Please use this identifier to cite or link to this item:
Title: Regeneration of a conjugated sp2 graphene system through selective defunctionalization of epoxides by using a proven synthetic chemistry mechanism
Authors: Chua, Chun Kiang
Pumera, Martin
Keywords: DRNTU::Science::Chemistry
Issue Date: 2014
Source: Chua, C. K., & Pumera, M. (2014). Regeneration of a conjugated sp2 graphene system through selective defunctionalization of epoxides by using a proven synthetic chemistry mechanism. Chemistry - A European Journal, 20(7), 1871-1877.
Series/Report no.: Chemistry - a European journal
Abstract: Graphene is a promising material capable of driving technological advancement. It is, however, a challenge to obtain pristine graphene in large quantities given the limitation of current synthetic methods. Among the numerous methods available, the chemical approach provides an optimistic outlook and has garnered much interest within the graphene community as a potential alternative. One of the most crucial steps of the chemical approach is the chemical reduction of graphene oxide as this dictates the final quality of the graphene sheets. In recent years, much of the focus has shifted to the usage of established reducing agents or oxygen removal reagents, frequently applied in organic chemistry, onto a graphene oxide platform. Herein, the selective removal of epoxide groups and subsequent regeneration of disrupted conjugated sp2 system is highlighted, based on the synergistic effect of indium and indium(I) chloride. The morphological, structural, and electrical properties of the resulting graphene were fully characterized with X-ray photoelectron, Fourier transform IR, solid-state 13C NMR, and Raman spectroscopy; thermogravimetric analysis; scanning electron microscopy; and conductivity measurements. The as-prepared graphene showed a tenfold increase in conductivity against conventional graphene treated with hydrazine reducing agent and demonstrated a high dispersion stability in ethanol. Moreover, the selective defunctionalization of the epoxide groups provides opportunities for potential tailoring of graphene properties for prospective applications.
ISSN: 0947-6539
DOI: 10.1002/chem.201304131
Rights: © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

Citations 10

Updated on Mar 7, 2021

Citations 10

Updated on Mar 7, 2021

Page view(s) 50

Updated on Apr 11, 2021

Google ScholarTM




Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.