Search results for " DFT"

showing 10 items of 97 documents

Growth of Palladium Clusters on a Boron Nitride Nanotube Support

2015

We demonstrated that the migration process of a single palladium atom on the BNNT is not highly energy demanding and can be represented as a hopping mechanism between boron and nitrogen. A model was finally found for the interpretation of the growth energetics, showing that the process is generally favoured increasing the cluster size.

Palladium Boron Nitride Supported Catalyst DFT
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Spinorial formulation of the GW-BSE equations and spin properties of excitons in two-dimensional transition metal dichalcogenides

2021

In many paradigmatic materials, such as transition metal dichalcogenides, the role played by the spin degrees of freedom is as important as the one played by the electron-electron interaction. Thus an accurate treatment of the two effects and of their interaction is necessary for an accurate and predictive study of the optical and electronic properties of these materials. Despite the fact that the GW-BSE approach correctly accounts for electronic correlations, the spin-orbit coupling effect is often neglected or treated perturbatively. Recently, spinorial formulations of GW-BSE have become available in different flavors in material-science codes. However, an accurate validation and comparis…

PhysicsWork (thermodynamics)Settore FIS/03ExcitonDegrees of freedom (physics and chemistry)02 engineering and technology021001 nanoscience & nanotechnologyCoupling (probability)01 natural sciencesPartícules (Física nuclear)Coupling effectTransition metalQuantum mechanics0103 physical sciencesmany-body perturbation theory non collinear spin spin-orbit coupling Hedin's equations GW BSE DFT MoS2 electronic properties optical properties010306 general physics0210 nano-technologyMaterialsMixing (physics)Spin-½
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Shape-Dependence of Pd Nanocrystal Carburization during Acetylene Hydrogenation

2015

This interdisciplinary work combines the use of shape- and size-defined Pd nanocrystals (cubes of 10 and 18 nm, and octahedra of 37 nm) with in situ techniques and DFT calculations to unravel the dynamic phenomena with respect to Pd reconstruction taking place during acetylene hydrogenation. Notably, it was found that the reacting Pd surface evolved at a different pace depending on the shape of the Pd nanocrystals, due to their specific propensity to form carbides under reaction conditions. Indeed, Pd cubes (Pd(100)) reacted with acetylene to form a PdC0.13 phase at a rate roughly 6-fold higher than that of octahedra (Pd(111)), resulting in nanocrystals with different degrees of carburizati…

Reaction conditionsMaterials scienceNanotechnologyPd Nanocrystal Acetylene Hydrogenation DFT structure sensitivitySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAcetylene hydrogenationCarbidechemistry.chemical_compoundGeneral EnergyAcetylenechemistryNanocrystalOctahedronSettore CHIM/03 - Chimica Generale E InorganicaLattice (order)Physical chemistryPhysical and Theoretical Chemistry
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Benzyl alcohol to benzaldehyde oxidation on MnOx clusters: Unraveling atomistic features

2021

Abstract The catalytic oxidation of benzyl alcohol with O 2 is a promising option for the production of benzaldehyde, from both environmental and economical viewpoints. In particular, highly dispersed MnO x systems feature good activity and selectivity in a wide range of temperatures, although deactivation phenomena by over-oxidation and/or poisoning of active sites are generally recorded. On this account, a density functional theory study was performed on cluster-sized catalyst models, namely Mn 4 O 8 and over-oxygenated Mn 4 O 9 fragments, to predict the reactivity pattern of MnO x catalysts in the selective aerobic oxidation of benzyl alcohol. Several pathways concur to determine the who…

Reaction mechanismCatalyst deactivationReaction mechanismsProcess Chemistry and TechnologyMnOx based catalystsPhotochemistryDFTCatalysisCatalysisBenzaldehydechemistry.chemical_compoundchemistryCatalytic oxidationBenzyl alcoholAlcohol oxidationCatalyst deactivation; DFT; MnO; x; based catalysts; Oxidative dehydrogenation; Reaction mechanismsReactivity (chemistry)Physical and Theoretical ChemistryOxidative dehydrogenationSettore CHIM/02 - Chimica FisicaBenzoic acidMolecular Catalysis
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Water Splitting on Multifaceted SrTiO3 Nanocrystals: Calculations of Raman Vibrational Spectrum

2022

The financial support of M-ERA.net SunToChem project is greatly acknowledged by L.L.R. and Y.A.M. This paper is partly based upon COST (European Cooperation in Science and Technology) Action 18234 Short Term Scientific Mission. The support is greatly acknowledged by E.K. and V.K. The Institute of Solid State Physics, University of Latvia (Latvia) as the Centre of Excellence has received funding from the European Union’s Horizon 2020 Frame-work Programme H2020-WIDESPREAD-01-2016-2017-Teaming Phase2 under grant agreement No. 739508, project CAMART2. The computer resources were provided by the Stuttgart Supercomputing Center (HLRS project DEFTD 12939) and Latvian Super Cluster (LASC).

