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Abstract
Fe4N thin films with (001) texture were prepared by reactive sputtering on MgO substrates, utilizing either a Cr or Ag buffer layer to facilitate the epitaxial growth. X-ray diffraction, atomic force microscopy, and vibrating sample magnetometry measurements show that the Fe4N thin film grown on the Ag buffer layer is superior to that grown on the Cr buffer layer. The point contact Andreev reflection measurement was then conducted, and the spin polarizations were determined to be 61.1% and 81.3% for Fe4N thin films with Cr and Ag buffer layers, respectively. The 81.3% spin polarization is significantly higher than the ratio reported previously for Fe4N and is comparable with that of state-of-the-art Heusler alloys. This result is in agreement with the theoretical prediction on the discrepancy between the two differently defined spin polarizations for Fe4N. Moreover, our study indicates that an optimized growth process for Fe4N thin films is crucial for achieving a high spin polarization and that true half-metallicity could potentially be realized with Fe4N. The high spin polarization of Fe4N combined with its low fabrication temperature and simple composition makes Fe4N a competitive candidate to be a half-metallic ferromagnet in spintronic devices.
Original language | English (US) |
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Article number | 162407 |
Journal | Applied Physics Letters |
Volume | 112 |
Issue number | 16 |
DOIs | |
State | Published - Apr 16 2018 |
Bibliographical note
Funding Information:The authors thank the useful discussion with Dr. Qunwen Leng. This work was supported by Western Digital Corporation. Part of this work was carried out at the Characterization Facility, University of Minnesota, a member of the NSF-funded Materials Research Facilities Network (www.mrfn.org) via the NSF MRSEC Program under Award No. DMR-0819885. The PCAR testing was supported as part of SHINES, an EFRC center funded by the U. S. Department of Energy, Office of Science, Basic Energy Science, under Award No. SC0012670.
Publisher Copyright:
© 2018 Author(s).
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