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G. Urbasch

Researcher at University of Marburg

Publications -  33
Citations -  1166

G. Urbasch is an academic researcher from University of Marburg. The author has contributed to research in topics: Laser & Femtosecond. The author has an hindex of 14, co-authored 33 publications receiving 1100 citations. Previous affiliations of G. Urbasch include RWTH Aachen University.

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Correlated electron emission in multiphoton double ionization

TL;DR: A strong correlation is reported between the magnitude and the direction of the momentum of two electrons that are emitted from an argon atom, driven by a femtosecond laser pulse (at 38 TW cm-2).
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Recoil-Ion momentum distributions for single and double ionization of helium in strong laser fields

TL;DR: The momentum distributions of singly and doubly charged helium ions created in the focus of 220 fs, 800 nm laser pulses at intensities of (2.9-6.6)x10(14) W/cm(2) are measured.
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Picosecond laser ablation of thin copper films

TL;DR: In this article, the ablation area of thin copper films on fused silica by picosecond laser pulses is characterized using optical and scanning electron microscopy, and the experimental ablation rate per pulse is compared to heat-flow calculations based on the two-temperature model for ultrafast laser heating.
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Sequential and nonsequential contributions to double ionization in strong laser fields

TL;DR: In this paper, the difference between a sequential interaction of a femtosecond laser field with two electrons and a non-sequential process of double ionization mediated by electron-electron correlation was demonstrated by observing the momentum distribution of doubly charged argon ions created in the laser field.
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Unusual mechanism for H3(+) formation from ethane as obtained by femtosecond laser pulse ionization and quantum chemical calculations.

TL;DR: A combined theoretical and experimental investigation is presented providing for the first time an understanding of the mechanism of H(3)(+) formation at the molecular level, with a surprising result that the transition state of the process can be formally regarded as a H( 2) molecule attached to a C(2)H(4)(2+) entity but IRC calculations show that it belongs to the reaction channel.