The effect of Co2+ ions on zinc deposition from acidic sulfate electrolytes
is investigated on the basis of steady-state polarization curves and imped
ance measurements. Hydrogen evolution is shown to be enhanced by adsorbed c
obalt on both the zinc deposit and the aluminium substrate, and this stimul
ation occurs in combination with the catalytic effect of adsorbed species o
riginating from anodic products. Hydrogen evolution involves a diffusion-co
ntrolled step and a slow adsorption process which is the rate-determining s
tep. It also induces the redissolution of the zinc deposit observable from
the potential dependencies of current, charge transfer resistance and doubl
e layer capacitance.