Search results for "electron spectroscopy"

showing 10 items of 525 documents

Determination of absolute internal conversion coefficients using the SAGE spectrometer

2016

A non-reference based method to determine internal conversion coefficients using the SAGE spectrometer is carried out for transitions in the nuclei of 154Sm, 152Sm and 166Yb. The Normalised-Peak-to-Gamma method is in general an efficient tool to extract internal conversion coefficients. However, in many cases the required well-known reference transitions are not available. The data analysis steps required to determine absolute internal conversion coefficients with the SAGE spectrometer are presented. In addition, several background suppression methods are introduced and an example of how ancillary detectors can be used to select specific reaction products is given. The results obtained for …

electron spectroscopyinternal conversion coefficientsilicon detectorbackground subtractionenergy reconstruction
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“Supported Co3O4-CeO2 monoliths: effect of preparation method and Pd-Pt promotion on the CO/CH4 oxidation activity”

2006

Abstract Two structured composite oxides, Co3O4(30wt%)-CeO2(70wt%), have been prepared by washcoating commercial cordierite monoliths with a CeO2-γAl2O3 layer, on which the active phase Co3O4-CeO2 was added through two different methods: dip-coating from a suspension containing the preformed active oxide or impregnation with a solution of the cobalt and cerium precursors. Morphological characterizations of the monoliths have been performed by BET, and SEM-EDAX analyses. Electronic and reduction properties have been evaluated by XPS and H2-TPR, respectively. The effect of the preparation method has been investigated in the catalytic oxidation of CO, whereas the promotion by a low content of …

geographygeography.geographical_feature_categoryMaterials scienceInorganic chemistryOxidechemistry.chemical_elementHeterogeneous catalysisCatalysischemistry.chemical_compoundCeriumX-ray photoelectron spectroscopyCatalytic oxidationchemistryMonolithCobaltNuclear chemistry
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Oxidation-Induced Changes in the ALD-Al2O3/InAs(100) Interface and Control of the Changes for Device Processing

2018

InAs crystals are emerging materials for various devices like radio frequency transistors and infrared sensors. Control of oxidation-induced changes is essential for decreasing amounts of the harmful InAs surface (or interface) defects because it is hard to avoid the energetically favored oxidation of InAs surface parts in device processing. We have characterized atomic-layer-deposition (ALD) grown Al2O3/InAs interfaces, preoxidized differently, with synchrotron hard X-ray photoelectron spectroscopy (HAXPES), low-energy electron diffraction, scanning tunneling microscopy, and time-of-flight elastic recoil detection analysis. The chemical environment and core-level shifts are clarified for w…

hapetusMaterials science02 engineering and technologyHigh-electron-mobility transistor01 natural sciences114 Physical scienceslaw.inventionAtomic layer depositionX-ray photoelectron spectroscopyInAslawsynchrotron0103 physical sciencesGeneral Materials Science010302 applied physicsta114business.industryDangling bondatomikerroskasvatus021001 nanoscience & nanotechnologyIII-V semiconductorCrystallographic defectElastic recoil detectionoxidation (active)Electron diffractionatomic layer depositionOptoelectronicsScanning tunneling microscope0210 nano-technologybusinessphotoelectron
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Reduction-oxidation dynamics of oxidized graphene: Functional group composition dependent path to reduction

2018

Micrometer-sized oxidation patterns containing varying composition of functional groups including epoxy, ether, hydroxyl, carbonyl, carboxyl, were created in chemical vapor deposition grown graphene through scanning probe lithography and pulsed laser two-photon oxidation. The oxidized graphene films were then reduced by a focused x-ray beam. Through in-situ x-ray photoelectron spectroscopy measurement, we found that the path to complete reduction depends critically on the total oxygen coverage and concentration of epoxy and ether groups. Over the threshold concentrations, a complex reduction-oxidation process involving conversion of functional groups of lower binding energy to higher bindin…

hapetusMaterials sciencekemiax-ray examinationBinding energyOxideEther02 engineering and technologyChemical vapor depositionchemistry010402 general chemistryPhotochemistry01 natural sciencesRedoxepoxylaw.inventionchemistry.chemical_compoundX-ray photoelectron spectroscopylawgrafeeniGeneral Materials Sciencefysiikkata116ta114GraphenegrapheneepoksiGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesröntgenkuvausoxidation (active)chemistryreduction-oxidation processes0210 nano-technologyphysicsScanning probe lithographyCarbon
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Co-reductive fabrication of carbon nanodots with high quantum yield for bioimaging of bacteria

