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A four-coordinate cobalt(II) single-ion magnet with coercivity and a very high energy barrier

机译:具有矫顽力和极高能量垒的四坐标钴(II)单离子磁体

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摘要

Single-molecule magnets display magnetic bistability of molecular origin, which may one day be exploited in magnetic data storage devices. Recently it was realised that increasing the magnetic moment of polynuclear molecules does not automatically lead to a substantial increase in magnetic bistability. Attention has thus increasingly focussed on ions with large magnetic anisotropies, especially lanthanides. In spite of large effective energy barriers towards relaxation of the magnetic moment, this has so far not led to a big increase in magnetic bistability. Here we present a comprehensive study of a mononuclear, tetrahedrally coordinated cobalt(II) single-molecule magnet, which has a very high effective energy barrier and displays pronounced magnetic bistability. The combined experimental-theoretical approach enables an in-depth understanding of the origin of these favourable properties, which are shown to arise from a strong ligand field in combination with axial distortion. Our findings allow formulation of clear design principles for improved materials.
机译:单分子磁体显示出分子起源的磁性双稳性,有一天可能会在磁性数据存储设备中加以利用。最近,人们认识到增加多核分子的磁矩不会自动导致磁双稳性的显着提高。因此,注意力越来越集中在具有大磁各向异性的离子上,尤其是镧系元素。尽管有很大的有效能量壁垒可缓解磁矩,但迄今为止,这并没有导致磁双稳态的大幅提高。在这里,我们对单核,四面体配位的钴(II)单分子磁体进行全面研究,该磁体具有非常高的有效能垒并显示出明显的双稳态。结合实验理论方法可以深入了解这些有利特性的起源,这些特性表明是由于强大的配体场结合轴向变形而产生的。我们的发现可为改进材料制定清晰的设计原则。

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