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用于深蓝色磷光体的三重态激子上转换蓝色激基复合物主体

Triplet Exciton Upconverting Blue Exciplex Host for Deep Blue Phosphors.

作者信息

Hui Yun Ju, Lim Junseop, Yeob Lee Jun, Lee Yoonkyoo, Chu Changwoong

机构信息

School of Chemical Engineering, Sungkyunkwan University, 2066, Seobu-ro, Jangan-gu, Suwon-si, Gyeonggi-do, 16419, Korea.

Display Research Center, Samsung Display Co., 1 Samsung-ro, Giheung-gu, Yongin, Gyeonggi-do, Korea.

出版信息

Chemistry. 2021 Sep 1;27(49):12642-12648. doi: 10.1002/chem.202101819. Epub 2021 Jul 30.

DOI:10.1002/chem.202101819
PMID:34240481
Abstract

A thermally activated delayed fluorescence (TADF)-type exciplex host employing a novel electron-transport type (n-type) type host managing positive polarons and stabilizing excitons was developed to elongate the device lifetime of deep blue phosphorescent organic light-emitting diodes (PhOLEDs). The bipolar n-type host was designed to prevent hole leakage and secure hole stability while being stabilized under excitons by introducing a CN-modified carbazole moiety as a weak donor. The TADF-type exciplex host-based blue PhOLEDs showed high (above 20 %) quantum efficiency with a deep blue color coordinate of (0.14, 0.16) and elongated device lifetime. The device operational lifetime of the blue PhOLEDs bearing the TADF-type exciplex host was extended by more than twice compared to that of the exciplex-free unipolar host. This work suggested a design concept of the n-type host to develop the TADF-type exciplex host for deep blue phosphors to reach a long lifespan in the deep blue PhOLEDs.

摘要

为了延长深蓝色磷光有机发光二极管(PhOLED)的器件寿命,开发了一种热激活延迟荧光(TADF)型激基复合物主体,该主体采用了一种新型的电子传输型(n型)主体,用于管理正极化子并稳定激子。通过引入作为弱供体的CN修饰咔唑部分,设计了双极性n型主体,以防止空穴泄漏并确保空穴稳定性,同时在激子作用下保持稳定。基于TADF型激基复合物主体的蓝色PhOLED显示出高(超过20%)的量子效率,色坐标为深蓝色(0.14, 0.16),并且器件寿命得以延长。与无激基复合物的单极性主体相比,带有TADF型激基复合物主体的蓝色PhOLED的器件工作寿命延长了两倍多。这项工作提出了一种n型主体的设计概念,以开发用于深蓝色磷光体的TADF型激基复合物主体,从而在深蓝色PhOLED中实现长寿命。

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引用本文的文献

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Advances in Blue Exciplex-Based Organic Light-Emitting Materials and Devices.基于蓝色激基复合物的有机发光材料与器件的进展
Front Chem. 2022 Jul 12;10:952116. doi: 10.3389/fchem.2022.952116. eCollection 2022.