Thin-film stabilization of LiNbO3-type ZnSnO3 and MgSnO3 by molecular-beam epitaxy
Source abstract
Abstract
In polar crystals, cooperative ionic displacement produces a macroscopic spontaneous polarization. Among such polar materials, LiNbO3-type wide bandgap oxides are particularly appealing because they offer useful ferroelectric properties and also potentially lead to multiferroic materials. Using molecular-beam epitaxy, we investigated the thin-film growth of high-pressure phase LiNbO3-type ZnSnO3 and discovered a polar oxide candidate, MgSnO3. We found that LiNbO3-type substrates play an essential role in the crystallization of these compounds, though corundum-type Al2O3 substrates also have the identical crystallographic arrangement of oxygen sublattice. Optical transmittance and electrical transport measurements revealed their potential as a transparent conducting oxide. Establishment of a thin-film synthetic route would be the basis for exploration of functional polar oxides and research on conduction at ferroelectric interfaces and domain walls.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Multiferroics and related materials · Ferroelectric and Piezoelectric Materials · Magnetic and transport properties of perovskites and related materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute for Materials Research, Tohoku University 1 , Sendai 980-8577, Japan
Institute of Engineering Innovation, The University of Tokyo 2 , Tokyo 113-8656, Japan
Funding
Kato Foundation for Promotion of Science · Japan Society for the Promotion of Science
References (23)
Show source-provided references
1. Chem. Mater. · 1998 · 10 · 275310.1021/cm980140w ↗
2. 2009
3. Chem. Mater. · 1994 · 6 · 36510.1021/cm00040a007 ↗
4. Chem. Mater. · 1998 · 10 · 278710.1021/cm9801901 ↗
5. J. Am. Chem. Soc. · 2008 · 130 · 670410.1021/ja801843v ↗
6. Inorg. Chem. · 2011 · 50 · 639210.1021/ic201006q ↗
7. J. Am. Chem. Soc. · 2014 · 136 · 274810.1021/ja408931v ↗
8. Inorg. Chem. · 2015 · 54 · 1140510.1021/acs.inorgchem.5b02049 ↗
9. J. Appl. Phys. · 2015 · 118 · 09410310.1063/1.4930034 ↗
10. Phys. Rev. Lett. · 2009 · 103 · 04760110.1103/physrevlett.103.047601 ↗
11. Chem. Mater. · 2016 · 28 · 664410.1021/acs.chemmater.6b02783 ↗
12. Phys. Rev. B · 2016 · 93 · 13430310.1103/physrevb.93.134303 ↗
13. ACS Appl. Mater. Interfaces · 2017 · 9 · 2187910.1021/acsami.7b04481 ↗
14. Adv. Condens. Matter Phys. · 2015 · 49304510.1155/2015/493045 ↗
15. J. Am. Chem. Soc. · 2009 · 131 · 838610.1021/ja903133n ↗
16. J. Am. Ceram. Soc. · 2008 · 91 · 242910.1111/j.1551-2916.2008.02556.x ↗
17. AIP Adv. · 2018 · 8 · 05532710.1063/1.5034403 ↗
18. Int. J. Mod. Phys. B · 2014 · 28 · 145022410.1142/s0217979214502245 ↗
19. Appl. Phys. Lett. · 1993 · 62 · 95210.1063/1.108530 ↗
20. Jpn. J. Appl. Phys., Part 1 · 2004 · 43 · 530710.1143/jjap.43.5307 ↗
21. Solid State Commun. · 2009 · 149 · 184910.1016/j.ssc.2009.07.009 ↗
22. APL Mater. · 2015 · 3 · 06250510.1063/1.4919564 ↗
23. J. Appl. Crystallogr. · 2011 · 44 · 127210.1107/s0021889811038970 ↗