Search results for "quench"

showing 10 items of 306 documents

Phosphine oxide functionalized pyrenes as efficient blue light emitting multifunctional materials for organic light emitting diodes

2015

In a search for blue light emitting multifunctional materials, the electron transport enhancing diphenyl phosphine–oxide (Ph2PO) group has been appended to blue light emitting pyrene derivatives. This design, we observe, leads to highly efficient electron transporting blue-emitters for non-doped organic light emitting devices (OLEDs) with good film formation characteristics. The superior performance is attributed to enhanced charge transport and formation of pyrene excimers assisted by thermally activated delayed fluorescence (TADF) in the device. We report the synthesis and characterization using experimental and computational methods of six such pyrene derivatives. Although three of these…

Materials scienceQuenching (fluorescence)business.industryStackingGeneral ChemistryPhotochemistryExcimerFluorescencechemistry.chemical_compoundchemistryMaterials ChemistryOLEDOptoelectronicsPyreneThin filmbusinessLuminescenceJournal of Materials Chemistry C
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Carrier-induced quenching processes on the erbium luminescence in silicon nanocluster devices

2006

The luminescence-quenching processes limiting quantum efficiency in Er-doped silicon nanocluster light-emitting devices are investigated and identified. It is found that carrier injection, while needed to excite Er ions through electron-hole recombination, at the same time produces an efficient nonradiative Auger deexcitation with trapped carriers. This phenomenon is studied in detail and, on the basis of its understanding, we propose device structures in which sequential injection of electrons and holes can improve quantum efficiency by avoiding Auger processes. © 2006 The American Physical Society.

Materials scienceSiliconAstrophysics::High Energy Astrophysical Phenomenalight-emitting deviceschemistry.chemical_elementElectronElectroluminescenceSettore ING-INF/01 - ElettronicaSettore FIS/03 - Fisica Della MateriaAugerErbiumCondensed Matter::Materials ScienceELECTROLUMINESCENCEPhysics::Atomic and Molecular ClustersPhysics::Atomic PhysicsQuenchingOPTICAL GAINbusiness.industryCondensed Matter PhysicsElectronic Optical and Magnetic Materials1.54 MU-MchemistryOptoelectronicsQuantum efficiencySI NANOCRYSTALSENERGY-TRANSFERLuminescencebusinessPhysical Review B
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Axialisation, cooling and quenching of $\mathsf{Ba^+}$ ions in a Penning trap

1998

Collisions of ions, stored in a Penning trap, with neutral background molecules usually lead to rapid ion loss from the trap unless the ions are excited by the sum of the frequencies of the reduced cyclotron and magnetron motion. Then the ions are cooled by collisions and are driven to the trap centre leading to substantial increase of the storage time. Furthermore in a three level system including a long living metastable state collisions deexcite this metastable state and increase the population density in the ionic ground state. In a laser spectroscopic experiment we demonstrate the advantages of collisions on Ba+ ions stored in a Penning trap. The combined action of metastable state que…

Materials scienceZeeman effectQuenching (fluorescence)Penning trapAtomic and Molecular Physics and OpticsIonsymbols.namesakeExcited stateMetastabilitysymbolsPhysics::Atomic PhysicsIon trapAtomic physicsGround stateThe European Physical Journal D - Atomic, Molecular and Optical Physics
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Effect of doping and crystallite size on the electrochemical performance of Li4Ti5O12

2016

Abstract Defect spinel phase lithium titanate (Li 4 Ti 5 O 12 ) has been suggested as a promising negative electrode material for next generation lithium ion batteries. Flame spray pyrolysis has been shown to be a viable fast, one-step process for synthesis of nanoparticulate Li 4 Ti 5 O 12 . However, due to the rapid quenching that is integral to the process the crystallite size remain very small and non-uniform. To overcome this shortcoming a vertical flow tube furnace was used to increase the high-temperature residence time. This resulted in an increase in the crystallite size and crystallinity of the product. As a result of this increase the electrochemical performance of the Li 4 Ti 5 …

Materials sciencesynthesista221Nanoparticlechemistry.chemical_elementNanotechnology02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesCrystallinitychemistry.chemical_compoundMaterials ChemistryLi-ion batteryLithium titanateta216ta116QuenchingMechanical EngineeringDopingSpinelMetals and Alloys021001 nanoscience & nanotechnology0104 chemical sciencesphase compositionchemistryChemical engineeringMechanics of MaterialsengineeringLithiumnanoparticlesCrystallite0210 nano-technologyJournal of Alloys and Compounds
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Long-Lived Luminescence and Slow Carrier Diffusion in Metal Halide Perovskites as a result of Multiple Trapping and De-Trapping by Shallow Non-Quench…

2018

MetalQuenching (fluorescence)Materials scienceChemical physicsvisual_artvisual_art.visual_art_mediumHalideTrappingDiffusion (business)LuminescenceProceedings of the nanoGe Fall Meeting 2018
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Influence of a continuous quenching procedure on the initial stages of spinodal decomposition

1986

Instead of the standard assumption in the theory of phase separation where an instantaneous quench from an initial equilibrium state to the final state in the two-phase region is assumed, we consider the more realistic situation that the change of the external control parameter (e.g. temperature) can only be performed with finite rates. During the initial stages of spinodal decomposition the system then has some “memory” of the states intermediate between the initial and the final one. This influence of the finite quench rate in continuous quenching procedures is studied within the linearized theory of spinodal decomposition, with the Langer-Baron-Miller decoupling, and with Monte Carlo sim…

Metallic alloyQuenchingSpinodalMaterials scienceSpinodal decompositionThermodynamic equilibriumMonte Carlo methodThermodynamicsGeneral Materials ScienceState (functional analysis)Decoupling (cosmology)Condensed Matter PhysicsElectronic Optical and Magnetic MaterialsZeitschrift f�r Physik B Condensed Matter
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Tryptophan quenching as linear sensor for oxygen binding of arthropod hemocyanins.

