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Local symmetry-reduction in tetragonal (La,Fe)-codoped Pb[Zr0.4Ti0.6]O3 piezoelectric ceramics

Emre Erdem1, Rüdiger-A Eichel1, Hans Kungl2, Michael J Hoffmann2, Andrew Ozarowski3, Hans van Tol3 and Louis Claude Brunel3

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Ferroelectric Pb[Zr0.4Ti0.6]O3 ceramics codoped with La3+ and Fe3+ at dopant concentrations of 1.0 and 0.5 mol. %, respectively, were investigated by means of multifrequency electron paramagnetic resonance (EPR) spectroscopy. The results prove that iron is incorporated at the [Zr,Ti]-site, acts as an acceptor and favors the creation of charged (Fe ' Zr, Ti- VO••) defect dipoles that may give rise to internal bias fields also for 'soft' piezoelectric compounds. In particular, the iron functional center site symmetry was investigated. A multi-site situation was observed in which the orientation of the (Fe ' Zr, Ti- VO••) defect dipole with respect to the orientation of spontaneous polarization is responsible for a (Fe ' Zr, Ti- VO••) center of 'tetragonal' and a different center of 'rhombic' local site symmetry.


PACS

77.84.Dy Niobates, titanates, tantalates, PZT ceramics, etc.

61.72.J- Point defects and defect clusters

76.30.Fc Iron group (3d) ions and impurities (Ti-Cu)

77.22.Ej Polarization and depolarization

61.72.S- Impurities in crystals

Subjects

Condensed matter: electrical, magnetic and optical

Condensed matter: structural, mechanical & thermal

Dates

Issue T129 (December 2007)

Received 31 March 2007, accepted for publication 17 August 2007

Published 22 November 2007



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