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Träfflista för sökning "WFRF:(Wolff Max) srt2:(2010-2014)"

Sökning: WFRF:(Wolff Max) > (2010-2014)

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1.
  • Wolff, Nicole, et al. (författare)
  • Temperature dependent cubic and hexagonal close packing in micellar structures
  • 2014
  • Ingår i: Soft Matter. - : Royal Society of Chemistry (RSC). - 1744-683X .- 1744-6848. ; 10:42, s. 8420-8426
  • Tidskriftsartikel (refereegranskat)abstract
    • The interfacial structure and phase diagram of a micellar solution formed by the three block copolymer ( EO20-PO70-EO20) also known as P123 solved in deuterated water close to a solid boundary is investigated with respect to temperature. We find a hysteretic behavior of the d-spacing of the micellar crystal and a spontaneous change in the lateral correlation length going hand in hand with a structural reorganization between cubic and hexagonal. The phase transitions may be initiated by a change in the shape of the micelles from spherical to elongated together with a minimization of the polymer water interface.
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2.
  • Bruessing, F., et al. (författare)
  • Magnetization and magnetization reversal in epitaxial Fe/Cr/Co asymmetric spin-valve systems
  • 2012
  • Ingår i: Physical Review B. Condensed Matter and Materials Physics. - 1098-0121 .- 1550-235X. ; 85:17, s. 174409-
  • Tidskriftsartikel (refereegranskat)abstract
    • We have investigated asymmetric Fe/Cr/Co/Cr superlattices with two magnetic layers of Fe and Co, which are different with respect to their magnetic properties: magnetization, coercivity, and magnetic anisotropy. The magnetic layers are weakly coupled via a mediating Cr spacer layer providing an antiferromagnetic alignment of adjacent layers. The magnetic structure of these spin-valve-like Fe/Cr/Co/Cr superlattices was analyzed from the remanent state up to saturation via polarized neutron scattering and polarized neutron reflectivity (PNR). Furthermore, the domain structure in remanence was imaged via polarized x-ray photoemission electron microscopy (XPEEM). This analysis reveals that the Co magnetization strongly affects the Fe domain structure, while the layer magnetization is collinear from the remanent antiparallel state up to the ferromagnetic saturation state. However, for certain Co layer thicknesses, the as-grown remanent state exhibits a noncollinear antiferromagnetic spin structure, which cannot be recovered after applying a magnetic field. However, the noncollinear structure is reproducible with freshly grown superlattices.
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3.
  • Delavari, Hamid H., et al. (författare)
  • Modeling of self-controlling hyperthermia based on nickel alloy ferrofluids : Proposition of new nanoparticles
  • 2013
  • Ingår i: Journal of Magnetism and Magnetic Materials. - : Elsevier BV. - 0304-8853 .- 1873-4766. ; 335, s. 59-63
  • Tidskriftsartikel (refereegranskat)abstract
    • In order to provide sufficient heat without overheating healthy tissue in magnetic fluid hyperthermia (MFH), a careful design of the magnetic properties of nanoparticles is essential. We perform a systematic calculation of magnetic properties of Ni-alloy nanoparticles. Stoner-Wohlfarth model based theories (SWMBTs) are considered and the linear response theory (LRT) is used to extract the hysteresis loop of nickel alloy nanoparticles in alternating magnetic fields. It is demonstrated that in the safe range of magnetic field intensity and frequency the LRT cannot be used for the calculation of the area in the hysteresis for magnetic fields relevant for hyperthermia. The best composition and particle size for self-controlling hyperthermia with nickel alloys is determined based on SWMBTs. It is concluded that Ni-V and Ni-Zn are good candidates for self-controlling hyperthermia.
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4.
