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

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
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引用次数: 0

摘要

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