单斜晶系
铁磁性
铜
晶体结构
卤化物
结晶学
材料科学
极地的
空间组
带隙
Crystal(编程语言)
化学
化学物理
无机化学
光电子学
X射线晶体学
衍射
凝聚态物理
有机化学
光学
程序设计语言
物理
天文
计算机科学
作者
Ceng Han,Alasdair J. Bradford,Jason A. McNulty,Weiguo Zhang,P. Shiv Halasyamani,Alexandra M. Z. Slawin,Finlay D. Morrison,Stephen Lee,Philip Lightfoot
标识
DOI:10.1021/acs.chemmater.2c00107
摘要
Two-dimensional (2D) organic-inorganic hybrid copper halide perovskites have drawn tremendous attention as promising multifunctional materials. Herein, by incorporating ortho-, meta-, and para-chlorine substitutions in the benzylamine structure, we first report the influence of positional isomerism on the crystal structures of chlorobenzylammonium copper(II) chloride perovskites A2CuCl4. 2D polar ferromagnets (3-ClbaH)2CuCl4 and (4-ClbaH)2CuCl4 (ClbaH+ = chlorobenzylammonium) are successfully obtained. They both adopt a polar monoclinic space group Cc at room temperature, displaying significant differences in crystal structures. In contrast, (2-ClbaH)2CuCl4 adopts a centrosymmetric space group P 21/ c at room temperature. This associated structural evolution successfully enhances the physical properties of the two polar compounds with high thermal stability, discernible second harmonic generation (SHG) signals, ferromagnetism, and narrow optical band gaps. These findings demonstrate that the introduction of chlorine atoms into the interlayer organic species is a powerful tool to tune crystal symmetries and physical properties, and this inspires further exploration of designing high-performance multifunctional copper-based materials.
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