journal article·2017-03-01Open access

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

Nabadyuti Barman, Priyank Singh, Chandrabhas Narayana, K. B. R. Varma

AIP Advances· Volume 7· Issue 3

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.
Source: crossref · Quality: baseline

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 ↗