journal article·2013-05

Semiconductivity in Acceptor‐Doped BaTi 1− x Ho x O 3− x /2−δ/2

Yang Liu, Anthony R West

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Abstract

Acceptor‐doped BaTiO 3 powders of formula: BaTi 1− x Ho x O 3− x /2−δ/2 : x = 0.0001, 0.001, 0.01, 0.03, and 0.07, were prepared by sol‐gel synthesis, fired at 800°C–1500°C and either quenched or slow‐cooled to room temperature. Electrical properties of ceramics depended on firing conditions, Ho content, and cooling rate. Pellets of all x values fired at 800°C–1000°C were insulating and, from the presence of OH bands in the IR spectra, charge balance appeared to involve co‐doping of Ho 3+ and H + ions without necessity for oxygen vacancy creation. At higher firing temperatures, OH bands were absent. Pellets fired at 1400°C in air and slow cooled were insulating for both low x (0.0001) and high x (0.07) but at intermediate x (0.001 and 0.01) passed through a resistivity minimum of 20–30 Ω cm at room temperature, attributed to the presence of Ti 3+ ions; it is suggested that, for these dilute Ho contents, each oxygen vacancy is charge compensated by one Ho 3+ and one Ti 3+ ion. At higher x , charge compensation is by Ho 3+ ions and samples are insulating. A second, more general mechanism to generate Ti 3+ ions, and a modest level of semiconductivity, involves reversible oxygen loss at high temperatures.
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Research context

OpenAlex topics: Ferroelectric and Piezoelectric Materials · Electronic and Structural Properties of Oxides · Dielectric properties of ceramics

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

Affiliations

Department of Materials Science and Engineering University of Sheffield Mappin St Sheffield S1 3JD UK

Funding

EPSRC

References (29)

Show source-provided references
1. 10.1143/JJAP.42.110.1143/JJAP.42.1 ↗
2. 10.1111/j.1151-2916.2004.tb07729.x10.1111/j.1151-2916.2004.tb07729.x ↗
3. 10.1016/j.jeurceramsoc.2009.05.03310.1016/j.jeurceramsoc.2009.05.033 ↗
4. 10.1016/0038-1101(64)90068-110.1016/0038-1101(64)90068-1 ↗
5. 10.1007/BF0055009410.1007/BF00550094 ↗
6. Smyth D. M. · 2006 · 253
7. 10.1111/j.1151-2916.2001.tb00684.x10.1111/j.1151-2916.2001.tb00684.x ↗
8. 10.1111/j.1151-2916.2001.tb00694.x10.1111/j.1151-2916.2001.tb00694.x ↗
9. Defect Chemistry of BaTiO3
10. 10.1023/A:102321320890410.1023/A:1023213208904 ↗
11. 10.1111/j.1151-2916.1986.tb07453.x10.1111/j.1151-2916.1986.tb07453.x ↗
12. Defect Chemistry and Electrical Conductivity of Doped Barium Titanate Ceramics
13. 10.1111/j.1151-2916.1984.tb18849.x10.1111/j.1151-2916.1984.tb18849.x ↗
14. 10.1143/JPSJ.14.115910.1143/JPSJ.14.1159 ↗
15. 10.1111/j.1151-2916.1961.tb13742.x10.1111/j.1151-2916.1961.tb13742.x ↗
16. The Nature of Deffects in Semiconducting BaTiO3
17. 10.1111/j.1151-2916.1988.tb05780.x10.1111/j.1151-2916.1988.tb05780.x ↗
18. 10.1111/j.1151-2916.1994.tb05362.x10.1111/j.1151-2916.1994.tb05362.x ↗
19. 10.1063/1.208915810.1063/1.2089158 ↗
20. 10.1063/1.137447610.1063/1.1374476 ↗
21. 10.1111/j.1551-2916.2008.02397.x10.1111/j.1551-2916.2008.02397.x ↗
22. 10.1023/A:101221882673310.1023/A:1012218826733 ↗
23. 10.1039/jm993030043310.1039/jm9930300433 ↗
24. 10.1002/tcr.2008610.1002/tcr.20086 ↗
25. 10.1111/j.1551-2916.2011.04623.x10.1111/j.1551-2916.2011.04623.x ↗
26. 10.1002/adma.1990002030410.1002/adma.19900020304 ↗
27. 10.1111/j.1151-2916.2004.tb06370.x10.1111/j.1151-2916.2004.tb06370.x ↗
28. 10.1149/1.211977810.1149/1.2119778 ↗
29. 10.1039/b822785c10.1039/b822785c ↗