Search results for "porous material"

showing 10 items of 361 documents

The influence of the anatase nanoparticles boundaries on the titania activity performance

2014

Metal oxides structures, formed by ordered self-assembling of crystalline nanoparticles aggregates, are attracting growing attention in fields such as catalysis or solar cells. The properties of these structures are influenced not only by their morphology and nanoparticles composition but also by the assembled particles boundaries. In order to determine the influence of these boundaries on the structures properties, the present investigation has been devoted to study the characteristics of anatase nanoparticles boundaries in titania aggregates prepared by TiCl4 hydrolysis at low temperature. Proton magic angle spinning nuclear magnetic resonance and high resolution transmission electron mic…

AnataseHRTEMDopantChemistryinter-particles electron transfer [Anatase nanoparticles boundaries]Inorganic chemistryNanoparticleCatalysisCatalysisAmorphous solidChemical engineering4-Methoxybenzyl alcohol partial oxidationMagic angle spinningPhysical and Theoretical ChemistryHigh-resolution transmission electron microscopyMesoporous materialAnatase nanoparticles boundaries: inter-particles electron transferAmorphous titaniaJournal of Catalysis 309: 97-104 (2014)
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Mesocrystalline anatase nanoparticles synthesized using a simple hydrothermal approach with enhanced light harvesting for gas-phase reaction

2018

Mesocrystalline TiO2 nanoparticles were synthesized using a hydrothermal approach. A simple two-step procedure at low temperature (<140 °C) allowed the nucleation of primary particles sized 2–4 nm and their subsequent assembly as almost spherical aggregates sized ≈20 nm. X-ray powder diffraction (XRD), Raman and X-ray photoelectron spectroscopy (XPS) studies, and HRTEM studies confirmed anatase as the unique TiO2 crystalline phase. The mesocrystalline structure of the anatase aggregates was clearly evidenced by HRTEM and SAED results. The mesocrystalline nanopowders exhibit a mesoporous structure with a surface area and pore volume of 63.5 m2 g−1 and 0.22 cm3 g−1, respectively. Ultraviolet …

AnataseMaterials scienceNanoparticle02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesHydrothermal circulation0104 chemical sciencesInorganic ChemistryX-ray photoelectron spectroscopyChemical engineeringPhotocatalysisSelected area diffraction0210 nano-technologyHigh-resolution transmission electron microscopyMesoporous materialDalton Transactions
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2018

We report a novel multi-step method for the preparation of ordered mesoporous titania scaffolds and show an illustrative example of their application to solar cells. The method is based on (monolayer) colloidal nanosphere lithography that makes use of polystyrene nanoparticles organised at a water–air interface and subsequently transferred onto a solid substrate. A titania precursor solution (titanium(IV) isopropoxide in ethanol) is then drop-cast onto the monolayer and left to “incubate” overnight. Surprisingly, instead of the expected inverse monolayer-structure, a subsequent calcination step of the precursor yields an ordered monolayer of hollow titania nanospheres with a wall thickness …

AnataseMaterials scienceNanoparticle02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesNanocrystalline material0104 chemical scienceschemistry.chemical_compoundchemistryX-ray photoelectron spectroscopyChemical engineeringMonolayerMaterials ChemistryNanosphere lithographyPolystyrene0210 nano-technologyMesoporous materialJournal of Materials Chemistry C
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Anionic Organic Guests Incorporated in Zeolites: Adsorption and Reactivity of a Meisenheimer Complex in Faujasites

2005

Zeolites are suitable microporous hosts for positively charged organic species, but it is believed that they cannot adsorb organic anions. Pure Meisenheimer complex, derived from reduction of 2,4-dinitroaniline with NaBH4, was adsorbed inside faujasite cavities. Evidence for the internal incorporation of this negatively charged reaction intermediate comes from 1) XPS elemental analysis as a function of the depth of penetration into the particle, 2) the remarkable blue shift in lambda(max) of the Meisenheimer complex adsorbed on zeolite (ca. 470 nm) as compared to that in acetonitrile (580 nm) and 3) from the lack of reactivity with size-excluded hydride-acceptor reagents. Evidence is provid…

AnionsAniline CompoundsMolecular StructurebiologyChemistryOrganic ChemistryInorganic chemistryGeneral ChemistryReaction intermediateMicroporous materialFaujasiteengineering.materialCatalysisMeisenheimer complexAdsorptionZeolitesbiology.proteinengineeringReactivity (chemistry)AdsorptionZeoliteOxidation-ReductionOrganic anionChemistry - A European Journal
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Borate-driven gatelike scaffolding using mesoporous materials functionalised with saccharides.

2009

We report the development of an MCM-41 mesoporous support that is functionalised with saccharides at the pore outlets and contains the dye [Ru(bipy)(3)](2+) in the pores (solid S1; bipy = 2,2'-bipyridyl). For this hybrid system, the inhibition of mass transport of the dye from the pore voids to the bulk solution in the presence of borate is demonstrated in water at neutral pH. The formation of the corresponding boroester derivative is related to the selective reaction of borate with the appended saccharides. This control is selective and only anion borate, among several anions and cations, can act as a molecular tap and inhibit the delivery of the entrapped guest. Additionally, the S1-borat…

AnionsModels MolecularNanostructureOrganic ChemistryInorganic chemistrychemistry.chemical_elementSpectrometry X-Ray EmissionGeneral ChemistryMesoporous silicaSilicon DioxideCatalysisNanostructuresHydrolysisMolecular dynamicsNanoporechemistryPolysaccharidesPolymer chemistryBoratesHybrid materialMesoporous materialBoronChemistry (Weinheim an der Bergstrasse, Germany)
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Sequestering aromatic molecules with a spin-crossover Fe(II) microporous coordination polymer.

