Controllable β-phase formation in poly(9,9-dioctylfluorene) by dip-coating for blue polymer light-emitting diodes

•The β-phase poly(9,9-dioctylfluorene) film was realized by direct dip-coating.•β-phase content can be tailored by controlling the withdrawal speed.•Efficiency and color purity can be simultaneously improved.•About 3.6 times enhancement of current efficiency was achieved for the β-phase device. The...

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Veröffentlicht in:Thin solid films 2022-03, Vol.746, p.139118, Article 139118
Hauptverfasser: Chen, Yuehua, Zhang, Xiaoliang, Wang, Yangcheng, Lu, Wenjuan, Wang, Ruiting, Fan, Lixiang, Xu, Yanan, Lou, Hui, Zhang, Xinwen
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Sprache:eng
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Zusammenfassung:•The β-phase poly(9,9-dioctylfluorene) film was realized by direct dip-coating.•β-phase content can be tailored by controlling the withdrawal speed.•Efficiency and color purity can be simultaneously improved.•About 3.6 times enhancement of current efficiency was achieved for the β-phase device. The performance of polymer light-emitting diodes based on poly(9,9-dioctylfluorene) (PFO) is strongly affected by the presence of β-phase in the polymer films. In this work, β-phase PFO films were developed by a facile method dip-coating in one step. Absorption spectra with an additional peak at 435 nm and red-shifted emission spectra demonstrate the formation of β-phase in the dip-coated films. Notably, β-phase content in the PFO films can be tailored by controlling the withdrawal speed. The experimental results show that the content of β-phase in PFO films increases from 1.4 % to 23.2 % with the decreasing of the withdrawal speed from 60 mm/min to 5 mm/min, and the device efficiency and color purity for the blue emission get improved due to the formation of β-phase. When the withdrawal speed is 5 mm/min, the devices possess the optimal performance with a current efficiency of 2.47 cd/A, which is 3.6 times as high as that of the device with the spin-coated PFO film as emitting layer. These results demonstrate that as a simple methodology, the dip-coating technology can effectively induce the molecular chain orientation in the film to regulate the optoelectronic properties for applications in efficient optoelectronic devices.
ISSN:0040-6090
1879-2731
DOI:10.1016/j.tsf.2022.139118