Advances In Electrochemical Sensors Research Articles

Electrochemical sensing platform for anticonvulsant drug carbamazepine detection based on graphitic carbon nitride and tetrabutylammonium chloride ionic liquid

The development of a rapid and straightforward electrochemical approach for the quantification of the anticonvulsant drug carbamazepine (CBZ) is herein presented. Carbon paste electrode (CPE) was bulk modified with a type of two-dimensional conjugated polymer, i.e., graphitic carbon nitride (g-C3N4), and additionally with an ionic liquid tetrabutylammonium chloride (TBACl) to obtain advanced electrochemical sensor for CBZ. Synthesized g-C3N4 material was structurally and morphologically characterized by Raman spectroscopic, FTIR, and SEM/EDX methods. CV experiments showed that the resulting electrode (TBACl-g-C3N4-CPE) has an improved electrochemical response compared to unmodified CPE and g-C3N4-CPE due to the synergistic effect of electrode modifiers, as well as that the CBZ oxidation process is irreversible and diffusion-controlled. After optimization steps concerning the amount of electrode modifiers and the selection of pH of the supporting electrolyte, the analytical performance of TBACl-g-C3N4-CPE was investigated by direct anodic square-wave voltammetry (SWV). The most intensive peak of the target analyte was obtained in Britton-Robinson buffer solution at pH 7.0, whereby the developed SWV method was characterized by a linear concentration range of CBZ from 0.42 to 9.31 µmoL L−1, limit of detection (LOD) of 0.13 µmoL L−1, and relative standard deviation lower than 3%. The interference study showed that TBACl-g-C3N4-CPE exhibits adequate selectivity for CBZ in the presence of ions/compounds commonly present in the urine matrix. The developed sensor was utilized to determine CBZ in pharmaceuticals and spiked human urine sample with excellent recovery and reproducibility, indicating a good application capability of TBACl-g-C3N4-CPE for monitoring CBZ in different matrices.

Ferulic acid detection in honey using carbon paste electrode modified by C-C3N4/Li2CoMn3O8 nanocomposite

Honey is regarded as a valuable food commodity which has many and varied components, including phenolic compounds. Ferulic acid (FA) is one of these compounds, which possesses activities such as antioxidant, anti-inflammatory, anti-diabetic, haemolytic, antiviral, anti-cancer, etc. In view of these unique characteristics, a quick, sensitive, simple and inexpensive method for FA identification is required. This research developed a novel electrochemical sensor for measuring FA in honey samples. The sensor utilizes a C-C3N4/Li2CoMn3O8 nanocomposite modified carbon paste electrode (C-C3N4/LCMO/CPE) to enhance the sensitivity and detection. The synthesized nanocomposite exhibits remarkable properties, featuring an abundance of electrochemically active sites and enhanced electron transfer rates, making it ideal for developing advanced electrochemical sensors. The XRD, SEM and EDX analysis were used to examine and look like the synthesised nanocomposite structure. Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) methods were used to evaluate the electrochemical behavior of C-C3N4/LCMO/CPE sensor for FA detection and optimized by adjusting pH, and potential scan rate. FA was measured in a phosphate buffered saline (PBS; 0.1 M, pH 4.0) by DPV with the detection limit of 3.6 nM and quantitative limit of 0.009 µM in the linear response ranges of 0.009–3.000 and 5.00–100 µM. Chronoamperometry was utilized to calculate the diffusion coefficient of FA (D = 3.45 (±0.11) × 10−6 cm2.s−1) on the surface of the C-C3N4/LCMO/CPE, as well as the electron transfer coefficient (α = 0.68). The sensor’s high sensitivity for accurately assessing FA in real samples was demonstrated by recovery values ranging from 96.96 to 102.36 %.

