journal article·2017-02-28

Identifying and Visualizing the Edge Terminations of Single-Layer MoSe2 Island Epitaxially Grown on Au(111)

Jianchen Lu, De-Liang Bao, Kai Qian, Shuai Zhang, Hui Chen, Xiao Lin, Shi-Xuan Du, Hong-Jun Gao

ACS Nano· Volume 11· Issue 2
Publisher page

Abstract

Recently, single-layer transition-metal dichalcogenides have drawn significant attention due to their remarkable physical properties in the monolayer as well as at the edges. Here, we constructed high-quality, single-layer MoSe 2 islands on the Au(111) surfaces in ultrahigh vacuum by molecular beam epitaxy. All of the islands have hexagonal or triangular shapes with two kinds of well-defined edges. Scanning tunneling spectroscopy (STS) curves show notable differences in positive sample bias for the two types of edges. Density functional theory calculations for several edge configurations of MoSe 2 confirm that the STS differences are attributed to the coupling between the p z orbital of Se atoms and the d xz orbital of Mo atoms, and the two types of observed edge terminations are the bare Se edge and selenium-saturated Mo edge.
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Research context

OpenAlex topics: 2D Materials and Applications · Graphene research and applications · Quantum Dots Synthesis And Properties

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Affiliations

Institute of Physics & University of Chinese Academy of Sciences, Chinese Academy of Sciences, Beijing 100190, P. R. China

Funding

Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Chinese Academy of Sciences

References (41)

Show source-provided references
1. 10.1038/nchem.158910.1038/nchem.1589 ↗
2. 10.1038/nnano.2012.19310.1038/nnano.2012.193 ↗
3. 10.1103/PhysRevB.83.24521310.1103/PhysRevB.83.245213 ↗
4. 10.1103/PhysRevLett.105.13680510.1103/PhysRevLett.105.136805 ↗
5. 10.1021/nn400203810.1021/nn4002038 ↗
6. 10.1038/nphys294210.1038/nphys2942 ↗
7. 10.1103/PhysRevLett.108.19680210.1103/PhysRevLett.108.196802 ↗
8. 10.1021/nl302584w10.1021/nl302584w ↗
9. 10.1063/1.172248310.1063/1.1722483 ↗
10. 10.1038/nnano.2013.27710.1038/nnano.2013.277 ↗
11. 10.1103/PhysRevB.84.15340210.1103/PhysRevB.84.153402 ↗
12. 10.1021/nl903868w10.1021/nl903868w ↗
13. 10.1038/ncomms188210.1038/ncomms1882 ↗
14. 10.1038/nnano.2012.9510.1038/nnano.2012.95 ↗
15. 10.1038/nmat406110.1038/nmat4061 ↗
16. 10.1038/nature1383110.1038/nature13831 ↗
17. 10.1080/0161494890935134710.1080/01614948909351347 ↗
18. 10.1016/0013-4686(79)87055-310.1016/0013-4686(79)87055-3 ↗
19. 10.1021/ja050469010.1021/ja0504690 ↗
20. 10.1126/science.114148310.1126/science.1141483 ↗
21. 10.1126/science.121586810.1126/science.1215868 ↗
22. 10.1016/j.jcat.2003.09.01510.1016/j.jcat.2003.09.015 ↗
23. 10.1039/c4cp01237b10.1039/c4cp01237b ↗
24. 10.1021/nn502812n10.1021/nn502812n ↗
25. 10.1021/acs.langmuir.5b0253310.1021/acs.langmuir.5b02533 ↗
26. 10.1016/0039-6028(94)90210-010.1016/0039-6028(94)90210-0 ↗
27. 10.1103/PhysRevLett.84.95110.1103/PhysRevLett.84.951 ↗
28. 10.1007/s10853-005-2104-710.1007/s10853-005-2104-7 ↗
29. 10.1039/C4NR03817G10.1039/C4NR03817G ↗
30. 10.1038/srep0406310.1038/srep04063 ↗
31. 10.1038/srep0107210.1038/srep01072 ↗
32. 10.1039/C6NR06194J10.1039/C6NR06194J ↗
33. 10.1103/PhysRevLett.87.19680310.1103/PhysRevLett.87.196803 ↗
34. 10.1063/1.243241010.1063/1.2432410 ↗
35. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
36. 10.1103/PhysRevB.46.667110.1103/PhysRevB.46.6671 ↗
37. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
38. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
39. 10.1103/PhysRevB.41.789210.1103/PhysRevB.41.7892 ↗
40. 10.1021/jp106469x10.1021/jp106469x ↗
41. 10.1063/1.218700610.1063/1.2187006 ↗