摘要
The potential of sustainable hydrogen production technology through water splitting necessitates the rational design of oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) bi-functional electrocatalysts . In this context, we initially synthesized and empirically evaluated ultralow Ru-doped NiMoO 4 @Ni 3 (PO 4 ) 2 core-shell nanostructures on nickel foam (Ru-NiMoO 4 @Ni 3 (PO 4 ) 2 /NF). The hydrous NiMoO 4 nanopillars were hydrothermally grown on NF, followed by successive RuCl 3 etching and subsequent phosphorylation processes, leading to the final Ru-NiMoO 4 @Ni 3 (PO 4 ) 2 /NF. The catalyst demonstrated impressive HER overpotential values of −14.8 and −57.1 mV at 10 and 100 mA cm −2 , respectively, with a Tafel slope of 35.8 mV dec −1 . For OER at 100 mA cm −2 , an overpotential of 259.7 mV was observed, with a Tafel slope of 21.6 mV dec −1 . The cell voltage required for overall water splitting was 1.43 V at 10 mA cm −2 and 1.68 V at 100 mA cm −2 . Moreover, the catalyst exhibited superior stability for 150 h, emphasizing its practical utility for long-term applications. Subsequent density functional theory calculations aligned with these empirical findings, indicating a low water dissociation energy barrier (Δ G b = 0.46 eV), near-zero free adsorption energy for HER (Δ G *H = 0.02 eV), and suitable free adsorption energy for OER (Δ G *OOH − Δ G *OH = 2.74 eV), alongside a high density of states near the Fermi level . These results, informed by both experimental evaluation and theoretical validation, highlight the potential of Ru-NiMoO 4 @Ni 3 (PO 4 ) 2 /NF as a high-performance catalyst for water splitting, setting a solid foundation for advancements in sustainable energy technologies.
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