Alberto Rodríguez-Velamazán José, Fabelo Óscar, Millán Ángel, Campo Javier, Johnson Roger D, Chapon Laurent
Instituto de Ciencia de Materiales de Aragón (ICMA), CSIC - Universidad de Zaragoza, 50009 Zaragoza, Spain.
nstitut Laue-Langevin, 38042 Grenoble Cedex 9, France.
Sci Rep. 2015 Sep 29;5:14475. doi: 10.1038/srep14475.
The number of magnetoelectric multiferroic materials reported to date is scarce, as magnetic structures that break inversion symmetry and induce an improper ferroelectric polarization typically arise through subtle competition between different magnetic interactions. The (NH4)2[FeCl5(H2O)] compound is a rare case where such improper ferroelectricity has been observed in a molecular material. We have used single crystal and powder neutron diffraction to obtain detailed solutions for the crystal and magnetic structures of (NH4)2[FeCl5(H2O)], from which we determined the mechanism of multiferroicity. From the crystal structure analysis, we observed an order-disorder phase transition related to the ordering of the ammonium counterion. We have determined the magnetic structure below TN, at 2 K and zero magnetic field, which corresponds to a cycloidal spin arrangement with magnetic moments contained in the ac-plane, propagating parallel to the c-axis. The observed ferroelectricity can be explained, from the obtained magnetic structure, via the inverse Dzyaloshinskii-Moriya mechanism.
迄今为止报道的磁电多铁性材料数量稀少,因为打破反演对称性并诱导非本征铁电极化的磁结构通常是通过不同磁相互作用之间的微妙竞争而产生的。(NH4)2[FeCl5(H2O)]化合物是在分子材料中观察到这种非本征铁电性的罕见例子。我们使用单晶和粉末中子衍射来获得(NH4)2[FeCl5(H2O)]晶体和磁结构的详细解析,从中我们确定了多铁性的机制。通过晶体结构分析,我们观察到与铵抗衡离子有序化相关的有序-无序相变。我们已经确定了在2K和零磁场下低于TN的磁结构,它对应于一个摆线自旋排列,磁矩包含在ac平面内,沿c轴平行传播。从获得的磁结构来看,观察到的铁电性可以通过逆Dzyaloshinskii-Moriya机制来解释。