Research Article | Open Access
Ruma Gupta, Kavitha Jayachandran, J. S. Gamare, B. Rajeshwari, Santosh K. Gupta, J. V. Kamat, "Novel Electrochemical Synthesis of Polypyrrole/Ag Nanocomposite and Its Electrocatalytic Performance towards Hydrogen Peroxide Reduction", Journal of Nanoparticles, vol. 2015, Article ID 149406, 6 pages, 2015. https://doi.org/10.1155/2015/149406
Novel Electrochemical Synthesis of Polypyrrole/Ag Nanocomposite and Its Electrocatalytic Performance towards Hydrogen Peroxide Reduction
A simple electrochemical method of synthesis of polypyrrole/silver (PPy/Ag) nanocomposite is presented. The method is based on potentiodynamic polymerization of pyrrole followed by electrodeposition of silver employing a single potentiostatic pulse. The synthesized PPy film has embedded Ag nanocubes. The morphology and structure of the resulting nanocomposite were characterized by field emission scanning electron microscopy and X-ray diffraction. Electron paramagnetic resonance studies showed that silver nanoparticle deposition on polypyrrole leads to an increase in carrier density, indicative of enhanced conductivity of the resulting composite. Electrocatalytic performance of the prepared composite was examined for reduction of hydrogen peroxide and was compared with corresponding PPy film and bare glassy carbon electrode.
In recent years, the electrically conducting composites have attracted attention of researchers because of their potential applications in various fields, such as sensors, actuators, and electric devices [1–4]. These include electrically conducting polymers such as polypyrrole (PPy) [5, 6], polyaniline [7–9], polythiophene , poly(3,4-ethylenedioxythiophene) , and poly(p-phenylene vinylene) . PPy is known as one of the most important conducting polymers owing to its high conductivity, easy preparation, good environmental tolerance, and a large variety of applications . Various nanoparticles of different metals such as Au, Ag, Pd, Cu, and Pt can be incorporated into the polymer matrix to obtain a composite material with new properties [14–17]. Chemical and electrochemical polymerizations are used to prepare conducting polymer composites. One possible way of preparation of nanocomposite material is to use a spontaneous redox reaction of monomer and metal ion, sometimes in the presence of supporting reagent [18–20]. Another one is the chemical polymerization of monomer dissolved in a solution of colloidal metal particles in the presence of an oxidant [21, 22]. Metal nanoparticles/conducting polymer composites can also be obtained by using the electrochemical methods. These methods of preparation give a possibility of better control of the synthesis process compared to the chemical methods, because the structure, quantity, and properties of both electrodeposited components, that is, nanoparticles and polymer, depend not only on the composition of the solution, but also on the electrolysis potential and time [23, 24]. Electrochemical deposition is advantageous because of the least requirement of the additives and absence of any interfering products generated during the electrodeposition of silver metal. It is interesting to note that the deposition of Ag nanoparticles on polypyrrole film has not been attempted electrochemically so far. To the best of our knowledge, this is the first effort for the electrosynthesis of polypyrrole and then electrochemically depositing Ag nanoparticles on it. Such approach, in comparison with DC deposition, permits obtaining a more homogeneous polymer surface  and more homogenously distributed silver grains . This necessitates the optimization of different parameters to achieve the desired quality of the polypyrrole film and silver nanoparticles. It was, therefore, of interest to develop a strategy for the electrochemical synthesis of Ag nanoparticles on a polypyrrole film and their characterization. The results of these studies are reported in this paper.
All the chemicals, namely, pyrrole (C4H5N), sulphuric acid (H2SO4), potassium chloride (KCl), silver nitrate (AgNO3), and hydrogen peroxide (H2O2), were of GR (Guaranteed Reagent) grade. Cyclic voltammetry (CV), chronoamperometry, and differential pulse voltammetry were performed using CHI 760D electrochemical workstation with a three-electrode voltammetric cell having glassy carbon disk working electrode (area, cm2), platinum wire counter electrode, and Hg/Hg2SO4 reference electrode. All potentials are quoted with respect to Hg/Hg2SO4 reference electrode. All the experiments were carried out at room temperature (). Morphology of the composite was recorded by Auriga make field emission scanning electron microscope (FESEM). X-ray diffraction (XRD) patterns were recorded in air atmosphere by STOE-Theta-X-ray diffractometer using graphite monochromatic Cu Kα radiation ( nm). Electron paramagnetic resonance (EPR) measurements were done at room temperature using Bruker EPR spectrometer operated at X-band frequency (9.6 GHz). Polypyrrole (PPy) film was electrodeposited onto glassy carbon electrode by optimized procedure from aqueous 0.06 M pyrrole solution, using 0.1 M KCl as supporting electrolyte by potentiodynamic polymerization of pyrrole. A potential sweep from −0.9 V to 1 V was applied at a scan rate of 100 mV s−1 to the working electrode for a total of 30 sweep segments. 1 mM aqueous solution of AgNO3 containing 1 M H2SO4 was used to deposit silver nanoparticles onto PPy modified working electrode by applying a fixed potential of −0.38 V for 10 seconds.
