Is There a Relationship Between the M=O Bond length (strength) of Bulk Mixed Metal Oxides and Their Catalytic Activity?

KAMALAKANTA ROUTRAY; LAURA E. BRIAND; ISRAEL E. WACHS

JOURNAL OF CATALYSIS

Elsevier B.V.

Lugar: Amsterdam; Año: 2008 vol. 256 p. 145 - 153

0021-9517

It is widely accepted in the catalysis literature that the bulk M=O bond of bulk mixed metal oxides controls catalytic activity. In the present study, for the first time, the bulk M=O bond lengths (strengths) and the surface catalytic activity of bulk metal vanadates and molybdates were quantitatively compared to allow examination of this long-standing hypothesis. The bulk M=O bond lengths were obtained from crystallographic studies and also determined by Raman spectroscopy. The surface catalytic activity was determined by CH3OH-temperature programmed surface reaction (TPSR) spectroscopy and steady-state methanol oxidation. The CH3OH-TPSR experiments provided the first-order rate constants for breaking of the C?H bond for the decomposition of the surface CH3O* intermediate to H2CO and the number of catalytic active sites Ns. The corresponding steady-state methanol oxidation studies provided the equilibrium adsorption constant Kads for breaking the methanol OH bond and the specific reaction rate (TOF). The findings clearly demonstrate the lack of correlations among krds, Kads, TOF, and the bulk M=O bond length (strength). This finding is not so surprising when one considers that the adsorption step involves breaking the methanol OH bond and the rate-determining step involves breaking the surface methoxy CH bond on surface MO sites, not bulk M=O bond-breaking.