Search results for "HIF"

showing 10 items of 1515 documents

Estimation of line parameters under line mixing effect: the nu3 band of CH4 in helium

2001

International audience; Spectra of CH4-He mixtures were measured in the P and R branch regions of nu3 vibration-rotation band at lower pressures of 0.26-1.0 bar and for the whole band at higher pressures up to 90 bar. The line broadening coefficients were found from lower pressure data for the lines of the P branch. These coefficients were calculated in the framework of the Robert and Bonamy semi-classical approach. In general, they agree with the experimental ones, but a small J-dependent deviation was observed. Line mixing effects were observed at all pressures. At higher pressures they were interpreted in terms of the adjusted branch-coupling model. At lower pressures line mixing effects…

Materials science010504 meteorology & atmospheric sciences[ PHYS.QPHY ] Physics [physics]/Quantum Physics [quant-ph]chemistry.chemical_element01 natural sciencesSpectral lineOptics[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]Infrared gas spectra0103 physical sciencesLine broadeningSpectroscopyMixing (physics)Helium0105 earth and related environmental sciencesLine (formation)Radiation010304 chemical physicsbusiness.industryAtomic and Molecular Physics and OpticschemistryLower pressureAtomic physicsbusinessLine shiftingLine mixing effectBar (unit)
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Transient absorption with a femtosecond tunable excitation pump reveals the emission kinetics of color centers in amorphous silica.

2021

We report a set of femtosecond (fs) transient absorption (TA) measurements following the dynamics of the so-called nonbridging oxygen hole center in silica, a model color center in wide bandgap amorphous solids, characterized by a very large Stokes shift between the UV excitation and its associated red emission at 1.9 eV. The changes in the TA spectrum were probed in the UV-visible range at various delays after photoexcitation and analyzed as a function of the UV excitation energy, in single-photon absorption conditions. The combination of the experiments helps to clarify the defect photocycle, highlighting how TA measurements with tunable UV excitation could represent a powerful tool to in…

Materials scienceAbsorption spectroscopytransient absorption02 engineering and technology01 natural sciencesMolecular physics010309 opticssymbols.namesakeOpticsStokes shift0103 physical sciencesUltrafast laser spectroscopyluminescenceAbsorption (electromagnetic radiation)ultra-fast laser spectroscopyComputingMilieux_MISCELLANEOUS[PHYS.PHYS]Physics [physics]/Physics [physics]business.industrypoint defect021001 nanoscience & nanotechnologyAtomic and Molecular Physics and OpticsAmorphous solidPhotoexcitationsilicaFemtosecondsymbols0210 nano-technologybusinessExcitationOptics letters
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Crystallographic Visualization of a Double Water Molecule Addition on a Pt 1 ‐MOF during the Low‐temperature Water‐Gas Shift Reaction

2021

[EN] The low-temperature water-gas shift reaction (WGSR, CO+H2O H-2+CO2) is considered a very promising reaction -candidate for fuel cells- despite an efficient and robust catalyst is still desirable. One of the more prominent catalysts for this reaction is based on single Pt atoms (Pt-1) on different supports, which are supposed to manifold the reaction by the accepted mechanism for the general WGSR, i. e. by addition of one H2O molecule to CO, with generation of CO2 and H-2. Here we show, experimentally, that not one but two H2O molecules are added to CO on the Pt-1 catalyst, as assessed by a combination of reactivity experiments with soluble Pt catalysts, kinetic and spectroscopic measur…

Materials scienceAigua QuímicaMetal-organic frameworkSingle atom catalystchemistry.chemical_element010402 general chemistry01 natural sciences7. Clean energyCatalysisWater-gas shift reactionInorganic ChemistryCatàlisiMoleculePhysical and Theoretical ChemistryPlatinumWater gas shift reactionCrystallography010405 organic chemistryOrganic Chemistry0104 chemical sciencesVisualizationCrystallographychemistryMetal-organic frameworkCristallsPlatinumChemCatChem
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Photoelectrochemical evidence of inhomogeneous composition at nm length scale of anodic films on valve metals alloys

2016

Abstract Anodic films of different thickness (∼30 nm and 70 nm) were grown by anodizing sputtering-deposited Ta-19at% Al to different formation voltages. N incorporation into the anodic films was inducing by performing the anodizing process in ammonium containing solutions. Layered anodic films were prepared by a double formation procedure with a first anodizing step in ammonium biborate solution and second anodizing step in borate buffer solution, or vice versa. Glow Discharge Optical Emission Spectroscopy was employed to show the distribution of N across the oxide. Photoelectrochemical measurements evidenced a red shift of the light absorption threshold due to N incorporation. A model was…

Materials scienceBand gap020209 energyGeneral Chemical EngineeringPhotoelectrochemistryAnalytical chemistryOxideQuantum yield02 engineering and technologyPhoton energyAnodizingElectrochemistryN incorporationchemistry.chemical_compoundPhotoelectrochemistry0202 electrical engineering electronic engineering information engineeringElectrochemistryChemical Engineering (all)Double-layered anodic filmAnodizingMetallurgy021001 nanoscience & nanotechnologyAnodeRed shiftSettore ING-IND/23 - Chimica Fisica Applicatachemistry0210 nano-technology
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Strain effects and phonon-plasmon coupled modes in Si-doped AlN

2009

The E 2h and A 1 (LO) phonon modes of AlN films grown on sapphire are analyzed by Raman scattering as a function of silicon doping for concentrations covering from 5.5 x 10 19 cm ―3 to 5.2 x 10 21 cm ―3 . For high doping levels the appearance of a mode around 520 cm ―1 indicates the precipitation of crystalline silicon in the samples and its inhomogeneous incorporation to the AlN layer. The frequency of this mode shifts to lower energies with doping, indicating that the silicon crystals are embedded in the AlN lattice and under tensile strain. On the other hand, the AlN phonon modes are blue-shifted due to the compressive strain as a result of the silicon incorporation. This strain is parti…

