This paper describes the use of ammonia-containing baths for Zn-Ni alloy el
ectrodeposition. Buffering properties of the ammonia/ammonium couple limit
the local change in pH in the vicinity of the electrode surface caused by s
imultaneous hydrogen evolution. In addition, it is shown that the divalent
zinc and nickel species exist in the form of Zn(NH3)(4)(2+) and Ni(NH3)(6)(
2+) complexes over a large pH range. The electrochemistry of the deposition
at pH 10 was investigated by galvanostatic experiments and cyclic voltamme
try, and compared with deposition from ammonium chloride baths at pH 5. The
Ni content in the alloys were found to be 40-60% higher from the ammonia-c
ontaining bath than from the acidic baths. Reduction of divalent ions and h
ydrogen evolution were shown to occur at potentials 250 mV more cathodic th
an with baths at pH 5; the deposition mechanism may be affected by complexa
tion of the metal cations by ammonia.