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Escanhoela, C. A.; Fabbris, G.; Sun, F.
Argonne National Laboratory (ANL), Argonne, IL (United States). Funding organisation: USDOE Office of Science - SC, Basic Energy Sciences (BES) (SC-22) (United States); USDOE National Nuclear Security Administration (NNSA) (United States)2018
Argonne National Laboratory (ANL), Argonne, IL (United States). Funding organisation: USDOE Office of Science - SC, Basic Energy Sciences (BES) (SC-22) (United States); USDOE National Nuclear Security Administration (NNSA) (United States)2018
AbstractAbstract
[en] We studied the effect of physical pressure on the electronic and magnetic properties of ferrimagnetic double perovskites A2FeReO6 (A = Ca, Ba) using Re L2,3 edge x-ray absorption spectroscopy and powder diffraction measurements. Volume compression is shown to dramatically increase the magnetic coercivity (Hc) in polycrystalline samples of both compounds with ΔHc/ΔV similar to 150-200 Oe/Å3. A nearly eight-fold increase in Hc, from 0.2 to 1.55 T, is obtained in Ba2FeReO6 at P = 29 GPa. While no signs of structural phase transitions are seen in either sample to similar to 30 GPa, the structural data points to a pressure-driven increase in tetragonal distortion of ReO6 octahedra. A sizable but pressure-independent Re orbital-to-spin magnetic moment ratio is observed, pointing to the critical role of spin-orbit interactions at Re sites. We present a J(eff) description of the electronic structure that combines effects of crystal field and spin-orbit coupling on the Re 5d2 orbitals and use this description to provide insight into the pressure-induced enhancement of magnetic anisotropy.
Source
OSTIID--1465770; AC02-06CH11357; AC-02-06CH11357; FG02-99ER45775; FG02-03ER46097; NA0001974; Available from https://www.osti.gov/servlets/purl/1465770; DOE Accepted Manuscript full text, or the publishers Best Available Version will be available free of charge after the embargo period
Record Type
Journal Article
Journal
Physical Review B; ISSN 2469-9950;
; v. 98(5); vp

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