journal article·2022-07-06

Highly Efficient Artificial Light-Harvesting Systems Constructed in an Aqueous Solution Based on Twisted Cucurbit[14]Uril

Yang Luo, Wei Zhang, Qian Ren, Zhu Tao, Xin Xiao

ACS Applied Materials & Interfaces· Volume 14· Issue 26
Publisher page

Abstract

Relying on the supramolecular self-assembly of twisted cucurbit[14]urils (tQ[14]), anthracene derivatives (ADPy), Nile red (NiR), and rhodamine B (RB), highly efficient light-harvesting systems have been successfully designed in an aqueous medium. The addition of tQ[14] causes ADPy to aggregate through supramolecular self-assembly to form a supramolecular polymer (ADPy@tQ[14]) with excellent aggregation-induced fluorescence and an interesting spherical external morphology, making it a remarkable energy donor. Consequently, efficient energy-transfer processes have occurred between ADPy@tQ[14] assembly and NiR and RB, which both serve as effective energy acceptors while being loaded onto ADPy@tQ[14]. In the case of NiR, the energy-transfer efficiency is up to 72.45%, and the antenna effect is near 55.4 at a donor/acceptor ratio of 100:1, making it close to the light-harvesting systems in nature. As a result, effective water-soluble artificial light-harvesting systems are showing enormous prospective as versatile platforms for simulating photosynthesis.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Supramolecular Chemistry and Complexes · Supramolecular Self-Assembly in Materials

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

Affiliations

State Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Macrocyclic and Supramolecular Chemistry of Guizhou Province, Guizhou University, Guiyang 550025, China

Funding

National Natural Science Foundation of China · Guizhou Province

References (34)

Show source-provided references
1. 10.1002/ange.20180017510.1002/ange.201800175 ↗
2. 10.1002/anie.20181214610.1002/anie.201812146 ↗
3. 10.1021/jz101424p10.1021/jz101424p ↗
4. 10.1002/adma.20160171910.1002/adma.201601719 ↗
5. 10.1021/acs.chemmater.9b0133810.1021/acs.chemmater.9b01338 ↗
6. 10.1002/anie.20190440710.1002/anie.201904407 ↗
7. 10.1021/acsami.0c0491710.1021/acsami.0c04917 ↗
8. 10.1002/adfm.20180436210.1002/adfm.201804362 ↗
9. 10.1038/s41467-020-14792-110.1038/s41467-020-14792-1 ↗
10. 10.1002/anie.20191210210.1002/anie.201912102 ↗
11. 10.1039/C8CS00278A10.1039/C8CS00278A ↗
12. 10.1039/D0CC01292K10.1039/D0CC01292K ↗
13. 10.1002/anie.20050387310.1002/anie.200503873 ↗
14. 10.1016/j.dyepig.2019.10765210.1016/j.dyepig.2019.107652 ↗
15. 10.1002/anie.20200358510.1002/anie.202003585 ↗
16. 10.1039/C9CC00097F10.1039/C9CC00097F ↗
17. 10.1039/D0TA03169K10.1039/D0TA03169K ↗
18. 10.1002/adom.20200170210.1002/adom.202001702 ↗
19. 10.1016/j.gresc.2021.01.00310.1016/j.gresc.2021.01.003 ↗
20. 10.1021/ar500013310.1021/ar5000133 ↗
21. 10.1021/acsami.0c2029210.1021/acsami.0c20292 ↗
22. 10.1016/j.cclet.2020.02.02310.1016/j.cclet.2020.02.023 ↗
23. 10.1016/j.snb.2018.12.02410.1016/j.snb.2018.12.024 ↗
24. 10.1016/j.ccr.2020.21373310.1016/j.ccr.2020.213733 ↗
25. 10.1016/j.ccr.2020.21374110.1016/j.ccr.2020.213741 ↗
26. 10.1002/anie.20121026710.1002/anie.201210267 ↗
27. 10.1016/j.cclet.2021.11.05310.1016/j.cclet.2021.11.053 ↗
28. 10.1039/C6QO00310A10.1039/C6QO00310A ↗
29. 10.1016/j.microc.2022.10736410.1016/j.microc.2022.107364 ↗
30. 10.1021/acs.macromol.2c0007510.1021/acs.macromol.2c00075 ↗
31. 10.1002/anie.20160450810.1002/anie.201604508 ↗
32. 10.1002/adma.20170190510.1002/adma.201701905 ↗
33. 10.1002/anie.20200342710.1002/anie.202003427 ↗
34. 10.1039/D0TC05243D10.1039/D0TC05243D ↗