336 research outputs found
Modulated excitation extended X-ray absorption fine structure spectroscopy
The sensitivity of extended X-ray absorption fine structure spectroscopy (EXAFS) for minute structural
changes can be enhanced by combination with the modulated excitation approach and making use of
phase sensitive analysis. A modulated EXAFS experiment of a reversible periodic Pd to PdO partial oxidation
has been simulated in order to understand the effect of the phase sensitive analysis on the shape and
meaning of the resulting phase-resolved EXAFS spectra. In particular, the simulation comprises either a
synchronous or a delayed sinusoidal variation of the EXAFS parameters, i.e. coordination number (N),
interatomic distance (R) and Debye\u2013Waller factor (s2
), of first Pd\u2013Pd, first Pd\u2013O, and second Pd\u2013(O)\u2013Pd
coordination shells. The effect of these variations on the resulting phase-resolved Fourier transform EXAFS
spectra is discussed. The results of the simulation are validated by an in situ EXAFS experiment at the
Pd K-edge over 1.6 wt% Pd/Al2O3 undergoing reversible partial oxidation in a H2 vs. O2 modulation at 573 K.
It is shown that phase sensitive detection (PSD) is able to separate the minor contribution at ca. 2.8 \uc5
corresponding to the growth of the Pd\u2013(O)\u2013Pd shell that is otherwise hidden under the static signal of the
Pd\u2013Pd shell of reduced Pd particles. The fitting of the phase-resolved EXAFS spectra suggests that the fast
H2 to O2 switch leads the partial oxidation of the Pd surface with the formation of a PdO shell covering a
metallic Pd core. Therefore, the dynamics of the full system can be described with greater detail than in
conventional EXAFS. The intention of this work is to provide the tools and therefore a solid guidance to
qualitatively and quantitatively understand the nature of the shape of phase-resolved FT-EXAFS spectra that
may prove helpful in the analysis of a wide range of functional materials
In situ attenuated total reflection infrared spectroscopy study of the photocatalytic steam reforming of methanol on Pt/TiO2
The effect of Pt deposition on TiO2 and of Pt particle size on the photocatalytic steam reforming of methanol was studied by in situ attenuated total reflectance infrared spectroscopy (ATR-IR). Two 0.5 wt.% Pt/TiO2 samples were investigated, one possessing Pt nanoparticles of ca. 4 nm mean size, the other Pt clusters of ca. 1.3 nm mean size showing significantly different photoactivity in terms of both hydrogen production rate and selectivity to CO, CO2 and all other by-products. The presence of Pt nanoparticles strongly affected both the adsorption/desorption and the reactivity properties of the TiO2 surface. Moreover, the variation of the IR spectrum background upon UV\u2013vis irradiation proved that the photopromoted
electrons can be trapped by the Pt particles with the consequent increase of electron-hole separation.
Reducing the Pt size from nanoparticles to clusters increased the rate of methanol and water absorption and hindered the detrimental formation of irreversibly adsorbed CO on Pt. All of these aspects contribute to increase the photocatalytic performance of Pt cluster-decorated TiO2 with respect to Pt nanoparticles containing TiO2. Finally, prolonged exposure of all samples to methanol/water vapour in the dark led to the formation of unreactive formate which persisted also under UV\u2013vis irradiation. By contrast, this spectator species did not form when the sample was exposed to methanol/water vapour
under UV\u2013vis irradiation
Quantum statistical information contained in a semi-classical Fisher--Husimi measure
We study here the difference between quantum statistical treatments and
semi-classical ones, using as the main research tool a semi-classical,
shift-invariant Fisher information measure built up with Husimi distributions.
Its semi-classical character notwithstanding, this measure also contains
information of a purely quantal nature.
