4.6 Article

Delayed thermal depolarization of Bi0.5Na0.5TiO3-BaTiO3 by doping acceptor Zn2+ with large ionic polarizability

期刊

JOURNAL OF APPLIED PHYSICS
卷 122, 期 20, 页码 -

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AMER INST PHYSICS
DOI: 10.1063/1.5012889

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资金

  1. Beijing Municipal High Level Innovative Team Building Program [IDHT20170502]
  2. Jing-Hua Talents Project of the Beijing University of Technology [2015-JH-L04]
  3. National Natural Science Foundation of China [51602012, 51677001]
  4. Natural Science Foundation of Beijing [4164078]
  5. Ri-Xin Talents Project of the Beijing University of Technology [2017-RX(1)-15]

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In this paper, (Bi0.5Na0.5)(0.94)Ba0.06Ti1-xZnxO3 ceramics (0 <= x <= 0.06 ) were prepared by the solid oxide reaction route. The doping of Zn2+ into Bi0.5Na0.5TiO3-6BaTiO(3) delays the crossover from nonergodic to ergodic states, and the thermal depolarization temperature T-d is delayed from 85 degrees C for pure samples to 120 degrees C for samples doped by 6% Zn2+, as confirmed by temperature-dependent dielectric and ferroelectric measurements. It suggests that the variation of the T-d could be ascribed to the reformation of the long-range ferroelectric order due to the large ionic polarizability of Zn2+. The high ionic polarizability of Zn2+ can result in a large dipole moment of BO6 octahedra, thus strengthening the coherence of neighboring dipoles and suppressing the ferroelectric-relaxor transition. These results improve our understanding on the thermal depolarization of Bi0.5Na0.5TiO3-based ferroelectrics. Published by MP Publishing.

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