We have studied coadsorbed CO and H on the stepped Pt(335) surface wit
h electron energy loss spectroscopy and temperature-programmed desorpt
ion. Radically different coadsorption behavior is found on the step ed
ges and the terraces. Along the edge coadsorbed H strongly affects CO'
s vibrational spectrum, shifting CO from atop to bridge sites and enha
ncing the cross section of bridge CO. On the terrace coadsorbed H has
virtually no effect on CO's spectrum, even at very high H coverage. Bo
th of these behaviors differ from the interactions observed on Pt(111)
. Possible explanations are discussed.