Search results for "Auger electron spectroscopy"

showing 10 items of 32 documents

Structural properties of the quaternary Heusler alloy Co2Cr1−xFexAl

2007

The quarternary substitutional series Co2Cr1?xFexAl was investigated by means of surface and bulk sensitive techniques in order to exploit its structural and compositional properties. Both bulk and powder samples of the alloy series were investigated to obtain specific information about this material.The long range order was determined by means of x-ray diffraction and neutron diffraction, while the site specific (short range) order was proved by extended x-ray absorption fine structure spectroscopy. The magnetic structure was investigated by M?ssbauer spectroscopy in transmission and scattering modes in order to compare and separate powder and bulk properties. The chemical composition was …

Auger electron spectroscopyAcoustics and UltrasonicsMagnetic structureChemistryNeutron diffractionOxideCondensed Matter PhysicsSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographyChemical physicsEmission spectrumThin filmAbsorption (electromagnetic radiation)SpectroscopyJournal of Physics D: Applied Physics
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Surface spectroscopic study of the corrosion of ultrathin57Fe-evaporated and Langmuir-Blodgett films in humid SO2 environments

2000

Integral conversion electron Mossbauer spectroscopy (ICEMS), x-ray photoelectron spectroscopy (XPS), Auger electron spectroscopy (AES) and scanning electron microscopy (SEM) have been used to carry out a comparative study of the corrosion resistance against humid SO2-aggressive environments of ultrathin 57Fe films. These films, having a thickness ≤ 2.5 nm, have been prepared by evaporation of 57Fe under vacuum and by 57Fe coating by a Langmuir–Blodgett (LB) technique on SiO2/Si wafers. The results have shown that the corrosion resistance of the evaporated films is similar to that of massive Fe. However, the LB films show a remarkably higher corrosion resistance. Thus, although the Fe films …

Auger electron spectroscopyChemistryScanning electron microscopeAnalytical chemistrySurfaces and InterfacesGeneral Chemistryengineering.materialCondensed Matter PhysicsEvaporation (deposition)Langmuir–Blodgett filmSurfaces Coatings and FilmsCorrosionX-ray photoelectron spectroscopyCoatingConversion electron mössbauer spectroscopyMaterials ChemistryengineeringSurface and Interface Analysis
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Reactivity of H2S and H2S/H2 Mixture With Molybdenum Oxide Thin Films Epitaxied on CoO (100) : Characterization by Rheed and Auger Spectroscopy

2010

Molybdenum-Cobalt composite oxide films were prepared by the evaporation of molybdenum trioxide on a fresh cleaved CoO (100) surface (Thickness = 10 A). The MoO3-CoO interface has been characterized simultaneously by reflexion high electron diffraction (RHEED) and Auger Electron Spectroscopy (AES). The thin film structure and composition depend on the annealing temperature. After a 300°C treatment, metallic cobalt islands nucleate at the interface thin film - CoO (100) and crystallize with the cubic FCC symmetry. After a 700°C treatment cobalt molybdate (a CoMoO4) islands grow. The metastable crystallites are epitaxied on CoO (100). After a 900°C treatment, the thin film consists of flat tw…

Auger electron spectroscopyCrystallographychemistry.chemical_compoundReflection high-energy electron diffractionChemistrychemistry.chemical_elementGeneral ChemistryCrystalliteThin filmMolybdateCobaltAmorphous solidMolybdenum trioxideBulletin des Sociétés Chimiques Belges
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Functionalization using biocompatible carboxylated cyclodextrins of iron-based nanoMIL-100

2021

9 pags., 7 figs., 1 tab.

Auger electron spectroscopyCyclodextrinsCyclodextrin applicationsNanoparticleMetal-organic frameworksInorganic ChemistryThermogravimetrychemistry.chemical_compoundMonomerchemistryPolymer chemistrypolycyclic compoundsMaterials ChemistrySurface modified nanoparticlesMössbauerSurface modificationCarboxylatePhysical and Theoretical ChemistryPorosityLinkerMaterials
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SVET, AFM and AES study of pitting corrosion initiated on MnS inclusions by microinjection

2003

As pitting is a random phenomenon, it is difficult to predict where a pit will appear on the surface and consequently the use of local probes is rendered difficult. In this work, a new method to study pitting corrosion on a MnS inclusion on 316L stainless steel is proposed. It consists in modifying locally the chemistry in its vicinity by injecting with a microcapillary an aggressive solution of NaCl, H2SO4 or HCl. Once a pit appears, scanning vibrating electrode technique (SVET) is used to follow the current fluctuations over and around the pit when the metal is polarized at a passive potential. In another series of experiments the effect of local activation of MnS inclusion was studied ex…

Auger electron spectroscopyGeneral Chemical EngineeringChloric acidMetallurgyInorganic chemistryHydrochloric acidGeneral Chemistryengineering.materialCorrosionCathodic protectionchemistry.chemical_compoundchemistryPitting corrosionengineeringGeneral Materials ScienceAustenitic stainless steelDissolutionCorrosion Science
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Iron deposition on TiO2(110): effect of the surface stoichiometry and roughness

