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首页> 外文期刊>Physical review >Spin structure at zero magnetic field and field-induced spin reorientation transitions in a layered organic canted antiferromagnet bordering a superconducting phase
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Spin structure at zero magnetic field and field-induced spin reorientation transitions in a layered organic canted antiferromagnet bordering a superconducting phase

机译:旋转结构处于零磁场和场诱导的自旋重新定向转换,层状有机倾斜反霉菌抗逆式转换,边界超导相

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摘要

We attempted to assign the spin structure of a layered organic antiferromagnet, κ-(d8-BEDT-TTF)_2Cu[N(CN)_2]Br. which is a key material located closest to the Mott boundary at ambient pressure among this family of compounds, by investigating its macroscopic magnetization thoroughly, motivated by a recent successful assignment of the spin structure of an isostructural material, κ-(BEDT-TTF)_2Cu[N(CN)_2]Cl [BEDT-TTF and d8-BEDT-TTF are bis(ethylenedithio)tetrathiafulvalene and its deuterated molecule, respectively]. We measured the isothermal magnetization after careful choice of the measurement temperatures and cooling speed at around 80 K. so that the magnetism of the antiferromagnetic phase can be effectively extracted. Consequently, we observed hysteresis loops signifying ferromagnetism and steplike behavior when the magnetic field applied parallel to the crystallographic b and a axes was swept, respectively. The possible spin structure consistent with these results was discussed in terms of probable interactions between the spins, such as exchange interactions and the Dzyaloshinskii-Moriya interaction. Eventually, we asserted that κ-(d8-BEDT-TTF)_2Cu[N(CN)_2]Br has a spin structure with the easy axis being the c axis and the net canted moment parallel to the b axis, which is surprisingly different from that of κ-(BEDT-TTF)_2Cu[N(CN)_2]Cl. We suggested that this difference originates from the difference of the sign of the interlayer interaction between the two materials. We also elucidated the overall picture of the magnetization processes of this material under the magnetic fields parallel to the three principle axes, which are also in contrast to those of κ-(BEDT-TTF)_2Cu[N(CN)_2]Cl. In particular, the spin-reverse transition at which half of the spins rotate by 180° was not induced by the b-axis magnetic field, as in the case of κ-(BEDT-TTF)_2Cu[N(CN)_2]Cl. but by the α-axis magnetic field. Finally, numerical simulations and magnetic symmetry analysis enabled us to confirm the validity of the spin structures proposed for the two antiferromagnets under zero and high magnetic fields.
机译:我们试图分配层状有机反霉菌,κ-(D8-BEDT-TTF)_2CU [N(CN)_2] BR的旋转结构。这是一种钥匙材料,该关键材料通过彻底研究其宏观磁化,通过彻底的宏观结构的宏观结构的旋转结构,κ-(bedt-ttf)_2cu的旋转结构的成功分配,其位于该化合物中最近的宏观磁化的关键材料。 [N(CN)_2] Cl [卧床TTF和D8-BEDT-TTF分别是双(乙基噻嗪)四血红素和其氘代分子]。我们在仔细选择测量温度和约80k的冷却速度之后测量等温磁化。从而可以有效地提取反铁磁相的磁性。因此,当平行于晶体B和轴施加的磁场分别扫描时,我们观察了磁滞回路,表示铁磁场和温度镜的行为。与这些结果一致的可能的旋转结构在于旋转之间的可能相互作用,例如交换相互作用和Dzyaloshinskii-Moriya相互作用。最终,我们断言κ-(d8-bedt-ttf)_2cu [n(cn)_2] br具有旋转结构,简单的轴是C轴和平行于B轴的净倾斜瞬间,令人惊讶的是从κ-(bedt-ttf)_2cu [n(cn)_2] cl的那个。我们建议这种差异来自两种材料之间层间相互作用的符号的差异。我们还阐明了在平行于三个原理轴的磁场下该材料的磁化过程的整体图像,这也与κ-(床TTF)_2CU [N(CN)_2] Cl相反。特别地,旋转反转转变,其中一半的旋转旋转180°的B轴磁场诱导,如κ-(卧TTF)_2cu [n(cn)_2] cl的情况下。但是通过α轴磁场。最后,数值模拟和磁对称分析使我们能够确认为零和高磁场下的两个反铁磁磁带所提出的旋转结构的有效性。

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  • 来源
    《Physical review》 |2020年第3期|035102.1-035102.14|共14页
  • 作者单位

    Graduate School of Science and Engineering Saitama University Saitama 338-8570 Japan;

    Graduate School of Science and Engineering Saitama University Saitama 338-8570 Japan;

    Graduate School of Science and Engineering Saitama University Saitama 338-8570 Japan;

    Graduate School of Science and Engineering Saitama University Saitama 338-8570 Japan;

    Graduate School of Science and Engineering Saitama University Saitama 338-8570 Japan;

    Graduate School of Science and Engineering Saitama University Saitama 338-8570 Japan;

    Graduate School of Science and Engineering Saitama University Saitama 338-8570 Japan;

    Meson Science Laboratory Nishina Center for Accelerator-Based Science Institute of Physical and Chemical Research (RIKEN) 2-1 Hirosawa Wako 351-0198 Japan;

    Meson Science Laboratory Nishina Center for Accelerator-Based Science Institute of Physical and Chemical Research (RIKEN) 2-1 Hirosawa Wako 351-0198 Japan;

    Department of Physics College of Engineering Shibaura Institute of Technology Saitama 337-8570 Japan;

    Faculty of Medicine Kanazawa University Kodatsuno 5-11-89 Kanazawa 920-0942 Japan;

    Department of Applied Physics Tokyo University of Science Tokyo 125-8585 Japan;

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