Defect‐Driven Enhancement of Electrochemical Oxygen Evolution on Fe–Co–Al Ternary Hydroxides

Efficient, abundant and low‐cost catalysts for the oxygen evolution reaction (OER) are required for energy conversion and storage. In this study, a doping–etching route has been developed to access defect rich Fe–Co–Al (Fe–Co–Al‐AE) ternary hydroxide nanosheets for superior electrochemical oxygen evolution. After partial etching of Al, ultrathin Fe 3 Co 2 Al 2 ‐AE electrocatalysts with a rich pore structure are obtained with a shift of the cobalt valence state towards higher valence (Co 2+ →Co 3+ ), along with a substantial improvement in the catalytic performance. Fe 3 Co 2 Al 2 ‐AE shows a notably lower overpotential of only 284 mV at a current density of 10 mA cm −2 and double the OER mass activity of the etching‐free Fe 3 Co 2 Al 2 with an overpotential of 350 mV. Density functional theory shows the leaching of Al changes the rate‐determining step of the OER from conversion of *OOH into O 2 on Fe 3 Co 2 Al 2 to formation of OOH from *O on the Al‐defective catalysts. This work demonstrates an effective route to design and synthesize transition metal electrocatalysts and provides a promising alternative for the further development of oxygen evolution catalysts.