Enhanced Triplet–Triplet Annihilation of Blue Fluorescent Organic Light-Emitting Diodes by Generating Excitons in Trapped Charge-Free Regions
Source abstract
Abstract
Three new anthracene-cored molecules, 3,3'-(5-(10-(naphthalen-1-yl)anthracen-9-yl)-1,3-phenylene)dipyridine (AP3Py-Na), 3,3'-(5-(10-(naphthalen-2-yl)anthracen-9-yl)-1,3-phenylene)dipyridine (AP3Py-2Na), and 9,10-bis(3,5-di(pyridin-3-yl)phenyl)anthracene (ADP3Py), were synthesized to be used as an efficiency-enhancement layer (EEL) in blue fluorescent organic light-emitting diodes. Insertion of a very thin EEL (3 nm) between the deep blue emitting layer (EML) and the electron transport layer enhanced the external quantum efficiency (EQE) of the blue device by 44% compared to the device without the EEL, resulting in an EQE of 7.9% and a current efficiency of 9.0 cd A-1 at 1000 cd m-2; the CIE coordinates of the emitting color were (0.13, 0.14). The transient electroluminescence showed that the efficiency enhancement originates from the triplet-triplet annihilation (TTA) process in the EEL, followed by energy transfer to the emitting dye in the EML.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Luminescence and Fluorescent Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science and Engineering, Gyeongsang National University, 501, Jinju-daero, Jinju-si 660-701, Gyeongsangnam-do, South Korea
Samsung Display Company, Limited, 95 Samsung 2-ro, Giheung-gu, Yongin-si 446-711, Gyeonggi-Do, South Korea
Funding
National Research Foundation of Korea · Ministry of Trade, Industry and Energy · GNU-Samsung Display Center
References (34)
Show source-provided references
1. 10.1063/1.151512910.1063/1.1515129 ↗
2. 10.1063/1.281836210.1063/1.2818362 ↗
3. 10.1063/1.327340710.1063/1.3273407 ↗
4. 10.1103/physrevb.85.04520910.1103/physrevb.85.045209 ↗
5. 10.1063/1.180423210.1063/1.1804232 ↗
6. 10.1002/adfm.20120175010.1002/adfm.201201750 ↗
7. 10.1039/b805062g10.1039/b805062g ↗
8. 10.1016/j.synthmet.2014.10.01910.1016/j.synthmet.2014.10.019 ↗
9. 10.1039/b918739a10.1039/b918739a ↗
10. 10.1039/c1jm14482k10.1039/c1jm14482k ↗
11. 10.1039/c2tc00185c10.1039/c2tc00185c ↗
12. 10.1039/c8tc05707a10.1039/c8tc05707a ↗
13. 10.1039/c6cc05076j10.1039/c6cc05076j ↗
14. 10.1063/1.193105210.1063/1.1931052 ↗
15. 10.1021/acsami.8b0901310.1021/acsami.8b09013 ↗
16. 10.1016/j.orgel.2010.02.00910.1016/j.orgel.2010.02.009 ↗
17. 10.1002/1521-4095(200111)13:22<1690::aid-adma1690>3.0.co;2-k10.1002/1521-4095(200111)13:22<1690::aid-adma1690>3.0.co;2-k ↗
18. 10.1016/j.orgel.2012.03.01910.1016/j.orgel.2012.03.019 ↗
19. 10.1016/j.orgel.2015.02.01810.1016/j.orgel.2015.02.018 ↗
20. 10.1039/c6sc00100a10.1039/c6sc00100a ↗
21. 10.1039/c4cc01851f10.1039/c4cc01851f ↗
22. 10.1016/j.dyepig.2015.04.02010.1016/j.dyepig.2015.04.020 ↗
23. 10.1002/adfm.20130290710.1002/adfm.201302907 ↗
24. 10.1002/adma.20110440310.1002/adma.201104403 ↗
25. 10.1889/1.350052810.1889/1.3500528 ↗
26. 10.7567/jjap.53.05210210.7567/jjap.53.052102 ↗
27. 10.1038/s41467-018-07432-210.1038/s41467-018-07432-2 ↗
28. 10.1080/1542140680808293010.1080/15421406808082930 ↗
29. 10.1016/j.orgel.2015.11.02610.1016/j.orgel.2015.11.026 ↗
30. 10.1002/adfm.20090232910.1002/adfm.200902329 ↗
31. Mott N. F. · 1964
32. 10.1088/0022-3727/3/2/30810.1088/0022-3727/3/2/308 ↗
33. 10.1038/s41467-019-10260-710.1038/s41467-019-10260-7 ↗
34. 10.1098/rsta.2014.032110.1098/rsta.2014.0321 ↗