Surface step edge-assisted monolayer epitaxy of α-antimonene on SnSe2 substrate
Source abstract
Abstract
We demonstrate a strategy of van der Waals (vdW) epitaxy assisted by surface step edges. Different from the usual vdW epitaxy where the growth is initiated by the vdW interactions with the substrate, the step edge-assisted epitaxy is most likely initiated by the formation of a strong valence bond at the periphery of surface step edges, thus allowing for the growth of strained vdW monolayers. With this strategy, we have successfully grown the α-antimonene monolayer with a puckered honeycomb lattice on the SnSe2 substrate with a high density of surface step edges, thus forming a horizontal heterostructure. This study paves a way toward tuning the morphology and properties of epitaxial vdW materials via a strong valence bond at the boundary between the epilayer and substrate.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: 2D Materials and Applications · Graphene research and applications · Topological Materials and Phenomena
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Physics, Nanjing University 1 , Nanjing 210093, China
National Laboratory of Solid State Microstructures, Collaborative Innovation Center of Advanced Microstructures, Nanjing University 2 , Nanjing 210093, China
Department of Materials Science and Engineering, Nanjing University 3 , Nanjing 210093, China
Jiangsu Provincial Key Laboratory for Nanotechnology, Nanjing University 4 , Nanjing 210093, China
Funding
National Natural Science Foundation of China
References (41)
Show source-provided references
1. Chem. Rev. · 2017 · 117 · 622510.1021/acs.chemrev.6b00558 ↗
2. Phys. Rev. Lett. · 2005 · 95 · 14680210.1103/physrevlett.95.146802 ↗
3. Phys. Rev. Lett. · 2011 · 107 · 07680210.1103/physrevlett.107.076802 ↗
4. Phys. Rev. Lett. · 2013 · 111 · 13680410.1103/physrevlett.111.136804 ↗
5. Nat. Mater. · 2015 · 14 · 102010.1038/nmat4384 ↗
6. Science · 2014 · 346 · 134410.1126/science.1256815 ↗
7. Phys. Rev. B · 2017 · 96 · 04110810.1103/physrevb.96.041108 ↗
8. Science · 2017 · 357 · 28710.1126/science.aai8142 ↗
9. Nat. Nanotechnol. · 2015 · 10 · 76510.1038/nnano.2015.143 ↗
10. Chin. Phys. Lett. · 2012 · 29 · 03740210.1088/0256-307x/29/3/037402 ↗
11. Chin. Phys. Lett. · 2014 · 31 · 01740110.1088/0256-307x/31/1/017401 ↗
12. Nature · 2017 · 546 · 26510.1038/nature22060 ↗
13. Nature · 2017 · 546 · 27010.1038/nature22391 ↗
14. Chin. Phys. Lett. · 2020 · 37 · 07750210.1088/0256-307x/37/7/077502 ↗
15. Science · 2004 · 306 · 66610.1126/science.1102896 ↗
16. Rev. Mod. Phys. · 2009 · 81 · 10910.1103/revmodphys.81.109 ↗
17. Nat. Nanotechnol. · 2015 · 10 · 60810.1038/nnano.2015.91 ↗
18. Phys. Rev. Lett. · 2015 · 115 · 18640310.1103/physrevlett.115.186403 ↗
19. Science · 2015 · 349 · 72310.1126/science.aaa6486 ↗
20. Nat. Nanotechnol. · 2015 · 10 · 51710.1038/nnano.2015.71 ↗
21. Nat. Commun. · 2014 · 5 · 447510.1038/ncomms5475 ↗
22. Acta Phys. Sin. · 2021 · 70 · 14810110.7498/aps.70.20210638 ↗
23. Chem. Soc. Rev. · 2018 · 47 · 98210.1039/c7cs00125h ↗
24. Adv. Mater. · 2016 · 28 · 633210.1002/adma.201602128 ↗
25. Angew. Chem., Int. Ed. · 2016 · 55 · 1434510.1002/anie.201605298 ↗
26. Nat. Commun. · 2016 · 7 · 1335210.1038/ncomms13352 ↗
27. Nano Lett. · 2017 · 17 · 497010.1021/acs.nanolett.7b02111 ↗
28. Adv. Mater. · 2017 · 29 · 160540710.1002/adma.201605407 ↗
29. Adv. Mater. · 2019 · 32 · 190687310.1002/adma.201906873 ↗
30. Front. Phys. · 2018 · 13 · 13810610.1007/s11467-018-0757-3 ↗
31. Nano Lett. · 2018 · 18 · 213310.1021/acs.nanolett.8b00429 ↗
32. Angew. Chem., Int. Ed. · 2015 · 54 · 311210.1002/anie.201411246 ↗
33. Adv. Mater. · 2019 · 31 · 190260610.1002/adma.201902606 ↗
34. Adv. Mater. · 2019 · 31 · 180613010.1002/adma.201806130 ↗
35. Nano Lett. · 2020 · 20 · 840810.1021/acs.nanolett.0c03704 ↗
36. ACS Nano · 2020 · 14 · 1675510.1021/acsnano.0c04620 ↗
37. Jpn. J. Appl. Phys., Part 1 · 2021 · 60 · SE080510.35848/1347-4065/abf74e ↗
38. ACS Nano · 2015 · 9 · 836810.1021/acsnano.5b03043 ↗
39. New J. Phys. · 2020 · 22 · 07305010.1088/1367-2630/ab9b59 ↗
40. Phys. Rev. B · 2000 · 62 · 1581510.1103/physrevb.62.15815 ↗
41. Phys. Rev. B · 2015 · 91 · 23544610.1103/physrevb.91.235446 ↗