English
 
User Manual Privacy Policy Disclaimer Contact us
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Angle-Resolved Electron Spectroscopy of Laser-Assisted Auger Decay Induced by a Few-Femtosecond X-Ray Pulse

MPS-Authors
/persons/resource/persons61064

Maier,  Andreas R.
Laboratory for Attosecond Physics, Max Planck Institute of Quantum Optics, Max Planck Society;
Ludwig-Maximilians Universität München, Department of Physics, Am Coulombwall 1, 85748 Garching, Germany;

/persons/resource/persons60612

Kienberger,  Reinhard
Attosecond Dynamics, Laboratory for Attosecond Physics, Max Planck Institute of Quantum Optics, Max Planck Society;

Fulltext (public)

PhysRevLett.108.063007.pdf
(Publisher version), 616KB

Supplementary Material (public)
There is no public supplementary material available
Citation

Meyer, M., Radcliffe, P., Tschentscher, T., Costello, J. T., Cavalieri, A. L., Grguraš, I., et al. (2012). Angle-Resolved Electron Spectroscopy of Laser-Assisted Auger Decay Induced by a Few-Femtosecond X-Ray Pulse. Physical Review Letters, 108(6): 063007. doi:10.1103/PhysRevLett.108.063007.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0028-15BD-C
Abstract
Two-color (x−ray+infrared) electron spectroscopy is used for investigating laser-assisted KLL Auger decay following 1s photoionization of atomic Ne with few-femtosecond x-ray pulses from the Linac Coherent Light Source. In an angle-resolved experiment, the overall width of the laser-modified Auger-electron spectrum and its structure change significantly as a function of the emission angle. The spectra are characterized by a strong intensity variation of the sidebands revealing a gross structure. This variation is caused, as predicted by theory, by the interference of electrons emitted at different times within the duration of one optical cycle of the infrared dressing laser, which almost coincides with the lifetime of the Ne 1s vacancy.