An inverted singlet-triplet excited state in a pentaazaphenalene derivative (5AP-N(C12)2)

被引:9
作者
Kusakabe, Yu [1 ]
Shizu, Katsuyuki [1 ]
Tanaka, Hiroyuki [1 ]
Tanaka, Kazuo [2 ]
Kaji, Hironori [1 ]
机构
[1] Kyoto Univ, Inst Chem Res, Uji, Kyoto 6110011, Japan
[2] Kyoto Univ, Grad Sch Engn, Dept Polymer Chem, Nishikyo Ku, Kyoto 6158510, Japan
基金
日本学术振兴会;
关键词
organic light-emitting diodes; thermally activated delayed fluorescence; reverse intersystem crossing; inverted singlet-triplet excited states; pentaazaphenalene; ACTIVATED DELAYED FLUORESCENCE; LIGHT-EMITTING DIODE; HYBRID DENSITY FUNCTIONALS; S-TRIAZINO HETEROCYCLES; EFFICIENCY; EMITTERS; 1,3,4,6,9B-PENTAAZAPHENALENES; MOLECULES; GAPS;
D O I
10.35848/1882-0786/ad4e96
中图分类号
O59 [应用物理学];
学科分类号
摘要
The characteristic of inverted singlet-triplet excited states, in which the lowest singlet excited state (S-1) is lower than the lowest triplet state (T-1) in energy, was observed in a dialkylamine-substituted pentaazaphenalene derivative, 5AP-N(C12)(2). The transient photoluminescence measurements showed that the reverse intersystem crossing has virtually zero activation energy, whereas the intersystem crossing is proceeded by a thermal activation process. T-1 was located energetically above S-1 with a negative energy gap between S-1 and T-1 (Delta E-ST) of -37 meV. Fluorescence and phosphorescence spectra also confirmed the negative Delta E-ST of -46 to -32 meV. (c) 2024 The Author(s). Published on behalf ofThe Japan Society of Applied Physics by IOP Publishing Ltd
引用
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页数:4
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