Issue 21, 2014

Facile synthesis and enhanced catalytic performance of graphene-supported Ni nanocatalyst from a layered double hydroxide-based composite precursor

Abstract

In this paper, graphene-supported Ni nanocatalyst (Ni/G) was prepared via self-reduction of a hybrid Ni–Al layered double hydroxide/graphene (NiAl-LDH/G) composite precursor. NiAl-LDH/G nanocomposite was assembled via a facile one-step coprecipitation route, which involved the nucleation and growth of NiAl-LDH, simultaneously accompanied by the reduction of graphene oxide without the addition of any reducing agents. The characterization results demonstrated that NiAl-LDH nanoplatelets were homogeneously dispersed on both sides of an exfoliated, structurally flexible graphene The graphene component in the precursor, serving as reducing agent, could in situ reduce Ni2+ species to Ni0 on heating under an inert atmosphere, thus facilitating the formation of highly dispersed Ni nanoparticles with a uniform size. Compared with those prepared by conventional methods, as-formed graphene-supported Ni nanocatalyst exhibited superior catalytic performance in the liquid phase selective hydrogenation of cinnamaldehyde to hydrocinnamaldehyde owing to the much higher metal dispersion and smaller size of Ni nanoparticles in the catalyst. The present finding provides a simple approach to fabricate new types of graphene-supported, metal-based heterogeneous catalysts with advanced catalytic performance.

Graphical abstract: Facile synthesis and enhanced catalytic performance of graphene-supported Ni nanocatalyst from a layered double hydroxide-based composite precursor

Supplementary files

Article information

Article type
Paper
Submitted
22 Jan 2014
Accepted
24 Mar 2014
First published
25 Mar 2014

J. Mater. Chem. A, 2014,2, 7880-7889

Facile synthesis and enhanced catalytic performance of graphene-supported Ni nanocatalyst from a layered double hydroxide-based composite precursor

R. Xie, G. Fan, Q. Ma, L. Yang and F. Li, J. Mater. Chem. A, 2014, 2, 7880 DOI: 10.1039/C4TA00395K

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