Diphenylsulfone-based hosts for electroluminescent devices: Effect of donor substituents
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Author
Bezvikonnyi, Oleksandr
Gudeika, Dalius
Volyniuk, Dmytro
Rutkis, Martins
Grazulevicius, Juozas V.
Date
2020Metadata
Show full item recordAbstract
In this work, we report on a series of diphenylsulfone derivatives substituted by 2-(trifluoromethyl)-phenothiazinyl, 10,11-dihydro-5H-dibenz[b,f]azepinyl, 5H-dibenz[b,f]azepinyl, 4-methoxy-carbazolyl and 1,2,3,4-tetrahydrocarbazolyl moieties. Utilization of such donating units provided high triplet levels (2.99–3.12 eV) of the designed compounds. The compounds were characterized by glass-forming properties (with glass transition temperatures of 68–162 °C) and ionization potentials of 5.61–5.99 eV. Depending on the donor substitution pattern, either hole or electron transport was observed for the studied compounds with charge mobilities in the range from 5.3 × 10−6 to 2.8 × 10−4 cm2/V at electric fields higher than 3.1·105 V/cm. Hosting properties of the compounds were studied using widely known emitter exhibiting thermally activated delayed fluorescence. Among the studied compounds, bis(4-(4-methoxy-9H-carbazole-9-yl)phenyl)sulfone showed the best performances in both guest:host solid films (photoluminescence quantum yield of 87%) and electroluminescent devices (maximum external quantum efficiency over 20%).