Sparfloxacin/Gold Nanoparticles Modified Electrochemical Sensor for the Determination of Dopamine

Background: The development of facile, reliable, and sensitive electrochemical sensors for neurotransmitter detection is of utmost importance in biomedical research. Objectives: In this study, we proposed a novel approach for the synthesis of gold nanoparticles (AuNPs) using sparfloxacin as a reducing and stabilizing agent and further utilized as-prepared AuNPs for the construction of an electrochemical sensor to detect dopamine. Methods: The synthesis of AuNPs was achieved through a simple method where sparfloxacin acted as both a reducing and stabilizing agent. The AuNPs were investigated by using UV-visible spectroscopy, field emission scanning electron microscopy (FESEM), energy dispersive spectroscopy (EDS), elemental mapping (Emap), and X-ray diffraction (XRD). Results: The synthesised AuNPs were used to develop an electrochemical sensor for the detection of dopamine molecules. The fabricated electrochemical sensor demonstrated remarkable sensitivity and selectivity toward dopamine sensing. This sensor exhibited a good linear detection of dopamine in micromolar concentrations. Moreover, the sensor showed excellent stability and reproducibility. Conclusion: This novel electrochemical sensor holds significant potential for practical applications in neuroscience and clinical diagnosis, offering a rapid and sensitive method for dopamine detection. The utilization of sparfloxacin/AuNPs provides a promising avenue for the development of advanced electrochemical sensors with enhanced performance and wider applications in the detection of other neurotransmitters and biomolecules.

Sensitive and fast electrochemical recognition of nitroaromatic explosives in liquid phase using ultrathin graphitic carbon nitride nanotubes

In the present work, a simple, effective method to synthesis high-quality carbon nitride nanotubes with ∼90 nm diameter and 5–9 nm in thickness along with a high-yield (63 %) via template-free hydrothermal synthesis is reported. By using these graphitic carbon nitride nanotubes an advanced electrochemical sensor was demonstrated to selectively sense explosive 2,4-dinitrotoluene. It is demonstrated that bigger linear range towards 2,4-dinitrotoluene, sensing up to 425 μM is reported. Furthermore, the experiments demonstrated that this sensor possesses a high sensitivity not only for 2,4-dinitrotoluene but also for other nitroaromatic explosives.

Electrochemical sensor based on hollow Au/Pd/Ag dendrites prepared by galvanic replacement from a choline chloride-ethylene glycol deep eutectic solvent

This study presents a simple approach to fabricating a hollow dendritic Au/Pd/Ag electrode through a galvanic replacement reaction (GRR) in a choline chloride-ethylene glycol deep eutectic solvent. The resulting electrode's morphological, structural, and compositional features were characterized using SEM, TEM, XRD, and XPS techniques, with the XPS depth profile providing insights into metal content ratio variations along the electrode's depth. The results emphasize the significant impact of immersion time on both morphological evolution and composition. Cyclic voltammetry investigations revealed significantly enhanced current density in furaltadone (FTD) detection compared to bimetallic and single metallic electrodes. The proposed electrochemical sensor exhibited a dynamic linear range for FTD spanning 1.67–625 μM, accompanied by a low detection limit of 91.7 nM, as confirmed by differential pulse voltammetry (DPV) quantitative experiments. The selectivity, reproducibility, stability, and recovery of the as-prepared sensors were evaluated, particularly in aquaculture water samples, underscoring the practical applicability of the electrodes for furaltadone sensing. This innovative trimetallic electrode design opens avenues for advanced electrochemical sensors with enhanced performance characteristics.

Carrageenan derived polyelectrolyte complexes material: An effective bifunctional for electrochemical sensing of sulfamethazine and antibacterial activity

Biopolymer-derived polyelectrolyte complexes (PECs) are a class of materials that have emerged as promising candidates for developing advanced electrochemical sensors due to their tunable properties, biocompatibility, cost-effective production, and high surface area. PECs are formed by combining positively and negatively charged polymers, resulting in a network with intriguing properties that can be tailored for specific sensing applications. The resultant PECs-based nanocomposites were used to modify the glassy carbon electrode (GCE) to detect the sulfamethazine (SFZ) antibiotic drug. In addition, electrochemical studies using electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and differential pulse voltammetry (DPV) are used to evaluate the SFZ detection ability. Similarly, various microscopic and spectroscopic studies investigated the nano composite's structural features and morphological behavior. The κ-CGN/P(Am-co-DMDAAc)-GO modified GCE demonstrated excellent detection ability of SFZ with the nano molar range and without interference with similar structural components. Furthermore, the newly fabricated electrode κ-CGN/P(Am-co-DMDAAc)-GO was derived from naturally available materials, water-soluble, low cost, biocompatible, exhibits good conductivity, and excellent catalytic properties. Finally, κ-CGN/P(Am-co-DMDAAc)-GO- modified GCE has versatile, practical applications for detecting SFZ in real-time samples and determining the efficacy of an antibacterial activity.

