Search results for " surface"

showing 10 items of 2838 documents

On the approximation of the similarity-transformed Hamiltonian in single-reference and multireference coupled cluster theory

2012

Abstract We consider the recursive single commutator (RSC) approximation of the Baker–Campbell–Hausdorff expansion introduced by Yanai and Chan [T. Yanai, G.K.-L. Chan, J. Chem. Phys. 124 (2006) 194106] and apply it in order to approximate the similarity transformation of the Hamiltonian in both traditional and unitary coupled cluster theory. The equilibrium bond distance, harmonic vibrational frequency, and anharmonic constant of H2, HF, N2, CuH, and Cu2 were computed using the coupled cluster approach with single and double excitations (CCSD) and CCSD with the RSC approximation of the similarity-transformed Hamiltonian (CCSD-RSC). Our results demonstrate that the RSC approximation introdu…

ChemistryAnharmonicityGeneral Physics and AstronomyPotential energyMatrix similarityBond lengthsymbols.namesakeCoupled clusterQuantum mechanicsMolecular vibrationPotential energy surfacesymbolsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryHamiltonian (quantum mechanics)Chemical Physics
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Electrocrystallization of Monolayer-Protected Gold Clusters : Opening the Door to Quality, Quantity, and New Structures

2017

Thiolate-protected metal clusters are materials of ever-growing importance in fundamental and applied research. Knowledge of their single-crystal X-ray structures has been instrumental to enable advanced molecular understanding of their intriguing properties. So far, however, a general, reliable, chemically clean approach to prepare single crystals suitable for accurate crystallographic analysis was missing. Here we show that single crystals of thiolate-protected clusters can be grown in large quantity and very high quality by electrocrystallization. This method relies on the fact that charged clusters display a higher solubility in polar solvents than their neutral counterparts. Nucleation…

ChemistryChemistry (all)Nucleation02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCatalysis; Chemistry (all); Biochemistry; Colloid and Surface Chemistry01 natural sciencesBiochemistrygold clustersCatalysis0104 chemical sciencesCrystallographyColloid and Surface ChemistryQuality (physics)Chemical physicsElectrodeMonolayerCluster (physics)PolarSolubility0210 nano-technologyta116Metal clusters
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Full configuration interaction calculation of BeH adiabatic states.

2008

An all-electron full configuration interaction (FCI) calculation of the adiabatic potential energy curves of some of the lower states of BeH molecule is presented. A moderately large ANO basis set of atomic natural orbitals (ANO) augmented with Rydberg functions has been used in order to describe the valence and Rydberg states and their interactions. The Rydberg set of ANOs has been placed on the Be at all bond distances. So, the basis set can be described as 4s3p2d1f3s2p1d(BeH)+4s4p2d(Be). The dipole moments of several states and transition dipole strengths from the ground state are also reported as a function of the R(Be-H) distance. The position and the number of states involved in sever…

ChemistryConfiguration interactionsGeneral Physics and AstronomyBond lengthsBeryllium compounds ; Bond lengths ; Configuration interactions ; Ground states ; Molecular moments ; Potential energy surfaces ; Rydberg states ; Vibrational statesRydberg statesPotential energyFull configuration interactionGround statesUNESCO::FÍSICA::Química físicaDipolesymbols.namesakeAtomic orbitalBeryllium compoundsPotential energy surfacesRydberg formulasymbolsMolecular momentsVibrational statesPhysical and Theoretical ChemistryAtomic physicsGround stateAdiabatic process:FÍSICA::Química física [UNESCO]Basis setThe Journal of chemical physics
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Analysis and parametric sensitivity of the behavior of overshoots in the concentration of a charged adsorbate in the adsorbed phase of charged adsorb…

2003

In this work, an analysis of the parametric sensitivity of the overshoot in the concentration of the adsorbate in the adsorbed phase, which occurs under certain conditions during an ion-exchange adsorption process, is presented and used to suggest practical implications of the concentration overshoot phenomenon on operational policies and configurations of chromatographic columns and finite bath adsorption systems. The results presented in this work demonstrate and explain how the development of an overshoot in the concentration of the adsorbate in the adsorbed phase could be enhanced or suppressed by (i) varying the diffusion coefficient, D3, of the adsorbate relative to the diffusion coef…

ChemistryDiffusionAnalytical chemistryLangmuir adsorption modelThermodynamicsElectrolyteCharged particleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialssymbols.namesakeColloid and Surface ChemistryAdsorptionIonic strengthPhase (matter)symbolsDebye lengthJournal of Colloid and Interface Science
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Solution Synthesis of a New Thermoelectric Zn1-xSb Nanophase and Its Structure Determination Using Automated Electron Diffraction Tomography

2010

Engineering materials with specific physical properties have recently focused on the effect of nanoscopic inhomogeneities at the 10 nm scale. Such features are expected to scatter medium- and long-wavelength phonons thereby lowering the thermal conductivity of the system. Low thermal conductivity is a prerequisite for effective thermoelectric materials, and the challenge is to limit the transport of heat by phonons, without simultaneously decreasing charge transport. A solution-phase technique was devised for synthesis of thermoelectric "Zn(4)Sb(3)" nanocrystals as a precursor for phase segregation into ZnSb and a new Zn-Sb intermetallic phase, Zn(1+delta)Sb, in a peritectoid reaction. Our …

