1. Stability of ferroelectric phase and structural characteristics in oriented PbTiO3 ceramic coating formed by aerosol deposition method
- Author
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Lin Wu, Sangwook Kim, Chikako Moriyoshi, Muneyasu Suzuki, Kentaro Shinoda, Rintaro Aoyagi, Jun Akedo, and Yoshihiro Kuroiwa
- Subjects
Physics and Astronomy (miscellaneous) - Abstract
Temperature-dependent structural variations of ceramic coatings of lead titanate PbTiO3 (PT) formed at room temperature (RT) via aerosol deposition (AD) have been investigated to evaluate the stability of the ferroelectric phase. Synchrotron radiation x-ray diffraction experiments in the as-deposited state showed a polycrystalline film oriented preferentially along the c-axis of the perovskite-type ferroelectric tetragonal structure on the quartz glass substrate. The c-axis orientation may be attributed to the anisotropic structural characteristics of the crystal with a layered structure composed of a two-dimensional (2D) covalent bonding network in the ferroelectric phase at RT. The 2D interfaces of the ceramic particles in the aerosol, which are chemically activated by collision with the substrate, are most likely to recombine during the AD process and form a dense and hard coating at RT. When the PT film was heated to the paraelectric phase with a cubic structure at 1000 K, the c-axis orientation observed in the as-deposited state disappeared upon cooling owing to the degree of freedom in selecting the polar axis associated with the cubic-tetragonal phase transition. The spontaneous lattice distortion of the AD film at RT was smaller than that of the bulk ceramic. However, the phase transition temperature ( TC) was approximately 100 K higher only during the first heating process from the c-oriented as-deposited state. The AD method stabilizes the ferroelectric phase up to a higher temperature, although the spontaneous polarization is suppressed. The ferroelectric ceramic materials synthesized mainly via particle collisions are assumed to have low ferroelectricity but high TC.
- Published
- 2023
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