https://doi.org/10.1140/epjd/e2005-00077-9
Environmental influence on the IR fluorescence of Xe2* molecules in electron beam excited Ar–Xe mixture at high density
1
Istituto Nazionale per la Fisica della Materia,
Dept. of Physics, University of Padua, via
F. Marzolo 8, 35131 Padua, Italy
2
Istituto Nazionale di
Fisica Nucleare, via F. Marzolo 8, 35131 Padua, Italy
3
Harvard University,
Division of Engineering and Applied Sciences, 9 Oxford St., Cambridge, MA 02138, USA
4
Istituto Nazionale di Fisica Nucleare,
Dept. of Physics, University of Padua, via
F. Marzolo 8, 35131 Padua, Italy
Corresponding author: a borghesani@padova.infm.it
Received:
18
March
2005
Published online:
7
June
2005
We report new measurements of the near infrared (NIR) Xe2* excimer fluorescence in an electron–beam–excited Ar (90%)–Xe (10 %) mixture at room temperature. Previous measurements up to a density m-3 discovered a broad excimer fluorescence band at
cm
whose center is red–shifted by increasing N [A.F. Borghesani, G. Bressi, G. Carugno, E. Conti, D. Iannuzzi, J. Chem. Phys. 115, 6042 (2001)]. The shift has been explained by assuming that the energy of the optical active electron in the molecule is shifted by the density–dependent Fermi shift and by accounting for the solvation effect due to the environment. We have extended the density range up to
m
confirming the previous measurements and extending the validity of the interpretative model. A detailed analysis of the width of the fluorescence band gives a value of 2.85 nm for the size of the investigated excimer state. Such a large value lends credibility to the validity of the proposed explanation of the experimental findings.
PACS: 34.50.Gb – Electronic excitation and ionization of molecules; intermediate molecular states (including lifetimes, state mixing, etc.) / 33.70.Jg – Line and band widths, shapes, and shifts / 33.20.Ea – Infrared spectra
© EDP Sciences, Società Italiana di Fisica, Springer-Verlag, 2005