Ion-Imprinted Electrochemical Sensor Based on Copper Nanoparticles-Polyaniline Matrix for Nitrate Detection

1Laboratory of Interfaces and Advanced Materials, University of Monastir, Faculty of Sciences of Monastir, 5000 Monastir, Tunisia 2Laboratoire Matériaux, Traitement et Analyse, INRAP, Biotechpole Sidi-Thabet, 2020, Ariana, Tunisia 3Université de Tunis El Manar, Faculté des Sciences de Tunis, Campus Universitaire Farhat Hached, 1068 Tunis, Tunisia 4Chair for Measurement and Sensor Technology, Technische Universitat Chemnitz, Reichenhainer Str. 70, 09126 Chemnitz, Germany


Introduction
Nitrate is recognized as a significant contaminant in ground water because of its high environmental and human health risks.It is mostly present in aquatic ecosystems and food products [1][2][3].The Environmental Protection Agency (EPA) recommended maximum limit for nitrate concentration in drinking water is 10 mg.L −1 [4,5].The negatively charged nitrogen oxide compound NO 3 − can accelerate the growth of algae and, thus, causes lakes and rivers eutrophication.Several studies revealed that the presence of higher levels of nitrate in drinking water leads to harmful diseases such as methemoglobinemia [6][7][8], gastrointestinal tumors [9], and stomach cancer [10][11][12].Moreover, nitrate can be readily reduced to nitrites and ammonia, even more toxic, by microbial reduction in food products [13].These compounds can also cause a large decrease in oxygen carrying capacity of hemoglobin, which may lead to death.Generally, the levels of nitrate are measured with analytical techniques such as ultraviolet (UV) spectrometry [14,15], ion chromatography [16,17], Raman spectroscopy [18], chemiluminescence [19], and electrochemical techniques [20][21][22], but most of these methods have few disadvantages, related to high instruments cost, low reproducibility, and time consuming [23].Therefore, it is needful to establish an easy, rapid, and credible method to detect nitrate in water.For emphasizing these matters, Molecular Imprinting technique has induced a considerable research interest thanks to its good manageability, innocuous nature, high selectivity, low cost, high stability, and quick response [24,25].This technique is based on a complex formation between a template molecule and monomer(s) and, then, the use of this template as an artificial receptor to produce cavities which are able to recognize only the same template molecule of interest.The same strategy is obedient to the selective recognition of ions.[26,27].Up to now, surface ion imprinting technique has found interesting applications in sensors, membrane separation of imprint metal ions, and solid-phase extractions [28,29].Over the last few years, various materials involving conductive polymers, carbon nanotube metal, metal oxide nanoparticles, and graphene have been explored for the modification of the electrode aiming at increasing the sensitivity and selectivity of the imprinted electrochemical sensor.Among the materials used for the electroreduction of nitrate, polyaniline (PANI) is one of the most conducting polymers in the field of electrochemical sensing.PANI is considered as metal nanoparticles stabilizer and a good electrocatalyst due to its high chemical stability, high conductivity, low cost, and environmental stability [30][31][32].It has been demonstrated that copper nanosheets on WO 3 /PANI composite can be used to detect the reduction of nitrate with a good sensitivity and low detection limit [33].In comparison with conventional methods, electrochemical deposition is simple, convenient, and reproducible for the deposition of IIP film on the surface of the electrode.Similarly, as far as the electrochemical reduction of nitrate is concerned, metal nanoparticles such as palladium [34], rhodium [35], copper [36], platinum [37], and silver [38,39] can not only offer marked improvements in sensitivity and selectivity but also be manufactured easily and reproducibly.Therefore, this kind of catalyst has been widely studied and used in electrochemical sensors for nitrate detection.Copper nanoparticles have been vastly used in electrode modification thanks to their extraordinary catalytic activities, good electrical properties, biocompatibility, large specific surface area, and high conductivity [40,41].Indeed, many chemically modified coppers metal nanoparticles in non-IIP films have recently been reported for the detection of nitrate ions in different environments.Some researchers have demonstrated that copper nanoparticles electrochemically deposited on platinum electrode are useful in the detection of nitrate ions.In this work, we report a novel, rapid, and highly sensitive ion-imprinted electrochemical sensor based on copper nanoparticles and polyaniline (Cu-NPs/PANI) nanocomposites for the determination of nitrate ions.The electrochemical behavior of the deposit matrix on the electrode surface was investigated by cyclic voltammetry, electrochemical impedance spectroscopy, and linear sweep voltammetry.The proposed sensor exhibits good analytical performances such as sensitivity, selectivity, and high binding affinity toward nitrate determination., and CO 3 2− were all obtained from Sigma-Aldrich.Ferricyanide (K 4 (Fe(CN) 6 ) and ferrocyanide (K 3 (Fe(CN) 6 ) were obtained from Fluka.All chemicals used in this work were of analytical grade and used as received without further purification.

