English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Photoelectron-Auger electron coincidence spectroscopy of free molecules: New experiments

MPS-Authors
/persons/resource/persons21810

Lischke,  Toralf
Molecular Physics, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21399

Bradshaw,  Alex M.
Theory, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21622

Hergenhahn,  Uwe
Molecular Physics, Fritz Haber Institute, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)

ecoinc-app-edoc.pdf
(Preprint), 5MB

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

Ulrich, V., Barth, S., Lischke, T., Joshi, S., Arion, T., Mucke, M., et al. (2011). Photoelectron-Auger electron coincidence spectroscopy of free molecules: New experiments. Journal of Electron Spectroscopy and Related Phenomena, 183(1-3), 70-79. doi:10.1016/j.elspec.2010.03.001.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-F6CE-C
Abstract
Photoelectron-Auger electron coincidence spectroscopy probes the dicationic states produced by Auger decay following the photoionization of core or inner valence levels in atoms, molecules or clusters. Moreover, the technique provides valuable insight into the dynamics of core hole decay. This paper serves the dual purpose of demonstrating the additional information obtained by this technique compared to Auger spectroscopy alone as well as of describing the new IPP/FHI apparatus at the BESSY II synchrotron radiation source. The distinguishing feature of the latter is the capability to record both the photoelectron and Auger electron with good energy and angle resolution, for which purpose a large hemispherical electrostatic analyser is combined with several linear time-of-flight spectrometers. Results are reported for the K-shell photoionization of oxygen (O2) and the subsequent K-VV Auger decay. Calculations in the literature for non-coincident O2 Auger spectra are found to be in moderately good agreement with the new data.