Multimodal analysis of Zr substitution effects on magnetic and crystallographic properties in (Sm1-xZrx)(Fe0.8Co0.2)12 compounds with ThMn12 structure

SmFe12-based compounds containing Zr atoms have been recognized as candidates for novel high-performance permanent magnet materials with a high saturation magnetization. Partial substitution of Sm with Zr in (Sm1 -xZrx)(Fe0.8Co0.2)(12) has been known to enhance the magnetization of the compound. This study focused on (Sm1 -xZrx)(Fe0.8Co0.2)(12) single-crystalline films to evaluate the effects of Zr sub-stitution for Sm on their structural and magnetic properties via systematic multimodal analysis. X-ray absorption fine structure (XAFS) and scanning transmission electron microscopy indicated a selective oc-cupation of the Sm site by Zr atoms without disturbing the Fe sublattices. The chemical shift in the Zr-K edge XAFS spectra suggested electron transfer from Zr to the Fe band. Soft X-ray magnetic circu-lar dichroism analysis proved that the magnetic moment of Sm was two orders of magnitude smaller than the magnetic moments of Fe and Co, and its contribution to the total magnetization was negligible. The partial substitution of Sm with Zr resulted in a volumetric expansion and c-axis length elongation despite Zr having a smaller atomic radius, which is unique to (Sm1 -xZrx)(Fe0.8Co0.2)(12) without structure -stabilizing elements such as Ti, V, and Si. This anisotropic expansion is explained by an increase in the magnetic moment and magnetic interactions in the Fe8f site, which is induced by the electron transfer from Zr to Fe8f atoms. Thus, we conclude that the electron transfer from Zr to the Fe8f atoms principally drives magnetization enhancement in (Sm1 -xZrx)(Fe0.8Co0.2)(12) single-crystalline films. (c) 2022 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

Automated summary

This study focused on the effects of Zr substitution for Sm in (Sm1-xZrx)(Fe0.8Co0.2)(12) single-crystalline films on their structural and magnetic properties. The results showed that Zr selectively occupied the Sm site without disturbing the Fe sublattices. Electron transfer from Zr to the Fe band increased the magnetic moment and magnetic interactions in the Fe8f site, leading to magnetization enhancement in (Sm1-xZrx)(Fe0.8Co0.2)(12) single-crystalline films.