Functionalization of Defect Sites in Graphene with RuO2 for High Capacitive Performance
Source abstract
Abstract
Graphene is an attractive material for its physicochemical properties, but for many applications only chemically synthesized forms such as graphene oxide (GO) and reduced graphene oxide (rGO) can be produced in sufficient amounts. If considered as electrode material, the intrinsic defects of GO or rGO may have negative influence on the conductivity and electrochemical properties. Such defects are commonly oxidized sites that offer the possibility to be functionalized with other materials in order to improve performance. In this work, we demonstrate how such ultimately efficient functionalization can be achieved: namely, through controlled binding of very small amount of materials such as RuO2 to rGO by atomic layer deposition (ALD), in this way substituting the native defect sites with RuO2 defects. For the example of a supercapacitor, we show that defect functionalization results in significantly enhanced specific capacitance of the electrode and that its energy density can be stabilized even at high consumption rates.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Supercapacitor Materials and Fabrication · Graphene research and applications · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
CIC nanoGUNE Consolider, Tolosa Hiribidea 76, 20018 Donostia−San Sebastian, Spain
Centro de Física de Materiales, Paseo Manuel de Lardizabal 5, 20018 Donostia−San Sebastian, Spain
Donostia International Physics Center, Paseo Manuel de Lardizabal 4, 20018 Donostia−San Sebastian, Spain
Ikerbasque, Basque Foundation for Science, Maria Diaz de Haro 3, 48013 Bilbao, Spain
Funding
Directorate-General for Research and Innovation · Eusko Jaurlaritza · Ministerio de Economía y Competitividad
References (36)
Show source-provided references
1. 10.1002/adma.20120148210.1002/adma.201201482 ↗
2. 10.1016/j.nanoen.2012.05.00110.1016/j.nanoen.2012.05.001 ↗
3. 10.1039/c3ta12193c10.1039/c3ta12193c ↗
4. 10.1039/c000417k10.1039/c000417k ↗
5. 10.1146/annurev-matsci-070214-02090110.1146/annurev-matsci-070214-020901 ↗
6. 10.1002/adma.20130120710.1002/adma.201301207 ↗
7. 10.1021/ar300203n10.1021/ar300203n ↗
8. 10.1002/adma.20100106810.1002/adma.201001068 ↗
9. 10.1039/c3ee43526a10.1039/c3ee43526a ↗
10. 10.1039/c3cs00009e10.1039/c3cs00009e ↗
11. 10.1039/C2NR32040A10.1039/C2NR32040A ↗
12. 10.1038/nmat229710.1038/nmat2297 ↗
13. 10.1039/c3ta10436b10.1039/c3ta10436b ↗
14. 10.1021/jp902214f10.1021/jp902214f ↗
15. 10.1021/nl102661q10.1021/nl102661q ↗
16. 10.1021/nl202663510.1021/nl2026635 ↗
17. 10.1016/j.jpowsour.2008.09.01410.1016/j.jpowsour.2008.09.014 ↗
18. 10.1002/adfm.20100105410.1002/adfm.201001054 ↗
19. 10.1039/c3ra47641c10.1039/c3ra47641c ↗
20. 10.1002/adma.20070007910.1002/adma.200700079 ↗
21. 10.1021/cr900056b10.1021/cr900056b ↗
22. 10.3938/jkps.55.3210.3938/jkps.55.32 ↗
23. 10.1063/1.293805210.1063/1.2938052 ↗
24. 10.1149/1.164063310.1149/1.1640633 ↗
25. 10.1016/j.mee.2007.01.23910.1016/j.mee.2007.01.239 ↗
26. 10.1149/2.001303jss10.1149/2.001303jss ↗
27. Pinna N. · 201110.1002/9783527639915 ↗
28. 10.1002/smll.20120083910.1002/smll.201200839 ↗
29. 10.1063/1.181019310.1063/1.1810193 ↗
30. 10.1038/ncomms578110.1038/ncomms5781 ↗
31. 10.1038/ncomms349110.1038/ncomms3491 ↗
32. 10.1016/j.electacta.2004.03.01710.1016/j.electacta.2004.03.017 ↗
33. 10.1002/aenm.20130002410.1002/aenm.201300024 ↗
34. 10.1039/c2jm31226c10.1039/c2jm31226c ↗
35. 10.1038/nnano.2011.1310.1038/nnano.2011.13 ↗
36. 10.1149/1.163902010.1149/1.1639020 ↗