Search results for "EFF"

showing 10 items of 13980 documents

Optical properties and microstructure of 2.02-3.30 eV ZnCdO nanowires: effect of thermal annealing

2013

International audience; ZnCdO nanowires with up to 45% Cd are demonstrated showing room temperature photoluminescence (PL) down to 2.02 eV and a radiative efficiency similar to that of ZnO nanowires. Analysis of the microstructure in individual nanowires confirms the presence of a single wurtzite phase even at the highest Cd contents, with a homogeneous distribution of Cd both in the longitudinal and transverse directions. Thermal annealing at 550 C yields an overall improvement of the PL, which is blue-shifted as a result of the homogeneous decrease of Cd throughout the nanowire, but the single wurtzite structure is fully maintained.

010302 applied physicsTelecomunicacionesPhotoluminescenceMaterials sciencePhysics and Astronomy (miscellaneous)Annealing (metallurgy)business.industryWide-bandgap semiconductorNanowire02 engineering and technology021001 nanoscience & nanotechnologyMicrostructure01 natural sciencesHomogeneous distributionRadiative efficiency0103 physical sciences[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]Optoelectronics0210 nano-technologybusinessWurtzite crystal structure
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Long term stability testing of oxide unicouple thermoelectric modules

2019

Thermoelectric devices based on oxides are good candidates for energy harvesting technologies for use in aggressive conditions where the materials should withstand high temperatures and corrosive environments over prolonged time. This leads to a natural concern for the stability of the electrical contacts, especially on the hot side of the module. In this work, we have assembled several prototype unicouple thermoelectric modules made by pyrolyzed and spark plasma sintered n-type CaMnO3 and p-type Ca3Co4O9 and then tested under different conditions mimicking end-user applications. For baseline experiments we have chosen to use nickel as the contact material in order to show the effect of its…

010302 applied physicsWork (thermodynamics)Materials scienceOxidechemistry.chemical_element02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesElectrical contactsNickelchemistry.chemical_compoundVDP::Teknologi: 500Thermoelectric generatorchemistry0103 physical sciencesThermoelectric effectComposite material0210 nano-technologyEnergy harvestingPower density
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Simulation of IQE tuning of individual cells for DC-balancing multijunction tandem cells

2016

In the present work, the performance of stacks of cells connected in series is examined at different levels of internal quantum efficiency (IQE). Incident photons, generated by employing the ASTM G173-03 data set, are accounted for individually as they interact with the stack of cells. The efficiencies of the devices studied are dependent upon the DC balance throughout the stack of cells. It is demonstrated that reducing the internal quantum efficiency of upper cells can lead to a better DC balance and thereby higher efficiency.

010302 applied physicsWork (thermodynamics)Materials sciencePhotonTandembusiness.industryMonte Carlo methodElectrical engineering02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesStack (abstract data type)0103 physical sciencesOptoelectronicsQuantum efficiencyPhotonics0210 nano-technologybusinessPhotonic crystal2016 IEEE 43rd Photovoltaic Specialists Conference (PVSC)
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Fourier-transform spectroscopy and deperturbation analysis of the spin-orbit coupled A(1)Σ(+) and b(3)Π states of KRb.

2016

Fourier-transform A(1)Σ(+) - b(3)Π → X(1)Σ(+) laser-induced fluorescence spectra were recorded for the natural mixture of (39,41)K(85,87)Rb isotopologues produced in a heatpipe oven. Overall 4200 rovibronic term values of the spin-orbit coupled A(1)Σ(+) and b(3)Π states were determined with an uncertainty of about 0.01 cm(-1) in the energy range [10 850, 14 200] cm(-1) covering rotational quantum numbers J' ∈ [3, 280]. Direct deperturbation analysis of the A ∼ b complex performed within the framework of the A(1)Σ(+) ∼ b(3)ΠΩ=0,1,2 coupled-channel approach reproduced experimental data with a standard deviation of 0.004 cm(-1). Initial parameters of the internuclear potentials and spin-orbit …

010304 chemical physicsChemistryGeneral Physics and AstronomyElectronic structureQuantum number01 natural sciencesFourier transform spectroscopyB vitamins0103 physical sciencesKinetic isotope effectIsotopologueEmission spectrumPhysical and Theoretical ChemistryAtomic physics010306 general physicsSpectroscopyThe Journal of chemical physics
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Unexpected Substituent Effects in the Iso-Heterocyclic Boulton-Katritzky Rearrangement of 3-Aroylamino-5-methyl-1,2,4-oxadiazoles: A Mechanistic Stud…

2019

The kinetics of the iso-heterocyclic mononuclear rearrangement of some 3-aroylamino-5-methyl-1,2,4-ozadiazoles was carefully examined under largely variable acidic or alkaline conditions. This reaction may proceed via two different mechanistic pathways (an uncatalyzed and a base-catalyzed one), as accounted for also by the evaluation of the relevant activation parameters. Substituent effects, as quantified by means of the Hammett’s equation, appear relatively modest; however, they reveal some interesting anomalies, which enabled us to draw a very precise picture of the intimate reaction course.

