Doped MoS 2 Polymorph for an Improved Hydrogen Evolution Reaction.

Green hydrogen produced from solar energy could be one of the solutions to the growing energy shortage as non-renewable energy sources are phased out. However, the current catalyst materials used for photocatalytic water splitting (PWS) cannot compete with other renewable technologies when it comes to efficiency and production cost. Transition-metal dichalcogenides, such as molybdenum disulfides (MoS 2 ), have previously proven to have electronic and optical properties that could tackle these challenges. In this work, optical properties, the d-band center, and Gibbs free energy are calculated for seven MoS 2 polymorphs using first-principles calculations and density functional theory (DFT) to show that they could be suitable as photocatalysts for PWS. Out of the seven, the two polymorphs 3H a and 2R 1 were shown to have d-band center values closest to the optimal value, while the Gibbs free energy for all seven polymorphs was within 5% of each other. In a previous study, we found that 3H b had the highest electron mobility among all seven polymorphs and an optimal bandgap for photocatalytic reactions. The 3H b polymorphs were therefore selected for further study. An in-depth analysis of the enhancement of the electronic properties and the Gibbs free energy through substitutional doping with Al, Co, N, and Ni was carried out. For the very first time, substitutional doping of MoS 2 was attempted. We found that replacing one Mo atom with Al, Co, I, N, and Ni lowered the Gibbs free energy by a factor of 10, which would increase the hydrogen evolution reaction of the catalyst. Our study further shows that 3H b with one S atom replaced with Al, Co, I, N, or Ni is dynamically and mechanically stable, while for 3H b , replacing one Mo atom with Al and Ni makes the structure stable. Based on the low Gibbs free energy, stability, and electronic bandgap 3H b , MoS 2 doped with Al for one Mo atom emerges as a promising candidate for photocatalytic water splitting.