4.7 Article

Origin of thermally stable ferroelectricity in a porous barium titanate thin film synthesized through block copolymer templating

Journal

APL MATERIALS
Volume 5, Issue 7, Pages -

Publisher

AMER INST PHYSICS
DOI: 10.1063/1.4995650

Keywords

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Funding

  1. Japan Society for the Promotion of Science (JSPS) [26810126]
  2. Innovation-Boosting Equipment Common (IBEC) Innovation Platform, National Institute of Advanced Industrial Science and Technology (AIST), Japan
  3. Deanship of Scientific Research, King Saud University
  4. service of The Pore Fabrication Pty Ltd. (Australia)
  5. Wollongong City Council (Australia)
  6. Grants-in-Aid for Scientific Research [26810126, 16K17966] Funding Source: KAKEN

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A porous barium titanate (BaTiO3) thin film was chemically synthesized using a surfactant-assisted sol-gel method in which micelles of amphipathic diblock copolymers served as structure-directing agents. In the Raman spectrum of the porous BaTiO3 thin film, a peak corresponding to the ferroelectric tetragonal phase was observed at around 710 cm(-1), and it remained stable at much higher temperature than the Curie temperature of bulk single-crystal BaTiO3 (similar to 130 degrees C). Measurements revealed that the ferroelectricity of the BaTiO3 thin film has high thermal stability. By analyzing high-resolution transmission electron microscope images of the BaTiO3 thin film by the fast Fourier transform mapping method, the spatial distribution of stress in the BaTiO3 framework was clearly visualized. Careful analysis also indicated that the porosity in the BaTiO3 thin film introduced anisotropic compressive stress, which deformed the crystals. The resulting elongated unit cell caused further displacement of the Ti4+ cation from the center of the lattice. This displacement increased the electric dipole moment of the BaTiO3 thin film, effectively enhancing its ferro(piezo) electricity. (C) 2017 Author(s).

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