Investigation on electrically-driven semiconductor-metal transition of polycrystalline VO2 thin films on two kinds of substrates
Source abstract
Abstract
Electrical driving is one of frequently-used stimuli for the semiconductor-metal transition (SMT) of VO2. But the driving mechanism is still under debate. We investigated the DC electrically-driven SMT features of polycrystalline VO2 thin films deposited on two kinds of substrates (quartz and silicon) with obviously-different thermal conductivity and the influence of cooling by a thermo electric cooler (TEC) on the SMT of VO2. Interestingly, the SMT doesn’t happen at a high voltage at very start, but at a relatively low one. Moreover, the SMT of VO2 thin films on silicon substrate is completely restrained by cooling through a TEC although the electric field strength across VO2 reaches 1.1×107 V/m. Our findings reveal that the Joule-heating effect plays an important role in the DC electrically-driven SMT of VO2.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Transition Metal Oxide Nanomaterials · Advanced Memory and Neural Computing · Ga2O3 and related materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Optoelectronic Information, University of Electronic Science and Technology of China , 610054 Chengdu, Sichuan, People’s Republic of China
Funding
National Natural Science Foundation of China
References (27)
Show source-provided references
1. Phys. Rev. Lett. · 1959 · 3 · 3410.1103/physrevlett.3.34 ↗
2. Adv. Mater. · 2013 · 25 · 612810.1002/adma.201302046 ↗
3. Nat. Mater. · 2013 · 12 · 11410.1038/nmat3510 ↗
4. Adv. Mater. · 2007 · 19 · 7310.1002/adma.200700251 ↗
5. Nature · 2012 · 487 · 34510.1038/nature11231 ↗
6. Nano Lett. · 2016 · 16 · 302910.1021/acs.nanolett.5b05313 ↗
7. Nano Lett. · 2009 · 9 · 339210.1021/nl900841k ↗
8. Appl. Phys. Lett. · 2007 · 90 · 02351510.1063/1.2431456 ↗
9. Phys. Rev. B · 2008 · 78 · 03310610.1103/physrevb.78.033106 ↗
10. Phys. Rev. Lett. · 2013 · 110 · 05660110.1103/physrevlett.110.056601 ↗
11. Phys. Rev. B · 2012 · 86 · 09420310.1103/physrevb.86.094203 ↗
12. J. Phys. D: Appl. Phys. · 2014 · 47 · 29510110.1088/0022-3727/47/29/295101 ↗
13. Solid State Electron. · 1980 · 23 · 64910.1016/0038-1101(80)90050-7 ↗
14. Phys. Rev. B · 2011 · 84 · 241410(R)10.1103/physrevb.84.241410 ↗
15. Appl. Phys. Lett. · 2008 · 92 · 16290310.1063/1.2911745 ↗
16. Science · 2007 · 318 · 175010.1126/science.1150124 ↗
17. Appl. Phys. Lett. · 2007 · 91 · 13350910.1063/1.2790830 ↗
18. Nat. Commun. · 2015 · 6 · 684910.1038/ncomms7849 ↗
19. Nat. Nanotechnol. · 2009 · 4 · 42010.1038/nnano.2009.141 ↗
20. J Phys. Chem. Solids · 2000 · 61 · 77910.1016/s0022-3697(99)00268-1 ↗
21. Phys. Rev. B · 2017 · 95 · 16540710.1103/physrevb.95.165407 ↗
22. Appl. Phys. Lett. · 2005 · 87 · 05191010.1063/1.2001139 ↗
23. Phys. Rev. B · 2002 · 65 · 22411310.1103/physrevb.65.224113 ↗
24. J. Phys. Chem. C · 2010 · 114 · 190110.1021/jp909009w ↗
25. Appl. Surf. Sci. · 2012 · 259 · 25610.1016/j.apsusc.2012.07.028 ↗
26. J Appl. Phys. · 2017 · 121 · 15510310.1063/1.4981241 ↗
27. Appl. Phys. Lett. · 2005 · 86 · 24210110.1063/1.1941478 ↗