The density of badger setts in a natural river corridor (NE Italy)

The European badger Meles meles (Linnaeus, 1758) is a common semifossorial mustelid species widely distributed throughout Europe. It also shows a high degree of plasticity, adapting its spatial and temporal behaviour to live in highly disturbed environments. Badgers live in social groups occupying underground systems called setts, which could be classified as “main” (i.e., the complex systems with a great number of entrances), and as “outliers”, “annexes” and “subsidiary” (i.e., the other burrows with a low number of entrances). An extensive scientific literature occurs on the ecology and biology of this species, and some information is available also for setts density in Europe and in Italy, too. However, since badgers may inhabit a wide variety of habitats, the setts density varies significantly both locally and on a large scale. We aimed to provide setts density in a river basin in the North-East of Italy. From January to March 2022, a sett survey was conducted in the eastern plain of Friuli Venezia Giulia Region (NE Italy), along the floodplains of the lowest reaches of Isonzo/Soca river basin, from Pavia di Udine (Torre river) to the Isonzo river mouth, a natural corridor surrounded by a highly human-modified matrix. Transects to collect setts information were made in the entire area of 27.82 km2 by two or three operators. For each sett, we recorded the geo-referenced location, the type (main, subsidiary and outliers), the habitat, and the number of entrances. To estimate the density, we only considered active main setts, dividing their number by the area. A total of 22 main setts were identified within the floodplains, corresponding to a density of 0.79 setts/km2. The mean number of entrances was 13.67 (min: 5, max: 28) and they were mainly recorded in forested patches (riverine forests and transitional woodlands-shrublands). We founded other 14 subsidiaries and 13 outliers setts. The density estimated in our study area is remarkably high compared to those estimated in similar environmental conditions (e.g., Po plain area, NW Italy), but considerably lower than those reported for natural habitats (e.g., Alpine area). Even if we did not specifically analyse habitat selection of the badger for the location of setts, our results confirm the importance of the forested area and specifically riverine forests for the badgers in agricultural matrices. Furthermore, it is known that several mammals use the complex burrow system of the European badger as shelter or as a reproductive site. In a highly fragmented and disturbed area, the high density of badger setts could favour the expansion and the survival of other species, some of which are of conservation interest (e.g., European wildcat Felis silvestris and golden jackal Canis aureus) and some other invasive species (e.g., the raccoon dog Nyctereutes procyonoides)

Mobile setup for synchrotron based in situ characterization during thermal and plasma-enhanced atomic layer deposition

We report the design of a mobile setup for synchrotron based in situ studies during atomic layer processing. The system was designed to facilitate in situ grazing incidence small angle x-ray scattering (GISAXS), x-ray fluorescence (XRF), and x-ray absorption spectroscopy measurements at synchrotron facilities. The setup consists of a compact high vacuum pump-type reactor for atomic layer deposition (ALD). The presence of a remote radio frequency plasma source enables in situ experiments during both thermal as well as plasma-enhanced ALD. The system has been successfully installed at different beam line end stations at the European Synchrotron Radiation Facility and SOLEIL synchrotrons. Examples are discussed of in situ GISAXS and XRF measurements during thermal and plasma-enhanced ALD growth of ruthenium from RuO4 (ToRuS™, Air Liquide) and H2 or H2 plasma, providing insights in the nucleation behavior of these processes

EXAFS analysis of the L3 edge of Ce in CeO2: effects of multi‐electron excitations and final‐state mixed valence

Cerium oxide (IV) (CeO2) is extensively employed in heterogeneous catalysis, particularly as a promoter of noble metal action in three-way catalysts. For this reason there is a great scientific and economical interest in the development of any possible chemical or structural analysis technique that could provide information on these systems. EXAFS spectroscopy has revealed itself as a powerful technique for structural characterization of such catalysts. Unfortunately, good quality K-edge spectra of cerium are not yet easily obtainable because of the high photon energy required (>40 keV). On the other hand, at lower energies it is easy to collect very good spectra of the L3 edge (5.5 keV), but L3-edge spectra of cerium (IV) are characterized by the presence of two undesired additional phenomena that interfere with EXAFS analysis: final-state mixed-valence behaviour and intense multi-electron excitations. Here, a comparative analysis of the K, L3, L2 and L1 edges of Ce in CeO2 has been made and a procedure for obtaining structural parameters from L3-edge EXAFS, even in the presence of these features, has been developed. This procedure could allow further studies of catalytic compounds containing tetravalent cerium surrounded by oxygen ligands

A Novel Electrochemical Flow-Cell for Operando XAS Investigations On X-ray Opaque Supports

