Search results for "Surfaces"

showing 10 items of 2837 documents

Photoluminescence quantum yield exceeding 80% in low dimensional perovskite thin-films via passivation control

2017

Quasi-2D perovskites with the BA : MA molar ratio equal to 3 : 3 show a remarkable PLQY exceeding 80%, thanks to the use of an electron donor as the passivating agent. These films have been applied in LEDs that exhibit high brightness exceeding 1000 cd m−2 and current efficiencies >3 cd A−1.

BrightnessPhotoluminescenceMaterials sciencePassivationQuantum yieldElectron donor02 engineering and technology010402 general chemistry01 natural sciencesCatalysislaw.inventionchemistry.chemical_compoundlawMaterials ChemistryThin filmPerovskite (structure)business.industryMetals and AlloysGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCeramics and CompositesOptoelectronics0210 nano-technologybusinessLight-emitting diodeChemical Communications
researchProduct

Formation of an unprecedented (CuBr)5 cluster and a zeolite-type 2D-coordination polymer: a surprising halide effect

2013

A unique pentanuclear cluster within a zeolite-type polymer ([Cu5(μ4-Br)(μ3-Br)2(μ2-Br)2](μ2-MeSPr)3)n (1; void space >81%) and a luminescent 1D ([Cu(μ3-I)]4(MeSPr)3)n polymer, 2, are formed when MeSPr reacts with CuBr and CuI.

BromidesModels MolecularPolymersCoordination polymerInorganic chemistryHalide010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundHalogensPolymer chemistryMaterials ChemistryCluster (physics)ZeoliteComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationLuminescent Agents010405 organic chemistryMetals and AlloysGeneral ChemistryPolymer3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryVoid spaceZeolitesCeramics and CompositesLuminescenceCopperChemical Communications
researchProduct

Cationic and Zwitterionic Polymerizable Surfactants:  Quaternary Ammonium Dialkyl Maleates. 1. Synthesis and Characterization

1999

Cationic and zwitterionic reactive dialkyl maleates with different hydrophobic chain lengths (R = C10H21, C12H25, C16H33, and C18H37), and some similar surfactants without double bonds were synthesized with an aim to use them as stabilizers in the batch and seeded emulsion copolymerization of styrene and butyl acrylate (part 2 of this series). Surfactants are obtained in a three-step synthesis, starting from ring opening of maleic anhydride, followed by O alkylation with an aminoalkyl compound, and finishing with quaternization of the amino group in the hydrophilic part of the molecule. The chemical structure of surfactants was confirmed by 1H NMR. Melting points and critical micelle concen…

Butyl acrylateCationic polymerizationMaleic anhydrideSurfaces and InterfacesCondensed Matter PhysicsMicelleStyrenechemistry.chemical_compoundPulmonary surfactantchemistryElectrochemistryCopolymerOrganic chemistryGeneral Materials SciencePolystyreneSpectroscopyLangmuir
researchProduct

Chemical Identification at the Solid–Liquid Interface

2017

Solid-liquid interfaces are decisive for a wide range of natural and technological processes, including fields as diverse as geochemistry and environmental science as well as catalysis and corrosion protection. Dynamic atomic force microscopy nowadays provides unparalleled structural insights into solid-liquid interfaces, including the solvation structure above the surface. In contrast, chemical identification of individual interfacial atoms still remains a considerable challenge. So far, an identification of chemically alike atoms in a surface alloy has only been demonstrated under well-controlled ultrahigh vacuum conditions. In liquids, the recent advent of three-dimensional force mapping…

CALCIUM-CARBONATEMOLECULAR-DYNAMICS SIMULATIONSSURFACEInterface (Java)AlloyNanotechnology02 engineering and technologyengineering.material010402 general chemistry53001 natural sciencesAQUEOUS-SOLUTIONCorrosionElectrochemistryWATERGeneral Materials ScienceFIELDSpectroscopySpectroscopySolid liquidATOMIC-FORCE MICROSCOPYta114ChemistryAtomic force microscopyHYDRATIONSolvationSurfaces and Interfaces021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesRESOLUTIONengineeringIdentification (biology)0210 nano-technologyLangmuir
researchProduct

Molecular Self-Assembly Versus Surface Restructuring During Calcite Dissolution.

2016

Organic additives are known to alter the mineral-water interface in various ways. On the one hand, organic molecules can self assemble into ordered structures wetting the surface. On the other hand, their presence can affect the interfacial morphology, referred to as surface restructuring. Here, we investigate the impact, of a class of calcium-complexing azo dyes on the dissolution of calcite (10.4) using high-resolution atomic force microscopy operated in aqueous solution, with a focus on the two constitutional isomers Eriochrome Black T and Eriochrome Black A. A very pronounced surface restructuring is observed in the presence of the dye solution, irrespective of the specific dye used and…

CalciteAqueous solutionMorphology (linguistics)Chemistry02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences5300104 chemical sciencesEriochrome Black Tchemistry.chemical_compoundChemical engineeringElectrochemistryMolecular self-assemblyOrganic chemistryMoleculeGeneral Materials ScienceWetting0210 nano-technologyDissolutionSpectroscopyLangmuir : the ACS journal of surfaces and colloids
researchProduct

