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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Phase transitions and dielectric properties of a hexagonal ABX(3) perovskite-type organic-inorganic hybrid compound: [C3H4NS][CdBr3]
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Phase transitions and dielectric properties of a hexagonal ABX(3) perovskite-type organic-inorganic hybrid compound: [C3H4NS][CdBr3]

机译:六方ABX(3)钙钛矿型有机-无机杂化化合物[C3H4NS] [CdBr3]的相变和介电性能

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摘要

A new organic-inorganic hexagonal perovskite-type compound with the formula ABX(3), thiazolium tribromocadmate(II) (1), in which thiazolium cations are situated in the space between the one-dimensional chains of face-sharing CdBr6 octahedra, has been successfully synthesized. Systematic characterizations including differential scanning calorimetry measurements, variable-temperature structural analyses, and dielectric measurements reveal that it undergoes two structural phase transitions, at 180 and 146 K. These phase transitions are accompanied by remarkable dielectric relaxation and anisotropy. The thiazolium cations remain orientationally disordered during the two phase transition processes. The origins of the phase transitions at 180 and 146 K are ascribed to the slowing down and reorientation of the molecular motions of the cations, respectively. Moreover, the dielectric relaxation process well described by the Cole-Cole equation and the prominent dielectric anisotropy are also connected with the dynamics of the dipolar thiazolium cations.
机译:一种新的具有式ABX(3)的有机-无机六方钙钛矿型化合物,三溴环十二烷噻唑鎓(II)(1),其中噻唑鎓阳离子位于面部共享CdBr6八面体的一维链之间的空间中。已成功合成。包括差示扫描量热法测量,可变温度结构分析和介电测量在内的系统表征表明,它在180和146 K处经历了两个结构相变。这些相变伴随着显着的介电弛豫和各向异性。噻唑鎓阳离子在两个相变过程中保持定向无序。 180和146 K处相变的起源分别归因于阳离子分子运动的减慢和重新取向。此外,很好地由Cole-Cole方程描述的介电弛豫过程和显着的介电各向异性也与偶极噻唑阳离子的动力学有关。

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