及其共聚物因其高介电常数、优异的机械与电化学稳定性及宽电化学窗口,在准固态钠离子电池聚合物电解质领域展现出重要的应用前景。然而,其室温离子电导率偏低及电极/电解质界面不稳定问题,制约了其在高安全性、长寿命储能体系中的实际应用。本文系统梳理了PVDF的共聚特性、多晶型结构及分子构象,重点分析液体环境调控、功能性填料引入及正负极界面改性提升电化学性能的三大策略。在液体环境方面,分析溶剂优选、残留溶剂比例调控及多功能添加剂协同对稳定固体电解质界面(SEI)构建的影响;在填料方面,对比活性填料与惰性填料的作用机制及表面改性技术对分散性的提升效果;在界面改性方面,阐述PVDF在负极侧生成富无机SEI及在正极侧作为柔性缓冲层的双重角色。指出通过构建“机械增强-离子传导-界面调控”多功能网络实现全链条优化的技术路径。通过对改性策略的系统比较与性能提升路径的深入探讨,为高稳定性、高能量密度PVDF基准固态钠离子电池的开发提供了系统参考与思路支持。

【Abstract】 Polyvinylidene fluoride(PVDF)and its copolymers have shown important application prospects in the field of polymer electrolytes for quasi-solid-state sodium ion batteries due to their high dielectric constant,excellent mechanical and electrochemical stability and wide electrochemical window. However,its low ionic conductivity at room temperature and unstable electrodes-electrolyte interface restrict its practical application in high-security and long-life energy storage systems. In this review,the copolymerization characteristics,the polymorphic structures,and molecular conformation of PVDF are systematically reviewed. Three main strategies for improving the electrochemical performance of PVDF,including liquid environment regulation,introduction of functional fillers and interface modification of positive and negative electrodes,are emphatically analyzed. In the aspect of liquid environment,the effects of solvent optimization,residual solvent ratio regulation and multi-functional additive synergy on the construction of stable solid electrolyte interphase(SEI)are analyzed. In terms of fillers,the mechanism of interaction with the PVDF of active fillers and inert fillers and the improvement effect of surface modification technology on dispersion are compared. In terms of interface modification,the dual roles of PVDF in forming inorganic-rich SEI on the negative side and acting as a flexible buffer layer on the positive side are described. The technical path of realizing the whole chain optimization by constructing a multi-functional network of “mechanical enhancement-ion conduction-interface regulation” is pointed out. Through the systematic comparison of modification strategies and the in-depth discussion of performance improvement paths,it provides a system reference and idea support for the development of high stability and high energy density PVDF based quasi-solid-state sodium ion batteries.

【基金】 河南省自然科学基金(No.252300423746)
  • 【文献出处】 生态产业科学与磷氟工程 ,Eco-industry Science & Phosphorus Fluorine Engineering , 编辑部邮箱 ,2026年03期
  • 【分类号】TM912;TQ325.4
  • 【下载频次】55
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