Four Dibenzofuran-Terminated High-Triplet-Energy Hole Transporters for High-Efficiency and Long-Life Organic Light-Emitting Devices |
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Authors: | Prof. Hisahiro Sasabe Suguru Araki Shoki Abe Nozomi Ito Kengo Kumada Taito Noda Yoshihito Sukegawa Prof. Daisuke Yokoyama Prof. Junji Kido |
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Affiliation: | 1. Department of Organic Materials Science, Yamagata University, 4-3-16 Jonan, Yonezawa, Yamagata, 992-8510 Japan;2. Department of Organic Materials Science, Yamagata University, 4-3-16 Jonan, Yonezawa, Yamagata, 992-8510 Japan Research Center of Organic Electronics (ROEL), Yamagata University, 4-3-16 Jonan, Yonezawa, Yamagata, 992-8510 Japan |
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Abstract: | The weak stability of a hole-transporter upon approaching the anion state is one of the major bottlenecks for developing long-life organic light-emitting devices (OLEDs). Therefore, in this study, we developed a series of thermally and electrically stable hole-transporters that are end-capped with four dibenzofuran units. These materials exhibit i) high bond dissociation energy (BDE) toward the anion state, ii) a high glass transition temperature (Tg>130 °C), and iii) high triplet energy (ET>2.7 eV), thereby enabling approximately 20 % high external quantum efficiency (EQE) and significantly prolonging the stability of both thermally activated delayed fluorescent (TADF) and phosphorescent OLEDs with an operation lifetime at 50 % (LT50) of 20 000–30 000 h at 1000 cd m−2. In addition, investigating their structure-property relationship revealed that ionization potential (IP), BDE, and Tg are critical prerequisites for the hole-transporter to prolong lifetime in OLEDs. |
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Keywords: | arylamine derivatives hole transporter long lifetimes phosphorescence thermally activated delayed fluorescence |
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