0000000000650927

AUTHOR

Gustavo Brunetto

showing 2 related works from this author

A TDDFT-based Study on the Proton-DNA Collision

2019

The interaction of heavy charged particles with DNA is of interest for several areas, from hadrontherapy to aero-space industry. In this paper, a TD-DFT study on the interaction of a 4 keV proton with an isolated DNA base pair was carried out. Ehrenfest dynamics was used to study the evolution of the system during and after the proton impact up to about 193 fs. This time was long enough to observe the dissociation of the target, which occurs between 80-100 fs. The effect of base pair linking to the DNA double helix was emulated by fixing the four O3' atoms responsible for the attachment. The base pair tends to dissociate into its main components, namely the phosphate groups, sugars and nitr…

Models MolecularBase pairFirst-principlesFOS: Physical sciences02 engineering and technology010402 general chemistry01 natural sciencesDissociation (chemistry)Settore FIS/03 - Fisica Della Materiachemistry.chemical_compoundFragmentationPhysics - Chemical PhysicsMaterials ChemistryPhysics - Biological PhysicsPhysical and Theoretical ChemistryBase PairingChemical Physics (physics.chem-ph)ChemistryTime-dependent density functional theoryDNA021001 nanoscience & nanotechnologyCollisionPhosphateCharged particle0104 chemical sciencesSurfaces Coatings and FilmsEnergy TransferBiological Physics (physics.bio-ph)Chemical physicsQuantum TheoryDensity functional theoryProtonsAtomic physics0210 nano-technologyDNADNA Damage
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Simulating pump-probe photo-electron and absorption spectroscopy on the attosecond time-scale with time-dependent density-functional theory

2013

Molecular absorption and photoelectron spectra can be efficiently predicted with real-time time-dependent density functional theory. We show herein how these techniques can be easily extended to study time-resolved pump-probe experiments, in which a system response (absorption or electron emission) to a probe pulse is measured in an excited state. This simulation tool helps with the interpretation of fast-evolving attosecond time-resolved spectroscopic experiments, in which electronic motion must be followed at its natural timescale. We show how the extra degrees of freedom (pump-pulse duration, intensity, frequency, and time delay), which are absent in a conventional steady-state experimen…

Time-resolved spectroscopyTime FactorsAbsorption spectroscopyAtomic Physics (physics.atom-ph)AttosecondAttosecond dynamicsFOS: Physical sciencesPump probesingle-molecule studies01 natural sciencestime-resolved spectroscopySettore FIS/03 - Fisica Della MateriaPhysics - Atomic PhysicsAb initio quantum chemistry methodsPhysics - Chemical Physics0103 physical sciencesPhysics - Atomic and Molecular ClustersLaser spectroscopyPhysical and Theoretical Chemistry010306 general physicsSpectroscopyPhysicsChemical Physics (physics.chem-ph)010304 chemical physicsEuropean researchab initio calculationsPhotoelectron SpectroscopySingle-molecule studiesattosecond dynamicsTime-dependent density functional theoryAtomic and Molecular Physics and OpticsPhysics - Plasma PhysicsPlasma Physics (physics.plasm-ph)X-Ray Absorption Spectroscopylaser spectroscopyQuantum TheoryAtomic physicsTime-resolved spectroscopyAtomic and Molecular Clusters (physics.atm-clus)
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