2018

A simple and straightforward synthetic approach for carbon nanodots (C-dots) is proposed. The strategy is based on a one-step hydrothermal chemical reduction with thiourea and urea, leading to high quantum yield C-dots. The obtained C-dots are well-dispersed with a uniform size and a graphite-like structure. A synergistic reduction mechanism was investigated using Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The findings show that using both thiourea and urea during the one-pot synthesis enhances the luminescence of the generated C-dots. Moreover, the prepared C-dots have a high distribution of functional groups on their surface. In this work, C-dots proved …

hydrothermalMaterials scienceGeneral Physics and AstronomyQuantum yield02 engineering and technologylcsh:Chemical technologyCarbon nanodots010402 general chemistrylcsh:Technology01 natural sciencesFull Research PaperHydrothermal circulationNanomaterialschemistry.chemical_compoundX-ray photoelectron spectroscopyNanotechnologylcsh:TP1-1185General Materials Sciencecarbon nanodotsbioimagingElectrical and Electronic EngineeringFourier transform infrared spectroscopylcsh:Sciencecollaborative reductionlcsh:TCondensed Matter::Mesoscopic Systems and Quantum Hall Effect021001 nanoscience & nanotechnologyBioimagingHydrothermallcsh:QC1-9990104 chemical sciencesNanoscienceChemical engineeringThioureachemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoCollaborative reductionUrealcsh:Q0210 nano-technologyLuminescencelcsh:PhysicsBeilstein Journal of Nanotechnology
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Improvement of catalytic activity over Cu--Fe modified Al-rich Beta catalyst for the selective catalytic reduction of NOx with NH3

2016

Copper and iron bimetal modified Al-rich Beta zeolites from template-free synthesis were prepared for selective catalytic reduction (SCR) of NOx with NH3 in exhaust gas streams. Comparing to the Cu-based and Fe-based mono-component Beta catalysts, Cu(3.0)-Fe(1.3)-Beta bi-component catalyst shows better low-temperature activity and wider reaction-temperature window. Over 80% of NO conversion can be achieved at the temperature region of 125–500 °C. Due to the synergistic effect of copper and iron evidenced by XRD, UV–Vis–NIR, EPR and XPS measurements, the dispersion state of active components as well as the ratio of Cu2+/Cu+ and Fe3+/Fe2+ were improved over Cu(3.0)-Fe(1.3)-Beta. Isolated Cu2+…

inorganic chemicalsInorganic chemistryCu--Fe-Betachemistry.chemical_elementNanotechnology02 engineering and technology010402 general chemistryDispersion (geology)01 natural sciencesCatalysisBimetalAl-rich BetaX-ray photoelectron spectroscopyGeneral Materials ScienceNOxSelective catalytic reductionGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsCopperSulfur0104 chemical scienceschemistryMechanics of MaterialsSynergistic effect0210 nano-technologyNH3-SCR
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Surface Study of Pumice Supported Nickel Catalysts Used in the Hydrogenation of CO

