Search results for "Ionization Energy"

showing 10 items of 83 documents

Untersuchungen von polymeren im massenspektrometer, 5. Fragmentierungsreaktionen oligomerer oxy- und thio-1,4-phenylene

1975

Als Modellverbindungen zur Differenzierung von thermischen und elektronenstosinduzierten Abbaureaktionen von entsprechenden Polymeren im Massenspektrometer wurden die Fragmentierungsreaktionen oligomerer 1,4-Phenylene mit Sauerstoff-, Schwefel- und Disulfidbrucken sowie eine Reihe alternierender Co-oligomersysteme untersucht. Bei verringerter Ionisationsenergie (15 eV) treten in den Massenspektren aller unzersetzt fluchtigen Oligomeren die Molekulionen als intensivste Peaks auf, so das–bei strukturell gleichen Polymeren–eine eindeutige Identifizierung von thermischen Abbauprodukten erwartet werden kann. In Abhangigkeit von den Bruckenatomen werden charakteristische Unterschiede in den Inten…

Fragmentation (mass spectrometry)ChemistryPolymer chemistryMass spectrumMoleculeIonization energyIsostructuralMass spectrometryElectron ionizationDie Makromolekulare Chemie
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Redox potentials and acidity constants from density functional theory based molecular dynamics.

2014

CONSPECTUS: All-atom methods treat solute and solvent at the same level of electronic structure theory and statistical mechanics. All-atom computation of acidity constants (pKa) and redox potentials is still a challenge. In this Account, we review such a method combining density functional theory based molecular dynamics (DFTMD) and free energy perturbation (FEP) methods. The key computational tool is a FEP based method for reversible insertion of a proton or electron in a periodic DFTMD model system. The free energy of insertion (work function) is computed by thermodynamic integration of vertical energy gaps obtained from total energy differences. The problem of the loss of a physical refe…

Free energy perturbationMolecular dynamicsStandard hydrogen electrodeChemistryPeriodic boundary conditionsThermodynamicsThermodynamic integrationPhysical chemistryDensity functional theoryGeneral MedicineGeneral ChemistryElectronic structureIonization energyAccounts of chemical research
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Levels of self-consistency in the GW approximation

2009

We perform $GW$ calculations on atoms and diatomic molecules at different levels of self-consistency and investigate the effects of self-consistency on total energies, ionization potentials and on particle number conservation. We further propose a partially self-consistent $GW$ scheme in which we keep the correlation part of the self-energy fixed within the self-consistency cycle. This approximation is compared to the fully self-consistent $GW$ results and to the $G W_0$ and the $G_0W_0$ approximations. Total energies, ionization potentials and two-electron removal energies obtained with our partially self-consistent $GW$ approximation are in excellent agreement with fully self-consistent $…

GW approximationSelf consistencyGeneral Physics and AstronomyFOS: Physical sciencesELECTRON-GASGreen's function methodsATOMSMOLECULESQuality (physics)IonizationPhysics - Chemical Physicsionisation potentialWAVE-FUNCTIONSKOOPMANS THEOREMPhysical and Theoretical ChemistryfysiikkaPhysicsChemical Physics (physics.chem-ph)total energyNONEQUILIBRIUM PROCESSESDiatomic moleculeTRANSPORTCondensed Matter - Other Condensed MatterYield (chemistry)GROUND-STATECORRELATION ENERGIESIonization energyAtomic physicsEXTENSIONOther Condensed Matter (cond-mat.other)
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Excited states of the water molecule: Analysis of the valence and Rydberg character

2008

The excited states of the water molecule have been analyzed by using the extended quantum-chemical multistate CASPT2 method, namely, MS-CASPT2, in conjunction with large one-electron basis sets of atomic natural orbital type. The study includes 13 singlet and triplet excited states, both valence and 3s-, 3p-, and 3d-members of the Rydberg series converging to the lowest ionization potential and the 3s- and 3p-Rydberg members converging to the second low-lying state of the cation, 1 math. The research has been focused on the analysis of the valence or Rydberg character of the low-lying states. The computation of the 1 math state of water at different geometries indicates that it has a predom…

