journal article·2023-09-27

Low-Temperature Cross-Linkable Hole Transport Materials for Solution-Processed Quantum Dot and Organic Light-Emitting Diodes with High Efficiency and Color Purity

Athithan Maheshwaran, Hyejeong Bae, Jaehyoung Park, Hyeonwoo Jung, Youngjun Hwang, Jongyoun Kim, Chaehyun Park, Byeongjae Kang, Myungkwan Song, Youngu Lee

ACS Applied Materials & Interfaces· Volume 15· Issue 38
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Abstract

Cross-linkable hole transport materials (HTMs) are ideal for improving the performance of solution-processed quantum dot light-emitting diodes (QLEDs) and phosphorescent light-emitting diodes (OLEDs). However, previously developed cross-linkable HTMs possessed poor hole transport properties, high cross-linking temperatures, and long curing times. To achieve efficient cross-linkable HTMs with high mobility, low cross-linking temperature, and short curing time, we designed and synthesized a series of low-temperature cross-linkable HTMs comprising dibenzofuran (DBF) and 4-divinyltriphenylamine (TPA) segments for highly efficient solution-processed QLEDs and OLEDs. The introduction of divinyl-functionalized TPA in various positions of the DBF core remarkably affected their chemical, physical, and electrochemical properties. In particular, cross-linked 4-(dibenzo[ b, d ]furan-3-yl)- N, N -bis(4-vinylphenyl)aniline (3-CDTPA) exhibited a deep highest occupied molecular orbital energy level (5.50 eV), high hole mobility (2.44 × 10 –4 cm 2 V –1 s –1 ), low cross-linking temperature (150 °C), and short curing time (30 min). Furthermore, a green QLED with 3-CDTPA as the hole transport layer (HTL) exhibited a notable maximum external quantum efficiency (EQE max ) of 18.59% with a remarkable maximum current efficiency (CE max ) of 78.48 cd A –1 . In addition, solution-processed green OLEDs with 3-CDTPA showed excellent device performance with an EQE max of 15.61%, a CE max of 52.51 cd A –1, and outstanding CIE( x, y ) color coordinates of (0.29, 0.61). This is one of the highest reported EQEs and CEs with high color purity for green solution-processed QLEDs and OLEDs using a divinyl-functionalized cross-linked HTM as the HTL. We believe that this study provides a new strategy for designing and synthesizing practical cross-linakable HTMs with enhanced performance for highly efficient solution-processed QLEDs and OLEDs.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Organic Light-Emitting Diodes Research · Perovskite Materials and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Energy Science & Engineering, Daegu Gyeongbuk Institute of Science and Technology (DGIST), 333, Techno Jungang Daero, Hyeonpung-Eup, Dalseong-Gun, Daegu 42988, Republic of Korea

Department of Energy & Electronic Materials, Korea Institute of Materials Science (KIMS), 797 Changwon-daero, Sungsan-gu, Changwon-si, Gyeongsangnam-do 51508, Republic of Korea

Funding

National Research Foundation of Korea · Korea Evaluation Institute of Industrial Technology

References (45)

Show source-provided references
1. 10.1080/15980316.2022.203583510.1080/15980316.2022.2035835 ↗
2. 10.1002/adma.20210788810.1002/adma.202107888 ↗
3. 10.1038/s41566-022-00999-910.1038/s41566-022-00999-9 ↗
4. 10.1038/s41467-021-24931-x10.1038/s41467-021-24931-x ↗
5. 10.1038/s41467-020-15481-910.1038/s41467-020-15481-9 ↗
6. 10.1002/smll.20180026510.1002/smll.201800265 ↗
7. 10.1002/smll.20170243310.1002/smll.201702433 ↗
8. 10.1038/nature1382910.1038/nature13829 ↗
9. 10.1007/s13233-021-9020-910.1007/s13233-021-9020-9 ↗
10. 10.1007/s13233-021-9017-410.1007/s13233-021-9017-4 ↗
11. 10.1007/s13233-021-9097-110.1007/s13233-021-9097-1 ↗
12. 10.1007/s13233-022-0053-510.1007/s13233-022-0053-5 ↗
13. 10.1002/adom.20220093510.1002/adom.202200935 ↗
14. 10.1007/s13233-022-0080-210.1007/s13233-022-0080-2 ↗
15. 10.1007/s13233-022-0069-x10.1007/s13233-022-0069-x ↗
16. 10.1016/j.dyepig.2020.10909110.1016/j.dyepig.2020.109091 ↗
17. 10.1002/adfm.20180471410.1002/adfm.201804714 ↗
18. 10.1039/C9TC03559A10.1039/C9TC03559A ↗
19. 10.1039/C9MH01053J10.1039/C9MH01053J ↗
20. 10.1016/j.orgel.2019.06.01610.1016/j.orgel.2019.06.016 ↗
21. 10.1002/adma.20070088710.1002/adma.200700887 ↗
22. 10.1002/chem.20160399410.1002/chem.201603994 ↗
23. 10.1021/cm102401k10.1021/cm102401k ↗
24. 10.1021/acsami.0c1733610.1021/acsami.0c17336 ↗
25. 10.1002/smll.20190011110.1002/smll.201900111 ↗
26. 10.1039/D0QM00591F10.1039/D0QM00591F ↗
27. 10.1021/acsami.7b0061510.1021/acsami.7b00615 ↗
28. 10.1002/adfm.20140195810.1002/adfm.201401958 ↗
29. 10.1016/j.cej.2019.12347910.1016/j.cej.2019.123479 ↗
30. 10.1021/acsami.6b0519710.1021/acsami.6b05197 ↗
31. 10.1016/j.orgel.2013.03.02810.1016/j.orgel.2013.03.028 ↗
32. 10.1021/cm071828o10.1021/cm071828o ↗
33. 10.1002/adma.20050276910.1002/adma.200502769 ↗
34. 10.1016/j.synthmet.2006.06.01110.1016/j.synthmet.2006.06.011 ↗
35. 10.1021/ol061642f10.1021/ol061642f ↗
36. 10.7536/PC18012810.7536/PC180128 ↗
37. 10.1016/j.dyepig.2020.10853410.1016/j.dyepig.2020.108534 ↗
38. 10.1039/C9TC02689D10.1039/C9TC02689D ↗
39. 10.1039/C8TC04900A10.1039/C8TC04900A ↗
40. 10.1016/j.dyepig.2019.10812110.1016/j.dyepig.2019.108121 ↗
41. 10.1039/D2TC02379B10.1039/D2TC02379B ↗
42. 10.1002/jsid.68110.1002/jsid.681 ↗
43. 10.1021/acsami.1c0183510.1021/acsami.1c01835 ↗
44. 10.1002/ejoc.20160040710.1002/ejoc.201600407 ↗
45. 10.1021/ma060808p10.1021/ma060808p ↗