The Preparation of Ion-Imprinted Electrodes toward
Nitrate Ions.Cyclic voltammetry and linear sweep voltammetry were performed using a potentiostat (DY200 POT Ecochimie) and an Autolab PGSTAT 320N potentiostat for electrochemical impedance measurements controlled by a computer using commercially available Nova version 1,5 software.The UV-Visible absorbance spectra were recorded in 67 series spectrophotometers models 6705 UV/Vis JENWAY ON indium-tin oxide (ITO) glass (10 ohm/mm) as working electrode to study UV-Visible spectral behavior.A typical three-electrode system was chosen to perform electrochemical measurements; a rotating glassy carbon electrode disk (GCE s ) was used as a working electrode, Ag/AgCl/3M KCl electrode as a reference electrode, and a Pt wire as a counter electrode.

Modification of the Working Electrode.
Before the modification of the working electrode, it was hand-polished with 1 and 0.05 휇m alumina-water slurry using a polishing cloth, washed, and then sonicated in acetone for 5 min to remove adsorbed particles.To ensure a clean surface, the bare GC disk electrode was rinsed with ultrapure water and subjected to 0.5 M sodium hydroxide by cycling the potential between 0.2 and 1.4 V until a stable cyclic voltammogram was obtained.The cleaned electrode was dried in air before use.The modification process consists in electrodepositing a fresh copper layer using the chronoamperometry method, onto the GCE surface by applying a potential step of -0.2 V for 120s in 0.1 M of Na 2 SO 4 solution.After depositing the copper layer on the GCE, it was rinsed with deionized water and allowed to dry in air.After deoxygenating the solution by bubbling nitrogen gas for about 10 min, the IIP was prepared by electropolymerization of 0.1 M of aniline in 0.5 M H 2 SO 4 solution as supporting electrolyte in presence of 1mM of sodium nitrate as template onto the Cu-NPs/GCE, through cyclic voltammetry by applying 10 successive polymerization cycles from -0.2 V to 1V with a scan rate of 100 mV/s.During the electrochemical polymerization process, the surface of the Cu-NPs/GCE gradually becomes green indicating the deposition of the PANI/NaNO 3 film.The resulting IIP-Cu-NPs/PAN/GCE was thoroughly washed with distilled water to remove unbound matter.The recognition sites in the imprinted matrix were formed after removing the template from the imprinted film.Therefore, the selection of a suitable solution and method to completely elute the template from the imprinted film is very important.To remove the nitrate ions the modified sensor was immersed in a solution of hydrochloric acid (0.5M) for 24 hours, leaving an impression on the surface shape corresponding to the template shape.Then, the imprinted Cu-NPs/PAN/GCE was rinsed with distilled water and dried under nitrogen for the following experiments.As a control, the nonimprinted polymer modified electrode (NIP) was also prepared using the same procedure but without nitrate.

