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Effect of the Ag-Doping on the Phase Structural Evolution, Dielectric and Ferroelectric Properties of Lead-Free Niobate Ceramics

Ionic doping is an important approach to modification of crystal structure and physical properties of the piezoelectric ceramics. In this work, the lead-free piezoelectric ceramic (1- x )K 0.18 Na 0.74 Li 0.08 NbO 3 - x AgNbO 3 (abbreviated as KNLN- x AN, 0 ≤ x ≤ 0.8) was prepared by conventional so...

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Published in:Electronic materials letters 2022, 18(2), , pp.159-167
Main Authors: Wang, Huining, Zhang, Zixin, Yang, QuanSen, Wang, Fangfang, Yan, Kang
Format: Article
Language:English
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Summary:Ionic doping is an important approach to modification of crystal structure and physical properties of the piezoelectric ceramics. In this work, the lead-free piezoelectric ceramic (1- x )K 0.18 Na 0.74 Li 0.08 NbO 3 - x AgNbO 3 (abbreviated as KNLN- x AN, 0 ≤ x ≤ 0.8) was prepared by conventional solid-state reaction method. The effect of the Ag doping on the phase structure, dielectric and ferroelectric properties of the KNLN-based ceramics was investigated by the XRD, DSC, dielectric and ferroelectric characterizations. It is found that all KNLN- x AN ceramics show single phase in perovskite structure because the ionic radii of dopant Ag close to the average ionic size at the A-site in KNLN. The KNLN- x AN exhibits the rhombohedral to orthorhombic phase transition at room temperature and the Curie temperature ( T C ) decreases to low temperature with increasing x value. A narrow tetragonal phase region and a wide orthorhombic phase region form for the compositions with x  ≥ 0.4, indicating that the Ag doping stabilizes orthorhombic phase in wide temperature for the KNLN. A ferroelectric anomalies due to high electrical field induced phase transition is found in the sample with x  = 0.1. When x  = 0.4, high Curie temperature ( T C  = 380 °C), large remnant polarization ( P r  = 24.4 μC/cm 2 ) and high dielectric constant ( ε r  = 10,000 at 1 kHz) at T C are achieved. Graphical abstract
ISSN:1738-8090
2093-6788
DOI:10.1007/s13391-021-00328-2