In this article we attempted to review the key issues relevant to tremendou
s oxidation activity of supported Au catalysts. We described in detail newl
y developed Au catalysts, remarkably active for low-temperature CO oxidatio
n, using Au phosphine complexes and clusters as precursors for gold metal p
articles and as-precipitated wet metal hydroxides as precursors for oxide s
upports. Particular attention was placed on chemical interaction of the Au
complexes and clusters with the oxide surfaces and its critical role in pre
paration of tremendously active supported Au. Simultaneous transformations
of both the gold and support precursors during temperature-programmed calci
nation provoked the formation of Au catalysts highly active for the low-tem
perature CO oxidation. A new aspect of CO oxidation mechanisms was also dis
cussed. (C) 1999 Elsevier Science B.V. All rights reserved.