Real Samples Preparation.
Water samples were used for environmental sample testing.The well water and mineral water were used without any pretreatment.The samples were first filtered and mixed with 0.1M Na 2 SO 4 electrolyte solution (pH=5).The water samples were spiked with NO 3 − .EIS method was employed to electrochemically detect nitrate, at optimum conditions.

Results and Discussion
3.1.Characterization of IIP.New ion-imprinted polymer for the electrochemical detection of nitrate was synthesized and characterized.In the first step Copper NPs were electrodeposited on the GCE surface via chronoamperometry technique by using CuSO 4 .As sensing substrate, the obtained nanoparticles further exhibited excellent benefit for the electropolymerization of PANI owing to the good absorption between the Cu-NPs and the PANI polymer.In the second step the electrodeposition of PANI on the modified electrode through cyclic voltammetry technique with good stability mechanical flexibility and electrical conductivity was successfully achieved on Cu-NPs coated electrode surface.The overall modification process was schematically presented in Scheme 1.In order to characterize the prepared copper nanoparticles and molecular imprinted films, different techniques involving SEM and UV-vis were conducted.

Morphological Characterization (SEM).
To investigate the morphology of the modified GCE surface, SEM images were recorded.Figure 1 displays the SEM images of the GCE/Cu-NPs (a, b), the GCE/Cu-NPs/PANI (c, d), the NIP-GCE/Cu-NPs/PANI (e), and the IIP-GCE/Cu-NPs/PANI (f), respectively.Clear changes in the surface morphology of the GCE before and after the surface modification were observed.Figures 1(a) and 1(b) show typical SEM images of electrodeposited copper nanoparticles with small white spots and a uniform size distributed homogeneously on the GCE surface.
From Figures 1(c) and 1(d), it is clearly observed that the electropolymerized polyaniline film grown on the GCE/Cu-NPs surface exhibited a net structure change.Since PANI film was grown on the surface of Cu-NPs modified electrode, the film became more uniform and porous.The typical features corresponding to Cu-NPs are identified in Figure 1(d).Figures 1(e) and 1(f) illustrate the SEM images of the imprinted films modified with GCE/Cu-NPs/PANI before and after removing the template, respectively.Their surface morphologies were different, which indicates the exclusion of the template from the matrix.After the removal of NO 3 − ions (Figure 1(f)), the imprinted surface was extremely rough, with polymer decorated with the copper nanoparticles.In contrast, before the removal of NO 3 − ions, NO 3 − imprinted pores appeared on the surface of the electrode as shown in Figure 1(e).The roughness of the IIP membrane enhances the sensitivity and the rebinding efficiency of the sensor.

Ultraviolet-Visible Studies.
Figure 2 shows the UV-Vis spectrum of Cu-NPs, Cu-NPs/PANI, NIP-Cu-NPs/PANI, and IIP-Cu-NPs/PANI.The UV-Vis spectrum of Cu-NPs displays an absorption band in the range of 386-475 nm which is a characteristic band of copper nanoparticles which confirms the formation of metal nanoparticles.After the addition of PANI, the intensity of the peak at 475 nm increased and two new peaks appeared at 272 and 790 nm, respectively.The peak at 272 nm is attributed to the 휋 -휋 * transition of the benzenoid ring.The peaks at 475 and 790 nm are assigned to the polaron transition of the PANI matrix [45][46][47].A more significant change is observed in the composite spectrum as compared to Cu-NPs alone.The UV-Visible spectra of NIP-Cu-NPs/PANI and IIP-Cu-NPs/PANI are shown in Figure 2.After the incorporation of NO 3 − ions into the composite matrix, the intensity of the peak with 휆 max around 475 nm decreased as compared to that of Cu-NPs/PANI, which reveals the intercalation of the NO 3 − ions.In addition, a bathochromic shift from 272 to 325 nm indicates the strong interaction between the composite matrix and NO 3 − .After the removal of NO 3 − ions from the composite matrix, the spectrum being identical to that obtained for the Cu-NPs/PANI matrix without template.This result corroborates the formation of artificial complementary sites to recognize NO 3 − ions in solution.
(a)  surface of the electrode was thicker, uniform, conductive, and electroactive.For imprinted electropolymerization, the effect of nitrate ion can be easily distinguished.It was observed that oxidation and reduction peaks were lower when nitrate ions were present in the polymerization solution.The nitrate ions are trapped in the polymer matrix through noncovalent interactions between -NH 2 groups of the polymer and the oxygen atoms of the nitrate.

