有机发光二极管
材料科学
蒽
量子产额
二苯胺
电致发光
量子效率
光电子学
磷光
荧光
单重态
融合
产量(工程)
图层(电子)
二极管
光化学
纳米技术
光学
化学
原子物理学
物理
激发态
哲学
冶金
语言学
作者
Chien‐Jung Chiang,Alpay Kimyonok,Marc K. Etherington,Gareth C. Griffiths,Vygintas Jankus,Figen Türksoy,Andrew P. Monkman
标识
DOI:10.1002/adfm.201201750
摘要
Abstract A new family of anthracene core, highly fluorescent emitters is synthesized which include diphenylamine hole transport end groups. Using a very simple one or two layer organic light emitting diode (OLED) structure, devices without outcoupling achieve an external quantum efficiency of 6% and photonic efficiencies of 20 cd/A. The theoretical maximum efficiency of such devices should not exceed 3.55%. Detailed photophysical characterization shows that for these anthracene based emitters 2T 1 ≤T n and so in this special case, triplet fusion can achieve a singlet production yield of 0.5. Indeed, delayed electroluminescence measurements show that triplet fusion contributes 59% of all singlets produced in these devices. This demonstrates that when triplet fusion becomes very efficient, fluorescent OLEDs even with very simple structures can approach an internal singlet production yield close to the theoretical absolute maximum of 62.5% and rival phosphorescent‐based OLEDs with the added advantage of much improved stability.
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