Search results for "catalysts"

showing 10 items of 164 documents

Oxide-based nanomaterials for fuel cell catalysis:the interplay between supported single Pt atoms and particles

2017

The concept of single atom catalysis offers maximum noble metal efficiency for the development of low-cost catalytic materials. Among possible applications are catalytic materials for proton exchange membrane fuel cells. In the present review, recent efforts towards the fabrication of single atom catalysts on nanostructured ceria and their reactivity are discussed in the prospect of their employment as anode catalysts. The remarkable performance and the durability of the ceria-based anode catalysts with ultra-low Pt loading result from the interplay between two states associated with supported atomically dispersed Pt and sub-nanometer Pt particles. The occurrence of these two states is a co…

Materials sciencePHOTOELECTRON-SPECTROSCOPYReducing agentCatalitzadorsOxideProton exchange membrane fuel cellNanotechnology02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesRedoxPALLADIUM NANOPARTICLESCatalysisNanomaterialsCatalysischemistry.chemical_compoundAdsorptionPiles de combustibleD-METAL ATOMSFuel cellsCatalystsCEO2(111) SURFACECO OXIDATIONIN-SITUNanostructured materialsSILICON SUBSTRATE021001 nanoscience & nanotechnology0104 chemical scienceschemistryChemical engineeringGRAPHITE FOILengineeringTHIN-FILM CATALYSTSNoble metalMaterials nanoestructuratsCERIA-BASED OXIDE0210 nano-technology
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Au/CeO2-SBA-15 catalysts for CO oxidation: Effect of ceria loading on physic-chemical properties and catalytic performances

2012

In this work gold catalysts supported over SBA-15 with different CeO 2 loadings (5-30 wt%) were prepared, characterized by N 2 physisorption analyses, SAXS, XRD, STEM and XPS techniques and their catalytic performances were evaluated in the CO oxidation, chosen as reaction test. Over a selected catalyst, Au/CeO 2(20 wt%)-SBA-15, the effect of CO 2 and of the mixture (CO 2 + H 2O) on the CO conversion to CO 2 was also evaluated. Characterizations by SAXS, XRD, STEM and XPS were carried out on selected spent catalysts after CO oxidation. The results were discussed in terms of relationship between morphological, structural, electronic and catalytic properties as a function of the ceria loading…

Materials scienceSmall-angle X-ray scatteringOxideNucleationSinteringNanotechnologyGeneral ChemistryCatalysisCatalysischemistry.chemical_compoundAu CeO2 SBA-15 catalysts CO oxidationchemistryX-ray photoelectron spectroscopyChemical engineeringPhysisorptionParticle sizeCatalysis Today
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Nanostructured CdO thin films for water treatments

2016

Abstract CdO was the very first transparent conducting metal oxide discovered. CdO thin films show electrical and optical properties of interest as photosensitive anode materials for photochemical cells, phototransistors, photodiodes, window electrodes in liquid crystal displays, IR detectors, antireflection coatings, gas sensors and in other solar energy applications. In the present study we report on the spectroscopic, microscopic, electrical and photo-catalytic properties of CdO thin films prepared by a metal organic chemical vapor method. The degenerate semiconducting CdO thin films are useful as photocatalysts for water treatments.

Materials sciencegenetic structuresCdO; Film; photocatalystsOxideNanotechnologyCondensed Matter Physic02 engineering and technology010402 general chemistrySettore ING-INF/01 - Elettronica01 natural sciencesSettore FIS/03 - Fisica Della Materialaw.inventionphotocatalystsMetalchemistry.chemical_compoundlawWater treatmentGeneral Materials ScienceThin filmFilmCdOLiquid-crystal displaybusiness.industryMechanical EngineeringPhotocatalyst021001 nanoscience & nanotechnologyCondensed Matter PhysicsSolar energy0104 chemical sciencesAnodePhotodiodechemistrySettore CHIM/03 - Chimica Generale E InorganicaMechanics of Materialsvisual_artElectrodevisual_art.visual_art_mediumMaterials Science (all)sense organs0210 nano-technologybusinessMaterials Science in Semiconductor Processing
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H2 Transformations on Graphene Supported Palladium Cluster: DFT-MD Simulations and NEB Calculations

2020

Molecular dynamics simulations based on density functional theory were employed to investigate the fate of a hydrogen molecule shot with different kinetic energy toward a hydrogenated palladium cluster anchored on the vacant site of a defective graphene sheet. Hits resulting in H2 adsorption occur until the cluster is fully saturated. The influence of H content over Pd with respect to atomic hydrogen spillover onto graphene was investigated. Calculated energy barriers of ca. 1.6 eV for H-spillover suggest that the investigated Pd/graphene system is a good candidate for hydrogen storage.

