279 research outputs found

    Effects of the restoration actions to combat desertification on soils: the practice project study site in Pula (Sardinia, Italy)

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    Land Degradation and Desertification affect much of the world’s drylands, resulting in a significant loss of biological and economic productivity. Responding to desertification by improving the efficiency of land and resource management represents a crucial step towards social welfare in drylands. However, the evaluation of the actions to combat desertification remains limited. The PRACTICE EC-FP7 project develops and tests integrated evaluation protocols to assess the effectiveness of restoration practices in a network of study sites distributed among the most LD affected regions of the world

    Seismic Station Installations and Their Impact on the Recorded Signals and Derived Quantities

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    The role of local geology in controlling ground motion has long been acknowledged. Consequently, increasing attention is paid to the assessment of the geophysical properties of the soils at the seismic stations, which impact the station recordings and a series of related quantities, particularly those referring to seismic hazard estimates. Not the same level of attention is commonly dedicated to the seismic station installation, to the point that it is generally believed that housings and shelters containing seismic instruments are of no interest, because they can only affect frequencies well above the engineering range of interest. Using examples from seismometric and accelerometric stations, we describe the (1) housing, (2) foundation, and (3) pillar effects on the seismic records. We propose a simple working scheme to identify the existence of potential installation-related issues and to assess the frequency fidelity range of response of a seismic station to ground motion. Our scheme is developed mostly on ambient noise recordings and, thus, surface waves. The hope is that, besides the parameters that start to be routinely introduced in the seismic archives (VS30, soil classes, etc.), the assessment of the maximum reliable frequency, under which no soil–structure interaction is expected, also becomes a mandatory information. In our experience, for some installation sites, the maximum reliable frequency can even be less than a very few hert

    Morphology and luminescence of nanocrystalline Nb<sub>2</sub>O<sub>5</sub> doped with Eu<sup>3+</sup>

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    The synthesis of nanocrystalline Nb2O5:Eu3+ has been achieved by using a Pechini procedure. The obtained materials are single-phase niobia with the orthorhombic structure, average crystallite size around 25nm and average lattice strain of about 0.002. TEM images show that the particles are rectangular and reasonably isolated. The luminescence of the Eu3+ ions in the niobia lattice is efficient and affected by a strong inhomogeneous broadening, due to an important disorder around the lanthanide ions

    Correlated electron-hole plasma in organometal perovskites

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    Organic-inorganic perovskites are a class of solution-processed semiconductors holding promise for the realization of low-cost efficient solar cells and on-chip lasers. Despite the recent attention they have attracted, fundamental aspects of the photophysics underlying device operation still remain elusive. Here we use photoluminescence and transmission spectroscopy to show that photoexcitations give rise to a conducting plasma of unbound but Coulomb-correlated electron-hole pairs at all excitations of interest for light-energy conversion and stimulated optical amplification. The conductive nature of the photoexcited plasma has crucial consequences for perovskite-based devices: in solar cells, it ensures efficient charge separation and ambipolar transport while, concerning lasing, it provides a low threshold for light amplification and justifies a favourable outlook for the demonstration of an electrically driven laser. We find a significant trap density, whose cross-section for carrier capture is however low, yielding a minor impact on device performance

    Defect-assisted synthesis of magneto-plasmonic silver-spinel ferrite heterostructures in a flower-like architecture

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    Artificial nano-heterostructures (NHs) with controlled morphology, obtained by combining two or more components in several possible architectures, make them suitable for a wide range of applications. Here, we propose an oleate-based solvothermal approach to design silver-spinel ferrite flower-like NHs. Small oleate-coated silver nanoparticles were used as seeds for the growth of magnetic spinel ferrite (cobalt ferrite and spinel iron oxide) nanodomains on their surface. With the aim of producing homogeneous flower-like heterostructures, a careful study of the effect of the concentration of precursors, the reaction temperature, the presence of water, and the chemical nature of the spinel ferrite was carried out. The magnetic and optical properties of the NHs were also investigated. A heterogeneous growth of the spinel ferrite phase on the silver nanoparticles, through a possible defect-assisted mechanism, was suggested in the light of the high concentration of stacking faults (intrinsic and twins) in the silver seeds, revealed by Rietveld refinement of powder X-ray diffraction patterns and High-Resolution electron microscopy

