journal article·2024-04-01Open access

Phase coexistence induced surface roughness in V2O3/Ni magnetic heterostructures

K. Ignatova, E. Vlasov, S. D. Seddon, N. Gauquelin, J. Verbeeck, D. Wermeille, S. Bals, T. P. A. Hase, U. B. Arnalds

APL Materials· Volume 12· Issue 4

Abstract

We present an investigation of the microstructure changes in V2O3 as it goes through its inherent structural phase transition. Using V2O3 films with a well-defined crystal structure deposited by reactive magnetron sputtering on r-plane Al2O3 substrates, we study the phase coexistence region and its impact on the surface roughness of the films and the magnetic properties of overlying Ni magnetic layers in V2O3/Ni hybrid magnetic heterostructures. The simultaneous presence of two phases in V2O3 during its structural phase transition was identified with high resolution x-ray diffraction and led to an increase in surface roughness observed using x-ray reflectivity. The roughness reaches its maximum at the midpoint of the transition. In V2O3/Ni hybrid heterostructures, we find a concomitant increase in the coercivity of the magnetic layer correlated with the increased roughness of the V2O3 surface. The chemical homogeneity of the V2O3 is confirmed through transmission electron microscopy analysis. High-angle annular dark field imaging and electron energy loss spectroscopy reveal an atomically flat interface between Al2O3 and V2O3, as well as a sharp interface between V2O3 and Ni.
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Research context

OpenAlex topics: Transition Metal Oxide Nanomaterials · ZnO doping and properties · Magnetic properties of thin films

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Science Institute, University of Iceland 1 , Dunhaga 3, 107 Reykjavik, Iceland

EMAT and NANOlab Center of Excellence, University of Antwerp 2 , Groenenborgerlaan 171, Antwerp, Belgium

TU Dresden, Institute of Applied Physics 3 , Nöthnitzer Strasse 61, 01187 Dresden, Germany

XMaS, The UK Materials Science Facility, European Synchrotron Radiation Facility 4 , F-38043 Grenoble, France

Department of Physics, University of Liverpool, Oliver Lodge 5 , Liverpool L69 7ZE, United Kingdom

Department of Physics, University of Warwick 6 , Coventry CV4 7AL, United Kingdom

Funding

The University of Iceland Research Fund, The Icelandic Research Fund · The European Union’s Horizon 2020 - ESTEEM3

References (40)

Show source-provided references
1. J. Appl. Phys. · 1974 · 45 · 220110.1063/1.1663568 ↗
2. Science · 2018 · 362 · 103710.1126/science.aam9189 ↗
3. Sci. Rep. · 2016 · 6 · 2311910.1038/srep23119 ↗
4. APL Mater. · 2021 · 9 · 02111610.1063/5.0035865 ↗
5. Phys. Rev. B · 1990 · 41 · 499310.1103/physrevb.41.4993 ↗
6. Phys. Rev. B · 1972 · 5 · 254110.1103/physrevb.5.2541 ↗
7. Small · 2021 · 17 · 200665110.1002/smll.202006651 ↗
8. Adv. Funct. Mater. · 2022 · 32 · 211155510.1002/adfm.202111555 ↗
9. Rev. Mod. Phys. · 2018 · 90 · 01500510.1103/revmodphys.90.015005 ↗
10. Artif. Cells, Nanomed., Biotechnol. · 2018 · 46 · 5810.1080/21691401.2018.1452020 ↗
11. Mater. Today · 2019 · 28 · 6310.1016/j.mattod.2019.06.006 ↗
12. Proc. IEEE · 2015 · 103 · 128910.1109/jproc.2015.2431914 ↗
13. M. Lee , “New materials and techniques for resistive switching devices and neuromorphic computing,” Ph.D. thesis, UC San Diego, 2021.
14. J. Appl. Phys. · 2019 · 125 · 04450110.1063/1.5037990 ↗
15. Phys. Rev. Lett. · 2019 · 122 · 05760110.1103/physrevlett.122.057601 ↗
16. Phys. Rev. Mater. · 2022 · 6 · 06440810.1103/physrevmaterials.6.064408 ↗
17. Sci. Rep. · 2017 · 7 · 1347110.1038/s41598-017-12690-z ↗
18. Appl. Phys. Lett. · 2013 · 102 · 12240410.1063/1.4798293 ↗
19. Appl. Phys. Lett. · 2014 · 104 · 06241010.1063/1.4865587 ↗
20. J. Phys.: Condens. Matter · 2022 · 34 · 49500110.1088/1361-648x/ac9946 ↗
21. Nat. Phys. · 2017 · 13 · 8010.1038/nphys3882 ↗
22. Phys. Rev. Mater. · 2021 · 5 · 03441310.1103/physrevmaterials.5.034413 ↗
23. Appl. Phys. Lett. · 2019 · 114 · 01240710.1063/1.5058751 ↗
24. Rev. Sci. Instrum. · 2007 · 78 · 10390110.1063/1.2793508 ↗
25. Philos. Trans. R. Soc., A · 2019 · 377 · 2018023710.1098/rsta.2018.0237 ↗
26. J. Appl. Crystallogr. · 2007 · 40 · 117410.1107/s0021889807045086 ↗
27. Catal. Lett. · 2002 · 83 · 11510.1023/a:1021042232178 ↗
28. Microsc. Microanal. · 2009 · 15 · 100410.1017/s1431927609092770 ↗
29. Appl. Phys. Lett. · 2016 · 109 · 14390310.1063/1.4964432 ↗
30. J. Nucl. Mater. · 1967 · 21 · 35610.1016/0022-3115(67)90194-8 ↗
31. 1996
32. Acta Mater. · 2013 · 61 · 644310.1016/j.actamat.2013.07.022 ↗
33. Surf. Sci. · 2004 · 555 · 10110.1016/j.susc.2003.12.053 ↗
34. Phys. Rev. B · 2009 · 80 · 02411110.1103/physrevb.80.024111 ↗
35. Sci. Rep. · 2016 · 6 · 3829610.1038/srep38296 ↗
36. Phys. Rev. B · 1970 · 2 · 377110.1103/physrevb.2.3771 ↗
37. J. Appl. Phys. · 1973 · 44 · 347010.1063/1.1662787 ↗
38. Nature · 2022 · 602 · 24010.1038/s41586-021-04260-1 ↗
39. Nanoscale · 2021 · 13 · 498510.1039/d0nr08253h ↗
40. Appl. Phys. Lett. · 2018 · 112 · 16190210.1063/1.5023180 ↗