Search results for "quench"

showing 10 items of 306 documents

Optical quenching and recovery of photoconductivity in single-crystal diamond

2017

We study the photocurrent induced by pulsed-light illumination (pulse duration is several nanoseconds) of single-crystal diamond containing nitrogen impurities. Application of additional continuous-wave light of the same wavelength quenches pulsed photocurrent. Characterization of the optically quenched photocurrent and its recovery is important for the development of diamond based electronics and sensing. (C) 2017 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license. This work was supported by AFOSR and the DARPA QuASAR program, by NSF Grant No. ECCS-1202258, and by DFG through the DIP program (FO 703/2-1).

TechnologyPhysics and Astronomy (miscellaneous)FOS: Physical sciencesPhysics::Optics02 engineering and technologyengineering.material01 natural sciencesEngineeringOpticsImpuritycond-mat.mes-hall0103 physical sciencesMesoscale and Nanoscale Physics (cond-mat.mes-hall)010306 general physicsApplied PhysicsPhotocurrentPhysicsQuenchingCondensed Matter - Mesoscale and Nanoscale Physicsbusiness.industryCondensed Matter::OtherPhotoconductivityDiamondPulse durationQuantum PhysicsNanosecond021001 nanoscience & nanotechnologyCondensed Matter::Mesoscopic Systems and Quantum Hall EffectWavelengthPhysical SciencesengineeringOptoelectronicsphysics.optics0210 nano-technologybusinessOptics (physics.optics)Physics - Optics
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Synthesis and Characterization of New Fluorescent Styrene-Containing Carborane Derivatives: The Singular Quenching Role of a Phenyl Substituent

2011

A set of neutral and anionic carborane derivatives in which the styrenyl fragment is introduced as a fluorophore group has been successfully synthesized and characterized. The reaction of the monolithium salts of 1-Ph-1,2-C(2)B(10)H(11), 1-Me-1,2-C(2)B(10)H(11) and 1,2-C(2)B(10)H(12) with one equivalent of 4-vinylbenzyl chloride leads to the formation of compounds 1-3, whereas the reaction of the dilithium salt of 1,2-C(2)B(10)H(12) with two equivalents of 4-vinylbenzyl chloride gives disubstituted compound 4. The closo clusters were degraded using the classical method, KOH in EtOH, to afford the corresponding nido species, which were isolated as tetramethylammonium salts. The crystal struc…

TetramethylammoniumQuenching (fluorescence)Organic ChemistrySubstituentGeneral ChemistryCrystal structurePhotochemistryMedicinal chemistryFluorescenceCatalysisDilithiumchemistry.chemical_compoundchemistryCarboranePhenyl groupta116Chemistry : A European Journal
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Conceptual Design and Modeling of Fast Discharge Unit for Quench Protection of Superconducting Toroidal Field Magnets of DTT

2020

The paper deals with the modelling and simulation of a Fast Discharge Unit (FDU) for quench protection of the Toroidal Field (TF) magnets of the Divertor Tokamak Test, an experimental facility under design and construction in Frascati (Italy). The FDU is a safety key component that protects the superconducting magnets when a quench is detected through the fast extraction of the energy stored in superconducting magnets by adding in the TF magnets a dump (or discharge) resistor. In the paper, two different configurations of dump resistors (fixed and variable respectively) have been analysed and discussed. As a first result, it is possible to underline that the configuration with variable dump…

TokamakMaterials scienceNuclear engineeringFDUSuperconducting magnet01 natural sciences010305 fluids & plasmaslaw.inventionhybrid circuit breakerConceptual designPhysics::Plasma Physicslaw0103 physical sciencesdump resisto010306 general physicsSuperconductivityToroidal fieldDivertorquench protectionSettore ING-IND/33 - Sistemi Elettrici Per L'EnergiaSettore ING-IND/31 - ElettrotecnicaMagnetPhysics::Accelerator Physicssuperconducting magnetsResistorQPC2020 IEEE 20th Mediterranean Electrotechnical Conference ( MELECON)
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Exciton emission and defect formation in yttrium trifluoride

2005

Two intrinsic emission bands at 220 and 280 nm have been detected in nominally pure YF3 powders at 10 K. Excitation spectra for both emissions have a sharp peak at 12 eV near the edge of interband transition. Observed emissions are assigned to the radiative decay of self-trapped excitons in YF3. The strong thermal quenching of intrinsic luminescence was observed at temperature above 120 K. It was supposed that non-radiative decay of self-trapped exciton at high temperatures lead to defect formation in YF3. (© 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)

TrifluoridechemistryIntrinsic luminescenceExcitonExcitation spectraRadiative decaychemistry.chemical_elementYttriumAtomic physicsThermal quenchingphysica status solidi (c)
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Impact of buffer gas quenching on the $^1S_0$ $\to$ $^1P_1$ ground-state atomic transition in nobelium

2017

International audience; Using the sensitive Radiation Detected Resonance Ionization Spectroscopy (RADRIS) techniquean optical transition in neutral nobelium (No, Z = 102) was identified. A remnant signal when delaying the ionizing laser indicated the influence of a strong buffer gas induced de-excitation of the optically populated level. A subsequent investigation of the chemical homologue, ytterbium (Yb, Z = 70), enabled a detailed study of the atomic levels involved in this process, leading to the development of a rate equation model. This paves the way for characterizing resonance ionization spectroscopy (RIS) schemes used in the studyof nobelium and beyond, where atomic properties are c…

