化学
铁电性
卤化物
二次谐波产生
极地的
偶极子
碘化物
钙钛矿(结构)
结晶学
极化(电化学)
各向异性
电介质
无机化学
光电子学
光学
物理化学
材料科学
有机化学
激光器
物理
天文
作者
Weixin He,Yali Yang,Chuanzhao Li,Walter P. D. Wong,Fanica Cimpoesu,Ana Maria Toader,Zhenyue Wu,Xiao Wu,Zexin Lin,Qing‐Hua Xu,Kai Leng,Alessandro Stroppa,Kian Ping Loh
摘要
Ferroelectricity in two-dimensional hybrid (2D) organic–inorganic perovskites (HOIPs) can be engineered by tuning the chemical composition of the organic or inorganic components to lower the structural symmetry and order–disorder phase change. Less efforts are made toward understanding how the direction of the polar axis is affected by the chemical structure, which directly impacts the anisotropic charge order and nonlinear optical response. To date, the reported ferroelectric 2D Dion–Jacobson (DJ) [PbI4]2− perovskites exhibit exclusively out-of-plane polarization. Here, we discover that the polar axis in ferroelectric 2D Dion–Jacobson (DJ) perovskites can be tuned from the out-of-plane (OOP) to the in-plane (IP) direction by substituting the iodide with bromide in the lead halide layer. The spatial symmetry of the nonlinear optical response in bromide and iodide DJ perovskites was probed by polarized second harmonic generation (SHG). Density functional theory calculations revealed that the switching of the polar axis, synonymous with the change in the orientation of the sum of the dipole moments (DMs) of organic cations, is caused by the conformation change of organic cations induced by halide substitution.
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