Voltammetric study and electrochemical detection of hexavalent chromium at gold nanoparticle-electrodeposited indium tinoxide (ITO) electrodes in acidic media

The voltammetric behavior of hexavalent chromium species (Cr(VI)) was respectively studied at ITO, bulk Au, and Au-electrodeposited electrodes in 0.01 M NaCl aqueous solutions containing 0.01 M HCl. It was found that performance degradation of the ITO electrodes toward the reduction of Cr(VI) can be...

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Bibliographic Details
Published in:Talanta (Oxford) 2008-07, Vol.76 (3), p.533-539
Main Authors: Tsai, Ming-Chih, Chen, Po-Yu
Format: Article
Language:English
Subjects:
Acids
Analytical chemistry
Chemistry
Chromium - analysis
Electrochemical methods
Electrochemistry - methods
Electrochemistry - standards
Exact sciences and technology
Gold
Hexavalent chromium
Indium
Indium tinoxide
Ion-Selective Electrodes - standards
Metal Nanoparticles - chemistry
Modified electrode
Nanoparticle
Tin Compounds
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Summary:The voltammetric behavior of hexavalent chromium species (Cr(VI)) was respectively studied at ITO, bulk Au, and Au-electrodeposited electrodes in 0.01 M NaCl aqueous solutions containing 0.01 M HCl. It was found that performance degradation of the ITO electrodes toward the reduction of Cr(VI) can be suppressed by modifying the electrode surface with gold nanoparticles (AuNPs), which were formed on ITO electrodes by potential-sweeping or potential-step electrodeposition in a 0.01 M Na 2SO 4 solution containing 1 mM HAuCl 4·3H 2O and 0.01 M H 2SO 4. After the modification, the surface of ITO electrodes turned to the characteristically red or blue color exhibited by AuNPs. The gold nanoparticle-electrodeposited indium-tinoxide electrode (AuNP-ITO) demonstrates unique catalytic behavior, higher sensitivity and stability in the reduction of Cr(VI). Cr(VI) species was detected by either cyclic voltammetry or hydrodynamic amperometry. By cyclic voltammetry, the dependence of cathodic peak current on concentration was linear from 5 to 100 μM with a detection limit of 2 μM ( σ = 3), and linearity was obtained from 0.5 to 50 μM by hydrodynamic amperometry where a constant potential of +0.2 V ( vs. Ag/AgCl) was applied and a batch-injection cell was employed. For hydrodynamic amperometry, the detection limit was 0.1 μM ( σ = 3).
ISSN:0039-9140
1873-3573
DOI:10.1016/j.talanta.2008.03.043