Search Results (415)

Electrochemical chlorine production is of considerable industrial importance in areas such as water treatment, chemical manufacturing, and disinfection. However, conventional precious metal-based dimensionally stable anodes (DSAs), such as RuO₂- and IrO₂-based systems, are limited by high cost and resource constraints, motivating the development of low-cost alternative catalysts. In this study, Mn₃O₄ electrodes with controllable defect characteristics were fabricated by electrochemical deposition under various processing conditions. The effects of defect modulation and surface modification on the structural, electronic, and electrochemical properties of the electrodes were systematically evaluated. X-ray diffraction analysis confirmed that all deposited films retained a stable tetragonal Mn₃O₄ crystal structure, indicating that the deposition parameters primarily influenced defect states rather than the bulk phase. Mott–Schottky measurements revealed that the Mn₃O₄ electrodes exhibited p-type semiconducting behavior, with charge carrier densities on the order of 10¹⁴ cm⁻³, suggesting that oxygen vacancy-related defect states may contribute to the observed electronic properties of the electrodes. To further enhance anodic performance, Pt was introduced onto the Mn₃O₄ surface via sputtering, resulting in significantly improved charge transfer characteristics. Electrochemical measurements demonstrated that the best performing Pt/Mn₃O₄ electrodes delivered a current density exceeding 100 mA cm⁻² at an applied potential of 1.5 V versus Ag/AgCl. More importantly, defect-enriched Pt/Mn₃O₄ electrodes exhibited markedly enhanced chlorine evolution activity, with the chlorine production rate increasing from approximately 14 µmol cm⁻² to 29 µmol cm⁻², corresponding to an enhancement of about 2.07-fold. Faradaic efficiency analysis further showed that sample (g) and sample (n) achieved chlorine evolution efficiencies of 59.2% and 74.6%, respectively, indicating a higher tendency toward chlorine evolution for the Pt-modified electrodes under the tested conditions. These findings suggest that the synergistic combination of defect engineering and surface modification effectively modulates the electronic structure of Mn₃O₄, providing a viable strategy for improving chlorine evolution performance. Full article

Antibiotics are extensively used in intensive livestock farming for disease prevention, resulting in the discharge of antibiotic-contaminated wastewater into aquatic environments. Addressing this issue, electrocatalytic oxidation has emerged as a promising alternative to conventional chemical oxidation due to its cost-effectiveness and minimal secondary pollution. Central to this technology is the development of catalytic electrodes with high specific surface area and superior electrocatalytic activity. In this work, an Fe₃O₄-modified activated carbon fiber electrode (Fe₃O₄@ACF) was fabricated via a co-precipitation method. The Fe₃O₄@ACF electrode exhibited a hierarchical porous structure with a specific surface area of 940.2 m²/g, and demonstrated significantly enhanced oxygen reduction reaction activity with a current density of 21.8 mA·cm⁻² at –3.25 V vs. Ag/AgCl, which is 2.3 times higher than that of pristine ACF. EIS analysis revealed a low charge transfer resistance of 7.18 Ω, indicating improved electron transfer kinetics. In electro-Fenton degradation of tetracycline, the electrode achieved 82% removal within 120 min with a first-order rate constant of 0.01335 min⁻¹, and maintained over 94% of its initial activity after ten cycles. This study offers a viable and sustainable strategy for the efficient treatment of antibiotic-containing medical wastewater. Full article

In the present study, an amperometric aflatoxin B1 sensor was constructed via modifying a nano-graphite carbon paste microelectrode with a cationic surfactant of cetyltrimethylammonium bromide (CTAB) and a perfluorosulfonic acid resin of Nafion through a simple and controllable electrochemical scanning method. The experiment results show that CTAB–Nafion composite film has a good catalytic effect on the electrochemical response of aflatoxin B1. The electrocatalytic mechanism was investigated with the aid of different analytical techniques, including square wave voltammetry, electrochemical impedance spectroscopy, chronocoulometry, energy-dispersive spectroscopy and scanning electron microscopy. Under the optimal conditions, the linear range of the sensor is from 0.1 nM to 100 nM, and its detection limit and sensitivity are 20 pM (S/N = 3) and (24.9 ± 1.51) μA/nM, respectively. The accurate and rapid detection of aflatoxin B1, which has strong carcinogenicity, is of great significance for food quality monitoring and the protection of human health. Therefore, finally, the sensor was used to detect the concentration of aflatoxin B1 in milk and soy sauce samples, and the favorable recovery results indicated its good application prospects. Full article

