Virtual unrolling and deciphering of Herculaneum papyri by X-ray phase-contrast tomography.

A collection of more than 1800 carbonized papyri, discovered in the Roman 'Villa dei Papiri' at Herculaneum is the unique classical library survived from antiquity. These papyri were charred during 79 A.D. Vesuvius eruption, a circumstance which providentially preserved them until now. This magnificent collection contains an impressive amount of treatises by Greek philosophers and, especially, Philodemus of Gadara, an Epicurean thinker of 1st century BC. We read many portions of text hidden inside carbonized Herculaneum papyri using enhanced X-ray phase-contrast tomography non-destructive technique and a new set of numerical algorithms for 'virtual-unrolling'. Our success lies in revealing the largest portion of Greek text ever detected so far inside unopened scrolls, with unprecedented spatial resolution and contrast, all without damaging these precious historical manuscripts. Parts of text have been decoded and the 'voice' of the Epicurean philosopher Philodemus is brought back again after 2000 years from Herculaneum papyri.

Evidence of composite plasmon­phonon modes in the electronic response of epitaxial graphene.

The electronic response of quasi-freestanding graphene on Pt(111) has been measured by high-resolution electron energy loss spectroscopy. Loss spectra reveal the existence of three distinct excitations: a dispersing feature due to the ordinary sheet plasmon and two dispersionless modes at 0.2 and 0.5­0.6 eV. The latter two features are assigned to the coupled plasmon­phonon excitation and to an interface plasmon, respectively. The complex interactions of plasmons with other particles have significant fundamental and practical implications on the electronic response of graphene and their knowledge is essential for tailoring upcoming graphene-based plasmonic devices.

Interplay between single-particle and plasmonic excitations in the electronic response of thin Ag films.

High-resolution electron energy loss spectroscopy is used to study the electronic properties of thin Ag layers on Ni(111). In addition to the ordinary surface plasmon at 3.8 eV, we observe a broad feature at 7-8 eV, whose nature is investigated as a function of scattering geometry and primary electron beam energy. Loss measurements unambiguously indicate that this mode has spectral components from both free-electron Ag plasmonic excitations (free-electron surface plasmons and multipole plasmons) and single-particle transitions.

The adsorption and co-adsorption of oxygen and carbon monoxide on Pt3Ni(111): a vibrational study.

High-resolution electron energy loss spectroscopy has been used to investigate the adsorption and co-adsorption of oxygen and CO on the Pt(3)Ni(111) surface. For the sake of comparison, similar measurements have also been performed on the Pt(111) surface. We find that CO adsorbs at the same manner on both surfaces. By contrast, significant differences between the two surfaces exist concerning the adsorption of O and the co-adsorption of O with CO.

Plasmonic modes confined in nanoscale thin silver films deposited onto metallic substrates.

Collective electronic excitations in nanoscale thin Ag layers adsorbed on Cu(111) and Ni(111) at room temperature have been investigated by high-resolution electron energy loss spectroscopy. Surface plasmon was found to be confined within grains on Ag thin films on Cu(111) nanostructured in islands. Annealing removed surface plasmon confinement and induced a negative linear term of the dispersion relation. On the other hand, on flat thin films on Ni(111) the dispersion of Ag surface plasmon is fully quadratic. Landau damping processes of the plasmonic excitation were found to be dependent on the growth mode. Ag multipole surface plasmon at 7.7 eV was observed only under stringent kinematic conditions enhancing surface sensitivity.

Collective excitations in nanoscale thin alkali films: Na/Cu(111).

The relationship between electron quantum confinement and the energy dispersion of the surface plasmon in nanoscale thin Na layers adsorbed on Cu(111) at room temperature have been studied by high resolution electron energy loss spectroscopy. Screening effects due to electron quantum confinement occurring in this system cause the lowering of the surface plasmon frequency and, moreover, make the energy range of its dispersion curve larger than in thick alkali films. Landau damping of the plasma excitation was unexpectedly very efficient at small momenta. The dispersion curve of the Na surface plasmon was found to depend on the primary electron beam energy. Multipole surface plasmon at 4.70 eV was observed only for higher impinging energies.

Comparative vibrational study on alkali coadsorption with CO and O on Ni(111) and Cu(111).

High-resolution electron energy loss spectroscopy was used to investigate alkali (Na, K) coadsorption with CO and O on Cu(111) and Ni(111). Measurements provided new insights in these systems. A CO-induced weakening of the alkali-substrate bond was revealed on both substrates. The effect is more pronounced for the Na+CO/Ni(111) system. Submonolayers of alkalis were found to promote the preferential population of the subsurface site for O/Cu(111) but not for O/Ni(111).

