TY - JOUR

T1 - An Ab initio study of magnetism in disordered Fe-Al alloys with thermal antiphase boundaries

AU - Friák, Martin

AU - Golian, Miroslav

AU - Holec, David

AU - Koutná, Nikola

AU - Šob, Mojmír

PY - 2019/12/23

Y1 - 2019/12/23

N2 - We have performed a quantum-mechanical study of a B2 phase of Fe 70Al 30 alloy with and without antiphase boundaries (APBs) with the {001} crystallographic orientation of APB interfaces. We used a supercell approach with the atoms distributed according to the special quasi-random structure (SQS) concept. Our study was motivated by experimental findings by Murakami et al. (Nature Comm. 5 (2014) 4133) who reported significantly higher magnetic flux density from A2-phase interlayers at the thermally-induced APBs in Fe 70Al 30 and suggested that the ferromagnetism is stabilized by the disorder in the A2 phase. Our computational study of sharp APBs (without any A2-phase interlayer) indicates that they have moderate APB energies (≈0.1 J/m 2) and cannot explain the experimentally detected increase in the ferromagnetism because they often induce a ferro-to-ferrimagnetic transition. When studying thermal APBs, we introduce a few atomic layers of A2 phase of Fe 70Al 30 into the interface of sharp APBs. The averaged computed magnetic moment of Fe atoms in the whole B2/A2 nanocomposite is then increased by 11.5% w.r.t. the B2 phase. The A2 phase itself (treated separately as a bulk) has the total magnetic moment even higher, by 17.5%, and this increase also applies if the A2 phase at APBs is sufficiently thick (the experimental value is 2–3 nm). We link the changes in the magnetism to the facts that (i) the Al atoms in the first nearest neighbor (1NN) shell of Fe atoms nonlinearly reduce their magnetic moments and (ii) there are on average less Al atoms in the 1NN shell of Fe atoms in the A2 phase. These effects synergically combine with the influence of APBs which provide local atomic configurations not existing in an APB-free bulk. The identified mechanism of increasing the magnetic properties by introducing APBs with disordered phases can be used as a designing principle when developing new magnetic materials.

AB - We have performed a quantum-mechanical study of a B2 phase of Fe 70Al 30 alloy with and without antiphase boundaries (APBs) with the {001} crystallographic orientation of APB interfaces. We used a supercell approach with the atoms distributed according to the special quasi-random structure (SQS) concept. Our study was motivated by experimental findings by Murakami et al. (Nature Comm. 5 (2014) 4133) who reported significantly higher magnetic flux density from A2-phase interlayers at the thermally-induced APBs in Fe 70Al 30 and suggested that the ferromagnetism is stabilized by the disorder in the A2 phase. Our computational study of sharp APBs (without any A2-phase interlayer) indicates that they have moderate APB energies (≈0.1 J/m 2) and cannot explain the experimentally detected increase in the ferromagnetism because they often induce a ferro-to-ferrimagnetic transition. When studying thermal APBs, we introduce a few atomic layers of A2 phase of Fe 70Al 30 into the interface of sharp APBs. The averaged computed magnetic moment of Fe atoms in the whole B2/A2 nanocomposite is then increased by 11.5% w.r.t. the B2 phase. The A2 phase itself (treated separately as a bulk) has the total magnetic moment even higher, by 17.5%, and this increase also applies if the A2 phase at APBs is sufficiently thick (the experimental value is 2–3 nm). We link the changes in the magnetism to the facts that (i) the Al atoms in the first nearest neighbor (1NN) shell of Fe atoms nonlinearly reduce their magnetic moments and (ii) there are on average less Al atoms in the 1NN shell of Fe atoms in the A2 phase. These effects synergically combine with the influence of APBs which provide local atomic configurations not existing in an APB-free bulk. The identified mechanism of increasing the magnetic properties by introducing APBs with disordered phases can be used as a designing principle when developing new magnetic materials.

UR - http://www.scopus.com/inward/record.url?scp=85077320003&partnerID=8YFLogxK

U2 - 10.3390/nano10010044

DO - 10.3390/nano10010044

M3 - Article

VL - 10.2020

JO - Nanomaterials

JF - Nanomaterials

SN - 2079-4991

IS - 1

M1 - 44

ER -