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showing 10 items of 3080 documents

Persistent photovoltage in methylammonium lead iodide perovskite solar cells

2014

Open circuit voltage decay measurements are performed on methylammonium lead iodide (CH3NH3PbI3) perovskite solar cells to investigate the charge carrier recombination dynamics. The measurements are compared to the two reference polymer-fullerene bulk heterojunction solar cells based on P3HT:PC60BM and PTB7:PC70BM blends. In the perovskite devices, two very different time domains of the voltage decay are found, with a first drop on a short time scale that is similar to the organic solar cells. However, two major differences are also observed. 65-70% of the maximum photovoltage persists on much longer timescales, and the recombination dynamics are dependent on the illumination intensity.

chemistry.chemical_classificationCondensed Matter - Materials ScienceMaterials scienceOrganic solar cellOpen-circuit voltagelcsh:BiotechnologyDrop (liquid)IodideGeneral EngineeringMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciences7. Clean energylcsh:QC1-999Polymer solar cell3. Good healthchemistryChemical physicslcsh:TP248.13-248.65General Materials ScienceCharge carrierddc:621lcsh:PhysicsVoltagePerovskite (structure)APL Materials
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Efficiency Boosting of Surfactants with Poly(ethylene oxide)-Poly(alkyl glycidyl ether)s: A New Class of Amphiphilic Polymers

2020

Twenty years ago, it was found that adding small amounts of amphiphilic block copolymers like poly(ethylene propylene)-co-poly(ethylene oxide) (PEP-b-PEO) to microemulsion systems strongly increases the efficiency of medium-chain surfactants to solubilize water and oil. Although being predestined to serve as a milestone in microemulsion research, the effect has only scarcely found its way into applications. In this work, we propose new types of efficiency boosters, namely, poly(ethylene oxide)-poly(alkyl glycidyl ether carbonate)s (PEO-b-PAlkGE) and their "carbonated" poly(ethylene oxide)-poly(carbonate alkyl glycidyl ether) analogs. Their synthesis via anionic ring-opening polymerization (…

chemistry.chemical_classificationEthylene oxideEther02 engineering and technologySurfaces and InterfacesPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryPolymerizationChemical engineeringAmphiphileddc:540ElectrochemistryGeneral Materials ScienceMicroemulsion0210 nano-technologyEthylene glycolSpectroscopyAlkyl
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Macroscopic persistent currents in YBa2Cu3O7

1988

Persistent currents in polycrystalline YBa2Cu3O7 rings have been investigated by measuring the spatial distribution of the magnetic flux trapped in field-cooled samples. The results unambiguously show that macroscopic persistent ring currents exist. The critical current density depends very sensitively on the sample quality, reachingj c ≈250 A/cm2 at 77 K for our best samples.

chemistry.chemical_classificationMaterials scienceHigh-temperature superconductivityCondensed matter physicspacs:68.35.JaPersistent currentCondensed Matter PhysicsRing (chemistry)Magnetic fluxElectronic Optical and Magnetic Materialslaw.inventionSample qualitychemistrypacs:67.70.+nlawCondensed Matter::Superconductivityddc:530General Materials ScienceCrystalliteCritical currentpacs:61.12.ExInorganic compoundZeitschrift f�r Physik B Condensed Matter
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Hybrid materials from organic polymers and inorganic salts

1994

The prepaparation of amorphous, homogeneous blends of zwitterionic polymers and transition metal salts was investigated. Homogeneous miscibility was achieved in many cases up to equimolar amounts of salt, depending on the anion and cation chosen. Various analytical techniques point to a solid state solution of the inorganic ions in the polymer matrix.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryInorganic chemistrySalt (chemistry)PolymerInorganic ionsCondensed Matter PhysicsMiscibilityAmorphous solidMatrix (chemical analysis)Transition metalchemistryddc:540Materials ChemistryInstitut für ChemieHybrid material
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Mixed polymeric monolayers and Langmuir-Blodgett multilayers with functional low molecular weight guest compounds

2008

Abstract Mixed monolayers and Langmuir-Blodgett multilayers of functional low molecular weight guest compounds, especially nonlinear optical (NLO) dyes, within the matrix of an amphotropic spacer polymer have been prepared. The polymer matrix enabled the transfer of guest compounds not capable of self-organizing at the air-water interface by themselves. The structure of the LB multilayers and the transfer process were studied by small angle X-ray scattering and UV-visible spectroscopy. Good NLO coefficients were found in the mixed films.

chemistry.chemical_classificationMaterials scienceScatteringMetals and AlloysSurfaces and InterfacesPolymerLangmuir–Blodgett filmSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMatrix (chemical analysis)Nonlinear opticalchemistryChemical engineeringMonolayerddc:540Materials ChemistryOrganic chemistryInstitut für ChemieSpectroscopy
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Preformed polymers for Langmuir-Blodgett films- molecular concepts

