journal article·2021-03

Employing Cholesterol Copolymerization Strategy for a Thermally Processable Organic Room‐Temperature Phosphorescence Material

Xin‐Shun Li, Yue Wu, Yiran Zhao, Zhen‐Qiang Yu

Advanced Optical Materials· Volume 9· Issue 6
Publisher page

Abstract

Abstract Development of pure organic room‐temperature phosphorescent (RTP) materials with strong emission and decent processability is highly desirable. However, in the pursuit of high quantum yield (QY) of phosphorescence, the processability of RTP materials is suppressed unwarily. Here, a liquid crystalline (LC) copolymer is envisioned, NpA‐Chol, comprising bromonaphthalimide as the phosphor and cholesterol as the LC mesogen. NpA‐Chol exhibits LC flexibility at high temperatures, thus enabling the material to possess decent processability. In addition, the liquid crystallinity of NpA‐Chol could be improved remarkably after thermal annealing, making a 7.5‐fold increase in phosphorescence QY. This cholesterol copolymerization strategy paves a general avenue for addressing the major defect well: highly efficient RTP materials always suffer from suppression of thermal processability.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Organic Light-Emitting Diodes Research · Perovskite Materials and Applications

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

Affiliations

College of Chemistry and Environmental Engineering Shenzhen University Xueyuan Road 1066 Shenzhen 518071 China

Department of Technical Support Zolix Instruments CO., LTD LDUV 68B Beijing 101102 China

Funding

National Natural Science Foundation of China · Natural Science Foundation of Guangdong Province

References (39)

Show source-provided references
1. 10.1002/anie.20200734310.1002/anie.202007343 ↗
2. 10.1039/c0cs00114g10.1039/c0cs00114g ↗
3. 10.1016/j.trac.2006.07.00910.1016/j.trac.2006.07.009 ↗
4. 10.1080/0010220070142177110.1080/00102200701421771 ↗
5. 10.1021/acssensors.6b0053310.1021/acssensors.6b00533 ↗
6. 10.1038/s41467-018-03236-610.1038/s41467-018-03236-6 ↗
7. 10.1038/nmat250910.1038/nmat2509 ↗
8. 10.1039/c3cc48376b10.1039/c3cc48376b ↗
9. 10.1021/acsami.5b0924410.1021/acsami.5b09244 ↗
10. 10.1002/adma.20180722210.1002/adma.201807222 ↗
11. 10.1002/asia.20190165810.1002/asia.201901658 ↗
12. 10.1002/adma.20080203410.1002/adma.200802034 ↗
13. 10.1007/s11426-016-0155-y10.1007/s11426-016-0155-y ↗
14. 10.1002/anie.20161076210.1002/anie.201610762 ↗
15. 10.1002/adma.20190326910.1002/adma.201903269 ↗
16. 10.1002/anie.20170578510.1002/anie.201705785 ↗
17. 10.1039/C6SC00563B10.1039/C6SC00563B ↗
18. 10.1038/ncomms994710.1038/ncomms9947 ↗
19. 10.1021/ja401769g10.1021/ja401769g ↗
20. 10.1021/ja501458s10.1021/ja501458s ↗
21. Tao P. · Adv. Opt. Mater. · 2020 · 8 · 200985
22. 10.1038/nchem.98410.1038/nchem.984 ↗
23. 10.1038/nchem.125610.1038/nchem.1256 ↗
24. 10.1021/acs.jpclett.7b0050310.1021/acs.jpclett.7b00503 ↗
25. 10.1039/C5CP01203A10.1039/C5CP01203A ↗
26. 10.1002/anie.20090328510.1002/anie.200903285 ↗
27. 10.1021/jp909388y10.1021/jp909388y ↗
28. 10.1002/adma.20150244210.1002/adma.201502442 ↗
29. 10.1039/C5SC00253B10.1039/C5SC00253B ↗
30. 10.1002/anie.20191555610.1002/anie.201915556 ↗
31. 10.1021/jacs.8b1122410.1021/jacs.8b11224 ↗
32. 10.1002/chem.20180281910.1002/chem.201802819 ↗
33. 10.1002/adom.20170011610.1002/adom.201700116 ↗
34. 10.1039/C8TC01007B10.1039/C8TC01007B ↗
35. 10.1002/adma.20160260410.1002/adma.201602604 ↗
36. 10.1002/adfm.20180265710.1002/adfm.201802657 ↗
37. 10.1002/adom.20160042710.1002/adom.201600427 ↗
38. 10.1002/adom.20190127710.1002/adom.201901277 ↗
39. Lin X. H. · Angew. Chem., Int. Ed. · 2020