Robust Spirobifluorene Core Based Hole Transporters with High Mobility for Long-Life Green Phosphorescent Organic Light-Emitting Devices

被引:5
|
作者
Nagamura, Natsuo [1 ]
Sasabe, Hisahiro [1 ,2 ,3 ]
Sato, Hiroki [4 ]
Ito, Nozomi [1 ]
Abe, Shoki [1 ]
Sukegawa, Yoshihito [1 ]
Yokoyama, Daisuke [1 ,2 ]
Kaji, Hironori [4 ]
Kido, Junji [1 ,2 ,3 ]
机构
[1] Yamagata Univ, Dept Organ Mat Sci, 4-3-16 Jonan, Yonezawa, Yamagata 9928510, Japan
[2] Yamagata Univ, Res Ctr Organ Elect ROEL, 4-3-16 Jonan, Yonezawa, Yamagata 9928510, Japan
[3] Yamagata Univ, Frontier Ctr Organ Mat FROM, 4-3-16 Jonan, Yonezawa, Yamagata 9928510, Japan
[4] Kyoto Univ, Inst Chem Res, Uji, Kyoto 6110011, Japan
基金
日本科学技术振兴机构;
关键词
hole transporter; long lifetime; multiscale simulation; phosphorescence; spirobifluorene derivative; MOLECULAR-ORIENTATION; MULTISCALE SIMULATION; CHARGE-TRANSPORT; EFFICIENT; DEGRADATION; MECHANISMS; STABILITY; BALANCE; DESIGN; ENERGY;
D O I
10.1002/chem.202202636
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Using a tailored high triplet energy hole transport layer (HTL) is a suitable way to improve the efficiency and extend the lifetime of organic light-emitting devices (OLEDs), which can use all molecular excitons of singlets and triplets. In this study, dibenzofuran (DBF)-end-capped and spirobifluorene (SBF) core-based HTLs referred as TDBFSBF1 and TDBFSBF2 were effectively developed. TDBFSBF1 exhibited a high glass transition temperature of 178 degrees C and triplet energy of 2.5 eV. Moreover, a high external quantum efficiency of 22.0 %, long operational lifetime at 50 % of the initial luminance of 89,000 h, and low driving voltage at 1000 cd m(-2) of 2.95 V were achieved in green phosphorescent OLEDs using TDBFSBF1. Further, a high-hole mobility mu(h) value of 1.9x10(-3) cm(2) V-1 s(-1) was recorded in TDBFSBF2. A multiscale simulation successfully reproduced the experimental mu(h) values and indicated that the reorganization energy was the primary factor in determining the mobility differences among these SBF core based HTLs.
引用
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页数:8
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