A novel representative in the rare family of trivanadates, KMn2V3O10: synthesis, crystal structure and magnetic properties

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

Abstract

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.
稀有三钒酸盐家族的新代表KMn2V3O10:合成、晶体结构和磁性能
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。
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