Atomic-Resolution Cinematography of Catalytic Intermediates over a Single-Site Heterogeneous Catalyst

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":null,"pages":null},"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.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
单位点异相催化剂上催化中间产物的原子分辨率电影摄影技术
异相催化剂在化学工业中占主导地位,但其活性位点通常多种多样,定义不完整。因此,与均相催化剂不同,描述结构-活性关系仍然具有挑战性。相比之下,分子定义的单位点异相催化剂(SSHC)利用适当的工具,有望解决这些难题,并为催化研究和开发提供新的途径。本研究探讨了在碳纳米角(CNHs)上支持的离散 MO2 位点介导的环保型 H2 生产,该位点对乙醇脱氢具有活性。虽然信息丰富,但仅靠详细的集合 EXAFS/XANES、XPS、动力学测量和 DFT 分析并不能提供反应途径的完整分子图景。在这里,我们利用单分子原子分辨时间分辨电子显微镜(SMART-EM)确定了锚定在 CNHs 上的四个关键催化中间体,并发现了一条涉及氧化烷/半缩醛平衡和缩醛低聚的新反应途径。这些中间产物完全是通过理论和 SMART-EM 确定的,这一进展凸显了 SMART-EM 在建立和验证催化机理假设方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Exascale Quantum Mechanical Simulations: Navigating the Shifting Sands of Hardware and Software Hybrid synthesis of AMFC-derived amides using supported gold nanoparticles and acyl-coenzyme A ligases Non-covalent spin labelling of TRPC5 ion channels enables EPR studies of protein-ligand interactions An Efficient RI-MP2 Algorithm for Distributed Many-GPU Architectures Unusual Confinement-Induced Basicity and Proton-Mediated CH Activity of an Adipic Acid-Ammonium Cluster
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1