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      Spin-Lattice Coupling and Frustrated Magnetism in Fe-doped Hexagonal LuMnO3

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          Abstract

          Strong spin-lattice coupling and prominent frustration effects observed in the 50\(\%\) Fe-doped frustrated hexagonal (\(h\))LuMnO\(_3\) are reported. A N\'{e}el transition at \(T_{\mathrm N} \approx\) 112~K and a possible spin re-orientation transition at \(T_{\mathrm {SR}} \approx\) 55~K are observed in the magnetization data. From neutron powder diffraction data, the nuclear structure at and below 300~K was refined in polar \(P6_3cm\) space group. While the magnetic structure of LuMnO\(_3\) belongs to the \(\Gamma_4\) (\(P6'_3c'm\)) representation, that of LuFe\(_{0.5}\)Mn\(_{0.5}\)O\(_3\) belongs to \(\Gamma_1\) (\(P6_3cm\)) which is supported by the strong intensity for the \(\mathbf{(100)}\) reflection and also judging by the presence of spin-lattice coupling. The refined atomic positions for Lu and Mn/Fe indicate significant atomic displacements at \(T_{\mathrm N}\) and \(T_{\mathrm {SR}}\) which confirms strong spin-lattice coupling. Our results complement the discovery of room temperature multiferroicity in thin films of \(h\)LuFeO\(_3\) and would give impetus to study LuFe\(_{1-x}\)Mn\(_x\)O\(_3\) systems as potential multiferroics where electric polarization is linked to giant atomic displacements.

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          Magnetic phase control by an electric field.

          The quest for higher data density in information storage is motivating investigations into approaches for manipulating magnetization by means other than magnetic fields. This is evidenced by the recent boom in magnetoelectronics and 'spintronics', where phenomena such as carrier effects in magnetic semiconductors and high-correlation effects in colossal magnetoresistive compounds are studied for their device potential. The linear magnetoelectric effect-the induction of polarization by a magnetic field and of magnetization by an electric field-provides another route for linking magnetic and electric properties. It was recently discovered that composite materials and magnetic ferroelectrics exhibit magnetoelectric effects that exceed previously known effects by orders of magnitude, with the potential to trigger magnetic or electric phase transitions. Here we report a system whose magnetic phase can be controlled by an external electric field: ferromagnetic ordering in hexagonal HoMnO3 is reversibly switched on and off by the applied field via magnetoelectric interactions. We monitor this process using magneto-optical techniques and reveal its microscopic origin by neutron and X-ray diffraction. From our results, we identify basic requirements for other candidate materials to exhibit magnetoelectric phase control.
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            Giant magneto-elastic coupling in multiferroic hexagonal manganites

            The motion of atoms in a solid always responds to cooling or heating in a way that is consistent with the symmetry of the given space group of the solid to which they belong. When the atoms move, the electronic structure of the solid changes, leading to different physical properties. Therefore, the determination of where atoms are and what atoms do is a cornerstone of modern solid-state physics. However, experimental observations of atomic displacements measured as a function of temperature are very rare, because those displacements are, in almost all cases, exceedingly small. Here we show, using a combination of diffraction techniques, that the hexagonal manganites RMnO3 (where R is a rare-earth element) undergo an isostructural transition with exceptionally large atomic displacements: two orders of magnitude larger than those seen in any other magnetic material, resulting in an unusually strong magneto-elastic coupling. We follow the exact atomic displacements of all the atoms in the unit cell as a function of temperature and find consistency with theoretical predictions based on group theories. We argue that this gigantic magneto-elastic coupling in RMnO3 holds the key to the recently observed magneto-electric phenomenon in this intriguing class of materials.
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              Author and article information

              Journal
              2015-12-23
              Article
              10.1209/0295-5075/110/37007
              1512.07539
              6e6fcff8-5266-47a3-8440-7dcd5ffd3b7a

              http://arxiv.org/licenses/nonexclusive-distrib/1.0/

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              cond-mat.str-el

              Condensed matter
              Condensed matter

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