Search results for "Substrate"

showing 10 items of 1018 documents

Nano-lithography by electron exposure using an Atomic Force Microscope

1999

Abstract We have used a conductive Atomic Force Microscope (AFM) tip to expose a very thin resist film. An exposing current of low energy electrons was induced from the tip to the substrate by applying a small bias voltage. Uniform resist films as thin as 10 nm were fabricated using the Langmuir–Blodgett technique. To orient the defined pattern and to make electrical connections a special larger scale alignment structure was first defined by conventional electron beam lithography, either directly in the Langmuir–Blodgett resist film or in a separate first lift-off process with a thicker resist. The results from the one resist process gave conducting 50 nm lines with a 60 A thick vacuum depo…

business.industryChemistryBiasingSubstrate (electronics)Condensed Matter PhysicsLangmuir–Blodgett filmAtomic and Molecular Physics and OpticsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOpticsResistTunnel junctionNano-OptoelectronicsElectrical and Electronic EngineeringbusinessLithographyElectron-beam lithographyMicroelectronic Engineering
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ZnO/CdTe/CuSCN, a promising heterostructure to act as inorganic eta-solar cell

2005

Abstract The ZnO/CdTe/CuSCN heterostructure was analyzed as a candidate to act as an inorganic eta -solar cell. A ZnO film consisting of single crystal nanocolumns was electrodeposited on a transparent conducting substrate which acts as n-type material. As absorber material we used CdTe, which was deposited on the ZnO columnar film by Metal Organic Chemical Vapor Deposition. In order to complete the eta -solar cell we deposited a CuSCN layer by chemical solution deposition. A conformal and uniform CdTe coverage of the ZnO columns was achieved, producing a very efficient light trapping effect. The effective absorption (∼87%) and effective reflectance (∼10%) of the complete heterostructure in…

business.industryChemistryInorganic chemistryMetals and AlloysHeterojunctionSurfaces and InterfacesPhotovoltaic effectSubstrate (electronics)Chemical vapor depositionCadmium telluride photovoltaicsSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionlawSolar cellMaterials ChemistryOptoelectronicsThin filmbusinessLayer (electronics)Thin Solid Films
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Synchrotron radiation multiple diffraction study of Al0.304Ga0.172In0.524As MOVPE grown onto InP(001)

1997

Synchrotron radiation multiple diffraction in Renninger scanning (RS) geometry is used to characterise an Al0.304Ga0.172In0.524 As hetero-epitaxial layer MOVPE grown onto InP(001). (006) RS data for bulk, InP substrate and the quaternary layer were obtained using a new experimental set-up on station 7.6 at the Daresbury synchrotron radiation source. Examination of the multiple diffraction peak profiles reveal the epitaxial layers to have a higher mosaic spread than the underlying substrate materials. Measurements of the layer parallel lattice parameter a∥ = 5.8755 ± 0.003 A, as deduced from the tetragonal distortion measured at the 6-beam case in the layer RS, agrees very well with that obt…

business.industryChemistrySynchrotron Radiation SourceAnalytical chemistrySynchrotron radiationSubstrate (electronics)Condensed Matter PhysicsEpitaxyInorganic ChemistryTetragonal crystal systemLattice constantOpticsMaterials ChemistryMetalorganic vapour phase epitaxybusinessLayer (electronics)Journal of Crystal Growth
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Influence of the U3O7 domain structure on cracking during the oxidation of UO2

2010

Abstract Cracking is observed when a UO 2 single crystal is oxidised in air. Previous studies led to the hypothesis that cracking occurs once a critical depth of U 3 O 7 oxidised layer is reached. We present some μ-Laue X-ray diffraction results, which evidence that the U 3 O 7 layer, grown by topotaxy on UO 2 , is made of domains with different crystalline orientations. This observation was used to perform a modelling of oxidation coupling chemical and mechanical parameters, which showed that the domain patterning induces stress localisation. This result is discussed in comparison with stress localisation observed in thin layer deposited on a substrate and used to propose an interpretation…

characterisationNuclear and High Energy PhysicsMaterials scienceoxidation[ SPI.MAT ] Engineering Sciences [physics]/MaterialsFOS: Physical sciences02 engineering and technologySubstrate (electronics)UO201 natural sciencesChemical reaction[SPI.MAT]Engineering Sciences [physics]/Materials[PHYS.MECA.MEMA]Physics [physics]/Mechanics [physics]/Mechanics of materials [physics.class-ph]Stress (mechanics)[SPI.MECA.MEMA]Engineering Sciences [physics]/Mechanics [physics.med-ph]/Mechanics of materials [physics.class-ph]0103 physical sciencesGeneral Materials ScienceThin film010302 applied physicsCondensed Matter - Materials SciencemodeldiffusionMaterials Science (cond-mat.mtrl-sci)[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyCrackingCrystallographyNuclear Energy and EngineeringChemical engineering[ CHIM.MATE ] Chemical Sciences/Material chemistry[ SPI.MECA.MEMA ] Engineering Sciences [physics]/Mechanics [physics.med-ph]/Mechanics of materials [physics.class-ph][ PHYS.MECA.MEMA ] Physics [physics]/Mechanics [physics]/Mechanics of materials [physics.class-ph]U3O7X-ray crystallography0210 nano-technologyLayer (electronics)Single crystalJournal of Nuclear Materials
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Engineering faster transglycosidases and their acceptor specificity

