Synergistic Manganese Cobalt Phosphide core-shell for the Electrochemical Detection of Methyl Parathion in Food Sample.

The development of a robust electrocatalyst for the electrochemical sensor for hazardous pesticides will reduce its effects on the ecosystem. Herein, we synthesized the robust manganese cobalt phosphide (MnCoP) - Core-shell as an electrochemical sensor for the determination of hazardous pesticide methyl parathion (MP). The MnCoP- Core-shell was prepared with the sustainable self-template route can help with the larger surface area. The Core-shell structure of MnCoP possesses a higher active surface area which increases the electrocatalytic performance and is utilized to improve the electrochemical MP reduction with the synergism of the core and shell structure. Remarkably, it realizes the higher sensitivity (0.014 µA µM-1 cm-2) of MnCoP- Core-shell/GCE achieves towards MP with lower limit of detection (LoD 50 nM) and exceptional recovery rate of MP in vegetable samples are achieved with the differential pulse voltammetry (DPV) technique. The MnCoP- Core-shell electrode reserved their superior electrochemical performances with high reproducibility and repeatability. This prominent activity of the MnCoP core-shell towards the MP in real sample analysis, makes it a promising electrochemical sensor for the detection of MP.

Design and fabrication of La-based perovskites incorporated with functionalized carbon nanofibers for the electrochemical detection of roxarsone in water and food samples.

The pentavalent arsenic compound roxarsone (RSN) is used as a feed additive in poultry for rapid growth, eventually ending up in poultry litter. Poultry litter contains chicken manure, which plays a vital role as an affordable fertilizer by providing rich nutrients to agricultural land. Consequently, the extensive use of poultry droppings serves as a conduit for the spread of toxic forms of arsenic in the soil and surface water. RSN can be easily oxidized to release highly carcinogenic As(III) and As(IV) species. Thus, investigations were conducted for the sensitive detection of RSN electrochemically by developing a sensor material based on lanthanum manganese oxide (LMO) and functionalized carbon nanofibers (f-CNFs). The successfully synthesised LMO/f-CNF composite was confirmed by chemical, compositional, and morphological studies. The electrochemical activity of the prepared composite material was examined using cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The obtained results confirmed that LMO/f-CNF showed enhanced electrocatalytic activity and improved current response with a good linear range (0.01-0.78 µM and 2.08-497 µM, respectively), exhibiting a low limit of detection (LOD) of 0.004 µM with a high sensitivity of 13.24 µA µM-1 cm-2 towards the detection of RSN. The noteworthy features of LMO/f-CNF composite with its superior electrochemical performance enabled reliable reproducibility, exceptional stability and reliable practical application in the analysis of tap water and food sample, affording a recovery range of 86.1-98.87%.

In-situ growth of MOF-derived Co3S4@MoS2 heterostructured electrocatalyst for the detection of furazolidone.

The over-exploitation of antibiotics in food and farming industries ruined the environmental and human health. Consequently, electrochemical sensors offer significant advantages in monitoring these compounds with high accuracy. Herein, MOF-derived hollow Co3S4@MoS2 (CS@MS) heterostructure has been prepared hydrothermally and applied to fabricate an electrochemical sensor to monitor nitrofuran class antibiotic drug. Various spectroscopic methodologies have been employed to elucidate the structural and morphological information. Our prepared electrocatalyst has better electrocatalytic performance than bare and other modified glassy carbon electrodes (GCE). Our CS@MS/GCE sensor exhibited a highly sensitive detection by offering a low limit of detection, good sensitivity, repeatability, reproducibility, and stability results. In addition, our sensor has shown a good selectivity towards the target analyte among other potential interferons. The practical reliability of the sensor was measured by analyzing various real-time environmental and biological samples and obtaining good recovery values. From the results, our fabricated CS@MS could be an active electrocatalyst material for an efficient electrochemical sensing application.

Development of Different Kinds of Electrocatalyst for the Electrochemical Reduction of Carbon Dioxide Reactions: An Overview.

