TY - JOUR
T1 - Band-Order Anomaly at the δ-Al2O3/SrTiO3Interface Drives the Electron-Mobility Boost
AU - Chikina, Alla
AU - Christensen, Dennis Valbjørn
AU - Borisov, Vladislav
AU - Husanu, Marius Adrian
AU - Chen, Yunzhong
AU - Wang, Xiaoqiang
AU - Schmitt, Thorsten
AU - Radovic, Milan
AU - Nagaosa, Naoto
AU - Mishchenko, Andrey S.
AU - Valentí, Roser
AU - Pryds, Nini
AU - Strocov, Vladimir N.
N1 - Publisher Copyright:
© 2021 The Authors. Published by American Chemical Society.
PY - 2021
Y1 - 2021
N2 - The rich functionalities of transition-metal oxides and their interfaces bear an enormous technological potential. Its realization in practical devices requires, however, a significant improvement of yet relatively low electron mobility in oxide materials. Recently, a mobility boost of about 2 orders of magnitude has been demonstrated at the spinel-perovskite γ-Al2O3/SrTiO3 interface compared to the paradigm perovskite-perovskite LaAlO3/SrTiO3 interface. We explore the fundamental physics behind this phenomenon from direct measurements of the momentum-resolved electronic structure of this interface using resonant soft-X-ray angle-resolved photoemission. We find an anomaly in orbital ordering of the mobile electrons in γ-Al2O3/SrTiO3 which depopulates electron states in the top SrTiO3 layer. This rearrangement of the mobile electron system pushes the electron density away from the interface, which reduces its overlap with the interfacial defects and weakens the electron-phonon interaction, both effects contributing to the mobility boost. A crystal-field analysis shows that the band order alters owing to the symmetry breaking between the spinel γ-Al2O3 and perovskite SrTiO3. Band-order engineering, exploiting the fundamental symmetry properties, emerges as another route to boost the performance of oxide devices.
AB - The rich functionalities of transition-metal oxides and their interfaces bear an enormous technological potential. Its realization in practical devices requires, however, a significant improvement of yet relatively low electron mobility in oxide materials. Recently, a mobility boost of about 2 orders of magnitude has been demonstrated at the spinel-perovskite γ-Al2O3/SrTiO3 interface compared to the paradigm perovskite-perovskite LaAlO3/SrTiO3 interface. We explore the fundamental physics behind this phenomenon from direct measurements of the momentum-resolved electronic structure of this interface using resonant soft-X-ray angle-resolved photoemission. We find an anomaly in orbital ordering of the mobile electrons in γ-Al2O3/SrTiO3 which depopulates electron states in the top SrTiO3 layer. This rearrangement of the mobile electron system pushes the electron density away from the interface, which reduces its overlap with the interfacial defects and weakens the electron-phonon interaction, both effects contributing to the mobility boost. A crystal-field analysis shows that the band order alters owing to the symmetry breaking between the spinel γ-Al2O3 and perovskite SrTiO3. Band-order engineering, exploiting the fundamental symmetry properties, emerges as another route to boost the performance of oxide devices.
KW - electron-phonon interactions
KW - electronic band structure
KW - heterostructures
KW - photoelectron spectroscopy
KW - transition-metal oxides
U2 - 10.1021/acsnano.0c07609
DO - 10.1021/acsnano.0c07609
M3 - Journal article
C2 - 33661601
AN - SCOPUS:85103460225
SN - 1936-0851
VL - 15
SP - 4347
EP - 4356
JO - ACS Nano
JF - ACS Nano
IS - 3
ER -