TY - JOUR
T1 - Surface triggered stabilization of metastable charge-ordered phase in SrTiO3
AU - Eom, Kitae
AU - Chung, Bongwook
AU - Oh, Sehoon
AU - Zhou, Hua
AU - Seo, Jinsol
AU - Oh, Sang Ho
AU - Jang, Jinhyuk
AU - Choi, Si Young
AU - Choi, Minsu
AU - Seo, Ilwan
AU - Lee, Yun Sang
AU - Kim, Youngmin
AU - Lee, Hyungwoo
AU - Lee, Jung Woo
AU - Lee, Kyoungjun
AU - Rzchowski, Mark
AU - Eom, Chang Beom
AU - Lee, Jaichan
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/2/8
Y1 - 2024/2/8
N2 - 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., d1-d0. 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.
AB - 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., d1-d0. 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.
UR - https://www.scopus.com/pages/publications/85185128116
U2 - 10.1038/s41467-024-45342-8
DO - 10.1038/s41467-024-45342-8
M3 - Article
C2 - 38332134
AN - SCOPUS:85185128116
SN - 2041-1723
VL - 15
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 1180
ER -