    Magnetic properties of cobalt ferrite-silica nanocomposites prepared by a sol-gel autocombustion technique

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    The magnetic properties of cobalt ferrite-silica nanocomposites with different concentrations (15, 30, and 50 wt %) and sizes (7, 16, and 28 nm) of ferrite particles have been studied by static magnetization measurements and Mossbauer spectroscopy. The results indicate a superparamagnetic behavior of the nanoparticles, with weak interactions slightly increasing with the cobalt ferrite content and with the particle size. From high-field Mossbauer spectra at low temperatures, the cationic distribution and the degree of spin canting have been estimated and both parameters are only slightly dependent on the particle size. The magnetic anisotropy constant increases with decreasing particle size, but in contrast to many other systems, the cobalt ferrite nanoparticles are found to have an anisotropy constant that is smaller than the bulk value. This can be explained by the distribution of the cations. The weak dependence of spin canting degree on particle size indicates that the spin canting is not simply a surface phenomenon but also occurs in the interiors of the particles. (c) 2006 American Institute of Physics

    Core-shell nano-architectures: the incorporation mechanism of hydrophobic nanoparticles into the aqueous core of a microemulsion

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    This work presents an in-depth investigation of the molecular interactions in the incorporation mechanism of colloidal hydrophobic-capped nanoparticles into the hydrophilic core of reverse microemulsions. 1H Nuclear Magnetic Resonance (NMR) was employed to obtain molecular level details of the interaction between the nanoparticles capping amphiphiles and the microemulsion surfactants. The model system of choice involved oleic acid (OAC) and oleylamine (OAM) as capping molecules, while igepal-CO520 was the surfactant. The former were studied both in their ‘‘free’’ state and ‘‘ligated’’ one, i.e., bound to nanoparticles. The latter was investigated either in cyclohexane (micellar solution) or in water/cyclohexane microemulsions. The approach was extremely useful to gain a deeper understanding of the equilibria involved in this complex system (oleic acid capped-Bi2S3 in igepal/water/cyclohexane microemulsions). In difference to previously proposed mechanisms, the experimental data showed that the high affinity of the capping ligands for the reverse micelle interior was the driving force for the incorporation of the nanoparticles. A simple ligand-exchange mechanism could be ruled out. The collected information about the nanoparticle incorporation mechanism is extremely useful to develop new synthetic routes with an improved/tuned coating efficiency, in order to tailor the core–shell structure preparation

    The sulphate ion in aqueous solution: an X-ray diffraction study of a ZnSO 4

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    The interplay between single particle anisotropy and interparticle interactions in ensembles of magnetic nanoparticles

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    This paper aims to analyze the competition of single particle anisotropy and interparticle interactions in nanoparticle ensembles using a random anisotropy model. The model is first applied to ideal systems of non-interacting and strongly dipolar interacting ensembles of maghemite nanoparticles. The investigation is then extended to more complex systems of pure cobalt ferrite CoFe2O4 (CFO) and mixed cobalt-nickel ferrite (Co,Ni)Fe2O4 (CNFO) nanoparticles. Both samples were synthetized by the polyol process and exhibit the same particle size (DTEM 48 5 nm), but with different interparticle interaction strengths and single particle anisotropy. The implementation of the random anisotropy model allows investigation of the influence of single particle anisotropy and interparticle interactions, and sheds light on their complex interplay as well as on their individual contribution. This analysis is of fundamental importance in order to understand the physics of these systems and to develop technological applications based on concentrated magnetic nanoparticles, where single and collective behaviors coexist

    Colloidal synthesis and characterization of Bi2S3 nanoparticles for photovoltaic applications

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    Bismuth sulfide is a promising n-type semiconductor for solar energy conversion. We have explored the colloidal synthesis of Bi2S3 nanocrystals, with the aim of employing them in the fabrication of solution-processable solar cells and to replace toxic heavy metals chalcogenides like PbS or CdS, that are currently employed in such devices. We compare different methods to obtain Bi2S3 colloidal quantum dots, including the use of environmentally benign reactants, through organometallic synthesis. Different sizes and shapes were obtained according to the synthesis parameters and the growth process has been rationalized by comparing the predicted morphology with systematic physical-chemistry characterization of nanocrystals by X-ray diffraction, FT-IR spectroscopy, Transmission Electron Microscopy (TEM)
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