Journal of Nanotechnology

Volume 2014 (2014), Article ID 304526, 7 pages

http://dx.doi.org/10.1155/2014/304526

Research Article

Graphene/Gold Nanocomposites-Based Thin Films as an Enhanced Sensing Platform for Voltammetric Detection of Cr(VI) Ions

Chella Santhosh, Murugan Saranya, Rajendran Ramachandran, Sathiyanathan Felix, Venugopal Velmurugan, and Andrews Nirmala Grace

Centre for Nanotechnology Research, VIT University, Vellore 632 014, India

Received 31 July 2013; Revised 15 November 2013; Accepted 23 December 2013; Published 5 February 2014

Academic Editor: Carlos R. Cabrera

Copyright © 2014 Chella Santhosh et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

A highly sensitive and selective Cr(VI) sensor with graphene-based nanocomposites film as an enhanced sensing platform is reported. The detection of chromium species is a challenging task because of the different possible oxidation states in which the element can occur. The sensing film was developed by homogenously distributing Au nanoparticles (AuNPs) onto the two-dimensional (2D) graphene nanosheet matrix by electrochemical method. Such nanostructured composite film platforms combine the advantages of AuNPs and graphene nanosheets because of the synergistic effect between them. This effect greatly facilitates the electron-transfer processes and the sensing behavior for Cr(VI) detection, leading to a remarkably improved sensitivity and selectivity. The interference from other heavy metal ions is studied in detail. Such sensing elements are very promising for practical environmental monitoring applications.

1. Introduction

Heavy metal ions are paid more attention in environmental, toxicological, pharmaceutical, and biomedical analysis point of view [1–3]. Among those, the detection of chromium is of particular interest owing to the high toxicity of chromium (VI) ions. The detection of chromium species is a challenging task because of the different possible oxidation states of the element. The most common valences are 0, +II, +III, and +VI. The two environmentally relevant valence states of chromium, namely, Cr(III) and Cr(VI), have a contrasting impact on environment and health. Trivalent chromium is relatively harmless, plays an essential role in biological processes, and is related to human glucose tolerance [4], whereas hexavalent chromium is about 100–1000 times more carcinogenic and toxic [5] because of its high oxidation potential and is limited in groundwater by WHO provisional guideline value of 0.05 mg L⁻¹ (50 ppb) [6]. The main sources of anthropogenic chromium pollution in ground water are plating industries, cooling towers, timber treatment [7], leather tanning, wood preservation, and steel manufacturing [8]. The major toxic effects of Cr(VI) are chronic ulcers, dermatitis, corrosive reaction in nasal septum, and local effects in the lungs [9].

There are several approaches for the detection of Cr(VI) ions like atomic absorption spectroscopy (AAS) [10], inductively coupled plasma atomic emission spectrometry (ICP-AES) [11], inductively coupled plasma mass spectroscopy (ICP-MS) [12], and colorimetry with 1,5-diphenylcarbazide [13] for the environmental analysis of chromium. To determine the total concentration of chromium, these methods are sensitive and accurate but they are time-consuming and expensive and require sophisticated techniques. Electrochemical methods are chosen for analytical purpose, as they are reliable and sensitive and require less expensive equipment [14, 15]. Voltammetric methods have been described in the literature for the detection of Cr(VI) using metallic nanoparticles modified carbon screen-printed electrodes [16], pyridinium-based sol-gel film [17], self-assembled monolayer [18], and modified electrodes [19, 20]. Metal nanoparticles have been extensively used in recent years for the development of highly sensitive nanodevices because of their unusual physical and chemical properties. Zayats and coworkers have successfully utilized the nanosized Au particles in the development of versatile biosensors [21]. The electrodeposited Au nanoparticles have been used for the detection of arsenic [22]. However, Au nanoparticles have not been used for the detection of carcinogenic Cr(VI), because Au is known to be very sensitive towards Cr(VI). Considering the importance of the measurement of Cr(VI) in groundwater, in the present investigation we have utilized Au nanoparticles for the voltammetric detection of Cr(VI).

