129 research outputs found

    Influence of the electrode nano/microstructure on the electrochemical properties of graphite in aluminum batteries

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    Herein we report on a detailed investigation of the irreversible capacity in the first cycle of pyrolytic graphite electrodes in aluminum batteries employing 1-ethyl-3-methylimidazolium chloride:aluminum trichloride (EMIMCl:AlCl3) as electrolyte. The reaction mechanism, involving the intercalation of AlCl4- in graphite, has been fully characterized by correlating the micro/nanostructural modification to the electrochemical performance. To achieve this aim a combination of X-ray diffraction (XRD), small angle X-ray scattering (SAXS) and computed tomography (CT) has been used. The reported results evidence that the irreversibility is caused by a very large decrease in the porosity, which consequently leads to microstructural changes resulting in the trapping of ions in the graphite. A powerful characterization methodology is established, which can also be applied more generally to carbon-based energy-related materials

    Calibration of the GLAST Burst Monitor detectors

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    The GLAST Burst Monitor (GBM) will augment the capabilities of GLAST for the detection of cosmic gamma-ray bursts by extending the energy range (20 MeV to > 300 GeV) of the Large Area Telescope (LAT) towards lower energies by 2 BGO-detectors (150 keV to 30 MeV) and 12 NaI(Tl) detectors (10 keV to 1 MeV). The physical detector response of the GBM instrument for GRBs is determined with the help of Monte Carlo simulations, which are supported and verified by on-ground calibration measurements, performed extensively with the individual detectors at the MPE in 2005. All flight and spare detectors were irradiated with calibrated radioactive sources in the laboratory (from 14 keV to 4.43 MeV). The energy/channel-relations, the dependences of energy resolution and effective areas on the energy and the angular responses were measured. Due to the low number of emission lines of radioactive sources below 100 keV, calibration measurements in the energy range from 10 keV to 60 keV were performed with the X-ray radiometry working group of the Physikalisch-Technische Bundesanstalt (PTB) at the BESSY synchrotron radiation facility, Berlin.Comment: 2 pages, 1 figure; to appear in the Proc. of the First Int. GLAST Symp. (Stanford, Feb. 5-8, 2007), eds. S.Ritz, P.F.Michelson, and C.Meegan, AIP Conf. Pro

    Influence of the electrode nano microstructure on the electrochemical properties of graphite in aluminum batteries

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    Herein we report on a detailed investigation of the irreversible capacity in the first cycle of pyrolytic graphite electrodes in aluminum batteries employing 1 ethyl 3 methylimidazolium chloride aluminum trichloride EMIMCl AlCl3 as electrolyte. The reaction mechanism, involving the intercalation of AlCl4 in graphite, 3 has been fully characterized by correlating the micro nano modification to the electrochemical performance. To achieve this aim a combination of X ray diffraction XRD , small angle X ray scattering SAXS and computed tomography CT has been used. The reported results evidence that the irreversibility is caused by a very large decrease in the porosity, which consequently leads to microstructural changes resulting in the trapping of ions in the graphite. A powerful characterization methodology is established, which can also be applied more generally to carbon based energy related material

    An accurate determination of the Avogadro constant by counting the atoms in a 28Si crystal

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    The Avogadro constant links the atomic and the macroscopic properties of matter. Since the molar Planck constant is well known via the measurement of the Rydberg constant, it is also closely related to the Planck constant. In addition, its accurate determination is of paramount importance for a definition of the kilogram in terms of a fundamental constant. We describe a new approach for its determination by "counting" the atoms in 1 kg single-crystal spheres, which are highly enriched with the 28Si isotope. It enabled isotope dilution mass spectroscopy to determine the molar mass of the silicon crystal with unprecedented accuracy. The value obtained, 6.02214084(18) x 10^23 mol^-1, is the most accurate input datum for a new definition of the kilogram.Comment: 4 pages, 5 figures, 3 table

    Dynamics of nonequilibrium quasiparticles in a double superconducting tunnel junction detector

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    We study a class of superconductive radiation detectors in which the absorption of energy occurs in a long superconductive strip while the redout stage is provided by superconductive tunnel junctions positioned at the two ends of the strip. Such a device is capable both of imaging and energy resolution. In the established current scheme, well studied from the theoretical and experimental point of view, a fundamental ingredient is considered the presence of traps, or regions adjacent to the junctions made of a superconducting material of lower gap. We reconsider the problem by investigating the dynamics of the radiation induced excess quasiparticles in a simpler device, i.e. one without traps. The nonequilibrium excess quasiparticles can be seen to obey a diffusion equation whose coefficients are discontinuous functions of the position. Based on the analytical solution to this equation, we follow the dynamics of the quasiparticles in the device, predict the signal formation of the detector and discuss the potentiality offered by this configuration.Comment: 16 pages, 5 figures Submitted to Superconducting Science and Technolog

    Scatterometry reference standards to improve tool matching and traceability in lithographical nanomanufacturing

