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首页> 外文期刊>Electrochimica Acta >Nitrogen doped carbon coated Mo modified TiO2 nanowires (NC@MTNWs-FI) with functionalized interfacial as advanced PtRu catalyst support for methanol electrooxidation
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Nitrogen doped carbon coated Mo modified TiO2 nanowires (NC@MTNWs-FI) with functionalized interfacial as advanced PtRu catalyst support for methanol electrooxidation

机译:氮掺杂碳涂覆的MO改性TiO2纳米线(NC @ MTNWS-Fi)具有官能化界面,作为甲醇电氧化的先进PTRU催化剂载体

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摘要

A strategy combining hydrothermal in-situ pre-carbonization coating and interfacial functionalization is proposed to prepare the nitrogen doped carbon coated Mo modified one-dimensional TiO2 nanowires (NC@MTNWs-FI) with functionalized interfacial core-shell structure as advanced carriers for PtRu nanoparticles towards methanol electrooxidation. Mo functional doping and chitosan pre-carbonization occur simultaneously on the surface of TiO2 nanowires (TNWs), resulting in a special concentric multi-layer one-dimensional (1D) structure with TiO2 core, Mo functionalized interface and an outer N-doped carbon layer. The mass activity of the prepared PtRu/NC@MTNWs-FI catalyst is increased to 1.23 A mg(-1) Pt for methanol electrooxidation, which is 2 times higher than that of the unmodified supported catalyst (PtRu/NC@TNWs) and the stability is increased by 15.9%. In addition, it is 2.24 times higher than that of the PtRu/C catalyst and the stability is increased by 23.2%. This excellent catalytic performance is attributed to the synergistic electron donating effect of the Mo functionalized interface and the nitrogen doped carbon layer on the supported PtRu as well as the stronger anchoring effect. This work reveals a new method for designing highly active and stable electrocatalytic support materials for the development of fuel cells. (c) 2019 Elsevier Ltd. All rights reserved.
机译:提出了一种结合水热原位预碳化涂层和界面官能化的策略,以制备氮掺杂碳涂覆的MO改性的一维TiO2纳米线(NC @ MTNWS-Fi),其具有官能化界面核心 - 壳结构,作为PTRU纳米粒子的先进载体朝向甲醇电氧化。 Mo功能掺杂和壳聚糖预碳化在TiO2纳米线(TNW)的表面上同时发生,导致具有TiO2芯,Mo官能化界面和外部N掺杂碳层的特殊同心多层一维(1D)结构。制备的PTRU / NC / NC-Fi催化剂的质量活性增加到甲醇电氧化的1.23毫克(-1)Pt,这是比未修改的负载催化剂(PTRU / NC @ TNW)高2倍。稳定性增加了15.9%。此外,比PTRU / C催化剂高2.24倍,稳定性增加23.2%。这种优异的催化性能归因于由支撑的PTRU上的Mo官能化界面和氮掺杂碳层的协同电子捐献效应以及较强的锚固效果。这项工作揭示了设计用于开发燃料电池的高活性和稳定的电催化支撑材料的新方法。 (c)2019 Elsevier Ltd.保留所有权利。

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