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ABX钙钛矿中具有高振动运动的A位阳离子有效地诱导了介电相变。

A-site cation with high vibrational motion in ABX perovskite effectively induces dielectric phase transition.

作者信息

Wang Yu-Zhen, Zhang Zhi-Xu, Su Chang-Yuan, Zhang Tie, Fu Da-Wei, Zhang Yi

机构信息

Ordered Matter Science Research Center, Jiangsu Key Laboratory for Science and Applications of Molecular Ferroelectrics, Southeast University, Nanjing 211189, P.R. China.

出版信息

Dalton Trans. 2021 Mar 21;50(11):3841-3847. doi: 10.1039/d0dt04415f. Epub 2021 Feb 25.

DOI:10.1039/d0dt04415f
PMID:33629085
Abstract

Organic-inorganic hybrid ABX perovskite (OIHPs) with phase transition have considerable application potential in multifunctional devices for their structural tunability and excellent photo/electric performance. Because the interaction between molecules during the crystallization process is difficult to predict and control, exploring targeted chemical design methods to synthesize phase change materials has been an interesting and challenging problem. As per the synergistic effect of anion and cation, we assemble a cation with high vibrational activity and an inorganic anion with large voids to successfully design a one-dimensional OIHPs phase change material. [FMPD][Cd(SCN)] (FMPD = 1-fluoroethyl-1-methylpiperidinium) undergoes two reversible phase transitions above room temperature with the substitution of methyl with fluoroethyl increasing the energy barrier of molecular motion. The individual crystal diffraction structures show that, unlike the phase change caused by the reorientation of organic cations in majority of known perovskites, this phase transition is triggered by the order/disorder of cations and anions related to the vibration increase by the introduction of fluoroethyl. The results provide a new design idea for the design and assembly of novel OIHPs-type phase change materials.

摘要

具有相变的有机-无机杂化ABX钙钛矿(OIHPs)因其结构可调性和优异的光/电性能在多功能器件中具有可观的应用潜力。由于结晶过程中分子间的相互作用难以预测和控制,探索有针对性的化学设计方法来合成相变材料一直是一个有趣且具有挑战性的问题。根据阴离子和阳离子的协同效应,我们组装了具有高振动活性的阳离子和具有大空隙的无机阴离子,成功设计了一种一维OIHPs相变材料。[FMPD][Cd(SCN)](FMPD = 1-氟乙基-1-甲基哌啶鎓)在室温以上经历两次可逆相变,氟乙基取代甲基增加了分子运动的能垒。单晶衍射结构表明,与大多数已知钙钛矿中有机阳离子重新取向引起的相变不同,这种相变是由与引入氟乙基导致振动增加相关的阳离子和阴离子的有序/无序引发的。该结果为新型OIHPs型相变材料的设计和组装提供了新的设计思路。

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