Search results for "Quantum"

showing 10 items of 9714 documents

Vibrations of a single adsorbed organic molecule: anharmonicity matters!

2010

Vibrational spectroscopy is a powerful tool to identify molecules and to characterise their chemical state. Inelastic electron tunnelling spectroscopy (IETS) combined with scanning tunnelling microscopy (STM) allows the application of vibrational analysis to a single molecule. Up to now, IETS was restricted to small species due to the complexity of vibration spectra for larger molecules. We extend the horizon of IETS for both experiment and theory by measuring the STM-IETS spectra of mercaptopyridine adsorbed on the (111) surface of gold and comparing it to theoretical spectra. Such complex spectra with more than 20 lines can be reliably determined and computed leading to completely new ins…

ChemistryAnharmonicityGeneral Physics and AstronomyInfrared spectroscopySelf-assembled monolayerElectronic structureSpectral linesymbols.namesakeComputational chemistryChemical physicssymbolsMoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistryRaman spectroscopyQuantum tunnellingPhysical chemistry chemical physics : PCCP
researchProduct

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
researchProduct

Ab initio study of the electronic and atomic structure of the wolframite-type ZnWO4

2009

Abstract Ab initio quantum chemistry calculations of the structural and electronic properties of monoclinic wolframite-type ZnWO 4 crystal have been performed within the periodic linear combination of atomic orbitals (LCAO) method using six different Hamiltonians, based on density functional theory (DFT) and hybrid Hartree-Fock-DFT theory. The obtained results for optimized structural parameters, band gap and partial density of states are compared with available experimental data, and the best agreement is observed for hybrid Hamiltonians. The calculations show that zinc tungstate is a wide band gap material, with the direct gap about 4.6 eV, whose valence band has largely O 2p character, w…

ChemistryBand gapAb initioGeneral ChemistryElectronic structureCondensed Matter PhysicsQuantum chemistryLinear combination of atomic orbitalsAb initio quantum chemistry methodsPhysics::Atomic and Molecular ClustersMaterials ChemistryDensity functional theoryAtomic physicsMonoclinic crystal systemSolid State Communications
researchProduct

Analytic second derivatives for the spin-free exact two-component theory

2011

The formulation and implementation of the spin-free (SF) exact two-component (X2c) theory at the one-electron level (SFX2c-1e) is extended in the present work to the analytic evaluation of second derivatives of the energy. In the X2c-1e scheme, the four-component one-electron Dirac Hamiltonian is block diagonalized in its matrix representation and the resulting "electrons-only" two-component Hamiltonian is then used together with untransformed two-electron interactions. The derivatives of the two-component Hamiltonian can thus be obtained by means of simple manipulations of the parent four-component Hamiltonian integrals and derivative integrals. The SF version of X2c-1e can furthermore exp…

ChemistryBent molecular geometryMatrix representationGeneral Physics and AstronomyEquilibrium geometryQuantum chemistrysymbols.namesakeQuantum mechanicssymbolsMoleculePhysical and Theoretical ChemistryHamiltonian (quantum mechanics)Ground stateSecond derivativeThe Journal of Chemical Physics
researchProduct

Ab initio modeling of copper adhesion on regular BaTiO3(001) surfaces

2005

Ab initio calculations have been performed for copper adsorption on a regular, defect-free TiO"2- and BaO-terminated (001) surfaces of a cubic BaTiO"3, using a posteriori HF-CC method as implemented into the CRYSTAL-03 computer code. To clarify the nature of the interfacial bonding, we use slab models of the Cu/BaTiO"3(001) interfaces with different one-side substrate coverages, varied from 1/8 monolayer (ML) up to 1/2 ML, over both TiO"2- and BaO-terminated surfaces. TiO"2 termination has been found to be energetically more favorable for the adsorption of copper atoms. In agreement with previous experimental and theoretical data, our calculations indicate essential contribution of atomic p…

ChemistryBinding energyAb initiochemistry.chemical_elementSubstrate (electronics)Electronic structureCondensed Matter PhysicsCopperAtomic and Molecular Physics and OpticsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAdsorptionAb initio quantum chemistry methodsChemical physicsMonolayerElectrical and Electronic EngineeringAtomic physicsMicroelectronic Engineering
researchProduct

Comparison of quantum dot-binding protein tags: Affinity determination by ultracentrifugation and FRET

2013

Abstract Background Hybrid complexes of proteins and colloidal semiconductor nanocrystals (quantum dots, QDs) are of increasing interest in various fields of biochemistry and biomedicine, for instance for biolabeling or drug transport. The usefulness of protein–QD complexes for such applications is dependent on the binding specificity and strength of the components. Often the binding properties of these components are difficult and time consuming to assess. Methods In this work we characterized the interaction between recombinant light harvesting chlorophyll a / b complex (LHCII) and CdTe/CdSe/ZnS QDs by using ultracentrifugation and fluorescence resonance energy transfer (FRET) assay exper…

