ABSTRACT Spinel‐type NiFe 2 O 4 exhibits promising application prospects as electrocatalysts for water electrolysis, but its intrinsic properties limit achieving industrial current densities at low voltages. Herein, a dual‐pronged approach is proposed, aimed at enhancing the bifunctional electroactivities of NiFe 2 O 4 toward the oxygen/hydrogen evolution reaction (O/HER) through the incorporation of MoS 4 2− ions. Studies show that the S 2− ligands in MoS 4 2− act as H adsorption sites with optimized adsorption energy, while the Mo 6+ ‐mediated electronic regulation of Ni/Fe active sites reduces the H 2 O dissociation energy, jointly boosting HER performance effectively. Moreover, MoS 4 2− drives controlled reconstruction: accelerates formation of defect‐rich MoO 4 2− /SO 4 2− modified‐NiOOH layer during OER to activate the lattice oxygen mechanism (LOM), and d‐π conjugation inhibits over‐oxidation/leaching of metal ions to enhance OER stability. Benefiting from the dual regulatory effects of MoS 4 2− , the NiFe 2 O 4 /MoS 4 /NF shows a substantial enhancement in performance, with low overpotentials of 200 and 290 mV for HER and OER at 0.2 A cm −2 , respectively, as well as high stability (140 h at 0.5 A cm −2 ). Furthermore, when NiFe 2 O 4 /MoS 4 /NF electrodes are employed as both the cathode and anode in an overall water splitting system, they can achieve 1.0 A cm −2 at 2.0 V. This research significantly expands the methodologies for the preparation of spinel oxide‐based bifunctional catalysts.
Zhao et al. (Sat,) studied this question.