This is the authors' abstract. We don't add key points for this paper.
Dynamic carburization is a common and important phenomenon in many industrial reactions. Finding the critical factor governing this process is significant for catalyst optimization, which is complicated due to the coherence between catalyst dynamics and reaction dynamics. In this work, we manipulate the in situ formation of fast carburization on the Pd-FeO x surface by revealing a domino effect between the reaction network and catalyst restructuring during long-term CO 2 hydrogenation reaction. We prepared catalysts of three sizes (5Pd-FeO x, 0.5Pd-FeO x, 0.05Pd-FeO x ) and found that the large size of Pd NP (5Pd-FeO x ) induces the reactive metal–support interaction, following the in situ Pd 3 Fe formation, the reaction route change, the fast surface carburization (Fe 5 C 2 ), and finally the superior catalytic performance. Among these changes, we identify that in situ alloying instead of the apparent size difference is crucial for the formation of the active Fe 5 C 2 phase. As a proof of concept, we further design a presynthesized Pd 3 Fe alloy on FeO x and find an enhanced activity with reduced Pd loading by controlled fast carburization. This work not only demonstrates the controllability of dynamic carburization but also presents a benchmark of optimizing catalysts through the comprehensive understanding of in situ catalyst changes.
Answers are grounded in this paper and cite their sources.
No takes yet. Share an insight, caveat, or question.
Du et al. (2025) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: