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Chlorinated organic compounds are useful chemicals or intermediates that are used extensively in both industry and agriculture. The 4-chlorophenol (4CP) in low concentration poses a serious environmental problem and causes many health issues, including cancer and liver disease. In this work, we demonstrated the detection of 4CP at carbon paste electrodes modified using tungsten oxide (WO 3 ) nanorods and reduced graphene oxide (rGO) nanoparticles. The significance of pH on the voltammetric response of 4CP was investigated, and it was discovered that an alkaline pH is an optimal condition for detecting substituted phenols. Moreover, parameters like heterogeneous rate constant, accumulation time, temperature effect, Gibb's free energy, scan rate, enthalpy, activation energy, and entropy were studied. The excellent catalytic and bulk properties of tungsten oxide nanostructures make it an effective modifier in electrochemical sensors. The employment of nanostructured WO 3 for the assay of 4CP offers excellent sensitivity, selectivity, and applicability. The WO 3 nanostructures are obtained hydrothermally and characterized in detail to understand the crystalline, quantitative and chemical properties. The electrochemical behavior of 4CP was studied utilizing voltammetry techniques. The CV technique was used to optimize and affect many factors in the electrochemical behavior of 4CP. The scan rate investigation helps to examine the physicochemical characteristics of the electrode process, and the electrooxidation of 4CP included 2 electrons and 2 protons. With 4CP, the modified electrode displayed a broad range of linearity. The limit of detection was determined to be 0.102 nM, while the limit of quantification was 0.3433 nM. The concentration of 4CP ranged between 0.1 × 10 -7  M and 3.5 × 10 -7  M. The fabricated electrode was also used to detect 4CP in soil and water samples. Good recoveries were obtained from the soil and water samples. The proposed electrode was used for analytical applications, including 4CP detection with high selectivity, low detection limit, sensitivity, and rapid response., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The antibiotic drug trimethoprim (TMP) is used to treat bacterial infections in humans and animals, and frequently TMP is used along with sulfonamides. However, a large portion of TMP is excreted in its active state, which poses a severe problem to humans and the environment. A sensitive, rapid, cost-effective analytical tool is required to monitor the TMP concentration in biological and environmental samples. Hence, this study proposed an analytical methodology to analyze TMP in clinical, biological and environmental samples. The investigations were carried out using a glucose-modified carbon paste electrode (G-CPE) employing voltammetric techniques. Electrochemical behavior was examined with 0.5 mM TMP solution at optimum pH 3.4 (Phosphate Buffer Solution, I = 0.2 M). The influence of scan rate on the electro-oxidation of TMP was studied within the range of 0.05 to 0.55 V/s. The effect of pH and scan rate variations revealed proton transfer during oxidation. Moreover, diffusion phenomena governed the irreversibility of the electrode reaction. A probable and suitable electrode interaction and reaction mechanism was proposed for the electrochemical oxidation of TMP. Further, the TMP was quantitatively estimated with the differential pulse voltammetry (DPV) technique in the concentration range from 9.0 × 10 -7 to 1.0 × 10 -4 M. The tablet, spiked water and urine analysis demonstrated that the selected method and developed electrode were rapid, simple, sensitive, and cost-effective.

