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

被引:109
作者
Tsai, Ming-Chih [1 ]
Chen, Po-Yu [1 ]
机构
[1] Kaohsiung Med Univ, Fac Med & Appl Chem, Kaohsiung 807, Taiwan
关键词
gold; nanoparticle; hexavalent chromium; indium tinoxide; modified electrode;
D O I
10.1016/j.talanta.2008.03.043
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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 Na2SO4 solution containing 1 mM HAuCl4 center dot 3H(2)O and 0.01 M H2SO4. 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 mu M with a detection limit of 2 mu M (or = 3), and linearity was obtained from 0.5 to 50 mu M 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 mu M (sigma = 3). (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:533 / 539
页数:7
相关论文
共 39 条
[1]   Reduction of hexavalent chromium by polypyrrole deposited on different carbon substrates [J].
Alatorre, MA ;
Gutierrez, S ;
Paramo, U ;
Ibanez, JG .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1998, 28 (05) :551-557
[2]   THE DETERMINATION OF THE CHROMIUM SPECIATION IN SEA-WATER USING CATALYTIC CATHODIC STRIPPING VOLTAMMETRY [J].
BOUSSEMART, M ;
VAN DEN BERG, CMG ;
GHADDAF, M .
ANALYTICA CHIMICA ACTA, 1992, 262 (01) :103-115
[3]   Dichromate reduction on gold and platinum electrodes in aqueous acid solutions [J].
Burke, LD ;
Nugent, PF .
ELECTROCHIMICA ACTA, 1997, 42 (03) :399-411
[4]   Preconcentration and speciation of chromium by the determination of total chromium and chromium(III) in natural waters by flame atomic absorption spectrometry with a chelating ion-exchange flow injection system [J].
CesponRomero, RM ;
YebraBiurrun, MC ;
BermejoBarrera, MP .
ANALYTICA CHIMICA ACTA, 1996, 327 (01) :37-45
[5]   Chemoselective immobilization of gold nanoparticles onto self assembled monolayers [J].
Chan, EWL ;
Yu, LP .
LANGMUIR, 2002, 18 (02) :311-313
[6]   VOLTAMMETRIC ION-SELECTIVE ELECTRODE FOR CHROMIUM(VI) [J].
COX, JA ;
KULESZA, PJ ;
MBUGWA, MA .
ANALYTICAL CHEMISTRY, 1982, 54 (04) :787-789
[7]   STRIPPING VOLTAMMETRY OF CHROMIUM(VI) AT A POLY(4-VINYLPYRIDINE)-COATED PLATINUM-ELECTRODE [J].
COX, JA ;
KULESZA, PJ .
ANALYTICA CHIMICA ACTA, 1983, 154 (NOV) :71-78
[8]   DETERMINATION OF CHROMIUM(VI) BY DIFFERENTIAL-PULSE POLAROGRAPHY WITH A SODIUM-FLUORIDE SUPPORTING ELECTROLYTE [J].
COX, JA ;
WEST, JL ;
KULESZA, PJ .
ANALYST, 1984, 109 (07) :927-930
[9]   DETERMINATION OF CHROMIUM(VI) IN NATURAL-WATERS BY DIFFERENTIAL PULSE POLAROGRAPHY [J].
CROSMUN, ST ;
MUELLER, TR .
ANALYTICA CHIMICA ACTA, 1975, 75 (01) :199-205
[10]  
Danilov FI, 1998, RUSS J ELECTROCHEM+, V34, P276