Understanding the structure–property relationships of the ferroelectric to relaxor transition of the (1 − x)BaTiO3–(x)BiInO3 lead-free piezoelectric system

Alicia Manjón-Sanz, Caitlin Berger, Michelle R. Dolgos

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

A structural and electromechanical investigation has been performed on (1 − x)BaTiO3–(x)BiInO3 in the region 0.03 ≤ x ≤ 0.12. A gradual structural phase transition has been observed where the structure changes from tetragonal (P4mm) and passes through two regions of coexisting phases: (1) P4mm + R3m in the range 0.03 ≤ x ≤ 0.075 and (2) Pm3 ¯ m + R3m for 0.10 ≤ x ≤ 0.12. The properties also transition from ferroelectric (x ≤ 0.03) to relaxor ferroelectric (x ≥ 0.05) as the dielectric permittivity maximum becomes temperature and frequency dependent. This transition was also confirmed via polarization-electric field measurements as well as strain-electric field measurements. At the critical composition of x = 0.065, a moderate strain of ~0.104% and an effective piezoelectric coefficient (d33 *) of 260 pm/V were observed. The original purpose of this study was to demonstrate the polarization extension mechanism as predicted in the literature, but due to the ferroelectric to relaxor transition, this mechanism was not found to be present in this system. However, this demonstrates that BaTiO3-based lead-free ceramics could be modified to obtain enhanced electromechanical properties for actuator applications.

Original languageEnglish
Pages (from-to)5309-5323
Number of pages15
JournalJournal of Materials Science
Volume52
Issue number9
DOIs
StatePublished - May 1 2017
Externally publishedYes

Funding

This material is based upon work supported by the National Science Foundation under Grant No. DMR-1606909. Use of the Advanced Photon Source at Argonne National Laboratory was supported by the U. S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357. This research used resources at the Spallation Neutron Source, a DOE Office of Science User Facility operated by the Oak Ridge National Laboratory. We would like to thank Saul Lapidus and Lynn Ribaud of 11-BM at the APS and Ashfia Huq, Pam Whitfield, and Melanie Kirkham of POWGEN at the SNS for their assistance with our mail-in samples. We would also like to thank David Cann at Oregon State University for use of his equipment for the permittivity measurements and helpful discussions.

FundersFunder number
National Science Foundation1606909, DMR-1606909
U.S. Department of Energy
Office of Science
Basic Energy SciencesDE-AC02-06CH11357

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