Bitte benutzen Sie diese Kennung, um auf die Ressource zu verweisen: http://dx.doi.org/10.18419/opus-4962
Autor(en): Womes, Manfred
Bihler, Eckardt
Eisenmenger, Wolfgang
Titel: Dynamics of polarization growth and reversal in PVDF films
Erscheinungsdatum: 1989
Dokumentart: Zeitschriftenartikel
Erschienen in: IEEE transactions on electrical insulation 24 (1989), S. 461-468. URL http://dx.doi.org./10.1109/14.30890
URI: http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-56087
http://elib.uni-stuttgart.de/handle/11682/4979
http://dx.doi.org/10.18419/opus-4962
Zusammenfassung: Measurements are presented of the time development of the dielectric displacement and the remanent polarization in polyvinylidene fluoride (PVDF) for poling times ranging from 1 μs to 1000 s and poling fields between 0.8 and 2.0 MV/cm. For longer times (0.1 to 1000 s), the time dependence of the polarization distribution across the film thickness is also determined. After application of a steep rectangular high-voltage pulse, the sample is shorted to zero voltage. The remanent polarization under the short-circuit conditions is compared to the maximum dielectric displacement under the external poling field. A significant time delay of the buildup of the remanent polarization was observed as compared to the dielectric displacement under field. This time delay depends significantly on the applied field strength and the crystallinity of the films. In the case of polarization reversal, a flipping back' of the polarization was observed for shorter poling times of up to 200 μs. Under these conditions, a large part of the polarization is reversed under the field, but after the removal of the field, most of the polarization returns to the original direction. The results can be explained by the ferroelectric cooperative coupling of oriented crystallite dipoles to charges trapped at the surface of polarized crystallites.
Enthalten in den Sammlungen:08 Fakultät Mathematik und Physik

Dateien zu dieser Ressource:
Datei Beschreibung GrößeFormat 
eis95.pdf1,62 MBAdobe PDFÖffnen/Anzeigen


Alle Ressourcen in diesem Repositorium sind urheberrechtlich geschützt.