STOCondensed Matter::Materials ScienceRaman calculation:NATURAL SCIENCES [Research Subject Categories]General Materials Sciencestepped surfacePhysics::Chemical PhysicsSTO; Raman calculation; DFT; stepped surfaceDFTMaterials
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DFT calculation of NMR δ(113Cd) in cadmium complexes

2016

Abstract We have tested several DFT protocols, at the non-relativistic and relativistic ZORA (scalar and spin–orbit) levels, for the calculation of the 113Cd chemical shifts, δ(113Cd), for a number of cadmium complexes accounting for both different local coordination environments on the metal center, involving N, O and S ligands, and different geometrical arrangements. Moreover, suitable models as reference compounds for δ(113Cd) evaluation have been set up in order to propose a complete computational approach to calculate δ(113Cd) for cadmium complexes. Inclusion of relativistic corrections did not lead to any sensible improvement in the quality of results and, in this context, non-relativ…

Scalar (mathematics)chemistry.chemical_element113Cd; NM; DFT; Relativistic; ZORA113 CdContext (language use)010402 general chemistryDFT01 natural sciences113Cd113; Cd; DFT; NMR; Relativistic; ZORAInorganic ChemistryMetalZORAComputational chemistryMaterials ChemistryOrder (group theory)RelativisticPhysical and Theoretical ChemistrySettore CHIM/02 - Chimica FisicaCadmium010405 organic chemistryChemistryChemical shiftNMR0104 chemical sciencesSettore CHIM/03 - Chimica Generale E Inorganicavisual_artvisual_art.visual_art_mediumPolyhedron
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Theoretical Investigation of Aqueous Phase Reforming of 1,2 Propanediol over a Pt catalyst

2015

Aqueous Phase Reforming (APR) process is one of the most efficient solution for producing hydrogen from biomass renewable feedstocks, such as polyalcohols. [1] Generally the reaction is catalyzed by supported platinoid metals and among these platinum has been recognized as the most active and selective toward the production of hydrogen. However, due to its really high complexity, the reaction mechanism is today poorly understood. DFT methods can be useful for understanding the APR catalytic mechanism at atomistic level. A detailed mechanistic study was carried out using a Pt30 cluster for the modelization of the catalyst and 1,2 propanediol (1,2PDO) as a model feedstock for the APR. Even fo…

Settore CHIM/03 - Chimica Generale E InorganicaAqueous Phase Reforming DFT Pt Catalyst
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Palladium clusters on BNNT as catalysts for biomass conversion

2015

The construction of a heterogeneous catalytic systems by a bottom-up approach is a fascinating strategy well assisted by molecular level characterizations. In this sense, DFT investigations can be used with predictive and descriptive purposes both for the treatment of the catalyst/support and for the substrate/catalyst characterization. This should be particularly useful for highly perspective but scarcely treated systems such as boron nitride based supports. Among these, boron nitride nanotubes (BNNT) have been demonstrated to have high chemical and thermal stability as well as great mechanical strength and high thermal conductivity.[1] Moreover, a high affinity toward hydrogen [2] as well…

Settore CHIM/03 - Chimica Generale E InorganicaBoron Nitride Nanotube DFT Biomass Conversion
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NAOs and vdW‐DF for simulating co‐adsorption of water and polyols on metal surfaces

2015

The computational approach employed in this study is based on the combined use of numerical atomic orbitals (NAOs), which are recognized as highly efficient basis sets, and different parameterization of vdW-DF exchange-correlation functionals, namely DRSLL and KBM as implemented in the SIESTA code.

Settore CHIM/03 - Chimica Generale E InorganicaPolyols metal surface DFT
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Reactivity of antitumor coinage metal-based N-heterocyclic carbene complexes with cysteine and selenocysteine protein sites

2021

Abstract The reaction of the antitumor M(I)-bis-N-heterocyclic carbene (M(I)-NHC) complexes, M = Cu, Ag, and Au, with their potential protein binding sites, i.e. cysteine and selenocysteine, was investigated by means of density functional theory approaches. Capped cysteine and selenocysteine were employed to better model the corresponding residues environment within peptide structures. By assuming the neutral or deprotonated form of the side chains of these amino acids and by considering the possible assistance of an external proton donor such as an adjacent acidic residue or the acidic component of the surrounding buffer environment, we devised five possible routes leading to the binding o…

SilverAnticancer; Copper(I) complexes; DFT calculations; Gold(I) complexes; N-heterocyclic carbenes; Silver(I) complexesStereochemistryCoinage metalsAntineoplastic AgentsProtonationLigandsDFT calculationsBiochemistrySilver(I) complexesInorganic Chemistrychemistry.chemical_compoundDeprotonationProtein structureCoordination ComplexesCysteineN-heterocyclic carbenesDensity Functional Theorychemistry.chemical_classificationMolecular StructureSelenocysteineCopper(I) complexesSelenocysteineAmino acidAnticancerGold(I) complexesModels ChemicalchemistryThermodynamicsGoldCarbeneCopperCysteineJournal of Inorganic Biochemistry
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