Improvement of electrochemical technologies is one of the most popular topics in the field of renewable energy. However, this process requires a deep understanding of the electrode electrolyte interface behavior under operando conditions. X-ray absorption spectroscopy (XAS) is widely employed to characterize electrode materials, providing element-selective oxidation state and local structure. Several existing cells allow studies as close as possible to realistic operating conditions, but most of them rely on the deposition of the electrodes on conductive and X-ray transparent materials, from where the radiation impinges the sample. In this work, we present a new electrochemical flow-cell for operando XAS that can be used with X-ray opaque substrates, since the signal is effectively detected from the electrode surface, as the radiation passes through a thin layer of electrolyte. The electrolyte can flow over the electrode, reducing bubble formation and avoiding strong reactant concentration gradients. We show that high-quality data can be obtained under operando conditions, thanks to the high efficiency of the cell from the hard X-ray regime down to 4 keV. We report as a case study the operando XAS investigation at the Fe and Ni K-edges on Ni-doped maghemite films, epitaxially grown on Pt substrates. The effect of the Ni content on the catalytic performances for the oxygen evolution reaction is discussed.Comment: 11 pages, 9 figures, available supporting informatio

Nanostructured Pd\u2013Pt nanoparticles: evidences of structure/performance relations in catalytic H2production reactions

A widespread approach to modulate the performances of heterogeneous catalysts is the use of bimetallic nanoparticles (NPs) as the active phase. However, studying the relationship between the NPs structure and catalytic properties requires well-defined systems, having uniform composition, size and nanostructure, which cannot be achieved by traditional methods (e.g. impregnation). Here, we developed wet-chemistry synthetic routes to prepare PdPt NPs or Pt-core@Pd-shell NPs of small size and well-controlled composition and structure, protected by mercaptoundecanoic acid (MUA) moieties. The pristine NPs were tested for H2 production by NH3BH3 hydrolysis, in order to systematically investigate the effect of composition and of synthetic route on the activity of the systems. Depending on the preparation method, two distinct trends of activity were observed, rationalized in terms of the extent of surface functionalization by MUA. The MUA protective layer was found to effectively stabilize the NPs dispersion while maintaining high activity in certain cases (Pt-rich NPs), and was demonstrated to be essential for catalyst recycling. In order to further study structure-activity relationships of PdPt NPs after ligand removal, nanostructured PdPt@CeO2-based catalysts were prepared by self-assembly route. Regardless of the starting NPs structure (alloy or core-shell), similar water gas shift reaction performances were observed, due to the structural rearrangements occurring upon oxidation and reduction thermal treatments, which led to the formation of Pt-rich core@PdPt-shell under reducing conditions

Size- and composition-controlled Pt–Sn bimetallic nanoparticles prepared by atomic layer deposition

Pt-Sn bimetallic nanoparticles (BMNPs) are used in a variety of catalytic reactions and are widely accepted as a model system for Pt-based bimetallics in fundamental catalysis research. Here, Pt-Sn BMNPs were prepared via a two-step synthesis procedure combining atomic layer deposition (ALD) and temperature programmed reduction (TPR). In situ X-ray diffraction measurements during TPR and ex situ X-ray absorption spectroscopy at the Pt L-III-edge revealed the formation of Pt-Sn bimetallic alloys with a phase determined by the Pt/(Pt + Sn) atomic ratio of the as-deposited bilayer. The size of the BMNPs could be tuned by changing the total thickness of the bilayers, while keeping the Pt/(Pt + Sn) atomic ratio constant. Due to the exceptional control over BMNP size and crystalline phase, the proposed method will enable highly systematic studies of the relation between the structure and the performance of Pt-Sn bimetallic catalysts

Active and Stable Embedded Au@CeO2 Catalysts for Preferential Oxidation of CO

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Visible-light-driven coproduction of diesel precursors and hydrogen from lignocellulose-derived methylfurans

Photocatalytic hydrogen production from biomass is a promising alternative to water splitting thanks to the oxidation half-reaction being more facile and its ability to simultaneously produce solar fuels and value-added chemicals. Here, we demonstrate the coproduction of H2 and diesel fuel precursors from lignocellulose-derived methylfurans via acceptorless dehydrogenative C 12C coupling, using a Ru-doped ZnIn2S4 catalyst and driven by visible light. With this chemistry, up to 1.04\u2009g\u2009gcatalyst 121\u2009h 121 of diesel fuel precursors (~41% of which are precursors of branched-chain alkanes) are produced with selectivity higher than 96%, together with 6.0\u2009mmol\u2009gcatalyst 121\u2009h 121 of H2. Subsequent hydrodeoxygenation reactions yield the desired diesel fuels comprising straight- and branched-chain alkanes. We suggest that Ru dopants, substituted in the position of indium ions in the ZnIn2S4 matrix, improve charge separation efficiency, thereby accelerating C 12H activation for the coproduction of H2 and diesel fuel precursors