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Size-Dependent Catalytic Activity and Dynamics of Gold Nanoparticles at the Single-Molecule Level

机译:单分子水平的金纳米颗粒的尺寸依赖性催化活性和动力学。

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Nanoparticles are important catalysts for petroleum processing, energy conversion, and pollutant removal. As compared to their bulk counterparts, their often superior or new catalytic properties result from their nanometer size, which gives them increased surface-to-volume ratios and chemical potentials. The size of nanoparticles is thus pivotal for their catalytic properties. Here, we use single-molecule fluorescence microscopy to study the size-dependent catalytic activity and dynamics of spherical Au-nanoparticles under ambient solution conditions. By monitoring the catalysis of individual Au-nanoparticles of three different sizes in real time with single-turnover resolution, we observe clear size-dependent activities in both the catalytic product formation reaction and the product dissociation reaction. Within a model of classical thermodynamics, these size-dependent activities of Au-nanoparticles can be accounted for by the changes in the adsorption free energies of the substrate resazurin and the product resorufin because of the nanosize effect. We also observe size-dependent differential selectivity of the Au-nanoparticles between two parallel product dissociation pathways, with larger nanoparticles less selective between the two pathways. The particle size also strongly influences the surface-restructuring-coupled catalytic dynamics; both the catalysis-induced and the spontaneous dynamic surface restructuring occur more readily for smaller Au-nanoparticles due to their higher surface energies. Using a simple thermodynamic model, we analyze the catalysis- and size-dependent dynamic surface restructuring quantitatively; the results provide estimates on the activation energies and time scales of spontaneous dynamic surface restructuring that are fundamental to heterogeneous catalysis in both the nano- and the macro-scale. This study further exemplifies the power of the single-molecule approach in probing the intricate workings of nanoscale catalysts.
机译:纳米颗粒是石油加工,能量转化和污染物去除的重要催化剂。与它们的同类产品相比,它们通常具有优越的或新的催化性能是由于其纳米尺寸,这使它们具有更高的表面积体积比和化学势。因此,纳米颗粒的尺寸对于它们的催化性能至关重要。在这里,我们使用单分子荧光显微镜研究球形金纳米颗粒在环境溶液条件下的尺寸依赖性催化活性和动力学。通过实时监测具有单个周转分辨率的三种不同尺寸的单个金纳米颗粒的催化作用,我们在催化产物形成反应和产物离解反应中观察到明显的尺寸依赖性活性。在经典的热力学模型中,由于纳米尺寸的影响,金纳米颗粒的这些与尺寸有关的活性可以通过底物刃天青和产物刃天青的吸附自由能的变化来解释。我们还观察到两个平行产物解离途径之间的金纳米颗粒的尺寸依赖性差异选择性,较大的纳米颗粒在两个途径之间的选择性较低。粒径也极大地影响了表面结构耦合的催化动力学。较小的金纳米粒子由于其较高的表面能而更容易发生催化诱导的和自发的动态表面重组。使用简单的热力学模型,我们定量分析了催化和尺寸相关的动态表面重构。结果提供了对自发动态表面重构的活化能和时间尺度的估计,这对于纳米尺度和宏观尺度的非均相催化都是至关重要的。这项研究进一步证明了单分子方法在探测纳米级催化剂复杂工作中的作用。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2010年第1期|138-146|共9页
  • 作者单位

    Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853;

    Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853;

    Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853;

    Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853;

  • 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);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 03:15:25

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