PH-Tuned Enantioselectivity Reversal in a Defective Chiral Metal Organic Framework.

The introduction of chirality into easy-scalable metal-organic frameworks (MOFs) gives rise to the development of advanced electrochemical sensors. However, integrating chirality by directly connecting metal ions and chiral ligands is unpredictable. Postmodification synthesis is a common method for synthesizing chiral MOFs, but it reduces the size of chiral channels and poses obstacles to the approach of chiral guest molecules. In this work, missing connection defects were introduced into the chiral MOFs through defect engineering strategies, which enhance the recognition of the target enantiomers. pH can tune enantioselectivity reversal in defective chiral MOFs. The chiral MOFs show enantioselectivity for d-Trp at pH = 5 and l-Trp at pH = 8. From the results of zeta potential, regardless of pH 5 or 8, the chiral MOF has a positive potential. The chiral MOFs are positively charged, while tryptophan is negatively charged when pH = 8. The difference in the positive and negative charge interactions between the two amino acids and chiral MOFs leads to chiral recognition. However, the difference in π-π interaction between chiral MOF and Trp enantiomers mainly drives chiral recognition under pH = 5. This study paves a pathway for the synthesis of defective chiral MOFs and highlights the pH-tuned enantioselectivity reversal.

Accurate and Rapid Determination of Ammonium in Water by Voltametric Analysis on a Novel Modified Electrode

The development of efficient and sensitive electrochemical sensors is of crucial for a wide range of applications, including environmental monitoring, chemical analysis, and biomedical diagnostics. In this study, we present on the development and characterization of a novel of electrochemical sensor, based on a silver/poly 1-aminoanthraquinone/glassy carbon modified electrode (Ag/PAAQ/GC), with high sensitivity and selectivity for the detection of ammonium ions (NH4 +) in water. The Ag/PAAQ/GC electrode was prepared by a simple and low- cost electrochemical co-deposition method, which enabled for a uniform and stable deposition of PAAQ and Ag ions on the surface of the GC electrode. The resulting electrode exhibited excellent electrocatalytic activity in the oxidation of NH4 + ions. The performance of the Ag/PAAQ/GC electrode as an electrochemical sensor for NH4 + was evaluated using square wave voltammetry (SWV) in aqueous solutions. The results showed that the Ag/PAAQ/GC electrode exhibited a linear response to NH4 + in a concentration range of 0.01 to 9 mgL−1, with a detection limit of 3 μgL−1 and a sensitivity of 0.0413 μA.Lmg−1. In addition, the Ag/PAAQ/GC electrode showed excellent selectivity for NH4 + over interfering ions such as K+, Na+, Ca2+, and Mg2+. Overall, our results show that the Ag/PAAQ/GC electrode is a promising platform for the development of advanced electrochemical sensors for the detection of NH4 + in water. Due to its high sensitivity, selectivity and stability, the Ag/PAAQ/GC electrode is suitable for a wide range of environmental and analytical applications, e.g., water quality monitoring, wastewater treatment and fertiliser analysis. The precision of the method was tested by analysing sixteen measurements of the same NH4 + concentration, yielding standard deviation (RSD) of 1.78%. Good recovery values were obtained when measuring spiked tap water samples analysed by the classical Colorimetric Nessler reagent methods and measuring natural water by the ion-selective electrode.

Recent Advances in Electrochemical Sensors for Formaldehyde.

Formaldehyde, a ubiquitous indoor air pollutant, plays a significant role in various biological processes, posing both environmental and health challenges. This comprehensive review delves into the latest advancements in electrochemical methods for detecting formaldehyde, a compound of growing concern due to its widespread use and potential health hazards. This review underscores the inherent advantages of electrochemical techniques, such as high sensitivity, selectivity, and capability for real-time analysis, making them highly effective for formaldehyde monitoring. We explore the fundamental principles, mechanisms, and diverse methodologies employed in electrochemical formaldehyde detection, highlighting the role of innovative sensing materials and electrodes. Special attention is given to recent developments in nanotechnology and sensor design, which significantly enhance the sensitivity and selectivity of these detection systems. Moreover, this review identifies current challenges and discusses future research directions. Our aim is to encourage ongoing research and innovation in this field, ultimately leading to the development of advanced, practical solutions for formaldehyde detection in various environmental and biological contexts.

