Boron nitride supported Ni nanoparticles as catalysts for hydrogen generation from hydrolysis of ammonia borane

We report on Ni nanoparticles supported on boron nitride spheres (BNSP) and sheets (BNSH) as catalysts for hydrogen generation via hydrolysis of ammonia borane (NH3BH3, AB). The Ni/BN catalysts were prepared through a redox replacement reaction. The structure, morphology, and chemical composition of...

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Published inJournal of alloys and compounds Vol. 693; pp. 642 - 649
Main Authors Yang, X.J., Li, L.L., Sang, W.L., Zhao, J.L., Wang, X.X., Yu, C., Zhang, X.H., Tang, C.C.
Format Journal Article
LanguageEnglish
Published Lausanne Elsevier B.V 05.02.2017
Elsevier BV
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Summary:We report on Ni nanoparticles supported on boron nitride spheres (BNSP) and sheets (BNSH) as catalysts for hydrogen generation via hydrolysis of ammonia borane (NH3BH3, AB). The Ni/BN catalysts were prepared through a redox replacement reaction. The structure, morphology, and chemical composition of the obtained samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) equipped with energy dispersive X-ray spectroscopy (EDX), and inductively coupled plasma emission spectroscopy (ICP). The characterization results showed that Ni nanoparticles were well dispersed on the BNSP and BNSH supports for the four Ni/BN catalysts prepared (Ni atomic contents of 6.8, 9.0, 9.2, and 12 wt%). The catalytic activity toward the hydrolysis of AB was found to correlate with the loading of the Ni/BN catalysts, which showed great cycle performance. Theoretical calculations revealed that BN sheets significantly influenced the electric character of Ni catalysts and thereby their catalytic properties. •The catalytic activities of Ni/BN is correlated with the loading of Ni content.•The catalytic activities of Ni/BN is much better than that of bare Ni.•The Ni/BN sheet catalysts show great cycle performance.•BN sheets influenced the electric character of Ni catalysts obviously.
ISSN:0925-8388
1873-4669
DOI:10.1016/j.jallcom.2016.09.204