J. Chem. Sci., Vol. 120, No. 5, September 2008, pp. 493498. Indian Academy of Sciences.

A study of nanostructured gold modified glassy carbon electrode for

the determination of trace Cr(VI)

BENZHI LIU, LIYUAN LU, MIN WANG and YANQIN ZI*

Department of Chemistry, Huaibei Coal Normal College, Huaibei, China 235000
e-mail: ziyanqin@163.com

MS received 7 July 2008; revised 31 July 2008

Abstract. A nanostructured gold modified glassy carbon electrode (Aunano/GCE) was employed for the
determination of trace chromium(VI). To prepare Aunano/GCE, the GCE was immersed into KAuCl4 solu-
tion and electrodeposition was conducted at the potential of 04 V (vs Ag/AgCl) for 600 s. Scanning
electron microscopy measurements show that the electrochemically synthesized gold nanoparticles were
deposited in aggregated form. Any undue effects caused by the presence of foreign ions in the solution
were also analysed to ensure that common interference in the determination of chromium(VI) by square
wave voltammetry, do not influence the electrochemical response of the latter element. The results show
that this method allows for Cr(VI) determinations with a much lower detection limit (001 g L1) in the
presence of excess of Cr(III) than the commonly used diethylenetriammine pentaacetic acid (DTPA)
method. The method was applied to determine levels of chromium(VI) in tap water and sewage water.

Keywords. Nanostructured gold modified glassy carbon electrode; square wave voltammetry; Cr(VI).

1. Introduction which have shown numerous advantages including

speed of analysis, good selectivity and sensitivity.1013
Chromium exists in natural samples in two main va- Metal nanoparticles have shown superior or advan-
lence states as Cr(III) and Cr(VI). The two environ- tageous properties for a wide range of technological
mentally relevant valence states of chromium Cr(III) applications,1417 and they provide three important
and Cr(VI) have a contrasting impact on environ- functions for electroanalysis: improved mass transport,
ment and health. Trivalent chromium is relatively high effective surface area, and catalytic properties.18
harmless and plays an essential role in biological Many methods were reported to synthesize metal
processes, whereas hexavalent chromium is about nanoparticles including reduction with different re-
1001000 times more toxic.1 Because of the differ- agents,19 UV light or electron-beam irradiation20 and
ent toxicities of these two valence states of chro- electrochemical methods.1417 The latter provides an
mium, it is necessary to determine Cr(VI) rather than easy and rapid alternative for the preparation of me-
the total concentration of Cr to estimate the toxicity tallic nanoparticle electrodes in a short span of time.
of the sample. Many sensitive methods have been In our work, nanostructured gold modified glassy
employed for the determination of chromium, such carbon electrode was prepared by the latter method,
as atomic adsorption spectrophotometry,2,3 plasma and it was applied for reduction detection of Cr(VI) in
mass spectrometry,4 spectrofluorimetry,5 chemilu- trace level by adsorptive stripping voltammetric with
minescence,6,7 spectrophotometry,8 but all these the aim of an improved analytical performance (lower
methods are time consuming and need high cost in- LOD and better reproducibility).
strument, and also atomic absorption spectrometry
(AAS) and inductively coupled plasma atomic emis-
sion spectrometry can only yield information on total 2. Experimental
Cr concentration.9 Therefore, electrochemical methods
have been applied for the determination of chromium, 2.1 Apparatus

Square wave voltammetry (SWV) experiments were

*For correspondence conducted using Electrochemical Workstation LK2005

493
494 Benzhi Liu et al

(LANLIK Instruments company, Tainjin, China). 3. Results and discussion

The nanostructured gold modified glassy carbon
electrode and gold electrode (disc diameter of 3 mm) 3.1 Deposition of gold at GCE surface
were used as working electrode with a Ag/AgCl
electrode (saturated KCl) reference electrode, and a It is known that the distribution of gold nanoparticle
platinum wire auxiliary electrode. All pH measure- is important to perform good sensitivity of stripping
ments were made with a Model pHS-23 acidity meter voltammetry. The size, shape and size distribution
(Shanghai Second Analytical Instruments, China). of gold nanoparticles deposited at GCE during the
SEM images were obtained from an XL 30 ESEM process of nucleation followed by particle growth
FEG SEM (Philips, Netherlands) by this procedure. were affected by the concentration of gold salt,
After the nanostructured gold modified GC electrode deposition time and deposition potential.21 To de-
was prepared, the glassy carbon head was taken down posit nanosize gold particles, the KAuCl4 solution was
and pasted onto the sample table of SEM, then SEM made in low concentration. However, if the gold salt
images were recorded. concentration was too low, the nucleation could not
be formed. In this experiment, according to literature,21
2.2 Reagents

Standard solutions of Cr(VI) and Cr(III) (1 gL1),

Potassium tetrachloroaurate(III)trihydrate (KAuCl4),
hydrogen chloride (HCl), and all other compounds
were purchased from Sinopharm Group Chemical
Reagents Co. Ltd, and used without any further puri-
fication. A solution of 50 M KAuCl4 in 01 M
H2SO4 was prepared for a solution stock to deposit
gold at the GCE surface. All reagents used were
analytical reagent-grade and double distilled water
was used throughout.

