{"title":"Diverse effects of ferromagnetic-paramagnetic phase transition on the activity and selectivity of ferromagnetic catalysts","authors":"Ya Chen , Yonghua Liu , Gaomou Xu , Tao Wang","doi":"10.1016/j.jcat.2024.115749","DOIUrl":null,"url":null,"abstract":"<div><p>Tuning the catalyst’s activity and selectivity is usually achieved by modifying the electronic structure through strategies such as alloying, doping, strain, and ligand modification, but inevitably accompanied by geometric structure changes of catalysts. It is challenging to modify a catalyst’s electronic structure without changing its geometric structure. Recent studies found that the second-order ferromagnetic to paramagnetic (FM-PM) phase transition could promote catalytic performance without altering the geometric structures of active sites, which was also known as the magneto-catalytic effect (MCE). However, the understanding of the MCE is still incomplete. Herein, we conducted systematic density functional theory (DFT) calculations to clarify the complex reaction mechanisms for conversions of nitrogen-containing small molecules on both FM and PM Ni (1<!--> <!-->1<!--> <!-->1) surfaces. Our microkinetic modeling (MKM) results demonstrate that FM-PM phase transition promotes the N<sub>2</sub>O decomposition activity of FM Ni catalyst but decreases its activity for NO decomposition while showing a negligible influence on the activity of ammonia decomposition. These results indicate the promotion, inhibition, and disappearance mechanisms of MCE on the catalytic activity, which further changes the selectivity of different products. We anticipate the MCE will work as an effective strategy for fine-tuning the activity and selectivity of ferromagnetic catalysts in heterogeneous catalysis, providing an extra basis for rational catalyst design.</p></div>","PeriodicalId":346,"journal":{"name":"Journal of Catalysis","volume":"439 ","pages":"Article 115749"},"PeriodicalIF":6.5000,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0021951724004627","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Tuning the catalyst’s activity and selectivity is usually achieved by modifying the electronic structure through strategies such as alloying, doping, strain, and ligand modification, but inevitably accompanied by geometric structure changes of catalysts. It is challenging to modify a catalyst’s electronic structure without changing its geometric structure. Recent studies found that the second-order ferromagnetic to paramagnetic (FM-PM) phase transition could promote catalytic performance without altering the geometric structures of active sites, which was also known as the magneto-catalytic effect (MCE). However, the understanding of the MCE is still incomplete. Herein, we conducted systematic density functional theory (DFT) calculations to clarify the complex reaction mechanisms for conversions of nitrogen-containing small molecules on both FM and PM Ni (1 1 1) surfaces. Our microkinetic modeling (MKM) results demonstrate that FM-PM phase transition promotes the N2O decomposition activity of FM Ni catalyst but decreases its activity for NO decomposition while showing a negligible influence on the activity of ammonia decomposition. These results indicate the promotion, inhibition, and disappearance mechanisms of MCE on the catalytic activity, which further changes the selectivity of different products. We anticipate the MCE will work as an effective strategy for fine-tuning the activity and selectivity of ferromagnetic catalysts in heterogeneous catalysis, providing an extra basis for rational catalyst design.
调整催化剂的活性和选择性通常是通过合金化、掺杂、应变和配体改性等策略改变电子结构来实现的,但不可避免地伴随着催化剂几何结构的改变。在不改变催化剂几何结构的情况下改变其电子结构是一项挑战。最近的研究发现,二阶铁磁到顺磁(FM-PM)相变可以在不改变活性位点几何结构的情况下提高催化性能,这也被称为磁催化效应(MCE)。然而,人们对磁催化效应的理解仍不全面。在此,我们进行了系统的密度泛函理论(DFT)计算,以阐明含氮小分子在调频和永磁镍(1 1 1)表面上转化的复杂反应机制。我们的微动力学建模(MKM)结果表明,FM-PM 相变促进了 FM Ni 催化剂的 N2O 分解活性,但降低了其 NO 分解活性,同时对氨分解活性的影响微乎其微。这些结果表明了 MCE 对催化活性的促进、抑制和消失机制,从而进一步改变了不同产物的选择性。我们预计 MCE 将成为微调铁磁催化剂在异相催化中的活性和选择性的有效策略,为催化剂的合理设计提供更多依据。
期刊介绍:
The Journal of Catalysis publishes scholarly articles on both heterogeneous and homogeneous catalysis, covering a wide range of chemical transformations. These include various types of catalysis, such as those mediated by photons, plasmons, and electrons. The focus of the studies is to understand the relationship between catalytic function and the underlying chemical properties of surfaces and metal complexes.
The articles in the journal offer innovative concepts and explore the synthesis and kinetics of inorganic solids and homogeneous complexes. Furthermore, they discuss spectroscopic techniques for characterizing catalysts, investigate the interaction of probes and reacting species with catalysts, and employ theoretical methods.
The research presented in the journal should have direct relevance to the field of catalytic processes, addressing either fundamental aspects or applications of catalysis.