Abstract
The development of highly productive, selective and stable propane dehydrogenation catalysts for propene production is strategic due to the increasing need for propene and the availability of shale gas, an abundant source of light alkanes. In that context, the combination of surface organometallic chemistry (SOMC) and a thermolytic molecular precursor (TMP) approach is used to prepare bimetallic subnanometric and narrowly distributed Pt-Zn alloyed particles supported on silica via grafting of a Pt precursor on surface OH groups present in a Zn single-site containing material followed by a H(2) reduction treatment. This material, that exhibits a Zn to Pt molar ratio of 3 : 2 in the form of alloyed Pt-Zn particles with a 0.2 to 0.4 fraction of the overall Zn amount remaining as Zn(II) sites on the silica surface, catalyzes propane dehydrogenation (PDH) with high productivity (703 g(C(3)H(6)) g(Pt) (-1) h(-1) to 375 g(C(3)H(6)) g(Pt) (-1) h(-1)) and very low deactivation rates (k (d) = 0.027 h(-1)) over 30 h at high WHSV (75 h(-1)). This study demonstrates how SOMC can provide access to highly efficient and tailored catalysts through the stepwise introduction of specific elements via grafting to generate small, homogeneously and narrowly distributed supported alloyed nanoparticles at controlled interfaces.