journal article·2019-03-01Open access

Growth control of corundum-derivative MnSnO3 thin films by pulsed-laser deposition

Kei Miura, Kohei Fujiwara, Atsushi Tsukazaki

AIP Advances· Volume 9· Issue 3

Abstract

The periodic arrangement of equimolar two cations in the corundum structure produces the ilmenite-type and LiNbO3-type orderings. The phase (polymorphism) control is one of the important topics in solid-state chemistry. Using a pulsed-laser deposition technique, we examined the formation of MnSnO3 films as a function of oxygen gas pressure. Under the optimal low oxygen gas pressure, c-axis oriented single-crystalline films of the ilmenite-type MnSnO3 were synthesized on Al2O3 (0001). We found that, with an increase of oxygen gas pressure, x-ray diffraction peaks characteristic of the ilmenite-type ordering disappeared and the c-axis length approached that of the LiNbO3-type MnSnO3 while the crystal structure retained basic features of corundum derivatives. The optical bandgap measurement revealed the decrease of bandgap in the LiNbO3-type (or disordered corundum-type) MnSnO3. The thin-film approach can add a new degree of freedom in the control of structural and physical properties in corundum-derivative oxides.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Electronic and Structural Properties of Oxides · ZnO doping and properties · Multiferroics and related materials

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

Affiliations

Institute for Materials Research, Tohoku University , Sendai 980-8577, Japan

Funding

Futaba Electronics Memorial Foundation · Japan Society for the Promotion of Science · Core Research for Evolutional Science and Technology

References (26)

Show source-provided references
1. J. Am. Chem. Soc. · 2008 · 130 · 670410.1021/ja801843v ↗
2. Phys. Rev. Lett. · 2009 · 103 · 04760110.1103/physrevlett.103.047601 ↗
3. Inorg. Chem. · 2011 · 50 · 639210.1021/ic201006q ↗
4. Chem. Mater. · 2016 · 28 · 664410.1021/acs.chemmater.6b02783 ↗
5. Phys. Rev. B · 2017 · 95 · 02442510.1103/physrevb.95.024425 ↗
6. Phys. Rev. Materials · 2018 · 2 · 05441110.1103/physrevmaterials.2.054411 ↗
7. J. Phys. Chem. C · 2013 · 117 · 1333910.1021/jp402046t ↗
8. Phys. Rev. B · 2016 · 93 · 13430310.1103/physrevb.93.134303 ↗
9. Chem. Mater · 2017 · 29 · 544710.1021/acs.chemmater.7b01567 ↗
10. Chem. Mater. · 1994 · 6 · 36510.1021/cm00040a007 ↗
11. Chem. Mater. · 1994 · 10 · 2787
12. J. Appl. Crystallogr. · 2011 · 44 · 127210.1107/s0021889811038970 ↗
13. Shiozaki · 2001 · 508
14. Solid State Commun. · 1969 · 7 · 71310.1016/0038-1098(69)90600-0 ↗
15. Mat. Res. Bull. · 1970 · 5 · 20710.1016/0025-5408(70)90008-5 ↗
16. Phys. Chem. Minerals · 1991 · 18 · 24410.1007/bf00202576 ↗
17. ACS Appl. Mater. Interfaces · 2017 · 9 · 2187910.1021/acsami.7b04481 ↗
18. APL Mater. · 2019 · 7 · 02250510.1063/1.5054289 ↗
19. Appl. Phys. Lett. · 2008 · 93 · 07250710.1063/1.2975373 ↗
20. J. Phys. Chem. · 2017 · 121 · 1871710.1021/acs.jpcc.7b06076 ↗
21. Appl. Surf. Sci. · 2011 · 257 · 271710.1016/j.apsusc.2010.10.051 ↗
22. J. Electron Spectrosc. Relat. Phenom. · 1975 · 7 · 46510.1016/0368-2048(75)85010-9 ↗
23. Mater. Chem. Phys. · 2016 · 180 · 7510.1016/j.matchemphys.2016.05.041 ↗
24. Appl. Phys. Lett. · 2017 · 111 · 05240910.1063/1.4997588 ↗
25. Appl. Phys. Lett. · 2017 · 110 · 26240110.1063/1.4989680 ↗
26. Appl. Phys. Lett. · 2018 · 112 · 13240110.1063/1.5019934 ↗