68
Views
14
CrossRef citations to date
0
Altmetric
Session D: Polymers and glass, amorphous and composites

Properties of thin ferroelectric polymer films

, , , &
Pages 61-66 | Received 08 Dec 1998, Published online: 09 Mar 2011
 

Abstract

The polymer polyvinylidene fluoride and its copolymers with trifluoroethylene are ferroelectric; they have switchable polarisation and display a Curie transition. These polymers are readily produced in the form of films with thickness down to 50 nm by conventional spin-casting.

The properties of these very thin films are remarkably similar to those of commercial films with thickness of 10 μm or more. The dielectric constant is virtually unchanged down to 100 nm. Hysteresis loops are readily obtained, which indicate a coercive field of around 50 MVm−1, meaning that the films can be poled with voltages of the order of 10 V. The pyro-electric and piezoelectric coefficients are also similar in magnitude to those in thicker films and, when measured with a varying bias field, display a field dependence which reflects the underlying ferroelectric switching.

The films show signs of fatigue after repetitive switching, with the polarisation dropping to half its normal value after a few thousand cycles.

The benign chemical nature of the polymers, coupled with their low poling voltage, makes such thin polymer films interesting candidates for applications in various types of integrated transducer.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.