Enhancing the dynamic electron transfer of Au species on wormhole-like TS-1 for boosting propene epoxidation performance with H2 and O2

Engineering unique electronic structure of catalyst to boost catalytic performance is of prime scientific and industrial importance. Herein, the identification of intrinsic electronic sensitivity for direct propene epoxidation was first achieved over highly stable Au/wormhole-like TS-1 catalyst. Results show that the electron transfer of Au species can be regulated by manipulating the dynamic evolutions and contents of Au valence states, thus resulting in different catalytic performance in 100 h time-on-stream. By DFT calculations, kinetic analysis and multi-characterizations, it is found that the Au0 species with higher electronic population can easily transfer more electrons to activate surface O2 compared with Au1+ and Au3+ species. Moreover, there is a positive correlation between Au0 content and activity. Based on this correlation, a facile strategy is further proposed to boost Au0 percentage, resulting in the reported highest PO formation rate without adding promoters. This work harbors tremendous guiding significance to the design of highly efficient Au/Ti-containing catalyst for propene epoxidation with H2 and O2. The identification of intrinsic electronic sensitivity for propene epoxidation with H2 and O2 is achieved and the enhanced dynamic electron transfer of Au0 species by increasing the Au0 content boost the reaction performance of green propene epoxidation. [Display omitted]