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Composition of Oxide Layers

Another mechanism is involved in the Cu(II)-containing solutions where Cu+ ions are generated due to the interaction between Cu and the metalhc phase of the copper electrode [Pg.243]

The latter process attains equilibrium, if the Cu concentration does not exceed some critical (maximum) value specified by the relation [30] [Pg.243]

Otherwise, an excess of Cu+ ions will react with OH yielding CU2O. The net [Pg.243]

3) and (10.5) refer to the main relationships that determine the conditions for formation of stabile CU2O. [Pg.243]

The largest amount of oxygen was found on the surface of all the samples this being the result of oxidation in the atmosphere. This surface layer is very thin (1 - 2 nm) and is easily removed by sputtering. The subsequent distribution of oxygen depends on the thickness of the oxide layer. As will be seen next, oxide layers may be destroyed to a large extent when the appropriate negative polarization is applied. [Pg.244]


SIMS analysis as carried out in our previous work [12,39] provides a qualitative analysis of Cr enrichment of the surface. Based on such qualitative analysis of Cr content, a Cr203 oxide layer was proposed to develop in nanocrystalline alloy, whereas, it was proposed that a mixed Fe-Cr oxide layer forms in case of microcrystalline alloy. A Future study quantifying the Cr, Fe and O contents of oxide layer and their oxidation states using techniques such as X-ray photoelectron spectroscopy (XPS) must provide a better understanding of the effect of nanocrystalline structure on the chemical composition of oxide layer. [Pg.232]


See other pages where Composition of Oxide Layers is mentioned: [Pg.243]    [Pg.243]    [Pg.244]   


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