Density functional theory study on water–gas-shift reaction over molybdenum disulfide

Density functional theory calculations have been carried out to investigate the adsorption of reaction intermediates appearing during water–gas-shift reaction at the sulfur covered MoS2 (1 0 0) surfaces, Mo-termination with 37.5% S coverage and S-termination with 50% S coverage using periodic slabs. The pathway for water–gas-shift reaction on both terminations has been carefully studied where the most favorable reaction path precedes the redox mechanism, namely the reaction takes place as follows: CO + H2O → CO + OH + H → CO + O + 2H → CO2 + H2. The most likely reaction candidates for the formate species HCOO formation is the surface CO2 reaction with H as a side reaction of CO2 desorption on S-termination with 50% S coverage. The formed HCOO species will react further with adsorbed hydrogen yielding H2COO followed by breaking its C–O bond to form the surface CH2O and O species.

Density functional theory calculations have been employed to investigate the water–gas-shift reaction mechanisms at sulfur covered MoS2 (1 0 0) surfaces using periodic slabs. The most favorable reaction path on both terminations precedes the redox mechanism, namely the reaction takes place as follows: CO + H2O → CO + OH + H → CO + O + 2H → CO2 + H2.Figure optionsDownload as PowerPoint slide