Structural and Electrochemical Identification of CoFe Pnictide Catalysts Affecting the Performance of the Oxygen Evolution Reaction

Abstract

The advance of efficient electrocatalysts for electrochemical water splitting is highly significant for the energy conversion system, but is hindered by the high overpotential of the oxygen evolution reaction (OER) by four-electron transfer. Herein, we report a variation of transition metal compound based on the Co-Fe Prussian blue analogue (PBA) precursor. CoP/FeP, Co2N/Fe3N, and CoFe catalysts are synthesized in N-2 atmosphere by phosphorization, nitridation, and calcination, respectively. After phosphorization, the synthesized mesoporous CoP/FeP nanocubes contribute to the improvement of the electrocatalyst performance by maintaining the shape of the precursor. The mesoporous structure of the CoP/FeP catalyst enhanced the electrochemically active surface area (ECSA) than other Co2N/Fe3N and CoFe catalysts, resulting in better OER performance with an overpotential of 279 mV at a current density of 10 mA center dot cm(-2), a Tafel slope of 74 mV center dot dec(-1), and good stability for 24 h with only 5.64% degradation in alkaline solution (1.0 M KOH).