Orthorhombic Ti2O3: A Polymorph-Dependent Narrow-Bandgap Ferromagnetic Oxide
Sarath Kumar, S. R.
Alshareef, Husam N.
Pennycook, Stephen J.
Breese, Mark B. H.
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AbstractMagnetic semiconductors are highly sought in spintronics, which allow not only the control of charge carriers like in traditional electronics, but also the control of spin states. However, almost all known magnetic semiconductors are featured with bandgaps larger than 1 eV, which limits their applications in long-wavelength regimes. In this work, the discovery of orthorhombic-structured Ti2O3 films is reported as a unique narrow-bandgap (≈0.1 eV) ferromagnetic oxide semiconductor. In contrast, the well-known corundum-structured Ti2O3 polymorph has an antiferromagnetic ground state. This comprehensive study on epitaxial Ti2O3 thin films reveals strong correlations between structure, electrical, and magnetic properties. The new orthorhombic Ti2O3 polymorph is found to be n-type with a very high electron concentration, while the bulk-type trigonal-structured Ti2O3 is p-type. More interestingly, in contrast to the antiferromagnetic ground state of trigonal bulk Ti2O3, unexpected ferromagnetism with a transition temperature well above room temperature is observed in the orthorhombic Ti2O3, which is confirmed by X-ray magnetic circular dichroism measurements. Using first-principles calculations, the ferromagnetism is attributed to a particular type of oxygen vacancies in the orthorhombic Ti2O3. The room-temperature ferromagnetism observed in orthorhombic-structured Ti2O3, demonstrates a new route toward controlling magnetism in epitaxial oxide films through selective stabilization of polymorph phases.
CitationLi Y, Weng Y, Yin X, Yu X, Kumar SRS, et al. (2017) Orthorhombic Ti2 O3 : A Polymorph-Dependent Narrow-Bandgap Ferromagnetic Oxide. Advanced Functional Materials: 1705657. Available: http://dx.doi.org/10.1002/adfm.201705657.
SponsorsThis work was supported by the King Abdullah University of Science and Technology (KAUST). Y.K.W. and S.D. were supported by National Natural Science Foundation of China (Grant No. 11674055). J.S.C. was supported by the Singapore National Research Foundation under CRP Award No. NRF-CRP10-2012-02 and IIP award No. NRF-IIP001-001.
JournalAdvanced Functional Materials