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Magnetic structure and dynamics of a strongly one-dimensional cobalt II metal-organic framework

机译:强一维钴II金属-有机骨架的磁性结构和动力学

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摘要

We investigate the magnetism of the CoII4(OH)2(C10H16O4)3 metal-organic framework, which displays complex inorganic chains separated from each other by distances of 1 to 2 nm and orders at 5.4 K. The zero-field magnetic structure is determined using neutron powder diffraction: it is mainly antiferromagnetic but possesses a ferromagnetic component along the c axis. This magnetic structure persists in presence of a magnetic field. Alternating current susceptibility measurements confirm the existence of a single thermally activated regime over seven decades in frequency (E/kB≈64 K), whereas time-dependent relaxation of the magnetization after saturation in an external field leads to a two times smaller energy barrier. These experiments probe the slow dynamics of domain walls within the chains: we propose that the ac measurements are sensitive to the motion of existing domain walls within the chains, while the magnetization measurements are governed by the creation of domain walls. © 2014 American Physical Society.
机译:我们研究了CoII4(OH)2(C10H16O4)3金属-有机骨架的磁性,该骨架显示复杂的无机链彼此隔开1到2 nm的距离,并且在5.4 K时有序。确定了零场磁结构使用中子粉末衍射:主要是反铁磁的,但沿c轴具有铁磁分量。该磁性结构在磁场存在下持续存在。交流电磁化率测量结果证实,在七年的时间里(E /kB≈64K),存在一个单一的热激活机制,而在外部磁场饱和后,磁化随时间的松弛导致能量垒减小了两倍。这些实验探究了链中畴壁的缓慢动力学:我们建议交流测量对链中现有畴壁的运动敏感,而磁化测量则受畴壁的形成支配。 ©2014美国物理学会。

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