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溶液处理有机发光二极管中通过界面电荷诱导过冲效应抑制初始降解

Suppression of Initial Degradation via an Interfacial Charge-Induced Overshooting Effect in Solution-Processed Organic Light-Emitting Diodes.

作者信息

Le Thi Na, Kim Yerin, Lee Kyu-Myung, Hong Jong-Am, Oh Jooyeon, Park Yongsup, Suh Min Chul

机构信息

Department of Information Display, College of Sciences, Kyung Hee University, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Republic of Korea.

Department of Physics, College of Sciences, Kyung Hee University, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2024 Dec 18;16(50):69636-69644. doi: 10.1021/acsami.4c11945. Epub 2024 Oct 10.

Abstract

As the chemical stability of organic materials in organic light-emitting diodes (OLEDs) greatly impacts devices' lifetime, a thoughtful and advanced design of materials and device structures is necessary. In our work, we have achieved lifetime enhancement at its initial stage for solution-processed OLEDs. This improvement was realized through the implementation of a double electron transporting layer (dETL) composed of 2-[4-(9,10-dinaphthalen-2-yl-anthracen-2-yl)-phenyl]-1-phenyl-1H-benzoimidazole (ET) and hydroxyquinolinolato-lithium (Liq). A giant surface potential was generated at the surface of a constituent electron transport layer (ETL) that contained a higher concentration of Liq with high polarity. This giant surface potential simultaneously promoted the injection of trapped/accumulated electrons through the interface within dETL and the injection of holes from the anode, generating more exciton recombination events and ultimately enhancing efficiency by 133.0% and lifetime LT95 (luminance dropped by 5%) by 300% with an overshooting effect. Additionally, the degradation at the emitting layer was mitigated by shifting the degradation zone to the dETL, which was evidenced by laser desorption/ionization-time-of-flight (LDI-TOF) mass spectroscopy.

摘要

由于有机发光二极管(OLED)中有机材料的化学稳定性对器件寿命有很大影响,因此需要对材料和器件结构进行精心且先进的设计。在我们的工作中,我们在溶液处理的OLED的初始阶段实现了寿命的延长。这种改进是通过实施由2-[4-(9,10-二萘-2-基-蒽-2-基)-苯基]-1-苯基-1H-苯并咪唑(ET)和羟基喹啉锂(Liq)组成的双电子传输层(dETL)来实现的。在含有高浓度具有高极性的Liq的组成电子传输层(ETL)表面产生了巨大的表面电势。这种巨大的表面电势同时促进了被困/积累电子通过dETL内的界面注入以及空穴从阳极的注入,产生了更多的激子复合事件,最终效率提高了133.0%,寿命LT95(亮度下降5%)提高了300%,并产生了过冲效应。此外,通过将降解区域转移到dETL减轻了发光层的降解,这通过激光解吸/电离飞行时间(LDI-TOF)质谱得到了证明。

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