  • Devishvili, A., et al. (författare)
  • SuperADAM : Upgraded polarized neutron reflectometer at the Institut Laue-Langevin
  • 2013
  • Ingår i: Review of Scientific Instruments. - : AIP Publishing. - 0034-6748 .- 1089-7623. ; 84:2, s. 025112-
  • Tidskriftsartikel (refereegranskat)abstract
    • A new neutron reflectometer SuperADAM has recently been built and commissioned at the Institut Laue-Langevin, Grenoble, France. It replaces the previous neutron reflectometer ADAM. The new instrument uses a solid state polarizer/wavelength filter providing a highly polarized (up to 98.6%) monochromatic neutron flux of 8 x 10(4) n cm(-2) s(-1) with monochromatization Delta lambda/lambda = 0.7% and angular divergence Delta alpha = 0.2 mrad. The instrument includes both single and position sensitive detectors. The position sensitive detector allows simultaneous measurement of specular reflection and off-specular scattering. Polarization analysis for both specular reflection and off-specular scattering is achieved using either mirror analyzers or a He-3 spin filter cell. High efficiency detectors, low background, and high flux provides a dynamic range of up to seven decades in reflectivity. Detailed specifications and the instrument capabilities are illustrated with examples of recently collected data in the fields of thin film magnetism and thin polymer films.
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5.
  • Gutfreund, Philipp, et al. (författare)
  • Depletion at solid/liquid interfaces : Flowing hexadecane on functionalized surfaces
  • 2011
  • Ingår i: Journal of Chemical Physics. - : AIP Publishing. - 0021-9606 .- 1089-7690. ; 134:6, s. 064711-
  • Tidskriftsartikel (refereegranskat)abstract
    • We present a neutron reflectivity study on interfaces in contact with flowing hexadecane, which is known to exhibit surface slip on functionalized solid surfaces. The single crystalline silicon substrates were either chemically cleaned Si(100) or Si(100) coated by octadecyl-trichlorosilane (OTS), which resulted in different interfacial energies. The liquid was sheared in situ and changes in reflectivity profiles were compared to the static case. For the OTS surface, the temperature dependence was also recorded. For both types of interfaces, density depletion of the liquid at the interface was observed. In the case of the bare Si substrate, shear load altered the structure of the depletion layer, whereas for the OTS covered surface no effect of shear was observed. Possible links between the depletion layer and surface slip are discussed. The results show that, in contrast to water, for hexadecane the enhancement of the depletion layer with temperature and interfacial energy reduces the amount of slip. Thus a density depletion cannot be the origin of surface slip in this system.
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6.
  • Kosogor, Anna, et al. (författare)
  • Landau theory for the phase transitions of interstitial hydrogen in strained vanadium
  • 2014
  • Ingår i: Physical Review B. Condensed Matter and Materials Physics. - 1098-0121 .- 1550-235X. ; 89:1, s. 014207-
  • Tidskriftsartikel (refereegranskat)abstract
    • A special version of the Landau theory of phase transitions has been developed, capturing the order-disorder phase transition in the bulk and elastically strained vanadium-hydrogen system. The equations for the solubility isotherms are obtained and the influence of biaxial strain on the critical temperature is determined. The critical temperature is found to change exponentially with strain. The calculated solubility isotherms agree well with experimental data for temperatures below, as well as above, the critical temperature. The influence of elastic strain on the solubility isotherm is analyzed and noticeable deviations from Sieverts' law, even at the extremely low concentrations, are obtained.
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7.
