Modification of nanostructured gold surfaces with organic functional groups using electrochemical and solid-phase synthesis methodologies

Celiktas, Ahmet, Ghanem, Mohamed A. and Bartlett, Philip N. (2012) Modification of nanostructured gold surfaces with organic functional groups using electrochemical and solid-phase synthesis methodologies. Journal of Electroanalytical Chemistry, 670, 42-49. (doi:10.1016/j.jelechem.2012.02.008).

Abstract

Anthraquinone and nitrobenzene redox probes were covalently attached to nanostructured sphere segment void (SSV) gold substrates prepared using templated electrodeposition. Anthraquinone was attached to the SSV gold surface through an (aminomethyl)phenyl (NH2CH2C6H4) linker using a combination of electrochemical coupling and solid-phase modification. The nitrobenzene probe was directly immobilized by electrochemical reduction of the corresponding diazonium salt or by self-assembly of 4-nitrobenzene thiol. The surface coverages and stabilities of the modified gold surfaces were characterised by electrochemical and surface enhanced Raman scattering (SERS) techniques. The results demonstrate that electrochemical coupling followed by solid phase coupling is a flexible method for the functionalisation of nanostructured SSV, or other, gold surfaces. The use of the SSV gold substrate allows us to follow the different steps in the modification process using SERS. We find that that diazonium attachment to gold gives greater stability than the more commonly used thiol self-assembly approach.

This record has no associated files available for download.

Contributors

Author: Philip N. Bartlett

Download statistics