Where Is the Most Hydrophobic Region? Benzopurpurine Self-Assembly at the Calcite–Water Interface

2017

Control of molecular self-assembly at solid–liquid interfaces is challenging due to the complex interplay between molecule–molecule, molecule–surface, molecule–solvent, surface–solvent, and solvent–solvent interactions. Here, we use in-situ dynamic atomic force microscopy to study the self-assembly of Benzopurpurine 4B into oblong islands with a highly ordered inner structure yet incommensurate with the underlying calcite (10.4) surface. Molecular dynamics and free energy calculations provide insights by showing that Benzopurpurine 4B molecules do not anchor to the surface directly but instead assemble on top of the second hydration layer. This seemingly peculiar behavior was then rationali…

CalciteChemistryAtomic force microscopy02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology53001 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsHydrophobeMolecular dynamicschemistry.chemical_compoundCrystallographyGeneral EnergyAdsorptionChemical physicsMoleculeSelf-assemblyPhysical and Theoretical Chemistry0210 nano-technologyLayer (electronics)The Journal of Physical Chemistry C
researchProduct

Stabilization of Polar Step Edges on Calcite (10.4) by the Adsorption of Congo Red

2015

In this work, we present the stabilization of polar step edges along the [010] direction of calcite (10.4) by the presence of a water-soluble organic molecule, namely Congo Red. While characteristic etch pits are observed on the surface in the absence of the additive, no etch pits can be found in the presence of the additive. Using atomic force microscopy, we can directly follow the restructuring of the surface. Upon addition of Congo Red, the charge-neutral step edges confining the characteristic etch pits vanish, while polar step edges along the [010] direction appear on the surface, which are entirely decorated by well-ordered molecular islands of the additive. After the restructuring ha…

CalciteChemistryDirect evidenceAtomic force microscopyMineralogySurfaces and InterfacesCondensed Matter Physics530Congo redchemistry.chemical_compoundAdsorptionChemical physicsElectrochemistryPolarStep edgesMoleculeGeneral Materials ScienceSpectroscopy
researchProduct

Reactivity of gypsum faces according to the relative humidity by scanning force microscopy

1997

Abstract This article reports the experimental observation of the stability of the different faces of calcium sulphate dihydrate (gypsum CaSO 4 .2H 2 O) according to the relative humidity. Scanning Force Microscopy experiments were carried out with a view to discerning the topography of the surfaces, the chemical compositional domains, and in an attempt to evaluate the friction and viscoelastic properties of the surface. Our results indicate that the (010) face of gypsum is hydrophilic and very reactive contrary to the less hydrophilic (120) and (101) faces which remain stable depending on the relative humidity. It is clear from our results that a precipitation like process can be induced b…

CalciteGypsumPrecipitation (chemistry)MuscoviteSurfaces and Interfacesengineering.materialCondensed Matter PhysicsSurfaces Coatings and Filmschemistry.chemical_compoundCrystallographychemistryMicroscopyMaterials ChemistryengineeringRelative humidityMicaWettingComposite materialSurface Science
researchProduct

Deposition order controls the first stages of a metal-organic coordination network on an insulator surface

2016

| openaire: EC/FP7/610446/EU//PAMS We report on first stages toward the formation of a surface-confined metal-organic coordination network (MOCN) by sequential deposition of biphenyl-4,4′-dicarboxylic acid and iron atoms on the surface of a bulk insulator, calcite (10.4). The influence of the deposition order on the structure formation is studied by noncontact atomic force microscopy operated in ultrahigh vacuum at room temperature. It is found that sequential deposition facilitates MOCN formation when the organic linker molecules are first adsorbed on the surface, followed by iron deposition. This observation is explained by first-principles computations, indicating that the metal-molecule…

CalciteStructure formationta114Atomic force microscopyIron deposition02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology53001 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistry.chemical_compoundGeneral EnergyAdsorptionchemistryChemical physicsLattice (order)Coordination networkMoleculePhysical and Theoretical Chemistry0210 nano-technologyJournal of Physical Chemistry C
researchProduct

Clear signature of the (2 x 1) reconstruction of calcite (1014).

2010

Calcite is a mineral of fundamental importance that plays a crucial role in many fields of research such as biomineralization, biomolecule adsorption, and reactivity as well as industrial and daily life applications. Consequently, the most stable cleavage plane of calcite has been studied extensively using both direct imaging techniques such as atomic force microscopy as well as spectroscopic and diffraction techniques. Several surface structures have been reported for the (10 (1) over bar4) cleavage plane of calcite differing from the simple bulk-truncated structure and an ongoing controversy exists in literature whether the cleavage plane exhibits a (2 x 1) reconstruction or not. We study…

CalciteSurface (mathematics)chemistry.chemical_classificationDiffractionMineralMaterials scienceBiomoleculeSurfaces and InterfacesCondensed Matter PhysicsMicroscopy Atomic Force530Calcium Carbonatechemistry.chemical_compoundCrystallographyAdsorptionCalcium carbonatechemistryChemical physicsElectrochemistryGeneral Materials ScienceSpectroscopyBiomineralizationLangmuir : the ACS journal of surfaces and colloids
researchProduct