2012

All in a spin: A series of three-dimensional porous coordination polymer {Fe(dpe)[Pt(CN)(4)]}⋅G (dpe = 1,2-di(4-pyridyl)ethylene; G = phenazine, anthracene, or naphthalene) exhibiting spin crossover and host-guest functions is reported. The magnetic properties of the framework are very sensitive to the chemical nature (aromatic or hydroxilic solvents) and the size of the included guest molecules.

AnthraceneEthyleneMolecular StructureCoordination polymerPolymersOrganic ChemistryPhenazineInorganic chemistryMolecular ConformationGeneral ChemistryMicroporous materialCrystallography X-RayCatalysischemistry.chemical_compoundMagneticschemistrySpin crossoverPolymer chemistryMoleculeFerrous CompoundsNaphthaleneChemistry (Weinheim an der Bergstrasse, Germany)
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Spectroelectrochemistry of cytochrome c and azurin immobilized in nanoporous antimony-doped tin oxide

2011

Stable immobilization of two redox proteins, cytochrome c and azurin, in a thin film of highly mesoporous antimony-doped tin oxide is demonstrated via UV-vis spectroscopic and electrochemical investigation.

AntimonyMaterials scienceInorganic chemistrychemistry.chemical_elementElectrochemistryRedoxCatalysisNanoporesAntimonyAzurinMaterials ChemistrybiologyNanoporousCytochrome ctechnology industry and agricultureMetals and AlloysCytochromes cTin CompoundsElectrochemical TechniquesGeneral Chemistryequipment and suppliesTin oxideSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsImmobilized ProteinschemistryCeramics and Compositesbiology.proteinSpectrophotometry UltravioletAdsorptionAzurinMesoporous materialChemical Communications
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Mesoporous aluminum phosphite

2009

Abstract High surface area pure mesoporous aluminum-phosphorus oxide-based derivatives have been synthesized through an S+I− surfactant-assisted cooperative mechanism by means of a one-pot preparative procedure from aqueous solution and starting from aluminum atrane complexes and phosphoric and/or phosphorous acids. A soft chemical extraction procedure allows opening the pore system of the parent as-prepared materials by exchanging the surfactant without mesostructure collapse. The nature of the pore wall can be modulated from mesoporous aluminum phosphate (ALPO) up to total incorporation of phosphite entities (mesoporous aluminum phosphite), which results in a gradual evolution of the acid…

Aqueous solutionInorganic chemistryOxideCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsInorganic ChemistryTemplate reactionMesoporous organosilicachemistry.chemical_compoundAtranechemistryMaterials ChemistryCeramics and CompositesPhysical and Theoretical ChemistryPhosphorous acidMesoporous materialPhosphoric acidJournal of Solid State Chemistry
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Mesoporous iron phosphate/phosphonate hybrid materials

2014

Abstract Relatively high surface area pure mesoporous iron-phosphorus oxide-based derivatives have been synthesized through an S + I − surfactant-assisted cooperative mechanism by means of a one-pot preparative procedure from aqueous solution and starting from iron atrane complexes and phosphoric and phosphonic acids. A soft chemical extraction procedure allows opening the pore system of the parent as-prepared materials by exchanging the surfactant without mesostructure collapse. The nature of the pore wall can be modulated from iron phosphate up to hybrids involving approximately 30% of organophosphorus entities (phosphonates or diphosphonates). X-ray powder diffraction, transmission elect…

Aqueous solutionInorganic chemistryOxideGeneral ChemistryCondensed Matter PhysicsPhosphonatechemistry.chemical_compoundAtranechemistryMechanics of MaterialsGeneral Materials ScienceIron phosphateHybrid materialMesoporous materialPowder diffractionMicroporous and Mesoporous Materials
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Tailored syntheses of nanostructured silicas: Control of particle morphology, particle size and pore size

1998

Ordered mesoporous silicas with spherical morphology and average particle size in the range between 100 nm and 2 μm were synthesised according to two novel routes. Both synthesis routes used tetraethoxysilane, water, alcohol and aqueous ammonia for producing spherical silica beads. The porosity was created by adding two different kinds of pore structure directing agents to the starting solution: one was an n-alkyltrialkoxysilane which was covalently bonded to the silica framework, the other was an n-alkylamine which acted as a nonionic template. After calcination and post treatment the resulting particles showed a specific surface area up to 1000 m2 g-1, a specific pore volume of up to 0.8 …

Aqueous solutionMaterials scienceDispersityGeneral EngineeringNanotechnologylaw.inventionChemical engineeringlawSpecific surface areaParticleCalcinationParticle sizePorosityMesoporous materialSupramolecular Science
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