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首页> 外文期刊>Physical review, B >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, kappa-(d8-BEDT-TTF)(2)Cu[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, kappa-(BEDT-TTF)(2)Cu[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 kappa-(d8-BEDT-TTF)(2)Cu[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 kappa-(BEDT-TTF)(2)Cu[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 kappa-(BEDT-TTF)(2)Cu[N(CN)(2)]Cl. In particular, the spin-reverse transition at which half of the spins rotate by 180 degrees was not induced by the b-axis magnetic field, as in the case of kappa-(BEDT-TTF)(2)Cu[N(CN)(2)]Cl, but by the a-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素,Kappa-(D8-Bedt-TTF)(2)Cu [N(CN)(2)] Br的旋转结构,该旋转结构是位于环境温度下最接近Mott边界的关键材料通过彻底研究其宏观磁化,通过彻底研究其近期成功分配旋转结构的旋转结构,Kappa-(Bedt-TTF)(2)Cu [N(CN)(2)] Cl [床型TTF和D8-BEDT-TTF分别是双(乙基噻嗪)四硫甲醛及其氘代分子]。在仔细选择测量温度和冷却速度约为80 k的冷却速度之后,我们测量了等温磁化,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,Kappa-(D8-Bedt-TTF)(2)Cu [N(CN)(2)] Br具有旋转结构,具有易轴是C轴和平行于B轴的净倾斜瞬间,这与Kappa-(Bedt-TTF)(2)Cu [N(CN)(2)] Cl的令人惊讶的不同。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。我们还阐明了与三个原理轴平行的磁场下该材料的磁化过程的整体图像,这也与Kappa-(Bedt-TTF)(2)Cu的磁场相反[n(CN)(2 )] cl。特别地,在kappa-(bedt-ttf)(2)Cu的情况下,不引起旋转旋转的旋转旋转旋转180度的旋转旋转180度的旋转旋转180度的旋转旋转180度,如[n(cn)的情况下(2)] CL,但由A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, B》 |2020年第3期|共14页
  • 作者单位

    Saitama Univ Grad Sch Sci &

    Engn Saitama 3388570 Japan;

    Saitama Univ Grad Sch Sci &

    Engn Saitama 3388570 Japan;

    Saitama Univ Grad Sch Sci &

    Engn Saitama 3388570 Japan;

    Saitama Univ Grad Sch Sci &

    Engn Saitama 3388570 Japan;

    Saitama Univ Grad Sch Sci &

    Engn Saitama 3388570 Japan;

    Saitama Univ Grad Sch Sci &

    Engn Saitama 3388570 Japan;

    Saitama Univ Grad Sch Sci &

    Engn Saitama 3388570 Japan;

    RIKEN Nishina Ctr Accelerator Based Sci Meson Sci Lab Inst Phys &

    Chem Res 2-1 Hirosawa Wako Saitama 3510198 Japan;

    RIKEN Nishina Ctr Accelerator Based Sci Meson Sci Lab Inst Phys &

    Chem Res 2-1 Hirosawa Wako Saitama 3510198 Japan;

    Shibaura Inst Technol Coll Engn Dept Phys Saitama 3378570 Japan;

    Kanazawa Univ Fac Med Kodatsuno 5-11-89 Kanazawa Ishikawa 9200942 Japan;

    Tokyo Univ Sci Dept Appl Phys Tokyo 1258585 Japan;

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  • 正文语种 eng
  • 中图分类 固体物理学;
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