2.3 preparation of the Aunano/GCE

The glassy carbon electrode was polished with a water

slurry of 05 mm Al2O3, rinsed with ethanol and water
and placed in an ultrasonic bath to remove any re-
sidual polishing material. The GCE was immersed into
KAuCl4 solution and deposition was conducted at
the potential of 04 V (vs Ag/AgCl) for 600 s.

2.4 Measurement procedure

SWVs were performed in 010 M HCl, if not stated

otherwise. The Cr(VI) solutions were spiked into the
cell and accumulation was carried out at 08 V with
stirring. After a 15 s equilibration period, the volt-
ammogram was recorded by applying a negative-
going square wave voltammetric potential scan from
06 to 00 V (with a step potential of 5 mV, ampli-
tude of 25 mV and frequency of 20 Hz). A 35 s con-
Figure 1. (a) SEM images of GCE and (b) gold
ditioning step at +01 V (with solution stirring) was nanoparticle-modified GCE. The GCE was immersed into
used to remove the Cr(VI) residual, prior to the next KAuCl4 solution and electrodeposition was conducted at
cycle. the potential of 04 V (vs Ag/AgCl) for 600 s.
 Determination of trace Cr(VI) 495

a concentration of 50 M gold salt and the deposi- in this work is one of the most extensively studied
tion time of 600 s in H2SO4 were used for all ex- redox couples in electrochemistry2327 and exhibits a
periments. Figure 1 shows the SEM image of gold heterogeneous one-electron transfer (n = 1). C is equal
nanoparticles at the GCE surface. As shown in figure to 10 mM, and the diffusion coefficient (D) is 6057
1, gold nanoparticles can be clearly observed decorat- 106 cm2/s. The value of the electroactive surface
ing the surface of GCE, and the particles were rela- area for optimized Aunano/GCE, and Au electrode
tively uniform, while the formation of gold film or were 041 cm2 and 019 cm2, respectively. A higher
agglomerates was not observed. peak current value also illustrated an increase in the
electroactive surface area for the Aunano/GCE, mainly
3.2 Electrochemical characterization of Aunano/ due to smaller size of Au nanoparticles distributed
GCE on the surface of GCE, which increased the large local
rates of mass transport to the Aunano/GCE.
The high effective surface area of Aunano/GCE was
studied by performing an electrochemical charac- 3.3 Electrochemical response of Cr(VI) on
terization using cyclic voltammetry. Figure 2 shows Aunano/GCE and Au electrode
steady CVs for (1) gold electrode and (2) Aunano/
GCE in 10 mM [Fe(CN)6]3/4 and 02 M KCl at Figure 3 shows the SWVs for 2 g L1 of Cr (VI)
20 mV/s. The well-defined oxidation and reduction determination with a Aunano/GCE (1) and Au electrode
peaks were observed at + 016 V and + 011 V due to (2). a well-defined peak was observed at ca. + 030 V
the [Fe(CN)6]3/4 redox couple in forward and reverse in the cathode scan at Au electrode, which was due
scans. The Aunano/GCE exhibited the high electroac- to the reduction of Cr(VI) to Cr(III), a well-defined
tive area according to the RandlesSevcikequation:22 peak takes 31% peak height enhancement over the
Au electrode was also observed when Aunano/GCE
Ip = 269 105 AD1/2n3/2v1/2 C. was used. The voltammetric current remarkably en-
hanced, which may be attributed to larger effective
In this equation, n is the number of electrons appear- surface area resulting from smaller size of Au nano-
ing in half-reaction for the redox couple, v is the rate particles supported on the surface of GCE. There-
at which the potential is swept (V/s), A is the elec- fore, measurement sensitivity could be improved
trode area (cm2), The [Fe(CN)6]3/4 redox system used by using Aunano/GCE for the determination of Cr
(VI).

