电容器
极化(电化学)
材料科学
介电强度
化学能
电介质
光电子学
储能
电气工程
聚合物
超级电容器
纳米技术
背景(考古学)
工程物理
铁电聚合物
功率密度
计算机数据存储
电子工程
电压
介电损耗
功率(物理)
节能
高效能源利用
电势能
高压
能量密度
聚合物电容器
能量转换
作者
Junhang Tang,Zepeng Mao,Han Zhang,Jun Zhang
标识
DOI:10.1016/j.rser.2025.116139
摘要
In the context of accelerated energy depletion, the efficient storage and release of energy has emerged as a pivotal concern. Dielectric capacitors have garnered significant attention for their high power density, rapid charging and discharging rates, and extended cycle life. With the development of electronic power equipment in the direction of lightweight and flexibility, all-organic dielectrics show a broad development prospect in the field of energy storage dielectric capacitors by virtue of their light weight, easy processing, high breakdown strength and other advantages. Among them, vinylidene fluoride (VDF)-based polymers exhibit high polarization characteristics, which are conducive to achieving high energy storage density ( U d ). However, severe polarization hysteresis leads to low charge/discharge efficiency. In response to these properties, this review explores various chemical and physical strategies to enhance the energy storage performance of VDF-based polymers based on three perspectives: modulation of polarization behavior, reduction of dielectric loss and enhancement of breakdown strength. The chemical strategy is centered on the design of the molecular chain structure, and the highest U d of 23.3 J/cm 3 was obtained by grafting linear polymers. The physical strategy focuses on modulating the structure of the aggregation state, and the special processing method of “Press & Folding” enables PVDF to achieve the highest U d of 39.8 J/cm 3 . Finally, suggestions are made for future research and development, as well as for the challenges that VDF-based all-organic dielectrics will have to overcome. • Energy storage performance can be optimized from three perspectives. • Chemical and physical strategies to enhance energy storage performance are reviewed. • Insights for future research on VDF-based all-organic dielectrics.
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