单斜晶系
钒酸盐
结晶学
反铁磁性
二聚体
发光
离子
化学
空间组
钒
晶体结构
固态
X射线晶体学
材料科学
无机化学
物理化学
物理
衍射
光电子学
有机化学
光学
凝聚态物理
作者
Nannan Wang,Zhangzhen He,Meiyan Cui,Wenbin Guo,Suyun Zhang,Ming Yang
摘要
A series of vanadate compounds Ba3M(V2O7)2 (M = Co, Mn, Mg, or Zn) are synthesized by a conventional high-temperature solid-state reaction. Four compounds are found to exhibit a similar structure, which all crystallize in the monoclinic system of space group P21/c. V5+ ions are tetrahedrally coordinated, forming corner-shared (V2O7)4– groups, while M2+ ions are octahedrally coordinated, forming edge-shared [M2O10] dimers. Isolated {M2V8O28}∞ clusters composed of [M2O10] dimer and (V2O7)4– groups form a pseudo-one-dimensional chain running along the a-axis. Magnetic measurements confirm that both Ba3Co(V2O7)2 and Ba3Mn(V2O7)2 show antiferromagnetic interaction exchanges in the systems, while luminescence measurements confirm that Ba3Mg(V2O7)2 and Ba3Zn(V2O7)2 have a broad emission band from 400 to 650 nm under 256 nm UV irradiation at room temperature.
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