Advances in electrochemical sensors for real-time glucose monitoring

This manuscript emphasizes advancements in electrochemical sensors for real-time glucose monitoring, showcasing their pivotal role in enhancing personalized healthcare through continuous, reliable measurement of biochemical markers.

Electrochemical sensors for analyte in saliva: recent update

Purpose This review provides an overview of recent advances in electrochemical sensors for analyte detection in saliva, highlighting their potential applications in diagnostics and health care. The purpose of this paper is to summarize the current state of the field, identify challenges and limitations and discuss future prospects for the development of saliva-based electrochemical sensors. Design/methodology/approach The paper reviews relevant literature and research articles to examine the latest developments in electrochemical sensing technologies for saliva analysis. It explores the use of various electrode materials, including carbon nanomaterial, metal nanoparticles and conducting polymers, as well as the integration of microfluidics, lab-on-a-chip (LOC) devices and wearable/implantable technologies. The design and fabrication methodologies used in these sensors are discussed, along with sample preparation techniques and biorecognition elements for enhancing sensor performance. Findings Electrochemical sensors for salivary analyte detection have demonstrated excellent potential for noninvasive, rapid and cost-effective diagnostics. Recent advancements have resulted in improved sensor selectivity, stability, sensitivity and compatibility with complex saliva samples. Integration with microfluidics and LOC technologies has shown promise in enhancing sensor efficiency and accuracy. In addition, wearable and implantable sensors enable continuous, real-time monitoring of salivary analytes, opening new avenues for personalized health care and disease management. Originality/value This review presents an up-to-date overview of electrochemical sensors for analyte detection in saliva, offering insights into their design, fabrication and performance. It highlights the originality and value of integrating electrochemical sensing with microfluidics, wearable/implantable technologies and point-of-care testing platforms. The review also identifies challenges and limitations, such as interference from other saliva components and the need for improved stability and reproducibility. Future prospects include the development of novel microfluidic devices, advanced materials and user-friendly diagnostic devices to unlock the full potential of saliva-based electrochemical sensing in clinical practice.

Gold particle-modified glassy carbon electrode: an advanced electrochemical sensor for dipyrone monitoring

This study presents the development and optimization of a gold particle-modified glassy carbon electrode (Au/GCE) as an advanced electrochemical sensor for monitoring dipyrone (DIP), a commonly used pharmaceutical compound. The objective of this study was to enhance the sensitivity and accuracy of DIP quantification through efficient experimental planning and the incorporation of gold particles onto the surface of the GCE. The electrodeposition of gold particles onto the GCE significantly improved the response of DIP in a 0.5 mol L−1 H2SO4 solution. By employing a design of experiments (DoE) approach, we optimized the differential pulse voltammetric (DPV) method, resulting in enhanced performance, including the achievement of a remarkably low limit of detection (0.15 µmol L−1). To assess the accuracy of the electroanalytical method, we conducted extensive recovery tests, which yielded recovery values ranging from 98.9% to 104% for DIP concentration in pharmaceutical formulations. These results emphasize the selectivity and robustness of the developed electroanalytical method, positioning it as a reliable tool for monitoring DIP. The comprehensive account of experimental procedures, optimization strategies, and analytical validation presented in this study establish the efficacy and potential applications of the developed sensor in pharmaceutical analysis. Overall, this research contributes valuable insights into the field of electrochemical sensing and offers promising prospects for its application in various pharmaceutical and clinical settings.

Recent Advances in and Applications of Electrochemical Sensors Based on Covalent Organic Frameworks for Food Safety Analysis.

The international community has been paying close attention to the issue of food safety as a matter of public health. The presence of a wide range of contaminants in food poses a significant threat to human health, making it vital to develop detection methods for monitoring these chemical contaminants. Electrochemical sensors using emerging materials have been widely employed to detect food-derived contaminants. Covalent organic frameworks (COFs) have the potential for extensive applications due to their unique structure, high surface area, and tunable pore sizes. The review summarizes and explores recent advances in electrochemical sensors modified with COFs for detecting pesticides, antibiotics, heavy metal ions, and other food contaminants. Furthermore, future challenges and possible solutions will be discussed regarding food safety analysis using COFs.

Zirconium Phosphate-Incorporated Polyaniline-Graphene Oxide Composite Modified Electrodes for Effective and Selective Detection of Nitrite.

