Covalent Functionalization of Surfactant-Wrapped Graphene Nanoribbons
Source abstract
Abstract
Using diazonium chemistry, two different covalent functionalization methods for graphene nanoribbons (GNRs) were developed. In addition to direct diazonium salt addition, which has been reported previously for functionalization of graphene sheets and single-walled carbon nanotubes, an in situ route using an organic nitrite was successfully applied. This new method broadens the possibilities of functionality type since anilines can be used instead of preprepared diazonium salts. The resulting functionalized GNRs (f-GNRs) are readily soluble in organic solvents such as N,N -dimethylformamide and N -methyl-2-pyrrolidinone, which increases their solution processability. The f-GNRs were also found to be in a reduced state, with minimal sp 2 carbon disruption, while keeping the ribbon shape. These organic-soluble ribbons might find applications in composites and thin film materials.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Graphene research and applications · Molecular Junctions and Nanostructures · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Departments of Chemistry and Mechanical Engineering and Materials Science and the Smalley Institute for Nanoscale Science and Technology, Rice University, MS 222, 6100 Main Street, Houston, Texas 77005
References (35)
Show source-provided references
1. Novoselov K. S. · Nature · 2005 · 438 · 19710.1038/nature04233 ↗
2. Geim A. K. · Nat. Mater. · 2007 · 6 · 18310.1038/nmat1849 ↗
3. Zhang Y. B. · Nature · 2005 · 438 · 20110.1038/nature04235 ↗
4. Areshkin D. A. · Nano Lett. · 2007 · 7 · 20410.1021/nl062132h ↗
5. Son Y. W. · Phys. Rev. Lett. · 2006 · 97 · 21680310.1103/PhysRevLett.97.216803 ↗
6. Nakada K. · Phys. Rev. B · 1996 · 54 · 1795410.1103/PhysRevB.54.17954 ↗
7. Han M. Y. · Phys. Rev. Lett. · 2007 · 98 · 20680510.1103/PhysRevLett.98.206805 ↗
8. Li X. · Science · 2008 · 319 · 122910.1126/science.1150878 ↗
9. Jiao L. · Nature · 2009 · 458 · 87710.1038/nature07919 ↗
10. Yang X. Y. · J. Am. Chem. Soc. · 2008 · 130 · 421610.1021/ja710234t ↗
11. Campos-Delgado J. · Nano Lett. · 2008 · 8 · 277310.1021/nl801316d ↗
12. Kosynkin D. V. · Nature · 2009 · 458 · 87210.1038/nature07872 ↗
13. Stankovich S. · J. Mater. Chem. · 2006 · 16 · 15510.1039/B512799H ↗
14. Stankovich S. · Nature · 2006 · 442 · 28210.1038/nature04969 ↗
15. Hill E. W. · IEEE Trans. Magn. · 2006 · 42 · 269410.1109/TMAG.2006.878852 ↗
16. Heersche H. B. · Nature · 2007 · 446 · 5610.1038/nature05555 ↗
17. Schedin F. · Nat. Mater. · 2007 · 6 · 65210.1038/nmat1967 ↗
18. Sofo J. O. · Phys. Rev. B · 2007 · 75 · 15340110.1103/PhysRevB.75.153401 ↗
19. Stoller M. D. · Nano Lett. · 2008 · 8 · 349810.1021/nl802558y ↗
20. Blake P. · Nano Lett. · 2008 · 8 · 170410.1021/nl080649i ↗
21. Lomeda J. R. · J. Am. Chem. Soc. · 2008 · 130 · 1620110.1021/ja806499w ↗
22. Bahr J. L. · J. Am. Chem. Soc. · 2001 · 123 · 653610.1021/ja010462s ↗
23. Bahr J. L. · Chem. Mater. · 2001 · 13 · 382310.1021/cm0109903 ↗
24. Dyke C. A. · Nano Lett. · 2003 · 3 · 121510.1021/nl034537x ↗
25. Price B. K. · J. Am. Chem. Soc. · 2006 · 128 · 1289910.1021/ja063609u ↗
26. Curtin D. Y. · J. Org. Chem. · 1956 · 21 · 122110.1021/jo01117a005 ↗
27. Li X. · Science · 2008 · 319 · 122910.1126/science.1150878 ↗
28. Si Y. · Nano Lett. · 2008 · 8 · 167910.1021/nl080604h ↗
29. Dyke C. A. · J. Am. Chem. Soc. · 2003 · 125 · 115610.1021/ja0289806 ↗
30. Becerril H. A. · ACS Nano · 2008 · 2 · 46310.1021/nn700375n ↗
31. Bekyarova E. · J. Am. Chem. Soc. · 2009 · 131 · 133610.1021/ja8057327 ↗
32. Li D. · Nat. Nanotechnol. · 2008 · 3 · 10110.1038/nnano.2007.451 ↗
33. Allongue P. · J. Am. Chem. Soc. · 1997 · 119 · 20110.1021/ja963354s ↗
34. Delamar M. · J. Am. Chem. Soc. · 1992 · 114 · 588310.1021/ja00040a074 ↗
35. Kotov N. A. · Adv. Mater. · 1996 · 8 · 63710.1002/adma.19960080806 ↗