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Facile design of Au@Pt core-shell nanostructures : formation of Pt submonolayers with tunable coverage and their applications in electrocatalysis

机译:Au @ Pt核壳纳米结构的简便设计:具有可调覆盖范围的Pt亚单分子层的形成及其在电催化中的应用

摘要

A facile design of Pt nanostructures from submonolayer to monolayer has been realized by ion adsorption-in situ electrochemical reduction on Au nanoparticles supported on multiwall carbon nanotubes (CNTs). The as prepared Au@Pt/CNTs catalysts display coverage-specific electrocatalysis. Au@Pt/CNTs with low Pt coverage is inactive towards methanol oxidation whereas it oxidizes formic acid effectively through a direct pathway with mass specific activity 90 times that of a commercial Pt/C catalyst. Due to its inertness to methanol, it shows high performance in the oxygen reduction reaction (ORR) with high methanol tolerance. In contrast, simply increasing the Pt coverage to above 40% switches the formic acid oxidation process to both direct and indirect catalytic pathways, and also results in high methanol oxidation activity. [Figure not available: see fulltext.]
机译:通过在多壁碳纳米管(CNTs)上负载的Au纳米粒子进行离子原位电化学还原,已经实现了从亚单层到单层的Pt纳米结构的简便设计。所制备的Au @ Pt / CNTs催化剂显示出特定于覆盖率的电催化作用。 Pt覆盖率低的Au @ Pt / CNT对甲醇氧化没有活性,而它通过质量比活度是商业Pt / C催化剂的90倍的直接途径有效地氧化甲酸。由于它对甲醇的惰性,因此在氧还原反应(ORR)中表现出很高的性能,并具有很高的甲醇耐受性。相反,仅将Pt覆盖率提高到40%以上,即可将甲酸氧化过程切换为直接和间接催化途径,并且还导致高甲醇氧化活性。 [图不可用:请参见全文。]

著录项

  • 作者

    Zheng F; Wong WT; Yung KF;

  • 作者单位
  • 年度 2014
  • 总页数
  • 原文格式 PDF
  • 正文语种 eng
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