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由有机阳离子的椅式到船式构象变化引发异常介电相变的无铅混合材料。

Lead-Free Hybrid Material with an Exceptional Dielectric Phase Transition Induced by a Chair-to-Boat Conformation Change of the Organic Cation.

作者信息

Han Shiguo, Zhang Jing, Sun Zhihua, Ji Chengmin, Zhang Weichuan, Wang Yuyin, Tao Kewen, Teng Bing, Luo Junhua

机构信息

State Key Laboratory of Structure Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences , Fuzhou 350002, P. R. China.

College of Physics, Qingdao University , Qingdao 266071, P. R. China.

出版信息

Inorg Chem. 2017 Nov 6;56(21):13078-13085. doi: 10.1021/acs.inorgchem.7b01863.

Abstract

Hybrid organic-inorganic perovskite materials have demonstrated great potential in the field of photovoltaics and photoelectronics. On the basis of the high degree of structural flexibility and compatibility, diverse molecular functional materials have been assembled by modifying the length of the organic components and/or dimensionality of the inorganic frameworks. In this paper, we present a chiral lead-free organic-inorganic hybrid, (piperidinium)SbCl (1), which follows the one-dimensional inorganic frameworks of the corner-sharing SbCl octahedra. Strikingly, 1 displays a dielectric phase transition at T = 338 K, changing from the chiral space group of P222 to polar Pna2 upon heating. Crystal structure analyses reveal that an unusual thermally activated conformation change of the piperidinium cations affords the driving force to the phase transition of 1. That is, organic piperidinium moieties display a chairlike conformation below T, which transforms to a boatlike structure above T. Such an unprecedented change is strongly coupled to the dielectric transition along with notable steplike anomalies, which suggest that 1 could be used as a potential switchable dielectric material. Besides, the temperature-dependent conductivity and theoretical analysis of its electronic structure disclose the semiconducting behavior of 1. This study paves the pathway to the design of new lead-free semiconducting perovskites with targeted properties for optoelectronic application.

摘要

有机-无机杂化钙钛矿材料在光伏和光电子领域已展现出巨大潜力。基于高度的结构灵活性和兼容性,通过改变有机组分的长度和/或无机骨架的维度,已组装出多种分子功能材料。在本文中,我们展示了一种手性无铅有机-无机杂化物(哌啶鎓)SbCl(1),它遵循角共享SbCl八面体的一维无机骨架。引人注目的是,1在T = 338 K时表现出介电相变,加热时从手性空间群P222转变为极性Pna2。晶体结构分析表明,哌啶鎓阳离子异常的热激活构象变化为1的相变提供了驱动力。也就是说,有机哌啶鎓部分在T以下呈现椅式构象,在T以上转变为船式结构。这种前所未有的变化与介电转变以及显著的阶梯状异常强烈耦合,这表明1可作为潜在的可切换介电材料。此外,其温度依赖性电导率和电子结构的理论分析揭示了1的半导体行为。本研究为设计具有用于光电子应用的目标特性的新型无铅半导体钙钛矿铺平了道路。

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