Rapid hydrogen adsorption-desorption at sulfur sites via an interstitial carbon strategy for efficient HER on MoS2

Molybdenum disulfide (MoS2), a noble-free material with plentiful unsaturated active edge sites, is expected to replace platinum catalysts for commercial electrocatalytic hydrogen production. However, efficient hydrogen adsorption-desorption processes on sulfur sites with full electron configuration still remain a challenge. Here, vertically oriented self-assembled metallic MoS2 nanospheres anchored by interstitial atomic carbon (Cia-MoS2) are proposed to achieve a rapid hydrogen adsorption-desorption process. In 0.5 M H2SO4 solution, Cia-MoS2 exhibits fast kinetics (Tafel slope of 45 mV dec−1 and overpotential of 87 mV at 10 mA cm−2), as well as a long-term durability over 72 h. As confirmed from X-ray absorption fine spectroscopy and density functional calculations, Cia significantly optimizes the overall HER performance by reconfiguring the charge landscape and re-splitting the energy level of surface S moiety, which provides a universal strategy for fabricating stable unsaturated 2D catalysts toward HER. [Display omitted] •Interstitial atomic carbon-doped MoS2 achieves a rapid hydrogen adsorption-desorption process.•Interstitial atomic carbon reconfigured the charge landscape and energy level splitting on sulfur.•The catalyst exhibits excellent thermodynamic stability in long-term hydrogen evolution catalysis.•The catalyst exhibits accelerated hydrogen generation kinetics.