296 research outputs found

    Archaeometric studies at the GILDA beamline at the European Synchrotron Radiation Facility

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    In the latest years archaeometry scientists have directed a growing interest to synchrotron radiation techniques. The Italian CRG beamline GILDA at the European Synchrotron Radiation Facility provides to the users the access to experimental techniques like X-ray absorption spectroscopy and diffraction that are of great potential usefulness in this field. Here we give a technical overview of the instrumentation available as well as some examples among the archaeometry studies presently in progress on the beamline

    Unveiling the atomic position of C in Mn5Ge3 Cx thin films

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    Heavily carbon-doped Mn5Ge3 is a unique compound for spintronics applications as it meets all the requirements for spin injection and detection in group-IV semiconductors. Despite the great improvement of the magnetic properties induced by C incorporation into Mn5Ge3 compounds, very little information is available on its structural properties and the genuine role played by C atoms. In this paper, we have used a combination of advanced techniques to extensively characterize the structural and magnetic properties of Mn5Ge3Cx films grown on Ge(111) by solid phase epitaxy as a function of C concentration. The increase of the Curie temperature induced by C doping up to 435 K is accompanied by a decrease of the out-of-plane c-lattice parameter. The Mn and C chemical environments and positions in the Mn5Ge3 lattice have been thoroughly investigated using x-ray absorption spectroscopy techniques (x-ray absorption near-edge structures and extended x-ray absorption fine structures) and scanning transmission electronic microscopy (STEM) combined to electron energy loss spectroscopy for the chemical analysis. The results have been systematically compared to a variety of structures that were identified as favorable in terms of formation energy by ab initio calculations. For x≤0.5, the C atoms are mainly located in the octahedral voids formed by Mn atoms, which is confirmed by simulations and seen for the first time in real space by STEM. However, the latter reveals an inhomogeneous C incorporation, which is qualitatively correlated to the broad magnetic transition temperature. A higher C concentration leads to the formation of manganese carbide clusters that we identified as Mn23C6. Interestingly, other types of defects, such as interstitial Ge atoms, vacancies of Mn, and their association into line defects have been detected. They take part in the strain relaxation process and are likely to be intimately related to the growth process. This paper provides a complete picture of the structure of Mn5Ge3Cx in thin films grown by solid phase epitaxy, which is essential for optimizing their magnetic properties

    Chemical variability of artificial stone powders in relation to their health effects

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    The occurrence of highly severe silica-related diseases among the resin- and silica-based artificial stone workers was claimed, associated to an extremely short latency. High levels of exposure and intrinsic properties of AS are thought to modulate the development of silicosis and auto-immune diseases. This study compares parent materials and processed dusts, to shed light on changes of AS occurring in the manufacturing process, through an XRF, EPR and XAS investigation. We point out the extremely wide variability of the materials, the occurrence of chemical signatures impressed by the processing techniques, and the unprecedented generation of stable radicals associated to the lysis of the Si-O chemical bond inside the resin coated respirable crystalline silica. These results suggest that the AS processing in industrial stone workshops can create respirable dusts with peculiar physical and chemical properties, to be correlated to the observed clinical evidences

    COPPER DIFFUSION IN ION-EXCHANGED SODA-LIME GLASS

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    Cu-alkali ion exchange in silicate glasses gives rise to a peculiar copper distribution, with the presence of both the Cu2+ and Cu+ oxidation states. Grazing incidence X-ray absorption near-edge structure spectroscopy and secondary ion mass spectrometry were performed on different ion-exchanged samples. The results show that the Cu2+/Cu+ ratio is strongly depth-dependent. The relative presence of the two species throughout the exchanged region turns out to be governed by their different diffusion regimes, while the chemistry of the redox process is shown to play a minor role. A phenomenological model is proposed to describe the diffusion process
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