An investigation into group 13 (Al, Ga, In) substituted (Na0.5Bi0.5)TiO3-BaTiO3 (NBT-BT) lead-free piezoelectrics

Ryan McQuade, Thomas Rowe, Alicia Manjón-Sanz, Lilibel de la Puente, Michelle R. Dolgos

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Ternary phase diagrams were explored for the systems (Na0.5Bi0.5)TiO3-BaTiO3-Bi(M)O3 M = Al, Ga, In to determine periodic trends as a function of substitution. The ferroelectric and piezoelectric properties were measured and compared to (Na0.5Bi0.5)TiO3-BaTiO3 (NBT-BT). X-ray synchrotron and neutron diffraction data were collected to determine the changes in structure as a function of substitution. Data showed that most systems behave in a similar manner to the parent (Na0.5Bi0.5)TiO3-BaTiO3. However, two specific compositions display interesting properties: the 2% BiGaO3 (BG2) substituted sample and the 4% BiAlO3 (BA4) substituted sample. The BG2 sample undergoes an irreversible electric-field induced phase transition, as seen in NBT-BT, but has a significantly larger high-field strain. The BA4 composition has a different strain mechanism than all the other composition studied. It displays incipient piezoelectricity which results in a giant high-field strain due to a reversible phase transition. This study highlights the difficulty in trying to improve the properties of the highly disordered NBT-BT material.

Original languageEnglish
Pages (from-to)378-388
Number of pages11
JournalJournal of Alloys and Compounds
Volume762
DOIs
StatePublished - Sep 25 2018
Externally publishedYes

Funding

Michelle Dolgos and Alicia Manjón-Sanz would like to thank the NSF for support ( DMR-1606909 ). The authors also thank Oregon State University for additional funding and use of instruments. 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 . A portion of 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 at 11-BM (APS) and Pam Whitfield, Ashfia Huq, and Melanie Kirkham of POWGEN (SNS) for their assistance and support in collecting high quality diffraction data. The authors would like to thank David Cann of the Materials Science division at Oregon State University, as well as Nitish Kumar, Noon Prasertpalichat, and Nopsiri Chaiyo for access to instrumentation and informative discussions about the complex world of relaxor ferroelectrics. Michelle Dolgos and Alicia Manjón-Sanz would like to thank the NSF for support (DMR-1606909). The authors also thank Oregon State University for additional funding and use of instruments. 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. A portion of 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 at 11-BM (APS) and Pam Whitfield, Ashfia Huq, and Melanie Kirkham of POWGEN (SNS) for their assistance and support in collecting high quality diffraction data. The authors would like to thank David Cann of the Materials Science division at Oregon State University, as well as Nitish Kumar, Noon Prasertpalichat, and Nopsiri Chaiyo for access to instrumentation and informative discussions about the complex world of relaxor ferroelectrics.

FundersFunder number
National Science FoundationDMR-1606909
U.S. Department of Energy
Office of Science
Basic Energy SciencesDE- AC02-06CH11357
National Stroke Foundation

    Keywords

    • Oxide
    • Perovskite
    • Piezoelectric
    • Relationships
    • Relaxor
    • Structure-property

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