Nearly 100% Exciton Utilization via Hybridized Inter‐ and Intramolecular Triplet Exciton Harvesting Channels in Blue Fluorescent Organic Light‐Emitting Diodes
Source abstract
Abstract
Abstract A highly efficient anthracene‐based 5‐(4‐(10‐phenylanthracen‐9‐yl)phenyl)‐5H‐benzofuro[3,2‐c]carbazole (ATDBF) with nearly 100% exciton utilization efficiency is developed for highly efficient nondoped blue organic light‐emitting diodes (OLEDs) through inter‐ and intramolecular triplet exciton up‐converting mechanisms. The ATDBF emitter opens hybridized hot excitons, triplet–triplet fusion (TTF), and mixed TTF/hot exciton channels for triplet exciton to singlet exciton conversion. The molecular design adopting a benzofuro[3,2‐c]carbazole (BFCz) donor manages the singlet and triplet excited states for hybridized triplet exciton up‐conversion mechanisms, which enable a high external quantum efficiency (EQE) of 7.93% in the ATDBF blue device with color coordinates of (0.15, 0.06). This is one of the best efficiencies of the nondoped blue OLEDs with a y color coordinate below 0.06.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Information Display Hongik University Seoul 04066 Korea
School of Chemical Engineering Sungkyunkwan University Suwon 16419 Korea
Department of Chemistry Korea Advanced Institute of Science and Technology Daejeon 34141 Korea
Department of Materials Science and Engineering Hongik University Sejong 30016 Korea
References (66)
Show source-provided references
1. 10.1063/1.9879910.1063/1.98799 ↗
2. 10.1002/anie.20150703110.1002/anie.201507031 ↗
3. 10.1002/adfm.20110219110.1002/adfm.201102191 ↗
4. 10.1002/advs.20200225410.1002/advs.202002254 ↗
5. 10.1002/adma.20180352410.1002/adma.201803524 ↗
6. 10.1021/acsami.8b0901310.1021/acsami.8b09013 ↗
7. 10.1002/adma.20120062710.1002/adma.201200627 ↗
8. 10.1002/ejoc.20130054410.1002/ejoc.201300544 ↗
9. 10.1002/adma.20180371410.1002/adma.201803714 ↗
10. 10.1002/adfm.20160300710.1002/adfm.201603007 ↗
11. 10.1039/C9TC00204A10.1039/C9TC00204A ↗
12. 10.1038/nature0464510.1038/nature04645 ↗
13. 10.1103/PhysRevLett.110.24740110.1103/PhysRevLett.110.247401 ↗
14. 10.1063/1.288453010.1063/1.2884530 ↗
15. 10.1039/C6CS00368K10.1039/C6CS00368K ↗
16. 10.1039/C7TC01133D10.1039/C7TC01133D ↗
17. 10.1039/C9CC02355K10.1039/C9CC02355K ↗
18. 10.1002/adom.20140015410.1002/adom.201400154 ↗
19. 10.1016/j.dyepig.2019.10786010.1016/j.dyepig.2019.107860 ↗
20. 10.1016/j.cclet.2016.06.00210.1016/j.cclet.2016.06.002 ↗
21. 10.1021/acs.jpclett.7b0286710.1021/acs.jpclett.7b02867 ↗
22. 10.1039/C4CC01851F10.1039/C4CC01851F ↗
23. Xing L. · Chem. Eng. J. · 2020 · 127748
24. 10.1016/j.cej.2021.13088910.1016/j.cej.2021.130889 ↗
25. 10.1016/j.mtener.2021.10072710.1016/j.mtener.2021.100727 ↗
26. 10.1039/D1QM00880C10.1039/D1QM00880C ↗
27. 10.1002/adom.20210050010.1002/adom.202100500 ↗
28. 10.1098/rsta.2014.032110.1098/rsta.2014.0321 ↗
29. 10.1002/adom.20190013010.1002/adom.201900130 ↗
30. 10.1039/C5RA02357B10.1039/C5RA02357B ↗
31. 10.1039/C8TC05013A10.1039/C8TC05013A ↗
32. 10.1016/j.synthmet.2016.03.02010.1016/j.synthmet.2016.03.020 ↗
33. 10.1039/C8TC05707A10.1039/C8TC05707A ↗
34. 10.1039/C6TC05308D10.1039/C6TC05308D ↗
35. 10.1039/c2jm16855c10.1039/c2jm16855c ↗
36. 10.1016/j.dyepig.2017.09.02710.1016/j.dyepig.2017.09.027 ↗
37. 10.1002/adfm.20210070410.1002/adfm.202100704 ↗
38. 10.1002/adom.20210096510.1002/adom.202100965 ↗
39. 10.1002/anie.20210854010.1002/anie.202108540 ↗
40. 10.1039/D1SC00272D10.1039/D1SC00272D ↗
41. 10.1021/acsami.9b1082310.1021/acsami.9b10823 ↗
42. 10.1002/adom.20180119010.1002/adom.201801190 ↗
43. 10.1039/D0CS00391C10.1039/D0CS00391C ↗
44. 10.1021/acsami.0c1587610.1021/acsami.0c15876 ↗
45. 10.1016/j.orgel.2016.04.00910.1016/j.orgel.2016.04.009 ↗
46. 10.1080/00268976.2014.95269610.1080/00268976.2014.952696 ↗
47. 10.1021/ct200936310.1021/ct2009363 ↗
48. 10.1021/jp101568f10.1021/jp101568f ↗
49. 10.1021/ct400450k10.1021/ct400450k ↗
50. 10.1021/acs.jctc.9b0101410.1021/acs.jctc.9b01014 ↗
51. 10.1021/jacsau.1c0017910.1021/jacsau.1c00179 ↗
52. 10.1016/j.displa.2015.05.00310.1016/j.displa.2015.05.003 ↗
53. 10.1021/acsami.9b2114310.1021/acsami.9b21143 ↗
54. 10.1016/j.cej.2020.12774810.1016/j.cej.2020.127748 ↗
55. 10.1002/hlca.19360190114510.1002/hlca.193601901145 ↗
56. 10.1063/1.327340710.1063/1.3273407 ↗
57. 10.1016/j.mser.2019.10051910.1016/j.mser.2019.100519 ↗
58. 10.1063/1.281836210.1063/1.2818362 ↗
59. 10.1002/ijch.20110012010.1002/ijch.201100120 ↗
60. 10.1016/j.synthmet.2014.10.00210.1016/j.synthmet.2014.10.002 ↗
61. 10.1039/D0TC05898J10.1039/D0TC05898J ↗
62. 10.1016/j.jsamd.2016.05.00210.1016/j.jsamd.2016.05.002 ↗
63. 10.1002/adom.20130042210.1002/adom.201300422 ↗
64. 10.1016/j.orgel.2018.06.02110.1016/j.orgel.2018.06.021 ↗
65. 10.1002/adma.20180738810.1002/adma.201807388 ↗
66. 10.1016/j.orgel.2011.04.01410.1016/j.orgel.2011.04.014 ↗