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|Title:||Gold-cluster sensors formed electrochemically at boron-doped-diamond electrodes: Detection of dopamine in the presence of ascorbic acid and thiols||Authors:||Weng, J.
|Issue Date:||Apr-2005||Citation:||Weng, J., Xue, J., Wang, J., Ye, J.-S., Cui, H., Sheu, F.-S., Zhang, Q. (2005-04). Gold-cluster sensors formed electrochemically at boron-doped-diamond electrodes: Detection of dopamine in the presence of ascorbic acid and thiols. Advanced Functional Materials 15 (4) : 639-647. ScholarBank@NUS Repository. https://doi.org/10.1002/adfm.200400049||Abstract:||Gold clusters have been electrodeposited on a boron-doped diamond (BDD) electrode by scanning the potential from 0.7 V to 0.0 V (vs. 3 M Kd-Ag/AgCl reference) in a solution of 0.5 mM KAuCl4 and 1.0 M KCl. The cluster-modified diamond (Au/ BDD) electrode has been used to investigate the oxidative properties of dopamine (DA) and ascorbate (AA). The modified diamond electrode shows a higher activity for DA oxidation than AA; the oxidation potential of DA shifted to a less-positive potential (0.11 V) than that of AA, which oxidized at 0.26 V, and DA possesses a much higher peak current than that of AA. The reversibility of the electrode reaction with DA is significantly improved at the Au/BDD electrode, which results in a large increase in the square-wave voltammetric peak current, with a detection limit of 0.1 μM in the presence of a large excess of AA. The Au/BDD electrode shows excellent sensitivity and good selectivity for DA detection. A self-assembled monolayer (SAM) of mercaptoacetic acid on the Au clusters was used to provide an antifouling effect as the negative CO2 - groups repulse negative ascorbate and attract positive dopamine in pH 7.4 buffer. After pre-absorption, the SAM/Au/BDD electrode could detect 1.0 nM DA in a linear range from 10 nM to 10 μM in the presence of 10-4 M AA. © 2005 WILEY-VCH Verlag GmbH &. Co. KGaA, Weinheim.||Source Title:||Advanced Functional Materials||URI:||http://scholarbank.nus.edu.sg/handle/10635/100784||ISSN:||1616301X||DOI:||10.1002/adfm.200400049|
|Appears in Collections:||Staff Publications|
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