Strain in Silica-Supported Ga(III) Sites: Neither Too Much nor Too Little for Propane Dehydrogenation Catalytic Activity

Well-defined Ga(III) sites on SiO2 are highly active, selective, and stable catalysts in the propane dehydrogenation (PDH) reaction. In this contribution, we evaluate the catalytic activity toward PDH of tricoordinated and tetracoordinated Ga(III) sites on SiO2 by means of first-principles calculations using realistic amorphous periodic SiO2 models. We evaluated the three reaction steps in PDH, namely, the C-H activation of propane to form propyl, the beta-hydride (beta-H) transfer to form propene and a gallium hydride, and the H-H coupling to release H-2, regenerating the initial Ga-O bond and closing the catalytic cycle. Our work shows how Bronsted-Evans-Polanyi relationships are followed to a certain extent for these three reaction steps on Ga(III) sites on SiO2 and highlights the role of the strain of the reactive Ga-O pairs on such sites of realistic amorphous SiO2 models. It also shows how transition-state scaling holds very well for the beta-H transfer step. While highly strained sites are very reactive sites for the initial C-H activation, they are more difficult to regenerate. The corresponding less strained sites are not reactive enough, pointing to the need for the right balance in strain to be an effective site for PDH. Overall, our work provides an understanding of the intrinsic activity of acidic Ga single sites toward the PDH reaction and paves the way toward the design and prediction of better single-site catalysts on SiO2 for the PDH reaction.

Automated summary

The study evaluates the catalytic activity of Ga(III) sites on SiO2 towards propane dehydrogenation (PDH) reaction using first-principles calculations. The research demonstrates the importance of strain on the reactivity of these sites, highlighting the need for a balance in strain for an effective catalytic site for PDH. Overall, the work provides insights into the intrinsic activity of acidic Ga single sites on SiO2 towards the PDH reaction and suggests potential for designing better single-site catalysts.