Optimization of the Experimental Conditions of Nitrate
Measurement.Different influencing factors including the electropolymerization scan cycles, the scan rate, the template concentration, and the monomer concentration were investigated to fabricate an efficient sensor.

Optimal Conditions for Monomer and Template Concentration.
The electrochemical performances of the IIP modified sensor can be affected by the monomer concentration during the electrodeposition process.In fact, the aptitude of the binding template molecules is substantially relying on the number of cavities created during the electropolymerization.Therefore, to determine the effect of monomer concentration on the response of the IIP sensor to NO 3 − , the films were grown in solutions containing constant concentration of NO 3 − ions, varying the aniline concentrations in the range from 1mM to 0,2M. Figure 4(a) is a plot of the R ct (electron transfer resistance) values and the current response as a function of aniline concentration.When the aniline concentration increased, the R ct values decreased and the current increased, whereas R ct increased with the decrease in the current when the concentration of aniline was up to 0.1M.It can be concluded that the optimum monomer concentration for the determination of nitrate was about 0,1M.Inadequate amount of functional monomer (aniline) led to insufficient number of available binding sites to combine template molecules.On the contrary, excessive monomers resulted in a thick IIP film, and consequently many binding sites were buried in the polymeric matrix and became noneffective.
To find the optimal composition for IIP-GCE/Cu-NPs/PANI which can produce the maximum sensitivity toward the detection of NO 3 − added to aniline in the electropolymerization system, different concentrations of nitrate ions ranging between 0.1 mM and 10 −2 M were studied (Figure 4(b)).When the concentration of NO 3 − increased, the R ct decreased and reached a minimum of 0.1mM and the current response increased and reached a maximum of 0.1mM.However, a rapid increase of R ct and a decrease in the current response can be observed when the nitrate concentration exceeded 0.1M, so this concentration was selected as the optimal value during the preparation of the IIP-GCE/Cu-NPs/PANI sensor.

Effect of Scan Rate and Electropolymerization Cycles.
Scan rate studies were carried out to determine whether the process on GCE/Cu-NPs/PANI was under diffusion control.The effect of scan rate on the peak current of NO 3 − was investigated by cyclic voltammetry technique in Na 2 SO 4 (pH 5.0) containing 10 −3 M of nitrate with different scan rates ranging from 1 to 1000 mV/s (Figure 5(a)).The oxidation peak currents increased with increasing the scan rate at the IIP in the nitrate solution, while their oxidation peak potentials gradually shift to positive values.This behavior indicates that the modified electrode reaction of NO 3 − is a surface confined process.Besides, a plot of I pa versus the square root of the scan rate (v 1/2 ) in the range of 10 to 1000 mV/s gave a straight line with a slope of 0.258, and a good correlation coefficient (R 2 =0.99963) was observed (insert Figure 5(a)).
The thickness of the imprinted film is an important factor which can affect the sensitivity and the stability of the imprinted sensors.increase with cyclic scanning number from 3 to 10, which indicates the successful formation of IIP films with a suitable thickness.When the scan number is less than ten, the imprinted polymer membrane becomes very thin and easy to break when extracting the template.If the cycles number is more than ten, the imprinted polymer membrane becomes too thick, and the template molecules cannot be completely removed from the film.Therefore, the number of cycles for the prepared IIP-GCE/Cu-NPs/PANI sensor was adjusted to 10 cycles in the following investigations.

