Electrofluorination and Room-Temperature Doping of Graphene Nanoribbons for Energy Storage Applications
Source abstract
Abstract
Multiwalled carbon nanotubes undergo a remarkable electrochemical transformation into graphene nanoribbons at room temperature in trifluoromethanesulfonic acid. More specifically, carbon nanotubes undergo oxidative unzipping in the first step in a potentiostatic manner to have several oxygen functionalities in the edges, while the second step ensures reductive transformation to graphene nanoribbons along with doping of fluorine. Such F-doped graphene nanoribbons are important for multifarious applications such as electrocatalysis, molecular electronics, biosensing, optoelectronics, photovoltaics, and energy storage. The open circuit potential of fluorinated graphene nanoribbons against anodes like sodium and lithium in standard battery electrolytes also suggests their potential utility in energy storage applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Graphene research and applications · Supercapacitor Materials and Fabrication · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Indian Institute of Science Education and Research, Tirupati Karakambadi Road, Ramireddy Nagar, Mangalam, Tirupati, Andhra Pradesh 517507, India
Electrodics and Electrocatalysis Division, CSIR-Central Electrochemical Research Institute, Karaikudi, College Road, Karaikudi, Tamilnadu 630003, India
Funding
Science and Engineering Research Board
References (44)
Show source-provided references
1. 10.1021/ja110173910.1021/ja1101739 ↗
2. 10.1126/science.113720110.1126/science.1137201 ↗
3. 10.1126/science.112592510.1126/science.1125925 ↗
4. 10.1038/nature0423310.1038/nature04233 ↗
5. 10.1126/science.120875910.1126/science.1208759 ↗
6. 10.1021/nl102112810.1021/nl1021128 ↗
7. 10.1039/C5TA00244C10.1039/C5TA00244C ↗
8. 10.1039/c3ee41444b10.1039/c3ee41444b ↗
9. 10.1039/C3TA14043A10.1039/C3TA14043A ↗
10. 10.1039/c3ee43463j10.1039/c3ee43463j ↗
11. 10.1021/jp201991j10.1021/jp201991j ↗
12. 10.1002/ange.20120954810.1002/ange.201209548 ↗
13. 10.1002/adma.20130275310.1002/adma.201302753 ↗
14. 10.1007/s40843-020-1551-x10.1007/s40843-020-1551-x ↗
15. 10.1002/ange.20180205510.1002/ange.201802055 ↗
16. 10.1039/C9TA04141A10.1039/C9TA04141A ↗
17. 10.1126/science.115087810.1126/science.1150878 ↗
18. 10.1038/nmat238210.1038/nmat2382 ↗
19. 10.1021/cm101027c10.1021/cm101027c ↗
20. 10.1038/nnano.2008.36510.1038/nnano.2008.365 ↗
21. 10.1038/nature0791910.1038/nature07919 ↗
22. 10.1039/c1nr10137d10.1039/c1nr10137d ↗
23. 10.1038/s43586-020-00005-y10.1038/s43586-020-00005-y ↗
24. 10.1021/nn403057t10.1021/nn403057t ↗
25. 10.1021/nn102326c10.1021/nn102326c ↗
26. 10.1002/macp.20120000110.1002/macp.201200001 ↗
27. 10.1038/srep2275510.1038/srep22755 ↗
28. 10.1021/acsami.5b0486410.1021/acsami.5b04864 ↗
29. 10.1039/C5TA03869C10.1039/C5TA03869C ↗
30. Olah G. A. · 200910.1002/9780470421604 ↗
31. 10.1139/v75-43310.1139/v75-433 ↗
32. 10.1038/srep0436310.1038/srep04363 ↗
33. 10.1021/acssuschemeng.3c0518210.1021/acssuschemeng.3c05182 ↗
34. 10.1039/c2ra20593a10.1039/c2ra20593a ↗
35. 10.1021/acsnano.9b0515710.1021/acsnano.9b05157 ↗
36. 10.1063/1.487186710.1063/1.4871867 ↗
37. 10.1063/1.175584910.1063/1.1755849 ↗
38. 10.1016/j.mencom.2020.01.02810.1016/j.mencom.2020.01.028 ↗
39. 10.1016/j.carbon.2012.11.02910.1016/j.carbon.2012.11.029 ↗
40. 10.1063/1.167410810.1063/1.1674108 ↗
41. 10.1039/c3ra22029j10.1039/c3ra22029j ↗
42. 10.1039/C8RA03451F10.1039/C8RA03451F ↗
43. 10.1021/acs.chemmater.1c0417010.1021/acs.chemmater.1c04170 ↗
44. 10.1039/C6TC04480H10.1039/C6TC04480H ↗