Abstract

X-ray free-electron lasers (XFELs) are now able to provide tunable pairs of intense sub-fs pulses in the soft x-ray regime, paving the way for time-resolved investigations of attosecond charge migration in molecules. However, the stochastic shot-to-shot variation of the XFEL pulses may degrade and eventually hide the observable features. We show by means of state-of-the-art calculations that the damping of the charge migration induced by 260 eV pulses in p-aminophenol due to the shot-to-shot variation of pulses generated at the Linac Coherent Light Source is negligible in comparison to the natural damping due to the intrinsic fluctuation of the initial molecular geometry. This result gives us confidence in the utility of XFEL sub-fs pulses for the measurement of charge migration and other ultrafast charge dynamics.

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