半最大全宽
有机发光二极管
材料科学
光致发光
量子产额
咔唑
光电子学
量子效率
荧光
光化学
化学
光学
纳米技术
物理
图层(电子)
作者
Paramasivam Palanisamy,Odugu Pavan Kumar,Hae Ung Kim,Kenkera Rayappa Naveen,JunYun Kim,Ji‐Ho Baek,Mi Young Chae,Jang Hyuk Kwon
标识
DOI:10.1016/j.cej.2024.148781
摘要
Multi-resonance boron-nitrogen-containing thermally activated delayed fluorescence (MR-TADF) emitters are well known for their high photoluminescence quantum yield (PLQY) and tuneable optoelectronic properties in organic light-emitting diodes (OLEDs). However, developing pure green emitters with narrow full-width at half-maximum (FWHM) reaching towards the Broadcast Service Television 2020 (BT2020) and National Television System Committee (NTSC) standards is still challenging. Herein, we demonstrated two highly symmetrical green MR-TADF scaffolds, namely, BpIC-DPA and BpIC-Cz, based on the rigidification and regulation of molecular orbitals (MO) engineering strategies. Both materials contain curvilinear indolocarbazole (pIC) donor, which enhances the rigidity of the whole MR-TADF skeletons. Furthermore, the MOs were regulated using the peripheral donors (such as tert-butyl substituted diphenylamine and carbazole moieties). Notably, both materials showed narrow FWHM below 25 nm and high PLQY in pure green emission. Consequently, the fabricated OLEDs based on BpIC-Cz showed maximum external quantum efficiency (EQEmax) of 25.7 % with alleviated efficiency roll-off characteristics (EQE1000 nits = 24.3 %). Mainly, the corresponding CIE coordinates reach almost towards BT2020 and NTSC green-colour industrial standards. Furthermore, the BpIC-Cz-based device resulted in a significantly longer device-lifetime (LT90) of 291 h at the initial luminance of 1000 nits, indicating their high stability.
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