手性(物理)
材料科学
钙钛矿(结构)
对映体
配体(生物化学)
激子
圆极化
超分子手性
卤化物
金属
化学物理
光子学
结晶学
超分子化学
立体化学
凝聚态物理
光电子学
晶体结构
光学
化学
物理
有机化学
手征异常
费米子
生物化学
受体
量子力学
Nambu–Jona Lasinio模型
冶金
微带线
作者
Bing Tang,Shixun Wang,Haochen Liu,Nanli Mou,Arsenii S. Portniagin,Peigang Chen,Ye Wu,Xiaoqing Gao,Dangyuan Lei,Andrey L. Rogach
标识
DOI:10.1002/adom.202301524
摘要
Abstract Owing to their attractive optical and chiroptical properties, chiral metal halide perovskites have received increasing attention, with potential applications ranging from photonics and optoelectronics to spintronics. Metal halide perovskite nanocrystals with either intrinsic or extrinsic (e.g., chiral ligand‐induced) chirality have been reported recently, and the interplay between these two types of chirality has yet to be addressed. Herein, the inversion and tuning of excitonic optical activity is reported in intrinsically chiral perovskite nanoplatelets, originating from interactions between their structural chirality (due to the spontaneously formed screw dislocations in the crystalline lattice) and the surface enantiomeric (R/S) chiral ligands R/S‐phenylethylammonium bromide. Through post‐preparative exposure of the perovskite nanoplatelets to these R/S ligands of varied contents, either chiral ligand‐induced intrinsic chirality inversion or negative and positive Cotton effects induced by the ligands via electronic coupling between the ligand and the nanoplatelets are identified. These findings deepen understanding of the modulation of excitonic optical activity in chiral perovskites and can guide the rational design and synthesis of novel chiral materials.
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