D. Bessas
Please Note
5 records found
1
Bulk Sr2PdO3 was synthesized by a modified solid state reaction and a detailed characterization was carried out using both microscopic and macroscopic experimental techniques. Pd site exhibits an electric field gradient of 5.9(1) ⋅ 1017 V/cm2 due to the anisotropic local atomic configuration. A Curie - paramagnetic susceptibility indicating antiferromagnetic interactions superimposed to a core diamagnetic state is confirmed. A linear volume thermal expansion with a coefficient of 3.0(1) ⋅ 10−5 K−1 at room temperature is extracted. A collection of Einstein oscillators, with an Einstein temperature of about 115 K, is involved in the thermal transport. Large atomic displacements were observed in Sr vibrations. No Pd or Sr valence change is observed up to 900 K. A moderate anharmonicity is identified and quantified in a macroscopic Grüneisen parameter of 2.5(1) at room temperature. The electrical resistivity reveals a semiconducting behaviour. A systematic reduction in electrical resistivity and a change in the conduction mechanism is observed upon thermal cycling which indicates that a peculiar electronic mechanism is involved.
Electric field controlled ion transport and interface formation of iron thin films on a BaTiO3 substrate have been investigated by in situ nuclear resonance scattering and x-ray reflectometry techniques. At early stage of deposition, an iron-II oxide interface layer was observed. The hyperfine parameters of the interface layer were found insensitive to the evaporated layer thickness. When an electric field was applied during growth, a 10 Å increase of the nonmagnetic/magnetic thickness threshold and an extended magnetic transition region was measured compared to the case where no field was applied. The interface layer was found stable under this threshold when further evaporation occurred, contrary to the magnetic layer where the magnitude and orientation of the hyperfine magnetic field vary continuously. The obtained results of the growth mechanism and of the electric field effect of the Fe/BTO system will allow the design of novel applications by creating custom oxide/metallic nanopatterns using laterally inhomogeneous electric fields during sample preparation.
The lattice dynamics in MnFe0.95Si0.50P0.50 were investigated experimentally using Fe57 nuclear inelastic scattering and inelastic x-ray scattering across the first-order magnetic transition which occurs close to room temperature. The lattice dynamics characterization was supported by a macroscopic magnetic characterization, an x-ray diffraction study, and a hyperfine interactions characterization using Mössbauer spectroscopy. The Fe specific and the x-ray generalized density of phonon states were obtained both in the ferromagnetic and in the paramagnetic state. A prominent shift, 2meV at 20meV, in the x-ray generalized density of phonon states across the first-order magnetic transition, that involves vibrations with essentially Fe character, is revealed corroborated by a change in the local environment quantified in the isomer shift and the quadrupole splitting. Above 35meV the vibrational modes are practically insensitive to the magnetic transition. The entropy change induced by a 1T magnetic field across the magnetic transition, ∼10J/K/kg, is only a fraction of the Fe vibrational entropy change, 62(21)J/K/kg.
The high pressure structural phase diagram of EuTiO3 is revisited by means of single crystal x-ray diffraction at pressures below 30GPa. We report a transition at about 3GPa with a surprisingly small lattice distortion. At 23GPa we have detected a yet unknown transition into a new orthorhombic phase (space group Ibam). Combining our observations on structures obtained on single crystals and polycrystalline samples with complementary methods, such as electrical resistivity and nuclear forward scattering of synchrotron radiation measured on polycrystalline samples, we address issues relevant to chemistry and disorder.
A versatile Lock-In digital Amplifier (LIdA)
The case of mechanical resonances
The assembly of a Lock-In digital Amplifier (LIdA) from widely accessible ready-made modules is presented. This equipment, which does not require any advanced knowledge of electronics or programming, may introduce the experimenter to resonant techniques by registering mechanical resonances. The freely available control program allows for general data acquisition and further data processing. The apparatus is versatile and may corroborate the science and engineering laboratory in elasticity measurements or in a series of experiments where a modulated signal is a prerequisite.