Publication Cover
Integrated Ferroelectrics
An International Journal
Volume 55, 2003 - Issue 1
24
Views
3
CrossRef citations to date
0
Altmetric
Original Articles

Structure and Dielectric Properties of Heteroepitaxial PMNT Thin Films

, , , , &
Pages 781-793 | Published online: 18 Jun 2010
 

Abstract

Thin films of PbMg1/3 Nb2/3O3(PMN) and (1 − x)PbMg1/3Nb2/3O3-xPbTiO3 (PMNT) with x = 0.1 to 0.3 were epitaxially grown on (100) MgO and (100) SrTiO3 (ST) substrates by magnetron sputtering. Typical film thickness was 300 to 900 nm. Pyrochlore free (001) PMN and (001) PMNT thin films were grown on the ST and MgO substrates at narrow temperature window of 500 ± 20°C. The cross-sectional TEM image showed that the sputtered PMN and PMNT thin films comprised high density and continuous structure. These sputtered films showed 3-dimensional epitaxy. The dielectric response of the sputtered thin films showed frequency dispersion similar to bulk relaxor-like behavior with a broad temperature anomaly. PMN-23PT (x = 0.23) thin films showed the temperature of maximum, Tm, at 80°C. The Tm coincided with that of corresponding bulk materials. However, the obtained maximum dielectric permittivity, ϵm, ϵm = 900 to 1000, was considerably smaller than that in the bulk. The relatively low dielectric permittivity was probably due to the presence of strained hetero-epitaxial layer having temperature independent dielectric properties.

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.