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Optically Induced Picosecond Lattice Compression in the Dielectric Component of a Strongly Coupled Ferroelectric/Dielectric Superlattice

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Abstract
Above-bandgap femtosecond optical excitation of a ferroelectric/dielectric BaTiO3/CaTiO3 superlattice leads to structural responses that are a consequence of the screening of the strong electrostatic coupling between the component layers. Time-resolved X-ray free-electron laser diffraction shows that the structural response to optical excitation includes a net lattice expansion of the superlattice consistent with depolarization-field screening driven by the photoexcited charge carriers. The depolarization-field-screening-driven expansion is separate from a photoacoustic pulse launched from the bottom electrode on which the superlattice is epitaxially grown. The distribution of diffracted intensity of superlattice X-ray reflections indicates that the depolarization-field-screening-induced strain includes a photoinduced expansion in the ferroelectric BaTiO3 and a contraction in CaTiO3. The magnitude of expansion in BaTiO3 layers is larger than the contraction in CaTiO3. The difference in the magnitude of depolarization-field-screening-driven strain in the BaTiO3 and CaTiO3 components can arise from the contribution of the oxygen octahedral rotation patterns at the BaTiO3/CaTiO3 interfaces to the polarization of CaTiO3. The depolarization-field-screening-driven polarization reduction in the CaTiO3 layers points to a new direction for the manipulation of polarization in the component layers of a strongly coupled ferroelectric/dielectric superlattice.
Author(s)
Gyan, Deepankar SriLee, Hyeon JunAhn, YoungjunCarson, River B.Carnis, JeromeKim, Tae YeonUnithrattil, SanjithLee, Jun YoungChun, Sae HwanKim, SunamEom, IntaeKim, MinseokPark, Sang-YounKim, Kyung SookLee, Ho NyungJo, Ji YoungEvans, Paul G.
Issued Date
2022-06
Type
Article
DOI
10.1002/aelm.202101051
URI
https://scholar.gist.ac.kr/handle/local/8684
Publisher
Wiley-VCH Verlag
Citation
Advanced Electronic Materials, v.8, no.6
ISSN
2199-160X
Appears in Collections:
Department of Materials Science and Engineering > 1. Journal Articles
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