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Structural, electrical and optical properties of lanthanide-doped Na0·4K0·1Bi0·5TiO3 ceramics

  • Jacem Zidani*
  • , Moneim Zannen*
  • , Mohammed Hadouchi
  • , Hassan A.H. Alzahrani
  • , Ēriks Birks
  • , Hamadi Khemakhem
  • , Mustapha Majdoub
  • , Mimoun El Marssi
  • , Abdelilah Lahmar
  • *Corresponding author for this work
  • University of Monastir
  • Université de Picardie Jules Verne
  • Mohammed V University in Rabat
  • Islamic University of Madinah
  • University of Jeddah
  • University of Sfax

Research output: Contribution to journalArticlepeer-review

14 Citations (Scopus)

Abstract

Lead-free Sodium–Potassium Bismuth Titanate (Na0·4K0·1Bi0·5TiO3; NKBT) ceramics doped with rare earth elements (RE: Ho, Pr, Nd, Er, Dy) were synthesized using the solid-state reaction technique. The X-ray diffraction analysis showed that the RE-doped NKBT ceramics crystallize in a pure perovskite phase with R3c as the space group. Interestingly, the doped ceramics exhibited low dielectric losses compared to the undoped NKBT, especially in the high temperature region. The dielectric permittivity of the NKBT-Dy ceramic at high temperatures was treated using the temperature coefficient of capacitance (TCC ± 20% with εstable = 2451 in a wide temperature range of 150 °C–470 °C). In addition, all samples showed higher ferroelectric polarization comparing with pure NKBT. Furthermore, the incorporation of RE3+ ions into the NKBT host lattice led to the luminescence properties in the visible region under different excitation wavelengths. The simultaneous presence of ferroelectric/dielectric and photoluminescence properties makes NKBT-RE a promising candidate for optoelectronic applications.

Original languageEnglish
Article number414680
JournalPhysica B: Condensed Matter
Volume653
DOIs
Publication statusPublished - 15 Mar 2023

OECD Field of Science

  • 1.3 Physical Sciences

Keywords

  • Dielectric properties
  • Ferroelectric properties
  • Photoluminescence
  • Sodium potassium bismuth titanate
  • Structural refinement

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