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Transition from SAMO to Rydberg State Ionization in C60 in Femtosecond Laser Fields.


ABSTRACT: The transition between two distinct ionization mechanisms in femtosecond laser fields at 785 nm is observed for C60 molecules. The transition occurs in the investigated intensity range from 3 to 20 TW/cm2 and is visualized in electron kinetic energy spectra below the one-photon energy (1.5 eV) obtained via velocity map imaging. Assignment of several observed broad spectral peaks to ionization from superatom molecular orbitals (SAMOs) and Rydberg states is based on time-dependent density functional theory simulations. We find that ionization from SAMOs dominates the spectra for intensities below 5 TW/cm2. As the intensity increases, Rydberg state ionization exceeds the prominence of SAMOs. Using short laser pulses (20 fs) allowed uncovering of distinct six-lobe photoelectron angular distributions with kinetic energies just above the threshold (below 0.2 eV), which we interpret as over-the-barrier ionization of shallow f-Rydberg states in C60.

SUBMITTER: Li H 

PROVIDER: S-EPMC5190148 | biostudies-literature | 2016 Nov

REPOSITORIES: biostudies-literature

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Transition from SAMO to Rydberg State Ionization in C<sub>60</sub> in Femtosecond Laser Fields.

Li H H   Mignolet B B   Wang Z Z   Betsch K J KJ   Carnes K D KD   Ben-Itzhak I I   Cocke C L CL   Remacle F F   Kling M F MF  

The journal of physical chemistry letters 20161107 22


The transition between two distinct ionization mechanisms in femtosecond laser fields at 785 nm is observed for C<sub>60</sub> molecules. The transition occurs in the investigated intensity range from 3 to 20 TW/cm<sup>2</sup> and is visualized in electron kinetic energy spectra below the one-photon energy (1.5 eV) obtained via velocity map imaging. Assignment of several observed broad spectral peaks to ionization from superatom molecular orbitals (SAMOs) and Rydberg states is based on time-depe  ...[more]

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