Ying Ting-Ting, Wan Ming-Yang, Wang Fang-Xin, Zhang Yu, Tang Yun-Zhi, Tan Yu-Hui, Liao Juan, Wang Li-Juan
Jiangxi Provincial Key Laboratory of, Functional Molecular Materials Chemistry, Jiangxi University of Science and Technology, 156 Hakka Avenue, Jiangxi, Ganzhou, 341000, China.
Chemistry. 2023 Mar 22;29(17):e202203893. doi: 10.1002/chem.202203893. Epub 2023 Feb 16.
One dimensional (1D) organic-inorganic halide hybrid perovskites have the advantages of excellent organic cation modifiability and diversity of inorganic framework structures, which cannot be ignored in the development of multi-functional phase-transition materials in photoelectric and photovoltaic devices. Here, we have successfully modified and synthesized an organic-inorganic hybrid perovskite photoelectric multifunctional phase-transition material: [C H ONCH F]⋅PbBr (1). The synergistic effect of the order double disorder transition of organic cations and the change of the degree of distortion of the inorganic framework leads to its high temperature reversible phase-transition point of T =374 K/346 K and its ultra-low loss high-quality dielectric switch response. Through in-depth research and calculation, compound 1 also has excellent semiconductor characteristics with a band gap of 3.06 eV and the photoluminescence characteristics of self-trapped exciton (STE) broadband emission. Undoubtedly, this modification strategy provides a new choice for the research field of organic-inorganic hybrid perovskite reversible phase-transition photoelectric multifunctional materials with rich coupling properties.
一维(1D)有机-无机卤化物杂化钙钛矿具有优异的有机阳离子可修饰性和无机骨架结构多样性的优点,这在光电和光伏器件中多功能相变材料的发展中不容忽视。在此,我们成功地改性并合成了一种有机-无机杂化钙钛矿光电多功能相变材料:[C₃H₇NH₃CH₂F]·PbBr₃(1)。有机阳离子的有序-双无序转变与无机骨架畸变程度变化的协同效应导致其高温可逆相变点为T = 374 K/346 K,以及超低损耗的高质量介电开关响应。通过深入研究和计算,化合物1还具有优异的半导体特性,带隙为3.06 eV,以及自陷激子(STE)宽带发射的光致发光特性。毫无疑问,这种改性策略为具有丰富耦合特性的有机-无机杂化钙钛矿可逆相变光电多功能材料的研究领域提供了新的选择。