Search results for "Faces"

showing 10 items of 3167 documents

Perovskite solar cells prepared by flash evaporation

2015

A simple vacuum deposition method for the preparation of high quality hybrid organic-inorganic methylammonium lead iodide perovskite thin films is reported. When sandwiched in between organic charge transporting layers, such films lead to solar cells with a power conversion efficiency of 12.2%.

chemistry.chemical_classificationMaterials scienceF100IodideInorganic chemistryEnergy conversion efficiencyF200Metals and AlloysFlash evaporationGeneral ChemistryHybrid solar cellCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryChemical engineeringVacuum depositionMaterials ChemistryCeramics and CompositesThin filmPerovskite (structure)Chemical Communications
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Solvent Determines Nature of Effective Interactions between Nanoparticles in Polymer Brushes

2015

We study the effective interaction between two parallel rod-like nanoparticles in swollen and collapsed polymer brushes as a function of penetration depth by 2D self-consistent field calculations. In vertical direction, the interaction is always attractive. In lateral direction, the behavior under good and poor solvent conditions is qualitatively different. In swollen brushes (good solvent), nanoparticles always repel each other. In collapsed brushes (poor solvent), we identify two different regimes: an immersed regime, where the nanoparticles are fully surrounded by the brush, and an interfacial regime, where they are located in the interface between brush and solvent. In the immersed regi…

chemistry.chemical_classificationMaterials scienceField (physics)BrushNanoparticleNanotechnologyPolymerSurfaces Coatings and Filmslaw.inventionSolventchemistrylawChemical physicsVertical directionMaterials ChemistryPhysical and Theoretical ChemistryPenetration depthThe Journal of Physical Chemistry B
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Affinity Distributions of a Molecularly Imprinted Polymer Calculated Numerically by the Expectation-Maximization Method

2003

Affinity distributions are calculated from adsorption isotherm data obtained for the enantiomers of L- and D-phenylalanine anilide (PA) on native and thermally annealed polymers molecularly imprinted with L-PA. The calculation is obtained with an iterative algorithm called expectation-maximization that does not require prior fit of the data to an isotherm model before inversion and thus yields a distribution indicative of the data only. The results show bimodal distributions, suggestive of a two-site model describing relatively selective and nonselective adsorption modes of the L-enantiomer and a corresponding unimodal/nonselective adsorption mode for the D-enantiomer. The nonselective adso…

chemistry.chemical_classificationMaterials scienceGaussianAnalytical chemistryMolecularly imprinted polymerSurfaces and InterfacesPolymerCondensed Matter Physicssymbols.namesakeAdsorptionDistribution (mathematics)chemistrySelective adsorptionExpectation–maximization algorithmElectrochemistrysymbolsGeneral Materials ScienceEnantiomerSpectroscopyLangmuir
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Single-Molecule Spectroscopy of MEH-PPV Polymer Molecules in Different Host Matrices

2009

Fluorescence emission and excitation spectra of single MEH-PPV molecules dispersed in three different host polymers (PMMA, PS, and Zeonex) have been recorded at 1.2 K. We observed only minor effects of the host matrix on the following parameters: the ratios of single-chromophoric to multichromophoric emission, the widths of the distributions of emission maxima, and the (generally very low) fraction of emission spectra with sharp zero-phonon lines. The differences are tentatively attributed to different conformations of MEH-PPV chains, subtle variations in local chromophore−matrix interactions, and/or different distributions of conjugation lengths of emitting chromophores, respectively. Usin…

chemistry.chemical_classificationMaterials scienceHost (biology)Analytical chemistryPolymerChromophoreMolecular physicsFluorescenceSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMatrix (mathematics)General EnergychemistryMoleculeEmission spectrumPhysical and Theoretical ChemistryMaximaThe Journal of Physical Chemistry C
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Ion bombardment of polyethylene—influence of polymer structure

2007

Abstract Polyethylenes of various macromolecular and supermolecular structures were studied from the point of view of their susceptibility to an ion beam treatment. An influence of molecular weight (Mw), molecular weight distribution (Mw/Mn) and the degree of branching were compared within the set of low-density polyethylenes (LDPE) studied. An influence of the length of branches was compared between LDPE, linear low-density (LLDPE) and high-density (HDPE) polyethylenes. An influence of the degree of crystallinity and the morphology of a crystalline phase were compared for HDPE samples solidified under various thermal conditions and ultra-high molecular weight polyethylene (UHMWPE). Plate p…

chemistry.chemical_classificationMaterials scienceIon beamPolymerPolyethyleneCondensed Matter PhysicsSurfaces Coatings and FilmsIonCondensed Matter::Soft Condensed MatterLinear low-density polyethyleneLow-density polyethylenechemistry.chemical_compoundCrystallinitychemistryChemical engineeringPolymer chemistryHigh-density polyethyleneInstrumentationVacuum
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Covalently attached polymer mono- and multilayers on silanized glass substrates

