Voltammetric behavior of submicron-thick electrodeposited Pt-Ru on gold support is studied in sulfuric acid solution as a function of deposition potential and Pt:Ru ratio in chloride bath. In contrast to Pt-Ru, deposition of pure Ru is observed only at potentials of hydrogen evolution. The reason is found to be of kinetic nature, namely an inhibition of Ru deposition in presence of chloride. Chloride ions remain adsorbed on Ru at more negative potentials than on Pt and An because of more negative ruthenium potential of zero free charge. Cu-UPD is applied to test the surface content of the oxidized Ru on pure Ru and various Pt-Ru surfaces. An enhancement of Ru oxohydroxides reduction in presence of Pt is observed. The electrocatalytic activity of Pt-Ru in respect to methanol oxidation correlates with the content of rechargeable surface Ru oxide. Ageing and 'training' of Pt-Ru electrodeposits under various modes is studied in order to determine the conditions of irreversible Ru oxidation. No manifestations of Ru dissolution from Pt-Ru electrodeposits in 0.5 M H2SO4 are found for anodic potential limits up to 1.1 V (RHE), in agreement with thermodynamic predictions. Electrodeposited Pt-Ru can be considered as a convenient model system for the study of Ru dissolution and crossover, as well as for determining the nature of the active surface species in the real composite catalysts for methanol oxidation. (c) 2006 Elsevier Ltd. All rights reserved.