Flexible electrode materials with tailored electrical and mechanical properties are essential for reliable electrocardiographic (ECG) sensing. In this work, p-toluenesulfonic-acid-doped polypyrrole (PPy–TSA) films were modified using polymeric and inorganic fillers, as well as their combinations (polyethylene glycol, graphene, carbon nanotubes, and zeolite), to tune their functional performance. The reference PPy–TSA film exhibits typical morphological and chemical characteristics of doped polypyrrole and serves as a reliable baseline for comparison. All composite films retain electrical conductivity within the range required for ECG applications while showing improved mechanical compliance (i.e., enhanced ability to conform to the skin and sustain deformation). Based on the optimized balance between electrical and mechanical properties, flexible ECG electrodes were fabricated using the TSA-doped PPy-based composite film. ECG recordings obtained with the several proposed electrodes show good agreement with those acquired using a commercial ECG electrode, demonstrating the potential of PPy-based composite films for flexible bioelectronic sensing applications. Full article

Ochratoxin A (OTA) is a highly toxic mycotoxin commonly detected in food and agricultural products, requiring sensitive analytical methods for reliable monitoring. Herein, we report an ultrasensitive turn-on electrochemical aptasensor for OTA detection based on a target-induced displacement of an aptamer–complementary DNA (cDNA) duplex assembled on an electrochemically reduced graphene oxide (ERGO)-modified glassy carbon electrode (GCE). In the absence of OTA, a methylene blue (MB)-labeled aptamer hybridized with cDNA is immobilized on the ERGO surface via π–π stacking interactions, forming a rigid duplex that suppresses electron transfer and yields a low electrochemical signal. Upon OTA binding, the aptamer undergoes a conformational transition into a G-quadruplex structure, leading to dissociation of the cDNA strand. This target-induced folding brings the MB redox tag into close proximity to the ERGO surface, markedly accelerating electron transfer and enhancing the cathodic reduction current of MB, thereby producing a pronounced signal-on response in square-wave voltammetry (SWV). The ERGO-modified electrode provides a conductive and stable interface without chemical linkers. Under optimized conditions, the aptasensor shows a linear response to OTA from 10 fM to 100 pM with an ultralow LOD of 0.67 fM, together with high selectivity, good reproducibility, and satisfactory stability. This work demonstrates a simple and effective turn-on aptasensing strategy for sensitive electrochemical detection of OTA. Full article

Glassy carbon electrodes (GCEs) have gained increased attention for the sensitive electrochemical detection of heavy metals due to their excellent chemical stability, wide potential window, and good electrical conductivity. These characteristics make GCEs an effective platform for sensor development. In particular, nanomaterial-modified GCEs have emerged as a promising strategy, offering enhanced sensitivity, selectivity, and faster response compared to conventional analytical techniques. This review summarizes recent advances over the past five years in the use of GCEs modified with chemically synthesized nanoparticles for the simultaneous detection of multiple heavy metal ions, including cadmium, lead, mercury, and chromium. It also includes how quantum chemical methods have aided our understanding of these phenomena. Heavy metals pose significant environmental and public health risks, with well-documented neurological, cardiovascular, reproductive, and carcinogenic effects, highlighting the need for accurate and rapid monitoring methods. Regulatory limits established by organizations such as the World Health Organization and the Environmental Protection Agency further emphasize the demand for highly sensitive detection technologies. This review examines the fundamental properties of GCEs, common nanomaterial modification techniques, and their application in multi-ion detection systems. Key advantages such as cost-effectiveness, portability, and adaptability to diverse sample matrices are highlighted. Current challenges, including electrode fouling, selectivity, and matrix interference, are also addressed, along with future perspectives for improving GCE-based sensors for real-world environmental monitoring. Full article

