4.7 Article

RuCu nanoparticles supported on graphene: A highly efficient catalyst for hydrolysis of ammonia borane

Journal

JOURNAL OF ALLOYS AND COMPOUNDS
Volume 590, Issue -, Pages 241-246

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2013.12.134

Keywords

Nanoparticles; Graphene; Hydrogen storage; Ammonia borane

Funding

  1. National Natural Science Foundation of China [21201134]
  2. Ph.D Programs Foundation of Ministry of Education of China [20120141120034]
  3. Natural Science Foundation of Jiangsu Province [BK20130370]
  4. Natural Science Foundation of Hubei Province [2013CFB288]
  5. Large-scale Instrument and Equipment Sharing Foundation of Wuhan University

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Well dispersed RuCu nanoparticles (NPs) supported on graphene were in situ synthesized by a one-step co-reduction of aqueous solution of ruthenium (III) chloride, cupric (II) chloride, and graphite oxide (GO) with ammonia borane (AB) under ambient condition. The nature of the NPs was fully characterized by TEM, HRTEM, XRD, energy dispersive spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS). The as-synthesized NPs exhibit much higher catalytic activity for hydrolytic dehydrogenation of AB than the monometallic Ru and Cu, bimetallic RuCu/graphene reduced by NaBH4, and graphene free RuCu counterparts. Additionally, the as-synthesized NPs supported on graphene exhibit higher catalytic activity than the catalysts with other conventional supports, such as SiO2, gamma-Al2O3, and carbon black. The activity of Ru1Cu7.5/graphene NPs in terms of turnover frequency (TOF) is 135 mol H-2 min(-1) (mol Ru)(-1), which is higher than Ru/graphene, and most reported Ru-based or other noble metal-based NPs for the catalytic hydrolysis of AB. The activation energy for hydrolysis of AB in the presence of Ru1Cu7.5/graphene NPs was determined as 30.59 kJ mol(-1), which is lower than most of the reported catalysts. Furthermore, the as-prepared NPs exert satisfied durable stability for the hydrolytic dehydrogenation of AB. (C) 2013 Elsevier B.V. All rights reserved.

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