期刊
JOURNAL OF MATERIALS CHEMISTRY C
卷 6, 期 16, 页码 4409-4417出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8tc00592c
关键词
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资金
- National Key Basic Research and Development Program of China (973 program) [2015CB655001, 2014CB643504]
- National Natural Science Foundation of China [51473162, 51773195, 51325303, 21334006]
- Strategic Priority Research Program of the Chinese Academy of Sciences [XDB12030200]
Exciplexes consisting of a combination of hole-transporting and electron-transporting materials and exhibiting narrow HOMO-LUMO gaps and bipolar transport ability are promising host choices in solution-processed phosphorescent organic light-emitting diodes (s-PhOLEDs). However, till date, there have been just a few reports on power-efficient s-PhOLEDs that use such an exciplex host structure. Herein, we successfully fabricated ultralow driving-voltage and power-efficient red s-PhOLEDs with a common hole-transporting and electron-transporting material combination, i.e. m-MTDATA:OXD-7 as exciplex co-host and Ir(MDQ)(2)acac as red dopant. The resultant s-PhOLEDs achieve satisfactory overall electroluminescent (EL) performance, i.e., light turn-on voltage at 2.4 V, maximum luminance of 26 385 cd m(-2), peak external quantum efficiency (EQE) of 15.5% and peak power efficiency (PE) of 36.9 lm W-1, respectively. However, a s-PhOLED using an exciplex-forming co-host couple of m-MTDATA:TmPyPB displays high turn-on voltage of 4.4 V and low EQE and PE of 9.4% and 10.1 lm W-1, respectively. The mechanism accounting for such an EL difference of s-PhOLEDs using m-MTDATA:OXD-7 or m-MTDATA:TmPyPB exciplex host were explored. It is found that the intrinsic incompatibility between m-MTDATA and TmPyPB does play a key role, which significantly deteriorates the bipolar charge transport capability of the solution-processed exciplex co-host matrix and consequently the EL performance of the resultant s-PhOLEDs.
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