YtterbiumQuenching (fluorescence)Materials scienceBuffer gaschemistry.chemical_elementRate equation[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]01 natural sciencesAtomic and Molecular Physics and OpticsSpectral line010305 fluids & plasmaschemistry0103 physical sciencesAtomic Physicsddc:530NobeliumPhysics::Atomic PhysicsAtomic physics010306 general physicsGround stateSpectroscopy
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Cyclotriveratrylene-Containing Porphyrins

2016

International audience; The C-3-symmetric cyclotriveratrylene (CTV) was covalently bonded via click chemistry to 1, 2, 3, and 6 zinc(II) porphyrin units to various host for C-60. The binding constants, Ka, were measured from the quenching of the porphyrin fluorescence by C-60. These constants vary between 400 and 4000 M-1 and are considered weak. Computer modeling demonstrated that the zinc(II) porphyrin units, [Zn], exhibit a strong tendency to occupy the CTV cavity, hence blocking the access for C-60 to land on this site. Instead, the pincer of the type [Zn]-[Zn] and in one case [Zn]-CTV, were found to be the most probable geometry to promote host-guest associations in these systems.

cagesStereochemistrychemistry.chemical_elementCyclotriveratryleneZinc010402 general chemistry01 natural sciences[ CHIM ] Chemical Sciencessupramolecular chemistrydendrimersInorganic Chemistrychemistry.chemical_compoundc-60[CHIM]Chemical SciencesmoleculesctvPhysical and Theoretical Chemistryinclusion complexesQuenching (fluorescence)010405 organic chemistryfullereneFluorescencePorphyrin0104 chemical sciencesPincer movementCrystallographychemistryCovalent bondClick chemistryderivativeshosts
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1989

Poly(9,10-dihydroanthrylenetrimethylene) (2) comprises a novel chain-type structure in which 9,10-dihydroanthracene units are linked by flexible spacer groups. Upon dehydrogenation with sulfur at elevated temperature, polymer 2 is converted into the corresponding polyanthrylene system 3. NMR- and UV-spectroscopic data provide firm evidence for the dehydrogenation process. The polymer 3 was subjected to reduction with active lithium, and the resulting polyanions were characterized by NMR spectroscopy and by quenching experiments. It appears that each anthracene unit of the chain can be charged with two electrons.

chemistry.chemical_classificationAnthraceneQuenching (fluorescence)chemistry.chemical_elementNuclear magnetic resonance spectroscopyPolymerElectron acceptorPhotochemistrySulfurchemistry.chemical_compoundchemistryPolymer chemistryLithiumDehydrogenationDie Makromolekulare Chemie
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A Simple and Versatile Route to Stable Quantum Dot−Dye Hybrids in Nonaqueous and Aqueous Solutions

2008

Hybrid systems consisting of core/shell semiconductor quantum dots (QDs) and organic rylene dyes have been prepared and characterized. Complex formation is mediated by bidentate carboxylate moieties covalently linked to the dye molecules. The complexes were very stable with respect to time (at least months), dilution (sub nM), and precipitation. After preparation in organic solvent, complexes could be easily transferred into water. The strong quenching of QD emission by the dye molecules (transfer efficiencies up to 95%) was satisfactorily modeled by an FRET process. Single complexes immobilized in thin polymer films were imaged by confocal fluorescence microscopy.

chemistry.chemical_classificationAqueous solutionQuenching (fluorescence)Inorganic chemistryGeneral ChemistryPolymerBiochemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryFörster resonance energy transferchemistryCovalent bondQuantum dotMoleculeCarboxylateJournal of the American Chemical Society
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Characterization of interaction between tricyclic structures containing pharmaceuticals, their models and humic substances.

2011

Their persistence and wide consumption identify pharmaceuticals as “emerging pollutants”. The complexation of pharmaceuticals containing adamantine ring structures and their model substances with humic acids (HA) of different origins was compared using fluorescence spectroscopy as a function of pH, humic acid concentration, ionic strength, and molecular mass of HA. Binding constants between the studied pharmaceuticals and humic acids were calculated. A combination of dynamic and static quenching processes as indicated by nonlinear Stern-Volmer plots and high Kd values were positively correlated with the concentration of carboxyl groups in the studied humic acids. For basic functional group-…

chemistry.chemical_classificationEnvironmental EngineeringQuenching (fluorescence)Molecular massMolecular Structurecomplex mixturesWaste Disposal FluidFluorescence spectroscopyCharacterization (materials science)Water PurificationHydrophobic effectchemistryPharmaceutical PreparationsIonic strengthOrganic chemistryHumic acidHumic SubstancesWater Pollutants ChemicalWater Science and TechnologyTricyclicWater science and technology : a journal of the International Association on Water Pollution Research
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New molecular catalysts for ATP cleavage. Criteria of size complementarity

2000

The interaction of the cyclophane receptor 2,5,8,11,14,17-hexaaza[18]metacyclophane (L) with the nucleotides ATP, ADP and AMP is described. L yields one of the largest rate enhancements for hydrolytic ATP cleavage observed in macrocyclic polyamines. The process is specific for the formation of ADP and involves a high degree of geometrical complementarity between host and guest species. The analogue compound 24-hydroxy-2,5,8,11,14,17-hexaaza[18]metacyclophane (L11) shows also a high degree of ATP activation. However, in this case deprotonation of the hydroxy group results in almost complete quenching of the ATPase activity above pH 7.0.

chemistry.chemical_classificationHydrolysischemistry.chemical_compoundDeprotonationQuenching (fluorescence)chemistryStereochemistryNucleotideReceptorCleavage (embryo)CyclophaneCatalysis
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