A novel method to control atomic defects in graphene sheets, by selective surface reactions
Source abstract
Abstract
Abstract Behaviors of atomic defects in graphene sheets in air at high temperature are studied. Results indicate that the number of defects in graphene sheets decreases after high temperature treatment in air. Mechanism for the behaviors are studied by molecular simulations and interpreted as follows. Charge distributions of atoms in graphene sheets are relatively uniform due to large conjugated π bond, but atomic defects in the graphene sheets change the uniform charge distributions. The change of charge distributions makes these defect-regions have higher chemical activities, thus these defect-regions are easy to be eroded selectively by O 2 in air, which makes the number of them decrease. Thus, high temperature treatment in air can be used as a novel method to control atomic defects in graphene sheets. However, in order to obtain the graphene sheets after reactions, two problems should be dealt with: one is sufficient contact between air and graphene sheets during reaction; the other is transfer and enrichment of graphene sheets after reaction. Our method dealt with the two problems.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Graphene research and applications · Carbon Nanotubes in Composites · Graphene and Nanomaterials Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (28)
Show source-provided references
1. Jia · Nanoscale · 2011 · 3 · 8610.1039/C0NR00600A ↗
2. Ansari · Superlattices and Microstructures · 2012 · 51 · 27410.1016/j.spmi.2011.11.019 ↗
3. Ansari · Solid State Communications · 2011 · 151 · 114110.1016/j.ssc.2011.05.021 ↗
4. Wang · Computational Materials Science · 2012 · 54 · 23610.1016/j.commatsci.2011.10.032 ↗
5. Qi · Applied Surface Science · 2012 · 259 · 19510.1016/j.apsusc.2012.07.018 ↗
6. Yang · Applied Surface Science · 2012 · 258 · 992610.1016/j.apsusc.2012.06.052 ↗
7. Banhart · ACS Nano · 2011 · 5 · 2610.1021/nn102598m ↗
8. Cheng · Carbon · 2012 · 50 · 258110.1016/j.carbon.2012.02.016 ↗
9. Bao · Chemical Physics Letters · 2011 · 510 · 24610.1016/j.cplett.2011.05.056 ↗
10. Zhang · Materials Letters · 2012 · 89 · 22610.1016/j.matlet.2012.08.113 ↗
11. Novoselov · Science · 2004 · 306 · 66610.1126/science.1102896 ↗
12. Wintterlin · Surface Science · 2009 · 603 · 184110.1016/j.susc.2008.08.037 ↗
13. Koh · Diamond and Related Materials · 2012 · 25 · 9810.1016/j.diamond.2012.02.014 ↗
14. Higginbotham · ACS Nano · 2010 · 4 · 205910.1021/nn100118m ↗
15. Hu · Materials Letters · 2011 · 65 · 258210.1016/j.matlet.2011.05.053 ↗
16. Chen · Advanced Materials · 2009 · 21 · 300710.1002/adma.200803726 ↗
17. Hummers · Journal of the American Chemical Society · 1958 · 80 · 133910.1021/ja01539a017 ↗
18. Glendening · 1996
19. Frisch · 2009
20. Cuong · Materials Letters · 2010 · 64 · 76510.1016/j.matlet.2010.01.009 ↗
21. McAllister · Chemistry of Materials · 2007 · 19 · 439610.1021/cm0630800 ↗
22. Wu · Carbon · 2009 · 47 · 49310.1016/j.carbon.2008.10.031 ↗
23. Ding · Diamond and Related Materials · 2012 · 21 · 1110.1016/j.diamond.2011.08.004 ↗
24. Tuinstra · The Journal of Chemical Physics · 1970 · 53 · 112610.1063/1.1674108 ↗
25. Sheng · New Carbon Materials · 2011 · 26 · 910.1016/S1872-5805(11)60062-0 ↗
26. Yang · Carbon · 2009 · 47 · 14510.1016/j.carbon.2008.09.045 ↗
27. Balden · Journal of Nuclear Materials · 2005 · 341 · 3110.1016/j.jnucmat.2005.01.006 ↗
28. Wang · Nanoscale · 2012 · 4 · 265110.1039/c2nr00055e ↗