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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.
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页码:6347 / 6353
页数:7
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