Pyrenyl substituted 1,8-naphthalimide as a new material for weak efficiency-roll-off red OLEDs: a theoretical and experimental study

Based on the theoretical calculations of excited states and semiconducting properties, a new 1,8-naphthalimide derivative having an electron-donating 1-pyrenyl group at the C-4 position was designed and synthesized. This derivative exhibited an excellent thermal stability and bipolar charge carrier...

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Bibliographic Details
Published inNew journal of chemistry Vol. 42; no. 15; pp. 12492 - 12502
Main Authors Bezvikonnyi, Oleksandr, Gudeika, Dalius, Volyniuk, Dmytro, Grazulevicius, Juozas, Bagdziunas, Gintautas
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 2018
Royal Society of Chemistry
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Summary:Based on the theoretical calculations of excited states and semiconducting properties, a new 1,8-naphthalimide derivative having an electron-donating 1-pyrenyl group at the C-4 position was designed and synthesized. This derivative exhibited an excellent thermal stability and bipolar charge carrier transport ability. It was successfully utilized as a host in red phosphorescent organic light-emitting diodes showing an efficient energy transfer from the host to the phosphorescent emitter. The derivative may be a single material electroplex-forming host for PhOLEDs. The best fabricated red emitting device demonstrated maximum current, power, and external quantum efficiencies of 10.8 cd A(-1), 7 lm W-1, and 13.6%, respectively. The best device exhibited a high brightness of 15 300 cd m(-2) and weak efficiency-roll-off.
ISSN:1144-0546
1369-9261
DOI:10.1039/c8nj01866a