Takayuki, Nakamuro, Yosi, Kratish, Yiqi, Liu, Jiaqi, Li, Anusheela, Das, Leighton, O. Jones, Amol, Agarwal, Qing, Ma, Michael, J. Bedzyk, George, C. Schatz, Eiichi, Nakamura, Tobin, J. Marks
{"title":"Atomic-Resolution Cinematography of Catalytic Intermediates over a Single-Site Heterogeneous Catalyst","authors":"Takayuki, Nakamuro, Yosi, Kratish, Yiqi, Liu, Jiaqi, Li, Anusheela, Das, Leighton, O. Jones, Amol, Agarwal, Qing, Ma, Michael, J. Bedzyk, George, C. Schatz, Eiichi, Nakamura, Tobin, J. Marks","doi":"10.26434/chemrxiv-2024-hpbl9","DOIUrl":null,"url":null,"abstract":"Heterogeneous catalysts dominate the chemical industry but typically feature diverse, incompletely defined active sites. Thus, describing structure-activity relationships, unlike homogeneous catalysts, remains challenging. In contrast, molecularly defined single-site heterogeneous catalysts (SSHCs), using appropriate tools, are poised to address these challenges and provide new avenues for catalysis research and development. The present study explores eco-friendly H2 production mediated by discrete MO2 sites supported on carbon nanohorns (CNHs) and active for alcohol dehydrogenation. While informative, detailed ensemble EXAFS/XANES, XPS, kinetic measurements, and DFT analysis alone cannot provide a full molecular picture of the reaction pathway. Here, using single-molecule atomic-resolution time-resolved electron microscopy (SMART-EM), we identify four key catalytic intermediates anchored to the CNHs and uncover a new reaction pathway involving alkoxide/hemiacetal equilibration and acetal oligomerization. These intermediates are identified solely by theory and SMART-EM, and this advance highlights the potential of SMART-EM to establish and verify mechanistic hypotheses in catalysis.","PeriodicalId":9813,"journal":{"name":"ChemRxiv","volume":"63 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemRxiv","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26434/chemrxiv-2024-hpbl9","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Heterogeneous catalysts dominate the chemical industry but typically feature diverse, incompletely defined active sites. Thus, describing structure-activity relationships, unlike homogeneous catalysts, remains challenging. In contrast, molecularly defined single-site heterogeneous catalysts (SSHCs), using appropriate tools, are poised to address these challenges and provide new avenues for catalysis research and development. The present study explores eco-friendly H2 production mediated by discrete MO2 sites supported on carbon nanohorns (CNHs) and active for alcohol dehydrogenation. While informative, detailed ensemble EXAFS/XANES, XPS, kinetic measurements, and DFT analysis alone cannot provide a full molecular picture of the reaction pathway. Here, using single-molecule atomic-resolution time-resolved electron microscopy (SMART-EM), we identify four key catalytic intermediates anchored to the CNHs and uncover a new reaction pathway involving alkoxide/hemiacetal equilibration and acetal oligomerization. These intermediates are identified solely by theory and SMART-EM, and this advance highlights the potential of SMART-EM to establish and verify mechanistic hypotheses in catalysis.