Spatial pattern formation and wave propagation in surface reactions ar
e often controlled by the chemical diffusion of adsorbed reactant spec
ies in mixed adlayers. We characterize the intrinsically coverage-depe
ndent and tensorial nature of such diffusion, emphasizing that these f
eatures result from the influence of site-blocking by coadsorbed speci
es, even in the absence of other interactions. The coverage dependence
is shown to depend on the relative hop rates of the various reactants
. These features are also shown to significantly influence the spatiot
emporal behavior in simple, atomistic lattice-gas models of surface re
actions. This is illustrated with two examples: trigger wave propagati
on in a bistable system characteristic of CO oxidation, and the remova
l of unstable NO+CO adlayers, controlled by dissociation-mediated NO r
eduction. (C) 1998 Elsevier Science B.V.