▎ 摘　　要

Molybdenum disulfide (MoS2) attracts attention as a highly efficient and low-cost photocatalyst for hydrogen production but suffers from low conductance and high recombination rate of photogenerated charge carriers. In this work, we investigate the MoS2 heterostructures with graphene variants (GVs), including graphene, graphene oxide, and their boron- and nitrogen-doped variants, by first-principles calculations. A systematic comparison between graphene and graphene oxide composites is performed, and the contrary effect of B and N doping on interface function and hydrogen evolution is clarified. We find that upon the formation of the interfaces, some amount of electronic charge transfers from the GV side to the MoS2 layer, inducing the creation of an interface dipole and the reduction of work function, which is more pronounced in the graphene oxide composites. Moreover, our results reveal that N doping enhances the interface functions by forming donor-type interface states, whereas B doping reduces those functions by forming acceptor-type interface states. However, the B-doped systems exhibit a lower Gibbs free energy difference for hydrogen adsorption on the GV side than the N-doped systems, which deserves much consideration in the design of new functional photocatalysts.