Information for : Imaging ultrafast molecular dynamics with laser-induced electron diffraction
Information for : Imaging ultrafast molecular dynamics with laser-induced electron diffraction
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发表时间:
2012
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通讯作者:
C. Blaga;Junliang Xu;A. DiChiara;E. Sistrunk;Kaikai Zhang;P. Agostini;T. Miller;L. DiMauro;C. Li
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作者:
C. Blaga;Junliang Xu;A. DiChiara;E. Sistrunk;Kaikai Zhang;P. Agostini;T. Miller;L. DiMauro;C. Li
The laser-induced electron diffraction (LIED) method aims at probing the femtosecond dynamics of gaseous molecules under conformal transformation with atomic-scale spatial resolution. In a typical pump-probe scheme, a pump pulse creates a dynamic system and then the LIED probe would map the time-dependent positions of atoms. In such experiment, the duration of the probe pulse defines the temporal resolution, while the spatial resolution is retrieved from the electron diffraction image accumulated during this time. In this Letter, we report on an approach that allows the application of a single laser pulse to interrogate the bond length change of simple homonuclear diatomic molecules. Our results show that sub-Angstrom spatial resolution (5 pm) is facilitated by using intense long wavelength sources (> 1 μm). In addition, variation of the wavelength is equivalent to changing the delay between pump and probe. In our case, the clock is initialized by tunnel ionization (pump) and the probe is a field-driven wave packet that rescatters (diffracts) with the parent molecular core at a later time, i.e. approximately one optical cycle. The LIED method bridges a number of concepts from strong-field rescattering physics and conventional electron diffraction (CED). This document summarizes the practical steps and theoretical tools used in LIED, the data analysis method and error assessment.