Abstract
Strong ferromagnetic materials at room temperature are of interest for various magnetic applications such as magnetic recording, sensors, and motors. Gigantic magnetism expected for α″-Fe16N2 thin films had been attracted much attention in terms of its large magnetization per weight in comparison to rare earth iron nitrides R2Fe17N3 because these films are made of only iron and nitrogen. It developed much straggling on iron nitride thin film research but inconsistent results were obtained using different preparation methods. A powdered α″-Fe16N2-like compound was prepared by the ammonolysis of fine α-Fe powder in low temperature below 200 °C to clarify the confusion; the magnetism was not large in α″-Fe16N2 itself but was increased in the intermediate ammonolysis dual-phase mixture product of the α″-Fe16N2-like compound and residual α-Fe. A way to control the magnetic coercivity was subsequently investigated to utilize the larger magnetization in the α″-Fe16N2-like compound mixture as magnetic materials similarly to Sm2Fe17N3 bonded magnet. Iron nitrides, zinc blende type γ″-FeN and rock-salt type γ‴-FeN, also decompose at around 500 °C. Thermal decomposition was a disadvantage in the preparation of the iron nitrides; however, iron nanoparticles dispersed composites in AlN matrix were derived from the iron nitrides (Fe,Al)N by thermal treatment including laser heating. Iron nitrides are thus promising magnetic materials for their potential applications in science and technology.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.