A comparative test of different density functionals for calculations of NH3-SCR over Cu-Chabazite

Abstract

A general challenge in density functional theory calculations is to simultaneously account for different types of bonds. One such example is reactions in zeolites where both van der Waals and chemical bonds should be described accurately. Here, we use different exchange–correlation functionals to explore O₂ dissociation over pairs of Cu(NH₃)₂⁺ complexes in Cu-Chabazite. This is an important part of selective catalytic reduction of NO_x using NH₃ as a reducing agent. The investigated functionals are PBE, PBE+U, PBE+D, PBE+U+D, PBE-cx, BEEF and HSE06+D. We find that the potential energy landscape for O₂ activation and dissociation depends critically on the choice of functional. However, the van der Waals contributions are similarly described by the functionals accounting for this interaction. The discrepancies in the potential energy surface are instead related to different descriptions of the Cu–O chemical bond. By investigating the electronic, structural and energetic properties of reference systems including bulk copper oxides and (Cu₂O₂)²⁺ enzymatic crystals, we find that the PBE+U approach together with van der Waals corrections provides a reasonable simultaneous accuracy of the different bonds in the systems.