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Abstract: The electrochemical response of 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS) on aryl-modified glassy carbon (GC) electrodes has been investigated. The electrochemical modification of GC surface with 4-nitrophenyl (NP) and 4-carboxyphenyl (CP) groups was performed using the diazonium reduction method. The 4-aminophenyl-modified GC electrodes were obtained by electroreduction of NP films. The surface coverage of aryl groups was altered by varying the number of potential scans during electrografting experiments. The electrochemical behaviour of ABTS was studied on bare and aryl-modified GC electrodes using cyclic voltammetry and the rotating disk electrode (RDE) methods. Electrochemical measurements were performed in acetate and phosphate buffers (pH=4–8) to study the effect of pH on the electron transfer process. The response of ABTS was independent of pH for bare GC and GC/NP electrodes (modified by 20 electrografting scans), whereas a slight pH-dependence was observed for other electrodes. The strongest blocking action was observed for the NP-modified GC electrodes of higher surface coverage and the lowest for reduced NP films (modified by a single electrografting scan). [Copyright &y& Elsevier]

This work focuses on investigating the electrografting of chemical vapour deposition (CVD) graphene electrodes grown onto Ni foil (Ni/Gra) with different diazonium salts (including azobenzene diazonium tetrafluoroborate, Fast Garnet GBC sulphate salt, Fast Black K salt, 4-bromobenzene diazonium tetrafluoroborate and 4-nitrobenzenediazonium tetrafluoroborate). Various grafting conditions (e.g. “normal” electrografting in the narrow potential range and redox grafting in the wider potential range) were used. The electrochemical grafting behaviour was similar for all diazonium compounds used, except for the 4-nitrobenzenediazonium tetrafluoroborate when redox grafting was applied. The X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM) and Raman spectroscopy results confirmed the presence of the corresponding aryl layers on Ni/Gra surfaces. The formation of multilayers on Ni/Gra substrates was in evidence since the thickness of different aryl layers varied from few to 30 nm depending on the modification procedures as well as the diazonium compounds used and the XPS analysis revealed a peak at about 400 eV for all aryl-modified Ni/Gra samples suggesting the multilayer formation also through azo linkages. [ABSTRACT FROM AUTHOR]