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Surface triggered stabilization of metastable charge-ordered phase in SrTiO<sub>3</sub>open access

Authors
Eom, KitaeChung, BongwookOh, SehoonZhou, HuaSeo, JinsolOh, Sang HoJang, JinhyukChoi, Si-YoungChoi, MinsuSeo, IlwanLee, Yun SangKim, YoungminLee, HyungwooLee, Jung-WooLee, KyoungjunRzchowski, MarkEom, Chang-BeomLee, Jaichan
Issue Date
8-Feb-2024
Publisher
NATURE PORTFOLIO
Citation
NATURE COMMUNICATIONS, v.15, no.1
Indexed
SCIE
SCOPUS
Journal Title
NATURE COMMUNICATIONS
Volume
15
Number
1
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/110120
DOI
10.1038/s41467-024-45342-8
ISSN
2041-1723
2041-1723
Abstract
Charge ordering (CO), characterized by a periodic modulation of electron density and lattice distortion, has been a fundamental topic in condensed matter physics, serving as a potential platform for inducing novel functional properties. The charge-ordered phase is known to occur in a doped system with high d-electron occupancy, rather than low occupancy. Here, we report the realization of the charge-ordered phase in electron-doped (100) SrTiO3 epitaxial thin films that have the lowest d-electron occupancy i.e., d(1)-d(0). Theoretical calculation predicts the presence of a metastable CO state in the bulk state of electron-doped SrTiO3. Atomic scale analysis reveals that (100) surface distortion favors electron-lattice coupling for the charge-ordered state, and triggering the stabilization of the CO phase from a correlated metal state. This stabilization extends up to six unit cells from the top surface to the interior. Our approach offers an insight into the means of stabilizing a new phase of matter, extending CO phase to the lowest electron occupancy and encompassing a wide range of 3d transition metal oxides.
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