General Physics and AstronomyElectronssymbols.namesakeAb initio quantum chemistry methodsMoleculePhysics::Atomic PhysicsSinglet statePhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Valence (chemistry)ChemistryAb initio calculations ; Molecular configurations ; Orbital calculations ; Quantum chemistry ; Rydberg states ; SCF calculations ; Valency ; WaterValencyWaterRydberg statesMolecular configurationsUNESCO::FÍSICA::Química físicaOrbital calculationsExcited stateRydberg atomRydberg formulasymbolsQuantum TheorySCF calculationsAb initio calculationsIonization energyAtomic physicsQuantum chemistryAlgorithmsThe Journal of Chemical Physics
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Electronic structure of tetraphenyldithiapyranylidene : A valence effective Hamiltonian theoretical investigation

1992

We present a theoretical investigation of the electronic structure of tetraphenyldithiapyranylidene (DIPSΦ4) using the nonempirical valence effective Hamiltonian (VEH) method. Molecular geometries are optimized at the semiempirical PM3 level which predicts an alternating nonaromatic structure for the dithiapyranylidene (DIPS) framework. The VEH one‐electron energy level distribution calculated for DIPSΦ4 is presented as a theoretical XPS simulation and is analyzed by comparison to the electronic structure of its molecular components DIPS and benzene. The theoretical VEH spectrum is found to be fully consistent with the experimental solid‐state x‐ray photoelectron spectroscopy (XPS) spectrum…

HamiltoniansOptimizationValence (chemistry)ChemistryPhotoemission spectroscopyGaussian orbitalPhenyl RadicalsGeometryGeneral Physics and AstronomyElectronic structureMoleculesMolecular physicsUNESCO::FÍSICA::Química físicasymbols.namesakeMolecular geometryElectronic StructureX-ray photoelectron spectroscopyComputational chemistrysymbolsPhysical and Theoretical ChemistryIonization energy:FÍSICA::Química física [UNESCO]Hamiltonian (quantum mechanics)Phenyl Radicals ; Electronic Structure ; Pyrans ; Hamiltonians ; Geometry ; Optimization ; MoleculesPyrans
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Tellurium( II ) Dialkanethiolates: n p (S)‐σ*(Te−S′) Orbital Interactions Determine the 125 Te NMR Chemical Shift, and the Molecular and Crystal Stru…

2003

Tellurium(II) dimethanethiolate, Te(SMe)(2), and tellurium(II) diethanethiolate, Te(SEt)(2), were synthesized by reaction of TeO2 and Te(OiPr)(4) with HSMe and HSEt, respectively. In the solid state, Te(SMe)(2) exhibits a cis-conformation of the methyl groups with respect to the TeS2 plane - an unprecedented situation for nonfunctionalized organotrichalcogenides - whereas Te(SEt)(2) shows a trans-conformation. Ab initio calculations performed for Te(SMe)(2) and Te(SEt)(2) show that the cis- and trans-conformers represent minima on the potential energy surface and are stabilized by intramolecular pi-type n(S)-sigma* (Te-S') orbital interactions. In the solid state, the molecules of each comp…

Inorganic Chemistrychemistry.chemical_classificationCrystallographychemistryStereochemistryAb initio quantum chemistry methodsChemical shiftIntramolecular forceIntermolecular forceNon-covalent interactionsNuclear magnetic resonance spectroscopyDihedral angleIonization energyEuropean Journal of Inorganic Chemistry
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DFT study of a singleF center in cubic SrTiO3 perovskite

