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Surface Composition Tuning of Au-Pt Bimetallic Nanoparticles for Enhanced Carbon Monoxide and Methanol Electro-oxidation

机译:用于增强一氧化碳和甲醇电氧化的Au-Pt双金属纳米颗粒的表面组成调整

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摘要

The ability to direct bimetallic nanoparticles to express desirable surface composition is a crucial step toward effective heterogeneous catalysis, sensing, and bionanotechnology applications. Here we report surface composition tuning of bimetallic Au-Pt electrocatalysts for carbon monoxide and methanol oxidation reactions. We establish a direct correlation between the surface composition of Au—Pt nanoparticles and their catalytic activities. We find that the intrinsic activities of Au-Pt nanoparticles with the same bulk composition of Au_(0.5)Pt_(0.5) can be enhanced by orders of magnitude by simply controlling the surface composition. We attribute this enhancement to the weakened CO binding on Pt in discrete Pt or Pt-rich dusters surrounded by surface Au atoms. Our finding demonstrates the importance of surface composition control at the nanoscale in harnessing the true electrocatalytic potential of bimetallic nanoparticles and opens up strategies for the development of highly active bimetallic nanoparticles for electrochemical energy conversion.
机译:引导双金属纳米颗粒表达所需表面成分的能力是迈向有效的多相催化,传感和仿生技术应用的关键一步。在这里,我们报告了用于一氧化碳和甲醇氧化反应的双金属Au-Pt电催化剂的表面组成调整。我们建立了Au-Pt纳米颗粒的表面组成与其催化活性之间的直接关联。我们发现,通过简单地控制表面组成,可以将具有相同体积组成的Au_(0.5)Pt_(0.5)的Au-Pt纳米粒子的固有活性提高几个数量级。我们将此增强归因于被表面金原子包围的离散Pt或富含Pt的除尘器中Pt上的CO结合力减弱。我们的发现证明了在利用双金属纳米颗粒的真实电催化潜力的情况下控制纳米级表面组成的重要性,并为开发用于电化学能量转换的高活性双金属纳米颗粒开辟了战略。

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  • 来源
    《Journal of the American Chemical Society》 |2013年第21期|7985-7991|共7页
  • 作者单位

    Department of Materials Science and Engineering,Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States;

    Department of Mechanical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States;

    Department of Mechanical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States;

    Department of Mechanical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States;

    Department of Materials Science and Engineering,Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States;

    Department of Mechanical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States;

    Department of Materials Science and Engineering,Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States;

    Department of Materials Science and Engineering,Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States,Theory and Simulation of Materials, Ecole Polytechnique Federale de Lausanne, 1015 Lausanne, Switzerland;

    Microscopy Group, Oak Ridge National Laboratory, 1 Bethel Valley Road, Building 4515, Oak Ridge, Tennessee 37831, United States;

    Department of Mechanical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States,Department of Chemistry, Technische Universitaet Muenchen,Lichtenbergstrasse 4, D 85747 Garching, Germany;

    Department of Mechanical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States,Department of Biological Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States;

    Department of Materials Science and Engineering,Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States,Department of Mechanical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States;

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