Inversion Symmetry Breaking by Oxygen Octahedral Rotations in the Ruddlesden-Popper<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline"><mml:mrow><mml:mi>Na</mml:mi><mml:mi>R</mml:mi><mml:msub><mml:mrow><mml:mi>TiO</mml:mi></mml:mrow><mml:mrow><mml:mn>4</mml:mn></mml:mrow></mml:msub></mml:mrow></mml:math>Family

2014 Physical Review Letters 76 citations

Abstract

Rotations of oxygen octahedra are ubiquitous, but they cannot break inversion symmetry in simple perovskites. However, in a layered oxide structure, this is possible, as we demonstrate here in A-site ordered Ruddlesden-Popper NaRTiO&lt;sub&gt;4&lt;/sub&gt; (R denotes rare-earth metal), previously believed to be centric. By revisiting this series via synchrotron x-ray diffraction, optical second-harmonic generation, piezoresponse force microscopy, and first-principles phonon calculations, we find that the low-temperature phase belongs to the acentric space group P4̄2&lt;sub&gt;1&lt;/sub&gt;m, which is piezoelectric and nonpolar. The mechanism underlying this large new family of acentric layered oxides is prevalent, and could lead to many more families of acentric oxides.

Keywords

Acentric factorOctahedronPoint reflectionCrystallographyMaterials scienceCondensed matter physicsCrystal structurePhysicsChemistry

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Publication Info

Year
2014
Type
article
Volume
112
Issue
18
Citations
76
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Closed

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Hirofumi Akamatsu, Koji Fujita, Toshihiro Kuge et al. (2014). Inversion Symmetry Breaking by Oxygen Octahedral Rotations in the Ruddlesden-Popper<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline"><mml:mrow><mml:mi>Na</mml:mi><mml:mi>R</mml:mi><mml:msub><mml:mrow><mml:mi>TiO</mml:mi></mml:mrow><mml:mrow><mml:mn>4</mml:mn></mml:mrow></mml:msub></mml:mrow></mml:math>Family. Physical Review Letters , 112 (18) . https://doi.org/10.1103/physrevlett.112.187602

Identifiers

DOI
10.1103/physrevlett.112.187602