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首页> 外文期刊>International journal of hydrogen energy >Nickel-based catalysts for hydrogen evolution by hydrolysis of sodium borohydride: from structured nickel hydrazine nitrate complexes to reduced counterparts
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Nickel-based catalysts for hydrogen evolution by hydrolysis of sodium borohydride: from structured nickel hydrazine nitrate complexes to reduced counterparts

机译:镍基催化剂,可通过硼氢化钠的水解而释放出氢气:从结构化的硝酸肼镍配合物到还原的配合物

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Nickel complexes have recently been presented as prospective catalytic materials for hydrogen H-2 evolution by hydrolysis of sodium borohydride NaBH4. An attractive complex is nickel hydrazine nitrate [Ni(N2H4)(3)][NO3](2) for which little variations in the synthesis procedure result in different morphologies like hexagonal plates, dews and discs. In our conditions, the dews have the better catalytic activity owing to more defects and more active sites. There is an effect of the morphology on the catalytic activity. However, the H-2 evolution curves (regardless the initial morphology) show an induction period during which the complex (purple violet in color) evolves into a catalytically active form (fine black powder). The evolution is featured by changes in morphology and chemical state of nickel. The catalytically active form is even more active than the pristine complex: it shows a higher H-2 generation rate (three times higher in the best case). The starting complexes and the "reduced" counterparts have been then characterized (e.g. SEM, FTIR, XRD, XPS) to better understand the aforementioned evolutions. One of our main conclusions is that there are some marked analogies between our nickel-based catalysts and the much-investigated cobalt-based catalysts. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:镍配合物最近被提出作为通过硼氢化钠NaBH4水解而释放氢H-2的潜在催化材料。有吸引力的配合物是硝酸肼镍[Ni(N2H4)(3)] [NO3](2),在合成过程中几乎没有变化,导致六方板,露珠和圆盘等不同形态。在我们的条件下,由于更多的缺陷和更多的活性位,露水具有更好的催化活性。形态对催化活性有影响。但是,H-2的演化曲线(无论初始形态如何)都显示出一个诱导期,在此期间,复合物(紫色紫色)演变成催化活性形式(精细的黑色粉末)。这种演变的特征是镍的形态和化学状态的变化。催化活性形式甚至比原始复合物更具活性:它显示出更高的H-2生成速率(最好的情况下,是三倍)。然后表征了起始复合物和“还原的”对应物(例如SEM,FTIR,XRD,XPS),以更好地理解上述演变。我们的主要结论之一是,在我们的镍基催化剂和经过广泛研究的钴基催化剂之间存在一些明显的类比。 (C)2018氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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