磷光
材料科学
发光
系统间交叉
光电子学
激发态
光化学
单重态
光学
荧光
物理
化学
核物理学
作者
Pengfei She,Yaxin Yu,Yanyan Qin,Yingjie Zhang,Feiyang Li,Yun Ma,Shujuan Liu,Wei Huang,Qiang Zhao
标识
DOI:10.1002/adom.201901437
摘要
Abstract Pure organic materials with tunable room temperature phosphorescence (RTP) have attracted considerable interest because they are promising candidates for a wide range of optoelectronic applications. Herein, a series of organic compounds of (4‐(9H‐carbazol‐9‐yl)butyl) triphenylphosphonium (CBTP) with different halide anions (CBTP‐Cl, CBTP‐Br, and CBTP‐I) are synthesized. They show emission color changes from blue to orange‐red in the solid state. Single‐crystal X‐ray diffraction analysis and theoretical calculations demonstrate that the RTP is primarily caused by the external heavy‐atom effect (EHE), which enhances the spin–orbit coupling between the singlet and triplet excited states to facilitate the intersystem crossing rate. Distinct white light emission can be achieved using the controllable RTP by doping a certain ratio of potassium iodide (KI) into a polymer matrix containing CBTP‐Cl. Moreover, luminescent information can be recorded on a paper substrate made from a polymer film containing CBTP‐Cl with KI aqueous solution as the ink. The results suggest that rational control of the EHE of these pure organic materials is promising for different optoelectronic applications, including solid‐state lighting, data recording, and security protection.
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