PtSe2/Pt Heterointerface with Reduced Coordination for Boosted Hydrogen Evolution Reaction

PtSe2 is a typical noble metal dichalcogenide (NMD) that holds promising possibility for next-generation electronics and photonics. However, when applied in hydrogen evolution reaction (HER), it exhibits sluggish kinetics due to the insufficient capability of absorbing active species. Here, we construct PtSe2/Pt heterointerface to boost the reaction dynamics of PtSe2, enabled by an in situ electrochemical method. It is found that Se vacancies are induced around the heterointerface, reducing the coordination environment. Correspondingly, the exposed Pt atoms at the very vicinity of Se vacancies are activated, with enhanced overlap with H 1s orbital. The adsorption of H-. intermediate is thus strengthened, achieving near thermoneutral free energy change. Consequently, the as-prepared PtSe2/Pt exhibits extraordinary HER activity even superior to Pt/C, with an overpotential of 42 mV at 10 mA cm(-2) and a Tafel slope of 53 mV dec(-1). This work raises attention on NMDs toward HER and provides insights for the rational construction of novel heterointerfaces.

Automated summary

Constructing PtSe2/Pt heterointerface can enhance the reaction kinetics of PtSe2, achieving near thermoneutral free energy change for hydrogen evolution reaction. The activated Pt atoms near Se vacancies strengthen the adsorption of H-. intermediate, leading to extraordinary activity even superior to Pt/C, demonstrating the potential of NMDs for HER and providing insights for constructing novel heterointerfaces.