Such a tool allows us to refine the celebrated Lieb bound for Wehrl entropies
and to discover thermodynamic-like relations that involve the degree of
delocalization. Fisher-related thermal uncertainty relations are developed and
the degree of purity of canonical distributions, regarded as mixed states, is
connected to this Fisher measure as well.Comment: 9 pages, 3 figures; chenged conten
Operando XANES study of simulated transient cycles on a Pd-only three-way catalyst
A model Pd-only three-way catalyst has been subjected to simulated driving conditions of natural gas and gasoline operation in an operando reactor cell for X-ray absorption spectroscopy that included alternated, but longer than real oscillations, rich and lean periods and a high temperature surge (850\u2013900 \ub0C). The X-ray absorption near edge structure (XANES) spectra indicated that metallic palladium is observed in the whole temperature range investigated (up to 900 \ub0C) and irrespective of the air/fuel ratio. In both natural gas and gasoline cycles, the XANES data show that the PdO reduced in the rich periods cannot be restored in the lean periods. With this background, activity for methane abatement in the high temperature regime is greatly affected by the oxidation state of palladium rather than by the change of air/fuel ratio. In the case of propene oxidation, while Pd also remains predominantly in the reduced state, activity is dictated by the oxygen concentration in the feedstock. Comparison between the two hydrocarbons demonstrates that the oxidation state of Pd may be responsible for observed methane emissions under realistic operating circumstances. Moreover, the experiments demonstrate that reduced Pd may be continuously present during operation in agreement with observations on real catalytic converters. Although this may be the average oxidation state of Pd, more advanced probes are certainly necessary to capture variations of oxidation state under the fast oscillatory conditions needed to imitate real operation
Synchrotron high energy X-ray methods coupled to phase sensitive analysis to characterize aging of solid catalysts with enhanced sensitivity
X-ray absorption spectroscopy and X-ray diffraction are suitable probes of the chemical state of a catalyst under working conditions but are limited to bulk information. Here we show in two case studies related to hydrothermal aging and chemical modification of model automotive catalysts that enhanced detailed information of structural changes can be obtained when the two methods are combined with a concentration modulated excitation (cME) approach and phase sensitive detection (PSD). The catalysts are subject to a modulation experiment consisting of the periodic variation of the gas feed composition to the catalyst and the time-resolved data are additionally treated by PSD. In the case of a 2 wt% Rh/Al2O3 catalyst, a very small fraction (ca. 2%) of Rh remaining exposed at the alumina surface after hydrothermal aging at 1273 K can be detected by PSD. This Rh is sensitive to the red-ox oscillations of the experiment and is likely responsible for the observed catalytic activity and selectivity during NO reduction by CO. In the case of a 1.6 wt% Pd/Al2O3-Ce1-xZrxO2 catalyst, preliminary results of cME-XRD demonstrate that access to the kinetics of the whole material at work can be obtained. Both the red-ox processes involving the oxygen storage support and the Pd component can be followed with great precision. PSD enables the differentiation between Pd deposited on Al2O3 or on Ce1-xZrxO2. Modification of the catalyst by phosphorous clearly induces loss of the structural dynamics required for oxygen storage capacity that is provided by the Ce4+/Ce3+ pair. The two case studies demonstrate that detailed kinetics of subtle changes can be uncovered by the combination of in situ X-ray absorption and high energy diffraction methods with PSD
Observation of long ionizing tracks with the ICARUS T600 first half-module
