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    Ultrafast Electric Field-Induced Phase Transition in Bulk Bi0.5Na0.5TiO3 under High-Intensity Terahertz Irradiation 
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    Ultrafast Electric Field-Induced Phase Transition in Bulk Bi0.5Na0.5TiO3 under High-Intensity Terahertz Irradiation

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    Accepted version
    Embargoed until: 2021-12-09
    Reason: Publisher Embargo
    Accepted version
    Embargoed until: 2021-12-09
    Reason: Publisher Embargo
    Publisher
    American Chemical Society (ACS)
    DOI
    10.1021/acsphotonics.0c01559
    Journal
    ACS Photonics
    ISSN
    2330-4022
    Metadata
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    Abstract
    Ultrafast polarization switching is being considered for the next generation of ferroelectric-based devices. Recently, the dynamics of the field-induced transitions associated with this switching have been difficult to explore, due to technological limitations. The advent of terahertz (THz) technology has now allowed for the study of these dynamic processes on the picosecond (ps) scale. In this paper, intense THz pulses were used as a high-frequency electric field to investigate ultrafast switching in the relaxor ferroelectric, Bi0.5Na0.5TiO3. Transient atomic-scale responses, which were evident as changes in reflectivity, were captured by THz probing. The high-energy THz pulses induce an increase in reflectivity, associated with an ultrafast field-induced phase transition from a weakly polar phase (Cc) to a strongly polar phase (R3c) within 20 ps at 200 K. This phase transition was confirmed using X-ray powder diffraction and by electrical measurements, which showed a decrease in the frequency dispersion of relative permittivity at low frequencies.
    Authors
    Zhang, M; McKinnon, RA; Viola, G; Yang, B; Zhang, D; Reece, MJ; Abrahams, I; Yan, H
    URI
    https://qmro.qmul.ac.uk/xmlui/handle/123456789/69703
    Collections
    • School of Engineering and Materials Science [1496]
    Language
    en
    Licence information
    This is a pre-copyedited, author-produced version of an article accepted for publication in ACS Photonics following peer review. The version of record is available https://pubs.acs.org/doi/10.1021/acsphotonics.0c01559
    Copyright statements
    © 2020 American Chemical Society
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