Chemical bonding state at grain boundaries in BaTiO3doped with a small amount of cation

T. Yamamoto; K. Hayashi; Yuichi Ikuhara; T. Sakuma

doi:10.1080/095008399177165

Chemical bonding state at grain boundaries in BaTiO₃doped with a small amount of cation

T. Yamamoto, K. Hayashi, Yuichi Ikuhara, T. Sakuma

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4 Citations (Scopus)

Abstract

The chemical bonding state at grain boundaries was examined with electron- energy-loss spectroscopy in BaTiO₃doped with a small amount of cations at a level of 0.001. In contrast with A-site excess compounds, the oxygen K-edge electron energy-loss near-edge structure spectra were different for grain interiors and for grain boundaries in B-site excess compounds. The difference is explained in terms of the linkage of TiO₆octahedra at grain boundaries in the B-site excess BaTiO₃.

Original language	English
Pages (from-to)	327-331
Number of pages	5
Journal	Philosophical Magazine Letters
Volume	79
Issue number	6
DOIs	https://doi.org/10.1080/095008399177165
Publication status	Published - 1999 Jan 1

ASJC Scopus subject areas

Condensed Matter Physics

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10.1080/095008399177165

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AU - Hayashi, K.

AU - Ikuhara, Yuichi

AU - Sakuma, T.

PY - 1999/1/1

Y1 - 1999/1/1

N2 - The chemical bonding state at grain boundaries was examined with electron- energy-loss spectroscopy in BaTiO3doped with a small amount of cations at a level of 0.001. In contrast with A-site excess compounds, the oxygen K-edge electron energy-loss near-edge structure spectra were different for grain interiors and for grain boundaries in B-site excess compounds. The difference is explained in terms of the linkage of TiO6octahedra at grain boundaries in the B-site excess BaTiO3.

AB - The chemical bonding state at grain boundaries was examined with electron- energy-loss spectroscopy in BaTiO3doped with a small amount of cations at a level of 0.001. In contrast with A-site excess compounds, the oxygen K-edge electron energy-loss near-edge structure spectra were different for grain interiors and for grain boundaries in B-site excess compounds. The difference is explained in terms of the linkage of TiO6octahedra at grain boundaries in the B-site excess BaTiO3.

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Chemical bonding state at grain boundaries in BaTiO₃doped with a small amount of cation

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