稀有三钒酸盐家族的新代表KMn2V3O10:合成、晶体结构和磁性能

O. Yakubovich, O. Yakubovich, O. Yakubovich, L. Shvanskaya, L. Shvanskaya, Z. Pchelkina, O. Dimitrova, A. Volkov, O. Volkova, O. Volkova, O. Volkova, A. Vasiliev, A. Vasiliev, A. Vasiliev
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引用次数: 5

摘要

采用水热法合成了三钒酸二锰钾KMn2V3O10,并通过单晶x射线衍射测定了其晶体结构。该新型相在空间群P\bar 1中具有三斜对称结晶,单位胞参数为a = 6.912 (5), b = 6.993 (5), c = 9.656 (5) a, α = 101.858 (5), β = 102.627 (5), γ = 100.669(5)°,Z = 2, V = 432.6 (5) A3。其结构由MnO6八面体共享边的四聚体和VO4四面体共享顶点的三聚体构成。这些主要的结构碎片连接在一个由钾离子占据的通道的三维框架中。讨论了这种结构向相互连接的NaCa3Mn(V3O10)(V2O7)结构的转变。由于锰八面体的四聚体与VO4四面体之间的磁交换相互作用,该化合物在TN = 8.2 K时具有反铁磁序。第一性原理计算表明磁耦合通过Mn-O-Mn和Mn-O-V-O-Mn途径进行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel representative in the rare family of trivanadates, KMn2V3O10: synthesis, crystal structure and magnetic properties
Potassium dimanganese trivanadate, KMn2V3O10, was synthesized hydro­thermally and its crystal structure was determined from single-crystal X-ray diffraction data. The novel phase crystallizes with triclinic symmetry in space group P\bar 1 with unit-cell parameters of a = 6.912 (5), b = 6.993 (5), c = 9.656 (5) A, α = 101.858 (5), β = 102.627 (5), γ = 100.669 (5)°, Z = 2 and V = 432.6 (5) A3. Its structure is built from tetramers of MnO6 octahedra sharing edges and trimers of VO4 tetrahedra sharing vertices. These main structural fragments are linked in a three-dimensional framework with channels occupied by potassium ions. The transformation of this structure to that of interconnected NaCa3Mn(V3O10)(V2O7) is discussed. The title compound orders antiferromagnetically at TN = 8.2 K due to the magnetic exchange interactions between tetramers of Mn octahedra through VO4 tetrahedra. First-principles calculations show the magnetic couplings via Mn—O—Mn and Mn—O—V—O—Mn pathways.
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