| 1. |
- Eyrich, C., et al.
(författare)
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Effects of substitution on the exchange stiffness and magnetization of Co films
- 2014
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Ingår i: Physical Review B. Condensed Matter and Materials Physics. - 1098-0121 .- 1550-235X. ; 90:23, s. 235408-
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Tidskriftsartikel (refereegranskat)abstract
- An antiferromagnetically coupled FM/NM/FM (FM = ferromagnet, NM = normal metal) trilayer structure responds to an external magnetic field by the formation of a magnetic-moment spring within the FM layers. We show that the exchange stiffness (A ex) of an FM layer can be determined by fitting the field-dependent magnetization, M(H), of the FM/NM/FM trilayer to a micromagnetic model. Using this method, we have measured the exchange stiffness of thin-film Co alloyed with Cr, Fe, Ni, Pd, Pt, and Ru. The results show that the rate at which a substituent element reduces the exchange stiffness is not directly related to its effect on the magnetization of the alloy. The observed trends have been understood by material-specific modeling based on density functional theory within the local density approximation. The stiffness measurements are in agreement with Brillouin light scattering carried out on thicker Co films.
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| 2. |
- Eyrich, C., et al.
(författare)
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Exchange stiffness in thin film Co alloys
- 2012
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Ingår i: Journal of Applied Physics. - : AIP Publishing. - 0021-8979 .- 1089-7550. ; 111:7, s. 07C919-
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Tidskriftsartikel (refereegranskat)abstract
- The exchange stiffness (A(ex)) is one of the key parameters controlling magnetization reversal in magnetic materials. We used a method based on the spin spiral formation in two ferromagnetic films antiferromagnetically coupled across a non-magnetic spacer layer and Brillouin scattering to measure A(ex) for a series of Co1-delta X delta (X=Cr, Ni, Ru, Pd, Pt) thin film alloys. The results show that A(ex) of Co alloys does not necessarily scale with M-s; A(ex) approximately decreases at the rate of 1.1%, 1.5%, 2.1%, 3.5%, and 5.6%, while M-s decreases at the rate of 1.1%, 0.5%, 1.1%, 3.7%, and 2.5% per addition of 1 at% of Pt, Ni, Pd, Cr, and Ru, respectively.
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| 3. |
- Girt, Erol, et al.
(författare)
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A method for measuring exchange stiffness in ferromagnetic films
- 2011
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Ingår i: Journal of Applied Physics. - : AIP Publishing. - 0021-8979 .- 1089-7550. ; 109:7, s. 07B765-
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Tidskriftsartikel (refereegranskat)abstract
- An exchange stiffness, A(ex), in ferromagnetic films is obtained by fitting the M(H) dependence of two ferromagnetic layers antiferromagnetically coupled across a nonmagnetic spacer layer with a simple micromagnetic model. In epitaxial and textured structures this method allows measuring A(ex) between the crystallographic planes perpendicular to the growth direction of ferromagnetic films. Our results show that A(ex) between [0001] planes in textured Co grains is 1.54 +/- 0.12 x 10(-11) J/m.
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| 4. |
- Mazumdar, Dipanjan, et al.
(författare)
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The valence band electronic structure of rhombohedral-like and tetragonal-like BiFeO3 thin films from hard X-ray photoelectron spectroscopy and first-principles theory
- 2016
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Ingår i: Journal of Electron Spectroscopy and Related Phenomena. - : Elsevier BV. - 0368-2048 .- 1873-2526. ; 208, s. 63-66
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Tidskriftsartikel (refereegranskat)abstract
- Abstract We investigate the electronic structure of rhombohedral-like (R) and tetragonal-like (T) BiFeO3 thin films using high energy X-ray photoelectron spectroscopy and first-principles electronic structure calculations. By exploiting the relative elemental cross sections to selectively probe the elemental composition of the valence band, we identify a strong Bi 6p contribution at the top of the valence band in both phases, overlapping in energy range with the O 2p states; this assignment is confirmed by our electronic structure calculations. We find that the measured occupied Bi 6p signal lies closer to the top of the valence band in the T phase than in the R phase, which we attribute, using our electronic structure calculations, to lower Bi–O hybridization in the T phase. We note, however, that our calculations of the corresponding densities of states underestimate the difference between the phases, suggesting that matrix element effects resulting from the different effective symmetries also contribute. Our results shed light on the chemical nature of the stereochemically active Bi lone pairs, which are responsible for the large ferroelectric polarization of BiFeO3.
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