English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Constant initial state (CIS) spectroscopy in the study of the decay of core-to-bound resonances in N2

MPS-Authors
/persons/resource/persons21708

Kempgens,  Brigitte
Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21836

Maier,  Klaus
Fritz Haber Institute, Max Planck Society;

/persons/resource/persons22029

Rüdel,  Andy
Fritz Haber Institute, Max Planck Society;

/persons/resource/persons109362

Hergenhahn,  Uwe
Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21399

Bradshaw,  Alexander M.
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)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Piancastelli, M. N., Kivimäki, A., Kempgens, B., Maier, K., Rüdel, A., Hergenhahn, U., et al. (1999). Constant initial state (CIS) spectroscopy in the study of the decay of core-to-bound resonances in N2. Journal of Physics B, 32(11), 2623-2628. doi:10.1088/0953-4075/32/11/311.


Cite as: https://hdl.handle.net/21.11116/0000-0008-C8F4-3
Abstract
Constant initial state (CIS) photoemission spectra of the N2 1πu−1 and 3σg-1 states have been measured in the photon energy range corresponding to the N 1s → π* core-to-bound transition, where they acquire intensity from participator decay. The resolution was sufficiently high that the spectra could be recorded individually for the first four vibrational components of the 1πu-1 state and for the first two vibrational components of the 3σg-1 state. Differences in the spectra for these two final states are discussed in terms of their potential curves compared to that of the intermediate neutral excited state. We point out the potential usefulness of the CIS method for elucidating the details of the molecular potential.