Low-Threshold Amplified Spontaneous Emission of Benzobisoxazole Derivatives in a Doped Film
Source abstract
Abstract
In this study, we focus on benzobisoxazole (BOX) derivatives with the aim of achieving large stimulated emission cross sections, which are expected to contribute to lower laser thresholds and high stability. While both optically and electrically pumped organic semiconductor lasers have the potential to provide miniaturized lasers with wavelength tunability from ultraviolet to infrared, the development of organic semiconductors with low laser thresholds remains crucial for realizing stable devices. We report a low amplified spontaneous emission (ASE) threshold of BOX derivatives, which are doped into 4,4′-bis(carbazol-9-yl)biphenyl (CBP) host layers, with values as low as approximately 1 μJ/cm 2 . Further, we demonstrate high photostability under continuous photoexcitation, suggesting that BOX derivatives are promising candidates as emitting materials for organic semiconductor lasers (OSLs).
Source: openalex_inverted_index · 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
Center for Organic Photonics and Electronics Research (OPERA), Kyushu University, 744 Motooka, Nishi, Fukuoka 819-0395, Japan
International Institute for Carbon Neutral Energy Research (I2CNER), Kyushu University, 744 Motooka, Nishi, Fukuoka 819-0395, Japan
Funding
Japan Society for the Promotion of Science
References (34)
Show source-provided references
1. 10.1002/pi.317310.1002/pi.3173 ↗
2. 10.1021/acs.chemrev.6b0017210.1021/acs.chemrev.6b00172 ↗
3. 10.7567/1882-0786/ab1b9010.7567/1882-0786/ab1b90 ↗
4. 10.1038/s41586-023-06488-510.1038/s41586-023-06488-5 ↗
5. 10.1063/1.149447310.1063/1.1494473 ↗
6. 10.1021/cr050152i10.1021/cr050152i ↗
7. 10.1021/acs.jpclett.1c0398310.1021/acs.jpclett.1c03983 ↗
8. 10.1063/1.169947910.1063/1.1699479 ↗
9. 10.1063/1.186755510.1063/1.1867555 ↗
10. 10.1063/1.348888310.1063/1.3488883 ↗
11. 10.1016/j.jlumin.2013.04.00110.1016/j.jlumin.2013.04.001 ↗
12. 10.1002/adom.20160000610.1002/adom.201600006 ↗
13. 10.1126/sciadv.160257010.1126/sciadv.1602570 ↗
14. 10.1063/1.291243310.1063/1.2912433 ↗
15. 10.1039/D0CS00037J10.1039/D0CS00037J ↗
16. 10.1021/acsmaterialslett.9b0053610.1021/acsmaterialslett.9b00536 ↗
17. 10.1021/ol802011y10.1021/ol802011y ↗
18. 10.1021/jo201078w10.1021/jo201078w ↗
19. 10.1351/PAC-CON-11-10-2310.1351/PAC-CON-11-10-23 ↗
20. 10.1246/cl.14105410.1246/cl.141054 ↗
21. 10.1039/C8CP03689F10.1039/C8CP03689F ↗
22. 10.1021/acs.chemmater.3c0210910.1021/acs.chemmater.3c02109 ↗
23. 10.1016/j.cej.2023.14495010.1016/j.cej.2023.144950 ↗
24. 10.1016/j.orgel.2008.12.01110.1016/j.orgel.2008.12.011 ↗
25. 10.1016/j.orgel.2015.01.03710.1016/j.orgel.2015.01.037 ↗
26. 10.1103/PhysRevLett.96.01740410.1103/PhysRevLett.96.017404 ↗
27. 10.1016/j.orgel.2008.10.01010.1016/j.orgel.2008.10.010 ↗
28. 10.1021/jp200771710.1021/jp2007717 ↗
29. 10.1021/acsphotonics.3c0161010.1021/acsphotonics.3c01610 ↗
30. 10.1002/adfm.20140049510.1002/adfm.201400495 ↗
31. 10.1002/adma.20240227510.1002/adma.202402275 ↗
32. 10.1038/s41598-017-08708-110.1038/s41598-017-08708-1 ↗
33. 10.1248/cpb.38.169210.1248/cpb.38.1692 ↗
34. 10.1038/ncomms1556610.1038/ncomms15566 ↗