This study has examined the effect of water on the electrodeposition of copper from a deep eutectic solvent (DES). Initial physiochemical measurements showed that the viscosity and resistivity of the DES decreased with added water in the range 1 -15 wt%. This reduction in viscosity resulted in an increase in the mass transfer limiting current, without narrowing the electrochemical window or altering the speciation of the copper chloro-complexes. This shows that metal deposition rates can be increased by water additions. The effect of water on the electrochemical kinetics of the Cu(I) and Cu(II) chloro-complexes was also studied. It was found that the kinetics of the Cu(I)/Cu(0) reaction is largely irreversible, while the Cu(II)/Cu(I) couple was quasi-reversible. The rate constants for Cu(II)/Cu(I) and Cu(I)/Cu(0) reactions were accelerated by water additions, although the transfer coefficients remained unchanged. The effect of increased deposition rates, electrolyte conductivity and reaction kinetics on deposit uniformity was estimated and subsequently verified by experiments. It was found that, although higher deposition rates could be achieved, the thickness of the deposit was non-uniform since the Wagner numbers remained relatively low.
An analysis of the anodic reaction occurring at soluble copper anodes during the electrodeposition of copper from an ethaline-based deep eutectic solvent (DES) has been performed. It was shown by UV-Vis spectroscopy and electrochemical measurements that the dominant anodic species produced is the CuCl 2 -complex. In pure ethaline the current efficiency of the anodic process is 100% and the dissolution valency is one. However, in the presence of Cu(II) species the apparent dissolution valency measured gravimetrically was typically less than unity, corresponding to an observed mass loss greater than that expected from Faraday's law.Moreover, the apparent dissolution valency showed a marked dependence on the electrode
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