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Formation of L10 Ordering in FeNi by Mechanical Alloying and Field-Assisted Heat Treatment: Synchrotron XRD Studies

Authors :
Mandal, Shuvam
Panigrahi, Ajit
Rath, Ashutosh
Bönisch, Matthias
Sengupta, Pradyut
Debata, Mayadhar
Basu, Suddhasatwa
Source :
ACS omega 8(15), 13690-13701 (2023). doi:10.1021/acsomega.2c07869
Publication Year :
2023
Publisher :
American Chemical Society (ACS), 2023.

Abstract

ACS omega 8(15), 13690 - 13701 (2023). doi:10.1021/acsomega.2c07869<br />L10-ordered FeNi, tetrataenite, found naturally in meteorites is a predilection for next-generation rare-earth free permanent magnetic materials. However, the synthesis of this phase remains unattainable in an industrially relevant time frame due to the sluggish diffusion of Fe and Ni near the order–disorder temperature (593 K) of L1$_0$ FeNi. The present work describes the synthesis of ordered L1$_0$ FeNi from elemental Fe and Ni powders by mechanical alloying up to 12 h and subsequent heat treatment at 623 K for 1000 h without a magnetic field and for 4 h in the presence of 1.5 T magnetic field. Also, to address the ambiguity of L1$_0$ phase identification caused by the low difference in the X-ray scattering factor of Fe and Ni, synchrotron-based X-ray diffraction is employed, which reveals that 6 h milling is sufficient to induce L1$_0$ FeNi formation. Further milling for 12 h is done to achieve a chemically homogeneous powder. The phase fraction of L1$_0$-ordered FeNi is quantified to ∼9 wt % for 12 h milled FeNi, which increases to ∼15 wt % after heat treatment. Heat treatment of the milled powder in a magnetic field increases the long-range order parameter (S) from 0.18 to 0.30. Further, the study of magnetic properties reveals a decrease in magnetic saturation and a slight increase in coercivity with the increase in milling duration. At the same time, heat treatment in the magnetic field shows a considerable increase in coercivity.<br />Published by ACS Publications, Washington, DC

Details

ISSN :
24701343
Volume :
8
Database :
OpenAIRE
Journal :
ACS Omega
Accession number :
edsair.doi.dedup.....5d271694138c983c1f4face5de84b857
Full Text :
https://doi.org/10.1021/acsomega.2c07869