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Journal Article

Valence-state reflectometry of complex oxide heterointerfaces

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Green,  Robert J.
Physics of Correlated Matter, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Haverkort,  Maurits W.
Maurits Haverkort, Physics of Correlated Matter, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Citation

Hamann-Borrero, J. E., Macke, S., Choi, W. S., Sutarto, R., He, F., Radi, A., et al. (2017). Valence-state reflectometry of complex oxide heterointerfaces. npj Quantum Materials, 1: 16013, pp. 1-6. doi:10.1038/npjquantmats.2016.13.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002D-D8DB-F
Abstract
Emergent phenomena in transition-metal-oxide heterostructures such as interface superconductivity and magnetism have been attributed to electronic reconstruction, which, however, is difficult to detect and characterise. Here we overcome the associated difficulties to simultaneously address the electronic degrees of freedom and distinguish interface from bulk effects by implementing a novel approach to resonant X-ray reflectivity (RXR). Our RXR study of the chemical and valance profiles along the polar (001) direction of a LaCoO3 film on NdGaO3 reveals a pronounced valence-state reconstruction from Co3+ in the bulk to Co2+ at the surface, with an areal density close to 0.5 Co2+ ions per unit cell. An identical film capped with polar (001) LaAlO3 maintains the Co3+ valence over its entire thickness. We interpret this as evidence for electronic reconstruction in the uncapped film, involving the transfer of 0.5e -per unit cell to the subsurface CoO2 layer at its LaO-terminated polar surface.