2008

Oxygen binding of hemocyanins results in an absorption band around 340nm and a strong quenching of the intrinsic tryptophan fluorescence. Our study analyses in detail the fluorescence quenching within two hemocyanins, a hexamer (Panulirus interruptus) and a 4 x 6-mer (Eurypelma californicum). Based on the comparison of calculated and measured transfer efficiencies we could show that: (1) For both hemocyanins FRET (fluorescence resonance energy transfer) is exclusively responsible for quenching of the tryptophan fluorescence upon oxygen binding. (2) Tryptophan quenching by FRET is independent of the oxy- or deoxy conformation of the protein. (3) The quenching takes place at the subunit level…

Models MolecularBiophysicschemistry.chemical_elementBiosensing TechniquesRandom hexamerPhotochemistryBiochemistryOxygenAbsorptionProtein structureAnimalsProtein Structure QuaternaryMolecular BiologyArthropodsQuenching (fluorescence)ChemistryTryptophanTryptophanFluorescenceOxygenFörster resonance energy transferSpectrometry FluorescenceEnergy TransferHemocyaninsOxygen bindingProtein BindingBiochimica et biophysica acta
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Modification of Nanocrystalline WO3 with a Dicationic Perylene Bisimide: Applications to Molecular Level Solar Water Splitting

2015

[(N,N?-Bis(2-(trimethylammonium)ethylene) perylene 3,4,9,10-tetracarboxylic acid bisimide)(PF6)2] (1) was observed to spontaneously adsorb on nanocrystalline WO3 surfaces via aggregation/hydrophobic forces. Under visible irradiation (? > 435 nm), the excited state of 1 underwent oxidative quenching by electron injection (kinj > 108 s-1) to WO3, leaving a strongly positive hole (Eox ? 1.7 V vs SCE), which allows to drive demanding photo-oxidation reactions in photoelectrochemical cells (PECs). The casting of IrO2 nanoparticles (NPs), acting as water oxidation catalysts (WOCs) on the sensitized electrodes, led to a 4-fold enhancement in photoanodic current, consistent with hole transfer from …

Models MolecularMolecular ConformationNanoparticleImidesPhotochemistryBiochemistryTungstenCatalysisNOCatalysiElectron Transportchemistry.chemical_compoundColloid and Surface ChemistryTheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYWO3ComputingMethodologies_SYMBOLICANDALGEBRAICMANIPULATIONperylenePhotoelectrochemical cellIrO2Quenching (fluorescence)Chemistry (all)charge transferWaterOxidesGeneral ChemistryPhotoelectrochemical cellPhotochemical ProcessesSolar fuelChemistry (all); Catalysis; Biochemistry; Colloid and Surface ChemistryNanocrystalline materialperylene WO3 charge transfer IrO2MicrosecondchemistryWater SplittingSunlightVISIBLE-LIGHT; ARTIFICIAL PHOTOSYNTHESIS; PHOTOELECTROCHEMICAL CELL; OXIDATION CATALYSTS; ELECTRON-TRANSFER; FABRICATIONNanoparticlesPerylene bisimideWater splittingPeryleneMathematicsofComputing_DISCRETEMATHEMATICS
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Singlet Excited-State Interactions in Naphthalene-Thymine Dyads

2004

Two thymidine-derived nucleosides 1 and 2 were prepared by attaching a chiral naphthalene to the positions 5′ and 3′ of the sugar. The resulting dyads, which contain key substructures present in drugs and nucleic acids, exhibit different spatial arrangements (transoid or cisoid) of the fluorophore relative to the thymine unit. Emission measurements on these compounds in the presence of ROH molecules revealed a remarkable intramolecular fluorescence quenching for dyad 1. The obtained results are consistent with quenching of the singlet excited state of 1 by hydrogen-bond donor solvents. Thus, a physical deactivation process (vibronically induced internal conversion) would be the pathway resp…

Models MolecularPhotolysisQuenching (fluorescence)ChemistryLasersMolecular ConformationNaphthalenesCrystallography X-RayInternal conversion (chemistry)PhotochemistryFluorescenceAtomic and Molecular Physics and OpticsThyminechemistry.chemical_compoundSpectrometry FluorescenceIntersystem crossingIntramolecular forceExcited stateSpectrophotometry UltravioletSinglet statePhysical and Theoretical ChemistryThymineChemPhysChem
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Design and Synthesis of Novel 1,3-Thiazole and 2-Hydrazinyl-1,3-Thiazole Derivatives as Anti-

2019

In the context of there being a limited number of clinically approved drugs for the treatment of Candida sp.-based infections, along with the rapid development of resistance to the existing antifungals, two novel series of 4-phenyl-1,3-thiazole and 2-hydrazinyl-4-phenyl-1,3-thiazole derivatives were synthesized and tested in vitro for their anti-Candida potential. Two compounds (7a and 7e) showed promising inhibitory activity against the pathogenic C. albicans strain, exhibiting substantially lower MIC values (7.81 μg/mL and 3.9 μg/mL, respectively) as compared with the reference drug fluconazole (15.62 μg/mL). Their anti-Candida activity is also supported by molecular docking studies, usin…

Molecular Docking Simulation13-thiazoleStructure-Activity RelationshipAntifungal Agentsbovine serum albuminfluorescence quenchingSerum Albumin Bovineanti-Candidamolecular dockingArticleCandidaMolecules (Basel, Switzerland)
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