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Exploring highly efficient and robust electrocatalysts to replace the noble metal-based electrocatalysts for alkaline oxygen evolution reaction (OER) is vital and challenging for the conversion of renewable energy. Herein, a novel element incorporation strategy is proposed to synthesize the multi-metallic selenide of (Ni,Fe,Co)Se 2 nanosheets anchored on a stainless steel mesh substrate (NiFeCoSe/SSM). The multi-metallic hybrid film (NiFeCo/SSM) obtained by a co-sputtering method is converted to the (Ni,Fe,Co)Se 2 nanosheets through an alloying-dealloying-selenization process, in which Co and Fe atoms replace part of Ni atoms in the NiSe 2 lattice. The as-obtained NiFeCoSe/SSM displays efficient OER performances in alkaline solutions with an overpotential of 228 mV at 20 mA cm−2 (268 mV at 50 mA cm−2), and a small Tafel slope of 69.8 mV dec−1 in 1.0 M KOH. Furthermore, the NiFeCoSe/SSM electrode demonstrates a remarkable catalytic stability as long as 24.0 h, and its initial nanosheet structure can be well retained after the durability test. Such excellent OER performances of NiFeCoSe/SSM can be attributed to the unique nanosheet structure and the optimized electronic structure due to the synergistic effect among different metallic elements. • A novel element incorporation strategy is proposed to obtain multi-metallic selenide. • Co and Fe atoms replace part of Ni atoms in the NiSe 2 lattice. • The NiFeCoSe/SSM displays efficient OER performances in alkaline solution. • Synergistic effect among metallic elements causes optimized electronic structure. [ABSTRACT FROM AUTHOR]

Antimony (Sb) as a low-toxic and cost-effective metal is a promising material to catalyse CO 2 electroreduction to formate with practical viability. However, monometallic Sb suffers from intrinsically low catalytic activity and the competing hydrogen evolution. Here, we report nanoporous Sb-Bi alloys for substantially improving the catalytic activity of Sb and suppressing hydrogen evolution. The optimal Sb-Bi alloy exhibits a maximum Faradaic efficiency of 95.8 % toward formate production, surpassing the 11.6 % of monometallic Sb counterpart. Operating the catalyst in the flow cell demonstrates a formate partial current density of 734 mA cm−2 and cathodic energy efficiency of 59 % at a moderate overpotential of 800 mV, representing a record formate-production performance so far. Experimental and theoretical studies indicate that the Sb-Bi interactions activate Sb sites to selectively stabilize *OCHO intermediates, facilitating CO 2 -to-formate conversion. This work offers insights in manipulating bimetallic interactions to transform inert materials into active catalysts for efficient electrocatalysis. [Display omitted] • Sb-Bi interactions induce electrocatalytic switching from HER to CO 2 ER. • Sb 2 Bi 6 exhibits a maximum formate selectivity of 95.8 % in an H-type cell. • Sb 2 Bi 6 achieves a record formate activity of 734 mA cm−2 in a flow cell. • Sb-Bi interactions facilitate Sb sites to stabilize *OCHO for formate formation. [ABSTRACT FROM AUTHOR]