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B Hjörvarsson

Publications and source records attributed to B Hjörvarsson.

11 recordsLinked to original sources

Competing exchange interactions in magnetic multilayers.

We have studied alloying of the nonmagnetic spacer layer with a magnetic material as a method of tuning the interlayer coupling in magnetic multilayers. We have specifically studied the Fe/V(100) system by alloying the spacer V with various amounts of Fe. For some Fe concentrations in the spacer, it is possible to create a competition between antiferromagnetic Ruderman-Kittel-Kasuya-Yoshida exchange and direct ferromagnetic exchange coupling. The exchange coupling and transport properties for a large span of systems with different spacer concentrations and thicknesses were calculated and measured experimentally and good agreement between observations and theory was observed. A reduction in magnetoresistance of about 50% was observed close to the switchover from antiferromagnetic to ferromagnetic coupling.

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Superconducting spin valve effect of a v layer coupled to an antiferromagnetic [Fe/V] superlattice.

We studied superconducting V layers deposited on an antiferromagnetically coupled [Fe(2)V(11)](20) superlattice. The parallel upper critical magnetic field exhibits an anomalous T dependence up to the ferromagnetic saturation field of the superlattice, indicating that the superconducting transition temperature T(S) decreases when rotating the relative sublattice magnetization directions of the superlattice from antiparallel to parallel. This proves that the pair breaking effect of a Fe2 layer is reduced if at a distance of 1.5 nm a second Fe2 layer with antiparallel spin orientation exists.

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On the sharpness of the interfaces in metallic multilayers.

We show that the three most relevant magnetic properties (magnetic moment, critical temperature, and interlayer exchange coupling) of metallic multilayers can be reproduced with good accuracy by first principles theory, provided that the picture of atomically sharp interfaces is abandoned and one allows instead for both interface alloying and interface roughness. The interface of a metallic multilayer (exemplified by the Fe/V system) is demonstrated to, at best, have interdiffusion essentially over two to three atomic layers on each side of the interface. Our conclusions are the result of combining experimental work with theoretical modeling, and we argue that this approach is the best avenue to obtain accurate information about the interface quality of metallic multilayers.

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Magnetic superlattices with variable interlayer exchange coupling: a new approach for the investigation of low-dimensional magnetism.

We have investigated the magnetic order in an [Fe(2)/(VHx)(13)] x 200 superlattice as a function of temperature and hydrogen content in the vanadium layers. A J(radially)-T magnetic phase diagram was established where J(radially) denotes the interlayer exchange coupling between adjacent Fe planes. We propose that Fe/V superlattices, in which the ratio of interlayer to intralayer coupling can be tuned continuously and reversibly via hydrogen in the nonmagnetic vanadium, offer a new approach for the study of low-dimensional magnetism and crossover effects near the transition from ferromagnetic to antiferromagnetic order.

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Hydrogen desorption from sand-blasted and acid-etched titanium surfaces after glow-discharge treatment.

Hydrogen desorption from argon plasma-treated titanium implants with a high surface roughness was studied. Implants with a high surface roughness have shown an increase in mechanical stability in bone tissue and a different behavior of osteoblasts in vitro. High surface roughness was produced by grit blasting and acid etching, resulting in an increase of the sub-surface hydrogen concentration and the formation of a titanium hydride. After an argon plasma treatment the surface oxide, which always covers titanum surfaces exposed to an oxygen-containing environment, and some of the hydrogen were sputtered away, decreasing the hydrogen concentration in the sub-surface region. Nuclear reaction analysis was used to determine the hydrogen concentration as a function of depth. The total amount of sub-surface (down to a depth of < or = 2 microm) hydrogen remaining after plasma treatment decreased with increasing plasma intensity to below the levels observed in non-acid-etched samples (approximately 1-2%). Thermal desorption spectroscopy was used for desorption studies and investigation of H(2) desorption activation energies. With a surface oxide present, the onset of hydrogen desorption is at ca 400 degrees C, which is the oxide decomposition temperature in vacuum, with an activation energy of ca 2 eV/molecule of H(2). After plasma treatment, that is, without surface oxide present, the onset of desorption was observed at ca 300 degrees C and with an activation energy of ca 0.8 eV/molecule of H(2), indicating a bulk diffusion-limited desorption.

Acids↗