journal article·2024

Photo-polymerization-induced tightened domain enhancing the room-temperature phosphorescence emission

Cheng Yuan, Sang Yup Lee, Jingyuan Huang, Yong Ho Cho, Yujie Liu, Dong June Ahn, Chunzhi Cui

Journal of Materials Chemistry C· Volume 12· Issue 33
Publisher page

Abstract

Diacetylene monomers are linked to pure organic phosphors (POPs), and the conjugated polydiacetylene formed by UV irradiation arranges the POPs tightly. This strategy significantly enhances the room-temperature phosphorescent efficiency of POPs.
Only a short abstract or summary was supplied by the source.
Source: crossref · Quality: short

Research context

OpenAlex topics: Polydiacetylene-based materials and applications · Luminescence and Fluorescent Materials · Antimicrobial Peptides and Activities

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

Affiliations

Department of Chemistry, Yanbian University, Yanji 133002, China

KU-KIST Graduate School of Converging Science and Technology, Korea University, Seoul 02841, Korea

Department of Chemical and Biological Engineering, Korea University, Seoul 02841, Korea

Funding

National Research Foundation of Korea · Overseas Expertise Introduction Project for Discipline Innovation · National Natural Science Foundation of China · Natural Science Foundation of Jilin Province

References (32)

Show source-provided references
1. Zhao · Nat. Rev. Mater. · 2020 · 5 · 86910.1038/s41578-020-0223-z ↗
2. Ma · Acc. Chem. Res. · 2021 · 54 · 340310.1021/acs.accounts.1c00336 ↗
3. Guo · Acc. Chem. Res. · 2022 · 55 · 116010.1021/acs.accounts.2c00038 ↗
4. Shao · Acc. Chem. Res. · 2022 · 55 · 157310.1021/acs.accounts.2c00146 ↗
5. Ding · Acc. Chem. Res. · 2023 · 4 · 827
6. Mukherjee · Chem. Commun. · 2015 · 51 · 1098810.1039/C5CC03114A ↗
7. Nidhankar · Chem. Sci. · 2021 · 12 · 421610.1039/D1SC00446H ↗
8. Kenry · Nat. Commun. · 2019 · 10 · 211110.1038/s41467-019-10033-2 ↗
9. Xu · Adv. Mater. · 2016 · 28 · 992010.1002/adma.201602604 ↗
10. Lower · Chem. Rev. · 1966 · 66 · 19910.1021/cr60240a004 ↗
11. El-Sayed · Acc. Chem. Res. · 1968 · 1 · 810.1021/ar50001a002 ↗
12. Bolton · Nat. Chem. · 2011 · 3 · 20510.1038/nchem.984 ↗
13. Baba · J. Phys. Chem. A · 2011 · 115 · 951410.1021/jp111892y ↗
14. Shao · Chem. Sci. · 2022 · 13 · 78910.1039/D1SC05689A ↗
15. Kwon · Nat. Commun. · 2015 · 6 · 894710.1038/ncomms9947 ↗
16. Baryshnikov · Chem. Rev. · 2017 · 117 · 650010.1021/acs.chemrev.7b00060 ↗
17. Huang · J. Mater. Chem. C · 2019 · 7 · 253010.1039/C8TC06202A ↗
18. Yan · Angew. Chem., Int. Ed. · 2021 · 60 · 1973510.1002/anie.202108025 ↗
19. Zhang · J. Am. Chem. Soc. · 2021 · 143 · 1367510.1021/jacs.1c05213 ↗
20. Scypinski · Anal. Chem. · 1984 · 56 · 32210.1021/ac00267a005 ↗
21. Yuan · ACS Appl. Mater. Interfaces · 2020 · 12 · 5205910.1021/acsami.0c17119 ↗
22. Schulman · Science · 1972 · 178 · 5310.1126/science.178.4056.53 ↗
23. Mitchell · J. Am. Chem. Soc. · 1998 · 120 · 972610.1021/ja981963p ↗
24. Ahn · Acc. Chem. Res. · 2008 · 41 · 80510.1021/ar7002489 ↗
25. Yoon · Chem. Soc. Rev. · 2009 · 38 · 195810.1039/b819539k ↗
26. Sun · Chem. Soc. Rev. · 2010 · 39 · 424410.1039/c001151g ↗
27. Okaniwa · Adv. Funct. Mater. · 2016 · 26 · 346310.1002/adfm.201600560 ↗
28. Lauher · Acc. Chem. Res. · 2008 · 41 · 121510.1021/ar8001427 ↗
29. Zhang · Ind. Eng. Chem. Res. · 2017 · 56 · 312310.1021/acs.iecr.7b00149 ↗
30. Xu · Chem. Commun. · 2013 · 49 · 844710.1039/c3cc44809f ↗
31. Lee · Chem. Mater. · 2020 · 32 · 258310.1021/acs.chemmater.0c00078 ↗
32. Choi · J. Mater. Chem. C · 2019 · 7 · 1313010.1039/C9TC03204E ↗