Abstract
Understanding the nature of active sites in heterogeneous catalysts and how to create them purposefully opens up the possibility of tailored catalyst design. Here we report mixed-valence subnanometre CoOx clusters, consisting of a few metallic Co0 atoms on top of Co2+, bound to a silicalite-1 support through lattice oxygen atoms as active species for non-oxidative propane dehydrogenation (PDH) to propene. Compared with commercial-like PtSn/Al2O3 and K-CrOx/Al2O3 catalysts also tested in the present study, as well as other state-of-the-art Pt- or Co-containing PDH catalysts, this system showed high on-stream stability, propene productivity and selectivity at close-to-equilibrium propane conversion. Moreover, it showed durability in a series of PDH/regeneration cycles between 500 and 550 °C. The performance of this catalyst system is industrially attractive in terms of propene production costs, as suggested by our initial techno-economic assessment. (Figure presented.)
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CITATION STYLE
Zhang, Q., Li, Y., Tian, X., Kondratenko, V. A., Fedorova, E. A., Yang, T., … Kondratenko, E. V. (2026). Mixed-valence Co0/IIOx clusters on silicalite-1 facilitate propane dehydrogenation to propene. Nature Catalysis, 9(3), 269–280. https://doi.org/10.1038/s41929-026-01488-w
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