Graphite Screen-printed Electrodes Research Articles

Electrochemistry of the synthetic tryptamine 5-MeO-MiPT at glassy carbon and screen-printed electrodes: A rapid and simple screening method for application in forensic analysis

5-Methoxy-N-methyl-N-isopropyltryptamine (5-MeO-MiPT), also known as moxy, is a synthetic tryptamine analogue used recreationally as a hallucinogenic drug. This work investigates the electrochemical behaviour of 5-MeO-MiPT using carbon electrodes for the first time. Although 5-MeO-MiPT showed only one irreversible oxidation process at a glassy carbon electrode, many electrochemical processes were exhibited on a graphite screen-printed electrode (SPE-Gr). The oxidation reaction of 5-MeO-MiPT on both carbon electrode surfaces involves an adsorption-controlled process with the loss of one electron and one proton. A voltammetric screening method for 5-MeO-MiPT was performed in 0.1 mol L−1 phosphate buffer solution at pH 7.0 on the SPE-Gr using differential pulse adsorptive stripping voltammetry (DPAdSV). The proposed method showed a wide linear range (0.05–30.0 µmol L−1) and a sufficiently low limit of detection (0.015 µmol L−1) for application to seized forensic samples containing 5-MeO-MiPT. Good stability of the electrochemical responses for 5-MeO-MiPT detection on SPE-Gr was obtained, using the same or different electrodes (N = 3) with a relative standard deviation of less than 4.0%. Interference studies with other drugs demonstrated that the proposed sensor is selective for electrochemical screening of 5-MeO-MiPT. In addition, 5-MeO-MiPT was identified in a biological sample of synthetic urine and in real seized samples by the proposed method and confirmed by GC-MS. The analytical performance of SPE-Gr with DPAdSV for 5-MeO-MiPT detection shows great potential as a simple, fast, and selective screening method in forensic scenarios.

Shedding light on the calculation of electrode electroactive area and heterogeneous electron transfer rate constants at graphite screen-printed electrodes

We present in detail the most known and commonly used methods for the calculation of electrode electroactive area (A) and heterogeneous electron transfer rate constants ({k}^{0}). The correct procedure for the calculation of these parameters is often disregarded due to either lack of a minimum theoretical background or oversimplification of each method’s limitations and prerequisites. The aim of this work is to provide the theoretical background as well as a detailed guide for the implementation of these measurements by impressing upon the electrochemists the parameters that need to be considered so that the obtained results are safe and useful. Using graphite screen-printed electrodes, A, and {k}^{0} were calculated with different methods and techniques. Data are compared and discussed.Graphical

Sensitive riboflavin sensing using silver nanoparticles deposited onto screen-printed electrodes via controlled-energy spark discharges

In this work, we elaborated the graphite screen-printed electrodes (SPEs) modification with metal nanoparticles formed as a result of spark discharges produced between a metal wire electrode and SPE that are connected to an Arduino board-based DC high voltage power supply. This sparking device allows, on the one hand, the toposelective formation of NPs of controlled dimensions through a direct and liquid-free approach, and on the other hand, controls the number and energy of the discharges delivered to the electrode surface during a single spark event. This way, the potential damage to the SPE surface by the action of heat evolved during the sparking process is considerably minimized compared with the standard setup in which each spark event consists of multiple electrical discharges. Data demonstrated that the sensing properties of the resulting electrodes are significantly improved compared with those achieved when conventional spark generators are employed, as demonstrated for silver-sparked SPEs that exhibit enhanced sensitivity to riboflavin. Sparked AgNp-SPEs were characterized using scanning electron microscopy and voltammetric measurements in alkaline conditions. The analytical performance of sparked AgNP-SPEs was evaluated by various electrochemical techniques. Under optimum conditions, the detection range for DPV was from 1.9 (LOQ) to 100nM riboflavin (R2=0.997), while a limit of detection (LOD, S/N 3) of 0.56nM was achieved. The analytical utility is demonstrated for the determination of riboflavin in the real matrices of B-complex pharmaceutical preparation and an energy drink.

Molybdenum Disulfide/Nickel-Metal Organic Framework Hybrid Nanosheets Based Disposable Electrochemical Sensor for Determination of 4-Aminophenol in Presence of Acetaminophen.

