Publication Cover
Materials Technology
Advanced Performance Materials
Volume 32, 2017 - Issue 9
202
Views
0
CrossRef citations to date
0
Altmetric
Research Paper

Structure, antiferro/ferro-electric transformation and relaxor behaviour in (1-x)Pb(Yb1/2Nb1/2)O3-xPb(Mg1/2W1/2)O3 ceramics

, ORCID Icon, , , , & show all
Pages 543-550 | Received 20 Dec 2016, Accepted 01 Apr 2017, Published online: 17 Apr 2017
 

Abstract

The superlattice structure and dielectric relaxor behaviour were simultaneously observed in (1-x)Pb(Yb1/2Nb1/2)O3-xPb(Mg1/2W1/2)O3 ((1-x)PYN-xPMW) ceramics composed by highly ordered end members. Orthorhombic perovskite structure was determined by X-ray diffraction for the compositions of x = 0·0–0·2 and 0·8–1·0 with two sets of superlattice. For intermediate compositions, the superlattice peaks were still preserved with weakening in intensity. Strong dielectric relaxor behaviour seemed to be independent with the superlattice and well fitted by Vogel–Fulcher equation for x = 0·3–0·7. It indicated that the polar microregions in (1-x)PYN-xPMW undergo the dipole glass-like and freezing state analogous to the prototypical relaxor Pb(Mg1/3Nb2/3)O3. Slim ferroelectric hysteresis loops, seemingly made up with ferroelectric and antiferroelectric together, were obtained for the relaxor compositions using huge external field. The antiferroelectric compositions related to superlattice were determined through double ferroelectric polarisation loops. A schematic diagram was sketched to describe the structure transform and generation of relaxor behaviour.

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.