Time-dependent oxidation of graphite and cobalt oxide nanoparticles as electrocatalysts for the oxygen evolution reaction

Abstract

• Co 3 O 4 /G OX was synthesized via a facile hydrothermal method for the OER. • Co 3 O 4 /G OX-10 catalyst showed the lowest overpotential of 250 mV at 10 mA cm −2 . • The optimal catalyst exhibited higher specific activity and turnover frequency. • Demonstrated improved electrical conductivity and small charge transfer resistance. • The optimal catalyst Exhibited excellent stability and durability. Water splitting is a promising way of producing hydrogen, but a highly efficient and durable electrocatalyst to accelerate the oxygen evolution reaction (OER) is required. In this study, we report cobalt oxide (Co 3 O 4 ) and oxidized graphite (G OX ) synthesized by a simple hydrothermal method to prepare a catalyst (Co 3 O 4 /G OX ) for the OER. Time-dependent oxidation of graphite (G) and Co 3 O 4 nanoparticles was observed by physical and electrochemical studies. The optimal catalyst (Co 3 O 4 /G OX-10 ) demonstrated the best catalytic OER performance with the lowest overpotential of 250 mV to reach 10 mA cm −2 and a small Tafel slope of 67 mV dec -1 , which is substantially smaller than that of pristine Co 3 O 4 and Co 3 O 4 /G. An efficient synergistic effect between Co 3 O 4 and G OX in the composite catalyst was observed compared to the individual catalysts. The optimal catalyst exhibited high specific activity (1.543 mA cm −2 ) and turnover frequency (0.474 s −1 ) compared to the other catalysts in this study. The high catalytic performance of the catalyst is attributed to the presence of oxygen functional groups, which induced a high electrochemical surface area, additional active site exposure, fast electron transfer, and enhanced dispersion of the catalyst. Thus, the synthesized Co 3 O 4 /G OX-10 catalyst can replace noble metals as an efficient OER electrocatalyst.