Donor-modified asymmetric N/B/O multi-resonance TADF emitters for high-performance deep-blue OLEDs with the BT.2020 color gamut

被引:2
|
作者
Jin, Jing [1 ]
He, Zhaolong [1 ]
Liu, Di [1 ]
Mei, Yongqiang [3 ]
Wang, Jiahui [3 ]
Wan, Huihui [4 ]
Li, Jiuyan [2 ,3 ]
机构
[1] Dalian Univ Technol, Coll Chem, Frontier Sci Ctr Smart Mat, 2 Linggong Rd, Dalian 116024, Peoples R China
[2] Yantai Econ & Technol Dev Zone, Shandong Lab Yantai Adv Mat & Green Mfg, 300 Changjiang Rd, Yantai, Peoples R China
[3] Dalian Univ Technol, Coll Chem Engn, Frontier Sci Ctr Smart Mat, 2 Linggong Rd, Dalian 116024, Peoples R China
[4] Dalian Univ Technol, Instrumental Anal Ctr, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
LIGHT-EMITTING-DIODES; ELECTROLUMINESCENCE;
D O I
10.1039/d4sc04896b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multi-resonance thermally activated delayed fluorescence (MR-TADF) materials of polycyclic heteroaromatics are attractive narrowband emitters in wide-color-gamut organic light-emitting diodes (OLEDs). However, deep-blue MR-TADF emitters with CIE coordinates fulfilling the BT.2020 standard and high efficiency still remain a significant challenge. Herein, two novel emitters NBO-mSAF and NBO-pSAF were developed by incorporating an electron donor, 10H-spiro[acridine-9,9 '-fluorene] (SAF), at the para-position of the oxygen atom and the para-position of the boron atom in the nitrogen/boron/oxygen (N/B/O) ternary doped asymmetric MR skeleton. With appropriate electron-donating capacity and rigid spiro-structure, SAF was selected as the donor so that the long-range charge transfer triplet state (3LRCT) is induced to accelerate the reverse intersystem crossing (RISC) process, while the 1LRCT aligns higher than the short-range CT state (1SRCT) of the N/B/O core to retain the MR characters. As a result, these optimized emitters exhibit deep-blue TADF with narrow spectra and a high RISC rate constant of 3.4 x 105 s-1. In hyperfluorescence OLEDs with a TADF emitter DMAC-DPS as the sensitizer and PPF as the host, NBO-mSAF and NBO-pSAF achieved maximum external quantum efficiencies (EQEmax) of 26.7% and 25.2%. Interestingly, improved performance was realized in a traditional device configuration with a single bipolar host 26DCzPPy but without any sensitizer, where NBO-mSAF realized a higher EQEmax of 29.5% and CIE (0.128, 0.114), and NBO-pSAF exhibited an EQEmax of 20.5% and CIE of (0.147, 0.048). Narrow full width at half maximum (FWHM) values of 26-28 nm were achieved in both devices. Among all the deep-blue N/B/O type MR-TADF emitters with CIEx <= 0.15 and CIEy <= 0.12 ever reported so far, NBO-mSAF exhibited a highest EQEmax of 29.5%, which is even higher than those obtained with sensitizers, while the CIEy = 0.048 of the NBO-pSAF device is close to the standard blue (0.046) according to BT.2020, with a decent EQE of 20%. Spiro-acridine modified N/B/O type MR-TADF emitters realized deep blue fluorescence with an EQEmax of 20.5% and CIE (0.147, 0.048), which is state-of-the-art efficiency for N/B/O type deep-blue MR emitters with CIEy approaching the BT.2020 standard.
引用
收藏
页码:18135 / 18145
页数:11
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