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JdE/dtj ¼ 2 mV sÀ1 (Reprinted with permission from Ref. [40]) monolayer. 2 V was assigned to a random adsorption of Cu atoms. Different voltammetric features appear in the case of Cu upd on a Au(100) substrate. 05 M H2S04 + 1 mM CuSO4 solution including also the Cu overpotential region [40]. A Cu monolayer formation was found in the region between 100 and 350 mV and two current density peaks pairs (corresponding to the Cu adsorption/desorption) were observed. The voltammogram obtained in the upd range between 50 and 500 mV is enlarged by a factor of 10 for clarity (dashed curve in the Figure).
115] analysed the effect of different amounts of chloride on the adsorption behaviour and adlayer structure in Cu upd on Au(111) in perchloric acid solutions. 67 Å, respectively, were observed. Both structures involved cooperative adsorption of Cu and Cl‾, but the (5 Â 5) adlattice predominated in most of the potential range and anion concentrations studied, while the (2 Â 2) adlattice became evident at particular potentials and if anion concentration did not exceed 10À6 M. More recently, Sieradski et al.
The upper scale corresponds to the hydrogen normal electrode, while the lower is referred to the bulk Ag deposition potential (Reprinted with permission from Ref. [13]) 20 2 Experimental Techniques and Structure of the Underpotential Deposition Phase Fig. 05 M H2SO4 solution. jdE/dtj ¼ 1 mV sÀ1. (b) Adsorption isotherm corresponding to (a), with a schematic view of the proposed Cu structures formed on Au(111) (Reprinted with permission from Ref. [39]) Cu upd on polycrystalline and single crystal gold surfaces, in particular on Au(111), is certainly one of the few systems that has been studied with a wide variety of in-situ techniques including electrochemical ones [19–28], Scanning Tunneling Microscopy [23, 29–31], Atomic Force Microscopy [32], Spectroscopic Methods [33–36] and Quartz Crystal Microbalance [25, 37], and Ex-Situ Techniques such as Low Energy Electron Diffraction, Auger Electron Spectroscopy and Reflection High Energy Electron Diffraction [21, 22, 38].