Time-of-flight (TOF) spectra of Be recoiled from clean and 0-adsorbed
polycrystalline Be surfaces were measured for low-energy (less-than-or
-equal-to 1 keV) Ne+ bombardment. Comparison of the TOF spectra for Be
0 (neutral Be) with those for Be0 + Be+ revealed that the Be+ fraction
increases upon O-adsorption and that it is larger for surface-recoile
d Be than for directly recoiled Be. It is suggested that the excitatio
n of the Be 2s electron in the Be-Be collision plays an important role
in the Be+ creation. The effect of 0 adsorption is possibly twofold.
Be becomes positively charged by bonding to O, which facilitates creat
ion of Be+ in the Be-Be collision. The decrease (increase) in neutrali
zation (ionization) rates of Be+ (excited Be) along the outgoing traje
ctory upon 0 adsorption also enhances the Be+ fraction.