The INFN-LNF present and future accelerator-based light facilities.

The INFN-Frascati National Laboratory (LNF) is nowadays running a 0.51 GeV electron-positron collider, DA Φ NE, that also represents the synchrotron radiation source of the beamlines of the DA Φ NE-Light facility. Not being DA Φ NE dedicated to synchrotron radiations activities, the DA Φ NE-Light facility can use it mainly in parasitic mode. Particle accelerators and high energy physics (HEP) have been and are the main core of the LNF research activity, but like other HEP international laboratories also LNF is now moving in the direction of developing a dedicated free electron laser (FEL) user facility, EuPRAXIA@SPARC_Lab, based on plasma acceleration. This new facility in the framework of the EuPRAXIA (European Plasma Research Accelerator with eXcellence in Applications) EU project should produce FEL radiation beams for a wide range of applications using a smaller accelerator compared to actual radio frequency-based accelerator sources dimensions.

Characterization of a Poly-4-Vinylpyridine-Supported CuPd Bimetallic Catalyst for Sonogashira Coupling Reactions.

CuPd bimetallic solvated metal atoms (SMA) synthesized by metal vapor synthesis (MVS) technique and supported on poly-4-vinylpyridine (PVPy) resin, showed significantly higher catalytic activity in Sonogashira-type carbon-carbon coupling reactions than the corresponding monometallic Cu and Pd systems as well as their physical mixture. The analysis of the bimetallic catalyst combining transmission electron microscopy techniques and X-ray absorption fine structure (XAFS) spectroscopy revealed the presence of small Pd nanoparticles (dm =2.5 nm) while the analysis of the X-ray absorption data, at the Cu K-edge suggests the formation of thin and incomplete Cu oxide layers around the Pd-rich cores.

Exploiting soft and hard X-ray absorption spectroscopy to characterize metallodrug/protein interactions: the binding of [trans-RuCl4(Im)(dimethylsulfoxide)][ImH] (Im = imidazole) to bovine serum albumin.

The reaction of bovine serum albumin (BSA) with [ trans-RuCl 4(Im)(dimethylsulfoxide)][ImH] (Im = imidazole) (NAMI-A), an experimental ruthenium(III) anticancer drug, and the formation of the respective NAMI-A/BSA adduct were investigated by X-ray absorption spectroscopy (XAS) at the sulfur and chlorine K-edges and at the ruthenium K- and L 3-edges. Ruthenium K and L 3-edge spectra proved unambiguously that the ruthenium center remains in the oxidation state +3 after protein binding. Comparative analysis of the chlorine K-edge XAS spectra of NAMI-A and NAMI-A/BSA, revealed that the chlorine environment is greatly perturbed upon protein binding. Only modest changes were observed in the sulfur K-edge spectra that are dominated by several protein sulfur groups. Overall, valuable information on the nature of this metallodrug/protein adduct and on the mechanism of its formation was gained; XAS spectroscopy turns out to be a very suitable method for the characterization of this kind of systems.

Qualitative detection of Mg content in a leaf of Hedera helix by using X-ray radiation from a laser plasma source.

In this article, a method to reveal the presence of Mg content inside the different parts of leaves of Hedera helix is presented. In fact a sample of a Hedera helix's leaf, commonly characterized by a green and a white side, is analyzed under X-ray radiation. The presence of two zones with different colors in the Hedera helix's leaf has not been explained. In this connection, there are presently three hypotheses to explain the characteristic double-color appearance of the leaf. The first hypothesis suggests a different cytoplasmic inheritance of chloroplasts at the cell division, the second a different allelic composition, homozygote and heterozygote, between the two zones, and finally the third the action of a virus which changes the color properties in the Hedera's leaves. The resulting effect is a different content of "something" between the green and the white side. We utilized X-ray radiation, obtained from a plasma source with a Mg target, to image Hedera helix leaves and we found that the green side of the leaf is highlighted. We may suppose that the reason why the X-rays from a Mg plasma source, allow us to pick up the green side is probably due to the greater presence of the amount of Mg (from chlorophyll or other complexes and/or salts) in the two sides, green and white, of the leaf.

Metal-support interaction and redox behavior of Pt(1 wt %)/Ce0.6Zr0.4O2.

The catalyst Pt(1 wt %)/Ce(0.6)Zr(0.4)O(2) is studied by CO-temperature programmed reduction (CO-TPR), isothermal oxygen storage complete capacity (OSCC), X-ray absorption spectroscopy (XAS) at the Pt L(III) edge, and in situ X-ray diffraction (in situ XRD), with the aim of elucidating the role of supported metal in CO oxidation by ceria-based three-way catalysts (TWC). The redox behavior of Pt(1 wt %)/Ce(0.6)Zr(0.4)O(2) is compared to that of bare ceria-zirconia. OSCC of redox-aged Pt/ceria-zirconia is twice that of bare ceria-zirconia, and the maximum of CO consumption occurs at a temperature about 300 K lower than redox-aged ceria-zirconia. XAS analysis allows one to evidence the formation of a platinum-cerium alloy in redox-aged samples and the stability of the metal particles toward oxidation and sintering during high-temperature treatments. Under CO flux at 773 K, bare ceria-zirconia shows a continuous drift of diffraction peaks toward smaller Bragg angles, due to a progressive increase of Ce(III) content. Under the same treatment, the structural rearrangement of Pt-supported ceria-zirconia starts after an induction time and takes place with an abrupt change of the lattice constant. The experimental evidence points to the role of supported Pt in modifying the redox properties of ceria-zirconia with respect to the bare support. It is proposed that the much faster bulk reduction observed by in situ XRD for redox-aged Pt/ceria-zirconia can be attributed to an easier release of reacted CO(2), producing a more effective turnover of reactants at the catalyst surface.

A new cell for the study of in situ chemical reactions using X-ray absorption spectroscopy.

An in situ cell for reductive and oxidative treatments at different temperatures that allows the possibility of recording data as a function of temperature has been designed and constructed for X-ray absorption experiments at the GILDA beamline BM08 of ESRF. The cell is linked to a mass quadrupole spectrometer providing control of the reaction gases and monitoring of the products. The apparatus allows measurements to be performed both in transmission and fluorescence geometry. The cell was tested by studying the CO oxidation reaction promoted by a Pt/ceria-zirconia-supported catalyst. The CO(2) yield is correlated with the structural results confirming the existence of a strong metal-support interaction between the Pt metal clusters and the ceria-zirconia support.