journal article·2015-11-01Open access

Preparation of meta-stable phases of barium titanate by Sol-hydrothermal method

Mahalakshmi Selvaraj, V. Venkatachalapathy, J. Mayandi, S. Karazhanov, J. M. Pearce

AIP Advances· Volume 5· Issue 11

Abstract

Two low-cost chemical methods of sol–gel and the hydrothermal process have been strategically combined to fabricate barium titanate (BaTiO3) nanopowders. This method was tested for various synthesis temperatures (100 °C to 250 °C) employing barium dichloride (BaCl2) and titanium tetrachloride (TiCl4) as precursors and sodium hydroxide (NaOH) as mineralizer for synthesis of BaTiO3 nanopowders. The as-prepared BaTiO3 powders were investigated for structural characteristics using x-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The overall analysis indicates that the hydrothermal conditions create a gentle environment to promote the formation of crystalline phase directly from amorphous phase at the very low processing temperatures investigated. XRD analysis showed phase transitions from cubic - tetragonal - orthorhombic - rhombohedral with increasing synthesis temperature and calculated grain sizes were 34 – 38 nm (using the Scherrer formula). SEM and TEM analysis verified that the BaTiO3 nanopowders synthesized by this method were spherical in shape and about 114 - 170 nm in size. The particle distribution in both SEM and TEM shows that as the reaction temperature increases from 100 °C to 250 °C, the particles agglomerate. Selective area electron diffraction (SAED) shows that the particles are crystalline in nature. The study shows that choosing suitable precursor and optimizing pressure and temperature; different meta-stable (ferroelectric) phases of undoped BaTiO3 nanopowders can be stabilized by the sol-hydrothermal method.
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Research context

OpenAlex topics: Ferroelectric and Piezoelectric Materials · Microwave Dielectric Ceramics Synthesis · Dielectric materials and actuators

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

Affiliations

R.D. Govt. Arts College 1 Department of Physics, , Tamilnadu, Sivaganga - 630561, India

Madurai Kamaraj University 2 Department of Material Science, School of Chemistry, , Tamilnadu Madurai-625 021, India

University of Oslo 3 Department of Physics/Centre for Materials Science and Nanotechnology, , P.O Box 1048 Blindern, NO-0316 Oslo, Norway

Michigan Technological University 4 Department of Materials Science & Engineering, , USA

Institute for Energy Technology 5 Department of Solar Energy, , P.O. Box 40, NO-2027 Kjeller, Norway

Michigan Technological University 6 Department of Electrical & Computer Engineering, , USA

Funding

University Grants Commission

References (38)

Show source-provided references
1. Adv. Mater. · 2008 · 20 · 364910.1002/adma.200800531 ↗
2. Nature. · 2004 · 432 · 73710.1038/nature03107 ↗
3. ACS Nano. · 2014 · 8 · 276610.1021/nn406481k ↗
4. J. Appl. Polym. Sci. · 2012 · 4 · 257710.1002/app.35362 ↗
5. Chem. Mater. · 2013 · 25 · 421510.1021/cm402092f ↗
6. Opt. Express. · 2012 · 20 · 2651110.1364/OE.20.026511 ↗
7. Mater. Lett. · 2008 · 62 · 213610.1016/j.matlet.2007.11.033 ↗
8. Mater. Lett. · 2008 · 62 · 295710.1016/j.matlet.2008.01.083 ↗
9. Mater. Lett. · 2006 · 60 · 97910.1016/j.matlet.2005.10.089 ↗
10. Nature. · 1992 · 358 · 13610.1038/358136a0 ↗
11. Renew. Sust. Energy Rev. · 2011 · 15 · 447010.1016/j.rser.2011.07.104 ↗
12. Energy. · 2009 · 34 · 194710.1016/j.energy.2009.08.012 ↗
13. Science. · 2011 · 334 · 92810.1126/science.1212741 ↗
14. J. Am. Ceram. Soc. · 1993 · 76 · 123310.1111/j.1151-2916.1993.tb03747.x ↗
15. J. Appl. Phys. · 1976 · 47 · 37110.1063/1.322330 ↗
16. J. Appl. Phys. · 1985 · 58 · 161910.1063/1.336051 ↗
17. J. Electro. Chem. Sci. · 2008 · 3 · 1196
18. Appl. Phys. Lett. · 2009 · 94 · 07290310.1063/1.3076125 ↗
19. Appl. Phys. Lett. · 2007 · 90 · 23290210.1063/1.2746066 ↗
20. J. Micromech. Microeng. · 2000 · 10 · 13610.1088/0960-1317/10/2/307 ↗
21. J. Mater. Chem. Phys. · 2008 · 111 · 20910.1016/j.matchemphys.2008.01.020 ↗
22. J. Alloys Compd. · 2007 · 440 · 7810.1016/j.jallcom.2006.09.023 ↗
23. Chem. Mater. · 2008 · 20 · 538110.1021/cm801638d ↗
24. J. Alloys Compd. · 2010 · 505 · 56810.1016/j.jallcom.2010.06.074 ↗
25. J. Am. Ceram. Soc. · 2000 · 83 · 86010.1111/j.1151-2916.2000.tb01286.x ↗
26. J. Phys. Chem. · 1993 · 97 · 236810.1021/j100112a043 ↗
27. J. Am. Ceram. Soc. · 1989 · 72 · 155510.1111/j.1151-2916.1989.tb07706.x ↗
28. J. Theor. Appl. Phys. · 2012 · 6 · 610.1186/2251-7235-6-6 ↗
29. Phys. Rev. · 1939 · 56 · 97810.1103/PhysRev.56.978 ↗
30. J. Am. Chem. Soc. · 2008 · 130 · 695510.1021/ja0758436 ↗
31. Phys. Rev. B. · 2015 · 91 · 10410410.1103/PhysRevB.91.104104 ↗
32. C. R. Acad. Sc. Paris · 1983 · 297 · 899
33. Fourth Euro Ceram. · 1995 · 5 · 203
34. J. Phys. IV. · 1998 · 8 · 85
35. Science. · 1998 · 281 · 164710.1126/science.281.5383.1647 ↗
36. Chem. Eng. · 1970 · 238 · CE 108
37. J. Mater. Sci. Eng. · 2011 · 8 · 2
38. J. Am. Ceram. Soc. · 2007 · 90 · 31110.1111/j.1551-2916.2006.01361.x ↗