Structural Optimization of 2,5-Diarylsiloles as Excellent Electron-Transporting Materials for Organic Electroluminescent Devices
Source abstract
Abstract
We have already reported that 2,5-di(2-pyridyl)silole (PySPy) has high performance as an electron-transporting material (ETM) for organic electroluminescent devices (OELDs). For the purpose of developing more practicable ETMs, we have now prepared three new 2,5-diarylsilole derivatives, PPySPyP, PyPySPyPy, and PyPSPPy, having 6-phenyl-2-pyridyl, 6-(2-pyridyl)-2-pyridyl, and 3-(2-pyridyl)phenyl as the aryl groups, respectively, and have studied their structure−properties relationships. These derivatives have higher glass transition temperatures when compared to PySPy. Among these compounds and tris(8-hydroxyquinolino)aluminum (Alq), the bipyridylsilole derivative, PyPySPyPy, showed the highest electron-transporting abilities. The efficiency of a device consisting of ITO/triphenyldiamine derivative/Alq/PyPySPyPy/MgAg reached 2.2 lm/W at 3.4 V. Furthermore, the half-life time of a device consisting of ITO/triphenylamine dimer derivative/Alq/PyPySPyPy/LiF/Al was nearly 3 times longer than that of the control device without PyPySPyPy under a constant current.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Conducting polymers and applications · Organic Electronics and Photovoltaics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Yokohama Research Center, Chisso Corporation, Kanazawa, Yokohama 236-8605, Japan, and Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan
References (13)
Show source-provided references
1. Tang C. W. · Appl. Phys. Lett. · 1987 · 51 · 91310.1063/1.98799 ↗
2. For · Mol. Cryst. Liq. Cryst. · 1996 · 280 · 33110.1080/10587259608040352 ↗
3. For · Chem. Lett. · 1993 · 905
4. For · Appl. Phys. Lett. · 1989 · 55 · 148910.1063/1.101586 ↗
5. Kido J. · Jpn. J. Appl. Phys. · 1993 · 32 · L91710.1143/JJAP.32.L917 ↗
6. Kido J. · Science · 1995 · 267 · 133210.1126/science.267.5202.1332 ↗
7. Naka S. · Appl. Phys. Lett. · 2000 · 7610.1063/1.125701 ↗
8. For · Synth. Met. · 1997 · 91 · 22310.1016/S0379-6779(98)80035-0 ↗
9. Tamao K. · J. Am. Chem. Soc. · 1996 · 118 · 1197410.1021/ja962829c ↗
10. Yamaguchi S. · Chem. Eur. J. · 2000 · 6 · 168410.1002/(SICI)1521-3765(20000502)6:9<1509::AID-CHEM1509>3.0.CO;2-8 ↗
11. Friend R. H. · Nature · 1999 · 397 · 12110.1038/16393 ↗
12. Hung L. S. · Appl. Phys. Lett. · 1997 · 70 · 15210.1063/1.118344 ↗
13. Mori T. · Appl. Phys. Lett. · 1998 · 73 · 276310.1063/1.122583 ↗