The complex oxygen evolution reaction (OER) is recognized as the most studied and explored electrochemical conversion, which plays a crucial role in energy-related applications. In this work, a series of metal−organic framework (MOF)derived FeNi oxides from a barrel-shaped Ni-based BMM-10 precursor are conveniently obtained to show an excellent OER performance. Under mild Fe(III) etching, a type of core−shell Fe 0.5 -BMM-10 can be well preserved and the coordination bond of the middle frame structure is decomposed. Furthermore, the Fe x -BMM-10-T series is successfully synthesized with a well-preserved morphology compared to precursors after direct oxidation. Finally, followed by initial electrochemical activation, the decomposition of FeNi oxides generates active Fe-doped nickel oxyhydroxides for efficient water oxidation. The improved OER performance stems from the high specific surface area and abundant exposed active centers, as well as the significant synergistic effect between iron and nickel, which is further verified by the theoretical calculation. This approach can be extended to precisely adjust the morphology of MOFs and their derivatives that can result in superior electrocatalytic properties in terms of energy conversion and storage applications.

The exploration of non-noble metal electrocatalysts with high catalytic activity and stability for oxygen evolution reaction (OER) has become particularly urgent. Here, FeNi-based Prussian blue analogues (PBAs) were obtained by adding different solvents, where PBA particles preferentially grew on the surface plane/edge of coordination polymer precursor (Ni-ABDC) with various polarities. This resulted in the formation of FeNi-PBAplane/edge morphologies, respectively. Notably, on account of more exposed PBAs, FeNi nanoparticles were uniformly supported on the porous N-doped carbon nanomaterials. Among them, the calcined FeNi-NC-800 underwent an interesting pre-activation process and exhibited a low overpotential of 281 mV at 10 mA cm À 2 and a small Tafel slope of 82 mV dec À 1 in 1.0 m KOH. This bimetallic sample showed superior OER activity and stability in comparison with control materials, which could be attributed to its abundant FeNi nanoparticles, high nitrogen content, large specific surface area, and synergistic effects between Fe and Ni atoms. In addition, relevant theoretical calculation on the optimal catalyst, FeNi-NC-800, further demonstrated its efficient OER performance with effective Fedoping in the Ni-based oxyhydroxides.

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