Journal of Catalysis, Vol.315, 48-58, 2014
Acid strength and bifunctional catalytic behavior of alloys comprised of noble metals and oxophilic metal promoters
The promotion of metal catalysts with partially oxidized oxophilic MOx species, such as ReOx-promoted Rh, has been demonstrated to produce Bronsted acid sites that can promote hydrogenolysis of oxygenate intermediates such as those found in biomass-derived species. A wide variety of alloy compositions and structures are examined in this work to investigate strongly acidic promoters by using DFT-calculated deprotonation energies (DPE) as a measure of acid strength. Sites with the highest acid strength had DPE less than 1100 kJ mol(-1), similar to DPE values of heteropolyacids or acid-containing zeolites, and were found on alloys composed of an oxophilic metal (such as Re or W) with a noble metal (such as Rh or Pt). NH3 adsorbs more strongly to sites with increasing acid strength and the activation barriers for acid-catalyzed ring opening of a furan ring decrease with increasing acid strength, which was also shown to be stronger for OH acid sites bound to multiple oxophilic metal atoms in a three-fold configuration rather than OH sites adsorbed in an atop configuration on one oxophilic metal, indicating that small MOx clusters may yield sites with the highest acid strength. (C) 2014 Published by Elsevier Inc.
Keywords:Hydrogenolysis;Ring opening cyclic ethers;DFT;bifunctional catalysis;Hydrodeoxygenation;Oxophilic metal promoters;Deprotonation energies;Hydroxymethyl tetrahydrofuran