Air Stable Organic Salt As an n-Type Dopant for Efficient and Stable Organic Light-Emitting Diodes
Source abstract
Abstract
Air-stable and low-temperature-evaporable n-type dopants are highly desired for efficient and stable organic light-emitting diodes (OLEDs). In this work, 2-(2-Methoxyphenyl)-1,3-dimethyl-1H-benzoimidazol-3-ium iodide (o-MeO-DMBI-I), a thermally decomposable precursor of organic radical o-MeO-DMBI, has been employed as a novel n-type dopant in OLEDs, because of its air stability, low decomposition temperature, and lack of atom diffusion. The n-type electrical doping is evidenced by the rapid increase in current density of electron-only devices and the large improvement in conductivity, originated from increased electron concentration in electron-transport layer (ETL) and reduced electron injection barrier. A highly efficient and stable OLED is created using o-MeO-DMBI as an n-type dopant in Bphen. Compared with the control device with its high-temperature-evaporable n-type dopant cesium carbonate (Cs2CO3), o-MeO-DMBI-doped device showed an incredible boom in current efficiency from 28.6 to 42.2 cd/A. Moreover, the lifetime (T(70%)) of o-MeO-DMBI-doped device is 45 h, more than 20 times longer than that of the Cs2CO3-doped device (2 h). The enhanced efficiency and stability are attributed to the improved balance of holes and electrons in the emissive layer, and the eliminated atom diffusion of cesium.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Organic Light-Emitting Diodes Research · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Lab of Organic Optoelectronics & Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing, 100084, People’s Republic of China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China
References (29)
Show source-provided references
1. Tang C. W. · Appl. Phys. Lett. · 1987 · 51 · 91310.1063/1.98799 ↗
2. Yook K. S. · Adv. Funct. Mater. · 2010 · 20 · 179710.1002/adfm.201000137 ↗
3. Zhou X. · Adv. Funct. Mater. · 2001 · 11 · 31010.1002/1616-3028(200108)11:4<310::AID-ADFM310>3.0.CO;2-D ↗
4. Greiner M. T. · Nat. Mater. · 2012 · 11 · 7610.1038/nmat3159 ↗
5. Zhou Y. · Science. · 2012 · 336 · 32710.1126/science.1218829 ↗
6. Parthasarathy G. · J. Appl. Phys. · 2001 · 89 · 498610.1063/1.1359161 ↗
7. Lee J.-H. · Chem. Phys. Lett. · 2005 · 416 · 23410.1016/j.cplett.2005.09.104 ↗
8. Naab B. D. · Adv. Mater. · 2014 · 26 · 426810.1002/adma.201400668 ↗
9. Yook K. S. · Adv. Funct. Mater. · 2010 · 20 · 179710.1002/adfm.201000137 ↗
10. Lee T.-W. · Appl. Phys. Lett. · 2008 · 92 · 04330110.1063/1.2837419 ↗
11. Chan C. K. · Adv. Funct. Mater. · 2006 · 16 · 83110.1002/adfm.200500402 ↗
12. Werner A. · Adv. Funct. Mater. · 2004 · 14 · 25510.1002/adfm.200305053 ↗
13. Li F. · J. Phys. Chem. B · 2004 · 108 · 1707610.1021/jp0478615 ↗
14. Wei P. · J. Am. Chem. Soc. · 2012 · 134 · 399910.1021/ja211382x ↗
15. Naab B. D. · J. Am. Chem. Soc. · 2013 · 135 · 1501810.1021/ja403906d ↗
16. Wei P. · Nano Lett. · 2013 · 13 · 189010.1021/nl303410g ↗
17. Li C. · J. Phys. Chem. C · 2012 · 116 · 1974810.1021/jp307951h ↗
18. Bassler H. · Phys. Status Solidi B · 1993 · 175 · 1510.1002/pssb.2221750102 ↗
19. Scher H. · Phys. Rev. B · 1975 · 12 · 245510.1103/PhysRevB.12.2455 ↗
20. Frisch, M. J.; Trucks, G. W.; Schelegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Scalmani, G.; Barone, V.; Mennucci, B.; Petersson, G. A.; Nakatsuji, H.; Caricato, M.; Li, X.; Hratchian, H. P.; Izmaylov, A. F.; Bloino, J.; Zheng, G.; Sonnenberg, J. L.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Vreven, T.; Montgomery, J. A., Jr.; Peralta, J. E.; Ogliaro, F.; Bearpark, M.; Heyd, J. J.; Brothers, E.; Kudin, K. N.; Staroverov, V. N.; Kobayashi, R.; Normand, J.; Raghavachari, K.; Rendell, A.; Burant, J. C.; Iyengar, S. S.; Tomasi, J.; Cossi, M.; Rega, N.; Millam, J. M.; Klene, M.; Knox, J. E.; Cross, J. B.; Bakken, V.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Morokuma, R. L. K.; Zakrzewski, V. G.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Dapprich, S.; Daniels, A. D.; Farkas, O.; Foresman, J. B.; Ortiz, J. V.; Cioslowski, J.; Fox, D. J.Gaussian 03, revision B.05.Gaussian Inc.:Wallingford, CT, 2004.
21. Fu Y. · J. Am. Chem. Soc. · 2005 · 127 · 722710.1021/ja0421856 ↗
22. Ha S. D. · Phys. Rev. B · 2009 · 80 · 19541010.1103/PhysRevB.80.195410 ↗
23. Maennig B. · Phys. Rev. B · 2001 · 64 · 19520810.1103/PhysRevB.64.195208 ↗
24. Naka S. · Appl. Phys. Lett. · 2000 · 76 · 19710.1063/1.125701 ↗
25. Borsenberger P. M. · J. Chem. Phys. · 1991 · 94 · 544710.1063/1.460506 ↗
26. Bin Z. · Org. Electron. · 2014 · 15 · 243910.1016/j.orgel.2014.07.002 ↗
27. Jia Y. · J. Phys. Chem. C · 2013 · 117 · 1376310.1021/jp400003m ↗
28. Zhang Q. · Adv. Mater. · 2014 · 26 · 682910.1002/adma.201305371 ↗
29. Aziz H. · Chem. Mater. · 2004 · 16 · 452210.1021/cm040081o ↗