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Comparative evaluation of hydrogen storage behavior of Pd doped carbon nanotubes prepared by wet impregnation and polyol methods

机译:湿法浸渍和多元醇制备的Pd掺杂碳纳米管储氢行为的比较评价

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The present manuscript deals with the hydrogen absorption properties of multiwalled carbon nano-tubes (MWCNTs) doped with Pd nanoparticles by the conventional wet impregnation method and the polyol method. In the latter method Pd nanoparticles are doped into CNTs based on polyhydroxy organic compounds (polyol) mediated functionalization. The polyol medium reduces palladium chloride to palladium nanoparticles, and also acts as a capping agent to stabilize the Pd nanoparticles. The samples have been characterized using X-ray diffraction (XRD), Energy Dispersive X-ray (EDX) and Infrared (IR) spectroscopy. Hydrogen absorption studies clearly illustrate that Pd doped MW-CNT's prepared by polyol mediated functionalization show much higher hydrogen storage capacity compared to the sample prepared by wet impregnation route. To determine the cause of this behavior, Transmission Electron Microscopic (TEM) studies of the samples were carried out. The results indicate that the dispersion of Pd nanoparticle on the MWCNT is much better for the sample prepared by the polyol route. An attempt was made to determine the existence of any metal-support interaction using Thermogravimetric Analysis (TGA). The investigation reveals that the higher dispersion of Pd nanoparticles on the CNT support plays a major role for the hydrogen adsorption. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
机译:本手稿通过常规的湿法浸渍法和多元醇法研究了掺杂Pd纳米颗粒的多壁碳纳米管(MWCNT)的吸氢性能。在后一种方法中,基于多羟基有机化合物(多元醇)介导的功能化,将Pd纳米颗粒掺杂到CNT中。多元醇介质将氯化钯还原为钯纳米粒子,并且还充当封端剂以稳定Pd纳米粒子。使用X射线衍射(XRD),能量色散X射线(EDX)和红外(IR)光谱对样品进行了表征。氢吸收研究清楚地表明,与通过湿法浸渍法制备的样品相比,通过多元醇介导的官能化制备的Pd掺杂的MW-CNT具有更高的储氢能力。为了确定此行为的原因,对样品进行了透射电子显微镜(TEM)研究。结果表明,对于通过多元醇路线制备的样品,Pd纳米颗粒在MWCNT上的分散性要好得多。尝试使用热重分析(TGA)确定是否存在任何金属-载体相互作用。研究表明,Pd纳米颗粒在CNT载体上的较高分散度对氢吸附起主要作用。 Hydrogen Energy Publications,LLC版权所有(C)2015。由Elsevier Ltd.出版。保留所有权利。

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