The toxicity of commonly used drugs, such as acetaminophen (ACAP) and its degradation-derived metabolite of 4-aminophenol (4-AP), underscores the need to achieve an effective approach in their simultaneous electrochemical determination. Hence, the present study attempts to introduce an ultra-sensitive disposable electrochemical 4-AP and ACAP sensor based on surface modification of a screen-printed graphite electrode (SPGE) with a combination of MoS2 nanosheets and a nickel-based metal organic framework (MoS2/Ni-MOF/SPGE sensor). A simple hydrothermal protocol was implemented to fabricate MoS2/Ni-MOF hybrid nanosheets, which was subsequently tested for properties using valid techniques including X-ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy (EDX), Fourier transformed infrared spectroscopy (FTIR), and N2 adsorption-desorption isotherm. The 4-AP detection behavior on MoS2/Ni-MOF/SPGE sensor was followed by cyclic voltammetry (CV), chronoamperometry and differential pulse voltammetry (DPV). Our experimental findings on the generated sensor confirmed a broad linear dynamic range (LDR) for 4-AP from 0.1 to 600 μM with a high sensitivity of 0.0666 μA/μM and a low limit of detection (LOD) of 0.04 μM. In addition, an analysis of real specimens such as tap water sample as well as a commercial sample (acetaminophen tablets) illuminated the successful applicability of as-developed sensor in determining ACAP and 4-AP, with an impressive recovery rate.

Voltammetric determination of vitamin B6 in the presence of vitamin C based on zinc ferrite nano-particles modified screen-printed graphite electrode.

The zinc ferrite nano-particles (ZnFe2O4) modified screen-printed graphite electrode (ZnFe2O4/SPGE) was used for the voltammetric determination of vitamin B6 in real samples, using differential pulse voltammetry (DPV). It has been found that the oxidation of vitamin B6 at the surface of such an electrode occurs at a potential about 150 mV less positive compared to an unmodified screen-printed graphite electrode. After optimization, a vitamin B6 sensor with a linear range from 0.8 to 585.0 μM and a detection limit of 0.17 μM. The ZnFe2O4/SPGE sensor exhibits good resolution between the voltammetric peaks of vitamin B6 and vitamin C, making it suitable for detecting vitamin B6 in the presence of vitamin C in real samples.

Determination of the standard rate constant for soluble-soluble quasi-reversible electrochemical systems by linear sweep voltammetry: Application to the electrochemical oxidation on screen-printed graphite electrodes

Semi-analytical approach was used for modeling and establishing Linear Sweep Voltammetry (LSV) profiles in the case of quasi-reversible electrochemical reactions involving soluble species. The effects of charge transfer coefficient (α) and dimensionless kinetic rate constant (Λ) on the shape and position of voltammograms were investigated. The combined effect on the LSV responses, peak current, half peak width and peak potential was also analyzed qualitatively and quantitatively. Kinetic curves were constructed in the form of the change in the LSV characteristics as a function of (α, Λ) and then modeled by the interpolation functions. The obtained equations are an easy-to-use tool in order to calculate the heterogeneous kinetic rate constant for quasi-reversible charge transfer. Experimental-theory validation has been performed on ferrocyanide oxidation on screen-printed graphite electrodes.

A Novel Electrochemical Immunosensor Based on Anti-IgY and PLA/PEG Nanofibrous Mats Used for Allergens Detection in Farinaceous Products

The present study focuses on the first electrochemical immunosensor built with polymeric mats enriched with nanomaterials, targeting the dust mite protein, for the detection of allergens in flour sources with important implications in allergic reactions. As a proof-of-concept, we have used the Blo t 5 allergen from Blomia tropicalis (target) and established electrochemical parameters to recognize and detect the specific allergen using a polyclonal immunoglobulin (Ig) Y (probe). Detection was performed in a portable potentiostat (EmStat) using a graphite screen-printed electrode. For that, the nanofibrous mats of poly(lactic acid)/poly(ethylene glycol) (PLA/PEG), and carbon nanotubes (CNTs) were placed in contact with the surface of the electrodes. The functionalization that occurs through the deposition of the polymer was induced through the passage of current. Subsequently, the modification was validated by cyclic voltammetry (CV) readings and ferri/ferrocyanide was used as a redox indicator in CV analyses. The novel immunosensor was able to discriminate between allergen-contaminated and uncontaminated farinaceous samples. The immunosensor displays high sensitivity detecting up to 50 μg ml−1 in the calibration curve with a linear response between 5 and 500 μg ml−1. The new biosensor shows great potential in the detection of farinaceous contaminants in laboratories, food factories and in the field.

