Theoretical and experimental investigations on site occupancy for palladium oxidation states in mesoporous Al-MCM-41 materials

Abstract

The site occupancy of the various oxidation state of palladium supported on mesostructured porous aluminosilica of Al-MCM-41 type was studied combining density functional theory (DFT), FTIR, and Raman investigations. The study focuses on the usual +2 oxidation state highly dispersed during palladium incorporation via template-ion exchange (TIE) but also on other oxidation states. The simulations of the IR spectra using silica clusters of different sizes confirm the Pd2+ preference for sites contained in 6- or 8-membered rings (band at 930cm−1). The calculations suggest that, after calcination, isolated oxidized palladium species such as [PdO]2+, [Pd(OH)2]2+ for the+4 oxidation state, as well as [PdOH]2+ for the+3 EPR active oxidation state may coexist. The match between experimental and calculated vibrational frequencies relies on the two intense Raman bands at 270 and 630cm−1. All these oxidized species are preferentially located on 8-membered rings and linked to three framework oxygen atoms.