4.7 Article

Crystallization kinetics and enhanced dielectric properties of free standing lead-free PVDF based composite films

Journal

POLYMER
Volume 121, Issue -, Pages 88-96

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.polymer.2017.06.009

Keywords

PVDF composites; Crystallization kinetics; Dielectric

Funding

  1. China Scholarship Council (CSC) [201306630008]

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Ferroelectric composites, integrating dielectric ceramic fillers with mechanically flexible polymers, are promising materials for flexible electronic applications. Plenty of research has demonstrated the enhanced dielectric and ferroelectric properties of composite materials. However, the mechanisms responsible for these enhancements are not completely understood. Herein, we used typical dielectric materials, poly(vinylidene fluoride) (PVDF) and BaTiO3 (BTO), to study the effect of a dielectric filler on the crystallization, phase transformation and dielectric properties of PVDF. The crystallization of beta-PVDF was not affected by the presence of BTO particles, but small amounts of BTO (< 3 vol %) made PVDF crystallize into larger spherulites. This is linked to crystallization kinetic studies, which showed that BTO acted as a nucleation agent for large full ring banded spherulites when its content was less than 1 vol %. Furthermore, solid state drawing in the presence of BTO particles promoted the formation of b-PVDF with more pronounced preferred crystalline orientation at high drawing temperatures (120 degrees C). The dielectric and ferroelectric properties were enhanced with BTO filling. The 100 degrees C oriented drawn PVDF tape exhibited a dielectric permittivity of 14 (100 Hz) and remnant polarization of 0.080 C/m(2) (10 Hz), which increased to 23 and 0.095 C/m(2), respectively, after filling with 5 vol % BTO; neither resulting in high dielectric loss tangent (similar to 0.02) nor obvious current leakage. Moreover, the coercive field decreased from 80 to 50 kV/mm with increasing BTO content from 0 to 5 vol %. Crown Copyright (C) 2017 Published by Elsevier Ltd. All rights reserved.

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