2006

Various properties of a cubic phase of SrTiO3 perovskite containing single F centers (neutral oxygen vacancies), including energies of their formation and migration, were simulated using different formalisms of density functional theory (DFT) as implemented into CRYSTAL-2003 and VASP computer codes. The lattice relaxation around the F center was found to be sensitive to both shape and size of supercells used. The larger the supercell, the closer the defect energy level in the bandgap lies to the conduction band bottom. It approaches the optical ionization energy of 0.49 eV for 270- and 320-atom supercells, where the distance between neighboring defects increases up to four lattice constants…

Lattice constantF-CenterCondensed matter physicsBand gapChemistryLattice (order)Density functional theorySupercellPhysical and Theoretical ChemistryIonization energyCondensed Matter PhysicsConduction bandAtomic and Molecular Physics and OpticsInternational Journal of Quantum Chemistry
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He-I and He-II excited photoelectron spectra of cyclohepttatrienetricarbonyl complexes of group via metals

1979

Abstract Photoelectron spectra of Group VIA metal complexes M(CO) 3 (η 6 -C 7 H 8 ) have been assigned using experimental criteria along with quantum-mechanical calculations. A general agreement between computed and measured ionization energies has been found for molecular orbitas mainly ligand in character. Similar correlations do not hold for the highest orbitals, mainly metal d based. The energies associated with ionization processes are, in this case, largely dominated by the relaxation terms. The variations of intensities of these bands on changing the energy of ionizing radiation were of crucial significance in the assignment

LigandChemistryOrganic ChemistryRelaxation (NMR)BiochemistrySpectral lineInorganic ChemistryMetalAtomic orbitalIonizationExcited statevisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical chemistryPhysical and Theoretical ChemistryIonization energyAtomic physics
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Charge injection and trapping at perovskite interfaces with organic hole transporting materials of different ionization energies

2019

The extraction of photogenerated holes from CH3NH3PbI3 is crucial in perovskite solar cells. Understanding the main parameters that influence this process is essential to design materials and devices with improved efficiency. A series of vacuum deposited hole transporting materials (HTMs) of different ionization energies, used in efficient photovoltaic devices, are studied here by means of femtosecond transient absorption spectroscopy. We find that ultrafast charge injection from the perovskite into the different HTMs (<100 fs) competes with carrier thermalization and occurs independently of their ionization energy. Our results prove that injection takes place from hot states in the valence…

Materials science530 Physicslcsh:Biotechnology02 engineering and technologyElectronTrapping7. Clean energy01 natural sciencesVacuum depositionlcsh:TP248.13-248.65540 Chemistry0103 physical sciencesUltrafast laser spectroscopyGeneral Materials ScienceMaterialsPerovskite (structure)010302 applied physicsGeneral EngineeringCarrier lifetime021001 nanoscience & nanotechnologylcsh:QC1-999SemiconductorsChemical physicsFemtosecondIonization energy0210 nano-technologylcsh:PhysicsAPL Materials
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Relation between molecule ionization energy, film thickness and morphology of two indandione derivatives thin films

2016

Abstract Nowadays most organic devices consist of thin (below 100 nm) layers. Information about the morphology and energy levels of thin films at such thickness is essential for the high efficiency devices. In this work we have investigated thin films of 2-(4-[N,N-dimethylamino]-benzylidene)-indene-1,3-dione (DMABI) and 2-(4-(bis(2-(trityloxy)ethyl)amino)benzylidene)-2H-indene-1,3-dione (DMABI-6Ph). DMABI-6Ph is the same DMABI molecule with attached bulky groups which assist formation of amorphous films from solutions. Polycrystalline structure was obtained for the DMABI thin films prepared by thermal evaporation in vacuum and amorphous structure for the DMABI-6Ph films prepared by spin-coa…

Materials scienceAnalytical chemistry02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesAmorphous solidElectrodeMoleculeGeneral Materials ScienceVacuum levelCrystalliteIonization energyThin film0210 nano-technologySpectroscopyJournal of Physics and Chemistry of Solids
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