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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/羟基桥接bridge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的2D layer层化合物,其中Dy3 +离子驻留在方形反棱镜配位环境中并连接通过羧酸盐/草酸盐/羟基桥联。磁性研究揭示了Dy3 +离子之间的铁磁相互作用,缓慢的磁弛豫以及在零直流磁场下的有效能垒U-eff为186 K,以及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Dy3 +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。另外,理论计算表明,由于Dy3 +离子与羟基之间的强相互作用,Dy3 +离子具有很强的Ising各向异性。

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