Significant advancements have been made in the development of CO2 reduction processes for applications such as electrosynthesis, energy storage, and environmental remediation. Several materials have demonstrated great potential in achieving high activity and selectivity for the desired reduction products. Nevertheless, these advancements have primarily been limited to small-scale laboratory settings, and the considerable technical obstacles associated with large-scale CO2 reduction have not received sufficient attention. Many of the researchers have been faced with persistent challenges in the catalytic process, primarily stemming from the low Faraday efficiency, high overpotential, and low limiting current density observed in the production of the desired target product. The highlighted materials possess the capability to transform CO2 into various oxygenates, including ethanol, methanol, and formates, as well as hydrocarbons such as methane and ethane. A comprehensive summary of the recent research progress on these discussed types of electrocatalysts is provided, highlighting the detailed examination of their electrocatalytic activity enhancement strategies. This serves as a valuable reference for the development of highly efficient electrocatalysts with different orientations. This review encompasses the latest developments in catalyst materials and cell designs, presenting the leading materials utilized for the conversion of CO2 into various valuable products. Corresponding designs of cells and reactors are also included to provide a comprehensive overview of the advancements in this field.

Novel Design of Perovskite-Structured Neodymium Cobalt Oxide Nanoparticle-Embedded Graphene Oxide Nanocomposites as Efficient Active Materials of Energy Storage Devices.

In recent years, electrochemical supercapacitors are expected to represent the future of energy storage device technology. Specifically, the excellent electrochemical performance with long cycle life, high energy, and power density is considered an essential criterion for commercial applications. Herein, we constructed a novel composite of neodymium cobalt oxide-encapsulated graphene oxide nanocomposite (NCO/GO) via a simple and robust method for a symmetric supercapacitor (SSC) device. The prepared samples were securitized by X-ray diffraction, Fourier transform infrared spectroscopy, Raman, X-ray photoelectron spectroscopy, field emission scanning electron microscopy, high-resolution transmission electron microscopy, and Brunauer-Emmett-Teller analysis. The as-synthesized NCO/GO is deposited on nickel foam (NF) and used as a supercapacitor electrode (NCO/GO/NF), which exhibits superior specific capacitance (Cs) of 1080.92 F g-1 at 1 A g-1 and fantastic cycling life with ∼89.42% retention after 10,000 cycles at 10 A g-1 in 1.0 M KOH aqueous electrolyte. A tremendous electrochemical performance of the hybrid nanocomposite electrode is obtained from the good redox activity and synergistic effects of the NCO spherical-like nanoparticles combined with the GO nanosheets. Furthermore, the assembled SSC device delivers significantly enhanced power density (932.93 Wh kg-1) and energy density (210.42 mWh kg-1). Moreover, the SSCs exhibit excellent cycling stability with ∼82.19% capacity retaining over 10,000 charge/discharge cycles. Remarkably, a 1.8 V red light-emitting diode (LED) can be lit up for more than 10 min by series connection SSCs. Thus, the obtained results indicated that the NCO/GO/NF//NCO/GO/NF symmetric device has a robust and cost-effective electrode material for high-performance supercapacitor systems.

Metal-Oxides- and Metal-Oxyhydroxides-Based Nanocomposites for Water Splitting: An Overview.

Water electrolysis is an important alternative technology for large-scale hydrogen production to facilitate the development of green energy technology. As such, many efforts have been devoted over the past three decades to producing novel electrocatalysis with strong electrochemical (EC) performance using inexpensive electrocatalysts. Transition metal oxyhydroxide (OxH)-based electrocatalysts have received substantial interest, and prominent results have been achieved for the hydrogen evolution reaction (HER) under alkaline conditions. Herein, the extensive research focusing on the discussion of OxH-based electrocatalysts is comprehensively highlighted. The general forms of the water-splitting mechanism are described to provide a profound understanding of the mechanism, and their scaling relation activities for OxH electrode materials are given. This paper summarizes the current developments on the EC performance of transition metal OxHs, rare metal OxHs, polymers, and MXene-supported OxH-based electrocatalysts. Additionally, an outline of the suggested HER, OER, and water-splitting processes on transition metal OxH-based electrocatalysts, their primary applications, existing problems, and their EC performance prospects are discussed. Furthermore, this review article discusses the production of energy sources from the proton and electron transfer processes. The highlighted electrocatalysts have received substantial interest to boost the synergetic electrochemical effects to improve the economy of the use of hydrogen, which is one of best ways to fulfill the global energy requirements and address environmental crises. This article also provides useful information regarding the development of OxH electrodes with a hierarchical nanostructure for the water-splitting reaction. Finally, the challenges with the reaction and perspectives for the future development of OxH are elaborated.