F. Arneodo, B. Bade"ek, A. Badertscher, B. Baiboussinov, M. Baldo Ceolin, G. Battistoni, B. Bekman, P. Benetti, E. Bernardini, M. Bischofberger, A. Borio di Tigliole, R. Brunetti, A. Bueno, E. Calligarich, M. Campanelli, C. Carpanese, D. Cavalli, F. Cavanna, P. Cennini, S. Centro, A. Cesana, C. Chen, D. Chen, D.B. Chen, Y. Chen, D. Cline, Z. Dai, C. De Vecchi, A. Dabrowska, R. Dolfini*, M. Felcini, A. Ferrari, F. Ferri, Y. Ge, A. Gigli Berzolari, I. Gil-Botella, K. Graczyk, L. Grandi, K. He, J. Holeczek, X. Huang, C. Juszczak, D. Kie"czewska, J. Kisiel, T. Koz"owski, H. Kuna-Ciska", M. Laffranchi, J. Łagoda, Z. Li, F. Lu, J. Ma, M. Markiewicz, A. Martinez de la Ossa, C. Matthey, F. Mauri, D. Mazza, G. Meng, M. Messina, C. Montanari, S. Muraro, S. Navas-Concha, M. Nicoletto, G. Nurzia, S. Otwinowski, Q. Ouyang, O. Palamara, D. Pascoli, L. Periale, G. Piano Mortari, A. Piazzoli, P. Picchi, F. Pietropaolo, W. P ! o"ch"opek, T. Rancati, A. Rappoldi, G.L. Raselli, J. Rico, E. Rondio, M. Rossella, A. Rubbia, C. Rubbia, P. Sala, D. Scannicchio, E. Segreto, F. Sergiampietri, J. Sobczyk, J. Stepaniak, M. Szeptycka, M. Szleper, M. Szarska, M. Terrani, S. Ventura, C. Vignoli, H. Wang, M. W ! ojcik, J. Woo, G. Xu, Z. Xu, A. Zalewska, J. Zalipska, C. Zhang, Q. Zhang, S. Zhen, W. Zipper a INFN Laboratori Nazionali del Gran Sasso, s.s. 17bis Km 18+910, Assergi (L'Aquila), Italy b Institute of Experimental Physics, Warsaw University, Warszawa, Poland c Institute for Particle Physics, ETH H . onggerberg, Z . urich, Switzerland Dipartimento di Fisica e INFN, Universit " a di Padova, via Marzolo 8, Padova, Italy Dipartimento di Fisica e INFN, Universit " a di Milano, via Celoria 16, Milano, Italy f Institute of Physics, University of Silesia, Katowice, Poland Dipartimento di Fisica e INFN, Universit " a di Pavia, via Bassi 6, Pavia, Italy Dpto de F!isica Te ! orica y del Cosmos & C.A.F.P.E., Universidad de Granada, Avda. Severo Ochoa s/n, Granada, Spain Dipartimento di Fisica e INFN, Universit " a dell'Aquila, via Vetoio, L'Aquila, Italy CERN, CH-1211 Geneva 23, Switzerland Politecnico di Milano (CESNEF), Universit " a di Milano, via Ponzio 34/3, Milano, Ital
Scientific rationale for Uranus and Neptune <i>in situ</i> explorations
The ice giants Uranus and Neptune are the least understood class of planets in our solar system but the most frequently observed type of exoplanets. Presumed to have a small rocky core, a deep interior comprising ∼70% heavy elements surrounded by a more dilute outer envelope of H2 and He, Uranus and Neptune are fundamentally different from the better-explored gas giants Jupiter and Saturn. Because of the lack of dedicated exploration missions, our knowledge of the composition and atmospheric processes of these distant worlds is primarily derived from remote sensing from Earth-based observatories and space telescopes. As a result, Uranus's and Neptune's physical and atmospheric properties remain poorly constrained and their roles in the evolution of the Solar System not well understood. Exploration of an ice giant system is therefore a high-priority science objective as these systems (including the magnetosphere, satellites, rings, atmosphere, and interior) challenge our understanding of planetary formation and evolution. Here we describe the main scientific goals to be addressed by a future in situ exploration of an ice giant. An atmospheric entry probe targeting the 10-bar level, about 5 scale heights beneath the tropopause, would yield insight into two broad themes: i) the formation history of the ice giants and, in a broader extent, that of the Solar System, and ii) the processes at play in planetary atmospheres. The probe would descend under parachute to measure composition, structure, and dynamics, with data returned to Earth using a Carrier Relay Spacecraft as a relay station. In addition, possible mission concepts and partnerships are presented, and a strawman ice-giant probe payload is described. An ice-giant atmospheric probe could represent a significant ESA contribution to a future NASA ice-giant flagship mission
Search for leptophobic Z ' bosons decaying into four-lepton final states in proton-proton collisions at root s=8 TeV
Peer reviewe
Search for black holes and other new phenomena in high-multiplicity final states in proton-proton collisions at root s=13 TeV
Peer reviewe
Search for high-mass diphoton resonances in proton-proton collisions at 13 TeV and combination with 8 TeV search
Peer reviewe
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