Structure–activity relationships for propane oxidative dehydrogenation by anatase-supported vanadium oxide monomers and dimers

To understand the importance of the effect of molecular structure on reactivity, we have studied the activity of anatase TiO2 (0 0 1) supported VOx catalytic sites for propane oxidative dehydrogenation (ODH). First, possible structures of monomeric and dimeric VOx species on anatase (0 0 1) after VO4H3 grafting and water elimination were determined. We then studied the conversion reaction of propane to propanol by the supported VOx to elucidate the structure–reactivity relationship. The coordination number of the vanadium atom was the key structural parameter in predicting the catalytic activity. This key structural difference alone resulted in an increase of up to 800 times in the reaction rate of CH bond activation (rate-determining for propane ODH) for the various vanadium oxide species at 600 K. These results demonstrate the remarkable sensitivity of the catalytic site activity to its geometric structure and its implications for achieving optimal catalyst performance.

Graphical abstractDensity functional calculations suggest that the coordination number of the vanadium atom in supported vanadium oxide clusters is a key structural parameter for predicting the catalytic activity of propane oxidative dehydrogenation.Figure optionsDownload full-size imageDownload high-quality image (75 K)Download as PowerPoint slideHighlights► Structures of monomeric and dimeric VOx species on anatase (0 0 1). ► Relationship of structure of VOx to the catalytic activity for propane oxidative dehydrogenation. ► Coordination environment of vanadium active site determines the activity of the catalytic site.