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Oxidation-resistant catalyst supports for proton exchange membrane fuel cells.

机译:用于质子交换膜燃料电池的抗氧化催化剂载体。

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摘要

In automotive applications, when proton exchange membrane fuel cells (PEMFCs) are subjected to frequent startup-shutdown cycles, a significant drop in performance is observed. One reason for this drop in performance is oxidation of the carbon in the catalyst layer when cathode potential excursions as high as 1.5V are observed. In this work, non-carbon based catalyst support materials were studied. The materials investigated include: tungsten carbide (WC), tungsten oxide (WOx), and niobium (Nb) or tungsten (W) doped titania.High surface area Nb and W doped titania materials synthesized using sol-gel techniques were subjected to several heat treatments and atmospheres, and their resulting physical properties characterized. The materials' phase changes and their impact on electrical conductivity were evaluated. W doped titania was found to be resistive, and for Nb doped titania, the rutile phase was found to be more conductive than the anatase phase. Conventionally, 10-50 wt% Pt is supported on carbon, but as the non-carbon catalyst support materials have different densities, similar mass ratios of catalyst to support will not result in directly comparable performances. It is recommended that the ratio of Pt surface area to the support surface area should be similar when comparing Pt supported on carbon to Pt supported on a non-carbon support. A normalization approach was investigated in this work, and the ORR performance of 40wt.%Pt/C was found to be similar to that of 10wt.%Pt/Nb-TiO2. Fuel cell performance tests showed significantly higher stability of Pt on Nb doped titania catalyst when compared to conventional Pt on carbon catalyst. It was found that, of the materials studied, only the rutile phase of Nb doped titania synthesized under reducing conditions is useful as a potential PEMFC catalyst support.Platinum was dispersed on commercial samples of WC and WO x. Stability tests were performed by stepping the materials between 0.6 to 1.8V. Higher stability of both WC and WOx was observed compared to carbon based commercial catalyst (HiSpec 4000). The performance of Pt supported on WC or WOx was found to be lower than that of Pt/C due to poor dispersion of Pt on these low surface area commercial powders.
机译:在汽车应用中,当质子交换膜燃料电池(PEMFC)经受频繁的启动-关闭循环时,性能会显着下降。性能下降的原因之一是,当观察到高达1.5V的阴极电位偏移时,催化剂层中的碳被氧化。在这项工作中,研究了非碳基催化剂载体材料。研究的材料包括:碳化钨(WC),氧化钨(WOx)和铌(Nb)或钨(W)掺杂的二氧化钛。使用溶胶-凝胶技术合成的高表面积Nb和W掺杂的二氧化钛材料要经受几次加热处理和气氛,以及由此产生的物理特性。评价了材料的相变及其对电导率的影响。 W掺杂的二氧化钛被发现是电阻性的,并且对于Nb掺杂的二氧化钛,发现金红石相比锐钛矿相更具导电性。常规地,在碳上负载10-50wt%的Pt,但是由于非碳催化剂载体材料具有不同的密度,相似的催化剂与载体的质量比将不会导致直接可比的性能。当比较负载在碳上的Pt和负载在非碳载体上的Pt时,建议Pt表面积与载体表面积的比率应相似。在这项工作中研究了归一化方法,发现40wt。%Pt / C的ORR性能与10wt。%Pt / Nb-TiO2的ORR性能相似。燃料电池性能测试表明,与传统的碳载Pt催化剂相比,掺Nb的二氧化钛催化剂上的Pt稳定性更高。发现在所研究的材料中,只有在还原条件下合成的掺Nb的二氧化钛金红石相可用作潜在的PEMFC催化剂载体。铂分散在WC和WO x的商业样品上。通过使材料在0.6V至1.8V之间步进来进行稳定性测试。与碳基商业催化剂(HiSpec 4000)相比,观察到WC和WOx的稳定性更高。发现由于在这些低表面积的商品粉末上Pt的分散性差,WC或WOx上负载的Pt的性能低于Pt / C的性能。

著录项

  • 作者

    Chhina, Harmeet.;

  • 作者单位

    University of Toronto (Canada).;

  • 授予单位 University of Toronto (Canada).;
  • 学科 Alternative Energy.Engineering Materials Science.Engineering Mechanical.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 259 p.
  • 总页数 259
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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