010304 chemical physicsChemistryKineticsSubstituent124-oxadiazoleSettore CHIM/06 - Chimica OrganicaMononuclear Heterocyclic Rearrangement010402 general chemistry01 natural sciences0104 chemical sciencesKineticschemistry.chemical_compoundSubstituent effectComputational chemistry0103 physical sciencesPhysical and Theoretical ChemistryReaction mechanismThe journal of physical chemistry. A
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Origin of Enzymatic Kinetic Isotope Effects in Human Purine Nucleoside Phosphorylase

2017

Here we report a study of the effect of heavy isotope labeling on the reaction catalyzed by human purine nucleoside phosphorylase (hPNP) to elucidate the origin of its catalytic effect and of the enzymatic kinetic isotope effect (EKIE). Using quantum mechanical and molecular mechanical (QM/MM) molecular dynamics (MD) simulations, we study the mechanism of the hPNP enzyme and the dynamic effects by means of the calculation of the recrossing transmission coefficient. A free energy surface (FES), as a function of both a chemical and an environmental coordinate, is obtained to show the role of the environment on the chemical reaction. Analysis of reactive and nonreactive trajectories allows us …

010304 chemical physicsChemistryPurine nucleoside phosphorylasevariational transition state theoryGeneral Chemistry010402 general chemistryenzyme catalysis01 natural sciencesChemical reactionCatalysis0104 chemical sciencesEnzyme catalysisCatalysisSolventMolecular dynamicsComputational chemistryenzymatic kinetic isotope effect0103 physical sciencesKinetic isotope effectMoleculeQM/MM methodsprotein motionsACS Catalysis
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A quantum dynamics study of the benzopyran ring opening guided by laser pulses

2014

Abstract The ring-opening photoisomerization of benzopyran, which occurs via a photochemical route involving a conical intersection, has been studied with quantum dynamics calculations using the multi-configuration time-dependent Hartree method (MCTDH). We introduce a mechanistic strategy to control the conversion of benzopyran to merocyanine with laser pulses. We use a six-dimensional model developed in a previous work for the potential energy surfaces (PES) based on an extension of the vibronic-coupling Hamiltonian model (diabatization method by ansatz), which depends on the most active degrees of freedom. The main objective of these quantum dynamics simulations is to provide a set of str…

010304 chemical physicsChemistryQuantum dynamicsDegrees of freedom (physics and chemistry)General Physics and AstronomyHartreeConical intersection010402 general chemistry01 natural sciencesPotential energyMolecular physics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrysymbols.namesakeStark effectComputational chemistry0103 physical sciences[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrysymbolsPhysical and Theoretical ChemistryGround stateAdiabatic processComputingMilieux_MISCELLANEOUS
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Quantum dynamics of 16O in collision with ortho- and para-17O17O

2017

Abstract We report full quantum dynamical observables, such as integral and differential cross sections and rate constants, for the 16 O +  17 O 17 O reactive collision process. We particularly emphasize the effect coming from the nonzero nuclear spin of 17 O, leading to two nuclear spin isomers of 34 O 2 , ortho- and para- 34 O 2 which can be studied independently and behave differently. A comparison with the 16 O +  18 O 18 O collision is given. We find that processes involving 17 O 17 O are always faster than with 18 O 18 O.

010304 chemical physicsChemistryQuantum dynamicsGeneral Physics and AstronomyObservable010402 general chemistryCollision01 natural sciences0104 chemical sciencesReaction rate constant0103 physical sciencesKinetic isotope effectPhysical chemistryPhysical and Theoretical ChemistryAtomic physicsQuantumChemical Physics Letters
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Full-dimensional control of the radiationless decay in pyrazine using the dynamic Stark effect

2014

We present a full quantum-mechanical study of the laser control of the radiationless decay between the B3u(nπ(*)) and B2u(ππ(*)) states of pyrazine using the dynamic Stark effect. In contrast to our previous study [Sala et al., J. Chem. Phys. 140, 194309 (2014)], where a four-dimensional model was used, all the 24 degrees of freedom are now included in order to test the robustness of the strategy of control. Using a vibronic coupling Hamiltonian model in a diabatic representation, the multi-layer version of the multi-configuration time-dependent Hartree method is exploited to propagate the corresponding wave packets. We still observe a trapping of the wavepacket on the B2u(ππ(*)) potential …

010304 chemical physicsChemistryWave packetDiabaticGeneral Physics and AstronomyHartree010402 general chemistry01 natural sciencesPotential energy0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryVibronic couplingsymbols.namesakeStark effectQuantum mechanicsExcited state[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistry0103 physical sciencesPotential energy surfacesymbolsPhysics::Atomic PhysicsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsComputingMilieux_MISCELLANEOUSThe Journal of Chemical Physics
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Heavy enzymes and the rational redesign of protein catalysts

2019

Abstract An unsolved mystery in biology concerns the link between enzyme catalysis and protein motions. Comparison between isotopically labelled “heavy” dihydrofolate reductases and their natural‐abundance counterparts has suggested that the coupling of protein motions to the chemistry of the catalysed reaction is minimised in the case of hydride transfer. In alcohol dehydrogenases, unnatural, bulky substrates that induce additional electrostatic rearrangements of the active site enhance coupled motions. This finding could provide a new route to engineering enzymes with altered substrate specificity, because amino acid residues responsible for dynamic coupling with a given substrate present…

010402 general chemistryProtein Engineering01 natural sciencesBiochemistryCatalysisEnzyme catalysisisotope effectsCatalytic DomainDihydrofolate reductaseMolecular BiologyAlcohol dehydrogenasechemistry.chemical_classificationalcohol dehydrogenasesCarbon Isotopesdihydrofolate reductasesbiologyBacteriaNitrogen Isotopes010405 organic chemistryConceptOrganic ChemistryAlcohol DehydrogenaseActive siteSubstrate (chemistry)Protein engineeringDeuteriumCombinatorial chemistrymolecular dynamics0104 chemical sciencesKineticsTetrahydrofolate Dehydrogenaseenzyme engineeringEnzymechemistrybiology.proteinBiocatalysisMolecular MedicineConcepts
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