Development of high-temperature ferromagnetism in SnO2 and paramagnetism in SnO by Fe doping

A. Punnoose, J. Hays, A. Thurber, M. H. Engelhard, R. K. Kukkadapu, C. Wang, V. Shutthanandan, and S. Thevuthasan
Phys. Rev. B 72, 054402 – Published 2 August 2005

Abstract

We report the development of room-temperature ferromagnetism in chemically synthesized powder samples of Sn1xFexO2 (0.005x0.05) and paramagnetic behavior in an identically synthesized set of Sn1xFexO. The ferromagnetic Sn0.99Fe0.01O2 showed a Curie temperature TC=850K, which is among the highest reported for transition-metal-doped semiconductor oxides. With increasing Fe doping, the lattice parameters of SnO2 decreased and the saturation magnetization increased, suggesting a strong structure-magnetic property relationship. When the Sn0.95Fe0.05O2 was prepared at different temperatures between 200 and 900°C, systematic changes in the magnetic properties were observed. Combined Mössbauer spectroscopy and magnetometry measurements showed a ferromagnetic behavior in Sn0.95Fe0.05O2 samples prepared at and above 350°C, but the ferromagnetic component decreased gradually as preparation temperature approached 600°C. All Sn0.95Fe0.05O2 samples prepared above 600°C were paramagnetic. X-ray photoelectron spectroscopy, magnetometry, and particle induced x-ray emission studies showed that the Fe dopants diffuse towards the surface of the particles in samples prepared at higher temperatures, gradually destroying the ferromagnetism. Mössbauer studies showed that the magnetically ordered Fe3+ spins observed in the Sn0.95Fe0.05O2 sample prepared at 350°C is only 24% of the uniformly incorporated Fe3+. No evidence of any iron oxide impurity phases were detected in Sn1xFexO2 or Sn1xFexO, suggesting that the emerging magnetic interactions in these systems are most likely related to the properties of the host systems SnO2 and SnO, and their oxygen stoichiometry.

    • Received 26 May 2005

    DOI:https://doi.org/10.1103/PhysRevB.72.054402

    ©2005 American Physical Society

    Authors & Affiliations

    A. Punnoose1,*, J. Hays1, A. Thurber1, M. H. Engelhard2, R. K. Kukkadapu2, C. Wang2, V. Shutthanandan2, and S. Thevuthasan2

    • 1Department of Physics, Boise State University, Boise, Idaho 83725-1570, USA
    • 2Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352, USA

    • *Corresponding author. Electronic address: apunnoos@boisestate.edu

    Article Text (Subscription Required)

    Click to Expand

    References (Subscription Required)

    Click to Expand
    Issue

    Vol. 72, Iss. 5 — 1 August 2005

    Reuse & Permissions
    Access Options
    Author publication services for translation and copyediting assistance advertisement

    Authorization Required


    ×
    ×

    Images

    ×

    Sign up to receive regular email alerts from Physical Review B

    Log In

    Cancel
    ×

    Search


    Article Lookup

    Paste a citation or DOI

    Enter a citation
    ×