Regulating the electronic structure of Pt SAs-Ni2P for enhanced hydrogen evolution reaction

The single atom catalysts (SACs) show immense promise as catalytic materials. By doping the single atoms (SAs) of precious metals onto substrates, the atomic utilization of these metals can be maximized, thereby reducing catalyst costs. The electronic structure of precious metal SAs is significantly influenced by compositions of doped substrates. Therefore, optimizing the electronic structure through appropriate doping of substrates can further enhance catalytic activity. Here, Pt single atoms (Pt SAs) are doped onto transition metal sulfide substrate NiS 2 (Pt SAs-NiS 2 ) and phosphide substrate Ni 2 P (Pt SAs-Ni 2 P) to design and prepare catalysts. Compared to the Pt SAs-NiS 2 catalyst, the Pt SAs-Ni 2 P catalyst exhibits better hydrogen evolution catalytic performance and stability. Under 1 M KOH conditions, the hydrogen evolution mass activity current density of the Pt SAs-Ni 2 P catalyst reaches 0.225 A mg Pt –1 at 50 mV, which is 33 times higher than that of commercial Pt/C catalysts. It requires only 44.9 mV to achieve a current density of 10 mA cm −2 . In contrast, for the Pt SAs-NiS 2 catalyst, the hydrogen evolution mass activity current density is 0.178 A mg Pt –1 , requiring 77.8 mV to achieve a current density of 10 mA cm −2 . Theoretical calculations indicate that in Pt SAs-Ni 2 P, the interaction between Pt SAs and the Ni 2 P substrate causes the Pt d-band center to shift downward, enhancing the H 2 O desorption and providing optimal H binding sites. Additionally, the hollow octahedral morphology of Ni 2 P provides a larger surface area, exposing more reactive sites and improving reaction kinetics. This study presents an effective pathway for preparing high-performance hydrogen evolution electrocatalysts by selecting appropriate doped substrates to control the electronic structure of Pt SAs.