Graphene, a single layer of sp² hybridized carbon atoms packed into a dense honeycomb two-dimensional lattice, has attracted tremendous attention from both experimental and theoretical scientific communities since it was experimentally produced in 2004 [23, 24]. Graphene-based materials hold great promise in fabricating enhanced electrochemical-sensing platforms. However, graphene-based nanocomposite film has never been used for the determination of Cr(VI). Herein, we report on an ultrasensitive Cr(VI) sensor by using nanocomposite film of monodispersed Au nanoparticles and graphene as the powerful platform. Uniform AuNPs were homogenously distributed onto the graphene nanosheet matrix, constructing a monodispersed AuNPs-based ensemble. It is worth noting that the as-prepared composite matrix in this work combines the advantages of the graphene nanosheets (unique electrical conductivity and enlarged active surface area) together with AuNPs (extraordinary catalytic activity and good conductivity). This should greatly facilitate the rapid, stable and sensitive measurement of Cr(VI). The performance of this novel platform for voltammetric detection of Cr(VI) is investigated in detail. Encouragingly, such a nanostructured composite film offers a remarkably improved sensitivity and selectivity and exhibits fine applicability for the detection of Cr(VI) in practical water samples.

2. Materials and Methods

2.1. Materials

Graphite powder, HAuCl₄4H₂O, polyvinylpyrrolidone (PVP), sodium nitrate, sulphuric acid (98%), potassium permanganate, hydrogen peroxide (30%), and hydrazine hydrate (35%), chitosan were purchased from SD-Fine, India. All reagents were of analytical reagent grade and were used without further purification. All the reagents were prepared using Milli-Q water.

2.2. Synthesis of Graphene Oxide

Graphene oxide was prepared from natural graphite powder using modified Hummers Jr. and Offeman method [25] as follows. In a typical synthesis, 1 g of graphite and 1 g of NaNO₃ were mixed with 46 mL of H₂SO₄ (98%) in a 250 mL flask in an ice bath. To it, 6 g of KMnO₄ was slowly added at below 20°C with vigorous stirring. The resulting mixture was stirred at room temperature for 1 h, diluted with 70 mL of water, and stirred at 95°C for 2 h. Then, the mixture was further diluted with 100 mL of water and deoxidized with 7 mL of H₂O₂ (30%). Finally, the product formed in the solution was separated out by centrifugation at 7000 rpm and then repeatedly washed with 600 mL of water for six times until the pH of supernatant was neutral. The graphene oxide (gray powder) was obtained by drying the product in vacuum at 60°C for 24 h.

2.3. Preparation of PVP Protected Grapheme

PVP protected graphene is prepared from the as-synthesized graphene oxide. In a typical synthesis, 100 mg of graphene oxide was dispersed in 50 mL of water containing 2.5% polyvinylpyrrolidone (PVP). Then, 0.2 mL of hydrazine hydrate (35%) in water was added with a subsequent addition of 1.5 mL aqueous ammonia (28%) into the graphene oxide solution. After the solution was held at 95°C for 1 h, the product formed in the solution was separated by centrifugation and washed with 100 mL of water for six times. Finally, graphene was obtained by drying the product in vacuum at 60°C for 24 h.

2.4. Fabrication of the Au@Graphene Films

Ultrasonic agitation for ca.30 min was used to disperse 4 mg of PVP protected graphene nanosheets into 0.5 mL of 0.03 mgm⁻¹ chitosan. Prior to the surface modification, the bare Au electrode was polished carefully with 0.05 μm alumina powder, rinsed with deionized water, followed by sonication in acetone and doubly distilled water successively, and dried under nitrogen. 20 μL of the resulting chi-graphene dispersion was dropped onto the surface of the cleaned gold electrode with a geometric surface area of 0.0707 cm² and was dried at room temperature (labeled as chi-graphene/Gold Electrode). Further modification of AuNPs onto chi-graphene/gold electrode was conducted by CV scanning from 0.2 to 1.0 V in 0.1 M KCl solution containing 2 mM HAuCl₄ at a scan rate of 50 mV/s for 8 cycles. After modification, the electrode (denoted as AuNPs-chi-graphene/Gold Electrode) was thoroughly rinsed with water and kept at room temperature for further use. The amount of Au loaded on the graphene matrix was calculated to be 0.746 wt%.

2.5. Instruments

The phase and the crystallographic structure were identified by X-ray diffraction (XRD, Philips X’Pert Pro, Cu-Kα: λ = 0.1540598 nm). The particle size and morphology of the products were studied by FE-Scanning Electron Microscopy (FE-SEM) (HITACHI SU6600 SEM). FT-IR spectra were recorded for studying the functional groups using KBr disks on a Shimadzu affinity spectrophotometer.

2.6. Electrochemical Setup

Electrochemical measurements were performed using CHI 660C model using a three-electrode type electrochemical cell. A three-electrode system was employed with a SCE-sat.KCl as reference electrode, a platinum wire as counter electrode and AuNPs-chi-graphene modified Au as working electrode respectively.

