4.7 Article

Control of electron recollision and molecular nonsequential double ionization

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COMMUNICATIONS PHYSICS
卷 3, 期 1, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s42005-020-0297-3

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  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Atomic, Molecular and Optical Sciences Program [DE-SC0002325, DE-FG02-86ER13491]
  2. U.S. Department of Energy (DOE) [DE-SC0002325] Funding Source: U.S. Department of Energy (DOE)

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Intense laser pulses lasting a few optical cycles, are able to ionize molecules via different mechanisms. One such mechanism involves a process whereby within one optical period an electron tunnels away from the molecule, and is then accelerated and driven back as the laser field reverses its direction, colliding with the parent molecule and causing correlated non-sequential double ionization (NSDI). Here we report control over NSDI via spectral-phase pulse shaping of femtosecond laser pulses. The measurements are carried out on ethane molecules using shaped pulses. We find that the shaped pulses can enhance or suppress the yield of dications resulting from electron recollision by factors of 3 to 6. This type of shaped pulses is likely to impact all phenomena stemming from electron recollision processes induced by strong laser fields such as above threshold ionization, high harmonic generation, attosecond pulse generation, and laser-induced electron diffraction. Controlling the ionisation process of molecules via ultrafast photoexcitation can provide insight into a number of nonlinear processes. This study employs shaped laser pulses to enhance or suppress dication yields resulting from electron recollision by up to a factor of six.

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