Contrast in Electron-Transfer Mediation between Graphene Oxide and Reduced Graphene Oxide

Wiphada Hongthani, Avinash J. Patil, Stephen Mann, David J. Fermin

Research output: Contribution to journalArticle (Academic Journal)peer-review

2 Citations (Scopus)

Abstract

The properties of graphene oxide (GO) and DNA-stabilised reduced graphene-oxide (rGO) sheets as electron-transfer mediators in partially blocked electrodes are evaluated employing electrochemical impedance spectroscopy. Evidences obtained from UV/Vis, Raman and FTIR spectroscopies, as well as atomic force microscopy, confirm that the reduction of exfoliated GO single sheets by hydrazine yields partially reduced graphene oxide featuring a high defect density. Two-dimensional assemblies of GO and rGO were formed through electrostatic adsorption at Au electrodes, sequentially modified with 11-mercaptoundecanoic acid (MUA) and poly-diallyldimethylammonium chloride (PDADMAC). The MUA:PDADMAC generates a strong blocking layer to the electron-transfer reaction involving the ferri/ferrocyanide redox couple. This blocking behaviour is not significantly affected upon adsorption of GO. However, adsorption of a sub-monolayer of rGO decreases the charge-transfer resistance by more than two orders of magnitude. Analysis of cyclic voltammograms and impedance spectra suggests that electron transfer in rGO assemblies is mediated by occupied states located just below the redox Fermi energy of the probe. These findings are discussed in the context of on-going controversies regarding the electrochemical reactivity of sp2-carbon basal planes.

Original languageEnglish
Pages (from-to)2956-2963
Number of pages8
JournalChemPhysChem
Volume13
Issue number12
DOIs
Publication statusPublished - 27 Aug 2012

Cite this