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首页> 外文期刊>Electrochimica Acta >Self-supported porous Ni-Fe-P composite as an efficient electrocatalyst for hydrogen evolution reaction in both acidic and alkaline medium
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Self-supported porous Ni-Fe-P composite as an efficient electrocatalyst for hydrogen evolution reaction in both acidic and alkaline medium

机译:自支撑多孔Ni-Fe-P复合材料,在酸性和碱性介质中均可作为有效的氢气分解反应的电催化剂

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Self-supported porous Ni-Fe-P nanocomposite cathode was fabricated via a direct reaction between metallic foam (Ni-Fe) and P vapor. Microstructure characterization results confirm that, after the reaction with P vapor, the metallic framework including Ni and Fe was converted into corresponding metallic phosphide compounds (i.e., Ni2P, Ni5P4 and Fe2P) and quantities of nanosheet arrays vertically-grown on the ligament. Both in acidic (0.5 M H2SO4) and alkaline (1.0 M KOH) media, the as-obtained Ni-Fe-P electrode demonstrates a quite high HER catalytic performance as compared with pristine Ni and Ni-Fe foam, even being almost close to state-of-the-art Pt/C. The as-evolved typical micro-nano hierarchical 3D integrated framework coupled with quantities of nanosheet arrays on it should be responsible for the great HER performance of this resulting composite cathode, which provides not only fast channels for electron transfer but also offers large electrochemical surface area so as to expose more active sites toward the electrocatalysis for HER. Meanwhile, the synergistic effect between the three active Ni2P, Ni5P4 and Fe2P phase may also play a crucial role in the as-revealed superior HER activity. These excellent results promise the potential application of this typical kind of multi-component Ni-Fe-P cathode toward electrochemical water splitting for large-scale hydrogen fuel production. (C) 2016 Elsevier Ltd. All rights reserved.
机译:通过金属泡沫(Ni-Fe)和P蒸气之间的直接反应,制备了自支撑多孔Ni-Fe-P纳米复合阴极。微观结构表征结果证实,与P蒸气反应后,包括Ni和Fe的金属骨架转化为相应的金属磷化物(即Ni2P,Ni5P4和Fe2P),并且在韧带上垂直生长了一定数量的纳米片阵列。无论是在酸性介质(0.5 M H2SO4)中还是在碱性介质(1.0 M KOH)中,与原始的Ni和Ni-Fe泡沫相比,所获得的Ni-Fe-P电极都具有相当高的HER催化性能。最新的Pt / C。不断发展的典型的微纳分层3D集成框架以及其上的大量纳米片阵列应归因于这种合成阴极的出色HER性能,该复合阴极不仅为电子转移提供了快速通道,而且还提供了较大的电化学表面积从而使更多的活性位点暴露于HER的电催化作用。同时,三个活性Ni2P,Ni5P4和Fe2P相之间的协同作用也可能在所揭示的优异HER活性中起关键作用。这些优异的结果保证了这种典型的多组分Ni-Fe-P阴极在大规模生产氢燃料的电化学水分解中的潜在应用。 (C)2016 Elsevier Ltd.保留所有权利。

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