z-logo
open-access-imgOpen Access
Probing doubly excited ionic states ofN2+via a triple excitation above the N1sthreshold in the
Author(s) -
R. Feifel,
K. Ueda,
A. De Fanis,
K. Okada,
S. Tanimoto,
Takuya Furuta,
H. Shindo,
M. Kitajima,
Hiroshi Tanaka,
Olle Björneholm,
Leif Karlsson,
S. Svensson,
S. L. Sörensen
Publication year - 2003
Publication title -
physical review a
Language(s) - English
Resource type - Journals
eISSN - 1094-1622
pISSN - 1050-2947
DOI - 10.1103/physreva.67.032504
Subject(s) - excited state , physics , atomic physics , valence (chemistry) , photoionization , electron , crystallography , ion , ionization , chemistry , quantum mechanics
Angle-resolved resonant Auger-electron spectroscopy has been carried out on the nitrogen molecule at selected photon energies around 419 eV, where a 1s core electron and two valence electrons are promoted into the lowest unoccupied molecular orbital 1pi(g). Significant enhancement of a specific band, which cannot be disentangled in direct photoionization, is observed at a binding energy of 37.6 eV, with a value of the anisotropy parameter beta much smaller than 2. We assign this new band to the transition to a doubly excited cationic state of N-2, in which two of the excited valence electrons remain in the 1pi(g) orbital, proposing a "double spectator" type decay mechanism. This observation shows how to preferentially probe multiply excited configurations of cations using multiple resonant excitation

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom