有机发光二极管
电致发光
材料科学
光电子学
光致发光
共发射极
激子
聚合物
二极管
激进的
兴奋剂
光发射
光化学
化学
图层(电子)
纳米技术
有机化学
量子力学
复合材料
物理
作者
Qinying Gu,Alim Abdurahman,Richard H. Friend,Feng Li
标识
DOI:10.1021/acs.jpclett.0c01399
摘要
Organic light-emitting radicals have developed rapidly due to their unique doublet emission and great potential in display technology. Although some organic light-emitting diodes (OLEDs) exploiting small-molecular radicals as the emitters have been reported, there is no report about the polymer-radical-based OLEDs until now. Herein, a kind of polymer radical, PS-CzTTM, is adopted as the emitter to fabricate solution-processed OLEDs. A maximum external quantum efficiency of 3.0% is achieved for a deep-red device with an emissive layer of PS-CzTTM lightly doped in 2,2′,2″-(1,3,5-benzinetriyl)-tris(1-phenyl-1H-benzimidazole) (TPBi). Temperature-dependent time-resolved photoluminescent spectra and transient electroluminescence of radical emitters and devices are first measured. The results demonstrate that the emission channels for both thin films and devices are from the transition of doublet excitons, indicating that the unique doublet emission mechanism of radicals is maintained in PS-CzTTM films and PS-CzTTM-based OLEDs.
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