4.7 Article

Dielectric response of BaTiO3 electronic states under AC fields via microsecond time-resolved X-ray absorption spectroscopy

期刊

ACTA MATERIALIA
卷 207, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.actamat.2021.116681

关键词

Ferroelectricity; Electrical properties; Electronic structure; External electric field; X-ray absorption spectroscopy

资金

  1. JSPS KAKENHI [18H01153, 19H02426, 18K19126]
  2. European Union [H2020-WIDESPREAD-01-2016-2017-TeamingPhase2, 739508]
  3. Grants-in-Aid for Scientific Research [18H01153] Funding Source: KAKEN

向作者/读者索取更多资源

For the first time, the dielectric response of a BaTiO3 thin film under an AC electric field was investigated using microsecond time-resolved X-ray absorption spectroscopy. The study revealed the correlated contributions of each constituent atom on the electronic states, with Ti 3d hybridizing with O 2p and Ti 4p, and Ba contributing to polarization reversal.
For the first time, the dielectric response of a BaTiO3 thin film under an AC electric field is investigated using microsecond time-resolved X-ray absorption spectroscopy at the Ti K-edge in order to clarify correlated contributions of each constituent atom on the electronic states. Intensities of the pre-edge e(g) peak and shoulder structure just below the main edge increase with an increase in the amplitude of the applied electric field, whereas that of the main peak decreases in an opposite manner. Based on the multiple scattering theory, the increase and decrease of the e(g) and main peaks are simulated for different Ti off-center displacements. Our results indicate that these spectral features reflect the inter- and intraatomic hybridization of Ti 3d with O 2p and Ti 4p, respectively. In contrast, the shoulder structure is not affected by changes in the Ti off-center displacement but is susceptible to the effect of the corner site Ba ions. This is the first experimental verification of electronic contribution of Ba to polarization reversal. (C) 2021 Acta Materialia Inc. Published by Elsevier Ltd.

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