Harnessing intrinsic electric fields in 2D Janus MoOX (X=S, Se, and Te) monolayers for enhanced photocatalytic hydrogen evolution

Two-dimensional (2D) Janus monolayers, distinguished by their intrinsic vertical electric fields, emerge as highly efficient and eco-friendly materials for advancing the field of hydrogen evolution reactions (HER). In this study, we explore, for the first time, the potential viability of the oxygenation phase of two-dimensional Janus transition metal dichalcogenides MoOX (X = S, Se, and Te) monolayers as an exceptionally efficient photocatalyst for hydrogen production. Based on first-principles computations, we demonstrate that all three monolayers exhibit semiconductor behavior, characterized by a band gap ranging from 0.66 to 1.55 eV. This narrow band gap renders the proposed materials highly efficient at absorbing light within the visible region. Excitingly, the introduction of an electrostatic potential difference Delta Phi has granted us the ability to surpass the conventional bandgap limit (E-g >= 1.23). Consequently, all monolayers exhibit favorable band alignment with respect to the vacuum level. Moreover, the calculated solar-to-hydrogen efficiency for the envisaged monolayer exceeds the established theoretical limit. Particularly, the MoOTe monolayer emerges as an infrared-lightdriven photocatalyst, demonstrating a remarkable solar-to-hydrogen efficiency limit of up to 25,21% when considering the entire solar spectrum. A thorough examination of the Gibbs free energy differences across these monolayers has revealed that the values during the oxygenation phase are significantly smaller and approach the optimum, in contrast to the parental two-dimensional Janus transition metal dichalcogenides. Our results conclusively establish that the proposed materials exhibit exceptional efficiency as photocatalysts for hydrogen evolution reactions. Notably, their efficacy is demonstrated even in the lack of co-catalysts or sacrificial agents.