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Sökning: WFRF:(Lepine J P)

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1.
  • Ballan, M., et al. (författare)
  • Nuclear physics midterm plan at Legnaro National Laboratories (LNL)
  • 2023
  • Ingår i: European Physical Journal Plus. - 2190-5444. ; 138:8, s. 3-26
  • Tidskriftsartikel (refereegranskat)abstract
    • The next years will see the completion of the radioactive ion beam facility SPES (Selective Production of Exotic Species) and the upgrade of the accelerators complex at Istituto Nazionale di Fisica Nucleare – Legnaro National Laboratories (LNL) opening up new possibilities in the fields of nuclear structure, nuclear dynamics, nuclear astrophysics, and applications. The nuclear physics community has organised a workshop to discuss the new physics opportunities that will be possible in the near future by employing state-of-the-art detection systems. A detailed discussion of the outcome from the workshop is presented in this report.
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2.
  • L'Huillier, A., et al. (författare)
  • Atomic physics with attosecond pulses
  • 2006
  • Ingår i: International Conference on Ultrafast Phenomena, UP 2006. - 1557528101 - 9781557528100
  • Konferensbidrag (refereegranskat)
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4.
  • Neidel, Ch, et al. (författare)
  • Probing Time-Dependent Molecular Dipoles on the Attosecond Time Scale
  • 2013
  • Ingår i: Physical Review Letters. - 1079-7114. ; 111:3
  • Tidskriftsartikel (refereegranskat)abstract
    • Photoinduced molecular processes start with the interaction of the instantaneous electric field of the incident light with the electronic degrees of freedom. This early attosecond electronic motion impacts the fate of the photoinduced reactions. We report the first observation of attosecond time scale electron dynamics in a series of small-and medium-sized neutral molecules (N-2, CO2, and C2H4), monitoring time-dependent variations of the parent molecular ion yield in the ionization by an attosecond pulse, and thereby probing the time-dependent dipole induced by a moderately strong near-infrared laser field. This approach can be generalized to other molecular species and may be regarded as a first example of molecular attosecond Stark spectroscopy.
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5.
  • Sansone, G., et al. (författare)
  • Attosecond excitation of electron wavepackets
  • 2008
  • Ingår i: Quantum Electronics and Laser Science Conference, QELS 2008. - 9781557528599
  • Konferensbidrag (refereegranskat)abstract
    • We present experiments, supported by time-dependent Schrödinger simulations, on the dynamics of Helium bound states after an attosecond excitation in the presence of a strong infrared laser field.
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6.
  • Barillot, T., et al. (författare)
  • Angular asymmetry and attosecond time delay from the giant plasmon resonance in C60 photoionization
  • 2015
  • Ingår i: Physical Review A. Atomic, Molecular, and Optical Physics. - 1050-2947 .- 1094-1622. ; 91
  • Tidskriftsartikel (refereegranskat)abstract
    • This combined experimental and theoretical study demonstrates that the surface plasmon resonance in C 60 alters the valence photoemission quantum phase, resulting in strong effects in the photoelectron angular distribution and emission time delay. Electron momentum imaging spectroscopy is used to measure the photoelectron angular distribution asymmetry parameter that agrees well with our calculations from the time-dependent local density approximation (TDLDA). Significant structure in the valence photoemission time delay is simultaneously calculated by TDLDA over the plasmon active energies. Results reveal a unified spatial and temporal asymmetry pattern driven by the plasmon resonance and offer a sensitive probe of electron correlation. A semiclassical approach facilitates further insights into this link that can be generalized and applied to other molecular systems and nanometer-sized metallic materials exhibiting plasmon resonances.
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8.
  • Kling, M. F., et al. (författare)
  • Attosecond control of electron localization in one- and two-color dissociative ionization of H2 and D2
  • 2008
  • Ingår i: 2008 Conference on Quantum Electronics and Laser Science Conference on Lasers and Electro-Optics, CLEO/QELS. - 9781557528599
  • Konferensbidrag (refereegranskat)abstract
    • We present one-color (IR) and two-color (single attosecond XUV pulse + IR) experiments where the sub-cycle evolution of the electric field of light is used to control the dissociative ionization of hydrogen and deuterium molecules.
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9.
  • Rouzee, A., et al. (författare)
  • Towards imaging of ultrafast molecular dynamics using FELs
  • 2013
  • Ingår i: Journal of Physics B: Atomic, Molecular and Optical Physics. - : IOP Publishing. - 0953-4075 .- 1361-6455. ; 46:16
  • Tidskriftsartikel (refereegranskat)abstract
    • The dissociation dynamics induced by a 100 fs, 400 nm laser pulse in a rotationally cold Br-2 sample was characterized by Coulomb explosion imaging (CEI) using a time-delayed extreme ultra-violet (XUV) FEL pulse, obtained from the Free electron LASer in Hamburg (FLASH). The momentum distribution of atomic fragments resulting from the 400 nm-induced dissociation was measured with a velocity map imaging spectrometer and used to monitor the internuclear distance as the molecule dissociated. By employing the simultaneously recorded in-house timing electro-optical sampling data, the time resolution of the final results could be improved to 300 fs, compared to the inherent 500 fs time-jitter of the FEL pulse. Before dissociation, the Br-2 molecules were transiently 'fixed in space' using laser-induced alignment. In addition, similar alignment techniques were used on CO2 molecules to allow the measurement of the photoelectron angular distribution (PAD) directly in the molecular frame (MF). Our results on MFPADs in aligned CO2 molecules, together with our investigation of the dissociation dynamics of the Br-2 molecules with CEI, show that information about the evolving molecular structure and electronic geometry can be retrieved from such experiments, therefore paving the way towards the study of complex non-adiabatic dynamics in molecules through XUV time-resolved photoion and photoelectron spectroscopy.
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  • Resultat 1-10 av 12

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