Application of the Heavy-Atom Effect for (Sub)microsecond Thermally Activated Delayed Fluorescence and an All-Organic Light-Emitting Device with Low-Efficiency Roll-off

系统间交叉 有机发光二极管 荧光 材料科学 微秒 共发射极 吩恶嗪 光化学 掺杂剂 光电子学 原子物理学 兴奋剂 化学 纳米技术 物理 光学 激发态 图层(电子) 医学 吩噻嗪 单重态 药理学
作者
Michał Mońka,Szymon Gogoc,Karol Kozakiewicz,Vladyslav Ievtukhov,Daria Grzywacz,Olga Ciupak,A. Kubicki,Piotr Bojarski,Przemysław Data,Illia E. Serdiuk
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
标识
DOI:10.1021/acsami.3c19627
摘要

The feature of abundant and environmentally friendly heavy atoms (HAs) like bromine to accelerate spin-forbidden transitions in organic molecules has been known for years. In combination with the easiness of incorporation, bromine derivatives of organic emitters showing thermally activated delayed fluorescence (TADF) emerge as a cheap and efficient solution for the slow reverse intersystem crossing (rISC) problem in such emitters and strong efficiency roll-off of all-organic light-emitting diodes (OLEDs). Here, we present a comprehensive photophysical study of a tri-PXZ-TRZ emitter reported previously and its hexabromo derivative showing a remarkable enhancement of rISC of up to 9 times and a short lifetime of delayed fluorescence of 2 μs. Analysis of the key molecular vibrations and TADF mechanism indicates almost compete blockage of the spin-flip transition between the charge-transfer states of different multiplicity 3CT → 1CT. In such a case, rISC as well as its enhancement by the HA is realized via the 3LE → 1CT transition, where 3LE is the triplet state localized on the same brominated phenoxazine donor involved in the formation of the 1CT state. Interestingly, the spin–orbit coupling (SOC) with two other 3LE states is negligible because they are localized on different donors and not involved in 1CT. We consider this as an example of an additional "localization" criterion that completes the well-known El Sayed rule on the different nature of states for nonzero SOC. The applicative potential of such a hexabromo emitter is tested in a "hyperfluorescent" system containing a red fluorescent dopant (tetraphenyldibenzoperiflanthene, DBP) as an acceptor of Förster resonance energy transfer, affording a narrow-band red-emitting system, with most of the emission in the submicrosecond domain. In fact, the fabricated red OLED devices show remarkable improvement of efficiency roll-off from 2–4 times depending on the luminance, mostly because of the increase of the rISC constant rate and the decrease of the overall delayed fluorescence lifetime thanks to the HA effect.
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