The oxidation of an Si(100) surface induced by photodissociation of adsorbe
d N2O has been studied by X-ray photoelectron spectroscopy, temperature-pro
grammed desorption, and angle-resolved time-of-flight (TOF) measurements. N
2O adsorbs in physisorption and chemisorption states on Si(100), The photoc
hemical oxidation is induced by the irradiation of light in the wavelength
range between 532 and 193 nm, The cross-sections of both adsorption states
at 193 nm are larger than that of gaseous N2O by about two orders of magnit
ude. Substrate-mediated excitation is considered to be responsible for the
photochemistry of N2O in the two adsorption states. Although the TOF distri
butions of N-2 fragments from the physisorbed N2O are almost identical in t
he wavelength region studied, those from the chemisorbed N2O show a marked
wavelength dependence. The interpretation is that there are multiple types
of chemisorbed states whose photodissociation dynamics and the wavelength d
ependence of the cross-section are different to each other. (C) 2000 Elsevi
er Science B,V, All rights reserved.