3. Results and Discussion
Figure 1 shows FESEM images of PPy film formed by potentiodynamic growth before (a) and after (b) electrodeposition of silver nanoparticles. The polymer exhibits the typical cauliflower-like nodular morphology. More changes in the structure and surface composition of the PPy/Ag could be noticed by using SEM backscattered electron detector (Figure 2). The contrast visible in the images reflects the surface composition of the material. The bright objects correspond to the positions where the silver structures are present, and the dark area is related to the polypyrrole matrix. Powder XRD pattern shown in Figure 3 also confirmed the presence of silver in the nanocomposites. All the diffraction peaks could be indexed to the cubic phase of silver (JCPDS card number 87-0717) having fcc lattice. The crystallographic data of the relatively intense peak () was indexed on a cubic system with space group Fm-3m and cell parameter Å. The XRD data are given in Table 1.
EPR spectrum of PPy (Figure 4(A)) showed a single Lorentzian line with a slight asymmetry line shape, asymmetry parameter as shown in Figure 4 at indicating the presence of polaron (charge carrier with spin due to unpaired electron). This value is close to the free electron value (). The small increase in value observed for PPy/Ag indicates that the unpaired electrons are present in the electron system for the conjugated polymers . Upon electrodepositing silver on polymer matrix, the EPR signal became more symmetric (). It was observed that Ag deposition leads to a corresponding increase in the area under the peak computed by double integration of the signal. This proves an increase in carrier density of the composite which is responsible for enhancement of catalytic activity . Figure 5 shows the schematic diagram of electrode modification process with polypyrrole and silver nanoparticles and its electrocatalytic application for hydrogen peroxide reduction.
Cyclic voltammetry (CV) was employed to monitor the polymerization of PPy and to investigate the kinetics of electrode process for electropolymerization. Figure 6 shows the first 15 cyclic voltammograms obtained during the potentiodynamic growth of PPy on a 3 mm diameter GC disc electrode as the potential was swept from −0.9 V to 1 V. The cathodic peaks obtained were significantly broader than the anodic peaks. The voltammograms are consistent with those reported previously . On the first scan, a single anodic wave was typically observed at approximately +0.5 V which is consistent with the oxidation of pyrrole monomer to produce the radical cation . On the second scan and all the subsequent oxidative scans, a new anodic wave is observed that is consistent with the oxidation of the newly formed polymer between −0.1 V and 0.5 V [29, 30]. With each successive scan, the peak current associated with the anodic as well as the cathodic peaks of the polymer increased and an increasingly thick, dark black coloured film was observed on the working electrode. The increase in charge passed between each cycle was approximately constant suggesting that the growth rate of the polymer is approximately constant. Depositing silver nanoparticles within the PPy film provides a convenient way to increase the area available for the electrocatalysis to take place and may improve the film conductivity.
Figure 7(a) shows CV of 1 mM aqueous solution of AgNO3 containing 1 M H2SO4 at PPy modified electrode. Based on the CV results, −0.38 V was chosen as the optimized potential to deposit silver nanoparticles. Differential pulse voltammogram (DPV) shown in Figure 7(b) was obtained with PPy/Ag composite electrode in 1 M H2SO4. The anodic peak observed at −0.068 V is responsible for the stripping of Ag+ from metallic Ag nanoparticles. This further confirmed the presence of Ag at polypyrrole matrix.
The electrochemical behavior of the synthesized PPy and PPy/Ag was examined by cyclic voltammetry to catalyse reduction of hydrogen peroxide. Figure 8 shows the cyclic voltammograms of bare-GC, PPy-GC, and PPy/Ag-GC coated electrodes in presence of 0.4 mM H2O2 in 1 M H2SO4. It is clearly seen that when bare glassy carbon electrode was used, no well-defined peak with very small current was observed in presence of H2O2. For PPy-GC electrode, although the current was high enough no substantial peak was seen for the reduction of hydrogen peroxide. Only a broad cathodic peak was observed between −0.5 V and −0.6 V. When silver nanoparticles were embedded in polypyrrole film (PPy/Ag), the silver modified PPy film electrode exhibited a considerable electrocatalytic behaviour towards the reduction of hydrogen peroxide and a reduction peak appeared at about −0.08 V () versus Hg/Hg2SO4 reference electrode. Another cathodic peak at around 0.2 V () was attributed to the reduction of AgOH in the PPy film. Typically, this reduction is preceded by uptake of H+ ions during reduction of PPy. We can conclude that, after addition of hydrogen peroxide to the solution, silver dispersed in the PPy film reacts chemically with hydrogen peroxide according to the following equation :
Step 1The second step is electrochemical reduction of silver hydroxide (peak ):
Step 2The peak present at 0.5 V is attributed to AgO stripping peak ().
Fabrication of PPy/Ag composite through electrosynthesis of polypyrrole and then electrochemically depositing Ag nanoparticles is presented. Such approach, in comparison with DC deposition, permits obtaining a more homogeneous polymer surface and more homogenously distributed silver grains. FESEM, XRD, and electrochemical measurements indicate that Ag/polypyrrole nanocomposite is successfully prepared in our experiments. This further showed electrocatalytic performance towards hydrogen peroxide reduction. We believe that the present method could be exploited for the fabrication of novel and inexpensive hydrogen peroxide sensor.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
The authors sincerely thank Dr. C. B. Basak of Glass and Advanced Ceramic Division, BARC, and Dr. Meera Keskar, Fuel Chemistry Division, BARC, for experimental support.
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