The Dion-Jacobson (DJ) family of perovskite-related materials have recently attracted interest due to their polar structures and properties, resulting from hybrid-improper mechanisms for ferroelectricity in = 2 systems and from proper mechanisms in = 3 CsBiTiNbO. We report here a combined experimental and computational study on analogous = 3 Cs TiNbO ( = La, Nd) materials. Density functional theory calculations reveal the shallow energy landscape in these systems and give an understanding of the competing structural models suggested by neutron and electron diffraction studies. The structural disorder resulting from the shallow energy landscape breaks inversion symmetry at a local level, consistent with the observed second-harmonic generation. This study reveals the potential to tune between proper and hybrid-improper mechanisms by composition in the DJ family. The disorder and shallow energy landscape have implications for designing functional materials with properties reliant on competing low-energy phases such as relaxors and antiferroelectrics.
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http://dx.doi.org/10.1021/acs.chemmater.0c03326 | DOI Listing |
ACS Omega
October 2024
Instituto de Nanociencia y Materiales de Aragón (INMA), CSIC-Universidad de Zaragoza, Zaragoza 50009, Spain.
We have studied the local structure and electronic and magnetic properties of hybrid improper ferroelectric CaMnO upon Ru substitution at the Mn site by a combination of atomic-selective X-ray absorption spectroscopies in the soft and hard X-ray energy regimes. Ru substitution enhances the macroscopic ferromagnetic contributions, whose origin is here elucidated. In particular, soft X-ray magnetic circular dichroism (XMCD) data indicate that the spin moments of Mn and Ru are aligned in opposite directions, with the effective magnetic moments of Ru being about 1 order of magnitude smaller than for Mn.
View Article and Find Full Text PDFJ Am Chem Soc
September 2024
Department of Materials Chemistry & Institute of Materials and Systems for Sustainability (IMaSS), Nagoya University, Nagoya 464-8601, Japan.
Recent advances in "hybrid-improper" ferroelectricity in Dion-Jacobson (DJ)-type layered perovskites have caused renewed interest in the search for new ferroelectrics. Here, we present an approach for the tailored synthesis of a new homologous series of DJ-type layered perovskites Cs(BiSr)(TiNb)O. Starting from CsBiTiNbO ( = 3), higher-order homologous phases with = 4 and 5 were successfully synthesized by repeated solid-state calcination with SrTiO.
View Article and Find Full Text PDFNat Commun
July 2024
Inner Mongolia Key Lab of Nanoscience and Nanotechnology & School of Physical Science and Technology, Inner Mongolia University, Hohhot, PR China.
Hybrid improper ferroelectricity can effectively avoid the intrinsic chemical incompatibility of electronic mechanism for multiferroics. Perovskite superlattices, as theoretically proposed hybrid improper ferroelectrics with simple structure and high technological compatibility, are conducive to device integration and miniaturization, but the experimental realization remains elusive. Here, we report a strain-driven oxygen octahedral distortion strategy for hybrid improper ferroelectricity in LaNiMnO/LaCoMnO double-perovskite superlattices.
View Article and Find Full Text PDFJ Am Chem Soc
February 2024
Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Katsura Nishikyo-ku, Kyoto 615-8510, Japan.
Rational design of ferroelectrics in layered perovskites, like = 2 Ruddlesden-Popper (RP) phase O, has been achieved by the hybrid-improper ferroelectric (HIF) mechanism, in which an electric polarization is induced via a trilinear coupling to nonpolar O octahedral rotation and tilt distortions around crystallographic axes. In the present work, hybrid improper ferroelectricity in = 2 RP-type LaSrScO induced by the disordering of Sr/La cations on the -sites in rocksalt ([Sr/La] = 25/75) and perovskite ([Sr/La] = 50/50) layers is demonstrated through experimental and theoretical investigations. The ferroelectric 2 structure ( in Glazer notation) at room temperature and the second-order phase transition to paraelectric structure () at ∼ 600 K are determined by a combination of X-ray and neutron diffraction and optical second harmonic generation.
View Article and Find Full Text PDFNat Commun
August 2022
Department of Materials Science and Engineering, The Pennsylvania State University, University Park, PA, 16802, USA.
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