化学
钙钛矿(结构)
二次谐波产生
相变
差示扫描量热法
卤化物
庚烷
电介质
相(物质)
结晶学
无机化学
光电子学
有机化学
凝聚态物理
光学
热力学
物理
激光器
作者
Bo Li,Wenjun Rao,Xiu-Li You,Pan Wang,Jing Wei,Zhenhong Wei,Haina Zhang,Hu Cai
标识
DOI:10.1021/acs.inorgchem.2c03740
摘要
Switchable second harmonic generation (SHG) materials have potential applications in information storage, signal processing, and so on because they can switch between SHG-on and SHG-off states. In this work, we designed and synthesized three organic-inorganic hybrid Rb halide three-dimensional (3D) perovskite materials [1S,4S 2,5-2.2.1-H2dabch]RbX3·0.5H2O (X = Cl, 1; Br, 2; I, 3) based on the chiral 1S,4S-2,5-diazabicyclo[2.2.1]heptane (1S,4S-2,5-2.2.1-dabch). The selection of homochiral organic cations ensures that the compounds 1∼3 crystallize in the noncentrosymmetric and chiral space group P212121, which further leads to reversible SHG responses of the three compounds. Through differential scanning calorimetry (DSC) and dielectric measurements, it revealed that the phase transition point of the compounds 1∼3 increased with RbCl, RbBr, and RbI. This is because the hydrogen interaction H···X between the inorganic framework [RbX3]n and the organic cation [1S,4S-2,5-2.2.1-H2dabch]2+ is increased with the order of I > Br > Cl. This study can provide an effective molecular design strategy for the exploration and construction of temperature-tunable SHG switching materials.
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