Q. Gao et al., UNUSUAL ADSORPTION SITE OCCUPATION SEQUENCE - NO ADSORPTION ON STEPPED PD(112), Journal of the American Chemical Society, 116(9), 1994, pp. 3901-3903
The adsorption of NO on a stepped Pd(112) surface has been investigate
d at 300-373 K with high resolution electron energy loss spectroscopy
(HREELS) and electron stimulated desorption ion angular distribution (
ESDIAD) techniques. At exposures below 5.7 X 10(14) NO/cm(2), NO molec
ules preferentially adsorb on the terrace sites, with an NO stretching
mode observed by HREELS at 1535-1550 cm(-1), and an O+ ESDIAD beam di
rected near the (111) terrace-normal direction. For NO exposures above
similar to 6 x 10(14) molecules/cm(2), step sites are occupied in add
ition to the terrace sites, with an NO stretching mode observed in HRE
ELS at similar to 1655-1670 cm(-1) and an additional O+ ESDIAD beam or
iented in the ''downstairs'' direction. This is an unusual reversal of
the site occupation sequence since one usually expects stronger adsor
bate bonding on the step sites causing the steps to fill first. The N-
O bond stretching frequencies observed in HREELS are indicative of wea
ker bonding of NO molecules on the step sites than on the terrace site
s.