Interface engineering and heterometal doping Co–Mo/FeS for oxygen evolution reaction

The sluggish kinetics of the oxygen evolution reaction (OER) limits the development of water electrolysis technology and the long-term efficiency of hydrogen energy production. In addition, it is important to evaluate the reconstruction performance of OER catalysts for actual water electrolysis. We created a self-supported electrode with FeS film coated Fe foam as a substrate, ordered resoluble molybdate (MoO42−) anions in interlayers, and Co-doped as a catalytically active phase for the OER. The catalyst is capable of electrochemical self-reconstruction (ECSR). With the dissolution of molybdate and sulfur ions, the catalyst surface cobalt iron oxide (CoFe2O4) forms an active amorphous FeCoOOH, which is favorable for alkaline OER. We realized the introduction of new active sites in the catalyst reconstruction process. Finally, the composite CoFeOx catalyst increased the specific surface area, promoted bubble transport, and enhanced electron mass transfer. The synergistic coupling effect of the catalyst makes it have excellent OER activity and stability. Remarkably, Co–Mo/FeS nanosheets afforded an electrocatalytic OER with a current density of 100 mA cm−2 at a low overpotential of 321 mV. These discoveries open up new opportunities for the application of doping and template-directed surface reconfiguration, which holds promise as an effective electrocatalyst for the OER.