Abstract
The influence of Mg incorporation into A- and B-sites of the perovskite lattice of SrTiO3 ceramics on the structural, microstructural and low-frequency dielectric properties is studied in this work. Compounds in the systems Sr1-xMgxTiO3 and SrTi 1-yMgyO3-δ were synthesised by a conventional solid-state method. The solid solubility of Mg is restricted to x < 1% for A-site occupancy (Sr1-xMgxTiO3) and to y < 15% for B-site occupancy (SrTi1-yMgyO 3-δ). The lattice parameter is found to increase with Mg content for the SrTi1-yMgyO3-δ system, while it is almost invariant in the Sr1-xMgxTiO 3 one. The dependence on the lattice-site occupancy is also verified for the grain growth of ceramics. For SrTi1-yMgyO 3-δ the average grain size markedly decreases with increasing Mg content. For Sr1-xMgxTiO3 the inverse dependence is observed. Contrary to expectations, Mg does not induce ferroelectricity or relaxor-like behaviour in strontium titanate, located in either A-or B-sites of the SrTiO3 lattice. Moreover, fitting the dielectric behaviour to Barrett's law demonstrates that B-site doping drives the system away from the ferroelectric instability. In Mg-doped strontium titanate ceramics the dielectric permittivity and dielectric losses decrease. The results are discussed based on the correlation between cation-site occupancy, charge and chemical stoichiometry in both systems.
| Original language | English |
|---|---|
| Pages (from-to) | 2013-2020 |
| Number of pages | 8 |
| Journal | Applied Physics A: Materials Science and Processing |
| Volume | 79 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - Dec 2004 |
| Externally published | Yes |
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