Alkali-promoted CO dissociation on Cu(111) and Ni(111) at room temperature.

The coadsorption of alkalis (K, Na) and CO on Cu(111) was investigated by high-resolution electron energy loss spectroscopy. Measurements performed at room temperature showed that CO adsorption is partially dissociative on a potassium-precovered Cu(111) surface and fully dissociative for Na/Cu(111). Carbon monoxide molecules occupy adsorption sites directly adjacent to those of alkali adatoms, as suggested by the absence of a threshold alkali precoverage for CO dissociation. On the contrary, for alkali+CO/Ni(111) a threshold alkali precoverage for CO dissociation was found to exist.

Electronic structure of cluster assembled nanostructured TiO(2) by resonant photoemission at the Ti L(2,3) edge.

The electronic structure of cluster assembled nanostructured TiO(2) thin films has been investigated by resonant photoemission experiments with photon energies across the Ti L(2,3) edge. The samples were produced by supersonic cluster beam deposition with a pulsed microplasma cluster source. The valence band shows resonance enhancements in the binding energy region between 4 and 8 eV, populated by O 2p and hybridized Ti 3d states, and in the region about 1 eV below the Fermi level associated with defects related Ti 3d states. The data show that in as-deposited films Ti atoms are mainly fully (sixfolds) coordinated to oxygen atoms in octahedral symmetry and only a small fraction is in a broken symmetry environment. Since resonant photoemission is closely linked to the local electronic and structural configurations around the Ti atom, it is possible to correlate the resonant photoemission intensity and lineshape with the presence of defects of the films and with the degree of hybridization between the titanium and oxygen atoms.

Evidences of alkali-induced softening of the oxygen-substrate bond.

The interaction of oxygen with alkalis (Na, K) on Ni(111) was studied by high-resolution electron energy loss spectroscopy. Loss measurements revealed for the first time a softening of the O-Ni bond and, simultaneously, a strengthening of the alkali-Ni bond in the alkali+O coadsorbed phase, in perfect agreement with recent theoretical calculations. The weakening of the O-Ni bond was ascribed to the alkali-induced filling of the O 2p(z) antibonding orbitals. Different physical mechanisms were discussed for explaining the strengthening of the alkali-substrate bond whenever alkalis are coadsorbed with O adatoms.

High resolution electron energy loss measurements of Na/Cu(111) and H2O/Na/Cu(111): dependence of water reactivity as a function of Na coverage.

Collective electronic excitations occurring in Na layers grown on Cu(111) and in H2O/Na/Cu(111) have been investigated at room temperature by high resolution electron energy loss spectroscopy. Loss spectra taken for a coverage between 0.55 and 0.70 ML of Na are characterized by a feature at 3.0 eV assigned to a Mie resonance. Further increasing the Na coverage leads to the appearance of the Na surface plasmon at 3.9 eV. Water molecules dissociate on Na layers as shown by the appearance of the OH-Na vibration. Upon water adsorption, relevant effects on both electronic excitations and vibrational modes were observed as a function of Na coverage.

Multiple scattering approach to DAFS.

In this article we outline a general approach to the anomalous correction to the atomic scattering factor "ab-initio" calculation based on the multiple scattering theory. This approach can be used for structural determination in any system and in particular in the surfaces where symmetry conditions make usual analysis impossible. We show as an application of the formalism calculations related to experimental data of bulk Ge.

Following local adsorption sites through a surface chemical reaction: CH3SH on Cu(111)

Studying the interaction of CH3SH, methanethiol, with Cu(111) as a model system, we demonstrate the ability of chemical-shift normal incidence x-ray standing wave field measurements to identify the local adsorption geometries of coadsorbed reaction products at different temperatures, a technical problem of broad chemical significance. In the present case the local geometries of four distinct S-containing adsorbate species (intact CH3SH, two thiolate (CH3S-) reaction intermediates and atomic S) are determined.

Trace element analysis on Si wafer surfaces by TXRF at the ID32 ESRF undulator beamline.

Synchrotron radiation total-reflection X-ray fluorescence (SR-TXRF) has been applied to the impurity analysis of Si wafers using a third-generation synchrotron radiation undulator source. A lower limit of detectability (LLD) for Ni atoms of 17 fg (1.7 x 10(8) atoms cm(-2)) has been achieved with an optical set-up based on an Si(111) double-crystal monochromator and a horizontal sample geometry. These first results are very promising for synchrotron radiation trace element analysis since we estimate that it is possible to lower the LLD by a factor of about 25 by employing appropriate optics and detectors. The use of a crystal monochromator opens new possibilities to perform absorption and scattering experiments (NEXAFS and X-ray standing-wave methods) for chemical and structural analysis of ultratrace elements.