Spin-induced multiferroicity in the binary perovskite manganite Mn2O3

Nature Communications Nature Publishing Group 9 (2018) 2996

Authors:

J Cong, K Zhai, Y Chai, D Shang, DD Khalyavin, Roger Johnson, DP Kozlenko, Kichanov, AM Abakumov, AA Tsirlin, L Dubrovinsky, X Xu, Z Sheng, SV Ovsyannikov, Y Sun

Abstract:

The ABO3 perovskite oxides exhibit a wide range of interesting physical phenomena remaining in the focus of extensive scientific investigations and various industrial applications. In order to form a perovskite structure, the cations occupying the A and B positions in the lattice, as a rule, should be different. Nevertheless, the unique binary perovskite manganite Mn2O3 containing the same element in both A and B positions can be synthesized under high-pressure high-temperature conditions. Here, we show that this material exhibits magnetically driven ferroelectricity and a pronounced magnetoelectric effect at low temperatures. Neutron powder diffraction revealed two intricate antiferromagnetic structures below 100 K, driven by a strong interplay between spin, charge, and orbital degrees of freedom. The peculiar multiferroicity in the Mn2O3 perovskite is ascribed to a combined effect involving several mechanisms. Our work demonstrates the potential of binary perovskite oxides for creating materials with highly promising electric and magnetic properties.

Magneto-orbital texture in the perovskite modification of Mn2O3

PHYSICAL REVIEW B 98:1 (2018) ARTN 014426

Authors:

Dmitry D Khalyavin, Roger D Johnson, Pascal Manuel, Alexander A Tsirlin, Artem M Abakumov, Denis P Kozlenko, Young Sun, Leonid Dubrovinsky, Sergey V Ovsyannikov

Intrinsic Triple Order in A-site Columnar-Ordered Quadruple Perovskites: Proof of Concept.

Chemphyschem : a European journal of chemical physics and physical chemistry (2018)

Authors:

Alexei A Belik, Dmitry D Khalyavin, Lei Zhang, Yoshitaka Matsushita, Yoshio Katsuya, Masahiko Tanaka, Roger D Johnson, Kazunari Yamaura

Abstract:

There is an emerging topic in the science of perovskite materials: A-site columnar-ordered A2 A'A''B4 O12 quadruple perovskites, which have an intrinsic triple order at the A sites. However, in many examples reported so far, A' and A'' cations are the same, and the intrinsic triple order is hidden. Here, we investigate structural properties of Dy2 CuMnMn4 O12 (1) and Ho2 MnGaMn4 O12 (2) by neutron and X-ray powder diffraction and prove the triple order at the A sites. The cation distributions determined are [Ho2 ]A [Mn]A' [Ga0.66 Mn0.34 ]A'' [Mn3.66 Ga0.34 ]B O12 and [Dy2 ]A [Cu0.73 Mn0.27 ]A' [Mn0.80 Dy0.20 ]A'' [Mn1.89 Cu0.11 ]B1 [Mn2 ]B2 O12 . There are clear signatures of Jahn-Teller distortions in 1 and 2, and the orbital pattern is combined with an original type of charge ordering in 1. Columnar-ordered quadruple perovskites represent a new playground to study complex interactions between different electronic degrees of freedom. No long-range magnetic order was found in 2 by neutron diffraction, and its magnetic properties in low fields are dominated by an impurity with negative magnetization or magnetization reversal. On the other hand, 1 shows three magnetic transitions at 21, 125, and 160 K.

Evolution of magneto-orbital order upon B-site electron doping in Na1−xCaxMn7O12 quadruple perovskite manganites

Physical Review Letters American Physical Society 120:25 (2018) 257202

Authors:

Roger Johnson, F Mezzadri, P Manuel, DD Khalyavin, E Gilioli, Paolo GR Radaelli

Abstract:

We present the discovery and refinement by neutron powder diffraction of a new magnetic phase in the Na1-xCaxMn7O12 quadruple perovskite phase diagram, which is the incommensurate analogue of the well-known pseudo-CE phase of the simple perovskite manganites. We demonstrate that incommensurate magnetic order arises in quadruple perovskites due to the exchange interactions between A and B sites. Furthermore, by constructing a simple mean field Heisenberg exchange model that generically describes both simple and quadruple perovskite systems, we show that this new magnetic phase unifies a picture of the interplay between charge, magnetic and orbital ordering across a wide range of compounds.

Observation of magnetic vortex pairs at room temperature in a planar α-Fe2O3/Co heterostructure

Nature Materials Nature Publishing Group 17 (2018) 581-585

Authors:

Francis Chmiel, Noah Waterfield Price, Roger Johnson, AD Lamirand, J Schad, G van der Laan, DT Harris, C-B Eom, Paolo Radaelli

Abstract:

Vortices, occurring whenever a flow field ‘whirls’ around a one-dimensional core, are among the simplest topological structures, ubiquitous to many branches of physics. In the crystalline state, vortex formation is rare, since it is generally hampered by long-range interactions: in ferroic materials (ferromagnetic and ferroelectric), vortices are observed only when the effects of the dipole–dipole interaction are modified by confinement at the nanoscale1,2,3, or when the parameter associated with the vorticity does not couple directly with strain4. Here, we observe an unprecedented form of vortices in antiferromagnetic haematite (α-Fe2O3) epitaxial films, in which the primary whirling parameter is the staggered magnetization. Remarkably, ferromagnetic topological objects with the same vorticity and winding number as the α-Fe2O3 vortices are imprinted onto an ultra-thin Co ferromagnetic over-layer by interfacial exchange. Our data suggest that the ferromagnetic vortices may be merons (half-skyrmions, carrying an out-of plane core magnetization), and indicate that the vortex/meron pairs can be manipulated by the application of an in-plane magnetic field, giving rise to large-scale vortex–antivortex annihilation.