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Research paper | Open Access

Spatially-resolved relaxor to ferroelectric phase switching in 0.93Na1/2Bi1/2TiO3-0.07BaTiO3 ceramics

Xi Shia( )Udo EcksteinaYizhe LibDavid HallbNeamul H. Khansura( )
Department of Materials Science and Engineering, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Erlangen, Germany
Department of Materials, University of Manchester, Manchester, UK

Peer review under responsibility of The Chinese Ceramic Society.

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Abstract

In situ, spatially-resolved synchrotron X-ray diffraction was utilized to investigate the electric field-induced heterogenous phase transformation of nonergodic relaxor 0.93Na1/2Bi1/2TiO3-0.07BaTiO3 ceramics. A Cu electrode was coated on one surface of a rectangular sample by aerosol deposition (AD), while a Pt layer was deposited on the opposite surface by sputter deposition. It is anticipated that a different stress state and/or domain morphology should occur on the AD deposited Cu electrode side due to the particle impact-consolidation deposition process. Under an electric field, different sample regions, i.e., AD, Middle, and Sputter sides, showed systematic changes in the relaxor to ferroelectric phase transition behavior. In particular, most < 001 > grains transformed at a sub-coercive field of 0.8 kV/mm, while the majority of the < 111 > grains only appeared to undergo transitions at a higher field (2.4 kV/mm). Also, the tetragonal phase became the dominant structure at higher field levels. Importantly, both < 111 > and < 001 > grains undergo phase switching at lower fields in the region close to the AD-processed layer. The study indicates that the AD process-induced stress can facilitate the electric field-induced relaxor to ferroelectric phase transition, i.e., the AD Cu side showed more significant lattice strain and domain texture than the sputter Pt side.

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Journal of Materiomics
Pages 976-981
Cite this article:
Shi X, Eckstein U, Li Y, et al. Spatially-resolved relaxor to ferroelectric phase switching in 0.93Na1/2Bi1/2TiO3-0.07BaTiO3 ceramics. Journal of Materiomics, 2022, 8(5): 976-981. https://doi.org/10.1016/j.jmat.2022.03.005

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Received: 22 January 2022
Revised: 16 March 2022
Accepted: 22 March 2022
Published: 29 March 2022
© 2022 The Chinese Ceramic Society.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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