Jihoon Kang , Soon Ok Jeon , Ha Lim Lee , Junseop Lim , Unhyeok Jo , Jun Yeob Lee
{"title":"高效窄带深蓝色有机发光二极管的扩展多共振结构","authors":"Jihoon Kang , Soon Ok Jeon , Ha Lim Lee , Junseop Lim , Unhyeok Jo , Jun Yeob Lee","doi":"10.1016/j.mattod.2023.09.002","DOIUrl":null,"url":null,"abstract":"<div><p><span>Excellent color purity and high external quantum efficiency<span> (EQE) are major requirements in the development of deep-blue organic light-emitting diodes (OLEDs). To achieve this, multiple-resonance (MR)–thermally activated delayed fluorescence (TADF) emitters have been considered as promising options. Herein, we suggest a novel expanded MR design strategy to fabricate deep-blue MR–TADF emitters derived from a fused indolo[3,2,1-</span></span><em>jk</em><span>]carbazole framework. The expanded MR structure managed a triplet excited state<span><span> for the accelerated spin–vibronic coupling-assisted reverse intersystem crossing and increased the emission dipole orientation while maintaining the high efficiency and deep-blue emission color. The rigid and </span>planar structure<span> of the MR core yielded a small full-width at half-maximum (FWHM; less than 16 nm), high photoluminescence<span> quantum yield (over 97%), and high horizontal emitting dipole orientation (over 90%), and facilitated a second-order spin–vibronic coupling-assisted triplet-to-singlet spin crossover. The fabricated MR–TADF OLEDs recorded a high EQE of 24.3% and FWHM of 21 nm at a CIE</span></span></span></span><sub>y</sub> of 0.044, thereby satisfying the BT.2020 blue standard. Additionally, further optimized device architecture provided an EQE of 26.8%.</p></div>","PeriodicalId":387,"journal":{"name":"Materials Today","volume":"69 ","pages":"Pages 88-96"},"PeriodicalIF":21.1000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Expanded multiple-resonance structure for highly efficient narrowband deep-blue organic light-emitting diodes\",\"authors\":\"Jihoon Kang , Soon Ok Jeon , Ha Lim Lee , Junseop Lim , Unhyeok Jo , Jun Yeob Lee\",\"doi\":\"10.1016/j.mattod.2023.09.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>Excellent color purity and high external quantum efficiency<span> (EQE) are major requirements in the development of deep-blue organic light-emitting diodes (OLEDs). To achieve this, multiple-resonance (MR)–thermally activated delayed fluorescence (TADF) emitters have been considered as promising options. Herein, we suggest a novel expanded MR design strategy to fabricate deep-blue MR–TADF emitters derived from a fused indolo[3,2,1-</span></span><em>jk</em><span>]carbazole framework. The expanded MR structure managed a triplet excited state<span><span> for the accelerated spin–vibronic coupling-assisted reverse intersystem crossing and increased the emission dipole orientation while maintaining the high efficiency and deep-blue emission color. The rigid and </span>planar structure<span> of the MR core yielded a small full-width at half-maximum (FWHM; less than 16 nm), high photoluminescence<span> quantum yield (over 97%), and high horizontal emitting dipole orientation (over 90%), and facilitated a second-order spin–vibronic coupling-assisted triplet-to-singlet spin crossover. The fabricated MR–TADF OLEDs recorded a high EQE of 24.3% and FWHM of 21 nm at a CIE</span></span></span></span><sub>y</sub> of 0.044, thereby satisfying the BT.2020 blue standard. Additionally, further optimized device architecture provided an EQE of 26.8%.</p></div>\",\"PeriodicalId\":387,\"journal\":{\"name\":\"Materials Today\",\"volume\":\"69 \",\"pages\":\"Pages 88-96\"},\"PeriodicalIF\":21.1000,\"publicationDate\":\"2023-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Materials Today\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S136970212300295X\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Today","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S136970212300295X","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Excellent color purity and high external quantum efficiency (EQE) are major requirements in the development of deep-blue organic light-emitting diodes (OLEDs). To achieve this, multiple-resonance (MR)–thermally activated delayed fluorescence (TADF) emitters have been considered as promising options. Herein, we suggest a novel expanded MR design strategy to fabricate deep-blue MR–TADF emitters derived from a fused indolo[3,2,1-jk]carbazole framework. The expanded MR structure managed a triplet excited state for the accelerated spin–vibronic coupling-assisted reverse intersystem crossing and increased the emission dipole orientation while maintaining the high efficiency and deep-blue emission color. The rigid and planar structure of the MR core yielded a small full-width at half-maximum (FWHM; less than 16 nm), high photoluminescence quantum yield (over 97%), and high horizontal emitting dipole orientation (over 90%), and facilitated a second-order spin–vibronic coupling-assisted triplet-to-singlet spin crossover. The fabricated MR–TADF OLEDs recorded a high EQE of 24.3% and FWHM of 21 nm at a CIEy of 0.044, thereby satisfying the BT.2020 blue standard. Additionally, further optimized device architecture provided an EQE of 26.8%.
期刊介绍:
Materials Today is the leading journal in the Materials Today family, focusing on the latest and most impactful work in the materials science community. With a reputation for excellence in news and reviews, the journal has now expanded its coverage to include original research and aims to be at the forefront of the field.
We welcome comprehensive articles, short communications, and review articles from established leaders in the rapidly evolving fields of materials science and related disciplines. We strive to provide authors with rigorous peer review, fast publication, and maximum exposure for their work. While we only accept the most significant manuscripts, our speedy evaluation process ensures that there are no unnecessary publication delays.