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首页> 外文期刊>International Journal of Quantum Chemistry >Structural disorder, octahedral coordination and two-dimensional ferromagnetism in anhydrous alums
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Structural disorder, octahedral coordination and two-dimensional ferromagnetism in anhydrous alums

机译:无水明矾中的结构紊乱,八面体配位和二维铁磁性

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The crystal structures of the triangular lattice, layered anhydrous alums KCr(SO4)(2), RbCr(SO4)(2) and KAl(SO4), are characterized by X-ray and neutron powder diffraction (NPD) at temperatures between 1.4 and 773 K. The compounds all crystallize in the space group P (3) over bar, with octahedral coordination of the trivalent cations. In all cases, small amounts of disorder in the stackirw of the triangular layers of corner Sharing MO,; octahedra and SO,, tetrahedra is seen, with the MO6-SO4,, network rotated in opposite directions between layers. The electron diffraction study of KCr(SO4)(4) supports this model, which on an average can he taken to imply trigonal prismatic coordination for the M3+ ions: as was previously reported for the prototype anhydrous alum, KAl(SO4)(2). The temperature-dependent magnetic susceptibilities for ACr(SO4)(2) (A = K, Rb, Cs) indicate the presence of predominantly ferromagnetic interactions. Low-temperature powder neutron diffraction reveals that the magnetic ordering is ferromagnetic in-plane, with antiferromagnetic ordering between planes below 3K. (C) 2008 Elsevier Inc. All rights reserved.
机译:三角形晶格,层状无水明矾KCr(SO4)(2),RbCr(SO4)(2)和KAl(SO4)的晶体结构通过X射线和中子粉末衍射(NPD)在1.4至1.4之间的温度下表征773 K.这些化合物全部在bar上的空间群P(3)中结晶,具有三价阳离子的八面体配位。在所有情况下,在共享MO角的三角层的堆叠层中出现少量混乱;八面体和SO(四面体)与MO6-SO4网络在层之间以相反的方向旋转。 KCr(SO4)(4)的电子衍射研究支持此模型,平均而言,他可以暗示M3 +离子的三角棱柱配位:如先前关于原型无水明矾KAl(SO4)(2)的报道。 。 ACr(SO4)(2)的温度依赖性磁化率(A = K,Rb,Cs)表明主要存在铁磁相互作用。低温粉末中子衍射显示,磁序为铁磁面内,在3K以下的平面之间为反铁磁序。 (C)2008 Elsevier Inc.保留所有权利。

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