Incorporating new pollutants and environmental pollution has become a formidable issue as new pollutants are introduced into it and have become a significant concern in recent years. Detection of such pollutants needs a susceptible, selective, and cost-effective sensor that can sense their presence and quantify them at a trace level. In the present study, we have designed a 2D graphene oxide (GO)-based glassy carbon electrode (GCE) electrochemical sensor (GO/GCE) and utilized it as a sensing material for the detection and determination of CRZ. The voltammetric behavior of CRZ was studied using cyclic voltammetry (CV) and square wave voltammetry (SWV) techniques. The SWV was applied to quantify and analyze CRZ in actual samples. A better response of CRZ was noticed at GO/GCE when phosphate buffer solution of pH 4.2 was used as a supporting electrolyte for to experiment. The SWV technique achieved trace-level detection of CRZ. A linearity plot was obtained for the concentration range of 1.0 × 10 -7  M to 2.5 × 10 -4  M with a limit of detection of 1.38 × 10 -8  M. The selectivity of the modified sensor was verified by the interference study of metal ions and other pesticides with CRZ. The agricultural and environmental significance of the developed method was successfully tested by estimating CRZ in water and soil samples., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Pramipexole (PMXL) belongs to the benzothiazole class of aromatic compounds and is used in treating Parkinson's disease; however, overdosage leads to some abnormal effects that could trigger severe side effects. Therefore, it demands a sensitive analytical tool for trace level detection. In this work, we successfully developed an electrochemical sensor for the trace level detection of PMXL, using the voltammetric method. For the analysis, graphitic carbon nitride (gCN) was opted and synthesized by using a high-temperature thermal condensation method. The synthesized nanoparticles were employed for surface characterization, using transmission electron microscopy (TEM), X-ray diffraction (XRD), and atomic force microscopy (AFM) techniques. The electrochemical characterization of the material was evaluated by using the electrochemical impedance spectroscopy (EIS) technique to evaluate the solution-electrode interface property. The cyclic voltammetry (CV) behavior of PMXL displayed an anodic peak in the forward scan, indicating that PMXL underwent electrooxidation, and an enhanced detection peak with lower detection potential was achieved for gCN-modified carbon paste electrode (gCN·CPE). The influence of different parameters on the electrochemical behavior was analyzed, revealing the diffusion governing the electrode process with an equal number of hydronium ions and electron involvement. For the fabricated gCN·CPE, good linearity range was noticed from 0.05 to 500 µM, and a lower detection limit (L D ) of 0.012 µM was achieved for the selected concentration range (0.5 to 30 µM). Selectivity of the electrode in PMXL detection was investigated by conducting an interference study, while the tablet sample analysis demonstrates the sensitive and real-time application of the electrode. The good recovery values for the analysis illustrate the efficiency of the electrode for PMXL analysis.

Graphene is an intriguing two-dimensional honeycomb-like carbon material with a unique basal plane structure, charge carrier mobility, thermal conductivity, wide electrochemical spectrum, and unusual physicochemical properties. Therefore, it has attracted considerable scientific interest in the field of nanoscience and bionanotechnology. The high specific surface area of graphene allows it to support high biomolecule loading for good detection sensitivity. As such, graphene, graphene oxide (GO), and reduced GO are excellent materials for the fabrication of new nanocomposites and electrochemical sensors. Graphene has been widely used as a chemical building block and/or scaffold with various materials to create highly sensitive and selective electrochemical sensing microdevices. Over the past decade, significant advancements have been made by utilizing graphene and graphene-based nanocomposites to design electrochemical sensors with enhanced analytical performance. This review focus on the synthetic strategies, as well as the structure-to-function studies of graphene, electrochemistry, novel multi nanocomposites combining graphene, limit of detection, stability, sensitivity, assay time. Finally, the review describes the challenges, strategies and outlook on the future development of graphene sensors technology that would be usable for the internet of things are also highlighted., (Copyright © 2022 Elsevier B.V. All rights reserved.)

