| Literature DB >> 28185447 |
Wen-Cheng Chen1, Yi Yuan2, Shao-Fei Ni3, Ze-Lin Zhu1, Jinfeng Zhang1, Zuo-Quan Jiang2, Liang-Sheng Liao2, Fu-Lung Wong1, Chun-Sing Lee1.
Abstract
Organic materials containing arylamines have been widely used as hole-transporting materials as well as emitters in organic light-emitting devices (OLEDs). However, it has been pointed out that the C-N bonds in these arylamines can easily suffer from degradation in excited states, especially in deep-blue OLEDs. In this work, phenanthro[9,10-d]imidazole (PI) is proposed as a potential donor with higher stability than those of arylamines. Using PI as the donor, a donor-acceptor type deep-blue fluorophore 1-phenyl-2-(4″-(1-phenyl-1H-benzo[d]imidazol-2-yl)-[1,1':4',1″-terphenyl]-4-yl)-1H-phenanthro[9,10-d]imidazole (BITPI) is designed and synthesized. Results from UV-aging test on neat films of BITPI and other three arylamine compounds demonstrate that PI is indeed a more stable donor comparing to common arylamines. An OLED using BITPI as an emitter exhibits good device performances (EQE over 7%) with stable deep-blue emission (color index: (0.15, 0.13)) and longer operation lifetime than the similarly structured device using arylamine-based emitter. Single-organic layer device based on BITPI also shows superior performances, which are comparable to the best results from the arylamine-based donor-acceptor emitters, suggesting that PI is a stable donor with good hole transport/injection capability.Entities:
Keywords: deep-blue OLED; donor−acceptor emitter; high efficiency; high stability; phenanthro[9,10-d]imidazole
Year: 2017 PMID: 28185447 DOI: 10.1021/acsami.6b14638
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229