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琥珀酰亚胺锂(I)杂化物中具有超大介电弛豫行为的可逆相变

Reversible Phase Transition with Ultralarge Dielectric Relaxation Behaviors in Succinimide Lithium(I) Hybrids.

作者信息

Tang Yun-Zhi, Wang Bin, Zhou Hai-Tao, Chen Shao-Peng, Tan Yu-Hui, Wang Chang-Feng, Yang Chang-Shan, Wen He-Rui

机构信息

School of Metallurgy and Chemical Engineering, Jiangxi University of Science and Technology , Ganzhou, 341000, P. R. China.

出版信息

Inorg Chem. 2018 Feb 5;57(3):1196-1202. doi: 10.1021/acs.inorgchem.7b02625. Epub 2018 Jan 22.

Abstract

Dielectric relaxations have widely applied on high permittivity capacitors, dielectric switches, ferroelectrics, pyroelectrics, and electrical insulating materials. However, few investigations of large dielectric relaxation behaviors on organic-inorganic hybrid materials have been documented before. Here we present a novel two-dimensional succinimide lithium(I) hybrid compound, [Li(PDD)ClO], 1, (PDD = 2,5-pyrrolidinedione = succinimide) which shows reversible phase transition behavior in the vicinity of 228 K accompanied by an unusual symmetry breaking from I4/amd to C2/c. X-ray single crystal diffractions analysis indicates the twist motion of pyrrolidine heterocycles, and order-disorder motion of ClO anions triggered the reversible phase transition. By means of an intuitive crystallographic model (rattling ion model), we further illustrated the mechanism of the interesting reversible phase transition. Particularly, 1 shows ultralarge dielectric relaxation behavior in the vicinity of the phase transition by its dielectric constant dependence on temperatures and frequencies as well as its Cole-Cole relation.

摘要

介电弛豫已广泛应用于高介电常数电容器、介电开关、铁电体、热电体和电绝缘材料。然而,此前关于有机-无机杂化材料中大介电弛豫行为的研究报道很少。在此,我们展示了一种新型的二维琥珀酰亚胺锂(I)杂化化合物[Li(PDD)ClO],1,(PDD = 2,5-吡咯烷二酮 = 琥珀酰亚胺),它在228 K附近表现出可逆相变行为,伴随着从I4/amd到C2/c的异常对称性破缺。X射线单晶衍射分析表明吡咯烷杂环的扭转运动以及ClO阴离子的有序-无序运动引发了可逆相变。通过一个直观的晶体学模型(晃动离子模型),我们进一步阐明了这种有趣的可逆相变的机制。特别地,1通过其介电常数对温度和频率的依赖性以及其科尔-科尔关系在相变附近表现出超大的介电弛豫行为。

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