For the co-adsorption of An and Cu on Ru(001), the Ru substrate promot
es the alloying of the noble metals by lowering the activation energy
required for the process. High-resolution photoemission spectroscopy w
ith synchrotron radiation and X-ray photoelectron spectroscopy have be
en used to investigate the core-level binding energy shifts and the va
lence-band behaviour in a series of Au and Cu overlayers on Ru(001): 1
ML Au, 1 ML Cu, 1 ML Au and 1 ML Cu, 3 ML Au and 1 ML Cu, as well as
1 ML Au and 3 ML Cu. A monolayer of Au in contact with Ru(001) has a A
u 4f(7/2) binding energy similar to 0.23 eV higher than that of Au sur
face atoms on pure Au but still similar to 0.1 eV smaller than that of
the bulk Au. In contrast a monolayer of Cu bonded to Ru(001) exhibits
a Cu 2p(7/2) binding energy similar to 0.1 eV lower than that of a Cu
surface atom on pure Cu. Most of the co-deposited Au-Cu systems forme
d ultrathin alloys on top of the Ru(001) surface. The strain and elect
ronic perturbations induced by the Ru substrate on the Au and Cu overl
ayers favour the formation of Au-Cu alloys, Binding energy shifts of t
he Au 5d band components and the accompanying change to the overall d-
band width were found to be very sensitive to the alloying process, as
has been observed in bulk Au-Cu alloys, The order of deposition, anne
aling, and the temperature of the substrate were all found to have an
effect on the formation of Au-Cu ultrathin alloys. These ultrathin all
oys exhibit Au 4f(7/2) and Cu 2p(3/2) binding energies that are signif
icantly different from those of bulk Au-Cu alloys as a consequence of
the interactions with the Ru(001) substrate.