Bioinspired multimetal electrocatalyst for selective methane oxidation

Selective partial electrooxidation of methane (CH4) to liquid oxygenates has been a long-sought goal. However, the high activation energy of C-H bonds and competing oxygen evolution reaction limit product selectivity and reaction rates. Inspired by iron (IV)-oxo containing metalloenzymes' functionality to activate the C-H bond, here we report on the design of a copper-iron-nickel catalyst for selective oxidation of CH4 to formate via a peroxide-assisted pathway. Each catalyst serves a specific role which is confirmed via electrochemical, in situ, and theoretical studies. A combination of electrochemical and in situ spectroelectrochemical studies revealed that H2O2 oxidation on nickel led to the formation of active oxygen species which trigger the formation of iron (IV) at low voltages. Density functional theory analysis helped reveal the role of iron (IV)-oxo species in reducing the activation energy barrier for CH4 deprotonation and the critical role of copper to suppress overoxidation. Our multimetal catalyst exhibits a formate faradaic efficiency of 42% at an applied potential of 0.9 V versus a reversible hydrogen electrode.