Selenium adsorption on Mo(110): A first-principles investigation

Abstract

Selenium adsorption on molybdenum surfaces is a relevant process in the production of thin-film solar cells, in particular as far as the formation of the layered compound MoSe${}_{2}$ is concerned. In this paper we investigate the energetics of Se adsorption on the (110) surface of molybdenum using first-principles calculations in the two limiting cases of low and high coverage, and we establish a comparison with the more extensively investigated case of sulfur adsorption at submonolayer coverage. The studied system provides the opportunity for testing the most crucial approximations, namely, the choice of the exchange-correlation functional and the pseudopotential generation. We find that semicore states of molybdenum have an influence on calculated surface energies and, to a lesser extent, on adsorption energies. We compare some more or less popular semilocal exchange-correlation functionals, including one recently proposed as an improvement for quasi-two-dimensional systems. The results show that the preferred adsorption site changes with coverage and suggest a strong variation of the adsorption energy with coverage.