4.7 Article

A rapid low-temperature synthetic method leading to large-scale carboxyl graphene

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 236, Issue -, Pages 471-479

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2013.10.060

Keywords

Graphene; Graphene oxide; Selective reduction

Funding

  1. National Natural Science Foundations of China [J1103315, 91023037]
  2. International Collaboration Project of Science and Technology Program of Sichuan Province, China [2010HH0008]
  3. Science and Technology Fund of CAEP [2011B0302052]
  4. National Fund for Fostering Talents of Basic Science [J1210004]
  5. Nordion Inc.

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We report a rapid, environmentally-friendly and cost-effective route for the preparation of a graphene-based nanomaterial, carboxyl graphene (aka. reduced graphene oxide, RGO) from graphene oxide (GO). Carboxyl graphene was prepared on the scale of several grams through the reduction of GO by thiourea dioxide (TUD) at a relatively low temperature (40 degrees C) in an alkaline medium (pH = 10). The reduction of GO was confirmed by FT-IR, UV-vis, X-ray photoelectron, and Raman spectroscopy. In addition, this reduction was also confirmed by thermal gravimetric analysis, X-ray diffraction, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and atomic force microscopy (AFM). Characterizations of these materials demonstrated that selective reduction of the epoxy and carbonyl groups occurred on the surface of GO, while carboxyl groups were left behind. In addition, the conjugation of the carbons in the structure was restored through this reduction and a single-layer of carboxyl graphene (with a thickness of 0.80 nm, as observed by AFM) was obtained under these conditions. Carboxyl graphene had a high surface area (of 454.52 m(2) g(-1)) and contained approximately 6.9 +/- 1.6 mmol of carboxyl groups per gram of material, as determined via Boehm titration. The mechanism for selective reduction of the epoxy and carbonyl groups on GO to form carboxyl graphene by TUD is proposed and discussed in detail. (C) 2013 Elsevier B.V. All rights reserved.

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