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Issue 5, 2019
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Anion-order driven polar interfaces at LaTiO2N surfaces

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Abstract

Perovskite oxynitrides have recently attracted attention for their ability to photocatalytically split water. Compared to oxides the arrangement of anions in the material represents a further structural degree of freedom. The bulk oxynitride LaTiO2N prefers a bonding-dominated cis nitrogen arrangement, while we have previously shown that the (001) surface prefers a non-polar trans order to compensate polarity. Here we consider, using density functional theory calculations, the polar/non-polar interface that would necessarily be present between the two anion orders. We show that the Ti-terminated surface will adopt up to two trans ordered surface layers, which has a beneficial effect on the oxygen evolution efficiency. We then consider the hypothetical case of a polar cis ordered surface layer atop a non-polar trans bulk and show that similar electronic reconstructions as in the LaAlO3/SrTiO3 interface can be expected when interfaces between different anion orders are engineered in one and the same oxynitride material.

Graphical abstract: Anion-order driven polar interfaces at LaTiO2N surfaces

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Publication details

The article was received on 24 Oct 2018, accepted on 26 Dec 2018 and first published on 10 Jan 2019


Article type: Paper
DOI: 10.1039/C8TA10230A
Citation: J. Mater. Chem. A, 2019,7, 2129-2134

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    Anion-order driven polar interfaces at LaTiO2N surfaces

    S. Ninova and U. Aschauer, J. Mater. Chem. A, 2019, 7, 2129
    DOI: 10.1039/C8TA10230A

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