ChemistryBinding proteinBiophysicsNanoparticleProtein tagBiochemistryCrystallographyB vitaminsFörster resonance energy transferQuantum dotQuantum DotsFluorescence Resonance Energy TransferNanoparticlesUltracentrifugeChlorophyll Binding ProteinsUltracentrifugationMolecular BiologyBinding selectivityProtein BindingBiochimica et Biophysica Acta (BBA) - General Subjects
researchProduct

The Reduction Pathway of End-on Coordinated Dinitrogen. I. Vibrational Spectra of Mo/W−N2, −NNH, and −NNH2 Complexes and Quantum Chemistry Assisted N…

1999

Infrared and Raman spectra of [M(N(2))(2)(dppe)(2)] (M = W, Mo) and the two protonated derivatives [WF(NNH)(dppe)(2)] and [WF(NNH(2))(dppe)(2)](+) (dppe = 1,2-bis(diphenylphosphino)ethane) are presented. Using isotope substituted compounds ((15)N and D) the vibrations of the Y-M-N(2)H(x)() (x = 0, 1, 2; Y = N(2), F) central unit are identified, in particular the M-N and N-N stretching modes. In case of the monoprotonated systems, an equilibrium between metal- and nitrogen-protonated species exists that is clearly detectable in the IR spectra. Making use of theoretical force fields, a quantum chemistry assisted normal coordinate analysis (QCA-NCA) is performed for all three tungsten systems …

ChemistryBond strengthInfraredInfrared spectroscopyProtonationQuantum chemistryInorganic ChemistryMetalsymbols.namesakeCrystallographyTransition metalComputational chemistryvisual_artsymbolsvisual_art.visual_art_mediumPhysical and Theoretical ChemistryRaman spectroscopyInorganic Chemistry
researchProduct

High resolution spectroscopy and potential determination of the (3)1Pi state of NaCs.

2006

The (3)(1)Pi state of the NaCs molecule was studied by high resolution Fourier-transform spectroscopy. The (3)(1)Pi--X (1)Sigma(+) laser induced fluorescence was excited by an Ar(+) ion laser or by a single-mode frequency-doubled cw Nd:YAG laser. The presence of argon buffer gas yielded rich rotational relaxation spectra allowing to enlarge the data set for the (3)(1)Pi state term values, as well as to observe Lambda splittings in a wide range of vibrational (v(')) and rotational (J(')) quantum numbers. The data field includes about 820 energy levels of (3)(1)Pi NaCs in the range from v(')=0 to 37 and from J(')=3 to 190, which corresponds to ca. 95% of the potential well depth. Direct fit o…

ChemistryBuffer gasGeneral Physics and AstronomyIon laserQuantum numberLaserPotential energylaw.inventionlawExcited statePhysical and Theoretical ChemistryAtomic physicsLaser-induced fluorescenceSpectroscopyThe Journal of chemical physics
researchProduct

Quantum chemical calculations of the electron center diffusion in MgO crystals

1996

Large-scale quantum chemical simulations of the diffusion hops of empty cation and anion vacancies, as well as F + and F centers in MgO crystals have been done. The atomic configurations for 224-site cluster and charge density distribution are analyzed for the equilibrium and saddle-point configurations during the defect hops. The relevant activation energy for diffusion increases monotonically in the series V a → F + → F center.

ChemistryCharge densityElectronActivation energyCondensed Matter PhysicsQuantum chemistryMolecular physicsElectronic Optical and Magnetic MaterialsIonPhysics::Atomic and Molecular ClustersCluster (physics)Physical chemistryDiffusion (business)Saddlephysica status solidi (b)
researchProduct

Quantum size effects in ambient CO oxidation catalysed by ligand-protected gold clusters

2009

Finely dispersed nanometre-scale gold particles are known to catalyse several oxidation reactions in aerobic, ambient conditions. The catalytic activity has been explained by various complementary mechanisms, including support effects, particle-size-dependent metal-insulator transition, charging effects, frontier orbital interactions and geometric fluxionality. We show, by considering a series of robust and structurally well-characterized ligand-protected gold clusters with diameters between 1.2 and 2.4 nm, that electronic quantum size effects, particularly the magnitude of the so-called HOMO-LUMO energy gap, has a decisive role in binding oxygen to the nano-catalyst in an activated form. T…

ChemistryColloidal goldLigandGeneral Chemical EngineeringExcited stateInorganic chemistryCluster (physics)NanoparticleGeneral ChemistryParticle sizeRedoxQuantum sizeNature Chemistry
researchProduct