Strong Electronic Coupling of Graphene Nanoribbons onto Basal Plane of a Glassy Carbon Electrode
Source abstract
Abstract
The grafting of molecular motifs to the conductive carbon represents a promising approach toward improved hybrid materials for electrocatalytic applications. Here, we investigate the electrochemical behavior of graphene nanoribbons (GNR) deposited onto a glassy carbon electrode using π–π stacking interactions. Using the bipyrimidine moiety on the nanoribbon edges as a reporter of the proton-coupled electron transfer chemistry, we illustrate that the simple electrochemical treatment of as-deposited nanoribbon generates a hybrid material that is in strong electronic communication with the conductive support. This work shows a strategy for modifying the basal plane of carbon materials and provides a potential platform for the incorporation of catalytic metal sites via coordination through the N-functionalities of GNR.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: CO2 Reduction Techniques and Catalysts · Electrocatalysts for Energy Conversion · Molecular Junctions and Nanostructures
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, University of Illinois at Chicago, Chicago, Illinois 60607, United States
Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, Illinois 60439, United States
Funding
National Science Foundation
References (46)
Show source-provided references
1. 10.1038/s41467-019-12886-z10.1038/s41467-019-12886-z ↗
2. 10.1002/ange.20190524110.1002/ange.201905241 ↗
3. Askins, E. J.; Zoric, M. R.; Li, K.; Luo, L.; Amine, K.; Glusac, K. D. Toward a mechanistic understanding of electrocatalytic nanocarbon. , 2020.10.1038/s41467-021-23486-1 ↗
4. 10.1021/ja106338h10.1021/ja106338h ↗
5. 10.1021/ja00040a07410.1021/ja00040a074 ↗
6. 10.1021/acsaem.9b0021610.1021/acsaem.9b00216 ↗
7. 10.1021/ja054958b10.1021/ja054958b ↗
8. 10.1039/C8CC00718G10.1039/C8CC00718G ↗
9. 10.1021/acs.organomet.8b0054710.1021/acs.organomet.8b00547 ↗
10. 10.1021/la204028u10.1021/la204028u ↗
11. 10.1021/acsaem.0c0033210.1021/acsaem.0c00332 ↗
12. 10.1021/jacs.5b1265210.1021/jacs.5b12652 ↗
13. 10.1002/anie.20110504410.1002/anie.201105044 ↗
14. 10.1021/ja409960910.1021/ja4099609 ↗
15. 10.1002/anie.20170492110.1002/anie.201704921 ↗
16. 10.1021/jacs.7b0626910.1021/jacs.7b06269 ↗
17. 10.1021/ja00345a02110.1021/ja00345a021 ↗
18. 10.1002/ange.20160916710.1002/ange.201609167 ↗
19. 10.1021/acscatal.0c0157710.1021/acscatal.0c01577 ↗
20. 10.1038/nchem.76110.1038/nchem.761 ↗
21. 10.1038/s41467-019-09626-810.1038/s41467-019-09626-8 ↗
22. 10.1021/cm071412a10.1021/cm071412a ↗
23. 10.1021/jacs.9b0498110.1021/jacs.9b04981 ↗
24. 10.1021/acs.accounts.9b0043910.1021/acs.accounts.9b00439 ↗
25. 10.1021/acscentsci.9b0011410.1021/acscentsci.9b00114 ↗
26. 10.1038/s41586-019-1760-810.1038/s41586-019-1760-8 ↗
27. 10.1002/anie.20200744510.1002/anie.202007445 ↗
28. 10.1038/s41560-020-0667-910.1038/s41560-020-0667-9 ↗
29. 10.1021/acsenergylett.8b0051910.1021/acsenergylett.8b00519 ↗
30. 10.1038/ncomms1467510.1038/ncomms14675 ↗
31. 10.1002/anie.20170110410.1002/anie.201701104 ↗
32. 10.1021/acssuschemeng.0c0279110.1021/acssuschemeng.0c02791 ↗
33. 10.1039/C9CC06574A10.1039/C9CC06574A ↗
34. 10.1021/acscatal.0c0136710.1021/acscatal.0c01367 ↗
35. 10.1021/acs.nanolett.5b0172310.1021/acs.nanolett.5b01723 ↗
36. 10.1002/anie.19970631110.1002/anie.199706311 ↗
37. 10.1038/ncomms418910.1038/ncomms4189 ↗
38. 10.1021/cr100085k10.1021/cr100085k ↗
39. 10.1021/acsenergylett.8b0235510.1021/acsenergylett.8b02355 ↗
40. 10.1038/s41563-020-0610-210.1038/s41563-020-0610-2 ↗
41. 10.1021/nn302906r10.1021/nn302906r ↗
42. 10.1002/sia.388010.1002/sia.3880 ↗
43. 10.1021/ja405149m10.1021/ja405149m ↗
44. 10.1021/acs.jpcc.9b0216310.1021/acs.jpcc.9b02163 ↗
45. 10.1021/jacs.7b1072310.1021/jacs.7b10723 ↗
46. 10.1021/jacs.5b0673710.1021/jacs.5b06737 ↗