2008

The use of preformed polymers for the preparation of Langmuir-Blodgett (LB) multilayers is reviewed. Principles for polymer self-organization are outlined and the appropriate molecular designs are discussed. Recent developments in the different classes of polymers for LB multilayers are presented, and their outstanding properties highlighted.

chemistry.chemical_classificationMaterials sciencechemistryPolymer scienceMechanics of MaterialsMechanical Engineeringddc:540Polymer chemistryInstitut für ChemieGeneral Materials SciencePolymerLangmuir–Blodgett filmAmphiphilic copolymerAdvanced Materials
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Cooperative formation of inorganic-organic interfaces in the synthesis of silicate mesostructures.

1993

A model is presented to explain the formation and morphologies of surfactant-silicate mesostructures. Three processes are identified: multidentate binding of silicate oligomers to the cationic surfactant, preferential silicate polymerization in the interface region, and charge density matching between the surfactant and the silicate. The model explains present experimental data, including the transformation between lamellar and hexagonal mesophases, and provides a guide for predicting conditions that favor the formation of lamellar, hexagonal, or cubic mesostructures. Model Q(230) proposed by Mariani and his co-workers satisfactorily fits the x-ray data collected on the cubic mesostructure …

chemistry.chemical_classificationMultidisciplinaryCationic polymerizationMineralogyMesophasePolymerSilicatechemistry.chemical_compoundPulmonary surfactantchemistryPolymerizationChemical engineeringddc:540Lamellar structureGyroidScience (New York, N.Y.)
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Citric Acid Based Carbon Dots with Amine Type Stabilizers: pH-Specific Luminescence and Quantum Yield Characteristics

2020

We report the synthesis and spectroscopic characteristics of two different sets of carbon dots (CDs) formed by hydrothermal reaction between citric acid and polyethylenimine (PEI) or 2,3-diaminopyridine (DAP). Although the formation of amide-based species and the presence of citrazinic acid type derivates assumed to be responsible for a blue emission is confirmed for both CDs by elemental analysis, infrared spectroscopy, and mass spectrometry, a higher abundance of sp2-hybridized nitrogen is observed for DAP-based CDs, which causes a red-shift of the n-π* absorption band relative to the one of PEI-based CDs. These CD systems possess high photoluminescence quantum yields (QY) of ∼40% and ∼48…

chemistry.chemical_classificationPolyethylenimineChemistryLigandQuantum yieldchemistry.chemical_element02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral Energyddc:530Amine gas treatingPhysical and Theoretical Chemistry0210 nano-technologyLuminescenceCitric acidCarbonNuclear chemistryThe Journal of Physical Chemistry C
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Oligoethyleneoxide spacer groups in polymerizable surfactants

1991

Cationic and zwitterionic polymerizable surfactants bearing tri- and tetraethyleneglycol spacer groups between the polymerizable moiety and the surfactant structure were prepared and polymerized. Monomers and polymers were investigated with respect to their aggregation behavior in aqueous systems and compared to analogous monomers and polymers lacking spacer groups. In the case of the monomeric surfactants, the spacer groups depress both the Kraffttemperature and the critical micelle concentration. the area occupied per molecule at the air-water interface is substantially enlarged by the spacers, whereas the depression of surface tension is nearly constant. Although the monomers with and wi…

chemistry.chemical_classificationPolymers and PlasticsCationic polymerizationPolymerMicelleKrafft temperaturechemistry.chemical_compoundColloid and Surface ChemistryMonomerPulmonary surfactantchemistryCritical micelle concentrationddc:540Polymer chemistryMaterials ChemistryInstitut für ChemieMoietyPhysical and Theoretical ChemistryColloid & Polymer Science
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Elastic properties of polymer interfaces: Aggregation of pure diblock, mixed diblock, and triblock copolymers

2002

Block copolymers adsorbing to an interface between two immiscible homopolymers modify the elastic constants of this interface. Within self-consistent field calculations for Gaussian chains, we determine how the bending constants vary in dependence on the block copolymer concentration and architecture. Four phenomena are discussed. (i) When a tricritical or isotropic Lifshitz critical point is approached in a ternary mixture by varying the concentration of diblock copolymers or changing temperature, the elastic constants vanish. We determine the corresponding power laws, and show that the de Gennes--Taupin criterium for the stability of lamellar phases against undulations and the Ginzburg-La…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceIsotropyThermodynamicsFlexural rigidityBendingPolymerJCondensed Matter::Soft Condensed MatterchemistryCritical point (thermodynamics)Copolymerddc:530Lamellar structureTernary operationPhysical Review E
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