Department of Fundamental Chemistry, Faculty of Sciences, University of A Coruña , 15071 A Coruña, Spain.
Department of Applied Physics, University of Santiago de Compostela , 15782 Santiago de Compostela, Spain.
J Am Chem Soc. 2016 Feb 3;138(4):1122-5. doi: 10.1021/jacs.5b11688. Epub 2016 Jan 20.
We present the first example of magnetic ordering-induced multiferroic behavior in a metal-organic framework magnet. This compound is [CH3NH3][Co(HCOO)3] with a perovskite-like structure. The A-site CH3NH3 cation strongly distorts the framework, allowing anisotropic magnetic and electric behavior and coupling between them to occur. This material is a spin canted antiferromagnet below 15.9 K with a weak ferromagnetic component attributable to Dzyaloshinskii-Moriya (DM) interactions and experiences a discontinuous hysteretic magnetic-field-induced switching along [010] and a more continuous hysteresis along [101]. Coupling between the magnetic and electric order is resolved when the field is applied along this [101]: a spin rearrangement occurs at a critical magnetic field in the ac plane that induces a change in the electric polarization along [101] and [10-1]. The electric polarization exhibits an unusual memory effect, as it remembers the direction of the previous two magnetic-field pulses applied. The data are consistent with an inverse-DM mechanism for multiferroic behavior.
我们首次在一个金属有机框架磁体中发现了磁有序诱导的多铁性行为。这种化合物是[CH3NH3][Co(HCOO)3],具有钙钛矿结构。A 位CH3NH3阳离子强烈扭曲了骨架,允许各向异性磁和电行为以及它们之间的耦合发生。这种材料在 15.9 K 以下是自旋倾斜反铁磁体,具有归因于 Dzyaloshinskii-Moriya (DM)相互作用的弱铁磁分量,并沿[010]经历不连续的磁滞磁场诱导开关,沿[101]经历更连续的磁滞。当磁场沿此[101]施加时,磁序和电序之间的耦合得以解决:在交流平面中的临界磁场下发生自旋重排,导致沿[101]和[10-1]的电极化发生变化。电极化表现出异常的记忆效应,因为它记住了前两个磁场脉冲的方向。这些数据与反 DM 机制一致,用于多铁性行为。