journal article·2021-08-04Open access

Fast Polymeric Functionalization Approach for the Covalent Coating of MoS 2 Layers

Iván Gómez-Muñoz, Sofiane Laghouati, Ramón Torres-Cavanillas, Marc Morant-Giner, Natalia V. Vassilyeva, Alicia Forment-Aliaga, Mónica Giménez-Marqués

ACS Applied Materials & Interfaces· Volume 13· Issue 30

Abstract

We present the covalent coating of chemically exfoliated molybdenum disulfide (MoS2) based on the polymerization of functional acryl molecules. The method relies on the efficient diazonium anchoring reaction to provoke the in situ radical polymerization and covalent adhesion of functional coatings. In particular, we successfully implement hydrophobicity on the exfoliated MoS2 in a direct, fast, and quantitative synthetic approach. The covalent functionalization is proved by multiple techniques including X-ray photoelectron spectroscopy and TGA-MS. This approach represents a simple and general protocol to reach dense and homogeneous functional coatings on 2D materials.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: 2D Materials and Applications · MXene and MAX Phase Materials · Advanced Photocatalysis Techniques

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

Affiliations

Instituto de Ciencia Molecular (ICMol), Universidad de Valencia, c/Catedrático José Beltrán 2, Paterna 46980, Spain

Funding

Ministerio de Ciencia e Innovaci??n · la Caixa Foundation · Generalitat Valenciana

References (47)

Show source-provided references
1. 10.1038/nchem.158910.1038/nchem.1589 ↗
2. 10.1039/C7TA04268J10.1039/C7TA04268J ↗
3. 10.1039/C6TA08089H10.1039/C6TA08089H ↗
4. 10.1039/C7NH00137A10.1039/C7NH00137A ↗
5. 10.1039/C8CP06535G10.1039/C8CP06535G ↗
6. 10.1039/C5NR05757D10.1039/C5NR05757D ↗
7. Avouris P. · 201710.1017/9781316681619 ↗
8. 10.1038/s41699-020-00162-410.1038/s41699-020-00162-4 ↗
9. 10.1139/p83-01310.1139/p83-013 ↗
10. 10.1021/acs.chemrev.6b0055810.1021/acs.chemrev.6b00558 ↗
11. 10.1021/acs.chemmater.5b0098610.1021/acs.chemmater.5b00986 ↗
12. 10.1002/adfm.20170612510.1002/adfm.201706125 ↗
13. 10.1039/C6NR09241A10.1039/C6NR09241A ↗
14. 10.1080/23746149.2019.162572310.1080/23746149.2019.1625723 ↗
15. 10.1039/C8CS00169C10.1039/C8CS00169C ↗
16. 10.1002/anie.20170821110.1002/anie.201708211 ↗
17. 10.1039/D0CC02371J10.1039/D0CC02371J ↗
18. 10.1002/chem.20200006810.1002/chem.202000068 ↗
19. 10.1021/acsnano.5b0096510.1021/acsnano.5b00965 ↗
20. 10.1038/nchem.210810.1038/nchem.2108 ↗
21. 10.1021/jacs.7b1124210.1021/jacs.7b11242 ↗
22. 10.1002/chem.20160417610.1002/chem.201604176 ↗
23. 10.1039/D0NR07310E10.1039/D0NR07310E ↗
24. 10.1039/C9TC03155C10.1039/C9TC03155C ↗
25. 10.1002/chem.20150501710.1002/chem.201505017 ↗
26. 10.1021/cm071371i10.1021/cm071371i ↗
27. 10.1039/c0jm03679j10.1039/c0jm03679j ↗
28. 10.1021/acsami.9b1182610.1021/acsami.9b11826 ↗
29. 10.1007/s10853-011-5709-z10.1007/s10853-011-5709-z ↗
30. 10.1002/smll.20180190010.1002/smll.201801900 ↗
31. 10.1021/acssuschemeng.8b0558710.1021/acssuschemeng.8b05587 ↗
32. 10.1021/acsnano.5b0158010.1021/acsnano.5b01580 ↗
33. 10.1021/cr00087a00410.1021/cr00087a004 ↗
34. 10.1016/0022-2860(82)80033-110.1016/0022-2860(82)80033-1 ↗
35. 10.1002/app.4357410.1002/app.43574 ↗
36. Aroney M. · J. Chem. Soc. · 1955 · 276
37. 10.1021/ja01595a02710.1021/ja01595a027 ↗
38. 10.1016/0371-1951(61)80030-110.1016/0371-1951(61)80030-1 ↗
39. 10.1002/chem.20150230310.1002/chem.201502303 ↗
40. 10.1021/jacs.8b1093010.1021/jacs.8b10930 ↗
41. 10.1039/C7TA08684A10.1039/C7TA08684A ↗
42. 10.1021/ma951782x10.1021/ma951782x ↗
43. 10.1021/la803742c10.1021/la803742c ↗
44. 10.1002/adfm.20120266210.1002/adfm.201202662 ↗
45. 10.1021/acsami.9b1731910.1021/acsami.9b17319 ↗
46. 10.1016/j.chempr.2018.05.02010.1016/j.chempr.2018.05.020 ↗
47. 10.1016/j.seppur.2019.11642010.1016/j.seppur.2019.116420 ↗