Hexagonally close-packed three-dimensional nano-flower entrapped on a heteroatom doped carbon sheets: A sensitive electro-catalyst to determine sulfonamide in environmental samples.

Sulfamethazine (SMZ) is one of the antibiotics frequently found with low concentrations in water bodies including drinking water sources and foodstuffs contamination, which affects the environmental ecosystem and humans. Therefore, the detection of SMZ is necessary to protect the biosphere. This work provides an investigation of the SMZ oxidation process using the electrochemical method by hydrothermally synthesized Barium doped Zinc oxide (BZO) with nitrogen and boron-doped reduced graphene oxide (NBRGO). The BZO/NBRGO composite was characterized using FESEM, EDAX, HR-TEM, Raman-spectroscopy, XRD, and XPS. Further, an electrochemical investigation has also made use of EIS, CV, and DPV. The limit of detection (LOD) of the SMZ has been found 0.003 µM with high sensitivity of 12.804 µA µM-1 cm-2 and a linear range (0.01-711 µM). Additionally, the repeatability, reproducibility, and stability of the BZO/NBRGO electrode have an excellent outcome compared with other electrodes. These prepared BZO/NBRGO electrodes have been used for the determination of SMZ in milk and water sample with acceptable recoveries.

In-situ formation of niobium oxide - Niobium carbide - Reduced graphene oxide ternary nanocomposite as an electrochemical sensor for sensitive detection of anticancer drug methotrexate.

Engineering the nanostructure of an electrocatalyst is crucial in developing a high-performance electrochemical sensor. This work exhibits the hydrothermal followed by annealing synthesis of niobium oxide/niobium carbide/reduced graphene oxide (NbO/NbC/rGO) ternary nanocomposite. The oval-shaped NbO/NbC nanoparticles cover the surface of rGO evenly, and the rGO nanosheets are interlinked to produce a micro-flower-like architecture. The NbO/NbC/rGO nanocomposite-modified electrode is presented here for the first time for the rapid and sensitive electrochemical detection of the anticancer drug methotrexate (MTX). Down-sized NbO/NbC nanoparticles and rGO's high surface area provide many active sites with a rapid electron transfer rate, making them ideal for MTX detection. In comparison to previously reported MTX sensors, the developed drug sensor exhibits a lower oxidation potential and a higher peak current responsiveness. The constructed sensors worked analytically well under optimal conditions, as shown by a low detection limit of 1.6 nM, a broad linear range of 0.1-850 µM, and significant recovery findings (∼98 %, (n = 3)) in real samples analysis. Thus, NbO/NbC/rGO nanocomposite material for high-performance electrochemical applications seems promising.

Development of an Amorphous Nickel Boride/Manganese Molybdate Heterostructure as an Efficient Electrode Material for a High-Performance Asymmetric Supercapacitor.

