Supramolecular Assembly of Hydrogen-Bonded Organic Frameworks with Carbon Dots: Realizing Ultralong Aqueous Room-Temperature Phosphorescence for Anticounterfeiting
Source abstract
Abstract
Room-temperature phosphorescent carbon dots (RTP-CDs) have received increasing attention due to their excellent optical properties and potential applications. Nevertheless, the realization of RTP-CDs in aqueous solutions remains a considerable challenge due to the water-molecule- and oxygen-induced deactivation of the triplet excitons, which leads to phosphorescence quenching. In this study, ultralong phosphorescence in water was achieved by in situ self-assembly of CDs encapsulated in a rigid hydrogen-bonded organic framework (HOF). The phosphorescence lifetime reaches an impressive 956.96 ms and exhibits long-lasting optical and structural stability in water for more than 90 days. The composite material not only has ultralong luminescence life and excellent luminescence stability but also has two-color phosphorescence emission, as well as excellent antiphotobleaching and phosphorescence stability in aqueous solution, which can solve the current problem that RTP is easily burst out by water and moisture. In addition, this study introduced a fluorescent dye based on the triplet-singlet Förster resonance energy transfer system (TS-FRET) to fine-tune the afterglow properties. This work will inspire the design of RTP systems with dual phosphor light sources and provide new strategies for the development of smart RTP materials in water.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Carbon and Quantum Dots Applications · Molecular Sensors and Ion Detection
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Chemistry, Chemical Engineering and Environment, Fujian Provincial Key Laboratory of Modern Analytical Science and Separation Technology, Minnan Normal University, Zhangzhou, Fujian 363000, PR China
Micro-Nano Organic Optical Materials Laboratory, Minnan Normal University, Zhangzhou, Fujian 363000, PR China
Funding
Natural Science Foundation of Fujian Province · National Natural Science Foundation of China · Minnan Normal University
References (55)
Show source-provided references
1. 10.1016/j.ccr.2019.21310710.1016/j.ccr.2019.213107 ↗
2. 10.1002/smll.20220740310.1002/smll.202207403 ↗
3. 10.1002/smll.20220122310.1002/smll.202201223 ↗
4. 10.1038/s41467-023-43133-110.1038/s41467-023-43133-1 ↗
5. 10.1002/adma.20220441510.1002/adma.202204415 ↗
6. 10.1002/adfm.20211194110.1002/adfm.202111941 ↗
7. 10.1002/anie.20220325410.1002/anie.202203254 ↗
8. 10.1002/anie.20160244510.1002/anie.201602445 ↗
9. 10.1038/s41467-024-47378-210.1038/s41467-024-47378-2 ↗
10. 10.1002/adfm.20150435710.1002/adfm.201504357 ↗
11. 10.1038/s41467-021-27914-010.1038/s41467-021-27914-0 ↗
12. 10.1002/adma.20200781110.1002/adma.202007811 ↗
13. 10.1021/acs.chemrev.3c0058110.1021/acs.chemrev.3c00581 ↗
14. 10.1016/j.nantod.2019.03.00510.1016/j.nantod.2019.03.005 ↗
15. 10.1016/j.tifs.2021.11.02910.1016/j.tifs.2021.11.029 ↗
16. 10.1002/adom.20207008610.1002/adom.202070086 ↗
17. 10.1021/jacs.7b0396310.1021/jacs.7b03963 ↗
18. 10.1002/adfm.20230073510.1002/adfm.202300735 ↗
19. 10.1002/agt2.12310.1002/agt2.123 ↗
20. 10.1016/j.mattod.2015.11.00810.1016/j.mattod.2015.11.008 ↗
21. 10.1002/smll.20180508710.1002/smll.201805087 ↗
22. 10.1016/j.cej.2023.14801810.1016/j.cej.2023.148018 ↗
23. 10.1016/j.jclepro.2023.13625010.1016/j.jclepro.2023.136250 ↗
24. 10.1016/j.snb.2022.13276110.1016/j.snb.2022.132761 ↗
25. 10.1016/j.talanta.2023.12439910.1016/j.talanta.2023.124399 ↗
26. 10.1002/advs.20210012510.1002/advs.202100125 ↗
27. 10.1002/anie.20161187910.1002/anie.201611879 ↗
28. 10.1016/j.bios.2023.11560710.1016/j.bios.2023.115607 ↗
29. 10.1021/acsami.3c1324410.1021/acsami.3c13244 ↗
30. 10.1016/j.jclepro.2017.07.18710.1016/j.jclepro.2017.07.187 ↗
31. 10.1016/j.nanoen.2023.10862310.1016/j.nanoen.2023.108623 ↗
32. 10.1038/s41565-021-01051-710.1038/s41565-021-01051-7 ↗
33. 10.1016/j.cej.2019.12320010.1016/j.cej.2019.123200 ↗
34. 10.1016/j.cej.2022.13652510.1016/j.cej.2022.136525 ↗
35. 10.1016/j.nanoen.2015.02.01310.1016/j.nanoen.2015.02.013 ↗
36. 10.1016/j.apcatb.2017.05.04910.1016/j.apcatb.2017.05.049 ↗
37. 10.1016/j.mattod.2021.07.02810.1016/j.mattod.2021.07.028 ↗
38. 10.1021/acsnano.8b0708710.1021/acsnano.8b07087 ↗
39. 10.1002/adma.20187009210.1002/adma.201870092 ↗
40. 10.1016/j.cej.2020.12764710.1016/j.cej.2020.127647 ↗
41. 10.1002/adma.20200134810.1002/adma.202001348 ↗
42. 10.1021/acscentsci.8b0084410.1021/acscentsci.8b00844 ↗
43. 10.1002/anie.20181462910.1002/anie.201814629 ↗
44. 10.1021/acsanm.8b0135510.1021/acsanm.8b01355 ↗
45. 10.1002/advs.20190131610.1002/advs.201901316 ↗
46. 10.1002/sstr.20220032710.1002/sstr.202200327 ↗
47. 10.1002/anie.20200410910.1002/anie.202004109 ↗
48. 10.1002/smll.20210337410.1002/smll.202103374 ↗
49. 10.1016/j.jcis.2021.10.01810.1016/j.jcis.2021.10.018 ↗
50. 10.1002/advs.20180079510.1002/advs.201800795 ↗
51. 10.1002/smll.20190116110.1002/smll.201901161 ↗
52. 10.1016/S0040-4020(02)00202-810.1016/S0040-4020(02)00202-8 ↗
53. 10.1021/jacs.8b0386710.1021/jacs.8b03867 ↗
54. 10.1038/s41467-020-18572-910.1038/s41467-020-18572-9 ↗
55. 10.1002/adma.20220671210.1002/adma.202206712 ↗