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Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Thermally activated delayed fluorescence emitters with dual conformations for white organic light-emitting diodes:
Feiyan Li1, Guanyu Jiang1, Muzhen Li1
1Shandong Key Laboratory of Medical Physics and Image Processing & Shandong Provincial Engineering and Technical Center of Light Manipulations, School of Physics and Electronics, Shandong Normal University, Jinan 250358, China. ckwang@sdnu.edu.cn linll@sdnu.edu.cn.
Abstract:
Thermally activated delayed fluorescence (TADF) molecules with dual emission have great potential for use as single emitters in white organic light-emitting diodes (WOLEDs). In this paper, the light-emitting mechanisms of PTZ-TTR and PTZ-Ph-TTR with blue-orange dual emission are studied systematically. The near-planar and near-orthogonal conformations are responsible for the blue and orange emission, respectively. For PTZ-TTR, the near-orthogonal conformation is only generated by the transformation from the near-planar conformation, while the near-orthogonal conformation of PTZ-Ph-TTR can be generated by both excitation and transformation. This results in relatively strong orange emission in PTZ-Ph-TTR. In addition, the TADF mechanism is investigated, and two up-conversion pathways are revealed for both molecules. Based on the comparison of the photophysical properties of PTZ-TTR in toluene and the aggregation state, we find that aggregation could induce a smaller energy gap between the first singlet excited state and the first triplet excited state. Besides, the substitution effect of donors on light-emitting properties is studied, and the design rules for emitters with dual conformations and compensatory emission are proposed. Our theoretical results would favor the understanding of the light-emitting mechanism as well as the design of new-type TADF emitters for WOLEDs.
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