Nitrite contamination in food, water, and environmental samples poses a substantial health hazard, owing to its capacity for transformation into carcinogenic compounds. Given the profound ecological and physiological implications, precise and highly sensitive surveillance of nitrite has emerged as an imperative area of concern, addressing the substantial detrimental impact that it can have on both terrestrial and aquatic ecosystems. The novel electroactive polyaniline-graphene oxide composite, incorporating hexagonal zirconium phosphate discs (PGZrP), was systematically engineered as a foundation for an advanced electrochemical sensor, enabling precise nitrite detection in diverse aqueous and biological matrices. At a specific potential peak of +0.85 V, observed within a pH 7.0 phosphate buffer solution, the PGZrP-modified glassy carbon electrode (GCE) exhibited exceptional electrocatalytic proficiency in the sensing nitrite ions (NO2-), surpassing the performance of alternative electrode configurations, including the zirconium phosphate-modified GCE (ZrP/GCE), graphene oxide-modified GCE (GO/GCE), polyaniline-graphene oxide-modified GCE (PG/GCE), and the unmodified bare glassy carbon electrode. The constructed sensor demonstrated an impressive limit of detection at 80 nM along with a broad and linear detection range spanning from 124 nM to 40 mM. The synergistic effect created by the close contact between ZrP and PG, which resulted in a well-enhanced electrochemical sensing capability, was responsible for this exceptional activity. The developed sensor exhibited an enhanced electrochemical performance characterized by an extended operational range, a heightened detection threshold, and exceptional sensitivity. The PGZrP/GCE sensor, as fabricated, consistently demonstrated commendable operational stability, robust reproducibility, and remarkable repeatability in its capacity for nitrite detection. Furthermore, its successful application in the precise quantification of nitrite levels within environmental water samples and blood specimens showcased an impressive recovery rate, establishing it as a promising tool for diverse analytical applications. These findings indicate the promising potential of the PGZrP composite for integration into electrochemical devices designed to deliver rapid response times, heightened sensitivity, and sustained stability, thereby placing it as a potential candidate for the production of cutting-edge sensors, particularly those employed for the precise recognition of nitrite in aquatic and biological specimens.

An Electrochemical Sensor Based on Cu-MOF-199@MWCNTs Laden with CuNPs for the Sensitive Detection of Creatinine.

In this study, the synthesis of Cu-MOF-199@multiwalled carbon nanotubes (Cu-MOF-199@MWCNTs) composites was achieved and utilized to create an advanced electrochemical sensor for creatinine (Cre) detection. The composites were modified on a glassy carbon electrode surface through direct drip coating, followed by the deposition of copper nanoparticles (CuNPs) via constant potential deposition. Characterized by various techniques and electrochemical analyses, the Cu-MOF-199@MWCNTs composite increased the CuNPs load, improving the detection sensitivity for Cre. Under optimal conditions, the modified electrode exhibited good linearity across a broad range of Cre concentrations (0.05-40.0 μM) with a low detection limit of 11.3 nM. The developed sensor demonstrated remarkable stability, reproducibility, and selectivity, showing promise in sensitive and accurate Cre detection in serum samples.

Advances in the Application of Nano-Enzymes in the Electrochemical Detection of Reactive Oxygen Species: A Review

Reactive oxygen species (ROS) play an important role in maintaining human health and are recognized as indicators of oxidative stress linked to various conditions such as neurodegenerative and cardiovascular diseases, as well as cancer. Consequently, detecting ROS levels in biological systems is crucial for biomedical and analytical research. Electrochemical approaches offer promising opportunities for ROS determination due to their exceptional sensitivity, speed, and simplicity of equipment. This review covers studies using advanced electrochemical nanozyme sensors for detecting ROS in biological samples that were published over the last ten years, from 2013 to 2023. Emphasis is placed on the sensor materials and different types of modifiers employed for selective ROS detection. Furthermore, a comprehensive analysis of the sensors’ selectivity was performed.

