Issue 26, 2015

Synthesis and characterization of arylamino end-capped silafluorenes for blue to deep-blue organic light-emitting diodes (OLEDs)

Abstract

Diphenylamino- or cabazolyl-endcapped silafluorene derivatives which show a wide energy band gap, a high fluorescence quantum yield and high stability have been designed, synthesized, and characterized. Double layer electroluminescent devices of these silafluorene derivatives exhibited efficient blue emission. The non-doped double layer OLEDs containing TDMS, TDPS, CDMS, or CDPS exhibited better electroluminescence efficiencies than those of the devices using the reference emitter DPFL-NPB, among which the best device was with TDPS, which showed a maximum current efficiency of 1.62 cd A−1 and an external quantum efficiency (EQE) of 1.36%. The solution processed device using TDPS as dopant exhibited a high performance with an EQE of 2.48% and an obviously low turn-on voltage of 4 V, when compared to the results of the reference device. The replacement of the carbon atom of the fluorene unit with a silicon atom could lower the energy gap effectively and improve the thermal stability as well as optical performances. The results indicate that the end-capped arylamino groups affect the organic light-emitting diode (OLED) performances greatly and aryl or alkyl substitution on the 9-position of a silafluorene unit is also crucial to the OLED performances of this kind of silafluorene.

Graphical abstract: Synthesis and characterization of arylamino end-capped silafluorenes for blue to deep-blue organic light-emitting diodes (OLEDs)

Supplementary files

Article information

Article type
Paper
Submitted
09 Feb 2015
Accepted
25 May 2015
First published
26 May 2015

J. Mater. Chem. C, 2015,3, 6822-6830

Author version available

Synthesis and characterization of arylamino end-capped silafluorenes for blue to deep-blue organic light-emitting diodes (OLEDs)

S. F. Chen, Y. Tian, J. Peng, H. Zhang, X. J. Feng, H. Zhang, X. Xu, L. Li and J. Gao, J. Mater. Chem. C, 2015, 3, 6822 DOI: 10.1039/C5TC00382B

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