The widespread use of methyl parathion (MP) and carbendazim (CBZ) as pesticide molecules for controlling pests and protect crops has added pollution issues; excess usage of these can lead to atmospheric pollution through contaminating water and soil sources. In the present study, detection of these compounds at the trace level was achieved by employing graphene oxide (GO) and graphitic carbon nitride (g-C 3 N 4 ) nanohybrid electrode assembly (GO/g-C 3 N 4 /GCE). The X-ray diffraction (XRD), Transmission Electron Microscopy (TEM), and Atomic Force Microscopy (AFM) techniques were also used to characterize the materials developed to reveal their purity, crystal structure, and morphology. The complete voltammetric behavior of these analytes was investigated using cyclic voltammetic (CV) and square wave voltammetry (SWV) techniques. The influence of pH was studied and it was noticed that electrochemical response was the highest at pH 7.0 for MP and at pH 4.2 for CBZ. Density Functional Theory (DFT) calculations could help us to understand the adsorption behavior of MP and CBZ onto the GO and g-C 3 N 4 before their degradation due to the electrochemical reactions. SWV technique was helpful in the trace level detection of MP and CBZ. Linearity plots were obtained in the range of concentration from 8.0 × 10 -8  M to 1.0 × 10 -4  M with a limit of detection 0.824 nM for MP and 1.0 × 10 -8  M to 2.5 × 10 -4  M for CBZ with the detection limit of 2.82 nM. Significance of the developed method in the field of agricultural and environmental domains was successfully investigated by monitoring MP and CBZ in water and soil samples, and the obtained results suggested the selectivity, stability, and reproducibility of the newly developed GO/g-C 3 N 4 /GCE electrode assembly., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Nano-size photocatalysts exhibit multifunctional properties that opened the door for improved efficiency in energy, environment, and health care applications. Among the diversity of catalyst Quantum dots are a class of nanomaterials having a particle size between 2 and 10 nm, showing unique optoelectrical properties that are limited to some of the metal, metal oxide, metal chalcogenides, and carbon-based nanostructures. These unique characteristics arise from either pristine or binary/ternary composites where noble metal/metal oxide/metal chalcogenide/carbon quantum dots are anchored on the surface of semiconductor photocatalyst. It emphasized that properties, as well as performance of photocatalytic materials, are greatly influenced by the choice of synthesis methods and experimental conditions. Among the chemical methods, photo-deposition, precipitation, and chemical reduction, are the three most influential synthesis approaches. Further, two types of quantum dots namely metal based and carbon-based materials have been highlighted. Based on the optical, electrical and surface properties, quantum dots based photocatalysts have been divided into three categories namely (a) photocatalyst (b) co-catalyst and (c) photo-sensitizer. They showed enhanced photocatalytic performance for hydrogen production under visible/UV-visible light irradiation. Often, pristine metal chalcogenides as well as metal/metal oxide/carbon quantum dots attached to a semiconductor particle exhibit enhanced the photocatalytic activity for hydrogen production through absorption of visible light. Alternatively, noble metal quantum dots, which provide plenty of defects/active sites facilitate continuous hydrogen production. For instance, production of hydrogen in the presence of sacrificial agents using metal chalcogenides, metal oxides, and coinage metals based catalysts such as CdS/MoS 2 (99,000 μmol h -1 g -1 ) TiO 2 -Ni(OH) 2 (47,195 μmol h -1 g -1 ) and Cu/Ag-TiO 2 nanotubes (56,167 μmol h -1 g -1 ) have been reported. Among the carbon-based nanostructures, graphitic C 3 N 4 and carbon quantum dots composites displayed enhanced hydrogen gas (116.1 μmol h -1 ) production via overall water splitting. This review accounts recent findings on various chemical approaches used for quantum dots synthesis and their improved materials properties leading to enhanced hydrogen production particularly under visible light irradiation. Finally, the avenue to improve quantum efficiency further is proposed., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

In recent years, various facile and low-cost methods have been developed for the synthesis of advanced nanostructured photocatalytic materials. These catalysts are required to mitigate the energy crisis, environmental deterioration, including water and air pollution. Among the various semiconductors explored, recently novel classes of polymeric graphitic carbon nitride (g-C 3 N 4 )-based heterogeneous photocatalysts have established much greater importance because of their unique physiochemical properties, large surface area, low price, and long service life, ease of synthesis, product scalability, controllable band gap properties, low toxicity, and high photocatalytic activity. The present comprehensive review focuses on recent achievements in a number of facile chemical synthesis methods for semiconducting polymeric carbon nitrides and their heterogeneous nanohybrids with various dopants, nanostructured metals, metal oxides, and nanocarbons, as well as the parameters influencing their physiochemical properties and photocatalytic efficiency, which are discussed with reference to various catalytic applications such as air (NO x ) purification, wastewater treatment, hydrogen generation, CO 2 reduction, and chemical transformation. The mechanisms for the superior photocatalytic activity of polymeric g-C 3 N 4 -based heterogeneous photocatalysts are also discussed. Finally, the challenges, prospects, and future directions for photocatalytic polymeric g-C 3 N 4 -based semiconducting materials are described., (Copyright © 2019 Elsevier Ltd. All rights reserved.)