  • Mooij, Lennard, et al. (författare)
  • The effect of microstructure on the hydrogenation of Mg/Fe thin film multilayers
  • 2014
  • Ingår i: International journal of hydrogen energy. - : Elsevier BV. - 0360-3199 .- 1879-3487. ; 39:30, s. 17092-17103
  • Tidskriftsartikel (refereegranskat)abstract
    • Nanoconfined magnesium hydride can be simultaneously protected and thermodynamically destabilized when interfaced with materials such as Ti and Fe. We study the hydrogenation of thin layers of Mg (<14 nm) nanoconfined in one dimension within thin film Fe/Mg/Fe/Pd multilayers by the optical technique Hydrogenography. The hydrogenation of nanosized magnesium layers in Fe/Mg/Fe multilayers surprisingly shows the presence of multiple plateau pressures, whose nature is thickness dependent. In contrast, hydrogen desorption occurs via a single plateau which does not depend on the Mg layer thickness. From structural and morphological analyses with X-ray diffraction/reflectometry and cross-section TEM, we find that the Mg layer roughness is large when deposited on Fe and furthermore contains high-angle grain boundaries (GB's). When grown on Ti, the Mg layer roughness is low and no high-angle GB's are detected. From a Ti/Mg/Fe multilayer, in which the Mg layer is flat and has little or no GB's, we conclude that MgH2 is indeed destabilized by the interface with Fe. In this case, both the ab- and desorption plateau pressures are increased by a factor two compared to the hydrogenation of Mg within Ti/Mg/Ti multilayers. We hypothesize that the GB's in the Fe/Mg/Fe multilayer act as diffusion pathways for Pd, which is known to greatly alter the hydrogenation behavior of Mg when the two materials share an interface. 
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8.
  • Pálsson, Gunnar K., et al. (författare)
  • Hydrogen site occupancy and strength of forces in nanosized metal hydrides
  • 2012
  • Ingår i: Physical Review B. Condensed Matter and Materials Physics. - 1098-0121 .- 1550-235X. ; 85:19, s. 195407-
  • Tidskriftsartikel (refereegranskat)abstract
    • The dipole force components in nanosized metal hydrides are quantitatively determined with curvature and x-ray diffraction measurements. Ab initio density functional theory is used to calculate the dipole components and the symmetry of the strain field. The hydrogen occupancy in a 100-nm-thick V film is shown to be tetrahedral with a slight asymmetry at low concentration, and a transition to octahedral occupancy is shown to take place at around 0.07 [H/V] at 360 K. When the thickness of the V layer is reduced to 3 nm and biaxially strained, in a Fe0.5V0.5/V superlattice, the hydrogen unequivocally occupies octahedral z-like sites, even at and below concentrations of 0.02 [H/V].
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9.
  • Pálsson, Gunnar K., et al. (författare)
  • Using light transmission to watch hydrogen diffuse
  • 2012
  • Ingår i: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 3, s. 892-
  • Tidskriftsartikel (refereegranskat)abstract
    • Because of its light weight and small size, hydrogen exhibits one of the fastest diffusion rates in solid materials, comparable to the diffusion rate of liquid water molecules at room temperature. The diffusion rate is determined by an intricate combination of quantum effects and dynamic interplay with the displacement of host atoms that is still only partially understood. Here we present direct observations of the spatial and temporal changes in the diffusion-induced concentration profiles in a vanadium single crystal and we show that the results represent the experimental counterpart of the full time and spatial solution of Fick's diffusion equation. We validate the approach by determining the diffusion rate of hydrogen in a single crystal vanadium (001) film, with net diffusion in the [110] direction.
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10.
  • Poulopoulos, P., et al. (författare)
  • Induced spin-polarization of EuS at room temperature in Ni/EuS multilayers
  • 2014
  • Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 104:11, s. 112411-
  • Tidskriftsartikel (refereegranskat)abstract
    • Ni/EuS multilayers with excellent multilayer sequencing are deposited via e-beam evaporation on the native oxide of Si(100) wafers at 4 x 10(-9) millibars. The samples have very small surface and interface roughness and show sharp interfaces. Ni layers are nanocrystalline 4-8 nm thick and EuS layers are 2-4 nm thick and are either amorphous or nanocrystalline. Unlike for Co/EuS multilayers, all Eu ions are in divalent (ferromagnetic) state. We show a direct antiferromagnetic coupling between EuS and Ni layers. At room temperature, the EuS layers are spin-polarized due to the proximity of Ni. Therefore, Ni/EuS is a candidate for room-temperature spintronics applications. (C) 2014 AIP Publishing LLC.
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