Electrocatalytic Water Oxidation Reaction Promoted by Cobalt-Prussian Blue and its Thermal Decomposition Product Under Mild Conditions

Cobalt-Prussian blue analogues are remarkable catalysts for the oxygen evolution reaction (water oxidation) under mild conditions such as neutral pH. Although there is extensive reports on literature about the application of these catalysts in water oxidation (the limiting step for hydrogen evolution) some limitations must be overcome in terms of improving the turnover frequency, oxygen production, long term stability, and elucidation of the mechanism. Another important feature to consider is the industrial processability of electrolytic cells for water splitting. For these reasons, we have reported herein a comparison of the electrochemical and chemical properties of three catalysts produced from Cobalt-Prussian Blue. Co-Co PBA 60 refers to Cobalt-Prussian blue heated up to 60 oC with a high content of water. Co-Co PBA 200 is the same starting material but heated up to 200 oC with a low water content. Finally, the Co3O4 is a thermal decomposition product from the heating Cobalt-Prussian blue up to 400 oC. Although the Co-Co PBA 60 has a higher overpotential for water oxidation than Co-Co PBA 200, this catalyst is kinetically faster than Co PBA 200. It is suggested that the water coordinated to the Co2+ in the Co-Co PBA 60 can accelerate the reaction and that there is a balance between thermodynamic and kinetic characteristics for the final properties of the catalyst on pH=7. Another important observation is that the Co3O¬4 catalyst has the best performance among the considered catalysts with the highest TON and TOF. This suggests that the different mechanisms and surface effects demonstrated by the Co3O4 catalyst are more conducive to efficient water oxidation than Prussian Blue. Further studies concerning the effect of water and surface on these catalysts under mild conditions are essential to developing a better understanding of the mechanism of water oxidation and to advancing the development of new catalysts.