The exploration of heterostructure materials with unique electronic properties is considered a desirable platform for fabricating electrode/surface interface relationships for constructing asymmetric supercapacitors (ASCs) with high energy density. In this work, a heterostructure based on amorphous nickel boride (NiXB) and crystalline square bar-like manganese molybdate (MnMoO4) was prepared by a simple synthesis strategy. The formation of the NiXB/MnMoO4 hybrid was confirmed by powder X-ray diffraction (p-XRD), field emission scanning electron microscopy (FE-SEM), field-emission transmission electron microscopy (FE-TEM), Brunauer-Emmett-Teller (BET), Raman, and X-ray photoelectron spectroscopy (XPS). In this hybrid system (NiXB/MnMoO4), the intact combination of NiXB and MnMoO4 leads to a large surface area with open porous channels and abundant crystalline/amorphous interfaces with a tunable electronic structure. This NiXB/MnMoO4 hybrid shows high specific capacitance (587.4 F g-1) at 1 A g-1, and it even retains a capacitance of 442.2 F g-1 at 10 A g-1, indicating superior electrochemical performance. The fabricated NiXB/MnMoO4 hybrid electrode also exhibited an excellent capacity retention of 124.4% (10000 cycles) and a Coulombic efficiency of 99.8% at a current density of 10 A g-1. In addition, the ASC device (NiXB/MnMoO4//activated carbon) achieved a specific capacitance of 104 F g-1 at 1 A g-1 and delivered a high energy density of 32.5 Wh.kg-1 with a power density of 750 W·kg-1. This exceptional electrochemical behavior is due to the ordered porous architecture and the strong synergistic effect of NiXB and MnMoO4, which enhances the accessibility and adsorption of OH- ions that improve electron transport. Moreover, the NiXB/MnMoO4//AC device exhibits excellent cyclic stability with a retention of 83.4% of the original capacitance after 10000 cycles, which is due to the heterojunction layer between NiXB and MnMoO4 that can improve the surface wettability without causing structural changes. Our results show that the metal boride/molybdate-based heterostructure is a new category of high-performance and promising material for the growth of advanced energy storage devices.

3D flower-like ceria silver co-doped zinc oxide catalyst assembled by nanorod for electrochemical sensing of zearalenone in food samples.

To ensure food safety and quality, the development of rapid detection of mycotoxins using sensitive and accurate methods is essential. Zearalenone is one of the mycotoxins found in cereals, and its toxicity poses a serious risk to humans. For this concern, a simple ceria silver co doped zinc oxide (Ce-Ag/ZnO) catalyst was prepared by coprecipitation approach. The physical properties of the catalyst were characterized by XRD, FTIR, XPS, FESEM, and TEM. The Ce-Ag/ZnO catalyst was used as an electrode material for the detection of ZEN in food samples due to its synergistic effect and high catalytic activity. The sensor exhibits good catalytic performance with a detection limit of 0.26 µg/mL. Moreover, the efficiency of the prepared sensor was confirmed by selectivity in interference studies and real-time analysis in food samples. Our research is an essential technique for using trimetallic heterostructures to study the construction of sensors.

Construction of an electrochemical sensor towards environmental hazardous 4-nitrophenol based on Nd(OH)3-embedded VSe2 nanocomposite.

The toxicity of 4-nitrophenol (4-NP) is one of the most common threats to the environment; therefore, developing a simple and sensitive analytical method to detect 4-NP is crucial. In this study, we prepared the Nd(OH)3/VSe2 nanocomposite using the simple hydrothermally assisted ultrasonication method and it was used to detect the 4-NP. Different characterization techniques were used to investigate the morphological and chemical compositions of Nd(OH)3/VSe2 nanocomposite. All of these investigations revealed that Nd(OH)3 nanoparticles were finely dispersed on the surface of the VSe2 nanosheet. The electrical conductivity of our prepared samples was evaluated by the electrochemical impedance spectroscopic technique. The CV and DPV methods were used to explore the electrochemical activity of 4-NP at the Nd(OH)3/VSe2/GCE sensor which exhibited a wide linear range (0.001 to 640 µM), low limit of detection (0.008 µM), and good sensitivity (0.41 µA µM-1 cm-2), respectively. Additionally, Nd(OH)3/VSe2/GCE sensor was tested in water samples for the detection of 4-NP, which exhibited good recovery results. The Nd(OH)3/VSe2 electrode material is a novel one for the electrochemical sensor field, and the obtained overall results also proved that our proposed material is an active material for sensor applications.

Hierarchical 3D Snowflake-like Iron Diselenide: A Robust Electrocatalyst for Furaltadone Detection.

