Crystal-structure dependence of electroactive properties in differently prepared poly(vinylidene fluoride/hexafluoropropylene) copolymer films

Citation
Ac. Jayasuriya et al., Crystal-structure dependence of electroactive properties in differently prepared poly(vinylidene fluoride/hexafluoropropylene) copolymer films, J POL SC PP, 39(22), 2001, pp. 2793-2799
Citations number
23
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS
ISSN journal
08876266 → ACNP
Volume
39
Issue
22
Year of publication
2001
Pages
2793 - 2799
Database
ISI
SICI code
0887-6266(20011115)39:22<2793:CDOEPI>2.0.ZU;2-9
Abstract
The electroactive properties of two random copolymers of vinylidene fluorid e (VDF) and hexafluoropropylene (HFP) were studied. The compositions were 9 5/5 and 85/15 mol % P(VDF/HFP). For each composition, three different film- preparation methods were used-solvent casting, melt-pressed quenched, and m elt-pressed slow-cooled. The ferroelectric properties observed were strongl y dependent on the preparation methods of the films as well as the HFP mola r content of the samples. The highest remanent polarizations (P-r) obtained from electric displacement versus electric field (D-E) hysteresis data are 80 and 50 mC/m(2) for the 5 and 15 % HFP solvent-cast samples, respectivel y. The slow-cooled samples do not exhibit any ferroelectric behavior for ei ther the 5 or 15% HFP copolymers. It was also observed that both the 5 and 15% HFP slow-cooled samples have a smaller electrostrictive response relati ve to the other two types of samples. Wide-angle X-ray diffraction and DSC results suggest that the 5% HFP sample has a higher crystallinity relative to the 15% HFP sample for each preparation method. In addition, different c rystal phases form in the samples resulting from the different preparation methods. Fourier transform infrared results suggest that the slow-cooled sa mples are in the nonpolar alpha phase, whereas the quenched and solvent-cas t samples are more likely in the polar beta phase. The slow-cooled samples do not show a switching peak in their nonpolar alpha -phase crystalline sta te. (C) 2001 John Wiley & Sons, Inc.