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.
Highlights
E similar oxygen frameworks and are suited to thin-film growth of oxides with triangular lattices
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 describe the decisive role of substrate in the crystallization and the thin-film synthesis of a new LiNbO3-type oxide, MgSnO3
Summary
E similar oxygen frameworks and are suited to thin-film growth of oxides with triangular lattices. Using molecular-beam epitaxy, we investigated the thin-film growth of high-pressure phase LiNbO3-type ZnSnO3 and discovered a polar oxide candidate, MgSnO3.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.