Crosslinking modification and hydrogen bonding synergy to achieve high breakdown strength and energy density of PMMA-co-GMA/PVDF dielectric composite films

材料科学 复合材料 电介质 复合数 聚合物 储能 甲基丙烯酸甲酯 甲基丙烯酸酯 光电子学 单体 功率(物理) 物理 量子力学 共聚物
作者
Shuo Zheng,Xuanchen Zhao,Junhao Xie,Shulin Sun
出处
期刊:Physical Chemistry Chemical Physics [Royal Society of Chemistry]
卷期号:25 (47): 32482-32492 被引量:7
标识
DOI:10.1039/d3cp04317g
摘要

Polymer-based dielectric materials have been used in film capacitors due to their rapid charge-discharge rate, lightness, and low cost. Nevertheless, the energy storage properties of these dielectric films were limited by their weak polarization ability and low discharge energy density. Herein, the solution casting method was used to prepare all-organic crosslinked composite films using linear methyl methacrylate-co-glycidyl methacrylate (MG) as the matrix and ferroelectric poly(vinylidene fluoride) (PVDF) as the organic filler. The crosslinked MG networks can enhance the breakdown strength, restrain dielectric loss, and keep high discharge efficiency. What's more, the presence of PVDF can compensate for the low electrical displacement, improve the permittivity, and overcome the brittleness of the crosslinked films. The optimal all-organic crosslinked dielectric film exhibited an ultrahigh breakdown strength of 800 MV m-1 and a high efficiency of 77.4%. The maximum energy density of the composite film reached up to 12.1 J cm-3, which was nearly 120% higher than the energy density of 5.6 J cm-3 of the pure MG film. The enhancement in energy storage properties is ascribed to the synergistic effects of chemical crosslinking and hydrogen bonding. This study offers a feasible method for all-organic polymer films to fabricate energy storage equipment.
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