2019

Transglycosidases are enzymes that have the potential to catalyze the synthesis of a wide range of high-value compounds starting from biomass-derived feedstocks. Improving their activity and broadening the substrate range are important goals to enable the widespread application of this family of biocatalysts. In this work, we engineered 20 mutants of the rice transglycosidase Os9BGlu31 and evaluated their catalysis in 462 reactions over 18 different substrates. This allowed us to identify mutants that expanded their substrate range and showed high activity, including W243L and W243N. We also developed double mutants that show very high activity on certain substrates and exceptional specific…

chemistry.chemical_classification010405 organic chemistryExternal validationSubstrate (chemistry)010402 general chemistry01 natural sciencesPollutionAcceptorCombinatorial chemistry0104 chemical sciencesCatalysisEnzymechemistryCheminformaticsEnvironmental ChemistryHigh activityGreen Chemistry
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Iron(II) complex of 2-(1H-pyrazol-1-yl)pyridine-4-carboxylic acid (ppCOOH) suitable for surface deposition

2018

The synthesis, structural and magnetic characterization of the tris iron(II) complex of 2-(1H-pyrazol-1-yl)pyridine-4-carboxylic acid (ppCOOH) ligand are reported in [Fe(ppCOOH)3](ClO4)2·0.5H2O·2EtOH. Single crystal structure and magnetic characterization of the bulk compound show that the low-spin state is dominant from 2 to 400 K. ESI-MS and UV–Vis spectroscopy experiments indicate that acetonitrile solutions of this complex are stable with time. ESI-MS confirms the presence of the tris complex in solution. This complex can be deposited onto SiO2 surfaces due to the presence of carboxylic acid groups by immersing the substrates into acetonitrile solutions of the complex. XPS spectra of th…

chemistry.chemical_classification010405 organic chemistryLigandCarboxylic acidSubstrate (chemistry)010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundCrystallographychemistrySpin crossoverPyridineMonolayerMaterials ChemistryPhysical and Theoretical ChemistryAcetonitrileSingle crystal
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Formation of Aroma by Hydrolysis of Glycosidically Bound Components

1992

SUMMARY Acid hydrolysis has been used in order to establish the presence of glycosidically bound components in fruits. During this treatment, rearrangement reactions of free monoterpene alcohols generally occur. This inconvenient may be avoided using enzymatic hydrolysis, however the specificity of enzymes requires the previous knowledge of the structures of compounds used as substrates in order to control the reaction. Several glycosidically bound components, glucosides, rutinosides and arabinoglucosides present in grapes and apricot were isolated, separated and identified using non destructive methods, MS-MS low energy CAD spectra and HPLC. s-D-glucosidase, α-L-rhamnosidase, α-L-arabinase…

chemistry.chemical_classification0303 health sciencesbiologyChemistry[SDV]Life Sciences [q-bio]Monoterpene010401 analytical chemistrySubstrate (chemistry)biology.organism_classification01 natural sciences0104 chemical sciences[SDV] Life Sciences [q-bio]03 medical and health sciencesHydrolysisEnzymeEnzymatic hydrolysisOrganic chemistryAcid hydrolysisNaringinaseComputingMilieux_MISCELLANEOUSAroma030304 developmental biology
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Silintaphin-1 - interaction with silicatein during structure-guiding bio-silica formation

2011

Silicateins are unique enzymes of sponges (phylum Porifera) that template and catalyze the polymerization of nanoscale silicate to siliceous skeletal elements. These multifunctional spicules are often elaborately shaped, with complex symmetries. They carry an axial proteinaceous filament, consisting of silicatein and the scaffold protein silintaphin-1, which guides silica deposition and subsequent spicular morphogenesis. In vivo, the synthesis of the axial filament very likely proceeds in three steps: (a) assembly of silicatein monomers to form one pentamer; (b) assembly of pentamers to form fractal-like structures; and finally (c) assembly of fractal-like structures to form filaments. The …

chemistry.chemical_classification0303 health sciencesbiologyStereochemistryPentamerSubstrate (chemistry)02 engineering and technologyCell BiologyPolymer021001 nanoscience & nanotechnologybiology.organism_classificationBiochemistryTetraethyl orthosilicateSuberites domunculaProtein filament03 medical and health scienceschemistry.chemical_compoundMonomerchemistryPolymerizationBiophysics0210 nano-technologyMolecular Biology030304 developmental biologyFEBS Journal
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Optical data storage in Langmuir-Blodgett-Kuhn multilayer assemblies of azo-dye side chain LC-polymers

1991

We describe the preparation of LB-films of novel polymers containing azobenzene dye side chains. X-ray refection measurements, surface-plasmon experiments were used to determine the structure of LB-films which had been transferred onto a substrate. Illumination with UV-light causes trans-cis isomerisation of the azobenzene side groups. This effect can be used for optical data storage and will be discussed in detail.

chemistry.chemical_classification3D optical data storageMaterials sciencePolymers and PlasticsOrganic ChemistryPolymerSubstrate (printing)Condensed Matter PhysicsLangmuir–Blodgett filmchemistry.chemical_compoundchemistryChemical engineeringAzobenzeneMaterials ChemistrySide chainOrganic chemistryIsomerizationMakromolekulare Chemie. Macromolecular Symposia
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Photochemical Functionalization of Allyl Benzoates by C-H Insertion

2013

The photoreactivity of allyl benzoates, containing an electron-rich double bond, has been explored by irradiation at 305 nm in different solvents. Solvent addition products arising from an insertion of the alpha H–C bonds of THF, dioxane, and i-PrOH to the allylic double bond was realized. The observed reactivity depended on reaction conditions and substitution pattern of the substrate. A DFT study on this unusual reaction was performed allowing the formulation of two mechanistic pathways.

chemistry.chemical_classificationAllylic rearrangementDouble bondChemistryOrganic ChemistryMechanistic organic photochemistrySubstrate (chemistry)Organic photochemistryPhotochemical synthesis THF reactivityBiochemistryMedicinal chemistryC-C bond formationDFTBenzoatesSolventDrug DiscoverySurface modificationReactivity (chemistry)C-H insertion
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