1998

A series of pumice supported nickel catalysts used in the CO hydrogenation reaction were characterised by X-ray photoelectron spectroscopy. Qualitative and quantitative analysis of the XPS peaks have shown the effect of the calcination conditions on the chemical state of the nickel before hydrogenation and the particle size of the metal after reduction. Calcination at high temperature determined enrichment of sodium ions on the surface of the support and also on the metal particles. After exposure to the gas mixture CO/H2, formation of nickel carbides and other carbon species was checked. The correlation found between the surface atomic ratio Na/Si and the activity and selectivity of the ca…

inorganic chemicalsInorganic chemistrychemistry.chemical_elementlaw.inventionCatalysisMetalNickelChemical statechemistry.chemical_compoundchemistryX-ray photoelectron spectroscopylawvisual_artvisual_art.visual_art_mediumCalcinationAtomic ratioCarbon monoxide
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X-ray Photoelectron-spectroscopy Investigation of Pumice-supported Nickel-catalysts

1995

Pumice-supported nickel catalysts, prepared by the method of slow homogeneous precipitation with urea, were analysed by x-ray photoelectron spectroscopy (XPS). By comparison with similarly prepared silica- and alumina-supported nickel catalysts, a preferential interaction of Ni2+ with Al3+ of the support has been determined. A quantitative XPS analysis indicated large segregation of nickel to the surface. The treatment with H2 at 673 K and 1073 K produced a partial reduction of Ni+2 to Ni0. The extent of the reduction was largest at 1073 K and in this case the reduced Ni in the metallic phase was detectable by x-ray diffraction. A decrease of the Ni 2p/Si 2p intensity ratio occurring in the…

inorganic chemicalsPrecipitation (chemistry)ChemistryAnalytical chemistrySinteringchemistry.chemical_elementSurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsSurfaces Coatings and FilmsCatalysisMetalNickelTransition metalX-ray photoelectron spectroscopyvisual_artX-ray crystallographyMaterials Chemistryvisual_art.visual_art_medium
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Study by static SIMS, XPS and UPS of the adsorption of cyanogen on (100) Ni surfaces

2000

Abstract The interaction of cyanogen with (100) Ni surfaces at room temperature was studied using secondary ion mass spectrometry in a static mode, and photoemission spectroscopies (XPS and UPS). It has been shown that cyanogen is adsorbed on this nickel surface in a dissociative mode: atomic carbon and nitrogen are present on the surface as well as CN fragments. These adsorbed species have been characterized by XPS and UPS. Increasing the temperature in the 400 K range increases the rate of the dissociation reaction of CN into atomic carbon and nitrogen. Moreover carbon is found to dissolved into the bulk for temperatures as low as 475 K. No evidence has been found of a polymerized form of…

inorganic chemicalsStatic secondary-ion mass spectrometryChemistryCyanogenAnalytical chemistrychemistry.chemical_elementSurfaces and InterfacesCondensed Matter PhysicsSurfaces Coatings and FilmsSecondary ion mass spectrometrychemistry.chemical_compoundNickelAdsorptionX-ray photoelectron spectroscopyChemisorptionMaterials ChemistryCarbonSurface Science
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Precatalyst or dosing-device? The [Pd2{μ-(C6H4) PPh2}2{μ-O2C(C6H5)}2] complex anchored on a carboxypolystyrene polymer as an effective supplier of pa…

2020

Abstract A new catalyst has been synthesized from the precursor [Pd2{μ-(C6H4) PPh2}2 {μ-O2C(C6H5)}2] immobilized on a carboxypolystyrene polymer that exhibits an excellent dispersion of the Pd (II) centers, reusability, and catalytic activity in front of phenyl bromides. The activity of this new material was studied in detail for the Suzuki-Miyaura reaction and compared to that of Pd nanoparticles (NPs) supported on UVM-7 (a mesoporous silica), and Pd NPs stabilized with polyvinylpirrolydone. The homogeneous/heterogeneous character of the catalytic process was determined from the results of the hot-filtration, centrifugation, poisoning, three phases tests, and from differential sensitivity …

inorganic chemicalschemistry.chemical_classification010405 organic chemistryNanoparticlechemistry.chemical_elementPolymerMesoporous silica010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistryX-ray photoelectron spectroscopyChemical engineeringCatalytic cycleOxidation statePhysical and Theoretical ChemistryPalladiumJournal of Catalysis
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