A conducting platinum cluster compound K1.64Pt(C2O4)(2) was electroche
mically synthesized on a glassy carbon electrode through the electroox
idation of K2Pt(C2O4)(2) in an aqueous medium using single potential s
tep and cyclic voltammetry methods. The precursor K2Pt(C2O4)(2) was pr
epared by a ligand exchange reaction between C2O42- and PtCl42-. Durin
g single potential step experiments, the electrolytic current correspo
nding to the oxidation of K2Pt(C2O4)(2) increased dramatically after a
sharp decrease at the beginning (due to the formation of conducting K
1.64Pt(C2O4)(2) on the surface of the working electrode). Two kinds of
mechanism account for the current transients at the different applied
potentials. Cyclic voltammetry was conducted with K1.64Pt(C2O4)(2) on
the surface of the working electrode and a steady-state diffusion cur
rent was observed. Since the material grew in a fibrous manner, each c
onducting fiber which was in contact with the electrode could serve as
an ultramicroelectrode. The behavior of the working electrode was thu
s changed from a plain to an ultramicroelectrode array.