F. Weik et E. Illenberger, INTERACTION OF LOW-ENERGY ELECTRONS WITH GASEOUS AND CONDENSED PERFLUORO COMPOUNDS, The Journal of chemical physics, 103(4), 1995, pp. 1406-1412
Formation of anions induced by collisions of low energy electrons (0-1
4 eV) with the perfluorinated compounds CF4, C2F6, C2F4, and C6F6 is s
tudied (a) in the gas phase under collision-free conditions in a beam
experiment, and (b) in the condensed phase where the electron beam int
eracts with the molecules deposited under ultrahigh vacuum conditions
in definite amounts on a cold (20 K) metallic substrate. In the gas ph
ase different fragment anions [F-, (M-F)(-), CF3-] are formed via diss
ociative attachment (DA). From condensed molecules, desorption of anio
ns is virtually restricted to F-. This can be explained by the polariz
ation interaction of the excess charge and the desorption kinematics p
referring desorption of light fragment ions. Below 10 eV F- desorption
is induced by DA at or near the surface while above 10 eV a nonresona
nt signal from dipolar dissociation is observed. The present results i
ndicate that the desorption cross section is essentially controlled by
the amount of translational energy released to F- in the dissociation
of the precursor anion (M(-)). In CF4 the precursor ion CF4- is assig
ned as the T-2 shape resonance with its pronounced sigma(CF) antibond
ing nature. This results in F- with high kinetic energy release, and,
consequently, a high desorption cross section. In C2F6 the decompositi
on of the transitory anion is less direct resulting in a comparatively
low desorption yield. In C2F4 and C6F6, on the other hand, electron c
apture proceeds via the pi system associated with indirect (statistic
al) decomposition processes. This results in a very low desorption cro
ss section for both compounds. (C) 1995 American Institute of Physics.