Effect of pH on the IIP Electrochemical Performances.
The electrochemical performances of the sensitive imprinted layer can be influenced by the working pH.Thus, to select a suitable pH for nitrate sensing, the effect of pH values was studied by a series of LSVs on the imprinted electrode in 10 −2 M of nitrate solution at different working pH values from 2 to 8, using 0.1 M Na 2 SO 4 as supporting electrolyte.As visualized in Figure 6, by increasing the pH from 2 to 5, the reduction peak current increased gradually and then decreased rapidly to reach a high peak at 5. These observations suggest that, at a strong acidic media, hydrogen evolution come at less negative potential and it can trouble the reduction peak of nitrate.To guarantee the optimal imprinted sensor performances toward nitrate detection the pH value of 5.0 was chosen as the appropriate pH.

Electrochemical Characterization of Various Modified
Electrodes.The electrochemical behavior of the modified electrodes was studied by cyclic voltammetry and impedance spectroscopy.CV is a convenient and effective technique used to investigate the modification processes of the electrodes.Figure 7(a) shows cyclic voltammograms of bare and modified GCE in 5.mM of [Fe(CN) 6 ] 3−/4− as a redox probe and 0.1 M KCl solution in a potential range -0.8 to 1V.The bare electrode shows a couple of quasi-reversible redox peaks at +0.26 V.As shown in curve B, after the electrode was modified with Cu-NPs, another redox peak appeared at +0.75 V and the peak current intensity at 0.26 V increased, which indicated the presence of copper nanoparticles on the surface of GCE.After electropolymerization of aniline in the surface of Cu-NPs/GCE (curve C), the Cu-NPs/PANI/GCE exhibited a much higher current response due to the excellent electrical conductivity of PANI and Cu-NPs.The decrease in the current response from curve C to curve D is related to the occupation of the imprinted cavities by NO 3 − after the rebinding process.However, the redox peaks of [Fe(CN) 6 ] 3−/4− decreased obviously after the electropolymerization of aniline in the presence of nitrate.This result indicates that the modified IIP film before the removal of the template is less conductive and can block the access of reactants to the electrode surface (curve D).
On the other hand, the current response of the electrode increased apparently when the nitrate was removed (curve E).This behavior is due to the increase of vacant recognition sites number after removing the template, which enhances the diffusion of [Fe(CN) 6 ] 3−/4− and promotes the redox reaction of the [Fe(CN) 6 ] 3−/4− on the sensor surface.
The relation between the peak current and electrode surface area obeys the Randles-Sevcik equation [45]: where I p is the peak current, n is the electron transfer number, A is the effective surface area (cm 2 ), D is the diffusion coefficient of K 3 [Fe(CN) 6 ] in the solution (0.650.10 −5 cm 2 s −1 ), C is the concentration of K 3 [Fe(CN) 6 ] (mol/cm 3 ), and v is the scan rate (mV s −1 ) [48,49].Based on (1), the effective surface areas of GCE, GCE/Cu-NPs, GCE/Cu-NPs/PANI, NIP-GCE/Cu-NPs/PANI, and IIP-GCE/Cu-NPs/PANI were calculated to be 0.035, 0.027, 0.04, 0.03, and 0.14 cm 2 , respectively.The results are shown in Figure 7(b) for which the peak currents of the bare GCE are lower than those theoretically calculated from the Randles-Sevcik (1).The peak current of Cu-NPs/PANI modified GCE presents higher redox signal than that of other electrodes.This result indicates that the redox reactions are not wholly under diffusion control.This is most possibly due to the adsorption of [Fe(CN) 6 ] 3−/4− leading to preconcentration within the modified composite layers because of the highly porous structure.
Consistent with CV study, electrochemical impedance spectroscopy (EIS) is an effective method to analyze the charge transfer resistance of the interface electrode/solution, which can be simulated using the Randles' equivalent circuit.Herein, EIS data were typically used to follow the R ct changes occurring at the interface after each stage of electrochemical modification.From the shape of an impedance spectrum, the electron transfer kinetics and the diffusion characteristics can be determined.In EIS studies, the semicircle portion at high frequency region represents the electron transfer resistance (R ct ) of the electrode, and the linear tail at lower frequencies indicates the diffusion limited process [50][51][52].Figure 7(c) depicts the Nyquist diagrams recorded at the frequency range from 0.1 to 10 5 Hz with 100 mV amplitude using bare and differently modified GC electrodes applying an excitation potential of 0.238V (vs.Ag/AgCl reference electrode.All EIS measurements were carried out using 5.10 −3 M [Fe(CN) 6 ] 3−/4− as redox probe in 0.1 M KCl solution.In the Nyquist plot, the diameter of the semicircle defines the electron transfer resistance (R ct ) [53][54][55].It is clearly observed that the GC electrode exhibits a small semicircle (curve A) indicating a fast charge transfer process.Compared with that observed for bare GCE, Cu-NPs modified GCE leads to an enhancement in the charge transfer resistance (curve B).After the electrodeposition of PANI layer, the semicircle diameter belonging to GCE/Cu-NPs/PANI decreases dramatically.And the corresponding R ct value is of the order of 71.7Ω (curve C).This value is attributed to the high conductivity of PANI that coated the surface of the modified electrode.Thus, it demonstrates obvious implementation of very fast charge transfer effect between the redox probe and the GCE/Cu-NPs/PANI modified electrode.With the modified electrode by the imprinted film (curve D), the diameter of the semicircle increased, which proves the nonconductivity of the film covering the electrode surface.However, after the removal of the template NO 3 − (curve E), the diameter of the semicircle of IIP-GCE/Cu-NPs/PANI decreased (R ct =108.7Ω),indicating the formation of a large number of the imprinted cavities on the film covering the electrode surface.And that enhances the diffusion rate of [Fe(CN) 6 ] 3−/4− through the membranes and makes electron transfer easy.

