Please use this identifier to cite or link to this item:
|Type:||Artigo de periódico|
|Title:||Electrochemical Behavior of Gold Nanoparticles Generated In Situ on 3-(1-Imidazolyl)propyl-silsesquioxane|
|Abstract:||Gold nanoparticles of different morphologies have been synthesized on a silica-based organic-inorganic hybrid material for catalytic applications. The gold nanoparticles formations proceed through in situ chemical reduction of the AuCl4- anions previously adsorbed on 3-(1-imidazolyl)propyl-silsesquioxane, which plays the role of substrate and stabilizer. Two distinct reducing agents, sodium citrate and sodium borohydride, were employed to generate gold nanoparticles of different sizes. UV-vis diffuse reflectance as well as transmission electron microscopy were employed to evaluate the particle's morphology. Modified carbon paste electrodes were prepared from these materials and their electrochemical behavior investigated using potassium ferrocyanide and 4-nitrophenol as redox model compounds. Both AuNPs-modified electrodes decreased the overpotential of 4-nitrophenol reduction by around 90mV compared to the unmodified electrode as evidenced by cyclic voltammetry experiment. However, the smaller diameter particles (borohydride-reduced) produced more significant catalytic effect as a consequence of their large surface area. Regarding the sensing parameters, the sensitivity is higher for the borohydride-reduced AuNPs while the values of limit of detection are of the same order of magnitude. Thus, the detection limit and sensitivity are 70.0 +/- 0.6nM and 187 mu A/mM for the citrate-reduced AuNPs; and 75.0 +/- 2.2nM and 238 mu A/mM for the borohydride-reduced AuNPs.|
|Editor:||Wiley-v C H Verlag Gmbh|
|Citation:||Electroanalysis. Wiley-v C H Verlag Gmbh, v. 25, n. 11, n. 2501, n. 2506, 2013.|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.