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      Structure of epitaxial SrIrO3 perovskite studied by interference between X-ray waves diffracted by the substrate and the thin film

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          Abstract

          A high-pressure metastable orthorhombic phase of SrIrO 3 perovskite has been epitaxially stabilized on several substrates (DyScO 3, GdScO 3, NdScO 3 and SrTiO 3) in the form of thin monocrystalline layers with (110) surface orientation. The unit-cell parameters of the pseudomorphic thin SrIrO 3 layers depend on the biaxial strain imposed by the various substrates due to the different lattice mismatches of the particular substrate and the bulk orthorhombic SrIrO 3 structure. Using X-ray diffractometry, it is shown that both compressive and tensile strain increase the lattice parameters a and b, while the angle γ scales with the applied strain, being smaller or larger than 90° for compressive or tensile strain, respectively, resulting in a small monoclinic distortion of the layer unit cell. Owing to the similarity of the substrate and layer lattices, the diffraction signals from the two structures overlap partially, which complicates structure determination by standard refinement methods using measured integrated intensities. The measured signal is composed of two interfering components corresponding to the waves diffracted by the substrate and by the layer, where the first component is calculated exactly using the known substrate structure, while the second one is determined by the unknown unit-cell parameters of the layer. The unit-cell parameters were refined in order to fit the experimental data with the simulation. The fractional coordinates of the atoms in the unit cell resulting from the fit are similar to those in the bulk structure.

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          Simple ways of determining perovskite structures

          A. Glazer (1975)
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            Electronic and ionic transport properties and other physical aspects of perovskites

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              Is Open Access

              Bandwidth-Controlled Insulator-Metal Transition and Correlated Metallic State in 5\(d\) Transition Metal Oxides Sr\(_{n+1}\)Ir\(_{n}\)O\(_{3n+1}\) (\(n\)=1, 2, and \(\infty\))

              We investigated the electronic structures of the 5\(d\) Ruddlesden-Popper series Sr\(_{n+1}\)Ir\(_{n}\)O\(_{3n+1}\) (\(n\)=1, 2, and \(\infty\)) using optical spectroscopy and first-principles calculations. As 5\(d\) orbitals are spatially more extended than 3\(d\) or 4\(d\) orbitals, it has been widely accepted that correlation effects are minimal in 5\(d\) compounds. However, we observed a bandwidth-controlled transition from a Mott insulator to a metal as we increased \(n\). In addition, the artificially synthesized perovskite SrIrO\(_{3}\) showed a very large mass enhancement of about 6, indicating that it was in a correlated metallic state.
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                Author and article information

                Journal
                JACGAR
                Journal of Applied Crystallography
                J Appl Crystallogr
                International Union of Crystallography (IUCr)
                1600-5767
                April 2017
                February 28 2017
                : 50
                : 2
                : 385-398
                Article
                10.1107/S1600576717000541
                51aa7a34-b5ad-4c9e-bce7-2bae27da2bae
                © 2017

                http://journals.iucr.org/services/copyrightpolicy.html

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