LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Relationship between ferromagnetism and, structure and morphology in un-doped ZnO and Fe-doped ZnO powders prepared by hydrothermal route

Photo from wikipedia

Abstract The magnetic properties, in the 5 K–350 K temperature range, were investigated in relationship with the structure and morphology of Zn 1−x Fe x O (x = 0, 0.01, 0.03) powders prepared by… Click to show full abstract

Abstract The magnetic properties, in the 5 K–350 K temperature range, were investigated in relationship with the structure and morphology of Zn 1−x Fe x O (x = 0, 0.01, 0.03) powders prepared by hydrothermal route. The magnetization measurements reveal that all powders are ferromagnetic at room temperature, with Curie temperature T c , higher than 350 K. The coercivity Hc takes values between 58 Oe and 107 Oe at 300 K and, between 217 Oe and 613 Oe at 5 K. The weak magnetization of the un-doped ZnO powder is temperature independent and was associated with the high surface to volume ratio of the powder particles (or the number of surface defects). The saturation magnetization M s was substantially enhanced (up to a factor of about 20 at 300 K and of about 200 at 5 K) at all temperatures as Fe concentration increased, in spite of reduction of the surface to volume ratio of the powder particles. The Hc vs. T and FC / ZFC curves for the un-doped ZnO show typical ferromagnetic behavior, whereas for the Fe doped powders exhibit Ruderman–Kittel–Kasuya–Yosida (RKKY) - like and spin-glass-like behavior. The observed magnetic phenomena in Fe doped ZnO can be explained on the basis of “donor defects concentration – magnetic cations concentration” phase diagram for dilute magnetic semiconductors.

Keywords: hydrothermal route; structure morphology; zno; powders prepared; prepared hydrothermal; doped zno

Journal Title: Current Applied Physics
Year Published: 2017

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.