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Structural Diversity and Magnetic Properties of Hybrid Ruthenium Halide Perovskites and Related Compounds

机译:杂交钌卤化物钙酸盐及相关化合物的结构分集和磁性

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There has been a great deal of recent interest in extended compounds containing Ru3+ and Ru4+ in light of their range of unusual physical properties. Many of these properties are displayed in compounds with the perovskite and related structures. Here we report an array of structurally diverse hybrid ruthenium halide perovskites and related compounds: MA(2)RuX(6) (X=Cl or Br), MA(2)MRuX(6) (M=Na, K or Ag; X=Cl or Br) and MA(3)Ru(2)X(9) (X=Br) based upon the use of methylammonium (MA=CH3NH3+) on the perovskite A site. The compounds MA(2)RuX(6) with Ru4+ crystallize in the trigonal space group R3?m and can be described as vacancy-ordered double-perovskites. The ordered compounds MA(2)MRuX(6) with M+ and Ru3+ crystallize in a structure related to BaNiO3 with alternating MX6 and RuX6 face-shared octahedra forming linear chains in the trigonal P3?m space group. The compound MA(3)Ru(2)Br(9) crystallizes in the orthorhombic Cmcm space group and displays pairs of face-sharing octahedra forming isolated Ru2Br9 moieties with very short Ru-Ru contacts of 2.789 angstrom. The structural details, including the role of hydrogen bonding and dimensionality, as well as the optical and magnetic properties of these compounds are described. The magnetic behavior of all three classes of compounds is influenced by spin-orbit coupling and their temperature-dependent behavior has been compared with the predictions of the appropriate Kotani models.
机译:据含有Ru3 +和Ru4 +的扩展化合物鉴于它们的不同性物理性质,近来有大量的兴趣。这些属性中的许多属性以钙钛矿和相关结构的化合物显示。在这里,我们报告了一系列结构不同的杂交钌卤化物钙酸盐和相关化合物:MA(2)Rux(6)(X = Cl或Br),MA(2)MRUX(6)(m = Na,K或Ag; x基于在钙钛矿网站上使用甲基铵(MA = CH 3 NH 3 +),= Cl或Br)和Ma(3)ru(2)x(9)(x = br)。化合物MA(2)Ru4 +中的Rux(6)在Trigonal Space Grous R 3ΔM中结晶,并且可以描述为空位有序的双钙酸盐。有序化合物MA(2)MA(2)MA +和RU3 +在与BANIO3相关的结构中结晶,其中交替的MX6和RUX6面部共用的八面体在Trigonal P3?M空间组中形成线性链。化合物MA(3)Ru(2)Br(9)在正交CMCM空间组中结晶,显示成对的面部共享八面体形成分离的Ru2BR9部分,其具有2.789埃的非常短的Ru-Ru接触。描述了结构细节,包括氢键和维度的作用,以及这些化合物的光学和磁性。所有三类化合物的磁性行为受自旋轨道耦合的影响,并且它们的温度依赖行为已经与适当的Kotani模型的预测进行了比较。

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