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Slow magnetic relaxation in a novel carboxylate/oxalate/hydroxyl bridged dysprosium layer

机译:新型羧酸盐/草酸盐/羟基桥合层中的慢磁弛豫

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摘要

A new 2D dysprosium layer compound has been successfully synthesized from reaction with 2-(3-pyridyl) pyrimidine-4-carboxylic acid (H3-py-4-pmc), in which the Dy3+ ions reside in square antiprismatic coordination environments and are connected by carboxylate/oxalate/hydroxyl bridges. Magnetic studies reveal ferromagnetic interactions between Dy3+ ions, slow magnetic relaxation with an effective energy barrier U eff of 186 K under zero dc field and pronounced hysteresis loops at low temperatures. Further dilution magnetic study suggests that the slow magnetic relaxation originates from the single-ion magnetic behavior of Dy3+ ion and that magnetic coupling suppresses the quantum tunneling of magnetization at low temperature. In addition, theoretical calculation indicates strong Ising anisotropy of the Dy3+ ion that is due to the strong interaction between Dy3+ ions and hydroxyl groups.
机译:通过与2-(3-吡啶基)嘧啶-4-羧酸(H3-py-4-pmc)反应,成功合成了一种新型的2D layer层化合物,其中Dy 3 + 离子驻留在方形反棱镜配位环境中,并通过羧酸根/草酸酯/羟基桥连接。磁性研究表明,Dy 3 + 离子之间存在铁磁相互作用,在零直流磁场下具有186 K的有效能垒U eff的缓慢磁弛豫和在低温下明显的磁滞回线。进一步的稀释磁研究表明,缓慢的磁弛豫源于Dy 3 + 离子的单离子磁行为,并且磁耦合抑制了低温下磁化的量子隧穿。此外,理论计算表明,Dy 3 + 离子具有较强的伊辛各向异性,这归因于Dy 3 + 离子与羟基之间的强相互作用。

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