Modulating the Oxygen Evolution Reaction of Single-Crystal Cobalt Carbonate Hydroxide via Surface Fe Doping and Facet Dependence.

The oxygen evolution reaction (OER) is a critical half-reaction in water splitting and metal-air cells. The sensitivity of the OER to the composition and structure of the electrocatalyst presents a significant challenge in elucidating the structure-property relationship. In this study, highly stable single-crystal cobalt carbonate hydroxide [Co(OH)CO, CoCH] was used as a model to investigate the correlations among structure, composition, and reactivity. Single-crystal CoCH nanowires (denoted as CoCH NWs) and Fe-doped CoCH nanowires (denoted as Fe-CoCH NWs) with an exposed (210) facet and Fe-doped CoCH nanosheets (denoted as Fe-CoCH NSs) with an exposed (2-13) facet were synthesized using electrochemical and one-step hydrothermal strategies, respectively. Their OER activity decreased in the following order: Fe-CoCH NWs > Fe-CoCH NSs > CoCH NWs. Theoretical investigation suggested that the doped Fe sites serve as active sites, and the crystal-facet dependence can finely adjust the 3d configuration of Fe sites, resulting in the optimal adsorption strengths and energy barriers for potential-determining steps on the (210) facet of CoCH. This renders the as-prepared Fe-CoCH NWs as some of the most promising Co-based OER catalysts.