3. Results and Discussion

3.1. XRD Spectrum

X-ray diffraction (XRD) pattern of raw graphite and graphene oxide is shown in Figure 1. In Figure 1(a), raw graphite has XRD diffraction peaks at 26.4, 44.3, and 54.5° corresponding to the hexagonal lattice of (002), (101), and (004) planes with an interplanar distance of 0.338 nm. After oxidation, the intense (002) peak of graphite powder disappears and an additional peak at 10.94° is observed, which corresponds to the (001) diffraction peak of graphene oxide. Graphite powder shows a sharp (002) peak at 26.4° with a typical interspacing of 3.38 A°; however, it is found that GO exhibits a strong peak at 10.94° corresponding to the (001) interplanar spacing of 8.2 Å, suggesting that graphite has been successfully oxidized by modified Hummers Jr. and Offeman method. The increase in interplanar distance in GO might be due to the presence of oxygen, carboxyl, and other functional groups in graphene oxide [26]. Oxidation of graphite leads to the increase in d-spacing, which can be attributed to the oxide induced oxygen containing functional groups and inserted water molecules.

Figure 1: XRD pattern for (a) raw graphite and (b) graphite oxide.

3.2. Morphology Characterization

The morphology of the AuNPs-chi-graphene was analyzed by SEM analysis. Figure 2 shows the corresponding FE-SEM image of AuNPs-chi-graphene deposited on ITO glass. From the image, it can be seen that the particles are deposited within the graphene matrix. Graphene seems to be crumbled and coiled and within the matrix, particles of Au are seen embedded.

(a)

(b)

(c)

(d)

Figure 2: FE-SEM images of AuNPs-chi-graphene deposited on ITO substrates at various magnifications.

3.3. Electrochemical Studies

3.3.1. Electroactivity of the Chromate Species-Electrolyte Analysis

An initial study of the reduction of Cr(VI) was carried out using cyclic voltammetry at gold (Au) and glassy carbon (GC) electrode materials at pH 1 (CVs not shown). When compared to GC electrode, Au electrode gave good response and because of this Au electrode was chosen for further investigations. Before probing the chromium detection, bare Au electrodes were tested by running a CV in two different electrolytes, namely, 0.1 M and 0.01 M HCl. To choose the pH of the electrolyte, CVs were run in different electrolytes, namely, 0.1 M and 0.01 M HCl. Figure 3 shows the corresponding cyclic voltammetry curves plotted as current versus potential obtained for 0.1 M HCl and 0.01 M HCl electrolyte using bare gold (Au) electrode at a scan rate of 50 mVs⁻¹. There were not any peaks except for the peak at higher potentials corresponding to the formation of Au oxides. The CV for 0.01 M HCl showed a large capacitive current and, in this regard, the detection of Cr(VI) ions will be uncertain. From the figure, it can be seen that 0.1 M HCl gave good response and hence 0.1 M HCl was taken as the standard electrolyte system.

(a)

(b)

Figure 3: Voltammetric responses of bare gold (Au) electrode in different electrolytes: (a) 0.1 M HCl and (b) 0.01 M HCl, respectively (scan rate = 50 mVs⁻¹).

3.3.2. Electrochemical Reduction of Cr(VI) Using Bare Au Electrode

Before probing the role AuNPs-chi-graphene modified electrode, bare Au electrode was checked for Cr(VI) ions reaction analysis. Figure 4 shows the corresponding cyclic voltammetry plotted as current versus potential in 0.1 M HCl electrolyte containing 200 μM Cr(VI) using bare gold (Au) electrode at a scan rate of 50 mVs⁻¹. It can be seen that the response of gold electrode to Cr(VI) in 0.1 M HCl gave a well-defined reduction peak at +0.314 V. The shape of the voltammogram might be preliminarily attributed to an electrochemically reversible process, whilst the absence of corresponding oxidation peak in the potential range studied indicates a chemically irreversible reaction.

Figure 4: Cyclic voltammograms detailing response of a bare Au electrode to 200 μM Cr(VI) in 0.1 M HCl (scan rate = 50 mVs⁻¹).

