Fröhlich Tobias, Stein Jonas, Bohatý Ladislav, Becker Petra, Gukasov Arsen, Braden Markus
II. Physikalisches Institut, Universität zu Köln, Zülpicher Straße 77, 50937 Köln, Germany.
J Phys Condens Matter. 2018 Jul 25;30(29):295403. doi: 10.1088/1361-648X/aaca6c. Epub 2018 Jun 5.
The compound [Formula: see text] is magnetoelectric but not multiferroic with an erythrosiderite-related structure. We present a comprehensive investigation of its structural and antiferromagnetic phase transitions by polarization microscopy, pyroelectric measurements, x-ray diffraction and neutron diffraction. At about [Formula: see text] K, the compound changes its symmetry from Cmcm to I2/c, with a doubling of the original c-axis. This transformation is associated with rotations of the [Formula: see text] octahedra and corresponds to an ordering of the [Formula: see text] molecules and of the related [Formula: see text] bonds. A significant ferroelectric polarization can be excluded for this transition by precise pyrocurrent measurements. The antiferromagnetic phase transition occurring at [Formula: see text] results in the magnetic space group [Formula: see text], which perfectly agrees with previous measurements of the linear magnetoelectric effect and magnetization.
化合物[化学式:见原文]具有磁电特性,但并非具有与红砷镍矿相关结构的多铁性材料。我们通过偏振显微镜、热释电测量、X射线衍射和中子衍射对其结构和反铁磁相变进行了全面研究。在约[化学式:见原文]K时,该化合物的对称性从Cmcm变为I2/c,原始c轴加倍。这种转变与[化学式:见原文]八面体的旋转相关,并且对应于[化学式:见原文]分子和相关[化学式:见原文]键的有序排列。通过精确的热电流测量可以排除该转变存在显著铁电极化的可能性。在[化学式:见原文]发生的反铁磁相变导致磁空间群为[化学式:见原文],这与先前对线性磁电效应和磁化强度的测量结果完全一致。