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摘要:
Influence of intramolecular π-π interaction on the luminescent properties of thermally activated delayed fluorescence (TADF) molecule (3,5-bis(3,6-di-tert-butyl-9H-carbazol-9-yl)-phenyl)(pyridin-4-yl) methanone (DTCBPY) is theoretically studied by using the density functional theory (DFT) and time-dependent density functional theory (TD-DFT).Four conformations (named as A,B,C,and D) of the DTCBPY can be found by relax scanning,and the configuration C corresponds to the luminescent molecule detected experimentally.Besides,we calculate the proportion of each conformation by Boltzmann distribution,high configuration ratios (44% and 52%) can be found for C and D.Moreover,C and D are found to exist with an intramolecular π-π interaction between one donor and the acceptor;the intramolecular interaction brings a smaller Huang-Rhys factor and reduced reorganization energy.Our work presents a rational explanation for the experimental results and demonstrates the importance of the intramolecular π-π interaction to the photophysical properties of TADF molecules.
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篇名 Luminescent properties of thermally activated delayed fluorescence molecule with intramolecular π-π interaction between donor and acceptor
来源期刊 中国物理B(英文版) 学科
关键词 thermally activated delayed fluorescence intramolecular π-π interaction Huang-Rhys factor and reorganization energy aggregation induced enhanced emission
年,卷(期) 2017,(11) 所属期刊栏目
研究方向 页码范围 544-549
页数 6页 分类号
字数 语种 英文
DOI 10.1088/1674-1056/26/11/118503
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thermally activated delayed fluorescence
intramolecular π-π interaction
Huang-Rhys factor and reorganization energy
aggregation induced enhanced emission
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中国物理B(英文版)
月刊
1674-1056
11-5639/O4
北京市中关村中国科学院物理研究所内
eng
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17050
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