Differential Pulse Voltammetric Analysis of Hydrazine in Water Samples by Using Screen-Printed Graphite Electrode Modified with Nitrogen-Doped Hollow Carbon Spheres

The present study introduces a facile and efficient voltammetric hydrazine sensor via the modification of screen-printed graphite electrode (SPGE) with nitrogen-doped hollow carbon spheres (N-HCSs). This work is the first report of the new method of electroanalytical determination of hydrazine through N-HCSs modified SPGE. The N-HCSs fabricated through the templating approach (hard template) were characterized by Fourier transform infrared (FT-IR) spectroscopy, field emission-scanning electron microscopy (FE-SEM), and energy-dispersive X-ray spectroscopy (EDS). Cyclic voltammetry (CV), chronoamperometry (CA), and differential pulse voltammetry (DPV) were employed for electrochemical determinations. The produced N-HCSs/SPGE had an appreciable electrocatalytic capacity for the hydrazine oxidation, with the least oxidation overpotential and elevated voltammetric peak currents. The peak current of hydrazine oxidation on N-HCSs/SPGE possessed a distinct linear association with its levels (0.02–380.0 μM) under the optimized experimental circumstances, with the limit of detection (LOD) as narrow as 0.007 μM. Good stability and acceptable reproducibility were also attained on the N-HCSs/SPGE. In addition, the developed technique exhibited good selectivity toward the detection of hydrazine in the presence of some interfering species. The practical applicability of proposed sensor was successful by sensing hydrazine in water samples.

Simultaneous Voltammetric Determination of Epinine and Venlafaxine Using Disposable Screen-Printed Graphite Electrode Modified by Bimetallic Ni-Co-Metal–Organic-Framework Nanosheets

We constructed two-dimensional NiCo-metal-organic-framework (NiCo-MOF) nanosheets based on a facile protocol and then characterized them using multiple approaches (X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), field emission-scanning electron microscopy (FE-SEM), and N2 adsorption/desorption isotherms techniques). As a sensitive electroactive material, the as-fabricated bimetallic NiCo-MOF nanosheets were employed to modify a screen-printed graphite electrode surface (NiCo-MOF/SPGE) for epinine electro-oxidation. According to the findings, there was a great improvement in the current responses of the epinine because of the appreciable electron transfer reaction and catalytic performance of the as-produced NiCo-MOF nanosheets. Differential pulse voltammetry (DPV), cyclic voltammetry (CV) and chronoamperometry were utilized to analyze the electrochemical activity of the epinine on the NiCo-MOF/SPGE. A linear calibration plot was obtained in the broad concentration range (0.07-335.0 µM) with a high sensitivity (0.1173 µA/µM) and a commendable correlation coefficient (0.9997). The limit of detection (S/N = 3) was estimated at 0.02 µM for the epinine. According to findings from DPV, the electrochemical sensor of the NiCo-MOF/SPGE could co-detect epinine and venlafaxine. The repeatability, reproducibility and stability of the NiCo-metal-organic-framework-nanosheets-modified electrode were investigated, and the relative standard deviations obtained indicated that the NiCo-MOF/SPGE had superior repeatability, reproducibility and stability. The as-constructed sensor was successfully applicable in sensing the study analytes in real specimens.

Screen-printed graphite electrode on polyvinyl chloride and parchment strips integrated with genetic programming for in situ nitrate sensing of aquaponic pond water

