Polarization and space charge performance in PVDF with MPB composition BCZT doped composite films. Issue 40 (16th June 2017)

• Record Type: Journal Article
• Authors: Lu, Haowei; Liu, Lizhu; Lin, Jiaqi; Yang, Wenlong; Weng, Ling; Zhang, Xiaorui; Chen, Gaoru; Huang, Wei
• Is Part Of: Journal of applied polymer science. Volume 134:Issue 40(2017)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2017-06-16
• Subjects: dielectric properties -- films -- theory and modeling -- thermal properties; Polymers -- Periodicals; Polymerization -- Periodicals; 668.9
• DOI: 10.1002/app.45362
• Languages: English
• ISSNs: 0021-8995

Abstract

ABSTRACT: The morphotropic phase boundary composition 47(Ba0.7 Ca0.3 )TiO3 –0.53Ba(Zr0.2 Ti0.8 )O3 (calcium barium zirconate titanate, BCZT) were doped in poly(vinylidene fluoride) matrix by solution casting method. The effect of BCZT particles on polarization characteristics of composite films were investigated through dielectric spectra, hysteresis, and thermally stimulated discharge current measurements. It reveals that relative dielectric constant, remnant polarization, and energy storage density gradually increase and reach the maximum value with 39 at 100 Hz, 1.17 μC/cm 2, and 3.69 J/cm 3 at the concentration of 20 vol % BCZT. The Gaussian method was employed to decompose thermally stimulated discharge current composite peaks and an approximate model was used to analyze the activation energy levels of these films. The results indicated that the introduction of BCZT is effective for the charge carrier traps and activation energy distribution in the relaxation process of composite films. The decreased molecular movements, and increased interfaces formed between the BCZT grains and the poly(vinylidene fluoride) matrix may be responsible for these performances. And a new relaxation peak appeared at about 370 K in composites when BCZT concentration exceeded 20 vol %, which was considered to be caused by the ferroelectric‐paraelectric phase transition of BCZT. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci.2017, 134, 45362. Abstract :