Incipient ferroelectric to a possible ferroelectric transition in Te4+ doped calcium copper titanate (CaCu3Ti4O12) ceramics at low temperature as evidenced by Raman and dielectric spectroscopy
Source abstract
Abstract
Partial replacement of Ti4+ by Te4+ ions in calcium copper titanate lattice improved its dielectric behaviour mostly due to cubic-to-tetragonal structural transformation and associated distortion in TiO6 octahedra. The relative permittivity values (23–30 x 103) of Te4+ doped ceramics is more than thrice that of un-doped ceramics (8 x 103) at 1 kHz. A decreasing trend in relative permittivity with increasing temperature (50–300 K) is observed for all the samples. Barrett’s formula, as a signature of incipient ferroelectricity, is invoked to rationalize the relative permittivity variation as a function of temperature. A systematic investigation supported by temperature dependent Raman studies reveal a possible ferroelectric transition in Te4+ doped ceramic samples below 120 K. The possible ferroelectric transition is attributed to the interactions between quasi-local vibrations associated with the micro-clusters comprising TiO6 and TeO6 structural units and indirect dipole-dipole interactions of off-center B–cations (Ti4+ and Te4+) in double perovskite lattice.
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Research context
OpenAlex topics: Dielectric properties of ceramics · Ferroelectric and Piezoelectric Materials · Multiferroics and related materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Indian Institute of Science 1 Materials Research Center, , Bangalore 560012, India
Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR) 2 Light Scattering Laboratory, Chemistry and Physics of Materials Unit, , Bangalore 560064, India
References (27)
Show source-provided references
1. Appl. Phys. Lett. · 1999 · 75 · 85610.1063/1.124536 ↗
2. Nat. Comm. · 2013 · 4 · 199010.1038/ncomms2990 ↗
3. Science · 2007 · 315 · 95410.1126/science.1129564 ↗
4. Nat. Comm. · 2016 · 7 · 1092010.1038/ncomms10920 ↗
5. Adv. Mater. · 2012 · 24 · 52310.1002/adma.201103717 ↗
6. Supercond. Sci. Technol. · 1995 · 8 · 75510.1088/0953-2048/8/10/003 ↗
7. Appl. Phys. Lett. · 1995 · 76 · 270810.1063/1.114300 ↗
8. J. Appl. Phys. · 1997 · 82 · 447510.1063/1.366180 ↗
9. Phys. Solid State · 2001 · 43 · 140110.1134/1.1395075 ↗
10. J. Phys. Cond. Mat · 1995 · 7 · 376510.1088/0953-8984/7/19/011 ↗
11. Appl. Phys. Lett. · 2002 · 81 · 88610.1063/1.1497199 ↗
12. J. Mater. Chem. · 2009 · 19 · 591610.1039/b910871h ↗
13. Appl. Phys. Lett. · 2007 · 91 · 13291110.1063/1.2769954 ↗
14. Phys. Rev. B. · 2010 · 81 · 22411210.1103/PhysRevB.81.224112 ↗
15. Solid State Comm. · 2016 · 241 · 710.1016/j.ssc.2016.04.018 ↗
16. Current Science · 2007 · 93 · 778
17. Chem. Mater. · 2010 · 22 · 610.1021/cm903220z ↗
18. Phys. Rev. · 1952 · 86 · 11810.1103/PhysRev.86.118 ↗
19. Appl. Phys. Lett. · 2007 · 91 · 02291010.1063/1.2757098 ↗
20. Phys. Rev. B. · 2010 · 81 · 22411210.1103/PhysRevB.81.224112 ↗
21. Phys. Rev. B · 2008 · 78 · 06050310.1103/PhysRevB.78.060503 ↗
22. Physica B · 2004 · 358 · 13810.1016/j.physb.2004.12.069 ↗
23. Mater. Chem. Phys. · 2009 · 117 · 19210.1016/j.matchemphys.2009.05.042 ↗
24. Phys. Rev. B. · 2002 · 65 · 05240610.1103/PhysRevB.65.052406 ↗
25. Ferroelectrics · 1998 · 218 · 8510.1080/00150199808227136 ↗
26. Phys. Rev. B. · 2014 · 89 · 14410410.1103/PhysRevB.89.144104 ↗
27. Phys. Rev. B. · 2015 · 91 · 17410310.1103/PhysRevB.91.174103 ↗