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Nanostructured Tio.7Mo_0.3O_2 Support Enhances Electron Transfer to Pt: High-Performance Catalyst for Oxygen Reduction Reaction

机译:纳米结构的Tio.7Mo_0.3O_2载体增强了电子向Pt的转移:高性能的氧还原反应催化剂

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摘要

The slow rate of the oxygen reduction reaction (ORR) and the instability of Pt-based catalysts are two of the most important issues that must be solved in order to make proton exchange membrane fuel cells (PEMFCs) a reality. Additionally, the serious carbon corrosion on the cathode side is a critical problem with respect to the durability of catalyst that limits its wide application. Here, we present a new approach by exploring robust noncarbon Ti_0.7Mo_0.3O_2 used as a novel functionalized cocatalytic support for Pt. This approach is based on the novel nanostructure Ti_0.7Mo_0.3O_2 support with "electronic transfer mechanism" from Ti_0.7Mo_0.3O_2 to Pt that can modify the surface electronic structure of Pt, owing to a shift in the d-band center of the surface Pt atoms. Furthermore, another benefit of Ti_0.7Mo_0.3O_2 is the extremely high stability of Ti_0.7Mo_0.3O_2during potential cycling, which is attributable to the strong metal/support interaction (SMSI) between Pt and Ti_0.7Mo_0.3O_2 This also enhances the inherent structural and chemical stability and the corrosion resistance of the TiO2-based oxide in acidic and oxidative environments. We also demonstrate that the ORR current densities generated using cocatalytic Ti_0.7Mo_0.3O_2 are respectively ~7- and 2.6-fold higher than those of commercial Pt/C and PtCo/C catalysts with the same Pt loading. This new approach opens a reliable path to the discovery advanced concept in designing new catalysts that can replace the traditional catalytic structure and motivate further research in the field.
机译:氧还原反应(ORR)的速度慢和Pt基催化剂的不稳定性是使质子交换膜燃料电池(PEMFC)成为现实必须解决的两个最重要的问题。另外,就催化剂的耐久性而言,在阴极侧的严重碳腐蚀是一个关键问题,这限制了其广泛的应用。在这里,我们通过探索鲁棒的非碳Ti_0.7Mo_0.3O_2作为Pt的新型功能化助催化剂,提出了一种新方法。该方法基于具有从Ti_0.7Mo_0.3O_2到Pt的“电子转移机制”的新型纳米结构Ti_0.7Mo_0.3O_2支撑,由于其d波段中心的偏移,该结构可以修饰Pt的表面电子结构。表面铂原子。此外,Ti_0.7Mo_0.3O_2的另一个好处是在电位循环期间Ti_0.7Mo_0.3O_2的极高稳定性,这归因于Pt和Ti_0.7Mo_0.3O_2之间的强金属/载体相互作用(SMSI),这也增强了固有的TiO2基氧化物在酸性和氧化性环境中的结构和化学稳定性以及耐腐蚀性。我们还证明了使用共催化Ti_0.7Mo_0.3O_2生成的ORR电流密度分别比相同Pt负载的商业Pt / C和PtCo / C催化剂高约7倍和2.6倍。这种新方法为设计新催化剂提供了一条通往探索高级概念的可靠途径,该新催化剂可以取代传统的催化剂结构并激发该领域的进一步研究。

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  • 来源
    《Journal of the American Chemical Society》 |2011年第30期|p.11716-11724|共9页
  • 作者单位

    NanoElectrochemistr)r Laboratory, Department of Chemical Engineering, National Taiwan University of Science and Technology,Taipei 106, Taiwan;

    NanoElectrochemistr)r Laboratory, Department of Chemical Engineering, National Taiwan University of Science and Technology,Taipei 106, Taiwan;

    NanoElectrochemistr)r Laboratory, Department of Chemical Engineering, National Taiwan University of Science and Technology,Taipei 106, Taiwan;

    NanoElectrochemistr)r Laboratory, Department of Chemical Engineering, National Taiwan University of Science and Technology,Taipei 106, Taiwan;

    NanoElectrochemistr)r Laboratory, Department of Chemical Engineering, National Taiwan University of Science and Technology,Taipei 106, Taiwan,National Synchrotron Radiation Research Center, Hsinchu 30076, Taiwan,National Taiwan University of Science and Technology, Taipei106, Taiwan;

  • 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
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  • 入库时间 2022-08-18 03:14:23

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