Supramolecular Hybrids of MoS2 and Graphene Nanosheets with Organic Chromophores for Optoelectronic Applications
Source abstract
Abstract
A novel supramolecular strategy based on host–guest chemistry has been proposed for the noncovalent functionalization of MoS2 nanosheets with organic chromophores. Stable ternary complexes are formed between benzyl imidazole functionalized MoS2 and chromophores in the presence of cucurbit[8]uril host, resulting in noncovalent anchoring of donor and acceptor chromophores on the surface. On the other hand, in the case of graphene, we observe π–π stacking resulting in the face-on organization of chromophore on the surface. The MoS2 and graphene hybrids have been characterized by various spectroscopic techniques. The present design opens up new possibilities for the noncovalent functionalization of transition metal dichalcogenides even in the absence of delocalized π-electrons which are essential to alter their optoelectronic properties. In addition, these novel supramolecular hybrid materials with strong electronic communication between noncovalently anchored chromophores and the 2D nanosheets may find applications in optoelectronics and related areas.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: 2D Materials and Applications · Graphene research and applications · Supramolecular Self-Assembly in Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Sheikh Saqr Laboratory, International Centre for Materials Science, School of Advanced Materials, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bangalore 560064, India
School of Advanced Materials and New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bangalore 560064, India
Funding
Council of Scientific and Industrial Research
References (47)
Show source-provided references
1. 10.1039/C7NR02025B10.1039/C7NR02025B ↗
2. 10.1038/nnano.2012.19310.1038/nnano.2012.193 ↗
3. 10.1038/nphoton.2015.28210.1038/nphoton.2015.282 ↗
4. 10.1038/nphoton.2014.27110.1038/nphoton.2014.271 ↗
5. 10.1126/science.110289610.1126/science.1102896 ↗
6. 10.1002/anie.20090167810.1002/anie.200901678 ↗
7. 10.1038/nature0496910.1038/nature04969 ↗
8. 10.1073/pnas.090584410610.1073/pnas.0905844106 ↗
9. 10.1126/science.115087810.1126/science.1150878 ↗
10. 10.1021/ja806262m10.1021/ja806262m ↗
11. Georgakalis, V. Functionalization of Graphene; Govindaraj, A., Rao, C. N. R., Eds. Wiley-VCH Verlag GmbH & Co. KGaA, 2014; Chapter 10, pp 283–358.
12. 10.1002/adma.20080380810.1002/adma.200803808 ↗
13. 10.1002/adma.20080316010.1002/adma.200803160 ↗
14. 10.1021/ar900056z10.1021/ar900056z ↗
15. 10.1039/b808955h10.1039/b808955h ↗
16. 10.1002/chem.20090282810.1002/chem.200902828 ↗
17. 10.1002/adma.20090157810.1002/adma.200901578 ↗
18. 10.1021/ja905032g10.1021/ja905032g ↗
19. 10.1088/0953-8984/20/47/47220410.1088/0953-8984/20/47/472204 ↗
20. 10.1021/jp907535510.1021/jp9075355 ↗
21. 10.1002/asia.20080048610.1002/asia.200800486 ↗
22. 10.1016/j.cplett.2011.03.03110.1016/j.cplett.2011.03.031 ↗
23. 10.1021/ja100190p10.1021/ja100190p ↗
24. 10.1039/b511541h10.1039/b511541h ↗
25. 10.1039/b406933a10.1039/b406933a ↗
26. 10.1038/nature0423310.1038/nature04233 ↗
27. 10.1038/nmat231810.1038/nmat2318 ↗
28. 10.1021/ar040238i10.1021/ar040238i ↗
29. 10.1021/ja016954m10.1021/ja016954m ↗
30. 10.1002/chem.20160417610.1002/chem.201604176 ↗
31. 10.1021/acsnano.5b0096510.1021/acsnano.5b00965 ↗
32. 10.1021/nn504784410.1021/nn5047844 ↗
33. 10.1038/nchem.210810.1038/nchem.2108 ↗
34. 10.1039/C6NR04326G10.1039/C6NR04326G ↗
35. 10.1021/acsnano.5b0745710.1021/acsnano.5b07457 ↗
36. 10.1002/cphc.20160051110.1002/cphc.201600511 ↗
37. 10.1038/nnano.2013.2010.1038/nnano.2013.20 ↗
38. 10.1002/asia.20130017410.1002/asia.201300174 ↗
39. 10.1016/j.ijhydene.2018.03.14810.1016/j.ijhydene.2018.03.148 ↗
40. 10.1021/ar040238i10.1021/ar040238i ↗
41. 10.1021/ja016954m10.1021/ja016954m ↗
42. 10.1021/ol060862q10.1021/ol060862q ↗
43. 10.1038/ncomms1455410.1038/ncomms14554 ↗
44. 10.1002/adma.20160532510.1002/adma.201605325 ↗
45. 10.1039/b716536f10.1039/b716536f ↗
46. 10.1038/s41598-017-10632-310.1038/s41598-017-10632-3 ↗
47. 10.1021/acs.chemmater.7b0353110.1021/acs.chemmater.7b03531 ↗