Nickel-iron alloys were electrodeposited using transient pulsed curren
ts on rotating disk electrodes. It was found that the influence of mas
s transfer on the nickel and iron deposition rates is through the chem
ical equilibrium of the respective surface electroactive species of ni
ckel and ferrous hydroxyl ions. The iron reduction rate increases with
the introduction of boric acid, while the nickel deposition rate decr
eases at larger applied pulsed currents. Further additions of surfacta
nts and complexing agents such as saccharin and ethylene diamine decre
ase both the nickel and iron deposition rates through a simple surface
-blocking and solution-chelating process.