Materials sciencespilloverhydrogen reactionchemistry.chemical_elementsupported metal catalysts02 engineering and technology010402 general chemistryKinetic energylcsh:Chemical technology01 natural sciencesDFTCatalysislaw.inventionlcsh:ChemistryMolecular dynamicsHydrogen storagelawCluster (physics)lcsh:TP1-1185Physical and Theoretical Chemistryhydrogenation elementary eventsGraphene021001 nanoscience & nanotechnology0104 chemical scienceschemistrylcsh:QD1-999Chemical physicsDensity functional theoryHydrogen spillover0210 nano-technologyPalladiumCatalysts
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New concepts in multidentate ligand chemistry: effects of multidentarity on catalytic and spectroscopic properties of ferrocenyl polyphosphines.

2008

This tutorial review devoted to ligand chemistry deals with the design and properties of ferrocenyl polyphosphines, an original class of multidentate ligands. The development of a varied library of ferrocenyl tetra-, tri- and diphosphine ligands is reviewed. The multidentate nature of these species has led to unique spectroscopic and catalytic properties, in which the spatial proximity of phosphorus atoms is crucial. Regarding their catalytic applications, the key issues of catalyst longevity and ultralow catalyst loadings are discussed. Another part is concerned with fundamental advances gained in physical chemistry for structure elucidation by the study of the intriguing “through-space” N…

Models MolecularDenticityMagnetic Resonance SpectroscopyMetallocenesferrocenyl polyphosphinesSuzukiMolecular ConformationSonogashira coupling010402 general chemistryLigands01 natural sciencescatalystsCatalysisCatalysis[ CHIM.CATA ] Chemical Sciences/Catalysisthrough-space interactionOrganometallic CompoundsOrganic chemistryCombinatorial Chemistry Techniques[CHIM.COOR]Chemical Sciences/Coordination chemistryFerrous CompoundsAminationComputingMilieux_MISCELLANEOUSGroup 2 organometallic chemistryCombinatorial Chemistry Techniquesnuclear spin-spin coupling010405 organic chemistryChemistryLigand[ CHIM.COOR ] Chemical Sciences/Coordination chemistrySonogashiraaminationStereoisomerismGeneral ChemistryNuclear magnetic resonance spectroscopy[CHIM.CATA]Chemical Sciences/CatalysisReference StandardsCombinatorial chemistry0104 chemical sciencesmultidentarityHeckChemical Society reviews
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Modification of Nanocrystalline WO3 with a Dicationic Perylene Bisimide: Applications to Molecular Level Solar Water Splitting

2015

[(N,N?-Bis(2-(trimethylammonium)ethylene) perylene 3,4,9,10-tetracarboxylic acid bisimide)(PF6)2] (1) was observed to spontaneously adsorb on nanocrystalline WO3 surfaces via aggregation/hydrophobic forces. Under visible irradiation (? > 435 nm), the excited state of 1 underwent oxidative quenching by electron injection (kinj > 108 s-1) to WO3, leaving a strongly positive hole (Eox ? 1.7 V vs SCE), which allows to drive demanding photo-oxidation reactions in photoelectrochemical cells (PECs). The casting of IrO2 nanoparticles (NPs), acting as water oxidation catalysts (WOCs) on the sensitized electrodes, led to a 4-fold enhancement in photoanodic current, consistent with hole transfer from …

Models MolecularMolecular ConformationNanoparticleImidesPhotochemistryBiochemistryTungstenCatalysisNOCatalysiElectron Transportchemistry.chemical_compoundColloid and Surface ChemistryTheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYWO3ComputingMethodologies_SYMBOLICANDALGEBRAICMANIPULATIONperylenePhotoelectrochemical cellIrO2Quenching (fluorescence)Chemistry (all)charge transferWaterOxidesGeneral ChemistryPhotoelectrochemical cellPhotochemical ProcessesSolar fuelChemistry (all); Catalysis; Biochemistry; Colloid and Surface ChemistryNanocrystalline materialperylene WO3 charge transfer IrO2MicrosecondchemistryWater SplittingSunlightVISIBLE-LIGHT; ARTIFICIAL PHOTOSYNTHESIS; PHOTOELECTROCHEMICAL CELL; OXIDATION CATALYSTS; ELECTRON-TRANSFER; FABRICATIONNanoparticlesPerylene bisimideWater splittingPeryleneMathematicsofComputing_DISCRETEMATHEMATICS
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Microstructure of ethylene-1-hexene and ethylene-1-octene copolymers obtained over Ziegler–Natta catalysts supported on MgCl 2 (THF) 2

