Abstract
The fabrication of a self-assembled monolayer (SAM) of a cyclopentadienylnickel(II) thiolato Schiff base compound, [Ni(SC 6 H 4 NC(H)C 6 H 4 OCH 2 CH 2 SMe)(η 5 -C 5 H 5 )] 2 on a gold electrode is described. Effective electronic communication between the Ni(II) centres and the gold surface was established by electrochemically cycling the Schiff base-doped Au electrode in 0.1 M NaOH from −200 mV to +600 mV. The SAM-modified electrode exhibited quasi-reversible electrochemistry. The integrity of this electrocatalytic SAM, with respect to its ability to block and electro-catalyse certain Faradaic processes, was interrogated using cyclic voltammetric experiments. The formal potential, E° ′, varied with pH to give a slope of about −30 mV pH −1 . The surface concentration, G , of the nickel redox centres was found to be 1.548×10 −11 mol cm −2 . By electrostatically doping the SAM using an applied potential of +700 mV versus Ag/AgCl, in the presence of horseradish peroxidase (HRP), it was fine-tuned for amperometric determination of H 2 O 2 . The electrocatalytic-type biosensor displayed typical Michaelis–Menten kinetics and the limit of detection was found to be 6.25 mM.
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