Hierarchical porous tri-metallic NiCoFe-Se/CFP derived from Ni-Co-Fe Prussian blue analogues as efficient electrocatalyst for oxygen evolution reaction

[Display omitted] •Trimetallic NiCoFe PBAs are electrodeposited homogeneously on CFP as precursors.•The NiCoFe-Se NCs grown on CFP as self-supported electrode for OER.•The NiCoFe-Se/CFP exhibits remarkable OER activity and desirable stability.•Trimetallic element regulation effectively improves the OER activity of selenides. The progress of inexpensive, high-efficiency, and steady oxygen evolution reaction (OER) electrocatalysts is of great importance to promoting water splitting for green hydrogen production. Herein, tri-metallic NiCoFe selenide catalyst backed up by carbon fiber paper (CFP) was synthesized by a facile selenization of NiCoFe Prussian blue analogues (PBAs) for OER in alkaline solutions. The NiCoFe-Se/CFP inherited the porous nanostructure of the metal-organic frameworks (MOFs) precursors prepared by rapid cyclic voltammetry electrodeposition. Benefiting from the 3D hierarchical porous structure, optimized electronic structure of NiCoFe selenides and high conductivity, the synthesized electrocatalyst exhibits outstanding catalytic activity to the corresponding mono-metallic or bi-metallic selenides. Specifically, the NiCoFe-Se/CFP electrode demands an overpotential of 221 mV to attain the 10 mA cm−2 current density in 1.0 M KOH solution and a low Tafel slope of 38.6 mV dec-1. The prepared catalyst also displays good stability and durability. These findings prove a feasible strategy to further improve the catalytic activities of non-precious metal based OER electrocatalysts by the cooperation of structure design and chemical component modification.