Search results for "Photoelectron spectroscopy"

showing 10 items of 439 documents

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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ORR Activity and Stability of Co-N/C Catalysts Based on Silicon Carbide Derived Carbon and the Impact of Loading in Acidic Media

2018

This work was supported by the EU through the European Regional Development Fund under projects TK141 “Advanced materials and high-technology devices for energy recuperation systems” (2014-2020.4.01.15-0011), NAMUR ”Nanomaterials - research and applications” (3.2.0304.12-0397) and by the Estonian institutional research grant No. IUT20-13.

inorganic chemicalschemistry.chemical_element02 engineering and technology010402 general chemistryElectrochemistry01 natural sciences7. Clean energyCatalysisElectron transferchemistry.chemical_compoundX-ray photoelectron spectroscopy:NATURAL SCIENCES:Physics [Research Subject Categories]Materials ChemistryElectrochemistrySilicon carbideheterocyclic compoundsRenewable Energy Sustainability and the EnvironmentChemistryorganic chemicals021001 nanoscience & nanotechnologyCondensed Matter PhysicsNitrogen0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical engineeringDegradation (geology)0210 nano-technologyCarbonJournal of The Electrochemical Society
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Structural Characterization of Surfactant-Coated Bimetallic Cobalt/Nickel Nanoclusters by XPS, EXAFS, WAXS, and SAXS

2011

Cobalt nickel bimetallic nanoparticles were synthesized by changing the sequence of the chemical reduction of Co(II) and Ni(II) ions confined in the core of bis(2-ethylhexyl)phosphate (2)., and Ni(DEHP)(2). The reduction was carried out by mixing, sequentially or contemporaneously, fixed amounts of n-heptane solution of Co(DEHP)2 and Ni(DEHP)2 micelles with a solution of sodium borohydride in ethanol at a fixed (reductant)/(total metal) molar ratio. This procedure involves the rapid formation of surfactant-coated nanoparticles, indicated as Co/Ni (Co after Ni), Ni/Co (Ni after Co), and Co + Ni (simultaneous), followed by their slow separation as nanostructures embedded in a sodium bis(2-eth…

inorganic chemicalsendocrine systemMaterials sciencechemistry.chemical_elementNanoparticleNanoclustersMetalSodium borohydridechemistry.chemical_compoundX-ray photoelectron spectroscopyNANOPARTICLESPARTICLESBimetallic Cobalt/Nickel Nanoclusters. XPS. EXAFS. WAXS. SAXS.GOLDPhysical and Theoretical ChemistryBimetallic stripMICELLESSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyNickelGeneral Energychemistryvisual_artNANOPARTICLES; PARTICLES; GOLD; MICELLESvisual_art.visual_art_mediumCobaltNuclear chemistry
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Study of the role of sulfur functionalities in humic acids for uranium(VI) complexation

2009

Humic substances influence the speciation and migration behavior of toxic and radiotoxic metal ions, such as actinides, in the environment. Depending on their origin, humic substances contain different amounts of sulfur ranging from 0.1 to 3.6% and 0.5 to 1.43% in soil and aquatic humic substances, respectively [1]. Reduced, intermediately oxidized and highly oxidized sulfur functionalities occur in humic substances [1]. Although sulfur functionalities occur in small concentrations, they can play an important role in the complexation of selected metal ions. Knowledge about the impact of sulfur functionalities on the metal ion complexation by humic substances and their significance compared …

inorganic chemicalsfs-TRLFScomplexationInorganic chemistryTRLFSchemistry.chemical_elementHumic substancesOxygencomplex mixturesFluorescence spectroscopysulfur functionalitiesfunctional groupsX-ray photoelectron spectroscopyXPSHumic acidPhysical and Theoretical Chemistrychemistry.chemical_classificationLigandUraniumSulfurhumic acidshumic acid model substanceschemistryHumic aciduranium(VI)sulfurThiol
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Total oxidation of naphthalene using bulk manganese oxide catalysts

2013

Several Mn2O3 catalysts have been synthesized using different preparation methods and tested for the total oxidation of naphthalene, a model polycyclic aromatic compound. The catalysts have been characterized by several physico-chemical techniques such as XRD, TPR, XPS, EDX and TEM. The surface area of the catalyst seems to be of paramount importance, since the mass normalized activity of catalysts increases as the surface area of the Mn2O3 catalysts increases. Consequently, a high surface area ordered mesoporous Mn2O3 catalyst, obtained through a nanocasting route using mesoporous KIT-6 silica as a hard template, was the most efficient catalyst for the deep oxidation of naphthalene. In add…

inorganic chemicalsorganic chemicalsProcess Chemistry and TechnologyCatalyst supportInorganic chemistryCatalysisCatalysisHopcalitechemistry.chemical_compoundchemistryCatalytic oxidationX-ray photoelectron spectroscopyPhase (matter)heterocyclic compoundsMesoporous materialNaphthaleneApplied Catalysis A: General
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