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