ABSTRACT:The effects of doping Co 3 O 4 with Ag 2 O (0.40-3.00 mol%) or .00 mol%) on the surface and catalytic properties of the solid were investigated via nitrogen adsorption at -196ºC and the decomposition of H 2 O 2 at 30-50ºC. Pure and doped samples were prepared by the thermal decomposition in air at 500-900ºC of pure cobalt carbonate and carbonate samples treated with different proportions of silver or zinc nitrates. The results showed that Ag 2 O doping followed by precalcination at 500-900ºC resulted in a significant decrease (ca. 25%) in the BET surface areas of the treated Co 3 O 4 samples. Treatment of Co 3 O 4 with ZnO followed by precalcination over the same temperature range effected a corresponding increase in the specific surface areas (ca. 28%). The addition of Ag 2 O to Co 3 O 4 effected a record increase in the corresponding catalytic activity towards the decomposition of H 2 O 2 . Thus, the maximum increase noted in the catalytic rate constant (k) measured at 30ºC over Co 3 O 4 doped with 3.00 mol% Ag 2 O exhibited a 36-fold, 26-fold and 3.5-fold increase for catalysts precalcined at 500ºC, 700ºC and 900ºC, respectively. Treatment of Co 3 O 4 with ZnO also effected an increase in the catalytic activity of the resulting solid. Thus, treatment of Co 3 O 4 with 6.00 mol% ZnO followed by precalcination at 500ºC, 700ºC and 900ºC effected an increase of 109%, 28% and 36%, respectively, in the catalytic activity expressed in terms of the reaction rate constant measured at 30ºC. The doping process did not modify the activation energy of the catalyzed reaction but increased the concentration of catalytically active constituents considerably without changing their energetic nature. Doping with Ag 2 O or ZnO led to an increase in the concentration of Co 3+ -Co 2+ ion pairs in the system and also generated corresponding Ag + -Co 2+ and Zn 2+ -Co 3+ ion pairs, thereby increasing the number of active constituents involved in the catalytic decomposition studied.