Simple excited-state modification toward a deep-blue hybridized local and charge-transfer (HLCT) fluorophore and non-doped organic light-emitting diodes

被引:16
|
作者
Huo, Yumiao [1 ,4 ]
Lv, Jichen [1 ]
Wang, Minghao [1 ]
Duan, Zuning [1 ]
Qi, Haoyuan [1 ]
Wang, Shengnan [1 ]
Liu, Yuchao [1 ]
Peng, Ling [2 ]
Ying, Shian [1 ]
Yan, Shouke [1 ,3 ]
机构
[1] Qingdao Univ Sci & Technol, Sch Polymer Sci & Engn, Key Lab Rubber Plast, Minist Educ, Qingdao 266042, Peoples R China
[2] Heze Univ, Coll Chem & Chem Engn, Heze 274015, Peoples R China
[3] Beijing Univ Chem Technol, Coll Mat Sci & Engn, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[4] Shandong Univ Sci & Technol, Coll Mat Sci & Engn, Qingdao 266590, Peoples R China
基金
中国国家自然科学基金;
关键词
HOST MATERIALS; DELAYED FLUORESCENCE; OLEDS; MOLECULE; EMITTERS;
D O I
10.1039/d3tc00574g
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Realizing high-performance deep-blue fluorophores and non-doped organic light-emitting diodes (OLEDs) with the Commission International de I'Eclairage (CIE) coordinates of CIEy < 0.046 is an important and challenging task for wide color-gamut displays. In this work, we report an efficient deep-blue hybridized local and charge-transfer (HLCT) fluorescent material with considerable fluorescence quantum yield and bipolar-transporting characteristics by managing the excited state and charge-transporting properties via a simple and novel acceptor p-difluorobenzene. The resulting non-doped OLED not only shows a high external quantum efficiency of 5.62%, but also exhibits stable deep-blue emission with the CIE coordinates of (0.163, 0.035) and a narrow full-width at half-maximum of 50 nm. This should be one of the state-of-the-art efficiencies achieved in the non-doped OLEDs with a CIEy of less than 0.046.
引用
收藏
页码:6347 / 6353
页数:7
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