Translator Disclaimer
24 August 2010 Orbital reconstruction at the LAO/STO interface investigated by x-ray spectroscopy
Author Affiliations +
Abstract
The appearance of high mobility electrons at the LaAlO3/SrTiO3 (LAO/STO) interface has raised strong interest in the material science community and a lively debate on the origin of the phenomenon. In particular, in view of the large band gaps of the two bulk single crystals constituting this heterostructure, the realization of a conducting system was totally unexpected. A possible explanation is an electronic reconstruction of the interface, realizing a transfer of electrons from the LaAlO3 surface to SrTiO3 near the interface, thereby avoiding the polarization catastrophe associated with the alternating polar layers of the LaAlO3 film. The predictions of theoretical models based on this idea are quite peculiar and need to be verified by specific experiments able to address the electronic properties of the LAO/STO buried interface. Here, by using x-ray spectroscopy techniques, we show that the appearance of an electron system is correlated to the removal of the degeneracy of the titanium 3d states, and doped electrons appear in a band preferentially created by the hybridization between 3dxy states of titanium and oxygen 2px,y states. This splitting is consistent with an ordering of the Ti 3dxy orbital belonging to the TiO6 octahedra close to the interface, as theoretically proposed. However, the valence of titanium ions remains prevalently 4+, therefore other mechanisms should be also considered for the stabilization of the system.
© (2010) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
G. Ghiringhelli, M. Moretti Sala, J. C. Cezar, N. B. Brookes, G. M. De Luca, and M. Salluzzo "Orbital reconstruction at the LAO/STO interface investigated by x-ray spectroscopy", Proc. SPIE 7760, Spintronics III, 77600V (24 August 2010); https://doi.org/10.1117/12.861465
PROCEEDINGS
9 PAGES


SHARE
Advertisement
Advertisement
Back to Top