Simplified Hybrid White Organic Light‐Emitting Diodes with a Mixed Fluorescent Blue Emitting Layer for Exciton Managing and Lifetime Improving
Source abstract
Abstract
The authors demonstrate a simple but effective way to manage the exciton, reduce the efficiency roll‐off, enhance the color stability and improve the lifetime of hybrid white organic light‐emitting diodes simultaneously. Red and green phosphorescent emission layers (EMLs) are connected by a mixed fluorescent blue‐emitting layer (MBL), which is composed of two self‐host fluorescent materials of N,N′‐di‐1‐naphthalenyl‐N,N′‐diphenyl‐[1,1′:4′,1″:4″,1″′‐quaterphenyl]‐4,4′″‐diamine and bis[2‐(2‐hydroxyphenyl)‐pyridine]beryllium. By adjusting the mixture ratio and the thickness of MBL, the intensity of blue and green emissions can be tuned independently. A maximum power efficiency of 41.1 lm W−1 and external quantum efficiency of 15.8% is obtained without any out‐coupling schemes or doping strategies. In addition, the device shows a stable electroluminescence spectrum with Commission International de L'Eclairage coordinates of (0.47, 0.43) in the practical range of 1000–5000 cd m−2. Furthermore, the fuzzy interfaces between MBL and phosphorescent EMLs, and the wide distribution of charges and excitons, result in four times prolonged device lifetime.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials · Organic Electronics and Photovoltaics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Jiangsu Key Laboratory for Carbon‐Based Functional Materials & Devices Institute of Functional Nano & Soft Materials (FUNSOM) Soochow University Suzhou Jiangsu 215123 China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Jiangsu Province
References (38)
Show source-provided references
1. 10.1038/nature0800310.1038/nature08003 ↗
2. 10.1002/adma.20090214810.1002/adma.200902148 ↗
3. 10.1002/adma.20100263610.1002/adma.201002636 ↗
4. 10.1103/RevModPhys.85.124510.1103/RevModPhys.85.1245 ↗
5. 10.1002/chem.20060127210.1002/chem.200601272 ↗
6. 10.1002/adma.20100312810.1002/adma.201003128 ↗
7. 10.1039/C4TC01619J10.1039/C4TC01619J ↗
8. 10.1002/adfm.20080150310.1002/adfm.200801503 ↗
9. 10.1038/nature0464510.1038/nature04645 ↗
10. 10.1016/j.orgel.2009.11.00110.1016/j.orgel.2009.11.001 ↗
11. 10.1063/1.288393510.1063/1.2883935 ↗
12. 10.1063/1.275709610.1063/1.2757096 ↗
13. Seo J. H. · Appl. Phys. Lett. · 2007 · 90 · 3507
14. 10.1063/1.297315110.1063/1.2973151 ↗
15. Gao C.‐H. · Int. J. Photoenergy · 2013 · 2013 · 831765
16. 10.1002/adma.20070064110.1002/adma.200700641 ↗
17. 10.1002/adma.20120112410.1002/adma.201201124 ↗
18. 10.1002/adma.20120472410.1002/adma.201204724 ↗
19. 10.1021/cm403318r10.1021/cm403318r ↗
20. 10.1039/C5TC00285K10.1039/C5TC00285K ↗
21. 10.1039/C4TC02459A10.1039/C4TC02459A ↗
22. 10.1038/nature1168710.1038/nature11687 ↗
23. 10.1038/srep0785910.1038/srep07859 ↗
24. 10.1002/adma.20150289710.1002/adma.201502897 ↗
25. 10.1002/adma.20130477910.1002/adma.201304779 ↗
26. 10.1002/adfm.20150560210.1002/adfm.201505602 ↗
27. 10.1063/1.240866310.1063/1.2408663 ↗
28. 10.1039/C3TC32301C10.1039/C3TC32301C ↗
29. 10.1016/j.orgel.2013.01.01910.1016/j.orgel.2013.01.019 ↗
30. 10.1103/PhysRevLett.96.01740410.1103/PhysRevLett.96.017404 ↗
31. 10.1002/pssa.20132910710.1002/pssa.201329107 ↗
32. 10.1103/PhysRevB.62.1096710.1103/PhysRevB.62.10967 ↗
33. 10.1103/PhysRevB.75.12532810.1103/PhysRevB.75.125328 ↗
34. 10.1002/adfm.20110094310.1002/adfm.201100943 ↗
35. 10.1063/1.354912810.1063/1.3549128 ↗
36. 10.1002/adfm.20130384010.1002/adfm.201303840 ↗
37. 10.1016/j.orgel.2015.03.03310.1016/j.orgel.2015.03.033 ↗
38. 10.1002/adma.20030215110.1002/adma.200302151 ↗