Nitrate is the primary water-soluble macronutrient essential for plant growth that is converted from excess fish feeds, fish effluents, and degrading biomaterials on the aquaponic pond floor, and when aquacultural malpractices occur, large amounts of it retain in the water system causing increase rate in eutrophication and toxifies fish and aquaculture plants. Recent nitrate sensor prototypes still require performing the additional steps of water sample deionization and dilution and were constructed with expensive materials. In response to the challenge of sensor enhancement and aquaponic water quality monitoring, this study developed sensitive, repeatable, and reproducible screen-printed graphite electrodes on polyvinyl chloride and parchment paper substrates with silver as electrode material and 60:40 graphite powder:nail polish formulated conductive ink for electrical traces, integrated with 9-gene genetic expression model as a function of peak anodic current and electrochemical test time for nitrate concentration prediction that is embedded into low-power Arduino ESP32 for in situ nitrate sensing in aquaponic pond water. Five SPE electrical traces were designed on the two types of substrates. Scanning electron microscopy with energy dispersive X-ray confirmed the electrode surface morphology. Electrochemical cyclic voltammetry using 10 to 100 mg/L KNO3 and water from three-depth regions of the actual pond established the electrochemical test time (10.5 s) and electrode potential (0.135 V) protocol necessary to produce peak current that corresponds to the strength of nitrate ions during redox. The findings from in situ testing revealed that the proposed sensors have strong linear predictions (R2 = 0.968 MSE = 1.659 for nSPEv and R2 = 0.966 MSE = 4.697 for nSPEp) in the range of 10 to 100 mg/L and best detection limit of 3.15 μg/L, which are comparable to other sensors of more complex construction. The developed three-electrode electrochemical nitrate sensor confirms that it is reliable for both biosensing in controlled solutions and in situ aquaponic pond water systems.

Smart Sensor for Lithium Detection: An Environmental Application

In this work, we propose a potentiometric smart sensor for lithium detection in environmental samples based on a screen-printed cell. The graphite screen-printed electrode (GSPE) was first modified by gold and silver nanoparticles to increase the conductivity, and then by an ion-selective membrane, which was directly deposited onto the nanostructured electrode surface. The potentiometric cell, thanks to its small size, was integrated with a portable instrument connected to a smartphone for decentralized analysis. The developed sensor was used in drop- and microflow-configurations and showed a high sensitivity for lithium with a low detection limit (1.6 µM). It was also applied in the analysis of real samples from the industrial recycling of automotive batteries and complex matrices, such as contaminated soils.

Investigating the electrochemical profile of methamphetamine to enable fast on-site detection in forensic analysis

Methamphetamine (MA) is a synthetic psychoactive drug which is consumed both licitly and illicitly. In some countries it is prescribed for attention-deficit and hyperactivity disorder, and short-term treatment of obesity. More often though, it is abused for its psychostimulant properties. Unfortunately, the spread and abuse of this synthetic drug have increased globally, being reported as the most widely consumed synthetic psychoactive drug in the world in 2019. Attempting to overcome the shortcomings of the currently used on-site methods for MA detection in suspected cargos, the present study explores the potential of electrochemical identification of MA by means of square wave voltammetry on disposable graphite screen-printed electrodes. Hence, the analytical characterization of the method was evaluated under optimal conditions exhibiting a linear range between 50 μM and 2.5 mM MA, a LOD of 16.7 μM, a LOQ of 50.0 μM and a sensitivity of 5.3 μA mM−1. Interestingly, two zones in the potential window were identified for the detection of MA, depending on its concentration in solution. Furthermore, the oxidative pathway of MA was elucidated employing liquid chromatography – mass spectrometry to understand the change in the electrochemical profile. Thereafter, the selectivity of the method towards MA in mixtures with other drugs of abuse as well as common adulterants/cutting agents was evaluated. Finally, the described method was employed for the analysis of MA in confiscated samples and compared with forensic methods, displaying its potential as a fast and easy-to-use method for on-site analysis.

Electrochemical sensing of methotrexate in the presence of folic acid using PAMAM dendrimer-functionalized multiwalled carbon nanotube-modified electrode.

This works presents a novel electrochemical sensor based on the third-generation poly(amidoamine) dendrimer (G3 PAMAM)-functionalized multiwalled carbon nanotube (MWCNT)-modified screen-printed graphite electrode (SPGE) for the simple and sensitive detection of methotrexate (MTX). The carboxylated MWCNTs were covalently functionalized with amino groups of G3 PAMAM and characterized using different techniques. The sensing ability of the designed nanosensor (MWCNTs-PAMAM/SPGE) was tested using differential pulse voltammetry (DPV), chronoamperometry (CHA), linear sweep voltammetry (LSV), and cyclic voltammetry (CV). To investigate the electrocatalytic activity of PAMAM-functionalized MWCNTs, a comparative electrochemical analysis was carried out and it was determined that PAMAM-functionalized MWCNT-modified SPGE showed good electrocatalytic performance for MTX oxidation compared to the unmodified SPGE. The MWCNT-PAMAM/SPGE lead to a reduced overpotential of MTX oxidation of about 300 mV and enhanced current of about 9 μA of the unmodified SPGE. Experiments were performed for the quantitative determination of MTX using the DPV technique. The response peak current linearly related against MTX concentration in the ranges from 0.01 to 110.0 μM and a limit of detection (LOD) equal to 0.003 μM. Also, MWCNT-PAMAM/SPGE exhibits good catalytic ability toward MTX determination in the presence of folic acid (FA), and the separation of their oxidation peaks (peak potential difference = 320 mV) simultaneously detected the above compounds. To prove the applicability of the MWCNT-PAMAM/SPGE sensor, the concentrations of MTX and FA in pharmaceutical products and biological samples were determined. The calculated recoveries were close to 100%, which indicates that the method might be assumed to be accurate.