1996

Abstract Applying grazing incidence FTIR and ellipsometry, the reaction of poly [(1-methyl-vinyl isocyanate)-alt-(maleic anhydride)](IAP) with amino-silanized glass and silicon oxide surfaces has been investigated. A reactive surface containing isocyanate and anhydride groups was formed after the adsorption of the polymer. The layer could be further functionalized using 2-aminoethanol. Multilayers could be built up by adsorbing a second layer of IAP onto an already reacted first layer of IAP.

chemistry.chemical_classificationMaterials scienceMetals and AlloysMaleic anhydrideSurfaces and InterfacesPolymerIsocyanateSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundAdsorptionchemistrySilanizationPolymer chemistryMaterials ChemistryFourier transform infrared spectroscopySilicon oxideLayer (electronics)Thin Solid Films
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Formation of nanorods by self-assembly of alkyl-substituted polyphenylene dendrimers on graphite

2000

Alkyl-substituted polyphenylene dendrimers with a tetrahedral or disk-like shape form self-assembled monolayers on graphite (HOPG) which show complex supramolecular structures, such as parallel rods of 6 nm diameter or two-dimensional crystals.

chemistry.chemical_classificationMaterials scienceMetals and AlloysSupramolecular chemistryNanotechnologyGeneral ChemistryCatalysisRodSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistryDendrimerMonolayerMaterials ChemistryCeramics and CompositesNanorodGraphiteSelf-assemblyAlkylChemical Communications
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Structured Nanoparticles from the Self-Assembly of Polymer Blends through Rapid Solvent Exchange

2017

Molecular dynamics simulations were performed to study systematically the rapid mixing of a polymer blend in solution with a miscible nonsolvent. In agreement with experiments, we observe that polymers self-assemble into complex nanoparticles, such as Janus and core-shell particles, when the good solvent is displaced by the poor solvent. The emerging structures can be predicted on the basis of the surface tensions between the polymers as well as between the polymers and the surrounding liquid. Furthermore, the size of the nanoparticles can be independently tuned through the mixing rate and the polymer concentration in the feed stream; meanwhile, the composition of the nanoparticles can be c…

chemistry.chemical_classificationMaterials scienceMixing (process engineering)Nanoparticle02 engineering and technologySurfaces and InterfacesPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesSolventMolecular dynamicsChemical engineeringchemistryPolymer chemistryElectrochemistryGeneral Materials ScienceParticle sizePolymer blendJanus0210 nano-technologySpectroscopyLangmuir
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On the Stability of Polymeric Nanoparticles Fabricated through Rapid Solvent Mixing.

2018

We study the stability of polymeric nanoparticles fabricated through the rapid mixing of polymers in a good solvent with a poor solvent that is miscible with the good solvent. In previous experiments where water was used as the poor solvent, a negative surface charge was measured on the precipitated nanoparticles, which led to the long-time stability of the dispersion. It was argued that these charges originate presumably from either water or hydroxide adsorption at the hydrophobic nanoparticle surface or from impurities in the feed streams that preferentially adsorb on the precipitated nanoparticles. To elucidate the origin of this stabilization mechanism, we performed experiments wherein …

chemistry.chemical_classificationMaterials scienceMixing (process engineering)Nanoparticle02 engineering and technologySurfaces and InterfacesPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesSolventchemistry.chemical_compoundAdsorptionChemical engineeringchemistryElectrochemistryHydroxideGeneral Materials ScienceSurface charge0210 nano-technologyDispersion (chemistry)SpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Effect of the Components Molar Mass and of the Mixing Conditions on the Compatibilization of PE/LCP Blends by PE-g-LCP Copolymers

1999

The rheology, morphology, and mechanical properties of blends of high-density polyethylene (HDPE) with a semiflexible liquid crystalline copolyester (SBH) were studied in order to assess the compatibilizing ability of added PE-g-SBH copolymers, and its dependence on the molar mass of the PE matrix, and on the technique used for blend preparation. The PE-g-SBH copolymers were synthesized as described in previous articles, either by the polycondensation of the SBH monomers in the presence of a functionalized PE sample containing free carboxyl groups, or by reactive blending of the latter polymer with preformed SBH. Two samples of HDPE having different molar masses, and two samples of SBH with…

chemistry.chemical_classificationMaterials scienceMolar massCondensation polymerPolymers and PlasticscompatibilizationGeneral ChemistryPolymerCompatibilizationPolyethyleneCopolyesterSurfaces Coatings and Filmschemistry.chemical_compoundchemistrypolyethylene-LCP blendmorphologyMaterials ChemistryCopolymerrheologyHigh-density polyethyleneComposite material
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