Materials scienceCondensed matter physicsSiliconPhononDopingAnalytical chemistrychemistry.chemical_elementSurfaces and InterfacesCondensed Matter PhysicsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBlueshiftsymbols.namesakechemistryMaterials ChemistrysymbolsSapphireCrystalline siliconElectrical and Electronic EngineeringRaman spectroscopyRaman scatteringphysica status solidi (a)
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A [Cr2Ni] coordination polymer: slow relaxation of magnetization in quasi-one-dimensional ferromagnetic chains

2018

The reaction of [Cr3IIIO(OAc)6(H2O)3]NO3·AcOH with 2-hydroxynaphthaldehyde, 2-amino-isobutyric acid and NiCl2·6H2O in MeOH, under basic and solvothermal conditions, led to the formation of the quasi-1D coordination polymer {[CrIII2NiII(L)4(MeOH)2]}n (where L = the dianion of the Schiff base between 2-hydroxynaphthaldehyde and 2-amino-isobutyric acid), which behaves as a ferromagnetic chain, displaying slow relaxation of magnetization.

Materials scienceCoordination polymer010402 general chemistry01 natural sciencesCatalysisMETAL-ORGANIC FRAMEWORKSchemistry.chemical_compoundMagnetizationChain (algebraic topology)SYSTEMSNANO-MAGNETSABSORPTIONMaterials ChemistryFIELDANTIFERROMAGNETSANISOTROPYMOSSBAUER RELAXATIONSchiff base010405 organic chemistryNONLINEAR EXCITATIONSMetals and AlloysGeneral ChemistrySINGLE-MOLECULE MAGNETS0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistryFerromagnetismCeramics and CompositesRelaxation (physics)Quasi one dimensional
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Photoactivity under visible light of metal loaded TiO2 catalysts prepared by low frequency ultrasound treatment

2017

Abstract Visible-light responsive bare and metal loaded (Pt, Ag, Rh, Pd) TiO 2 photocatalysts were prepared by using a simple ultrasound treatment. This method induced bulk oxygen deficiency resulting in a narrowing bandgap (from 3.18 to 3.04 eV) and in visible light absorption. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), BET specific surface area (SSA) and pore size distribution (PSD), UV–vis diffuse reflectance spectroscopy (DRS), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). The photocatalytic activity of the samples was evaluated by using the 4-nitrophenol oxidation reaction and the photocatalytic oxidation of glucose w…

Materials scienceDiffuse reflectance infrared fourier transformScanning electron microscopeAnalytical chemistryUltrasound treatment02 engineering and technology010402 general chemistry01 natural sciencesCatalysisCatalysisymbols.namesakeMetal loaded TiO2X-ray photoelectron spectroscopySpecific surface areaAbsorption (electromagnetic radiation)Chemistry (all)General Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesVisible-light active TiO2PhotocatalysissymbolsSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyRaman spectroscopyValence band edge shiftVisible spectrum
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XPS study of pumice-supported palladium and platinum catalysts

1992

An XPS study has been performed on samples of monometallic of palladium and platinum and on bimetallic Pd-Pt catalysts supported on pumice. A negative shift of about 0.5 eV in the Pd 3d and Pt 4f binding energies of the catalysis relative to the energies of the same levels in the pure metals suggested an increase in the electron density in both metals. A quantitative XPS analysis indicated that the supported metals did not modify the surface atomic composition of pumice

Materials scienceInorganic chemistryBinding energychemistry.chemical_elementSurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsSurfaces Coatings and FilmsCatalysisNegative shiftX-ray photoelectron spectroscopychemistryPumiceMaterials ChemistryPlatinumBimetallic stripPalladiumSurface and Interface Analysis
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Physicochemical properties of Ru(bpy)32+ entrapped in silicate bulks and fiber thin films prepared by the sol–gel method

1999

Silicate porous xerogels doped with ruthenium bipyridine (Ru(bpy)32+) complex have been obtained in the bulk form and in thin films on optical fibers. The hypsochromic shifts in the absorption and emission maxima are accompanied by fourfold increase in the lifetimes of the entrapped complex. The temperature-dependent lifetimes reveal that silicate xerogels induce two competing thermally activated processes in the excited state decay of the immobilized complex. The excited state lifetimes of the doped bulk xerogels and the fibers coated with thin films containing Ru(bpy)32+ are virtually identical to those obtained for the fibers coated with additional gas-impermeable layers.

Materials scienceInorganic chemistryGeneral Physics and Astronomychemistry.chemical_elementSilicateRutheniumBipyridinechemistry.chemical_compoundchemistryChemical engineeringHypsochromic shiftFiberPhysical and Theoretical ChemistryThin filmAbsorption (chemistry)Sol-gelChemical Physics Letters
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2016

Light shifts are an important source of noise and systematics in optically pumped magnetometers. We demonstrate that the long spin-coherence time in paraffin-coated cells leads to spatial averaging of the vector light shift over the entire cell volume. This renders the averaged vector light shift independent, under certain approximations, of the light-intensity distribution within the sensor cell. Importantly, the demonstrated averaging mechanism can be extended to other spatially varying phenomena in anti-relaxation-coated cells with long coherence times.

Materials scienceMagnetometerbusiness.industryAlkali metal01 natural sciencesMolecular physicsAtomic and Molecular Physics and Optics010305 fluids & plasmaslaw.inventionMagnetic fieldLight intensityOpticsLight Shiftlaw0103 physical sciences010306 general physicsbusinessLaser beamsEntire cellCoherence (physics)Optics Express
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