Voltammetric folic acid sensor based on nickel ferrite nanoparticles modified-screen printed graphite electrode

In this study, an electrochemical sensor for the quantification of folic acid with voltam­metric detection in physiological conditions was constructed. For this purpose, nickel ferrite (NiFe2O4) nanoparticles were used to modify the surface of a screen-printed graphite electrode (NiFe2O4/SPGE) and applied in the determination of folic acid. The modified electrode displays a strong electrochemical response to folic acid. Folic acid was determined electrochemically using the differential pulse voltammetry (DPV) technique with a detection limit of 0.09±0.001 µM in 0.2–147.0 µM linear range in phosphate buffer solution (PBS) at pH 7.0 with this NiFe2O4/SPGE sensor, which has the best electron transfer rate. Also, the sensitivity of the modified electrode was obtained as 0.1139 µA µM-1. The NiFe2O4/SPGE sensor was successfully applied for the determination of folic acid in real samples.

Novel electrochemical sensing platform for detection of hydrazine based on modified screen-printed graphite electrode

The current work aimed to fabricate a screen-printed graphite electrode (SPGE) modified by MnO2 nanorods (MnO2 NRs) for sensing hydrazine. Thus, a facile protocol was adopted to construct the MnO2 nanorods that were subsequently applied to modify the SPGE surface directly. As-synthesized MnO2 NRs/SPGE sensor exhibited a strong sensing behavior towards the hydrazine, with a large peak current and small oxidation potential. This electrochemical sensor in the optimized conditions to detect the hydrazine possessed a low detection limit (0.02 μM), a broad linear dynamic range (0.05–275.0 μM) and an admirable sensitivity (0.0625 μA μM-1). The sensor applicability was practically estimated in real water samples, which revealed successful recovery values.

Simple Preparation and Characterization of Hierarchical Flower-like NiCo2O4 Nanoplates: Applications for Sunset Yellow Electrochemical Analysis.

The current work was performed to construct a novel electrochemical sensing system for determination of sunset yellow via the modification of screen-printed graphite electrode modified with hierarchical flower-like NiCo2O4 nanoplates (NiCo2O4/SPGE). The prepared material (hierarchical flower-like NiCo2O4 nanoplates) was analyzed by diverse microscopic and spectroscopic approaches for the crystallinity, composition, and morphology. Chronoamperometry, differential pulse voltammetry, linear sweep voltammetry, and cyclic voltammetry were used for determination of the electrochemical behavior of sunset yellow. The as-fabricated sensor had appreciable electro-catalytic performance and current sensitivity in detecting the sunset yellow. There were some advantages for NiCo2O4/SPGE under the optimized circumstances of sunset yellow determination, including a broad dynamic linear between 0.02 and 145.0 µM, high sensitivity of 0.67 μA/(μM.cm2), and a narrow limit of detection of 0.008 μM. The practical applicability of the proposed sensor was verified by determining the sunset yellow in real matrices, with satisfactory recoveries.

Facile synthesis of nanostructured Prussian blue analogue for high performance symmetric supercapacitor device

Prussian blue analogues (PBAs) have received much attention in energy storage devices because of they offer three-dimensional open network, large surface area with tunable pore size distribution and low-cost constituents. Herein, nanostructured nickel hexacyanoferrate (III) (NCF) was easily synthesized by co-precipitation method and explored as a symmetrical supercapacitor device in different supporting electrolytes for the first time. Crystalline NCF nanoparticles (NPs) with an average size of 30 nm and large specific surface area (SBET) of 269 m2/g were obtained. Superior storage capabilities with battery-like behaviors were observed in 0.5 M KCl and 0.1 M KOH with specific capacitance values of 546 F/g and 1753 F/g at 5 A/g, respectively. Further, the NCF modified graphite screen-printed electrode (NCF/GSPE) showed excellent stability and storage retention even after 10,000 cycles. This significant achievement offers a promising strategy for achieving efficient, optimal and low-cost energy storage devices.

