

FOLLOWUS
a.Key Laboratory for Flexible Electronics & Institute of Advanced Materials (IAM), Jiangsu National Synergistic Innovation Center for Advanced Materials, Nanjing Tech University, Nanjing 211816, China
b.School of Chemistry and Chemical Engineering, Xuzhou Institute of Technology, Xuzhou 221111, China
c.Key Laboratory for Organic Electronics and Information Displays and Institute of Advanced Materials, Nanjing University of Posts and Telecommunications, Nanjing 210046, China
Xin-wen Zhang (张新稳), E-mail: iamxwzhang@njupt.edu.cn
Wei Huang (黄维), E-mail: iamwhuang@njtech.edu.cn
Received:01 September 2016,
Revised:2016-9-27,
Accepted:28 September 2016,
Published:2017-04
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Ling-yun Zhao, Ya-nan Liu, Shi-fan Wang, et al. Novel Hyperbranched Polymers as Host Materials for Green Thermally Activated Delayed Fluorescence OLEDs[J]. Chinese Journal of Polymer Science, 2017, 35(4): 490-502.
Ling-yun Zhao, Ya-nan Liu, Shi-fan Wang, et al. Novel Hyperbranched Polymers as Host Materials for Green Thermally Activated Delayed Fluorescence OLEDs[J]. Chinese Journal of Polymer Science, 2017, 35(4): 490-502. DOI: 10.1007/s10118-017-1881-1.
A series of novel hyperbranched polymers (HBPs) consisting of a 2
7-subsituted 9-(heptadecan-9-yl)-9
H
-carbazole unit (A
2
+A
2
') and a tetra-substituted green thermally activated delayed fluorescence (TADF) dye of 2
3
5
6-tetra (9
H
-carbazol-9-yl)-4-pyridinecarbonitrile (4CzCNPy
B
4
) have been synthesized
via
Suzuki cross-coupling reaction following an "A
2
+A
2
'+B
4
" method. The polymers are named according to the polymerization ratio of 4CzCNPy monomer (5 mol%
10 mol% and 15 mol% for HBPs of P2-P4 respectively
and 0 mol% for the control linear polymer P1). Their thermal
optoelectronic and electrochemical properties have been characterized by a combination of techniques. All the polymers exhibit high thermal stability with the decomposition temperatures (
T
d
) above 400℃ and glass transition temperatures (
T
g
) up to 98℃. Unfortunately
the incorporation of TADF moiety into these HBP materials induced non-TADF characteristics. However
when the HBPs functionalized as the host for our previously developed 4CzCNPy TADF dopant in solution processed devices
maximum external quantum efficiency of 5.7% and current efficiency of 17.9 cd/A have been achieved in P3-based device
which is significantly higher than those of 1.5% and 4.2 cd/A for the linear polymer P1.
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