Figure 3. SWVs of 2 g L1 Cr(VI) at Aunano/GCE (1)

Figure 2. Cyclic voltammetries of (1) gold electrode and Au electrode (2) in 01 M HCl. Accumulation for
and (2) Aunano/GCE in 10 mM [Fe(CN)6]3/4 and 02 M 80 s at +08 V, SWV detection conditions: step potential,
KCl at 20 mV/s. 5 mV; amplitude, 25 mV; frequency, 20 Hz.
496 Benzhi Liu et al

3.4 SWVs response of Cr(VI) in different acidity became unstable when the accumulation potential
was higher than +08 V, therefore, accumulation po-
The reduction of Cr(VI) was examined in various tential of +08 V was chosen in this experiment to
solutions containing different concentrations of hydro- keep chromium at hexavalent states. The accumula-
chloric acid (010001 M), which correspond to pH tion time was further studied, figure 5 shows the
13, respectively. Figure 4 illustrates the SWVs re- SWVs in various accumulation time in solution
sponse obtained in the solution containing 2 g L1 containing 2 g L1 Cr(VI). It can be seen that the
Cr(VI) in different acidity. It can be seen that the re- response increases nearly linearly with the accumula-
sponse of the Aunano/GCE to Cr(VI) in 01 M HCl tion time up to 80 s accumulation, and levels off
produced a well-defined peak, with a reduction peak thereafter, which reflecting the electrode surface
at +030 V, the sharply decreased peak current was saturation. Therefore, an accumulation time of 80 s
obtained in 001 M and 0001 M HCl in solution was utilized for all further measurements.
containing the same concentration of Cr(VI), with
peak potential at +026 V and +022 V, respectively.
Lower magnitude of reduction current and negative
peak potential indicating a proton-dependent proc-
ess, this is in accordance with the reported work.21
Therefore, the response of the electrode recorded in
0001 M HCl containing 2 g L1 Cr(VI) produced
very little analytical signal, possibly because of the
low concentration of protons.

3.5 Accumulation time

The reduction potential of Cr(VI) to Cr(III) was at

+030 V, in order to detect the whole Cr(VI) in solu-
tion, much higher potential was chosen to keep
chromium at hexavalent states, the accumulation po-
tential from +040 V to +10 V were investigated, re-
sults show that the highest peak current was occurred Figure 5. Effect of the accumulation time upon the re-
sponse to 2 g L1 Cr(VI). Other conditions as in figure 3.
at accumulation potential of +08 V, the peak current

Figure 6. SWVs on Aunano/GCE in 01 M HCl with dif-

Figure 4. SWVs response obtained in the solution con- ferent Cr(VI) concentration. (From 1 to 9: 0; 1; 3; 5; 7; 9;
taining 2 g L1 Cr(VI) in different acidity. Other condi- 11; 13; 15 g L1, respectively. Inset is plot of current ver-
tions as in figure 3. sus Cr(VI) concentration. Other conditions as in figure 3.
 Determination of trace Cr(VI) 497

Table 1. Determination of Cr(VI) in real samples.

This method DTPA method28 Added Found Recovery RSD(%)
Samples (g/L) (g/L) (g/L) (g/L) (%) (n = 5)
Tap water 0156 0151 02 0339 915 57
Sewage water 498 502 50 979 962 46

3.6 Calibration graph 3.8 Analytical applications

Calibration curves for the determination of Cr(VI) This method was applied to Cr(VI) determination in
on the Aunano/GCE was achieved by SWV under op- tap water (our laboratory) and sewage water sample
timal conditions. The SWVs for different concentra- (sewage water treatment station of Huaibei). The re-
tions of Cr(VI) were illustrated in figure 6. The sults are shown in table 1. Agreement between the
resulting calibration plots is linear over the range results obtained by this method with that obtained
from 013 to 45 g L1. The calibration curves and by DTPA method28 for tap water and sewage water
correlation coefficients are y = 0932 + 0115x and shows that this method can be used for determina-
r = 09988 with an accumulation time of 80 s, res- tion of Cr(VI) in real samples. The results show that
pectively. The limits of detection was 001 g L1 this method allows for Cr(VI) determinations with a
based on three times the standard deviation of the much lower detection limit in the presence of excess
baseline. The reproducibility of the electrode as- of Cr(III) than the commonly used DTPA method.28
prepared was estimated from the response to each
2 g L1 of Cr (VI) at 5 different electrodes by differ- 4. Conclusion
ent operating time. This series yield a mean current
response of 138 A, corresponding to relative stan- In this paper, a simple method for the fabrication of
dard deviation (R.S.D.) of 61%. The results demon- nanostructured gold modified glassy carbon elec-
strated that the Aunano/GCE could improve both the trode was presented. It has been shown that, after
sensitivity and the reproducibility for the determina- proper optimization of the experimental conditions,
tion of Cr (VI) by SWV. the electrode prepared was suitable for the determi-
nation of Cr(VI) with high sensitivity and good re-
producibility. The method developed was applied to
3.7 Effect of foreign ions real samples which gave satisfactory results.

The influence of foreign ions on the determination

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