Screen-Printed Graphite Electrode Modified with Graphene-Co3O4 Nanocomposite: Voltammetric Assay of Morphine in the Presence of Diclofenac in Pharmaceutical and Biological Samples.

This work focuses on the development of a novel electrochemical sensor for the determination of morphine in the presence of diclofenac. The facile synthesis of graphene-Co3O4 nanocomposite was performed. The prepared material (graphene-Co3O4 nanocomposite) was analyzed by diverse microscopic and spectroscopic approaches for its crystallinity, composition, and morphology. Concerning the electrochemical determinations, after drop-casting the as-fabricated graphene-Co3O4 nanocomposite on the surface of a screen-printed graphite electrode (SPGE), their electrochemical performance was scrutinized towards the morphine detection. It was also found that an SPGE modified by a graphene-Co3O4 nanocomposite exhibited better electrocatalytic activity for morphine oxidation than unmodified electrode. Under optimal conditions, the differential pulse voltammetry (DPV) was employed to explore the present sensor (graphene-Co3O4/SPGE), the findings of which revealed a linear dynamic range as broad as 0.02–575.0 µM and a limit of detection (LOD) as narrow as 0.007 μM. The sensitivity was estimated to be 0.4 µM/(µA cm2). Furthermore, the graphene-Co3O4/SPGE sensor demonstrated good analytical efficiency for sensing morphine in the presence of diclofenac in well-spaced anodic peaks. According to the DPV results, this sensor displayed two distinct peaks for the oxidation of morphine and diclofenac with 350 mV potential difference. In addition, the graphene-Co3O4/SPGE was explored for voltammetric determination of diclofenac and morphine in pharmaceutical and biological specimens of morphine ampoule, diclofenac tablet, and urine, where recovery rates close to 100% were recorded for all of the samples.

On spot detection of nickel and cobalt from exhausted batteries by a smart electrochemical sensor

This work presents the realization and the application of an user-friendly electrochemical platform based on screen-printed electrodes for the simultaneous determination of nickel and cobalt ions in real samples by means of square wave adsorptive stripping voltammetry (SWAdSV). The sensor was realized by electrodepositing in situ a bismuth film onto graphite screen-printed electrodes (GSPEs). The sensor surface was fully characterized by scanning electron microscopy (SEM), cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS).The experimental conditions for the determination of nickel and cobalt in the form of dimethylglyoximate complexes were studied and optimized. Linear calibration curves for Ni(II) and Co(II), determined individually and together, in the range 10–40 μg/L for nickel and 10–60 μg/L for cobalt, respectively, were obtained. The limits of detection for nickel and cobalt determination were 2.5 μg/L and 2.4 μg/L, respectively. The performance of the sensor in terms of reproducibility and selectivity was also studied. The applicability of the developed platform was assessed by determining nickel and cobalt in samples deriving from an industrial process of recycling exhausted batteries and in soil samples.

Construction of modified screen-printed graphite electrode for the application in electrochemical detection of sunset yellow in food samples

The current work introduced a novel electrochemical sensor (screen-printed graphite electrode (SPGE) modified with MnO2 nanorods anchored graphene oxide nanocomposite (MnO2 NRs/GO) for sensitive determination of sunset yellow. The characterization of MnO2 NRs/GO nanocomposite synthesized through a simple hydrothermal approach was determined employing varied analytical equipment like Field emission-scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FT-IR), and X-ray diffraction (XRD). Chronoamperometric measurements, differential pulse voltammetry (DPV), cyclic voltammetry (CV) and linear sweep voltammetry (LSV) were recruited to recognize the electrochemical oxidation of sunset yellow on the MnO2 NRs/GO/SPGE. The results of CV proved that the as-synthesized MnO2 NRs/GO nanocomposite has a good electrocatalytic activity toward sunset yellow. The MnO2 NRs/GO/SPGE electrode under optimized conditions using the DPV possessed a linear response for different concentrations of sunset yellow (between 0.01 and 115.0μM) with a low limit of detection (LOD) (0.008μM). Finally, the impressive applicability of this sensor was confirmed via real sample analysis with excellent recoveries (between 97.3 and 104.6%).