ChemistryDiffusionIntermetallicGeneral ChemistryThermoelectric materialsBiochemistryCatalysisCrystallographyColloid and Surface ChemistryThermal conductivityElectron diffractionChemical physicsPhase (matter)Thermoelectric effectNanoscopic scale
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Molecule Isomerism Modulates the Diradical Properties of Stable Singlet Diradicaloids

2019

Inclusion of quinoidal cores in conjugated hydrocarbons is a common strategy to modulate the properties of diradicaloids formed by aromaticity recovery within the quinoidal unit. Here we describe an alternative approach of tuning of diradical properties in indenoindenodibenzothiophenes upon anti → syn isomerism of the benzothiophene motif. This alters the relationship of the S atom with the radical center from linear to cross conjugation yet retains the same 2,6-naphtho conjugation pattern of the rearomatized core. We conduct a full comparison between the anti and syn derivatives based on structural, spectroscopic, theoretical, and magnetic measurements, showing that these systems are stabl…

ChemistryDiradicalBenzothiopheneAromaticityGeneral ChemistryConjugated system010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceschemistry.chemical_compoundColloid and Surface ChemistryMoleculeSinglet stateCross-conjugationTriplet stateJournal of the American Chemical Society
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Operational Mechanism of Conjugated Polyelectrolytes

2014

Conjugated polyelectrolytes (CPEs) are versatile materials used in a range of organic optoelectronic applications. Because of their ionic/electronic nature, characterizing these materials is nontrivial, and their operational mechanism is not fully understood. In this work we use a methodology that combines constant-voltage-driven current-density transient measurements with fast current vs voltage scans to allow decoupling of ionic and electronic phenomena. This technique is applied to diodes prepared with cationic CPEs having different charge-compensating anions. Our results indicate that the operational mechanism of these devices is governed by electrochemical doping of the CPE. On the bas…

ChemistryDopingIonic bondingNanotechnologyGeneral ChemistryBiochemistryConjugated PolyelectrolytesCatalysisIonColloid and Surface ChemistryDepletion regionDecoupling (electronics)DiodeVoltageJournal of the American Chemical Society
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Adsorbed CO on group 10 metal fragments: A DFT study

2009

DFT calculations on the helicopter and cartwheel rotations of one CO molecule adsorbed at the bridge site on metal-surface fragments, characterized by two (M(8)) or three (M(14)) metal-atom layers (M = Ni, Pd, Pt) were performed by the B3LYP[LANL2DZ+6-31 g(d,p)] method, to rationalize the adsorption energetics and the steric hindrance characteristics of surface CO molecules. Potential Energy Surfaces were obtained, either fixing the C-O bond-length or allowing it to change. The behavior of the three metals, as obtained from the study of the configurational space characterizing the CO adsorption on the fragments was explained on the basis of the interaction energies involved in the different…

ChemistryGeneral Chemical EngineeringDFT Infrared spectroscopy quantum chemistry metal surfaceInfrared spectroscopyGeneral ChemistryLibrary and Information SciencesQuantum chemistryComputer Science ApplicationsMetalCrystallographyAdsorptionGroup (periodic table)Settore CHIM/03 - Chimica Generale E Inorganicavisual_artvisual_art.visual_art_mediumMolecule
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Photocatalytic degradation of 4-Nitrophenol by g-C3N4-MCy: Mechanism study and kinetic modeling

2021

Abstract A graphitic carbon nitride (g-C3N4-MCy) photocatalyst was prepared by thermal condensation of melamine and cyanuric acid with equal proportions. The photocatalyst was characterized by Fourier transform infrared spectroscopy (FTIR), Specific surface area (SSA), X-ray diffraction (XRD), Field Emission Scanning Electron Microscope (FESEM), Transmission electron microscope (TEM), and DRS–UV–Vis spectroscopic methods. We studied the photo-degradation kinetics of 4-nitrophenol using a g-C3N4-MCy. Four parameters were applied including initial concentration of 4-nitrophenol, amount of catalyst, dissolved oxygen content, and photon flux. The reaction rate constant was shown to be correlate…

ChemistryGeneral Chemical EngineeringGraphitic carbon nitrideAnalytical chemistryGeneral Physics and Astronomy02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCatalysischemistry.chemical_compoundReaction rate constantSpecific surface areaPhotocatalysisFourier transform infrared spectroscopy0210 nano-technologyCyanuric acidMelamineJournal of Photochemistry and Photobiology A: Chemistry
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Magnetic Excitations in Polyoxometalate Clusters Observed by Inelastic Neutron Scattering:  Evidence for Anisotropic Ferromagnetic Exchange Interacti…

1999

The ground-state properties of the tetranuclear Co2+ cluster [Co4(H2O)2(PW9O34)2]10- were investigated by combining specific heat, magnetic susceptibility, and magnetization measurements with a detailed inelastic neutron scattering (INS) study on a fully deuterated sample of K10[Co4(H2O)2(PW9O34)2]·22H2O. As a result of the single ion anisotropy of the octahedral Co2+, the appropriate exchange Hamiltonian of the Co4 spin cluster is anisotropic. INS turns out to be essential for the determination of energy splittings in the ground state resulting from the coupling. Besides the energy pattern, INS provides information about the wave functions of the split ground-state components of the spin c…

ChemistryGeneral ChemistryBiochemistryMagnetic susceptibilityMolecular physicsCatalysisInelastic neutron scatteringMagnetizationsymbols.namesakeColloid and Surface ChemistryFerromagnetismsymbolsCluster (physics)Hamiltonian (quantum mechanics)AnisotropyGround stateJournal of the American Chemical Society
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