首页> 外文期刊>Journal of the American Chemical Society >The Atomic Structural Dynamics of γ-AI_2O_3 Supported Ir-Pt Nanocluster Catalysts Prepared from a Bimetallic Molecular Precursor:A Study Using Aberration-Corrected Electron Microscopy and X-ray Absorption Spectroscopy
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The Atomic Structural Dynamics of γ-AI_2O_3 Supported Ir-Pt Nanocluster Catalysts Prepared from a Bimetallic Molecular Precursor:A Study Using Aberration-Corrected Electron Microscopy and X-ray Absorption Spectroscopy

机译:双金属分子前驱体制备的γ-Al_2O_3负载的Ir-Pt纳米簇催化剂的原子结构动力学:像差校正电子显微镜和X射线吸收光谱研究

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摘要

This study describes a prototypical, bimetallic heterogeneous catalyst: compositionally well-defined Ir-Pt nanoclusters with sizes in the range of 1-2 nm supported on y-Al2O3. Deposition of the molecular bimetallic cluster [Ir_3Pt_3(μ-CO)_3(CO)_3(η-C_5Me_5)_3] on γ-A1_2O_3, and its subsequent reduction with hydrogen, provides highly dispersed supported bimetallic Ir-Pt nanoparticles. Using spherical aberration-corrected scanning transmission electron microscopy (Cs-STEM) and theoretical modeling of synchrotron-based X-ray absorption spectroscopy (XAS) measurements, our studies provide unambiguous structural assignments for this model catalytic system. The atomic resolution C_S-STEM images reveal strong and specific lattice-directed strains in the clusters that follow local bonding configurations of the γ-Al_2O_3 support. Combined nanobeam diffraction (NBD) and high-resolution transmission electron microscopy (HRTEM) data suggest the polycrystalline γ-Al_2O_3 support material predominantly exposes (001) and (011) surface planes (ones commensurate with the zone axis orientations frequently exhibited by the bimetallic clusters). The data reveal that the supported bimetallic clusters exhibit complex patterns of structural dynamics, ones evidencing perturbations of an underlying oblate/hemispherical cuboctahedral cluster-core geometry with cores that are enriched in Ir (a result consistent with models based on surface energetics, which favor an ambient cluster termination by Pt) due to the dynamical responses of the M-M bonding to the specifics of the adsorbate and metal-support interactions. Taken together, the data demonstrate that strong temperature-dependent charge-transfer effects occur that are likely mediated variably by the cluster-support, cluster-adsorbate, and intermetallic bonding interactions.
机译:这项研究描述了一种典型的双金属多相催化剂:在y-Al2O3上负载的,组成明确的Ir-Pt纳米团簇,尺寸在1-2 nm范围内。将分子双金属簇[Ir_3Pt_3(μ-CO)_3(CO)_3(η-C_5Me_5)_3]沉积在γ-A1_2O_3上,然后用氢还原,可得到高度分散的负载型双金属Ir-Pt纳米颗粒。使用球差校正的扫描透射电子显微镜(Cs-STEM)和基于同步加速器的X射线吸收光谱(XAS)测量的理论模型,我们的研究为该模型催化系统提供了明确的结构分配。原子分辨率C_S-STEM图像揭示了簇中遵循γ-Al_2O_3载体局部键合构型的强且特定的晶格定向应变。结合纳米束衍射(NBD)和高分辨率透射电子显微镜(HRTEM)数据表明,多晶γ-Al_2O_3载体材料主要暴露(001)和(011)表面(与双金属簇经常显示的区域轴方向相当的表面)。 )。数据显示,受支持的双金属团簇表现出复杂的结构动力学模式,这些团簇证明基础扁圆形/半球形立方八面体团簇-核的几何结构具有富于Ir的核(结果与基于表面能学的模型一致,这有利于由于MM键对被吸附物和金属与载体之间相互作用的动力学响应,动力学簇终止了Pt)。两者合计,数据表明发生强烈的温度依赖性电荷转移效应,其可能由簇-载体,簇-吸附物和金属间键合相互作用可变地介导。

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  • 来源
    《Journal of the American Chemical Society》 |2011年第10期|p.3582-3591|共10页
  • 作者单位

    School of Chemical Sciences and the F. Seitz Materials Research Laboratory, University of Illinois, Urbana, Illinois 61801, United States;

    School of Chemical Sciences and the F. Seitz Materials Research Laboratory, University of Illinois, Urbana, Illinois 61801, United States;

    Department of Chemistry, University of North Carolina, Chapel Hill, North Carolina 27599, United States;

    School of Chemical Sciences and the F. Seitz Materials Research Laboratory, University of Illinois, Urbana, Illinois 61801, United States,The Dow Chemical Company, Midland, Michigan 48667, United States;

    Physics Department, Yeshiva University, New York, New York 10016, United States;

    School of Chemical Sciences and the F. Seitz Materials Research Laboratory, University of Illinois, Urbana, Illinois 61801, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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