156 research outputs found
Two-Electron Effects in the Multiphoton Ionization of Magnesium with 400 nm 150 fs Pulses
The multiphoton ionization and photoelectron spectra of magnesium were
studied at laser intensities of up to 6x10^{13} Wcm^{-2} using 150 fs laser
pulses of a wavelength of 400 nm. The results indicated that a variety of
different ionization mechanisms played a role in both types of spectra. A
theoretical model describing the processes is presented and the routes to
ionization are identified. The work demonstrates the significance of the
two-electron nature of the atom in interpreting the experimental results.Comment: 14 pages, 9 figures, submitted to Physical Review
Molecular resolvent-operator method: Electronic and nuclear dynamics in strong-field ionization
We present an extension of the resolvent-operator method (ROM), originally designed for atomic systems, to extract differential photoelectron spectra (in photoelectron- and nuclear-kinetic energy) for diatomic molecules interacting with strong, ultrashort laser fields in the single active electron approximation. The method is applied to the study of H2+ photodissociation and photoionization by femtosecond laser pulses in the XUV-IR frequency range. In particular, the method is tested (i) in the perturbative regime, for few-photon absorption and bound-bound electronic transitions, and (ii) in the strong-field regime, in which multiphoton absorption and tunneling are present. In the latter case, we show how the differential ROM allows one to track the transition between both regimes. We also analyze isotopic effects by comparing the dynamics of H2+ and D2+ ionization for different pulses. © 2014 American Physical Society.This work was accomplished with an allocation of computer time from Mare Nostrum BSC and CCC-UAM and was partially supported by the MICINN Projects No. FIS2010- 15127 and No. CSD 2007-00010, ERA-Chemistry Project No. PIM2010EEC-00751, the European grants No. MC-ITN CORINF and No. MC-RG ATTOTREND, the European COST Action No. CM0702, and European Research Council Advanced Grant No. XCHEM 290853. R.E.F.S. acknowledges a Ph.D. contract from ITN CORINF and Grant No. SFRH/BD/84053/2012 from the Portuguese government. P.R. acknowledges a Juan de la Cierva contract grant from the Spanish MICIN
Correlated electron and nuclear dynamics in strong field photoionization of H2+
We present a theoretical study of H2+ ionization under strong IR femtosecond pulses by using a method designed to extract correlated (2D) photoelectron and proton kinetic energy spectra. The results show two distinct ionization mechanisms—tunnel and multiphoton ionization—in which electrons and nuclei do not share the energy from the field in the same way. Electrons produced in multiphoton ionization share part of their energy with the nuclei, an effect that shows up in the 2D spectra in the form of energy-conservation fringes similar to those observed in weak-field ionization of diatomic molecules. In contrast, tunneling electrons lead to fringes whose position does not depend on the proton kinetic energy. At high intensity, the two processes coexist and the 2D plots show a very rich behavior, suggesting that the correlation between electron and nuclear dynamics in strong field ionization is more complex than one would have anticipatedThis work was accomplished with an allocation of computer time from Mare Nostrum BSC and CCC-UAM, and was partially supported by the MICINN Projects No. FIS2010-15127, No. ACI2008-0777, and No. CSD 2007-00010, the ERA-Chemistry Project No. PIM2010EEC-00751, the European Grants No. MCITN CORINF and No. MC-RG ATTOTREND, the European COST Action CM0702, and the Advanced Grant of the European Research Council, Grant No. XCHEM 290853. R. E. F. S. acknowledges a Ph.D. contract from ITN CORINF. P. R. acknowledges a Juan de la Cierva contract grant from MICIN
Publisher Correction: Angle-dependent interferences in electron emission accompanying stimulated Compton scattering from molecules
Angle-dependent interferences in electron emission accompanying stimulated Compton scattering from molecules
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