An electrocatalyst with a large active site is critical for the development of a high-performance electrochemical sensor. This work demonstrates the fabrication of an iron diselenide (FeSe2)-modified screen-printed carbon electrode (SPCE) for the electrochemical determination of furaltadone (FLD). It has been prepared by the facile method and systematically characterized with various microscopic/spectroscopic approaches. Due to advantageous physiochemical properties, the FeSe2/SPCE showed a low charge-transfer resistance value of 200 Ω in 5.0 mM [Fe(CN)6]3-/4- containing 0.1 M KCl. More importantly, the FeSe2/SPCE exhibited superior catalytic performance compared to the bare SPCE for FLD sensing based on the electrochemical response in terms of a peak potential of -0.44 V (vs Ag/AgCl (sat. KCl)) and cathodic response current of -22.8 µA. Operating at optimal conditions, the FeSe2-modified electrode showed wide linearity from 0.01 to 252.2 µM with a limit of detection of 0.002 µM and sensitivity of 1.15 µA µM-1 cm-2. The analytical performance of the FeSe2-based platform is significantly higher than many previously reported FLD electrochemical sensors. Furthermore, the FeSe2/SPCE also has a promising platform for FLD detection with high sensitivity, good selectivity, excellent stability, and robust reproducibility. Thus, the finding above shows that the FeSe2/SPCE is a highly suitable candidate for the electrochemical determination of glucose levels for real-time applications such as in human urine and river water samples.

Fabrication of ZnWO4/Carbon Black Nanocomposites Modified Glassy Carbon Electrode for Enhanced Electrochemical Determination of Ciprofloxacin in Environmental Water Samples.

The major problem facing humanity in the world right now is the sustainable provision of water and electricity. Therefore, it is essential to advance methods for the long-term elimination or removal of organic contaminants in the biosphere. Ciprofloxacin (CIP) is one of the most harmful pollutants affecting human health through improper industrial usage. In this study, a zinc tungsten oxide (ZnWO4) nanomaterial was prepared with a simple hydrothermal synthesis. The ZnWO4/Carbon black nanocomposites were fabricated for the determination of CIP. The nanocomposites were characterized by field emission scanning electron microscopy, energy dispersion X-ray spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and electrochemical impedance spectroscopy. Electrochemical studies were done using cyclic voltammetry and differential pulse voltammetry methods. Based on the electrode preparation, the electrochemical detection of CIP was carried out, producing exceptional electrocatalytic performance with a limit of detection of 0.02 µM and an excellent sensitivity of (1.71 µA µM-1 cm-2). In addition, the modified electrode displayed great selectivity and acceptable recoveries in an environmental water sample analysis for CIP detection of 97.6% to 99.2%. The technique demonstrated high sensitivity, selectivity, outstanding consistency, and promise for use in ciprofloxacin detection. Ciprofloxacin was discovered using this brand-new voltammetry technique in a water sample analysis.

Design and synthesis of nickel-doped cobalt molybdate microrods: An effective electrocatalyst for the determination of antibiotic drug ronidazole.

Ronidazole (RDZ) is a veterinary antibiotic drug that has been used in animal husbandry as feed. However, improper disposal and illegal use of pharmaceuticals have severely polluted water resources. Doping/substitution of metal ions is an effective strategy to change the material's crystal phase, morphology, and electrocatalytic activity. In this work, nickel (Ni2+)-doped cobalt molybdate microrods (NCMO MRs) were prepared for the electrochemical detection of RDZ. The catalyst was prepared by reflux method followed by calcination at 500 °C. The prepared catalyst was confirmed by various spectroscopic and microscopic analyses. XRD and Raman spectroscopy demonstrated that the phase transition from ß-CoMoO4 to α-CoMoO4 was achieved by Ni2+ doping. The SEM analysis showed that cobalt molybdate (CMO) microrods were self-assembled during Ni2+ doping and formed an urchin-like structure, and the average diameter of the MRs was ±50 nm. The electrocatalytic activity of the catalysts was analyzed using the CV technique. The NCMO MRs/GCE exhibited the higher current response than the pristine CMO. The electron transfer coefficient (α = 0.56) and heterogeneous rate constant (ks = 0.32 s-1) of NCMO MRs/GCE were evaluated by kinetic studies. In addition, the diffusion coefficient of RDZ was determined to be 2.32 × 10-5 cm2/s. Moreover, NCMO MRs/GCE exhibits a low detection limit for RDZ (15 nM) as well as a higher sensitivity (1.57 µA µM-1 cm-2). The fabricated RDZ sensor was successfully applied to analysis of lake and tap water samples. Based on the results, we believe that the as-prepared NCMO MRs/GCE is a viable electrode material for RDZ sensors in environmental monitoring.