3.4. Electrochemical Reduction of Cr(VI) Using AuNPs-Chi-Graphene/Gold Electrode

3.4.1. Electrodeposition of Au Nanoparticles on Modified Gold Electrode

Figure 5 shows the CVs during electrodeposition of Au nanoparticles onto graphene modified Au electrode in 0.1 M HCl at a scan rate of 50 mVs⁻¹. Electrodepositing Au nanoparticles on the graphene modified Au electrode will facilitate the uniform dispersion of Au nanoparticles onto graphene matrix. Figure 5 shows the CV recorded during the course of electrodeposition of Au nanoparticles. From the figure, it can be clearly seen that a well-defined reduction peak with a peak potential at +0.34 V (versus SCE) is observed. This peak corresponds to the Au oxide/reduction peak, confirming that Au nanoparticles are deposited onto the graphene modified electrodes. The shape of the voltammograms might be preliminarily attributed to an electrochemical reversible process, whilst the absence of corresponding oxidation peak in the potential range studied indicates a chemically irreversible reaction.

Figure 5: Voltammetric responses during the deposition of Au nanoparticles to chi-graphene/gold electrode in 0.1 M HCl (scan rate = 50 mVs⁻¹).

3.4.2. Electrochemical Reduction of Cr(VI) on Modified Au Electrode

Figure 6 shows the corresponding cyclic voltammetric run in 0.1 M HCl containing 200 μM Cr(VI) using AuNPs-chi-graphene modified gold (Au) electrode at a scan rate of 50 mVs⁻¹. As can be seen, the response obtained at the modified gold (Au) electrode consists of a peak at +0.46 V. Comparing both modified and unmodified electrodes, the peak potential is quite good at the modified Au electrode which increases the sensitivity of hexavalent chromium ions. A comparison of unmodified and AuNPs-chi-graphene modified Au electrode (Figures 4 and 6) reveals that the reduction is enhanced 100 times in the presence of graphene/gold modified electrode surfaces. Compared to the bare Au electrode, the nanoparticle-modified electrodes exhibited typical voltammetric response for Cr(VI). The AuNPs-chi-graphene modified Au electrode shows well-defined voltammetric peaks for Cr(VI) at 0.4 V. The voltammetric response obtained is ascribed to the three-electron reduction of Cr(VI) to Cr(III). The unmodified Au electrode shows a reduction peak at 0.3 V. The shift in the reduction potential and increase in the peak current with respect to the unmodified electrode imply that the nanosized particles on graphene matrix efficiently catalyze the reduction of Cr(VI).

Figure 6: Cyclic voltammogram response of AuNPs-chi-graphene/gold electrode to 200 μM Cr(VI) in 0.1 M HCl (scan rate = 50 mVs⁻¹).

The voltammetric responses of 50 μM hexavalent chromium in 0.1 M HCl at various scan rates of 10 mV, 30 mV, 50 mV, 200 mV, and 400 mV were examined by cyclic voltammetry using modified gold electrode as shown in Figure 7. These reveal process with a peak potential at +0.46 V (100 mVs⁻¹), which was found to shift up to +0.4 V (400 mVs⁻¹) as the scan rate increases. The fact that peak potential is dependent on scan rate suggests that reaction is electrochemically reversible at the Au electrode.

Figure 7: Cyclic voltammograms detailing the response to different scan rates (10–400 mVs⁻¹) for the solution containing 50 μM Cr(VI) in 0.1 M HCl at a modified Au electrode.

In order to further validate the diffusional nature and, in particular, to test the analytical applicability of the reduction process, the response of Au electrode to increasing additions of Cr(VI) (5–800 μM) in 0.1 M HCl was examined. A plot of the change of reduction peak current as a function of hexavalent chromium added to the solution was found to be linear in the concentration range studied (slope = 1.313 and = 0.9756) consistent with a diffusion-controlled reaction (see Figure 8).

Figure 8: A plot of change in reduction current versus hexavalent chromium ion concentration.

4. Conclusions

The reduction of hexavalent chromium was examined at modified and unmodified gold electrodes. It was found that modified gold electrode (AuNPs-chi-graphene modified Au electrode) provided good voltammetric responses towards the addition of Cr(VI) in the electrolyte solutions. It was also verified that, in the presence of grapheme-/gold-based electrodes, the reduction process occurs at more positive potential when compared with that of unmodified gold electrode. The response of the electrode to addition of hexavalent chromium was found to be independent of common environmental interferences, such as Ni, Cu, and Cr(III). This investigation proved that the composites are good materials for electrochemical sensing of chromium ions.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The authors acknowledge the financial support of VIT University, Vellore, for supporting this work under the research associate fellowship. They thank DST-WTI, Government of India, for supporting this work under the Junior Research Fellowship.

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