Transition Metal‐Depleted Graphenes for Electrochemical Applications via Reduction of CO2 by Lithium
Source abstract
Abstract
Graphene has immense potential for future applications in the electrochemical field, such as in supercapacitors, fuel cells, batteries, or sensors. Graphene materials for such applications are typically fabricated through a top‐down approach towards oxidation of graphite to graphite oxide, with consequent exfoliation/reduction to yield reduced graphenes. Such a method allows the manufacture of graphenes in gram/kilogram quantities. However, graphenes prepared by this method can contain residual metallic impurities from graphite which dominate the electrochemical properties of the graphene formed. This dominance hampers their electrochemical application. The fabrication of transition metal‐depleted graphene is described, using ultrapure CO2 (with benefits of low cost and easy availability) and elemental lithium by means of reduction of CO2 to graphene. This preparation method produces graphene of high purity with electrochemical behavior that is not dominated by any residual transition metal impurities which would dramatically alter its electrochemical properties. Wide application of such methodology in industry and research laboratories is foreseen, especially where graphene is used for electrochemical devices.
Source: crossref · 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
Division of Chemistry & Biological Chemistry, School of Physical and Mathematical Sciences Nanyang Technological University Singapore 637371 Singapore
Institute of Chemical Technology, Department of Inorganic Chemistry 166 28 Prague 6 Czech Republic
References (31)
Show source-provided references
1. 10.1126/science.110289610.1126/science.1102896 ↗
2. 10.1038/nmat184910.1038/nmat1849 ↗
3. 10.1038/nnano.2008.11510.1038/nnano.2008.115 ↗
4. 10.1038/nature0496910.1038/nature04969 ↗
5. 10.1038/nnano.2008.9610.1038/nnano.2008.96 ↗
6. 10.1021/nl802558y10.1021/nl802558y ↗
7. 10.1021/ja803688x10.1021/ja803688x ↗
8. 10.1039/c002690p10.1039/c002690p ↗
9. 10.1039/C0EE00295J10.1039/C0EE00295J ↗
10. 10.1002/smll.20120289610.1002/smll.201202896 ↗
11. 10.1021/ja01539a01710.1021/ja01539a017 ↗
12. 10.1002/zaac.1937234040510.1002/zaac.19372340405 ↗
13. 10.1002/cber.1898031023710.1002/cber.18980310237 ↗
14. 10.1002/chem.20110111710.1002/chem.201101117 ↗
15. 10.1073/pnas.120538810910.1073/pnas.1205388109 ↗
16. 10.1021/nl304187e10.1021/nl304187e ↗
17. 10.1021/nl301952e10.1021/nl301952e ↗
18. 10.1002/anie.20110691710.1002/anie.201106917 ↗
19. 10.1039/c2sc21374e10.1039/c2sc21374e ↗
20. 10.1021/nl060366v10.1021/nl060366v ↗
21. 10.1002/anie.20060003310.1002/anie.200600033 ↗
22. Wiberg N. · 2001 · 807
23. 10.1039/c1jm11227a10.1039/c1jm11227a ↗
24. 10.1038/346255a010.1038/346255a0 ↗
25. 10.1021/jp210295e10.1021/jp210295e ↗
26. 10.1021/cm101027c10.1021/cm101027c ↗
27. 10.1039/c1jm11266j10.1039/c1jm11266j ↗
28. 10.1016/j.carbon.2007.02.03410.1016/j.carbon.2007.02.034 ↗
29. 10.1063/1.219605710.1063/1.2196057 ↗
30. 10.1021/la047597710.1021/la0475977 ↗
31. 10.1002/asia.20110031810.1002/asia.201100318 ↗