Issue 33, 2012

Synthesis of network reduced graphene oxide in polystyrene matrix by a two-step reduction method for superior conductivity of the composite

Abstract

Polymer/graphene composites have attracted much attention due to their unique organic–inorganic hybrid structure and exceptional properties. In this paper, we report the synthesis of polystyrene/reduced graphene oxide (PS/r-GO) composites by a two-step in situ reduction technique, which consists of a hydrazine hydrate reduction and a subsequent thermal reduction at 200 °C for 12 h. The structure and micromorphology of PS/r-GO composites were characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, Raman spectroscopy, X-ray photoelectron spectroscopy and thermogravimetric analysis. The results show that the GO can be efficiently reduced by the two-step in situ reduction method, and the r-GO sheets are well dispersed and ultimately form a continuous network structure in the polymer matrix. PS/r-GO composite films (5 wt% GO) are prepared by the hot press molding method, possessing a conductivity as high as 22.68 S m−1. The superior conductivity arises from the high reduction degree of GO and its high dispersion and the formation of a network structure in the polymer matrix. These polymer/r-GO composites are expected to be applied in multiple electric devices. The techniques for preparing polymer/r-GO composite films could be further extended to other similar systems.

Graphical abstract: Synthesis of network reduced graphene oxide in polystyrene matrix by a two-step reduction method for superior conductivity of the composite

Article information

Article type
Paper
Submitted
16 May 2012
Accepted
20 Jun 2012
First published
22 Jun 2012

J. Mater. Chem., 2012,22, 17254-17261

Synthesis of network reduced graphene oxide in polystyrene matrix by a two-step reduction method for superior conductivity of the composite

N. Wu, X. She, D. Yang, X. Wu, F. Su and Y. Chen, J. Mater. Chem., 2012, 22, 17254 DOI: 10.1039/C2JM33114D

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