Pressure and chemical doping induced phase transition and phonon dynamics of multiferroic Bi5Ti3FeO15 ceramics
Source abstract
Abstract
The external pressure and doping effect have been studied on the lattice structure of multiferroic Bi5Ti3−2xFe1+xNbxO15 (BTFNx) ceramics. Based on the x-ray diffraction and the Raman spectroscopic evidence, it is confirmed that the doping-induced lattice deformation is closely related to the concentrations of the Nb5+ and Fe3+ ions. The Bi5Ti3FeO15 (BTF) ceramic transits from orthorhombic (O, A21am) - O and tetragonal (T) - T (I4/mmm) with pressure, showing the intermediate phase coexistence at a wide pressure range of 4.5–14.8 GPa, while for BTFN0.6 ceramics, it is O (Fmm2) - O and T - T(I4/mmm) having the phase coexistence at 6–18 GPa. The ionic substitution, phase diagram and the evolution of phonon, lattice symmetry, and stability of BTFNx ceramics have been systematically observed and studied under the internal and external factors. Our work provides a comprehensive understanding of the structural and physical functionality for the development and optimization of multiferroic four-layer compounds BTF material systems.
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Research context
OpenAlex topics: Multiferroics and related materials · Ferroelectric and Piezoelectric Materials · Magnetic and transport properties of perovskites and related materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (28)
Show source-provided references
1. Phys. Rev. B · 1997 · 56 · 262310.1103/physrevb.56.2623 ↗
2. Nature · 2003 · 426 · 5510.1038/nature02018 ↗
3. Nature · 2004 · 429 · 39210.1038/nature02572 ↗
4. Ceram. Int. · 2014 · 40 · 263510.1016/j.ceramint.2013.10.063 ↗
5. Multiferroic and magnetoelectric materials10.1038/nature05023 ↗
6. Sci. Rep. · 2014 · 4 · 525510.1038/srep05255 ↗
7. Acta Phys. Pol., A · 2009 · 116 · 4710.12693/aphyspola.116.47 ↗
8. Ceram. Int. · 2014 · 40 · 745910.1016/j.ceramint.2013.12.094 ↗
9. Phys. Rev. B · 2014 · 90 · 21410910.1103/physrevb.90.214109 ↗
10. Phys. Rev. B · 2020 · 102 · 02410310.1103/physrevb.102.024103 ↗
11. J. Appl. Phys. · 2012 · 112 · 05201010.1063/1.4745936 ↗
12. Acta Crystallogr., Sect. B: Struct. Sci. · 2001 · 57 · 72510.1107/s0108768101015282 ↗
13. Appl. Phys. Lett. · 2020 · 117 · 02290110.1063/5.0019034 ↗
14. J. Appl. Phys. · 2014 · 115 · 14410110.1063/1.4870054 ↗
15. J. Appl. Phys. · 2014 · 116 · 14410110.1063/1.4897556 ↗
16. Appl. Phys. Lett. · 2021 · 119 · 13290510.1063/5.0060874 ↗
17. J. Phys. Chem. B · 2000 · 104 · 669410.1021/jp000114x ↗
18. Phys. Lett. A · 2007 · 362 · 47110.1016/j.physleta.2006.10.031 ↗
19. Ceram. Int. · 2019 · 45 · 748010.1016/j.ceramint.2019.01.040 ↗
20. Mater. Lett. · 2012 · 68 · 19010.1016/j.matlet.2011.09.113 ↗
21. J. Chem. Phys. · 1964 · 41 · 319910.1063/1.1725697 ↗
22. Ceram. Int. · 2017 · 43 · 1353010.1016/j.ceramint.2017.07.059 ↗
23. J. Appl. Phys. · 2013 · 113 · 03490110.1063/1.4775800 ↗
24. Adv. Mater. · 2017 · 29 · 170343510.1002/adma.201770317 ↗
25. Spectrochim. Acta A · 2021 · 225 · 11971610.1016/j.saa.2021.119716 ↗
26. Ceram. Int. · 2015 · 41 · s18510.1016/j.ceramint.2015.03.233 ↗
27. Phys. Rev. B · 2020 · 102 · 21410210.1103/physrevb.102.214102 ↗
28. Phys. Rev. B · 2021 · 104 · 22410510.1103/physrevb.104.224105 ↗