2001

Abstract The ethylene copolymerizations with 1-hexene or 1-octene in the presence of hydrogen using three catalysts, MgCl 2 (THF) 2 /VOCl 3 /Et 2 AlCl, MgCl 2 (THF) 2 /VCl 4 /Et 2 AlCl, MgCl 2 (THF) 2 /TiCl 4 /Et 2 AlCl, were investigated. It was found that the addition of hydrogen into the copolymerization feed reduces the molecular weight of the copolymers produced and decreases the activity of all the studied catalysts. The microstructure of the copolymers obtained was determined on the basis of 13 C NMR investigations and the reactivity ratios of the comonomers were calculated. The lack of tendency of the olefin comonomers to the creation of the polymer block was confirmed. It was found…

Olefin fiberEthyleneCopolymerization of ethylene with α-olefinPolymers and PlasticsComonomerOrganic ChemistryPolyethyleneMicrostructure of copolymers1-Hexenechemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryZiegler–Natta catalystsReactivity (chemistry)Ziegler–Natta catalyst1-OctenePolymer
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Ethylene/1-olefin copolymerization behaviour of vanadium and titanium complexes bearing salen-type ligand

2013

Ethylene/1-olefin copolymerization using vanadium and titanium complexes bearing tetradentate [O,N,N,O]-type ligand and EtAlCl2 or MAO as a cocatalyst is carried out. In the presence of the vanadium complex activated with EtAlCl2 is observed (a) negative “comonomer effect”, (b) high comonomer incorporation and narrow chemical composition distribution (CCD), (c) unexpected copolymer microstructure, and (d) increased molecular weight of copolymers when compared with the homopolymer. In contrast, titanium catalyst gives copolymers with lower 1-olefin content and broad CCD. Supported complexes show higher activity, lower 1-olefins incorporation and give copolymers with ultra high molecular weig…

Olefin fibersupportEthyleneMaterials scienceChemistry(all)Polymers and PlasticsComonomerVanadiumchemistry.chemical_elementGeneral Chemistrysalen-type complexCondensed Matter Physicscopolymer heterogeneitycatalystsPolyolefinCatalysiscopolymerizationchemistry.chemical_compoundchemistryPolymer chemistryCopolymerMaterials ChemistrypolyolefinTitaniumPolymer Bulletin
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Organocatalysts and metal-based catalysts: a journey toward the development of new catalytic materials

2015

Organocatalysis and metal-based catalysis represent two of the main pillars of catalytic reactions and have witnessed a huge interest in the last decade. Immobilization, recovery and reuse of these catalysts is of primary importance because of the large amount used especially in the case of organocatalysts. On the other hand, metal-based catalysts must be recovered even if used in low amount, in order to avoid contamination of the product. In this context, we started several years ago investigations on the use of supported ionic liquid phases for the asymmetric organocatalysis mediated by proline.1 This approach is an example of a “release and catch” catalytic system.2 Starting from this ex…

Organocatalysirecyclable catalystscatalysiSettore CHIM/06 - Chimica Organica
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Photoelectrochemical properties of doped lanthanum orthoferrites

2013

Abstract LaFeO 3 powders doped with Sr (20 mol%) and Cu (0-10-20 mol%) were prepared by citrate auto-combustion synthesis and investigated in terms of crystal structure, morphology, surface area and optical properties. All powders showed photocurrent response in the form of a pasted and annealed electrode and as slurry electrode; the highest value was obtained for undoped orthoferrite calcined at 600 °C. Their physical–chemical properties were related to photoelectrochemical behaviour. The position of the quasi-Fermi level of electrons for all the photocatalysts calcined in the range 600–980 °C is about the same within experimental error (between −0.62 and −0.67 V with respect to Ag/AgCl re…

OrthoferriteMaterials scienceGeneral Chemical EngineeringFerrites Photocatalysts Photocurrent response Quasi-Fermi levelAnalytical chemistryMineralogychemistry.chemical_elementPhotocatalysts; Photocurrent response; Quasi-Fermi level; Ferrites;Reference electrodelaw.inventionchemistry.chemical_compoundlawElectrochemistryLanthanumFerritesCalcinationPhotocurrentSettore ING-IND/24 - Principi Di Ingegneria ChimicaDopingPhotocatalystQuasi-Fermi levelCopperchemistryElectrodePhotocatalystsLanthanum orthoferritesPhotocurrent responseSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie
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