Permeability of Various Modified
Electrodes.The rotating disk electrode (RDE) experiments have been extensively used to investigate the intrinsic kinetics of the electrocatalytic process based on the suppression of the mass transfer control [56].Therefore, the mass transfer process through the bare and modified electrodes to the surface of the electrode was investigated by linear sweep voltammetry.The experiments were conducted using an RDE controller and rotator.The [Fe(CN) 6 ] 3−/4− couple was chosen for this study because it reacts in a simple, reversible electrochemical process and the diffusion properties in solution have been well documented.Figure 8(a) illustrates the voltammograms obtained for bare and modified rotating GCE, performed in aqueous 5mM [Fe(CN) 6 ] 3−/4− and 0.1 M KCl solution, recorded at 20 mV/s in the potential range from -0.8 to 1.0V.The response of the [Fe(CN) 6 ] 3−/4− redox probe gradually decreased after the modification steps.The permeability (P m ) of the modified electrodes was determined using the typical equations introduced by Gough and Leypoldt (2) [47]: where i  is the membrane diffusion limited current, A is the electrode area, D (1.8.10 −5 cm 2 s −1 ) corresponds to the  diffusion coefficients of the substrate in the bulk solution, C is the concentration of the probe, v (0.01 cm 2 s −1 ) is the kinetic viscosity of the solution, F is the Faraday constant, n is the number of electrons, and  is the rotation rate of the RDE [42].The intercept of a Koutecky-Levich plot of (1/i L ) versus (1/휔 −1/2 ) leads to (1/i  ) at the infinite rotation rate, the effect of diffusion of the probe in solution becomes negligible, and i  depends on the diffusion of the probe through the film [57].
The membrane diffusion limited current can be expressed by the relation given below.
To estimate the P m value of the different matrices under optimal condition, Koutecky-Levich plots of the inverse of the current (1/i  ) versus the inverse of the square root of the rotation rate (1/휔 −1/2 ) were explored for bare and modified rotating GC electrode, using the data extracted from the experimental curves plotted in Figure 8(b).Linear fittings were obtained for bare and modified electrodes and the straight lines were parallel to each other, which confirms that the redox reaction is irreversible.Table 1 summarizes the P m values obtained for the bare and the different modified electrodes.

