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Core-shell structured PtRu nanoparticles@FeP promoter with an efficient nanointerface for alcohol fuel electrooxidation

机译:核壳结构PtRu nanoparticles@FeP启动子与一个高效nanointerface酒精燃料电氧化

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In this study, a bottleneck was overcome for direct alcohol fuel cells using state-of-the-art PtRu catalysts for alcohol fuel oxidation. Herein, a core-shell structured PtRu catalyst system based on the emerging promoter FeP was developed that showed excellent catalytic performance for the oxidation of alcohol fuels. The surface spectrometric analysis and morphology observation confirmed the formation of a nanointerface of the PtRu shell and FeP core hybrid catalyst (PtRu@FeP), and efficient ligand effects and electronic effects were found to result from the noble metal active sites and adjacent promoter in the core-shell structure. The facile formation of oxygen-containing species and the strong electronic effects could activate the Pt active sites, leading to high catalytic performance. High anti-CO poisoning ability was found for this catalyst system when compared with the case of the benchmark commercial PtRu/C catalyst (110 mV less and 60 mV less as evaluated by the peak and onset potentials for CO oxidation, respectively). The PtRu@FeP catalysts also exhibited much higher catalytic activity and stability when compared with commercial and home-made PtRu/C catalysts; specifically, the peak current density of the PtRu@FeP 1 : 1 catalyst was about 2 and 3 times higher than those of the commercial PtRu/C catalyst and home-made PtRu/C for the oxidation of the alcohol fuels methanol and ethanol; moreover, high catalytic efficiency, improved by 2 times, was found, as expressed by the specific activity. Excellent catalytic stability as evaluated by 1000 cycles of cyclic voltammetry measurements was also demonstrated for the PtRu@FeP catalysts. The high catalytic performance could be attributed to the intimate nanointerface contact of the core-shell structured PtRu shell over the FeP core via a bi-functional catalytic mechanism and electronic effects based on the ligand effect in this catalyst system. The current study is a significant step to increase the PtRu catalytic performance via nanointerface construction by a core-shell structure on a novel promoter for direct alcohol fuel cells.
机译:在这项研究中,一个瓶颈是克服使用最先进的直接醇燃料电池PtRu酒精燃料的氧化催化剂。在此,核壳结构PtRu催化剂系统基于新兴的子聚全氟乙丙烯开发显示优秀的催化酒精燃料的氧化的性能。表面光谱分析和形态观察证实的形成nanointerface PtRu壳牌和聚全氟乙丙烯的核心混合催化剂(PtRu@FeP)和高效的配体效应和电子效应被发现结果从网站和贵金属活跃相邻的启动子的核壳结构。简单的含氧物种的形成和强烈的电子效应可以激活Pt活跃的网站,导致高的催化的性能。发现催化剂系统相比基准的情况下商业PtRu / C催化剂(110 mV少和60 mV评估发病高峰和潜力有限公司分别为氧化)。也表现出更高的催化活性和相比,商业和稳定自制PtRu / C催化剂;峰值电流密度PtRu@FeP 1: 1催化剂是2和3倍的商业PtRu / C和催化剂自制PtRu / C氧化的酒精燃料甲醇和乙醇;催化效率、提高了2倍发现,所表达的特定活动。优秀的催化稳定性评价1000次的循环伏安法测量也证明了PtRu@FeP催化剂。的高催化性能归因于nanointerface亲密接触的核壳结构PtRu壳了聚全氟乙丙烯通过bi-functional催化机制的核心基于配体效应和电子效应在这个催化剂体系。增加PtRu催化重要一步通过nanointerface建筑的性能核壳结构对小说启动子直接醇燃料电池。

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