Copper oxide nanoflowers/poly-l-glutamic acid modified advanced electrochemical sensor for selective detection of l-tryptophan in real samples

The main objective of this research work is to develop a low-cost sensor to detect l-tryptophan (L-tryp) in real sample medium based on a modified glassy carbon electrode. For this, copper oxide nanoflowers (CuONFs) and poly-l-glutamic acid (PGA) were used to modify GCE. The prepared NFs and PGA coated electrode was characterized using field emission scanning electron microscope (FE-SEM) with energy dispersive X-ray (EDX) and attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. Furthermore, the electrochemical activity was performed by cyclic voltammetry (CV), differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS). The modified electrode showed excellent electro-catalytic activity towards L-tryp detection in PBS solution at neutral pH 7.0. Based on the physiological pH condition, the proposed electrochemical sensor can detect L-tryp concentration with a linear range of 1.0 × 10−4-8.0 × 10−8 molL−1 with having a detection limit of 5.0 × 10−8 molL−1 and sensitivity of 0.6μA/μMcm2. The selectivity of L-tryp was tested with a mixture of salt and uric acid solution at the above conditions. Finally, this strategy demonstrated excellent recovery value in real sample analysis like milk and urine.

Recent advances in electrochemical sensors and biosensors for monitoring drugs and metabolites in pharmaceutical and biological samples.

Various applications of electrochemical sensors and biosensors have been reported in many fields. These include pharmaceuticals, drug detection, cancer detection, and analysis of toxic elements in tap water. Electrochemical sensors are characterised by their low cost, ease of manufacture, rapid analysis, small size and ability to detect multiple elements simultaneously. They also allow the reaction mechanisms of analytes, such as drugs, to be taken into account, giving a first indication of their fate in the body or their pharmaceutical preparation. Several materials are used in the construction of sensors, such as graphene, fullerene, carbon nanotubes, carbon graphite, glassy carbon, carbon clay, graphene oxide, reduced graphene oxide, and metals. This review covers the most recent progress in electrochemical sensors used to analyze drugs and metabolites in pharmaceutical and biological samples. We have highlighted carbon paste electrodes (CPE), glassy carbon electrodes (GCE), screen-printed carbon electrodes (SPCE) and reduced graphene oxide electrodes (rGOE). The sensitivity and analysis speed of electrochemical sensors can be improved by modifying them with conductive materials. Different materials used for modification have been reported and demonstrated, such as molecularly imprinted polymers, multiwalled carbon nanotubes, fullerene (C60), iron(III) nanoparticles (Fe3O4NP), and CuO micro-fragments (CuO MF). Manufacturing strategies and the detection limit of each sensor have been reported.

Advances in Electrochemical Sensors for Detecting Analytes in Biofluids

AbstractMore than half of all Americans suffer from chronic diseases, the leading causes of death and disability. However, prompt treatment of chronic diseases can lead to better patient outcomes and a reduced burden on the healthcare system. This highlights the urgent need for electrochemical (EC) sensors that provide non‐invasive, real‐time monitoring of disease‐indicating biomarkers. Due to their high sensitivity, high selectivity, and cost‐effectiveness, EC biosensors have recently shown tremendous promise for individualized health monitoring. This review explains the working principles of EC biosensors. It summarizes the recent advances and improvements of EC biosensors for detecting biomarkers in different biofluids, including tears, saliva, breath, urine, and sweat. Through a comprehensive overview of EC biosensor technologies, this article is expected to aid the development of flexible and wearable EC biosensing systems that have the potential to provide continuous, long‐term health monitoring for both clinical and at‐home use.

Fabrication and application of a 3D-rGO electrochemical sensor for SO2 detection in ionic liquids.

Sulfur dioxide (SO2) is a common atmospheric pollutant. Currently, most of the detection methods are based on chemical reactions and optical absorption principles. However, these methods have some limitations in their detection range and accuracy, especially in complex environments. In this work, sulfur dioxide was absorbed by an ionic liquid, and a new electrochemical sensor based on 3D-rGO/CB was developed for electrochemical detection. Specifically, carbon black (CB) nanoparticles were incorporated with graphene oxide (GO) sheets using spray drying technology to form a highly porous and interconnected 3D-GO/CB microsphere structure. Then, the 3D-rGO/CB/GCE electrochemical sensor was fabricated by electrochemical reduction of the composite material onto a glassy carbon electrode (GCE) surface and used to detect sulfur dioxide in ionic liquids. The results demonstrated that the sensor had excellent conductivity and mass transfer preferable performance catalytic activity for SO2 in ionic liquids, and a linear detection range of 100-3500 ppm. Besides, the detection limit was 52.3 ppm (S/N = 3). Moreover, it had high selectivity, stability, and repeatability. This work significantly contributed to the development of advanced electrochemical sensors with improved performance for detecting SO2 in ionic liquids and has a potential application prospect in the field of electrochemical gas detection.