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首页> 外文期刊>Advanced energy materials >Hierarchically Structured Ultraporous Iridium-Based Materials: A Novel Catalyst Architecture for Proton Exchange Membrane Water Electrolyzers
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Hierarchically Structured Ultraporous Iridium-Based Materials: A Novel Catalyst Architecture for Proton Exchange Membrane Water Electrolyzers

机译:分层结构的超多孔铱基材料:质子交换膜水电解槽的新型催化剂体系结构

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摘要

Iridium oxide is the gold-standard catalyst for the oxygen evolution reaction (OER) in acidic media due to its unmatched activity and stability. Here, a new catalyst architecture comprising a nanoneedle network of iridium-containing oxides assembled into macroporous micrometric particles with approximate to 75% of porosity is reported. The rationally designed porous hierarchical structure optimizes the accessibility of reactants and products to the surface of the nanoparticles and maximizes catalyst activity. The materials are easily prepared from aqueous solutions by an industrially viable spray-drying route through an evaporation self-assembly mechanism. The versatility of the process enables the preparation of mixed oxides with low iridium content, particles with tunable crystallinity, and various iridium surface species with high electrochemical activity. Highly porous Ir0.7Ru0.3O2 outperforms commercial iridium oxide. These materials also represent an ideal platform to assess the reactivity of the iridium and oxygen species involved in the oxygen evolution reaction. Furthermore, it is demonstrated that these highly porous particles are optimal building blocks to be integrated into catalyst layers, without the drawbacks associated with the use of discrete nanoparticles. Fresh- and end-of-test membrane-electrode assemblies' characterization shows that their particular architecture is preserved upon catalyst layer preparation and after operation in a proton-exchange membrane electrolysis cell.
机译:氧化铱因其无与伦比的活性和稳定性,是在酸性介质中进行氧气释放反应(OER)的金标准催化剂。在这里,报道了一种新的催化剂结构,该结构包括组装成大孔测微颗粒的含铱氧化物的纳米针状网络,其孔隙率约为75%。合理设计的多孔层级结构优化了反应物和产物对纳米颗粒表面的可及性,并使催化剂活性最大化。通过工业上可行的喷雾干燥路线,通过蒸发自组装机制,可以轻松地从水溶液中制备材料。该方法的多功能性使得能够制备具有低铱含量的混合氧化物,具有可调结晶度的颗粒以及具有高电化学活性的各种铱表面物质。高度多孔的Ir0.7Ru0.3O2优于商用氧化铱。这些材料还代表了一个理想的平台,可用来评估参与氧气逸出反应的铱和氧气物种的反应性。此外,已证明这些高度多孔的颗粒是整合到催化剂层中的最佳构件,而没有与使用离散纳米颗粒相关的缺点。新鲜和测试结束的膜电极组件的特性表明,在制备催化剂层时以及在质子交换膜电解池中运行后,它们的特定结构得以保留。

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  • 来源
    《Advanced energy materials》 |2019年第4期|1802136.1-1802136.11|共11页
  • 作者单位

    Sorbonne Univ, Coll France, CNRS, UMR 7574,Chim Matiere Condensee Paris, F-75005 Paris, France;

    Univ Paris Diderot, Sorbonne Paris Cite, UMR CNRS 7086, ITODYS, 15 Rue Jean Antoine de Baif, F-75205 Paris 13, France;

    Univ Montpellier, UMR 5253, Interfaces & Mat Energy, ICGM Aggregates, F-34095 Montpellier, France;

    Univ Montpellier, UMR 5253, Interfaces & Mat Energy, ICGM Aggregates, F-34095 Montpellier, France;

    Univ Montpellier, UMR 5253, Interfaces & Mat Energy, ICGM Aggregates, F-34095 Montpellier, France;

    Univ Paris Diderot, Sorbonne Paris Cite, Lab Electrochim Mol, Unite Mixte Rech Univ CNRS 7591, Batiment Lavoisier,15 Rue Jean de Baif, F-75205 Paris 13, France;

    Univ Paris Diderot, Sorbonne Paris Cite, UMR CNRS 7086, ITODYS, 15 Rue Jean Antoine de Baif, F-75205 Paris 13, France;

    Univ Strasbourg, IPCMS UMR 7504 CNRS, 23 Rue Loess,BP 43, F-67034 Strasbourg 2, France;

    Univ Strasbourg, IPCMS UMR 7504 CNRS, 23 Rue Loess,BP 43, F-67034 Strasbourg 2, France;

    Sorbonne Univ, Coll France, CNRS, UMR 7574,Chim Matiere Condensee Paris, F-75005 Paris, France;

    Sorbonne Univ, Coll France, CNRS, UMR 7574,Chim Matiere Condensee Paris, F-75005 Paris, France;

    Univ Paris Saclay, Ecole Polytech, CNRS, LCM, F-91128 Palaiseau, France;

    Univ Paris Diderot, Sorbonne Paris Cite, UMR CNRS 7086, ITODYS, 15 Rue Jean Antoine de Baif, F-75205 Paris 13, France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    anodes; electrolysis; hydrogen; nanoneedles; porous catalysts;

    机译:阳极;电解;氢;纳米酮;多孔催化剂;

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