Effect of the partial replacement of CaH2 with CaF2 in the Mixed System CaH2 + MgB2

In this work the effect of a partial replacement of CaH2 with CaF2 on the sorption properties of the system CaH2 + MgB2 has been studied. The first five hydrogen absorption and four desorption reactions of the CaH2 + MgB2 and 3CaH2 + CaF2 + 4MgB2 systems were investigated by means of volumetric measurements, high-pressure differential scanning calorimetric technique (HP-DSC), 11B and 19F MAS NMR spectroscopy, and in situ synchrotron radiation powder X-ray diffraction (SR-PXD). It was observed that already during the mixing of the reactants formation of a nonstoichiometric CaF2-xHx solid solution takes place. Formation of the CaF2-xHx solid solution sensibly affects the overall hydrogen sorption reactions of the system CaH2 + MgB2

Effect of Fe additive on the hydrogenation-dehydrogenation properties of 2LiH + MgB2/2LiBH4 + MgH2 system

Lithium reactive hydride composite 2LiBH4 + MgH2 (Li-RHC) has been lately investigated owing to its potential as hydrogen storage medium for mobile applications. However, the main problem associated with this material is its sluggish kinetic behavior. Thus, aiming to improve the kinetic properties, in the present work the effect of the addition of Fe to Li-RHC is investigated. The addition of Fe lowers the starting decomposition temperature of Li-RHC about 30 °C and leads to a considerably faster isothermal dehydrogenation rate during the first hydrogen sorption cycle. Upon hydrogenation, MgH2 and LiBH4 are formed whereas Fe appears not to take part in any reaction. Upon the first dehydrogenation, the formation of nanocrystalline, well distributed FeB reduces the overall hydrogen storage capacity of the system. Throughout cycling, the agglomeration of FeB particles causes a kinetic deterioration. An analysis of the hydrogen kinetic mechanism during cycling shows that the hydrogenation and dehydrogenation behavior is influenced by the activity of FeB as heterogeneous nucleation center for MgB2 and its non-homogenous distribution in the Li-RHC matrix.Fil: Puszkiel, Julián Atilio. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Helmholtz-zentrum Geesthacht - Zentrum Für Material- Und Küstenforschung Gmbh;Fil: Gennari, Fabiana Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Centro Atómico Bariloche; ArgentinaFil: Arneodo Larochette, Pierre Paul. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Centro Atómico Bariloche; ArgentinaFil: Ramallo Lopez, Jose Martin. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaFil: Vainio, U.. Helmholtz-zentrum Geesthacht - Zentrum Für Material- Und Küstenforschung Gmbh; . Deutsches Elektronen-Synchrotron; AlemaniaFil: Karimi, F.. Helmholtz-zentrum Geesthacht - Zentrum Für Material- Und Küstenforschung Gmbh;Fil: Pranzas, P. K.. Helmholtz-zentrum Geesthacht - Zentrum Für Material- Und Küstenforschung Gmbh;Fil: Troiani, Horacio Esteban. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Centro Atómico Bariloche; ArgentinaFil: Pistidda, C.. Helmholtz-zentrum Geesthacht - Zentrum Für Material- Und Küstenforschung Gmbh;Fil: Jepsen, J.. Helmholtz-zentrum Geesthacht - Zentrum Für Material- Und Küstenforschung Gmbh;Fil: Tolkiehn, M.. Deutsches Elektronen-Synchrotron; AlemaniaFil: Welter, E.. Deutsches Elektronen-Synchrotron; AlemaniaFil: Klassen, T.. Helmholtz-zentrum Geesthacht - Zentrum Für Material- Und Küstenforschung Gmbh;Fil: Bellosta Von Colbe, J.. Helmholtz-zentrum Geesthacht - Zentrum Für Material- Und Küstenforschung Gmbh;Fil: Dornheim, M.. Helmholtz-zentrum Geesthacht - Zentrum Für Material- Und Küstenforschung Gmbh

Neutron scattering and modeling of dipole-field-induced spin disorder in Nanoperm

We present magnetic-field-dependent small-angle neutron scattering data for the ferromagnetic nanocomposite Nanoperm (Fe89Zr7B3Cu1). The spin-misalignment scattering in the approach-to-saturation regime unexpectedly reveals pronounced lobes of high intensity at angles ±30−40° relative to the magnetic-field axis. Based on numerical calculations, the four-fold angular symmetry of the scattering pattern can be explained in terms of local spin misalignment, which originates from dipolar stray fields due to the mismatch of the saturation-magnetization values between the bcc Fe particles and the amorphous magnetic matrix

Dipolar correlations in a nanocomposite: A neutron scattering study of Nanoperm Fe89Zr7B3Cu

We present results for the magnetic-field, temperature, and neutron-polarization dependence of the small-angle neutron scattering intensity in the soft magnetic iron-based nanocomposite Nanoperm (Fe89Zr7B3Cu). An unusual “clover-leaf-shaped” intensity distribution on the detector is attributed to the dipolar stray fields around the nanosized iron particles, which are embedded in an amorphous magnetic matrix of lesser saturation magnetization. The dipole field induces spin disorder, correlating the spin misalignment of neighboring particles and matrix over several particle spacings. The clover-leaf-shaped anisotropy is observed over a wide range of applied magnetic field and momentum transfer. It persists up to several hundred degrees Kelvin above the Curie temperature of the matrix phase, indicating that some degree of magnetic coupling persists even when the matrix is paramagnetic

Temperature dependence of dipole-field scattering in Nanoperm

We present small-angle neutron scattering (SANS) data for the temperature variation of the recently observed dipole-field-induced spin-misalignment scattering in the soft magnetic nanocomposite Nanoperm (Fe89Zr7B3Cu1). The associated clover-leaf-shaped angular anisotropy of the SANS pattern, which is due to spin disorder arising from dipolar stray fields of the iron nanoparticles, persists up to several hundred Kelvin above the decoupling point of the intergranular amorphous matrix phase. This observation, in conjunction with the q-dependence of the scattering, suggests the existence of long-range magnetic correlations between the iron particles through the paramagnetic matrix, in agreement with previous investigations. The characteristic wavelength of the dipole-field-induced spin disorder appears to be temperature independent

Dipole-field-induced spin disorder in a nanocomposite soft magnet

We report on a study of a magnetic nanocomposite of the Nanoperm type (Fe89Zr7B3Cu1) by magnetic small-angle neutron scattering (SANS). The understanding of the magnetic microstructure of these materials leaves much to be desired since we lack techniques capable of resolving the spin structure in the bulk with nanoscale resolution. Here, we present an analysis of the SANS signal by which one cannot only characterise the nanoscale structure of the spin system, but which allows to identify origin and structure of the perturbing field. In Nanoperm, an unusual angular anisotropy of the scattering suggests that the local spin misalignment decorates, as the most important perturbing field, dipole stray fields around the crystalline phase of the composite