The Elettra 2.0 Beamlines

The Elettra 2.0 project was approved by the Italian Government in 2017, with plans for the new machine to commence serving external users in 2027. The design phase lead to a final version of Elettra 2.0 a fully transversely coherent source up to 0.5 keV-photon energy, more than doubling the total average current and increasing brightness by more than two orders of magnitude as compared to the current source, and maintaining a diversified beamline portfolio to allow experiments across a broad spectrum of photon energies, from a few tens of eV to several tens of keV, while substantially increasing the number of beamlines operating in the hard-X-ray range. In perspective, the possibility of producing picosecond-long light pulses at a MHz repetition rate across multiple beamlines simultaneously, without interference to standard multi-bunch operation is also being considered. Another important aspect of Elettra 2.0 is the high degree of transverse coherence in both the horizontal and vertical directions, projected to improve by a factor of 60 at 1 keV as compared to the current source

On the Origin of Metallicity and Stability of the Metastable Phase in Chemically Exfoliated MoS2_2

Chemical exfoliation of MoS$_2$ via Li-intercalation route has led to many desirable properties and spectacular applications due to the presence of a metastable state in addition to the stable H phase. However, the nature of the specific metastable phase formed, and its basic charge conduction properties have remained controversial. Using spatially resolved Raman spectroscopy (~1 micrometer resolution) and photoelectron spectroscopy (~120 nm resolution), we probe such chemically exfoliated MoS$_2$ samples in comparison to a mechanically exfoliated H phase sample and confirm that the dominant metastable state formed by this approach is a distorted T' state with a small semiconducting gap. Investigating two such samples with different extents of Li residues present, we establish that Li+ ions, not only help to exfoliate MoS$_2$ into few layer samples, but also contribute to enhancing the relative stability of the metastable state as well as dope the system with electrons, giving rise to a lightly doped small bandgap system with the T' structure, responsible for its spectacular properties.Comment: 34 pages, Main manuscript + Supplementary Materia

Effect of Carbon Nanotubes on the Na+ Intercalation Capacity of Binder Free Mn2V2O7-CNTs Electrode: A Structural Investigation

Improvements in sodium intercalation in sodium cathodes have been debated in recent years. In the present work, we delineate the significant effect of the carbon nanotubes (CNTs) and their weight percent in the intercalation capacity of the binder-free manganese vanadium oxide (MVO)-CNTs composite electrodes. The performance modification of the electrode is discussed taking into account the cathode electrolyte interphase (CEI) layer under optimal performance. We observe an intermittent distribution of the chemical phases on the CEI, formed on these electrodes after several cycles. The bulk and superficial structure of pristine and Na+ cycled electrodes were identified via micro-Raman scattering and Scanning X-ray Photoelectron Microscopy. We show that the inhomogeneous CEI layer distribution strongly depends on the CNTs weight percentage ratio in an electrode nano-composite. The capacity fading of MVO-CNTs appears to be associated with the dissolution of the Mn2O3 phase, leading to electrode deterioration. This effect is particularly observed in electrodes with low weight percentage of the CNTs in which the tubular topology of the CNTs are distorted due to the MVO decoration. These results can deepen the understanding of the CNTs role on the intercalation mechanism and capacity of the electrode, where there are variations in the mass ratio of CNTs and the active material

Contactless monitoring of the diameter-dependent conductivity of GaAs nanowires

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Chemical exfoliation of MoS2 leads to semiconducting 1T' phase and not the metallic 1T phase

A trigonal phase existing only as small patches on chemically exfoliated few layer, thermodynamically stable 1H phase of MoS2 is believed to influence critically properties of MoS2 based devices. This phase has been most often attributed to the metallic 1T phase. We investigate the electronic structure of chemically exfoliated MoS2 few layered systems using spatially resolved (lesser than 120 nm resolution) photoemission spectroscopy and Raman spectroscopy in conjunction with state-of-the-art electronic structure calculations. On the basis of these results, we establish that the ground state of this phase is a small gap (~90 meV) semiconductor in contrast to most claims in the literature; we also identify the specific trigonal (1T') structure it has among many suggested ones