Title: A solvent-resistant azide-based hole injection/transporting conjugated polymer for fluorescent and phosphorescent light-emitting diodes
Authors: Huang, Cheng-Wei
Chang, Feng-Chih
Chu, Yu-Lin
Lai, Cheng-Chang
Lin, Tzu-En
Zhu, Chao-Yuan
Kuo, Shiao-Wei
應用化學系
Department of Applied Chemistry
Issue Date: 1-Jan-2015
Abstract: Interfacial mixing of polymers is a critical issue when attempting to improve the charge transport and stabilize the operation of solution-processed organic light-emitting diodes (OLEDs). Herein, we describe a simple methodology for overcoming interfacial mixing, based on the use of a photo-crosslinkable hole injection/transporting material (HITM). We synthesized a conjugated polymer, PTCAzide, bearing ready crosslinking ability and investigated its suitability for use as an HITM. Photo-crosslinking of the PTCAzide copolymer gave X-PTCAzide, which exhibited much higher thermal stability (the glass transition temperature increased by 21 K relative to that of PTCAzide), remarkable electrochemical stability, and excellent solvent-resistance, thereby expanding the operation time of corresponding electronic devices. Such a tris(8-hydroxy-quinolinato) aluminum-based trilayer device reached a maximum brightness of 52 971 cd m(-2), and the maximum luminance efficiency (LE) and power efficiency (eta E) are both higher than those of the corresponding device based on commercial PEDOT:PSS. In addition, a solution-processed phosphorescent OLED device incorporating X-PTCAzide also exhibited good performance (external quantum efficiency: 7.93%; LE: 29.6 cd A(-1); eta E: 14.3 lm W-1; maximum brightness: 34484 cd m(-2)). The efficient and simple photocrosslinking without adding an initiator could facilitate the fabrication process. Thus, PTCAzide appears to be a promising next-generation HITM for the development of highly efficient and inexpensive OLEDs. Its photo-crosslinkable nature allows improvements in morphological stability and hole injection/transporting ability, leading to more stable devices with better operation, without disrupting molecular packing or charge transport.
URI: http://dx.doi.org/10.1039/c5tc01794g
http://hdl.handle.net/11536/128100
ISSN: 2050-7526
DOI: 10.1039/c5tc01794g
Journal: JOURNAL OF MATERIALS CHEMISTRY C
Issue: 31
Begin Page: 8142
End Page: 8151
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