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Issue 4, 2014
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Engineered spatial inversion symmetry breaking in an oxide heterostructure built from isosymmetric room-temperature magnetically ordered components

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Abstract

The oxide heterostructure [(YFeO3)5(LaFeO3)5]40, which is magnetically ordered and piezoelectric at room temperature, has been constructed from two weak ferromagnetic AFeO3 perovskites with different A cations using RHEED-monitored pulsed laser deposition. The polarisation arises through the removal of inversion centres present within the individual AFeO3 components. This symmetry reduction is a result of combining ordering on the A site, imposed by the periodicity of the grown structure, with appropriate orientations of the octahedral tilting characteristic of the perovskite units themselves, according to simple symmetry-controlled rules. The polarisation is robust against A site interdiffusion between the two layers which produces a sinusoidally modulated occupancy that retains the coupling of translational and point symmetries required to produce a polar structure. Magnetization and magneto-optical Kerr rotation measurements show that the heterostructure's magnetic structure is similar to that of the individual components. Evidence of the polarity was obtained from second harmonic generation and piezoelectric force microscopy measurements. Modeling of the piezoresponse allows extraction of d33 (approximately 10 pC N−1) of the heterostructure, which is in agreement with DFT calculations.

Graphical abstract: Engineered spatial inversion symmetry breaking in an oxide heterostructure built from isosymmetric room-temperature magnetically ordered components

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Publication details

The article was received on 26 Nov 2013, accepted on 20 Jan 2014 and first published on 20 Jan 2014


Article type: Edge Article
DOI: 10.1039/C3SC53248H
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Chem. Sci., 2014,5, 1599-1610

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    Engineered spatial inversion symmetry breaking in an oxide heterostructure built from isosymmetric room-temperature magnetically ordered components

    J. Alaria, P. Borisov, M. S. Dyer, T. D. Manning, S. Lepadatu, M. G. Cain, E. D. Mishina, N. E. Sherstyuk, N. A. Ilyin, J. Hadermann, D. Lederman, J. B. Claridge and M. J. Rosseinsky, Chem. Sci., 2014, 5, 1599
    DOI: 10.1039/C3SC53248H

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