氢键
分子间力
钙钛矿(结构)
相变
二次谐波产生
材料科学
化学物理
六方晶系
热稳定性
结晶学
相(物质)
高压
纳米技术
化学
凝聚态物理
热力学
分子
有机化学
光学
激光器
物理
作者
Hui Ye,Wang‐Hua Hu,Xiao‐Xian Chen,Bingqing Zhao,Wei‐Xiong Zhang,Xiao‐Ming Chen
标识
DOI:10.1002/asia.202300608
摘要
Abstract Endowing room‐temperature polymorphs with both long‐term stability and easy interconvertibility is a big challenge due to the complexity of intermolecular interactions. Herein, we present a chiral hexagonal perovskite ( R ‐3‐hydroxy‐1‐methylpiperidinium)[CdCl 3 ] having two room‐temperature crystalline forms featuring obviously distinct second‐harmonic‐generation (SHG) signals with a high switching contrast of ~18 times. The two room‐temperature forms could be long‐term stable yet easily interconvertible through an irreversible thermal‐induced phase transition and a pressure‐driven backward transition, by switching hydrogen bonds via collective reorientation of ordered homochiral cations. Based on the essential role of homochiral organic cations in inducing switchable hydrogen bond linkages, this present instance provides good evidence that relatively irregular organic cations could induce more obvious inorganic chain deformations, thus endowing polymorphs with significantly different SHG signals at room temperature.
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