Detection of nitroaromatic explosives is of paramount importance from security point of view. Graphene sheets obtained from the electrochemical anodic exfoliation of graphite foil in different electrolytes (LiClO4 and Na2SO4) were compared and tested as electrode material for the electrochemical detection of 2,4-dinitrotoluene (DNT) and 2,4,6-trinitrotoluene (TNT) in seawater. Voltammetry analysis demonstrated the superior electrochemical performance of graphene produced in LiClO4, resulting in higher sensitivity and linearity for the explosives detection and lower limit of detection (LOD) compared to the graphene obtained in Na2SO4. We attribute this to the presence of oxygen functionalities onto the graphene material obtained in LiClO4 which enable charge electrostatic interactions with the –NO2 groups of the analyte, in addition to π-π stacking interactions with the aromatic moiety. Research findings obtained from this study would assist in the development of portable devices for the on-site detection of nitroaromatic explosives.
Graphitic carbon nitride (g-C3 N4 ), synthesised by pyrolysis of different precursors (dicyandiamide, melamine and urea) under varying reaction conditions (air and nitrogen gas) is subjected to electrochemical studies for the elucidation of the inherent catalytic efficiency of the pristine material. Contrary to popular belief, pristine g-C3 N4 shows negligible, if any, enhancement in its electrochemical behaviour in this comprehensive study. Voltammetric analysis reveals g-C3 N4 to display similar catalytic efficiency to the unmodified glassy carbon electrode surface on which the bulk material was deposited. This highlights the non-catalytic nature of the pristine material and challenges the feasibility of using g-C3 N4 as a heterogeneous catalyst to deliver numerous promised applications.
Contrary to popular belief, pristine g‐C3N4 shows negligible, if any, enhancement in its electrochemical behavior in a comprehensive study. More information can be found in the Full Paper by M. Pumera et al. on page 481 in Issue 4, 2016 (DOI:10.1002/cphc.201501009).
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