Sulfone-Based HLCT Molecules with Efficient Orange and White Emission
Source abstract
Abstract
The hybrid local charge transfer (HLCT) state in the molecule opens up new avenues for achieving 100% exciton utilization by transforming high-energy triplet excitons into singlet excitons through reverse intersystem crossing. In this work, we designed and synthesized three D–A type HLCT materials without a π-bridge, PTZ-BTOBF, PXZ-BTOBF, as well as DMAC-BTOBF, using the BTOBF skeleton as the acceptor and phenothiazine (PTZ), phenoxazine (PXZ), and 9,9-dimethyl-9,10-dihydroacridine (DMAC) as donors. The molecules have HLCT excited-state characteristics, allowing for green to orange light emissions and exhibiting moderate PLQY. We fabricated a series of green to orange OLED devices and achieved the highest EQE of 4.99% and the lowest turn-on voltage of 3.05 V. Furthermore, by adjusting the doping concentration, single-emitter WOLEDs have been successfully fabricated and achieved an EQE of 1.82% with CIE coordinates of (0.30, 0.35). The result demonstrates a decent WOLED constructed with an HLCT molecule, which may have potential for practical application.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Organic Light-Emitting Diodes Research · Molecular Sensors and Ion Detection
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing 101408, PR China
Key Laboratory of Photochemical Conversion and Optoelectronic Materials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190, China
Funding
Natural Science Foundation of Beijing Municipality · Fundamental Research Funds for the Central Universities · National Natural Science Foundation of China · Chinese Academy of Sciences
References (56)
Show source-provided references
1. 10.1038/s41467-022-32967-w10.1038/s41467-022-32967-w ↗
2. 10.1002/adfm.20221496210.1002/adfm.202214962 ↗
3. 10.1002/advs.20220359610.1002/advs.202203596 ↗
4. 10.1002/anie.20140299210.1002/anie.201402992 ↗
5. 10.1002/anie.20150218010.1002/anie.201502180 ↗
6. 10.1016/j.jiec.2017.12.04410.1016/j.jiec.2017.12.044 ↗
7. 10.1038/ncomms329410.1038/ncomms3294 ↗
8. 10.1002/adma.20160544410.1002/adma.201605444 ↗
9. 10.1021/acssensors.0c0256210.1021/acssensors.0c02562 ↗
10. 10.1039/C4CS00110A10.1039/C4CS00110A ↗
11. 10.1002/chem.20200372110.1002/chem.202003721 ↗
12. 10.1002/advs.20190039710.1002/advs.201900397 ↗
13. 10.1021/ja411045r10.1021/ja411045r ↗
14. 10.1016/j.orgel.2021.10638910.1016/j.orgel.2021.106389 ↗
15. 10.1038/s41467-018-07670-410.1038/s41467-018-07670-4 ↗
16. 10.1002/adma.20190326910.1002/adma.201903269 ↗
17. 10.1002/advs.20190268810.1002/advs.201902688 ↗
18. 10.1007/s12274-019-2569-310.1007/s12274-019-2569-3 ↗
19. 10.1016/j.dyepig.2023.11113310.1016/j.dyepig.2023.111133 ↗
20. 10.1002/adom.20220091510.1002/adom.202200915 ↗
21. 10.1039/C8SC03753A10.1039/C8SC03753A ↗
22. 10.1016/j.dyepig.2020.10909010.1016/j.dyepig.2020.109090 ↗
23. 10.1016/j.orgel.2023.10684510.1016/j.orgel.2023.106845 ↗
24. 10.1016/j.dyepig.2024.11207510.1016/j.dyepig.2024.112075 ↗
25. 10.1021/ja310680x10.1021/ja310680x ↗
26. 10.1021/acs.orglett.9b0011510.1021/acs.orglett.9b00115 ↗
27. 10.1021/acs.jpca.6b0495410.1021/acs.jpca.6b04954 ↗
28. 10.1002/adfm.20170391810.1002/adfm.201703918 ↗
29. 10.1039/C8SC01915K10.1039/C8SC01915K ↗
30. 10.1039/C4TC02771J10.1039/C4TC02771J ↗
31. 10.1016/j.cclet.2023.10911810.1016/j.cclet.2023.109118 ↗
32. 10.1002/anie.20170386210.1002/anie.201703862 ↗
33. 10.1039/D0TC02205E10.1039/D0TC02205E ↗
34. 10.1038/s41586-021-03840-510.1038/s41586-021-03840-5 ↗
35. 10.1021/acsaem.3c0076110.1021/acsaem.3c00761 ↗
36. 10.1002/adma.20220053710.1002/adma.202200537 ↗
37. 10.1039/D0CS00391C10.1039/D0CS00391C ↗
38. 10.1002/anie.20210854010.1002/anie.202108540 ↗
39. 10.1016/j.ccr.2022.21476810.1016/j.ccr.2022.214768 ↗
40. 10.1021/acs.joc.7b0174510.1021/acs.joc.7b01745 ↗
41. 10.1039/C9RA00796B10.1039/C9RA00796B ↗
42. 10.1039/D1RA06985C10.1039/D1RA06985C ↗
43. 10.1039/D1RA06881D10.1039/D1RA06881D ↗
44. 10.1039/C9TC06790F10.1039/C9TC06790F ↗
45. 10.1016/j.dyepig.2023.11115310.1016/j.dyepig.2023.111153 ↗
46. 10.1039/b417717g10.1039/b417717g ↗
47. 10.1016/j.dyepig.2020.10858510.1016/j.dyepig.2020.108585 ↗
48. 10.1002/chem.20190524810.1002/chem.201905248 ↗
49. 10.1039/c3cc47130f10.1039/c3cc47130f ↗
50. 10.1021/cr940745l10.1021/cr940745l ↗
51. 10.1021/ol202107710.1021/ol2021077 ↗
52. 10.1002/adfm.20080080910.1002/adfm.200800809 ↗
53. 10.1002/adfm.20100125210.1002/adfm.201001252 ↗
54. 10.1002/adom.20180166710.1002/adom.201801667 ↗
55. 10.1021/acsami.9b2016210.1021/acsami.9b20162 ↗
56. 10.1063/1.226645210.1063/1.2266452 ↗