喹喔啉
接受者
荧光
材料科学
电子受体
光化学
部分
有机发光二极管
量子效率
电子供体
光电子学
纳米技术
化学
光学
有机化学
催化作用
物理
图层(电子)
凝聚态物理
作者
Shantaram Kothavale,Jun Yeob Lee,Jun Yeob Lee
标识
DOI:10.1021/acsami.9b02824
摘要
Highly efficient yellow and red thermally activated delayed fluorescent (TADF) organic light-emitting diodes were developed using two quinoxalinedicarbonitrile units, quinoxaline-6,7-dicarbonitrile (6,7-DCQx) and quinoxaline-5,8-dicarbonitrile (5,8-DCQx) as electron acceptors, and t-butylcarbazole or 9,9-dimethylacridan as electron donors. The strong electron-withdrawing capability of the 5,8-DCQx and 6,7-DCQx acceptors enabled from yellow to red emission in the TADF emitters. Comparing 5,8-DCQx and 6,7-DCQx, a red-shifted emission by about 40 nm was observed in the 5,8-DCQx acceptor-based emitters, but the external quantum efficiency of the TADF devices was over 20% irrespective of the acceptor, proving the usefulness of the two acceptor moieties as the building blocks of the TADF emitters. Therefore, the quinoxalinedicarbonitrile acceptors are promising as the acceptor moiety for designing yellow or red TADF emitters.
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