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    High quality scatterometry standard samples have been developed to improve the tool matching between different scatterometry methods and tools as well as with high resolution microscopic methods such as scanning electron microscopy or atomic force microscopy and to support traceable and absolute scatterometric critical dimension metrology in lithographic nanomanufacturing. First samples based on one dimensional Si or on Si 3 N 4 grating targets have been manufactured and characterized for this purpose. The etched gratings have periods down to 50 nm and contain areas of reduced density to enable AFM measurements for comparison. Each sample contains additionally at least one large area scatterometry target suitable for grazing incidence small angle X ray scattering. We present the current design and the characterization of structure details and the grating quality based on AFM, optical, EUV and X Ray scatterometry as well as spectroscopic ellipsometry measurements. The final traceable calibration of these standards is currently performed by applying and combining different scatterometric as well as imaging calibration methods. We present first calibration results and discuss the final design and the aimed specifications of the standard samples to face the tough requirements for future technology nodes in lithography

    Direct Observation of the Xenon Physisorption Process in Mesopores by Combining In Situ Anomalous Small Angle X ray Scattering and X ray Absorption Spectroscopy

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    The morphology and structural changes of confined matter are still far from being understood. This report deals with the development of a novel in situ method based on the combination of anomalous small angle X ray scattering ASAXS and X ray absorption near edge structure XANES spectroscopy to directly probe the evolution of the xenon adsorbate phase in mesoporous silicon during gas adsorption at 165 K. The interface area and size evolution of the confined xenon phase were determined via ASAXS demonstrating that filling and emptying the pores follow two distinct mechanisms. The mass density of the confined xenon was found to decrease prior to pore emptying. XANES analyses showed that Xe exists in two different states when confined in mesopores. This combination of methods provides a smart new tool for the study of nanoconfined matter for catalysis, gas, and energy storage application

    Improved measurement results for the Avogadro constant using a 28Si-enriched crystal

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    New results are reported from an ongoing international research effort to accurately determine the Avogadro constant by counting the atoms in an isotopically enriched silicon crystal. The surfaces of two 28Si-enriched spheres were decontaminated and reworked in order to produce an outer surface without metal contamination and improved sphericity. New measurements were then made on these two reconditioned spheres using improved methods and apparatuses. When combined with other recently refined parameter measurements, the Avogadro constant derived from these new results has a value of NA=6.02214076(12)×1023N_A = 6.022 140 76(12) \times 10^{23} mol1^{-1}. The X-ray crystal density method has thus achieved the target relative standard uncertainty of 2.0×1082.0 \times 10^{-8} necessary for the realization of the definition of the new kilogram.Comment: postprint, 22 page, 3 figures, 14 table

    Ground-based calibration and characterization of the Fermi Gamma-Ray Burst Monitor Detectors

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    One of the scientific objectives of NASA's Fermi Gamma-ray Space Telescope is the study of Gamma-Ray Bursts (GRBs). The Fermi Gamma-Ray Burst Monitor (GBM) was designed to detect and localize bursts for the Fermi mission. By means of an array of 12 NaI(Tl) (8 keV to 1 MeV) and two BGO (0.2 to 40 MeV) scintillation detectors, GBM extends the energy range (20 MeV to > 300 GeV) of Fermi's main instrument, the Large Area Telescope, into the traditional range of current GRB databases. The physical detector response of the GBM instrument to GRBs is determined with the help of Monte Carlo simulations, which are supported and verified by on-ground individual detector calibration measurements. We present the principal instrument properties, which have been determined as a function of energy and angle, including the channel-energy relation, the energy resolution, the effective area and the spatial homogeneity.Comment: 36 pages, 28 figures, accepted for publication in Experimental Astronom

    Hollow organosilica beads as reference particles for optical detection of extracellular vesicles

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    Background: The concentration of extracellular vesicles (EVs) in body fluids is a promising biomarker for disease, and flow cytometry remains the clinically most applicable method to identify the cellular origin of single EVs in suspension. To compare concentration measurements of EVs between flow cytometers, solid polystyrene reference beads and EVs were distributed in the first ISTH organized inter-laboratory comparison studies. The beads were used to set size gates based on light scatter, and the concentration of EVs was measured within the size gates. However, polystyrene beads lead to false size determination of EVs due to the mismatch in refractive index between beads and EVs. Moreover, polystyrene beads gate different EV sizes on different flow cytometers. Objective: To prepare, characterize and test hollow organosilica beads (HOBs) as reference beads to set EV size gates in flow cytometry investigations. Methods: HOBs were prepared by a hard template sol-gel method and extensively characterized for morphology, size and colloidal stability. The applicability of HOBs as reference particles was investigated by flow cytometry using HOBs and platelet-derived EVs. Results: HOBs proved monodisperse with homogeneous shell thickness. Two angle light scattering measurements by flow cytometry confirmed that HOBs have light scattering properties similar to platelet-derived EVs. Conclusions: Because HOBs resemble the structure and light scattering properties of EVs, HOBs with a given size will gate EVs of the same size. Therefore, HOBs are ideal reference beads to standardize optical measurements of the EV concentration within a predefined size range
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