Pengfei Du, Yafeng Zhang, Rui Qi, Qingqing Gu, Xiaoyan Xu, Aiqin Wang, Beien Zhu, Bing Yang, Tao Zhang
{"title":"Domino Effect of Catalysis: Coherence between Reaction Network and Catalyst Restructuring Accelerating Surface Carburization for CO2 Hydrogenation","authors":"Pengfei Du, Yafeng Zhang, Rui Qi, Qingqing Gu, Xiaoyan Xu, Aiqin Wang, Beien Zhu, Bing Yang, Tao Zhang","doi":"10.1021/jacs.5c01435","DOIUrl":null,"url":null,"abstract":"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 <i>in situ</i> formation of fast carburization on the Pd-FeO<sub><i>x</i></sub> surface by revealing a domino effect between the reaction network and catalyst restructuring during long-term CO<sub>2</sub> hydrogenation reaction. We prepared catalysts of three sizes (5Pd-FeO<sub><i>x</i></sub>, 0.5Pd-FeO<sub><i>x</i></sub>, 0.05Pd-FeO<sub><i>x</i></sub>) and found that the large size of Pd NP (5Pd-FeO<sub><i>x</i></sub>) induces the reactive metal–support interaction, following the <i>in situ</i> Pd<sub>3</sub>Fe formation, the reaction route change, the fast surface carburization (Fe<sub>5</sub>C<sub>2</sub>), and finally the superior catalytic performance. Among these changes, we identify that <i>in situ</i> alloying instead of the apparent size difference is crucial for the formation of the active Fe<sub>5</sub>C<sub>2</sub> phase. As a proof of concept, we further design a presynthesized Pd<sub>3</sub>Fe alloy on FeO<sub><i>x</i></sub> 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 <i>in situ</i> catalyst changes.","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"64 1","pages":""},"PeriodicalIF":14.4000,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/jacs.5c01435","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
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-FeOx surface by revealing a domino effect between the reaction network and catalyst restructuring during long-term CO2 hydrogenation reaction. We prepared catalysts of three sizes (5Pd-FeOx, 0.5Pd-FeOx, 0.05Pd-FeOx) and found that the large size of Pd NP (5Pd-FeOx) induces the reactive metal–support interaction, following the in situ Pd3Fe formation, the reaction route change, the fast surface carburization (Fe5C2), 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 Fe5C2 phase. As a proof of concept, we further design a presynthesized Pd3Fe alloy on FeOx 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.
期刊介绍:
The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.