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Improved piezoelectric performance via orientation regulation in novel BNT-BT-SBT thin film.

Authors :
Ni, Feier
Xu, Liuxue
Zhu, Kun
Yan, Hao
Shen, Bo
Zeng, Huarong
Zhai, Jiwei
Source :
Journal of Alloys & Compounds. Feb2023, Vol. 934, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

Lead-free piezoelectric thin films are urgently needed in microelectronic and microelectromechanical systems. In this work, (1- x)(0.94Bi 0.5 Na 0.5 TiO 3 -0.06BaTiO 3)- x (Sr 0.7 Bi 0.2 □ 0.1)TiO 3 (abbreviated as BNT-BT- x SBT) piezoelectric thin films were prepared successfully. The optimal piezoelectric performance can be achieved when x = 0.02 at morphotropic phase boundary (MPB). Further, to explore the impacts of orientation control on the properties of thin films, (100), (110), and (111)-oriented BNT-BT-0.02SBT thin films were prepared on Nb-SrTiO 3 single crystal. The (110) preferred orientation thin film can achieve a high inverse piezoelectric coefficient (d 33 *) of 170 pm/V, which has a great improvement contrasted with non-oriented films. From the perspective of engineering domain configuration, the high d 33 * of (110)-oriented thin film can be characterized that the ferroelectric domain can get a complete flip in the direction of non-easily polarized axes. In short, orientation regulation is of great importance in improving the piezoelectric properties of thin films and has important applications in microelectronic sensing. • BNT-BT- x SBT ternary thin films at MPB were prepared by sol-gel method. • (100), (110) and (111)-oriented thin films were prepared on Nb-SrTiO 3 single crystal. • Grain growth can be promoted along with the densely stacking plane orientation. • (110)-oriented thin film obtains the optimal inverse piezoelectric coefficient (170 pm/V). • The ferroelectric domain get complete flip in the direction of non-easily polarized axes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09258388
Volume :
934
Database :
Academic Search Index
Journal :
Journal of Alloys & Compounds
Publication Type :
Academic Journal
Accession number :
160581956
Full Text :
https://doi.org/10.1016/j.jallcom.2022.167936