Molecular beam epitaxy growth of antiferromagnetic Kagome metal FeSn
Abstract
FeSn is a room-temperature antiferromagnet expected to host Dirac fermions in its electronic structure. The interplay of the magnetic degree of freedom and the Dirac fermions makes FeSn an attractive platform for spintronics and electronic devices. While stabilization of thin film FeSn is needed for the development of such devices, there exist no previous reports of epitaxial growth of single crystalline FeSn. Here, we report the realization of epitaxial thin films of FeSn (001) grown by molecular beam epitaxy on single crystal SrTiO₃ (111) substrates. By combining X-ray diffraction, electrical transport, and torque magnetometry measurements, we demonstrate the high quality of these films with the residual resistivity ratio ρₓₓ(300K)/ρₓₓ(2K)=24 and antiferromagnetic ordering at T_N = 353 K. These developments open a pathway to manipulate the Dirac fermions in FeSn by both magnetic interactions and the electronic field effect for use in antiferromagnetic spintronics devices.
Copyright and License
© 2019 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Acknowledgement
We are grateful to R. Comin, M. Kang, J. van den Brink, S. Fang, and M. P. Ghimire for fruitful discussions.
Funding
This research was funded, in part, by the Gordon and Betty Moore Foundation EPiQS Initiative, Grant No. GBMF3848 to J.G.C. and ARO Grant No. W911NF-16-1-0034. L.Y. acknowledges support by the STC Center for Integrated Quantum Materials, NSF Grant No. DMR-1231319, and the Tsinghua Education Foundation. The authors acknowledge characterization facility support provided by the Materials Research Laboratory at the Massachusetts Institute of Technology, as well as fabrication facility support by the Microsystems Technology Laboratories at the Massachusetts Institute of Technology.
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Additional details
- ISSN
- 1077-3118
- Gordon and Betty Moore Foundation
- GBMF3848
- Army Research Office
- W911NF-16-1-0034
- National Science Foundation
- DMR-1231319