journal article·2012-10

Density variation and piezoelectric properties of Ba(Ti1 − x Sn x )O3 ceramics prepared from nanocrystalline powders

A K NATH, NIRMALI MEDHI

Bulletin of Materials Science· Volume 35· Issue 5
Publisher page

Abstract

Nanocrystalline powders of tin-doped barium titanate with different concentrations of tin have been synthesized by a combination of solid state reaction and high-energy ball milling. The average particle size of the milled powders as determined from TEM analysis was about 5·96 nm. Analysis of all the milled powders using X-ray diffraction method showed single phase perovskite structure. The density variation of the ceramics with sintering temperature has been studied by sintering the samples at different temperatures. Density variation results show that 1350°C is the optimum sintering temperature for tin-doped barium titanate ceramics. SEM micrographs show high density and increasing trend of grain size with increasing content of Sn. The ferroelectricity decreases with increasing concentration of Sn. The electromechanical coupling coefficient also decreases with increasing Sn content corroborating decreasing trend of ferroelectricity. The bipolar strain curves show piezoelectric properties of the prepared ceramics.
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Research context

OpenAlex topics: Ferroelectric and Piezoelectric Materials · Acoustic Wave Resonator Technologies · Microwave Dielectric Ceramics Synthesis

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

References (16)

Show source-provided references
1. Hennings D, Schreinemacher B and Schreinemacher H 1994 J. Eur. Ceram. Soc. 13 8110.1016/0955-2219(94)90062-0 ↗
2. Jaffe B, Cook W and Jaffe H 1972 Piezoelectric ceramics (New York: Academic Press) pp. 47
3. Jing Z, Ang C, Yu Z, Vilarinho P M and Baptista J L 1998 J. Appl. Phys. 84 98310.1063/1.368164 ↗
4. Kotnala R K, Verma V, Pandey V, Awana V P S, Aloysius R P and Kothari P C 2007 Solid State Commun. 143 52710.1016/j.ssc.2007.07.007 ↗
5. Kuwata J, Uchino K and Nomura S 1982 Jpn J. Appl. Phys. 21 129810.1143/JJAP.21.1298 ↗
6. Lu S G, Xu Z K and Chen H 2004 Appl. Phys. Lett. 85 531910.1063/1.1829794 ↗
7. Markovic S, Mitric M, Cvjeticanin N and Uskokovic D 2007 J. Eur. Ceram. Soc. 27 50510.1016/j.jeurceramsoc.2006.04.066 ↗
8. Park S E and Shrout T R 1997 J. Appl. Phys. 82 180410.1063/1.365983 ↗
9. Park S E, Wada S, Cross L E and Shrout T R 1999 J. Appl. Phys. 86 274610.1063/1.371120 ↗
10. Payne W H and Tennery V J 1965 J. Am. Ceram. Soc. 48 41310.1111/j.1151-2916.1965.tb14779.x ↗
11. Ravez J and Simon A 2001 J. Solid State Chem. 162 26010.1006/jssc.2001.9285 ↗
12. Smolenski G A 1970 J. Phys. Soc. Jpn 28 26
13. Wada S, Suzuki S, Noma T, Susuki T, Osada M, Kakihana M, Park S E, Cross L E and Shrout T R 1999 Jpn J. Appl. Phys. 38 550510.1143/JJAP.38.5505 ↗
14. Williamson G K and Hall W H 1953 Acta Metall. 1 2210.1016/0001-6160(53)90006-6 ↗
15. Wei X and Yao X 2007 Mater. Sci. Eng. B137 18410.1016/j.mseb.2006.11.012 ↗
16. Yasuda N, Ohwa H and Asano S H 1996 Jpn J. Appl. Phys. 35 509910.1143/JJAP.35.5099 ↗