535 research outputs found

    Longitudinal spin Seebeck coefficient: heat flux vs. temperature difference method

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    The determination of the longitudinal spin Seebeck effect (LSSE) coefficient is currently plagued by a large uncertainty due to the poor reproducibility of the experimental conditions used in its measurement. In this work we present a detailed analysis of two different methods used for the determination of the LSSE coefficient. We have performed LSSE experiments in different laboratories, by using different setups and employing both the temperature difference method and the heat flux method. We found that the lack of reproducibility can be mainly attributed to the thermal contact resistance between the sample and the thermal baths which generate the temperature gradient. Due to the variation of the thermal resistance, we found that the scaling of the LSSE voltage to the heat flux through the sample rather than to the temperature difference across the sample greatly reduces the uncertainty. The characteristics of a single YIG/Pt LSSE device obtained with two different setups was (1.143±0.007)⋅10−7(1.143\pm0.007)\cdot 10^{-7} Vm/W and (1.101±0.015)⋅10−7(1.101\pm0.015)\cdot 10^{-7} Vm/W with the heat flux method and (2.313±0.017)⋅10−7(2.313\pm0.017)\cdot 10^{-7} V/K and (4.956±0.005)⋅10−7(4.956\pm0.005)\cdot 10^{-7} V/K with the temperature difference method. This shows that systematic errors can be considerably reduced with the heat flux method.Comment: PDFLaTeX, 10 pages, 6 figure

    Electronic and magnetic structure of epitaxial NiO/Fe3_3O4_4(001) heterostructures grown on MgO(001) and Nb-doped SrTiO3_3(001)

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    We study the underlying chemical, electronic and magnetic properties of a number of magnetite based thin films. The main focus is placed onto NiO/Fe3_3O4_4(001) bilayers grown on MgO(001) and Nb-SrTiO3_3(001) substrates. We compare the results with those obtained on pure Fe3_3O4_4(001) thin films. It is found that the magnetite layers are oxidized and Fe3+^{3+} dominates at the surfaces due to maghemite (γ\gamma-Fe2_2O3_3) formation, which decreases with increasing magnetite layer thickness. From a layer thickness of around 20 nm on the cationic distribution is close to that of stoichiometric Fe3_3O4_4. At the interface between NiO and Fe3_3O4_4 we find the Ni to be in a divalent valence state, with unambiguous spectral features in the Ni 2p core level x-ray photoelectron spectra typical for NiO. The formation of a significant NiFe2_2O4_4 interlayer can be excluded by means of XMCD. Magneto optical Kerr effect measurements reveal significant higher coercive fields compared to magnetite thin films grown on MgO(001), and a 45∘^{\circ} rotated magnetic easy axis. We discuss the spin magnetic moments of the magnetite layers and find that the moment increases with increasing thin film thickness. At low thickness the NiO/Fe3_3O4_4 films grown on Nb-SrTiO3_3 exhibits a significantly decreased spin magnetic moments. A thickness of 20 nm or above leads to spin magnetic moments close to that of bulk magnetite

    Argon metastable dynamics in a filamentary jet micro-discharge at atmospheric pressure

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    Space and time resolved concentrations of Ar (3P2^{3}P_2) metastable atoms at the exit of an atmospheric pressure radio-frequency micro-plasma jet were measured using tunable diode laser absorption spectroscopy. The discharge features a coaxial geometry with a hollow capillary as an inner electrode and a ceramic tube with metal ring as outer electrode. Absorption profiles of metastable atoms as well as optical emission measurements reveal the dynamics and the filamentary structure of the discharge. The average spatial distribution of Ar metastables is characterized with and without a target in front of the jet, showing that the target potential and therewith the electric field distribution substantially changes the filaments' expansion. Together with the detailed analysis of the ignition phase and the discharge's behavior under pulsed operation, the results give an insight into the excitation and de-excitation mechanisms
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