The initial sticking probability
S0 of O
2 molecules on a Ti(0001)1×1 surface at room temperature was measured as a function of translational kinetic energy
Et by real-time photoelectron spectroscopy. The O 1s photoelectron spectra can be fitted well with three components A, B and C, where the chemical shift of component B and C are +0.7 and +1.6 eV relative to the binding energy of component A (528.8 eV). Upon exposing to the O
2 beam, component A and C appear dominantly and component B grows with an incubation time, indicating that two kinds of chemical adsorption states are concerned with dissociative adsorption of O
2 molecules at the initial stage. The
Et dependences of
S0 show quite different behaviors between component A and C:
S0 of component C decreases monotonously with
Et and is almost constant above 0.6 eV, while
S0 of component A shows a rapid decrease followed by a gradual increase with a minimum at ∼0.5 eV and then decreases two small maxima at ∼0.9 and ∼1.8 eV. The observed
Et dependences of
S0 for component A and C are discussed in terms of a trapping-mediated adsorption and an activated adsorption process and the chemical adsorption state corresponding to component A and C is also considered.
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