Synthesis of perovskite-type potassium niobate using deep eutectic solvents: A promising electrode material for detection of bisphenol A.

This study demonstrates a hydrothermal method to prepare perovskite-type potassium niobate (KNbO3) through deep eutectic solvent (DES), which is further used as an electrode material for the determination of bisphenol A (BPA). The as-synthesized KNbO3 was systematically characterized by different microscopic and spectroscopic techniques. The KNbO3-modified electrode demonstrates excellent electrocatalytic activity for BPA compared to the pristine electrode. The enhanced performance of the proposed sensor is attributed to the numerous active sites, large electrochemical surface area, high electrical conductivity, and rapid electron transfer. The fabricated sensor shows a wide detection range (0.01-84.3 µM), a low limit of detection (0.003 µM), a high sensitivity (0.51 µA µM-1 cm-2), and good anti-interference abilities towards the BPA detection by linear sweep voltammetry method. Besides, it was successfully applied to determining BPA in food samples, demonstrating good practicability. This design paves a new way to fabricate efficient electrode material for various electrochemical applications using a DES medium.

Effect of bismuth doping on zircon-type gadolinium vanadate: Effective electrocatalyst for determination of hazardous herbicide mesotrione.

Pesticides are used to promote the growth of plants and crops by killing weeds and other pests. On the other hand, overused and unused pesticides can leach into groundwater and agricultural lands, easily contaminating water, air, and soil resources. Doping with metal ions is an effective method to improve the catalytic activity of potential electrode materials. In the present study, an electrochemical sensor based on Bi3+-doped gadolinium vanadate nanoparticles (GVB NPs) was fabricated for sensitive and selective detection of harmful pesticide mesotrione (MST). The crystalline nature, functional groups, and elemental composition of the prepared electrocatalysts were confirmed by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. Field-emission scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HR-TEM) showed that the undoped gadolinium vanadate had a rice-like nanostructure and was designated as GV NRs, while GVB had the morphology of nanoparticles. The fabricated electrode exhibited a well-resolved MST reduction peak in cyclic voltammetry and linear sweep voltammetry (LSV). Bismuth doping effectively enhanced the MST reduction and produced a stronger cathodic current response than bare and GV NRs-modified GCE. Moreover, GVB NPs/GCE show a nanomolar detection limit of 45 nM with a sensitivity of 0.43 µA µM-1 cm-2. The proposed sensor showed good repeatability, reproducibility, and stability in LSV analysis. The fabricated MST sensor was successfully applied to the analysis of real samples (river water and corn) with good recovery results.

Enhancing catalytic activity through the construction of praseodymium tungstate decorated on hierarchical three-dimensional porous biocarbon for determination of furazolidone in aquatic samples.

Boosting catalytic performance as a vital role for an electrochemical sensor for monitoring various hazardous nitro drugs. Herein, an inexpensive, facile, and eco-friendly construction of praseodymium tungstate decorated on three dimensional porous biocarbon (PrW/3D-PBC) for electrochemical determination of carcinogenic residue furazolidone (FZ). The nanostructured PrW nanoparticles were prepared by solvent evaporation from peroxo-tungstic acid and 3D-PBC was prepared from biomass precursor under the carbonization method. Furthermore, the composite of PrW decorated on 3D-PBC was prepared by an ultrasonic-assisted wet chemical approach. Besides, the composite characterization of crystalline, functional group, degree of carbonization, chemical states, and morphology were utilized by theXRD, FTIR, RAMAN, XPS, and FESEM analysis. These 3D porous carbon decorated PrW nanoparticles facilitate the electrochemical anchoring sites, surface area, and ease of diffusion layers towards the detection of hazardous nitro pollutant FZ by using CV analysis. The low LOD and high sensitivity were achieved by FZ determination through using LSV and DPV techniques. The practical capability of the PrW/3D-PBC/GCE sensor was determined by using aquatic samples to achieve a good recovery result. These results instigate that the PrW/3D-PBC will be an efficient electrocatalytic material for FZ sensor in environmental aquatic samples.

