journal article·2021-07-05

Revisiting Carbazole: Origin, Impurity, and Properties

Chengjian Chen, Kok Chan Chong, Yutong Pan, Guobin Qi, Shidang Xu, Bin Liu

ACS Materials Letters· Volume 3· Issue 7
Publisher page

Abstract

Photoluminescence quantum yield (PLQY) is one of the most important characteristics for organic luminescent materials. However, when carbazole prepared from the lab was compared to that from a commercial source, a remarkable change of PLQY was observed to vary from 37.1% to 69.8%. Taking 9-(4-bromobenzyl)-9H-carbazole (CzBBr) as an example of carbazole derivatives, the PLQYs of CzBBr synthesized from different origins of carbazole were varied from 16.0% to 91.1%. Our studies demonstrated that efficient radiative transition pathways were activated for commercial carbazole based luminescence, leading to a large enhancement in PLQY with fluorescence (from 16.0% to 54.4%) and phosphorescence (from <1% to 36.7%) for CzBBr. These results suggest that the origin of carbazole plays a very important role in determining the optical properties of carbazole derivatives, alerting us to carefully revisit carbazole and its derivatives, especially those with record-high efficiency.
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

Department of Chemical and Biomolecular Engineering, National University of Singapore, Singapore 117585, Singapore

Joint School of National University of Singapore and Tianjin University, International Campus of Tianjin University, Binhai New City, Fuzhou 350207, China

Funding

National Research Foundation Singapore · National University of Singapore

References (28)

Show source-provided references
1. 10.1038/s41467-020-14669-310.1038/s41467-020-14669-3 ↗
2. 10.1002/anie.20200734310.1002/anie.202007343 ↗
3. 10.1002/anie.20201183010.1002/anie.202011830 ↗
4. 10.1021/acsmaterialslett.9b0036910.1021/acsmaterialslett.9b00369 ↗
5. 10.1021/jacs.0c1265910.1021/jacs.0c12659 ↗
6. 10.1038/s41467-019-10033-210.1038/s41467-019-10033-2 ↗
7. 10.1016/j.matt.2020.05.00510.1016/j.matt.2020.05.005 ↗
8. 10.1016/j.chempr.2016.08.01010.1016/j.chempr.2016.08.010 ↗
9. 10.1021/acsmaterialslett.0c0032010.1021/acsmaterialslett.0c00320 ↗
10. 10.1038/natrevmats.2018.2010.1038/natrevmats.2018.20 ↗
11. 10.1021/acsmaterialslett.9b0043310.1021/acsmaterialslett.9b00433 ↗
12. 10.1021/ie50641a00610.1021/ie50641a006 ↗
13. 10.1021/cr60127a00110.1021/cr60127a001 ↗
14. 10.1038/s41563-020-0797-210.1038/s41563-020-0797-2 ↗
15. 10.1021/ja055819x10.1021/ja055819x ↗
16. 10.1002/ejoc.20120016010.1002/ejoc.201200160 ↗
17. 10.1039/C7GC03392C10.1039/C7GC03392C ↗
18. 10.1021/jo050329910.1021/jo0503299 ↗
19. 10.1021/jp909388y10.1021/jp909388y ↗
20. 10.1038/nchem.98410.1038/nchem.984 ↗
21. 10.1002/anie.20190856710.1002/anie.201908567 ↗
22. 10.1038/271235a010.1038/271235a0 ↗
23. 10.26434/chemrxiv.13285589.v110.26434/chemrxiv.13285589.v1 ↗
24. 10.1002/adma.20200102610.1002/adma.202001026 ↗
25. 10.1038/s41467-018-03236-610.1038/s41467-018-03236-6 ↗
26. 10.1002/cphc.20180031010.1002/cphc.201800310 ↗
27. 10.1039/C7SC90048A10.1039/C7SC90048A ↗
28. 10.1002/anie.20180994510.1002/anie.201809945 ↗