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Ultrahighly-efficient and pure deep-blue thermally activated delayed fluorescence organic light-emitting devices based on dimethylacridine/thioxanthene-S,S-dioxide

Authors
Jeon, Young PyoKong, Byung KiLee, Eun JungYoo, Keon-HoKIM, TAE WHAN
Issue Date
May-2019
Publisher
ELSEVIER
Keywords
Thermally activated delayed fluorescence; Organic light-emitting devices; Deep-blue emission; Ultrahigh-efficiency; Thioxanthene-S,S-dioxide; Biphenyl
Citation
NANO ENERGY, v.59, pp.560 - 568
Indexed
SCIE
SCOPUS
Journal Title
NANO ENERGY
Volume
59
Start Page
560
End Page
568
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/14146
DOI
10.1016/j.nanoen.2019.02.067
ISSN
2211-2855
Abstract
A novel deep-blue emissive dopant material, 2,7-bis(9,9-dimethylacridine-10(9H)-yl)-9,9-diphenyl-9H-thioxanthene 10-,10-dioxide (DMA-ThX), is synthesized for use in highly-efficient thermally activated delayed fluorescence organic light-emitting devices (TADF OLEDs). The molecular design of DMA-ThX retains the overlap between the lowest singlet excited state (S-1) and the lowest triplet excited state (T-1) because of its twisted molecular structure. From photoluminescence emission measurements at low temperature, the difference between the S-1 and the T-1 energy levels of DMA-ThX is found to be 0.07 eV. Furthermore, the external quantum efficiency of the deep-blue-emitting TADF OLEDs with DMA-ThX-doped bis[2-(diphenylphosphino) phenyl] ether oxide is 18.4%, which is significant, and the Commission Internationale de l'Eclairage coordinates are (0.14, 0.14), indicative of very pure deep-blue emission.
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