Comparison of the Electrochemical Behaviors of IIP and
NIP for Nitrate Detection.The glassy carbon electrodes disk modified with IIP and NIP were incubated in different concentrations of NO 3 − solutions from 1 휇M to 0.1 M, while stirring the solution continuously.To investigate the detection ability of IIP and NIP, LSV and EIS techniques were applied to detect nitrate ions under optimum conditions.In EIS measurements, all the Nyquist plots are fitted by using the classical Randles' equivalent circuit [R(Q[RW])] depicted in Figure 9(a).The obtained results of the mentioned electrodes are shown in Figure 9(b) and Figure 9(c).Figure 9(b) shows a series of impedance spectra recorded for different NO 3 − concentrations ranging from 1 휇M to 0.1M in Na 2 SO 4 solution (0.1 M) at pH=5.It is reported that the electrochemical reduction of nitrate to nitrite ions on the surface of the IIP-GCE/Cu-NPs/PANI exhibited a twoelectron transfer process, as shown in the following equation.
The R ct (diameter of the semicircle) in the absence of NO 3 − is relatively small (35Ω).This value can be attributed to the free electron transfer at the interface electrode/solution.The increase of NO 3 − concentration induces the increase  good correlation (R 2 = 0.99).The sensitivity values were determined as 0.78 and 0.5 mA L.mol −1 with corresponding limit detection estimated as 5 휇M and 1.5 휇M for the IIP and NIP electrode, respectively.These electrochemical performances were better than those obtained using other electrochemical sensors listed in Table 2.

Reproducibility, Durability, and Interference Study.
To study the reproducibility of the sensor, the impedance signal for known nitrate concentration was carried out for 7 independent fabricated imprinted sensors.The relative standard deviation (RSD) of the sensors response to 1 mM nitrate was 3 %, indicating high reproducibility.Furthermore, the sensors were soaked in 0.1 M hydrochloric solution and then tested daily to measure durability.The RSD of the sensors' response to 1.0 mM of nitrate was 5 % during four weeks indicating high durability.
The selectivity of the IIP sensor was obtained by linear sweep voltammetry method in 0.1 mM of NO 3 − with the addition of various interference ions at fixed concentration of 10 mM.The comparison result is summarized in Figure 10.As expected, the determination of 0.1 mM of nitrate is not interfered by the presence of ions such as NO 2 − , Ca 2+ , PO 4 3− , Mg 2+ , and CO 3 2− in a 100-fold concentration; this may be attributed to the complementary cavities in the polymeric matrix which match the unique molecular structure of NO 3 − sterically and via multiple interactions between the functional groups in the imprinted matrix and the template.detect nitrate in well and mineral water to investigate the feasibility for practical values by performing recovery tests.The response of the sensor was evaluated using the impedance method with the addition of different concentrations of NO 3 − .It was observed that the R ct values increased with the increase of NO 3 − concentration such as 10 −5 , 10 −4 , and 10 −3 M. The recovery was calculated, and the results are summarized in Table 3.The results show that the imprinted sensor has a good recovery from 95.5 to 98.7 % to detect nitrate ions, which manifests IIP-Cu-NPs/PANI/GCE to be sensitive and a useful tool for nitrate quantification in real samples.

Figure 4 :Figure 5 :
Figure 4: (a) Effect of PANI, (b) NO 3 − concentration on the R ct values and peak currents of electrocatalytic reduction of nitrate in 0.1 M Na 2 SO 4 solution (pH=5).

Figure 6 :
Figure 6: LSV current as a function of pH of IIP-GCE/Cu-NPs/PANI in 10 mM nitrate solutions.

Table 2 :
Comparison of some characteristics of the different electrodes for the detection of NO 3 − .

Table 3 :
Recovery data for detection of NO 3 − in water samples using IIP-Cu-NPs/PANI/GCE in Na 2 SO 4 solution pH=5 as supporting electrolyte.