Issue 34, 2015

Stable and efficient deep-blue terfluorenes functionalized with carbazole dendrons for solution-processed organic light-emitting diodes

Abstract

A series of solution processible deep-blue fluorescent emitters TFPC0 ∼ TFPC2 have been designed and synthesized by incorporating different generation carbazole dendrons into the 9,9-positions of the terfluorene backbone. Compared with TFPC0, the dendritic TFPC1 and TFPC2 have the elevated glass transition temperatures as well as better solubility in common organic solvents, and their high quality amorphous films can be formed via spin-coating. Noticeably, with the increasing generation number, both the intermolecular aggregate and the formation of keto defects can be effectively suppressed to avoid the appearance of the unwanted long wavelength emission. Meanwhile, the highest occupied molecular orbital (HOMO) level is gradually enhanced from TFPC0 to TFPC2, facilitating the hole injection. As a result, TFPC2 with the second generation carbazole dendrons shows the best photoluminescence and electroluminescence stability among TFPC0 ∼ TFPC2. Its corresponding solution-processed undoped device gives a state-of-art external quantum efficiency as high as 2.02% and Commission International De L'Eclairge (CIE) coordinates of (0.16, 0.04). These results indicate that the introduction of oligocarbazole is a promising strategy towards solution processible deep-blue fluorene-containing oligomers simultaneously with high spectral stability and efficiency.

Graphical abstract: Stable and efficient deep-blue terfluorenes functionalized with carbazole dendrons for solution-processed organic light-emitting diodes

Supplementary files

Article information

Article type
Paper
Submitted
11 Jun 2015
Accepted
30 Jul 2015
First published
31 Jul 2015

J. Mater. Chem. C, 2015,3, 8895-8903

Author version available

Stable and efficient deep-blue terfluorenes functionalized with carbazole dendrons for solution-processed organic light-emitting diodes

L. Zhao, S. Wang, S. Shao, J. Ding, L. Wang, X. Jing and F. Wang, J. Mater. Chem. C, 2015, 3, 8895 DOI: 10.1039/C5TC01711D

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