In solution, the [(tim)Co](2+) complex (tim = 2,3,9,10-tetramethyl-1,4,8,11-tetraazacyclotetradeca-1,3,8,10-tetraene) reacts only slowly with O-2, but upon adsorption on graphite electrodes, it becomes an active catalyst for the reduction of O-2 to H2O2. The electroreduction of O-2 proceeds in a single voltammetric step at close to the diffusion-controlled rate at a relatively positive potential (0.25 V vs SCE). The remarkable enhancement in catalytic activity is attributed to a higher affinity for O-2 of the adsorbed complex as a result of its interactions with functional groups on the surface of roughened or oxidized graphite. A possible mechanism for the catalytic reduction of O-2 is proposed. It differs from the one employed by the analogous [(hmc)Co](2+) complex (hmc = C-meso-5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane) which operates at less positive potentials and exhibits two separated voltammetric steps in the reduction of O-2, via [(hmc)CoOOH](2+), to H2O2.