1999

Abstract Characterizations of ultra-thin iron films deposited on TiO 2 (110) surfaces with different stoichiometries, roughnesses and crystallinities have been carried out by X-ray photoelectron spectroscopy (XPS) and Auger electron spectroscopy (AES). For a high initial roughness of the substrate, a 2D growth mode is observed up to three monolayers. But, if the initial roughness is low, clusters grow on the TiO 2 surface. Whatever the initial surface stoichiometry, electronic exchanges occur between titanium and iron leading to a reduction of titanium and an oxidation of iron. This interaction between iron and titanium dioxide surface takes place only at the interface between the metal and…

Auger electron spectroscopyInorganic chemistrytechnology industry and agricultureOxidechemistry.chemical_elementSurfaces and InterfacesSurface finishCondensed Matter PhysicsSurfaces Coatings and Filmschemistry.chemical_compoundchemistryX-ray photoelectron spectroscopyTitanium dioxideMaterials ChemistryLayer (electronics)StoichiometryTitaniumSurface Science
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Structural properties of the quaternary Heusler compound Co2 Cr1−x Fex Al

2006

Abstract The structural and chemical properties of the quaternary Heusler compound Co2 Cr1−x Fex Al were investigated comparing powder and bulk samples. The long range order was determined by means of X-ray diffraction, while the site specific (short range) order was proved by the extended X-ray absorption fine structure method (EXAFS). The chemical composition was analysed by means of X-ray photo emission spectroscopy (XPS) combined with Auger electron spectroscopy (AES) depth profiling. The results from these methods are compared to get a detailed idea about the differences between surface and bulk properties and appearance of disorder in such alloys.

Auger electron spectroscopyMaterials scienceExtended X-ray absorption fine structureMechanical EngineeringMetals and AlloysAnalytical chemistryCrystal structureengineering.materialHeusler compoundCrystallographyX-ray photoelectron spectroscopyMechanics of MaterialsX-ray crystallographyMaterials ChemistryengineeringEmission spectrumAbsorption (electromagnetic radiation)Journal of Alloys and Compounds
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Relationships between strain, microstructure and oxide growth at the nano- and microscale

2008

In the present article, the relationships between oxidation processes, surface strains and the microstructure of duplex stainless steels were investigated. Specimens were oxidized at 500 °C under secondary vacuum for 1 h to form a thin oxide film (thickness in the range of 20-50 nm). Such specimens were considered as the model system for developing novel methods of analysis in understanding the behavior of passive films. The interfacial strain field after oxidation was measured experimentally at the microscale using the point grid method. On the other hand, the chemical composition of the oxide film was determined at the submicroscopic scale by means of local scanning Auger spectroscopy (wi…

Auger electron spectroscopyMaterials scienceMetallurgyOxideModel systemSurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsMicrostructureSurfaces Coatings and Filmschemistry.chemical_compoundchemistryNano-Materials ChemistryThin filmComposite materialChemical compositionMicroscale chemistrySurface and Interface Analysis
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Fabrication of layered nanostructures by successive electron beam induced deposition with two precursors: protective capping of metallic iron structu…

2011

We report on the stepwise generation of layered nanostructures via electron beam induced deposition (EBID) using organometallic precursor molecules in ultra-high vacuum (UHV). In a first step a metallic iron line structure was produced using iron pentacarbonyl; in a second step this nanostructure was then locally capped with a 2-3 nm thin titanium oxide-containing film fabricated from titanium tetraisopropoxide. The chemical composition of the deposited layers was analyzed by spatially resolved Auger electron spectroscopy. With spatially resolved x-ray absorption spectroscopy at the Fe L₃ edge, it was demonstrated that the thin capping layer prevents the iron structure from oxidation upon e…

Auger electron spectroscopyMaterials scienceNanostructureAbsorption spectroscopyMechanical Engineeringtechnology industry and agricultureAnalytical chemistrychemistry.chemical_elementBioengineeringGeneral ChemistryElectron spectroscopyIron pentacarbonylchemistry.chemical_compoundchemistryChemical engineeringMechanics of MaterialsGeneral Materials ScienceElectrical and Electronic EngineeringElectron beam-induced depositionLayer (electronics)TitaniumNanotechnology
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A CEMS/AES study of the passivation of iron

1989

The passivation of iron and steel (DIN 1623) was studied by integral and depth selective conversion electron Mossbauer spectroscopy and Auger electron spectroscopy. Thickness and phase composition of the passive layer formed in sulphate solution and in a phosphate buffer were determined in dependence on the anodic potential and the duration of the passivating procedure. The experimental results lead to the conclusion that not the whole oxidic layer is responsible for the passivity but only a very thin intermediate layer formed between the cubic substrate and the rhombic oxide (γ-FeOOH) cover.

Auger electron spectroscopyMaterials sciencePassivationClinical BiochemistryPassivityInorganic chemistryAnalytical chemistryOxideGeneral MedicineSubstrate (electronics)Analytical ChemistryAnodechemistry.chemical_compoundchemistryConversion electron mössbauer spectroscopyGeneral Materials ScienceLayer (electronics)Fresenius' Zeitschrift für analytische Chemie
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