| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1442463 | Synthetic Metals | 2009 | 6 Pages |
The utilization of a photoreactive hole injection/transport layer in multilayer electrophosphorescence polymer light-emitting diodes (PLEDs) is demonstrated in this study. A new photoreactive polymer was synthesized using 3,6-dibromo-9-(6-((3-methyloxetan-3-yl)methoxy)hexyl)-9H-carbazole and 2,4-dimethyl-N,N-bis(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)aniline via the Suzuki coupling reaction. When oxetane groups were photopolymerized in the presence of a cationic photoinitiator, the cured film showed good compatibility with PEDOT:PSS and the indium tin oxide (ITO) layer due to the hydrophilic nature of the cross-linked section. The resulting green light-emitting device bearing PVK:PBD:Ir(Cz-ppy)3 exhibits a maximum external quantum efficiency of 8.73%, corresponding to a luminous efficiency of 28.2 cd/A when using the device configuration of ITO/POx-TPACz/PEDOT:PSS/PVK:PBD:Ir(Cz-ppy)3/TAZ/Alq3/LiF/Al. These values are higher than those of PLEDs using conventional PEDOT:PSS as a single hole injection layer (HIL). The slight degree of improvement in device efficiency is due to the reduced hole injection barrier.
