反铁磁性
离子半径
凝聚态物理
铁磁性
半径
晶体结构
铷
结晶学
离子键合
Crystal(编程语言)
磁化
物理
化学
材料科学
离子
磁场
钾
量子力学
计算机科学
有机化学
程序设计语言
计算机安全
作者
O. V. Yakubovich,Galina V. Kiriukhina,Larisa Shvanskaya,Olga V. Maximova,А. С. Волков,О. В. Димитрова,Evgeniy A. Ovchenkov,O. B. Yumashev,Asif Iqbal,Badiur Rahaman,Tanusri Saha‐Dasgupta,A. N. Vasiliev
标识
DOI:10.1107/s2053229618006034
摘要
Rubidium tetramanganese tris(phosphate), RbMn 4 (PO 4 ) 3 , has been synthesized as single crystals under hydrothermal conditions. The crystal structure was refined in the space group Pnnm ( D 2 h 12 ). It is argued that the size factor R M / R A , i.e. the ratio of the A + ionic radius to the M 2+ ionic radius, within the morphotropic series AM 4 ( T O 4 ) 3 corresponds to a specific type of crystal structure. At low temperatures, the antiferromagnet superimposed on a buckled kagomé network in RbMn 4 (PO 4 ) 3 experiences a transition into a long-range ordered state with finite spontaneous magnetization. First principles calculations provide the dominant magnetic exchange interactions both within and between the kagomé layers. The analysis of these interactions allows us to suggest a model of alternating ferromagnetic and antiferromagnetic arrangements within chains of Mn3 atoms.
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