Crystalline GaSb Nanowires Synthesized on Amorphous Substrates: From the Formation Mechanism to p-Channel Transistor Applications
Source abstract
Abstract
In recent years, because of the narrow direct bandgap and outstanding carrier mobility, GaSb nanowires (NWs) have been extensively explored for various electronics and optoelectronics. Importantly, these p-channel nanowires can be potentially integrated with n-type InSb, InAs, or InGaAs NW devices via different NW transfer techniques to facilitate the III-V CMOS technology. However, until now, there have been very few works focusing on the electronic transport properties of GaSb NWs. Here, we successfully demonstrate the synthesis of crystalline, stoichiometric, and dense GaSb NWs on amorphous substrates, instead of the commonly used III-V crystalline substrates, InAs, or GaAs NW stems as others reported. The obtained NWs are found to grow via the VLS mechanism with a narrow distribution of diameter (220 ± 50 nm) uniformly along the entire NW length (>10 μm) with minimal tapering and surface coating. Notably, when configured into FETs, the NWs exhibit respectable electrical characteristics with the peak hole mobility of ~30 cm(2) V(-1) s(-1) and free hole concentration of ~9.7 × 10(17) cm(-3). All these have illustrated the promising potency of such NWs directly grown on amorphous substrates for various technological applications, as compared with the conventional MOCVD-grown GaSb NWs.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanowire Synthesis and Applications · Advancements in Semiconductor Devices and Circuit Design · Semiconductor materials and interfaces
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Cultivation Base for State Key Laboratory, Qingdao University, No. 308 Ningxia Road, Qingdao, People’s Republic of China
Shenzhen Research Institute, City University of Hong Kong, Shenzhen, People’s Republic of China
References (46)
Show source-provided references
1. Gudiksen M. S. · Nature · 2002 · 415 · 61710.1038/415617a ↗
2. Ford A. C. · Nano Lett. · 2010 · 10 · 50910.1021/nl903322s ↗
3. Lupan R. O. · ACS Appl. Mater. Interfaces · 2010 · 2 · 208310.1021/am100334c ↗
4. Alamo J. A. · Nature · 2011 · 479 · 31710.1038/nature10677 ↗
5. Weng W. Y. · ACS Appl. Mater. Interfaces · 2011 · 3 · 16210.1021/am100746c ↗
6. Hou J. J. · ACS Nano · 2012 · 6 · 362410.1021/nn300966j ↗
7. Wu P. M. · Nano Lett. · 2012 · 12 · 199010.1021/nl204552v ↗
8. Han N. · Adv. Mater. · 2013 · 25 · 444510.1002/adma.201301362 ↗
9. Borg B. M. · Nano Lett. · 2010 · 10 · 408010.1021/nl102145h ↗
10. Ganjipour B. · Appl. Phys. Lett. · 2011 · 99 · 26210410.1063/1.3673328 ↗
11. Dey A. W. · Nano Lett. · 2012 · 12 · 559310.1021/nl302658y ↗
12. Yan C. L. · Nano Lett. · 2012 · 12 · 179910.1021/nl203857h ↗
13. Xu W. · J. Appl. Phys. · 2012 · 111 · 10451510.1063/1.4720080 ↗
14. Borg B. M. · Nanotechnology · 2013 · 24 · 20200110.1088/0957-4484/24/20/202001 ↗
15. Bandyopadhyay S. · Appl. Phys. Lett. · 2013 · 102 · 10310810.1063/1.4795520 ↗
16. Zhang W. · Phys. Rev. B · 2006 · 74 · 20531310.1103/PhysRevB.74.205313 ↗
17. Zi Y. L. · ChemPhysChem · 2012 · 13 · 258510.1002/cphc.201101042 ↗
18. Ek M. · ACS Nano · 2013 · 7 · 366810.1021/nn400684p ↗
19. Aardvark A. · Prog. Cryst. Growth Charact. · 1997 · 35 · 20710.1016/S0960-8974(98)00004-7 ↗
20. Dimroth F. · J. Cryst. Growth · 2003 · 248 · 26510.1016/S0022-0248(02)01818-3 ↗
21. Jeppsson M. · J. Cryst. Growth · 2008 · 310 · 411510.1016/j.jcrysgro.2008.06.066 ↗
22. Caroff P. · Nanotechnology · 2009 · 20 · 49560610.1088/0957-4484/20/49/495606 ↗
23. Pozuelo M. · J. Cryst. Growth · 2011 · 329 · 610.1016/j.jcrysgro.2011.06.034 ↗
24. Mandl B. · Nanotechnology · 2011 · 22 · 14560310.1088/0957-4484/22/14/145603 ↗
25. Plissard S. R. · Nano Lett. · 2012 · 12 · 179410.1021/nl203846g ↗
26. Burke R. A. · J. Electron Mater. · 2010 · 39 · 35510.1007/s11664-010-1140-5 ↗
27. Ganjipour B. · Appl. Phys. Lett. · 2012 · 101 · 10350110.1063/1.4749283 ↗
28. Vaddiraju S. · J. Phys. Chem. C · 2007 · 111 · 733910.1021/jp068943r ↗
29. Jeppsson M. · J. Cryst. Growth · 2008 · 310 · 511910.1016/j.jcrysgro.2008.07.061 ↗
30. Xu G. W. · RSC Adv. · 2013 · 3 · 1983410.1039/c3ra43127d ↗
31. Ek M. · Cryst. Growth Des. · 2011 · 11 · 458810.1021/cg200829q ↗
32. Dey A. W. · Nano Lett. · 2012 · 12 · 559310.1021/nl302658y ↗
33. Guo Y. N. · Appl. Phys. Lett. · 2006 · 89 · 23191710.1063/1.2402234 ↗
34. Han N. · Nanotechnology · 2011 · 22 · 28560710.1088/0957-4484/22/28/285607 ↗
35. Johansson J. · J. Phys. Chem. B · 2005 · 109 · 1356710.1021/jp051702j ↗
36. Han N. · Cryst. Growth Des. · 2012 · 12 · 624310.1021/cg301452d ↗
37. Chung H. S. · Nano Lett. · 2009 · 9 · 239510.1021/nl9009765 ↗
38. Seifert W. · J. Cryst. Growth · 2004 · 272 · 21110.1016/j.jcrysgro.2004.09.023 ↗
39. Cooke C.J. · J. Less-Common Met. · 1966 · 10 · 4210.1016/0022-5088(66)90044-0 ↗
40. Poizot P. · Nature · 2000 · 407 · 49610.1038/35035045 ↗
41. Buffat P. · Phys. Rev. A · 1976 · 13 · 228710.1103/PhysRevA.13.2287 ↗
42. Ford A. C. · Nano Lett. · 2009 · 9 · 36010.1021/nl803154m ↗
43. Wiersma R. · J. Electron. Mater. · 2001 · 30 · 142910.1007/s11664-001-0197-6 ↗
44. Gutsche C. · J. Appl. Phys. · 2009 · 105 · 02430510.1063/1.3065536 ↗
45. Sørensen B. S. · Appl. Phys. Lett. · 2008 · 92 · 01211910.1063/1.2821372 ↗
46. Yang Z. X. · Nanoscale · 2013 · 5 · 967110.1039/c3nr03080f ↗