发光
材料科学
圆极化
光致发光
对映体
量子产额
手性(物理)
光学
光电子学
纳米技术
结晶学
荧光
立体化学
物理
量子力学
微带线
手征对称破缺
Nambu–Jona Lasinio模型
化学
夸克
作者
Chong Zhang,Zhi‐Ping Yan,Xi‐Yan Dong,Zhen Han,Si Li,Ting Fu,Yanyan Zhu,You‐Xuan Zheng,Yun‐Yin Niu,Shuang‐Quan Zang
标识
DOI:10.1002/adma.202002914
摘要
Abstract The host–guest chemistry of metal–organic frameworks (MOFs) has enabled the derivation of numerous new functionalities. However, intrinsically chiral MOFs (CMOFs) with helical channels have not been used to realize crystalline circularly polarized luminescence (CPL) materials. Herein, enantiomeric pairs of MOF crystals are reported, where achiral fluorophores adhere to the inner surface of helical channels via biology‐like H‐bonds and hence inherit the helicity of the host MOFs, eventually amplifying the luminescence dissymmetry factor ( g lum ) of the host l / d ‐CMOF (±1.50 × 10 −3 ) to a maximum of ±0.0115 for the composite l / d ‐CMOF⊃fluorophores. l / d ‐CMOF⊃fluorophores in pairs generate bright color‐tunable CPL and almost ideal white CPL (0.33, 0.32) with a record‐high photoluminescence quantum yield of ≈30%, which are further assembled into a white circularly polarized light‐emitting diode. The present strategy opens a new avenue for propagating the chirality of MOFs to realize universal chiroptical materials.
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