Self-organized growth of higher manganese silicide nanowires on Si(111), (110) and (001) surfaces
Source abstract
Abstract
Abstract Higher manganese silicide nanowires (NWs) with a large aspect ratio have been grown on three kinds of substrate, Si(1 1 1), (1 1 0) and (0 0 1), with the reactive epitaxy method at temperatures above ∼500 °C. The self-assembly of the NWs is confined along the Si〈1 1 0〉 directions, resulting in the NWs orienting with the long axis along one, two and three particular directions on the Si(1 1 0), (0 0 1) and (1 1 1) surfaces, respectively. Scanning tunneling spectroscopy and transmission electron microscopy (TEM) studies indicate unambiguously that the NWs are tetragonal MnSi1.7. The width of the NWs has a maximum or well-defined value on each kind of substrate, though the length varies greatly. In the plan-view TEM micrographs, the NWs exhibit two sets of Moire fringes: one is along the length direction and has a large periodicity, and the other is along the width direction and has a very small periodicity. These phenomena strongly indicate that the growth of NWs is governed by a strain-driven energetic mechanism and the NW shape results from anisotropic lattice mismatch between the silicide and the Si substrate. This research paves the way towards controllable growth of the silicide NWs on silicon substrates, which may help to advance the realization of practical applications of silicide NWs in nanoelectronics.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Semiconductor materials and interfaces · Surface and Thin Film Phenomena · Nanowire Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (27)
Show source-provided references
1. He · Phys Rev Lett · 2004 · 93 · 25610210.1103/PhysRevLett.93.256102 ↗
2. He · Appl Phys Lett · 2005 · 86 · 14311010.1063/1.1897424 ↗
3. Liang · Appl Phys Lett · 2006 · 88 · 11311110.1063/1.2185610 ↗
4. Preinesberger · J Appl Phys · 2002 · 91 · 169510.1063/1.1430540 ↗
5. Zhou · Nano Lett · 2007 · 7 · 164910.1021/nl0706143 ↗
6. Kobayashi · Phys Rev B · 2007 · 75 · 12540110.1103/PhysRevB.75.125401 ↗
7. Chen · J Appl Phys · 2002 · 91 · 321310.1063/1.1428807 ↗
8. Harrison · Surf Sci · 2005 · 594 · 9310.1016/j.susc.2005.07.014 ↗
9. Lee · Appl Phys Lett · 2003 · 82 · 261910.1063/1.1569654 ↗
10. Preinesberger · Appl Phys Lett · 2005 · 87 · 08310710.1063/1.2032620 ↗
11. Liu · J Appl Phys · 2003 · 93 · 59310.1063/1.1516621 ↗
12. Ohbuchi · Phys Rev B · 2002 · 66 · 16532310.1103/PhysRevB.66.165323 ↗
13. Lin · Appl Phys Lett · 2004 · 85 · 28110.1063/1.1769583 ↗
14. Hsu · Nano Lett · 2007 · 7 · 88510.1021/nl062465e ↗
15. He · Surf Sci · 2003 · 524 · 14810.1016/S0039-6028(02)02506-2 ↗
16. Stevens · J Appl Phys · 2003 · 93 · 567010.1063/1.1565173 ↗
17. Bennett · J Vac Sci Technol B · 2002 · 20 · 250010.1116/1.1525006 ↗
18. Zou · Appl Phys Lett · 2007 · 90 · 13311110.1063/1.2717580 ↗
19. Imai · Intermetallics · 2000 · 8 · 38110.1016/S0966-9795(99)00125-9 ↗
20. Mahan · Thin Solid Films · 2004 · 46 · 15210.1016/j.tsf.2004.02.090 ↗
21. Higgins · J Am Chem Soc · 2008 · 130 · 1608610.1021/ja8065122 ↗
22. Teichert · J Cryst Growth · 2001 · 227–228 · 88210.1016/S0022-0248(01)00922-8 ↗
23. Zhang · J Cryst Growth · 2002 · 237–239 · 195610.1016/S0022-0248(01)02283-7 ↗
24. Weir · Pure Appl Chem · 1999 · 71 · 121510.1351/pac199971071215 ↗
25. Zou · Phys Lett A · 2011 · 375 · 84910.1016/j.physleta.2010.12.039 ↗
26. Schwinge · Surf Sci · 2007 · 601 · 81010.1016/j.susc.2006.11.012 ↗
27. Tanaka · Appl Phys Lett · 2005 · 86 · 18310410.1063/1.1922576 ↗