journal article·2015-12-01Open access

Dramatic influence of Dy3+ doping on strain and domain structure in lead-free piezoelectric 0.935(Na1/2Bi1/2)TiO3−0.065BaTiO3 ceramics

C. Q. Li, Q. R. Yao, J. Z. Zhang, Z. G. Hu, F. F. Wang, A. Y. Liu, W. Z. Shi, J. H. Chu

AIP Advances· Volume 5· Issue 12

Abstract

An electric-field induced giant strain response and doping level dependent domain structural variations have been studied in the dysprosium (Dy3+)-modified 0.935(Na1/2Bi1/2)TiO3-0.065BaTiO3(xDy : NBBT) ceramics with the doping levels of 0%, 0.5%, 1%, and 2%. X-ray diffraction and Raman spectroscopy analyses not only demonstrates the change in ionic configurations induced by Dy3+ doping, but also shows the local crystal symmetry for x ≥ 0.5% doping levels to deviate from the idealized cubic structure. Piezoresponse force microscopy measurement exhibits the presence of an intermediate phase with orthorhombic symmetry at the critical Dy3+ doping level of 2%. Moreover, at this doping level, a giant recoverable nonlinear strain of ∼0.44% can be observed with high normalized strain (Smax/Emax) of 728 pm/V. At the same applied field, the strain exhibits a 175% increase than that of NBBT ceramic. Such a large strain stems from the varying coherence lengths of polar nanoregions (PNRs) and an unusual reversible 90° domain switching caused by the symmetry conforming property of point defects, where the restoring force is provided by unswitchable defects. The mechanism reveals a new possibility to achieve large electric-field strain effect for a wide range of ferroelectric systems, which can lead to applications in novel “on-off” actuators.
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Research context

OpenAlex topics: Ferroelectric and Piezoelectric Materials · Acoustic Wave Resonator Technologies · Multiferroics and related materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (31)

Show source-provided references
1. Adv. Mater. · 2002 · 21 · 4716
2. Chem. Mater. · 2015 · 27 · 62910.1021/cm504475k ↗
3. Chem. Mater. · 2011 · 23 · 21910.1021/cm102719k ↗
4. Phys. Rev. B · 2003 · 68 · 01411310.1103/PhysRevB.68.014113 ↗
5. Phys. Rev. B · 2012 · 85 · 02412110.1103/PhysRevB.85.024121 ↗
6. Phys. Rev. Lett. · 2009 · 103 · 25760210.1103/PhysRevLett.103.257602 ↗
7. J. Electroceram. · 2012 · 29 · 7110.1007/s10832-012-9742-3 ↗
8. Appl. Phys. Lett. · 2012 · 100 · 01290110.1063/1.3673832 ↗
9. Appl. Phys. Lett. · 2012 · 77 · 169810.1063/1.1308533 ↗
10. Appl. Phys. Lett. · 2012 · 101 · 14191210.1063/1.4757877 ↗
11. J. Am. Ceram. Soc. · 1977 · 60 · 9710.1111/j.1151-2916.1977.tb15479.x ↗
12. J. Alloys Compds. · 2013 · 555 · 5610.1016/j.jallcom.2012.12.002 ↗
13. Ferroelectrics · 1978 · 22 · 72910.1080/00150197808237382 ↗
14. J. Phys. Chem. Solids · 1970 · 31 · 178510.1016/0022-3697(70)90168-X ↗
15. Appl. Phys. Lett. · 2009 · 94 · 14290110.1063/1.3103313 ↗
16. J. Appl. Phys. · 2011 · 109 · 01411010.1063/1.3530737 ↗
17. Appl. Phys. Lett. · 2009 · 95 · 03290410.1063/1.3182679 ↗
18. Japan. J. Appl. Phys. · 2004 · 43 · 812610.1143/JJAP.43.8126 ↗
19. J. Appl. Phys. · 2010 · 108 · 08410210.1063/1.3490781 ↗
20. J. Phys: Condens. Matter · 2005 · 17 · 658710.1088/0953-8984/17/41/027 ↗
21. J. Phys: Condens. Matter · 2000 · 12 · 326710.1088/0953-8984/12/14/305 ↗
22. Scripta Mater. · 2014 · 75 · 5010.1016/j.scriptamat.2013.11.017 ↗
23. Phil. Mag. B · 2001 · 81 · 202110.1080/13642810108208556 ↗
24. J. Appl. Phys. · 2005 · 98 · 01410910.1063/1.1957130 ↗
25. Nature · 1997 · 389 · 57910.1038/39277 ↗
26. Mater. Lett. · 1994 · 21 · 27510.1016/0167-577X(94)90189-9 ↗
27. Phys. Rev. B · 2000 · 63 · 01210310.1103/PhysRevB.63.012103 ↗
28. J. Mech. Phys. Solids · 2004 · 52 · 171910.1016/j.jmps.2004.02.011 ↗
29. Nature Mater. · 2005 · 4 · 77610.1038/nmat1485 ↗
30. J. Appl. Phys. · 2013 · 113 · 11410110.1063/1.4792729 ↗
31. J. Mech. Phys. Solids · 2002 · 50 · 28310.1016/S0022-5096(01)00050-3 ↗