Contrary Effect of B and N Doping into Graphene and Graphene Oxide Heterostructures with MoS$_2$ on Interface Function and Hydrogen Evolution

TL;DR

This study uses first-principles calculations to explore how B and N doping in graphene-based heterostructures with MoS₂ affect interface properties and hydrogen evolution, revealing contrasting effects on charge transfer and catalytic activity.

Contribution

It provides a systematic comparison of B and N doping effects on graphene/MoS₂ heterostructures, clarifying their opposite impacts on interface function and hydrogen evolution.

Findings

N doping enhances interface functions via donor states

B doping reduces interface functions via acceptor states

B-doped systems show lower Gibbs free energy for hydrogen adsorption

Abstract

Molybdenum disulfide (MoS$_2$) attracts attention as a high efficient and low cost photocatalyst for hydrogen production, but suffers from low conductance and high recombination rate of photo-generated charge carriers. In this work, we investigate the MoS$_2$ heterostructures with graphene variants (GVs), including graphene, graphene oxide, and their boron- and nitrogen-doped variants, by using first-principles calculations. Systematic comparison between graphene and graphene oxide composites is performed, and 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 MoS$_2$ layer, inducing the creation of 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 lower Gibbs free energy difference for hydrogen adsorption on GV side than the N-doped systems, which deserves much consideration in the design of new functional photocatalysts.