Issue 30, 2019

In situ synthesis of Ni/NiO composites with defect-rich ultrathin nanosheets for highly efficient biomass-derivative selective hydrogenation

Abstract

Herein, a Ni/NiO composite catalyst was synthesized by a simple in situ reduction method, and its catalytic hydrogenation performance has been verified to be superior to that of noble metals. In particular, the catalysts can transform 2(5H)-furanone (HFO) to γ-butyrolactone (GBL) efficiently under mild conditions, which effectively upgrades the biomass-derivatives. The superior catalytic activity can be attributed to the synergism of the geometric construction and electronic regulation. Specifically, ultrathin NiO nanosheets contain plenty of surface defects and relatively large mesopores. Those defects can be helpful in the activation and dissociation of hydrogen, the adsorption of HFO molecules, as well as the enhancement of the local hydrogen concentration on the catalyst, while the pores can be considered as nano-reactors for hydrogenation. The strong interaction at the interface caused by the in situ synthesis can further tune its electronic structure and improve the hydrogen adsorption. In addition, the catalyst also displays great catalytic properties for p-nitrophenol (PNP) hydrogenation and non-enzymatic glucose sensing, which further supports the promising application potential of such catalysts with the unique mesostructures of Ni/NiO heterojunctions with defect-rich ultrathin nanosheets.

Graphical abstract: In situ synthesis of Ni/NiO composites with defect-rich ultrathin nanosheets for highly efficient biomass-derivative selective hydrogenation

Supplementary files

Article information

Article type
Paper
Submitted
30 Apr 2019
Accepted
18 Jun 2019
First published
18 Jun 2019

J. Mater. Chem. A, 2019,7, 17834-17841

In situ synthesis of Ni/NiO composites with defect-rich ultrathin nanosheets for highly efficient biomass-derivative selective hydrogenation

Y. Wang, F. Cao, W. Lin, F. Zhao, J. Zhou, S. Li and G. Qin, J. Mater. Chem. A, 2019, 7, 17834 DOI: 10.1039/C9TA04487F

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