We describe fabrication of microdimensional polyanilne films in a controlled manner by voltammetric potential cycling or controlled potential electrolysis on platinum microdisk electrodes. The film grows in a form of hemispherical microdeposits, and its size largely exceeds the size of a Pt microdisk. Consequently, the film covers both the Pt substrate as well as the surrounding glass seal. Since the adhering polyaniline layer is conducting, the latter situation may lead to an increase in the effective electrode surface area. The lateral growth of polyaniline films outside the microdisk has also been demonstrated by performing diagnostic voltammetric experiments with use of a double microdisk set-up in which independent polarization of each disk is feasible. Microelectrode-based chronocoulometry, that involves an uncomplicated well-defined reduction potential step starting from the emeraldine (conducting) form and ending at leucoemeraldine (nonconducting) form, yields (upon application of a sufficiently short pulse) a welldefined linear response of charge versus square root of time that is consistent with the linear effective diffusion as the predominant charge propagation mechanism. When describing the system kinetics in terms of the effective (apparent) diffusion coefficient, we expect this parameter to be on the level of 10 À8 cm 2 s À1 or lower. The relative changes in dynamics of charge transport are discussed with respect to the polyaniline film loading, the size of microdisk electrode, expansion of the active electrode area, and the choice of electrolyte (strong acid) anion. The results are consistent with the view that when Pt microelectrode is modified with PANI deposit exceeding the size of the microdisk substrate, it behaves in a way as if its surface area is effectively much larger than the geometric area of Pt microdisk.