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Anisotropic two-dimensional electron gas at the LaAlO3/SrTiO3 (110) interface.

Authors :
Annadi, A.
Zhang, Q.
Renshaw Wang, X.
Tuzla, N.
Gopinadhan, K.
Lü, W. M.
Roy Barman, A.
Liu, Z. Q.
Srivastava, A.
Saha, S.
Zhao, Y. L.
Zeng, S. W.
Dhar, S.
Olsson, E.
Gu, B.
Yunoki, S.
Maekawa, S.
Hilgenkamp, H.
Venkatesan, T.
Ariando
Source :
Nature Communications; May2013, Vol. 4 Issue 5, p1838, 01p
Publication Year :
2013

Abstract

The observation of a high-mobility two-dimensional electron gas between two insulating complex oxides, especially LaAlO<subscript>3</subscript>/SrTiO<subscript>3</subscript>, has enhanced the potential of oxides for electronics. The occurrence of this conductivity is believed to be driven by polarization discontinuity, leading to an electronic reconstruction. In this scenario, the crystal orientation has an important role and no conductivity would be expected, for example, for the interface between LaAlO<subscript>3</subscript> and (110)-oriented SrTiO<subscript>3</subscript>, which should not have a polarization discontinuity. Here we report the observation of unexpected conductivity at the LaAlO<subscript>3</subscript>/SrTiO<subscript>3</subscript> interface prepared on (110)-oriented SrTiO<subscript>3</subscript>, with a LaAlO<subscript>3</subscript>-layer thickness-dependent metal-insulator transition. Density functional theory calculation reveals that electronic reconstruction, and thus conductivity, is still possible at this (110) interface by considering the energetically favourable (110) interface structure, that is, buckled TiO<subscript>2</subscript>/LaO, in which the polarization discontinuity is still present. The conductivity was further found to be strongly anisotropic along the different crystallographic directions with potential for anisotropic superconductivity and magnetism, leading to possible new physics and applications. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
4
Issue :
5
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
87797636
Full Text :
https://doi.org/10.1038/ncomms2804