Abstract

SynopsisIn this work we explore the high-order harmonic generation in the H2+ molecule under the action of phase shaped pulses. To this end, quantum mechanical wavepacket calculations are performed within a collinear model of H2+. We analyze the effect of a chirp to the plateau extension of the HHG spectrum, observing significant differences with respect to the sign of the chirp parameter. This result is found to originate from a subtle electron recollision dynamics within the chirped laser pulses, as substantiated by classsical trajectory calculations. Extension of this work focuses on including the nuclear motion of H2+.

Highlights

  • The process of high harmonic generation has proven to be an effective source of extreme utraviolet and soft x-ray light with a crucial application to generate attosecond light pulses, which can be used in time-resolved pump-probe experiments

  • Since the up/down chirped pulses have the same spectrum, the observed asymmetry cannot be attributed to purely spectral arguments, using the three-step model, but is the result of a complex electron recombination dynamics

  • Quantum results are substantiated by classical trajectory calculations

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Summary

Introduction

The process of high harmonic generation has proven to be an effective source of extreme utraviolet and soft x-ray light with a crucial application to generate attosecond light pulses, which can be used in time-resolved pump-probe experiments. For the usual laser intensities, negative (down) chirp rates are found to be more efficient than positive (up) chirps.

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