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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Robust synthesis of ultrathin Au-Ag nanowires as a high-surface-area, synergistic substrate for constructing efficient Pt-based catalysts
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Robust synthesis of ultrathin Au-Ag nanowires as a high-surface-area, synergistic substrate for constructing efficient Pt-based catalysts

机译:超薄Au-Ag纳米线的鲁棒合成作为高表面积,用于构建高效Pt基催化剂的协同基材

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摘要

Ultrathin Au (or Ag) nanowires represent an excellent substrate for atomic layer deposition of Pt to afford highly active and cost-effective catalysts due to the large surface area and possible synergistic effect. An ideal synthesis of such nanowires should avoid using strong capping agents for convenient post-synthesis treatments and should be easily scaled up and reproduced in a high yield, which remains a challenge. Here, we report a novel strategy to synthesize sub-2 nm Au-Ag alloy nanowires with high quality in N,N-dimethyl formamide (DMF), which relies on Ag modification of the nanocrystal surface and Ag-halide interactions for regulating the one-dimensional growth of the nanowires, without involving strong capping agents that are usually required in conventional syntheses. Sub-monolayer Pt atoms were successfully deposited on these ultrathin Au-Ag alloy nanowires without forming ensembles despite a high loading amount (up to 20% in terms of Pt/(Au + Ag)) due to the large surface area. The resulting Au-Ag@Pt core/shell nanowires demonstrate superior activities in the formic acid oxidation reaction (FAOR) due to the synergistic ligand effect and the absence of Pt ensembles. We believe that the novel synthesis and the demonstration of these ultrathin Au-Ag alloy nanowires as a general platform for constructing cost-effective noble metal catalysts open new opportunities in designing catalysts for a broad range of reactions.
机译:超薄Au(或Ag)纳米线代表PT的原子层沉积的优异基材,得到由于大的表面积和可能的协同作用而提供高度活性和成本效率的催化剂。这种纳米线的理想合成应避免使用强封端剂,以方便合成后处理,并且应该以高产率容易地扩大并再现,这仍然是一个挑战。在此,我们报告了一种新的策略,以在N,N-二甲基甲酰胺(DMF)中具有高质量的亚2 NM Au-Ag合金纳米线,其依赖于纳米晶体表面和Ag卤化物相互作用来调节纳米晶体表面的Ag改性 - 纳米线的多级生长,而不涉及通常在常规合成中所需的强封端剂。亚单层Pt原子在这些超薄Au-Ag合金纳米线上成功地沉积,而不形成由于大的表面积的高负载量(在Pt /(Au + Ag)的高达20%,而不是形成高达20%)。由此产生的Au-Ag @ Pt核/壳纳米线在甲酸氧化反应(FAOR)上表现出优异的活性,由于协同配体效应和不存在PT合奏。我们认为,新的合成和这些超薄Au-Ag合金纳米线作为构建成本效益贵金属催化剂的一般平台,在设计催化剂方面为广泛的反应开辟了新的机会。

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    Xi An Jiao Tong Univ State Key Lab Multiphase Flow Power Engn Frontier Inst Sci &

    Technol Xian 710054 Shaanxi Peoples R China;

    Xi An Jiao Tong Univ State Key Lab Multiphase Flow Power Engn Frontier Inst Sci &

    Technol Xian 710054 Shaanxi Peoples R China;

    Xi An Jiao Tong Univ State Key Lab Multiphase Flow Power Engn Frontier Inst Sci &

    Technol Xian 710054 Shaanxi Peoples R China;

    Xi An Jiao Tong Univ State Key Lab Multiphase Flow Power Engn Frontier Inst Sci &

    Technol Xian 710054 Shaanxi Peoples R China;

    Xi An Jiao Tong Univ State Key Lab Multiphase Flow Power Engn Frontier Inst Sci &

    Technol Xian 710054 Shaanxi Peoples R China;

    Xi An Jiao Tong Univ State Key Lab Multiphase Flow Power Engn Frontier Inst Sci &

    Technol Xian 710054 Shaanxi Peoples R China;

    Xi An Jiao Tong Univ State Key Lab Multiphase Flow Power Engn Frontier Inst Sci &

    Technol Xian 710054 Shaanxi Peoples R China;

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  • 正文语种 eng
  • 中图分类 工程材料学;
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