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Oxidation of ethanol on platinum nanoparticles: surface structure and aggregation effects in alkaline medium

机译:铂纳米颗粒上乙醇的氧化:碱性介质中的表面结构和聚集效应

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摘要

The ethanol oxidation reaction in 0.1 M NaOH on Pt nanoparticles with different shapes and loadings was investigated using electrochemical and spectroscopic techniques. The surface structure effect on this reaction was studied using well-characterized platinum nanoparticles. Regardless of the type of Pt nanoparticles used, results show that acetate is the main product with negligible CO2 formation. From the different samples used, the nanoparticles with a large amount (111) of ordered domains have higher peak currents and a higher onset potential, in agreement with previous works with single crystal electrodes, In addition, spherical platinum nanoparticles supported on carbon with different loadings were used for studying possible diffusional problems of ethanol to the catalyst surface. The activity in these samples diminishes with the increase of Pt loading, due to diffusional problems of ethanol throughout the whole Pt nanoparticle layer, being the internal part of the catalyst layer inactive for the oxidation. To avoid this problem and prepare more dispersed nanoparticle catalyst layers, deposits were dried while the carbon support was rotated to favor the dispersion of the layer around the support. The improvement in the electrocatalytic activity for ethanol oxidation confirms the better performance of this procedure for depositing and drying.
机译:使用电化学和光谱技术研究了在0.1 M NaOH中不同形状和负载的Pt纳米颗粒上的乙醇氧化反应。使用表征良好的铂纳米粒子研究了该反应的表面结构效应。无论使用哪种类型的Pt纳米颗粒,结果都表明乙酸盐是主要产物,二氧化碳的生成量可忽略不计。通过使用不同的样品,与以前的单晶电极研究相一致,具有大量(111)有序域的纳米颗粒具有更高的峰值电流和更高的启动电位。此外,球形铂纳米颗粒负载在碳上的负载量也不同用于研究乙醇可能扩散到催化剂表面的问题。这些样品中的活性随着Pt负载的增加而降低,这归因于乙醇在整个Pt纳米颗粒层中扩散的问题,乙醇是催化剂层的内部对氧化不起活性的部分。为了避免该问题并制备更多分散的纳米颗粒催化剂层,将沉积物干燥,同时旋转碳载体以有利于该层在载体周围的分散。乙醇氧化的电催化活性的提高证实了该方法沉积和干燥的更好性能。

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