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Birefringence induced by antiferroelectric switching in transparent polycrystalline PbZr0.95Ti0.05O3 film

Pranab Parimal Biswas1,2,*, Cosme Milesi-Brault1,2,3,4, Alfredo Blázquez Martínez1,2,3, Naveen Aruchamy1,3, Longfei Song1,3, Veronika Kovacova2,3, Sebastjan Glinšek2,3, Torsten Granzow2,3, Emmanuel Defay2,3 et al.

Mael Guennou1,2,*

  • 1Department of Physics and Materials Science, University of Luxembourg, 41 rue du Brill, L-4422 Belvaux, Luxembourg
  • 2Inter-institutional Research Group Uni.lu–LIST on Ferroic Materials, 41 rue du Brill, L-4422 Belvaux, Luxembourg
  • 3Materials Research and Technology Department, Luxembourg Institute of Science and Technology, 41 rue du Brill, L-4422 Belvaux, Luxembourg
  • 4Institute of Physics of the Czech Academy of Sciences, Na Slovance 1999/2, 182 21 Prague, Czech Republic

  • *Authors to whom correspondence should be addressed: pranab.biswas@uni.lu, mael.guennou@uni.lu

Phys. Rev. Materials 6, L091403 – Published 20 September, 2022

DOI: https://doi.org/10.1103/PhysRevMaterials.6.L091403

Abstract

The most characteristic functional property of antiferroelectric materials is the possibility to induce a phase transition from a nonpolar to a polar phase by an electric field. Here, we investigate the effect of this field-induced phase transition on the birefringence change of PbZr0.95Ti0.05O3. We use a transparent polycrystalline PbZr0.95Ti0.05O3 film grown on PbTiO3/HfO2/SiO2 with interdigitated electrodes to directly investigate changes in birefringence in a simple transmission geometry. In spite of the polycrystalline nature of the film and its moderate thickness, the field-induced transition produces a sizable effect observable under a polarized microscope. The film in its polar phase is found to behave like a homogeneous birefringent medium. The time evolution of this field-induced birefringence provides information about irreversibilities in the antiferroelectric switching process and its slow dynamics. The change in birefringence has two main contributions: One that responds briskly and a slower one that rises and saturates over a period of as long as 30 min. Possible origins for this long saturation and relaxation times are discussed.

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