{"title":"Rh/Al2O3 and Pd/Al2O3 three-way catalysts show different thermal deactivation behaviors under real engine-aging conditions","authors":"Tomoya Muta , Rion Ohta , Masayuki Tsushida , Keisuke Awaya , Junya Ohyama , Rikuo Koinuma , Takeshi Miki , Masato Machida","doi":"10.1016/j.cattod.2025.115422","DOIUrl":null,"url":null,"abstract":"<div><div>Full-scale honeycomb three-way catalysts (TWCs) coated with Rh/Al<sub>2</sub>O<sub>3</sub> and Pd/Al<sub>2</sub>O<sub>3</sub> were engine-aged under different gas atmosphere and temperature conditions to systematically investigate their thermal deactivation behaviors. The average metal particle size was determined by electron microscope analysis (<em>d</em><sub>EM</sub>) and CO chemisorption (<em>d</em><sub>CO</sub>). For Pd/Al<sub>2</sub>O<sub>3</sub>, <em>d</em><sub>EM</sub> and <em>d</em><sub>CO</sub> were similar, suggesting the deactivation was simply associated with Pd sintering. The average Pd particle size increased significantly with aging temperature, from under 10 to over 100 nm. The effect of gas atmosphere on particle size was practically negligible. Contrastingly, for Rh/Al<sub>2</sub>O<sub>3</sub> the Rh particle size remained approximately one order of magnitude smaller than Pd, and the temperature dependence was not as noticeable because of a lower sintering rate. Interestingly, <em>d</em><sub>CO</sub> and <em>d</em><sub>EM</sub> differed substantially depending on the gas atmosphere. Such discrepancy was rationalized by the incorporation of Rh<sup>3</sup><sup>+</sup> into the Al<sub>2</sub>O<sub>3</sub> surface structure. Most likely, depending on the atmosphere, a strong anchoring effect at the Rh-Al<sub>2</sub>O<sub>3</sub> interface led to preserving highly dispersed metallic Rh nanoparticles on the Al<sub>2</sub>O<sub>3</sub> surface. The TWC deactivation behavior was remarkably different depending on the platinum group metal, Pd or Rh.</div></div>","PeriodicalId":264,"journal":{"name":"Catalysis Today","volume":"459 ","pages":"Article 115422"},"PeriodicalIF":5.2000,"publicationDate":"2025-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Today","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0920586125002408","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
Abstract
Full-scale honeycomb three-way catalysts (TWCs) coated with Rh/Al2O3 and Pd/Al2O3 were engine-aged under different gas atmosphere and temperature conditions to systematically investigate their thermal deactivation behaviors. The average metal particle size was determined by electron microscope analysis (dEM) and CO chemisorption (dCO). For Pd/Al2O3, dEM and dCO were similar, suggesting the deactivation was simply associated with Pd sintering. The average Pd particle size increased significantly with aging temperature, from under 10 to over 100 nm. The effect of gas atmosphere on particle size was practically negligible. Contrastingly, for Rh/Al2O3 the Rh particle size remained approximately one order of magnitude smaller than Pd, and the temperature dependence was not as noticeable because of a lower sintering rate. Interestingly, dCO and dEM differed substantially depending on the gas atmosphere. Such discrepancy was rationalized by the incorporation of Rh3+ into the Al2O3 surface structure. Most likely, depending on the atmosphere, a strong anchoring effect at the Rh-Al2O3 interface led to preserving highly dispersed metallic Rh nanoparticles on the Al2O3 surface. The TWC deactivation behavior was remarkably different depending on the platinum group metal, Pd or Rh.
期刊介绍:
Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues.
Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.