Complementary operando insights into the activation of multicomponent selective propylene oxidation catalysts

Two Bi-Mo-Co-Fe-O catalysts were synthesized by flame spray pyrolysis and tested for their catalytic performance in selective oxidation of propylene to acrolein. Pronounced structural changes during temperature-programmed oxidation and reaction were observed by operando X-ray absorption spectroscopy, X-ray diffraction, Raman spectroscopy, and thermogravimetric analysis. During oxidative treatment, mainly binary oxide phases (a-Bi2Mo3O12, b-CoMoO4, Fe2(MoO4)3) were observed, but single (MoO3) or ternary (Bi3(FeO4)(MoO4)2) oxides also formed depending on the relative elemental catalyst composition. During propylene oxidation, the reduction of Fe3+ to Fe2+ led to a strong rise in activity and induced further phase transformations. MoO3 was found to be unselective towards acrolein but was essential in binding other single oxides. The formation of b-Co0.7Fe0.3MoO4 and Bi3(FeO4)(MoO4)2 as well as their synergistic interplay with a-Bi2Mo3O12 are key factors for high performance. The combination of complementary operando methods was crucial to reveal new structure-activity/selectivity correlations, therefore bridging the knowledge gap between simplified model systems and complex applied catalysts. (c) 2021 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http:// creativecommons.org/licenses/by/4.0/).

Automated summary

In this study, two Bi-Mo-Co-Fe-O catalysts were synthesized and tested for their catalytic performance in selective oxidation of propylene to acrolein. The structural changes during oxidation and reaction processes were observed using various operando techniques. The formation of different oxide phases and the interaction between MoO3 and other oxides were found to be crucial for high performance. The combination of complementary operando methods bridged the knowledge gap between simplified model systems and complex catalysts.