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拉伸对齐氢键网络以制备机械坚固且高能量密度的聚(偏二氟乙烯-六氟丙烯)介电薄膜电容器。

Stretching Aligned Hydrogen Bonding Network to Evoke Mechanically Robust and High-Energy-Density P(VDF-HFP) Dielectric Film Capacitors.

作者信息

Wu Qi, Liu Xingang, Liu Yuanbo, Zhang Chuhong, Nie Min

机构信息

State Key Laboratory of Polymer Materials Engineering, Polymer Research Institute of Sichuan University, No. 24 South Section 1, Yihuan Road, Chengdu, 610065, China.

PetroChina Refining, Chemicals & New Materials Company, China.

出版信息

Small. 2024 Nov;20(45):e2404662. doi: 10.1002/smll.202404662. Epub 2024 Jul 28.

DOI:10.1002/smll.202404662
PMID:39073247
Abstract

Polymer-based dielectric film capacitors are essential energy storage components in electronic and power systems due to their ultrahigh power density and ultra-fast charge storage/release capability. Nonetheless, their relatively low energy density does not fully meet the requirements of power electronics and pulsed power systems. Herein, a scalable composite dielectric film based on a ferroelectric polymer with edge hydroxylated boron nitride nanosheets (BNNS-OH) is fabricated via the construction of a hydrogen bonding network and stretching orientation strategy. The presence of hydroxyl groups on boron nitride aids in forming a robust hydrogen bonding network within the ferroelectric polymer, leading to a significant increase in Young's modulus and superior dielectric performance. Furthermore, the stretching process aligns the BNNS-OH and the hydrogen bonding network along the drawing direction via covalent and hydrogen bonding interaction, resulting in a remarkable tensile strength (109 MPa), breakdown strength (688 MV m), and energy density (28.2 J cm), outperforming mostrepresentative polymer-based dielectric films. In combining the advantages of a simple preparation process, extraordinary energy storage performance, and low-cost raw materials, this strategy is viable for large-scale production of polymer-based dielectric films with high mechanical and dielectric performance and opens a new path for the development of next-generation energy storage applications.

摘要

基于聚合物的介电薄膜电容器因其超高的功率密度和超快的电荷存储/释放能力,在电子和电力系统中是必不可少的储能元件。然而,它们相对较低的能量密度并不能完全满足电力电子和脉冲功率系统的要求。在此,通过构建氢键网络和拉伸取向策略,制备了一种基于铁电聚合物与边缘羟基化氮化硼纳米片(BNNS-OH)的可扩展复合介电薄膜。氮化硼上羟基的存在有助于在铁电聚合物中形成强大的氢键网络,导致杨氏模量显著增加和优异的介电性能。此外,拉伸过程通过共价键和氢键相互作用使BNNS-OH和氢键网络沿拉伸方向排列,从而产生显著的拉伸强度(109MPa)、击穿强度(688MV m)和能量密度(28.2J cm),优于大多数代表性的基于聚合物的介电薄膜。结合制备工艺简单、储能性能优异和原材料成本低的优点,该策略对于大规模生产具有高机械和介电性能的基于聚合物的介电薄膜是可行的,并为下一代储能应用的发展开辟了一条新途径。

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