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首页> 外文期刊>Electrochimica Acta >Peptide templated AuPt alloyed nanoparticles as highly efficient bi-functional electrocatalysts for both oxygen reduction reaction and hydrogen evolution reaction
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Peptide templated AuPt alloyed nanoparticles as highly efficient bi-functional electrocatalysts for both oxygen reduction reaction and hydrogen evolution reaction

机译:肽模板包膜混合合金化纳米颗粒作为高效双官能电催化剂,用于氧还原反应和氢气进化反应

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摘要

AbstractPeptide driven metallic nanomaterials fabrication under mild conditions has become a significant research thrust recently, thanks to its capability to generate multifunctional materials with tunable electronic and catalytic properties. Herein, peptide Z1 is employed to fabricate a series of AuPt alloyed nanoparticles with different Au-to-Pt ratios. The morphology is examined by electron microscopic techniques, and well-defined peanut-shape is observed for Au33Pt67while spherical particles are obtained for the other samples. The AuPt alloys demonstrate effective electrocatalytic activity toward both oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER) and Au33Pt67exhibits the best bifunctional electrocatalytic performance. Its ORR activity is superior than commercial Pt/C in alkaline media, verified by the positive onset potential (+1.02?V vs. RHE) and large diffusion-limited current density, while its HER activity is comparable with Pt/C, evidenced by the small overpotential at 10?mA?cm?2(?171?mV vs. RHE) and low Tafel slope. Moreover, Au33Pt67exhibits markedly higher long-term durability than Pt/C for both ORR and HER. The excellent activity and stability for ORR and HER are ascribed to Au alloying Pt induced synergistic effects. The results highlight the advantages of using peptide to fabricate bi-functional or multiple functional electrocatalysts with desirable activity and robust stability.]]>
机译:<![CDATA [ 抽象 温和条件下肽从动金属纳米材料制造已成为显著研究推力最近,由于它的能力,以产生多功能具有可调谐电子性能和催化性能的材料。在此,肽Z1被用来制作一系列的AuPt合金具有不同的Au到的Pt比率的纳米颗粒。该形态通过电子显微镜技术检查,并且良好定义的花生形状观察的Au 33 的Pt 67 < / CE:INF>而球形颗粒被用于其它样品获得。所述的AuPt合金表现出对两者的氧还原反应(ORR)和析氢反应(HER)和Au有效的电催化活性 33 的Pt 67 展品的最佳双官能的电性能。其ORR活性比商业的Pt / C在碱性介质中,由正开始电位验证(1.02?V,相对于RHE)和大的扩散限制电流密度优异,同时其HER活性是有Pt / C相媲美,通过证明小的超电势在10mA厘米?2?:(?171 mV对RHE)和低的塔菲尔斜率。此外,金 33 的Pt 67 展品显着更高的长期耐久性比的Pt / C为两者ORR和她。优异的活性和稳定性为ORR和HER是归因于Au合金化的Pt诱导协同效应。结果突出显示使用肽以制造具有期望的活性和鲁棒稳定性的双功能或多个功能电催化剂的优点。 ]]>

著录项

  • 来源
    《Electrochimica Acta》 |2018年第2018期|共9页
  • 作者单位

    Guangzhou Key Laboratory for Surface Chemistry of Energy Materials New Energy Research Institute School of Environment and Energy South China University of Technology Guangzhou Higher Education Mega Centre;

    Guangzhou Key Laboratory for Surface Chemistry of Energy Materials New Energy Research Institute School of Environment and Energy South China University of Technology Guangzhou Higher Education Mega Centre;

    Guangzhou Key Laboratory for Surface Chemistry of Energy Materials New Energy Research Institute School of Environment and Energy South China University of Technology Guangzhou Higher Education Mega Centre;

    Department of Physics &

    Engineering Frostburg State University;

    Guangzhou Key Laboratory for Surface Chemistry of Energy Materials New Energy Research Institute School of Environment and Energy South China University of Technology Guangzhou Higher Education Mega Centre;

    Guangzhou Key Laboratory for Surface Chemistry of Energy Materials New Energy Research Institute School of Environment and Energy South China University of Technology Guangzhou Higher Education Mega Centre;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 电化学工业;物理化学(理论化学)、化学物理学;
  • 关键词

    Peptide Z1; AuPt alloys; Bi-functional electrocatalysts; Oxygen reduction reaction; Hydrogen evolution reaction;

    机译:肽Z1;消融合金;双功能电催化剂;氧还原反应;氢气进化反应;

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