余辉
材料科学
分子
单独一对
杂原子
有机发光二极管
荧光
纳米技术
咔唑
光化学
化学物理
化学
图层(电子)
物理
光学
有机化学
戒指(化学)
伽马射线暴
天文
作者
Zhongwei Man,Zhong Chen,Wenhao Tao,Zheng Lv,Feng Teng,Qiuhong Cui,Hongbing Fu,Qing Liao,Aiwei Tang
标识
DOI:10.1002/adfm.202412652
摘要
Abstract Unlocking the afterglow properties of the fluorescence molecules at room temperature is an urgent challenge. Herein, inks prepared with dimethyl terephthalate (DTT) and carbazole (Cz) analogs with heteroatom (C, S, and O) substituents on the N as host and guest molecules can be directly sprayed onto different substrates to unlock the excitation‐wavelength dependent (Ex‐De) afterglow characteristics of the guest compound. Additionally, with the increase in the number of lone pair electrons, spin‐orbit coupling (SOC) increases, resulting in a longer afterglow duration lasting up to 4.5 s with Φ p >27%. Theory calculations and experiments indicate that the afterglow originated from the interactions between the host and guest molecules restricting the non‐radiative transition of the triplet excitons. Different Ex (with watershed at 310 nm) lead to the variation in the conformation of the S 0 DTT and S 1 DTT , which in turn affects the strength of host‐guest interactions and contributes to the Ex‐De characteristics. Benefiting from facile preparation, substrate‐independent applicability, and Ex‐De characteristics, the afterglow samples are demonstrated for applications in multilevel information security fields. This work proposes a general strategy for unlocking the afterglow emission of traditional molecules, which is valuable for the discovery of high‐performance afterglow materials in the future.
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