手性(物理)
发光
圆二色性
材料科学
齿合度
超分子手性
圆极化
配体(生物化学)
分子间力
光化学
结晶学
超分子化学
晶体结构
化学
手征对称破缺
有机化学
光电子学
金属
物理
光学
分子
受体
生物化学
量子力学
冶金
Nambu–Jona Lasinio模型
微带线
夸克
作者
Shuhua Chen,Jie Fu,Congyang Zhang,Yiqi Hu,Yinghua Qiu,Jinxing Chen,Qiao Zhang,Muhan Cao
标识
DOI:10.1002/adom.202302883
摘要
Abstract Chiral ligand modification has emerged as a promising route to confer intrinsic chirality in perovskite nanocrystals (NCs), thereby imparting them with optically active properties and rendering great superiority in the next generation of circularly polarized luminescence. However, the functionalization of chiral ligand is not fully explored and the underlying mechanism governing chirality transfer remains elusive. Herein, tryptophan (Try), a naturally occurring chiral amino acid, is verified to serve as multidentate chiral ligands attaching on the surface of perovskite NCs. Such strong coordination favors the chirality imprinting on the electronic state of CsPbBr 3 , resulting in notable circular dichroism features and circularly polarized luminescence with a maximum g lum of 2.3 × 10 −3 . It is intriguing that the intermolecular interaction between Try ligands anchored on two neighboring NCs contribute to chiral optical properties as well. The RDG‐NCI analysis have confirmed the hydrogen bond between the amine and carboxylic groups on chiral Try, which may drive the chiral assembly of perovskite NCs.
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