Interaction of H_2S with perfect and S-covered Ni(110) surface: A first-principles study

摘要

First-Principles study based on Density functional theory (DFT) calculations are employed to investigate the dissociative mechanism of H2S adsorption and its dissociation on perfect, and sulfur covered Ni(110) surface. On both surfaces, we probe the site preference for H2S, HS, H, and S adsorption mechanisms. The results indicate that H2S is energetically adsorbed on their high symmetry adsorption sites with the preferred short-bridge (SB) site on both surfaces. Furthermore, we found that chemisorption of HS is stronger in contrast to H2S at favorable short-bridge (SB) with a binding energy of -3.59 eV on perfect Ni(110) surface, and on S-covered Ni(110) surface at the favorable hollow site having a binding energy of -3.57 eV. In the first H2S dehydrogenation, energy barriers for S-H bond breaking over the clean surface are 0.08-0.46 eV and a little bit higher on the S-covered surface are 0.1-0.78 eV, while in second dehydrogenation the energy barrier on a clean surface is 0.19 eV. For further detail, electronic densities of states and d-band center model are used to characterize the interaction of adsorbed H2S with both surfaces. Hence, our results show that decomposition of H2S over perfect and S-covered Ni(110) surface is exothermic and also an easy process. However, kinetically and thermodynamically, the subsistence of surface sulfur avoids the H-S bond breaking process. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.