Half-metallicity and wandering axis ferromagnetism in Fe$_2$Ti$_{1-x}$Mn$_x$Sn (0 $< x \leq$ 0.3) Heusler Alloys

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Hauptverfasser: Mishra, Kulbhushan, Pandey, Shishir Kumar, Chaudhuri, S., Rawat, Rajeev, Bhobe, P. A.
Format: Preprint
Veröffentlicht: 2024
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author Mishra, Kulbhushan
Pandey, Shishir Kumar
Chaudhuri, S.
Rawat, Rajeev
Bhobe, P. A.
author_facet Mishra, Kulbhushan
Pandey, Shishir Kumar
Chaudhuri, S.
Rawat, Rajeev
Bhobe, P. A.
contents We investigate the effect of Mn substitution in Fe$_2$Ti$_{1-x}$Mn$_x$Sn on electronic structure and magnetic and electrical transport properties. The spin-polarized density of states calculations using density-functional theory (DFT) yields a half-metallic ground state in Mn-rich compositions. Localized magnetic moments at Mn sites interacting through the cloud of conduction electrons formed by Fe and Ti atoms are also predicted. Electrical resistivity and magneto-transport measurements reveal a Kondo-like ground state at low temperatures and a peculiar linear negative temperature coefficient of resistance in the high-temperature regime with a predominant electron-phonon scattering mechanism. Analysis of room temperature powder X-ray diffraction data reveals a highly ordered L2$_1$ structure and reduction of antisite disorder upon Mn substitution. The temperature-dependent magnetization measurements reveal distinct features indicative of weak anisotropy in the system. Isothermal magnetization measured as a function of the applied field helps identify the unique magnetic ground state of the half-metallic Fe$_2$Ti$_{1-x}$Mn$_x$Sn composition as a ferromagnet with a wandering axis that distinctively orients in the direction of the applied magnetic field. The measurement of X-ray absorption fine structure (XAFS) reveals that the random anisotropy arises due to the local lattice distortion around Mn atoms in the prepared compositions. Our findings thus provide a new perspective for studying the mechanism of half-metallicity and associated magnetic order in Heuslers.
format Preprint
id arxiv_https___arxiv_org_abs_2407_11576
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle Half-metallicity and wandering axis ferromagnetism in Fe$_2$Ti$_{1-x}$Mn$_x$Sn (0 $< x \leq$ 0.3) Heusler Alloys
Mishra, Kulbhushan
Pandey, Shishir Kumar
Chaudhuri, S.
Rawat, Rajeev
Bhobe, P. A.
Materials Science
We investigate the effect of Mn substitution in Fe$_2$Ti$_{1-x}$Mn$_x$Sn on electronic structure and magnetic and electrical transport properties. The spin-polarized density of states calculations using density-functional theory (DFT) yields a half-metallic ground state in Mn-rich compositions. Localized magnetic moments at Mn sites interacting through the cloud of conduction electrons formed by Fe and Ti atoms are also predicted. Electrical resistivity and magneto-transport measurements reveal a Kondo-like ground state at low temperatures and a peculiar linear negative temperature coefficient of resistance in the high-temperature regime with a predominant electron-phonon scattering mechanism. Analysis of room temperature powder X-ray diffraction data reveals a highly ordered L2$_1$ structure and reduction of antisite disorder upon Mn substitution. The temperature-dependent magnetization measurements reveal distinct features indicative of weak anisotropy in the system. Isothermal magnetization measured as a function of the applied field helps identify the unique magnetic ground state of the half-metallic Fe$_2$Ti$_{1-x}$Mn$_x$Sn composition as a ferromagnet with a wandering axis that distinctively orients in the direction of the applied magnetic field. The measurement of X-ray absorption fine structure (XAFS) reveals that the random anisotropy arises due to the local lattice distortion around Mn atoms in the prepared compositions. Our findings thus provide a new perspective for studying the mechanism of half-metallicity and associated magnetic order in Heuslers.
title Half-metallicity and wandering axis ferromagnetism in Fe$_2$Ti$_{1-x}$Mn$_x$Sn (0 $< x \leq$ 0.3) Heusler Alloys
topic Materials Science
url https://arxiv.org/abs/2407.11576