journal article·2017

Capabilities of transition metals in retarding the bonding of carbon atoms to minimize dendritic graphene

Zhenwei Zhu, Linjie Zhan, Wen Wan, Zhijuan Zhao, Tien-Mo Shih, Weiwei Cai

Nanoscale· Volume 9· Issue 39
Publisher page

Abstract

The avoidance of growing dendritic graphene on the copper substrate during the chemical vapor deposition process is greatly desired. Here we have identified a mechanism, in which (1) transition metal plates placed inside the copper pockets reduce the majority of active carbon atoms to eventually suppress the graphene growth rate, and (2) transition metals etch graphene C-C bonds along defective edges to grow into zigzag-edge ending domains with higher priorities. Via isotopic labeling of the methane method, we have observed bright-dark-alternating hexagonal-shaped rings, which are shown in Raman mapping images. Under a hydrogen atmosphere, we are capable of acquiring hexagonal openings within graphene domains by means of transition-metal-driven catalytic etching. This methodology may work as a simple and convenient way to determine graphene size and crystal orientation, and may enable the etching of graphene into smooth and ordered zigzag edge nanoribbons without compromising the quality of graphene.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Graphene research and applications · Advanced Memory and Neural Computing · 2D Materials and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Physics

State Key Laboratory of Physical Chemistry of Solid Surfaces

Xiamen University

China

Institute for Complex Adaptive Matter

Funding

National Natural Science Foundation of China

References (33)

Show source-provided references
1. Li · Science · 2009 · 324 · 131210.1126/science.1171245 ↗
2. Bae · Nat. Nanotechnol. · 2010 · 5 · 57410.1038/nnano.2010.132 ↗
3. Yu · Nat. Mater. · 2011 · 10 · 44310.1038/nmat3010 ↗
4. Wu · Adv. Mater. · 2011 · 23 · 352210.1002/adma.201101746 ↗
5. Mohsin · ACS Nano · 2013 · 7 · 892410.1021/nn4034019 ↗
6. Luo · ACS Nano · 2011 · 5 · 915410.1021/nn203381k ↗
7. Wu · Sci. Rep. · 2015 · 5 · 903410.1038/srep09034 ↗
8. Robertson · Nano Lett. · 2011 · 11 · 118210.1021/nl104142k ↗
9. Vlassiouk · ACS Nano · 2011 · 5 · 606910.1021/nn201978y ↗
10. Wu · NPG Asia Mater. · 2013 · 5 · e3610.1038/am.2012.68 ↗
11. Das · Nanotechnology · 2017 · 28 · 10560110.1088/1361-6528/aa593b ↗
12. Geng · Proc. Natl. Acad. Sci. U. S. A. · 2012 · 109 · 799210.1073/pnas.1200339109 ↗
13. Geng · Adv. Mater. · 2014 · 26 · 642310.1002/adma.201401277 ↗
14. Hao · Science · 2013 · 342 · 72010.1126/science.1243879 ↗
15. Ma · Proc. Natl. Acad. Sci. U. S. A. · 2013 · 110 · 2038610.1073/pnas.1312802110 ↗
16. Jin · Sci. Rep. · 2015 · 5 · 961510.1038/srep09615 ↗
17. Wu · ACS Nano · 2012 · 6 · 773110.1021/nn301689m ↗
18. Gao · Nat. Commun. · 2012 · 3 · 69910.1038/ncomms1702 ↗
19. Ferrari · Phys. Rev. Lett. · 2006 · 97 · 18740110.1103/PhysRevLett.97.187401 ↗
20. Dresselhaus · Nano Lett. · 2010 · 10 · 75110.1021/nl904286r ↗
21. Hao · Nat. Nanotechnol. · 2016 · 11 · 42610.1038/nnano.2015.322 ↗
22. Dai · Nat. Commun. · 2011 · 2 · 52210.1038/ncomms1539 ↗
23. Wu · Carbon · 2012 · 50 · 522610.1016/j.carbon.2012.07.007 ↗
24. Rose · J. Phys. Chem. C · 2007 · 111 · 1905210.1021/jp075787v ↗
25. Pan · J. Catal. · 1990 · 123 · 20610.1016/0021-9517(90)90169-K ↗
26. Xue · Nano Res. · 2011 · 4 · 120810.1007/s12274-011-0171-4 ↗
27. Kim · Chem. Vap. Deposition · 2011 · 17 · 910.1002/cvde.201004296 ↗
28. Chae · Adv. Mater. · 2009 · 21 · 232810.1002/adma.200803016 ↗
29. Bhaviripudi · Nano Lett. · 2010 · 10 · 412810.1021/nl102355e ↗
30. Xu · Nat. Mater. · 2015 · 14 · 113510.1038/nmat4374 ↗
31. Wang · ACS Nano · 2016 · 10 · 450410.1021/acsnano.6b00270 ↗
32. Li · Nanoscale · 2014 · 6 · 1340210.1039/C4NR04455J ↗
33. Zhan · Nanotechnology · 2017 · 28 · 30560110.1088/1361-6528/aa77ec ↗