Transition Metal Chalcogenides/MXene Quantum Dot Heterostructure with Polyelectrolyte-Mediated Boosted Charge Separation for Photocatalytic Organic Transformation
Source abstract
Abstract
MXene quantum dots (QDs) possess the electron-withdrawing capability of MXene nanosheets (NSs) with more abundant active sites, rendering it an emerging charge mediator for photocatalysis. Nevertheless, few MXene QD-based photocatalytic systems have been explored, and the contribution of MXene QDs for the modulation of charge transfer remains elusive. Herein, we show the construction of cascade charge flow over transition metal chalcogenides (TMCs), which are coated via a polyelectrolyte layer of poly(dialyldimethylammonium chloride) (PDDA), followed by MXene QD deposition. It was unleashed that the intermediate PDDA layer serves as a charge relay medium to boost the electron transfer from TMC NSs to MXene QDs, boosting the charge transfer kinetics, promoting the interfacial charge separation, and endowing the TMCs@PDDA-M QD heterostructures with considerably enhanced visible-light-driven photoactivities for reduction of aromatic nitro compounds.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: MXene and MAX Phase Materials · Advanced Photocatalysis Techniques · Nanocluster Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Instrumental Measurement and Analysis Center, Fuzhou University, Fuzhou 350108, China
Funding
Natural Science Foundation of Fujian Province
References (40)
Show source-provided references
1. 10.1021/acsanm.0c0248110.1021/acsanm.0c02481 ↗
2. 10.1016/j.jmst.2020.02.03710.1016/j.jmst.2020.02.037 ↗
3. 10.1038/nature1397010.1038/nature13970 ↗
4. 10.1002/adma.20160484710.1002/adma.201604847 ↗
5. 10.1039/D0TA07235D10.1039/D0TA07235D ↗
6. 10.1039/C7NR06958H10.1039/C7NR06958H ↗
7. 10.1021/acsami.9b1498510.1021/acsami.9b14985 ↗
8. 10.1039/C9TA08107K10.1039/C9TA08107K ↗
9. 10.1002/smll.20230080410.1002/smll.202300804 ↗
10. 10.1002/smll.20230237210.1002/smll.202302372 ↗
11. 10.1039/D0TA05297C10.1039/D0TA05297C ↗
12. 10.1039/C8EE01487F10.1039/C8EE01487F ↗
13. 10.1039/D0TA02122A10.1039/D0TA02122A ↗
14. 10.1002/adfm.20180650010.1002/adfm.201806500 ↗
15. 10.1002/aenm.20120086810.1002/aenm.201200868 ↗
16. 10.1002/adfm.20180013610.1002/adfm.201800136 ↗
17. 10.1016/j.jhazmat.2016.08.02510.1016/j.jhazmat.2016.08.025 ↗
18. 10.1021/acscatal.8b0110510.1021/acscatal.8b01105 ↗
19. 10.1039/C7CC02366A10.1039/C7CC02366A ↗
20. 10.1021/acsnano.8b0684810.1021/acsnano.8b06848 ↗
21. 10.1002/adfm.20190849210.1002/adfm.201908492 ↗
22. 10.1002/adfm.20211084810.1002/adfm.202110848 ↗
23. 10.1039/C9TA07569K10.1039/C9TA07569K ↗
24. 10.1039/C8TA08841A10.1039/C8TA08841A ↗
25. 10.1039/D3TA01154B10.1039/D3TA01154B ↗
26. 10.1039/D2TA02755K10.1039/D2TA02755K ↗
27. 10.1002/admi.20170109810.1002/admi.201701098 ↗
28. 10.1039/D1TA10284B10.1039/D1TA10284B ↗
29. 10.1002/adfm.20210633810.1002/adfm.202106338 ↗
30. 10.1039/D2TA00572G10.1039/D2TA00572G ↗
31. 10.1021/acsami.9b1454310.1021/acsami.9b14543 ↗
32. 10.1039/C8TA10379H10.1039/C8TA10379H ↗
33. 10.1002/adfm.20221033210.1002/adfm.202210332 ↗
34. 10.1039/D2TA08547J10.1039/D2TA08547J ↗
35. 10.1039/C7TA04333C10.1039/C7TA04333C ↗
36. 10.1039/C7NR04802E10.1039/C7NR04802E ↗
37. 10.1021/acsomega.2c0513310.1021/acsomega.2c05133 ↗
38. 10.1016/j.jece.2023.11008810.1016/j.jece.2023.110088 ↗
39. 10.1021/acsomega.2c0775310.1021/acsomega.2c07753 ↗
40. 10.1016/j.surfin.2023.10271010.1016/j.surfin.2023.102710 ↗