The kinetics of electrode reactions in the Fe(CN)(6)(3-/4-) redox system is
studied on the platinum-doped (Pt content up to 15 at. %) amorphous diamon
d-like carbon thin-film electrodes. The wide-gap diamondlike carbon is elec
trochemically inactive per se; yet, it acquires the electrochemical activit
y on adding platinum to the film bulk during the film growth. The effect of
platinum is of a threshold character; at the same time, with increasing pl
atinum content, the electrode differential capacitance increases smoothly,
and the resistivity of the material remains practically constant. The effec
t is explained with a model which assumes that both the conductance in the
film bulk and the catalytic action of platinum on the charge transfer at th
e electrode/solution interface have a nonuniform character.