首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Displacement reaction of Pt on carbon-supported Ru nanoparticles in hexachloroplatinic acids
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Displacement reaction of Pt on carbon-supported Ru nanoparticles in hexachloroplatinic acids

机译:Pt在六氯铂酸中碳负载的Ru纳米颗粒上的置换反应

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摘要

The displacement reaction of Pt on Ru to form a Ru core and Pt shell (Ru@Pt) bimetallic structure is investigated by immersing the carbon-supported Ru nanoparticles in hexachloroplatinic acids with pH of 1, 2.2, and 8, followed by a hydrogen reduction treatment. Results from inductively coupled plasma mass spectrometry suggest that the dissolution of Ru is mostly caused by the reduction of Pt cations. Images from transmission electron microscopy demonstrate a uniform distribution of Ru@Pt in size of 3-5 nm. Spectra from X-ray absorption near edge structure and extended X-ray absorption fine structure confirm that the pH value of hexachloroplatinic acid determines the type of ligands complexing the Pt cations that affects their activity and consequently the severity of displacement reaction and alloying degree of Ru@Pt nanoparticles. As a result, the samples from pH 1 bath reveal a desirable core-shell structure that displays a reduced onset potential in CO stripping and stable catalytic performance for H2 oxidation while the samples from pH 8 bath indicate the formation of Pt clusters on the Ru surface that leads to poor CO stripping and H2 oxidation characteristics.
机译:通过将碳负载的Ru纳米颗粒浸入pH为1、2.2和8的六氯铂酸中,然后进行氢还原,研究了Pt在Ru上的置换反应,形成Ru核和Pt壳(Ru @ Pt)双金属结构。治疗。电感耦合等离子体质谱法的结果表明,Ru的溶解主要是由Pt阳离子的还原引起的。来自透射电子显微镜的图像表明Ru @ Pt的均匀分布为3-5 nm。 X射线吸收的边缘结构和扩展的X射线吸收精细结构的光谱证实,六氯铂酸的pH值决定了与Pt阳离子络合的配体类型,从而影响了其活性,因此置换反应的严重程度和Ru的合金化程度@Pt纳米粒子。结果,pH 1浴的样品显示出理想的核-壳结构,显示出降低的CO汽提起始电位和稳定的H2氧化催化性能,而pH 8浴的样品表明在Ru表面形成了Pt簇导致不良的CO汽提和H2氧化特性。

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