Issue 39, 2017

Enhanced dielectric properties due to space charge-induced interfacial polarization in multilayer polymer films

Abstract

With the recent advancement of power electronics, polymer film capacitors have become increasingly important. However, the low temperature rating (up to 85 °C) and low energy density (5 J cm−3 at breakdown) of state-of-the-art biaxially oriented polypropylene (BOPP) films have been limiting factors for advanced power electronics. Based on our recent work, multilayer films (MLFs), which consist of a high energy density polymer [e.g., poly(vinylidene fluoride) (PVDF)] and a high breakdown/low loss polymer [e.g., polycarbonate (PC)], have shown potential to achieve high energy density (13–17 J cm−3), enhanced breakdown strength, high temperature tolerance, and low loss simultaneously. In this study, the dielectric properties of PC/PVDF 50/50 32- and 256-layer (32L and 256L) films were investigated. The breakdown strength of the 32L film was as high as 800 MV m−1 at room temperature, as compared to 600 MV m−1 of PVDF and 750 MV m−1 of PC. The temperature rating of the 32L film reached 120 °C, higher than that of BOPP. In addition, it was observed that the 32L film with thicker PC layers exhibited a higher breakdown strength and a lower DC conductivity than the 256L film with thinner PC layers at elevated temperatures. These differences were attributed to the difference in the interfacial polarization of space charges, which was further verified by thermally stimulated depolarization current spectroscopy. From this study, we conclude that interfacial polarization endows MLFs with the desirable dielectric properties for next generation film capacitors.

Graphical abstract: Enhanced dielectric properties due to space charge-induced interfacial polarization in multilayer polymer films

Supplementary files

Article information

Article type
Paper
Submitted
12 Aug 2017
Accepted
14 Sep 2017
First published
15 Sep 2017

J. Mater. Chem. C, 2017,5, 10417-10426

Enhanced dielectric properties due to space charge-induced interfacial polarization in multilayer polymer films

X. Chen, J. Tseng, I. Treufeld, M. Mackey, D. E. Schuele, R. Li, M. Fukuto, E. Baer and L. Zhu, J. Mater. Chem. C, 2017, 5, 10417 DOI: 10.1039/C7TC03653A

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