N-substituted CQDs impregnated by Fe3O4 heterostructure: Bifunctional catalyst for electro-catalytic and photo-catalytic detection of an environmental hazardous organic pollutant.

ortho-Nitroaniline (o-NA) compounds are deemed to be a strongly toxic pollutant in nature and potentially carcinogenic; however, they are frequently utilized to synthesize dyes, pesticides, medicines, fungicides, pigments, and other organic chemicals. Their detection in an aqueous medium is fundamentally required to avoid the potential hazardous being created by these compounds. In this study, a novel sensor based on an Iron oxide (Fe3O4) containing highly dispersed nitrogen-doped carbon quantum dots (N-CQDs@Fe3O4 NFs) was demonstrated for the electrochemical detection of o-NA using differential pulse voltammetry (DPV) and cyclic voltammetry (CV) techniques. N-CQDs@Fe3O4 NFs were synthesized by hydrothermal method and studied by various analytical and spectroscopy techniques, which collectively reveal that the as-prepared composite has superior physical and chemical properties. The DPV study indicated that the o-NA sensor had a good limit of detection, linear range, and sensitivity in the range of 1.2 nm, 0.03-386.84 µM, and 36.5575 µA µM-1 cm-2, respectively, along with the sensor showed superior sensitivity when compared to the previously reported modified electrodes. Further, N-CQD/Fe3O4 NFs worked as heterogeneous catalysts for the photocatalytic reduction of o-NA to o-phenylenediamine (o-PD) in an aqueous medium. The reaction was examined under UV-Visible spectroscopy, and the complete photocatalytic reduction was observed for the N-CQD/Fe3O4 NFs in about 6 min with 96% as compared to other control samples; thus, authenticating the superiority of the synthesized composite in rendering the real-time applications.

Hexagonal nanosheets of pyrrochlore-type lanthanum stannate for sensitive detection of chlorinated pesticide in food and environmental samples.

2,4,6-Trichlorophenol (TCP) is the most widely used pesticide in the world and has a devastating effect on the environment and human health. As a result of the use of pyrochlore type La2Sn2O7 hexagonal nanosheet (La2Sn2O7 HNS) modified electrode, this work reports on the quick and sensitive electrochemical detection of TCP. The La2Sn2O7 HNS is reported here for the first time and has been made using a simple precipitation and calcination technique. The crystal structure and surface morphologies of La2Sn2O7 HNS have been characterized using XRD, XPS, HR-TEM, and FE-SEM analyses. Detection limits of 0.074 µM and sensitivity of 1.5 µA µM-1 cm-2 were achieved using the La2Sn2O7 HNS for TCP detection. It also showed decent selectivity among the common interfering molecules. Additionally, the La2Sn2O7 HNS/GCE sensor was able to detect TCP in water and vegetable samples with >90 % recovery, proving its appropriateness for quick TCP detection.

Recent development and challenges in fuel cells and water electrolyzer reactions: an overview.

Water electrolysis is the most promising method for the production of large scalable hydrogen (H2), which can fulfill the global energy demand of modern society. H2-based fuel cell transportation has been operating with zero greenhouse emission to improve both indoor and outdoor air quality, in addition to the development of economically viable sustainable green energy for widespread electrochemical applications. Many countries have been eagerly focusing on the development of renewable as well as H2-based energy storage infrastructure to fulfill their growing energy demands and sustainable goals. This review article mainly discusses the development of different kinds of fuel cell electrocatalysts, and their application in H2 production through various processes (chemical, refining, and electrochemical). The fuel cell parameters such as redox properties, cost-effectiveness, ecofriendlyness, conductivity, and better electrode stability have also been highlighted. In particular, a detailed discussion has been carried out with sufficient insights into the sustainable development of future green energy economy.