Antimony oxide nanoparticles (Sb₂O₃ NPs) were synthesized via a chemical vapor deposition (CVD) method and systematically characterized to evaluate their multifunctional performance. Powder X-ray diffraction (PXRD) confirmed the formation of an orthorhombic Sb₂O₃ phase with an average crystallite size of 53.50 nm, while SEM analysis revealed elongated nanostructures with diameters in the range of 20–100 nm. The stoichiometric composition of Sb₂O₃ (Sb:O ≈ 2:3) was verified by EDAX, and optical studies indicated a direct band gap of 3.10 eV. The electrochemical sensing capability of Sb₂O₃ NPs was investigated using a modified nickel mesh electrode for the detection of Metronidazole (MTZ) in 0.1 N KOH. The presence of Sb₂O₃ NPs resulted in an additional irreversible reduction peak at −0.14 V, confirming enhanced electrocatalytic activity toward MTZ, along with excellent cycling stability (94.36% retention after 10 cycles). In addition, the photocatalytic performance of Sb₂O₃ NPs was evaluated through the degradation of Acid Orange (AO) dye under UV-Vis irradiation, achieving a degradation efficiency of 73.31%. These results demonstrate that Sb₂O₃ nanoparticles are promising multifunctional materials for environmental remediation and electrochemical sensing applications, highlighting their potential for industrial implementation. Full article

This study presents a straightforward process for producing a hybrid ternary composite of silver nanoparticles (Ag NPs), small graphene oxide (s-GO), and zirconia (ZrO₂) and its use as an electrode material for electrochemical sensing. The physico-chemical properties of the ternary composite were analyzed by means of field emission scanning electron microscopy (FE-SEM), ultraviolet-visible (UV-vis) and FTIR spectroscopy, X-ray Photoelectron Spectrometry (XPS) and contact angle (CA) measurements. The synthesized hybrid nanomaterial was employed as an electrode modifier in the fabrication of a modified screen-printed carbon electrode (SPCE) and used for the simultaneous electrochemical sensing of key environmental pollutants such as hydroquinone (HQ) and catechol (CAT). The developed sensor exhibited linearity in the range of 0–100 µM for both HQ and CAT, with sensitivity values of 2640 µA·mM⁻¹·cm⁻² for HQ and 5120 µA·mM⁻¹·cm⁻² for CAT. The limits of detection (LOD) were 1.5 µM for HQ and 0.72 µM for CAT, respectively. The synergistic enhancement of electron transfer kinetics, the increased electroactive surface area, the strong anti-interference capability, and excellent reproducibility and stability establish these modified electrodes as promising candidates for environmental monitoring and real sample analysis. Full article

This study aims to enhance and develop the properties of materials used as supercapacitors. The synthesis of graphene oxide (GO) was achieved via a modified Hummer’s method, whereas the fabrication of polyaniline (PANI)/GO nanocomposites was conducted utilizing an in situ chemical polymerization technique. Subsequently, the PANI/GO layered films were deposited on fluorine-doped tin oxide (FTO) glass for supercapacitor applications. The materials were analyzed using X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), and cyclic voltammetry (CV). The experimental results demonstrated that a reaction time of 30 min, along with a weight ratio of aniline (ANI) monomer to GO of 1:1.5, yielded an optimal specific capacitance of 13.30 F/g. The robust electrochemical performance of the PANI/GO electrode may stem from the increased active sites for PANI deposition, attributable to the large surface areas of GO. Full article

Conducting polymers are extensively researched due to their remarkable characteristics, including adaptable and tunable electrical conductivity, straightforward manufacturing process, enhanced mechanical strength, lightweight composition, affordability, and convenience in handling. Furthermore, they demonstrate outstanding chemical stability and elevated thermal conductivity. Conducting polymers can be easily modified with other substances to create composites with improved performance. They are easy to integrate with other materials, such as metal oxide, metal sulfide, and metal nitride. In the energy sector, especially concerning electrochemical energy storage systems such as lithium-ion batteries (LIBs), conducting polymer composites with metal oxide, phosphate, and sulfide have shown considerable promise as electrode materials. These composites leverage synergistic effects that improve electrical conductivity, increase surface area, and prevent electrode pulverization, ultimately resulting in faster charge and discharge cycles, higher energy density, and enhanced cycling performance. This review offers a comprehensive examination of different types of conducting polymers used in LIB electrodes, provides hints regarding several synthesis methods for producing conducting polymer composites with metal oxide, phosphate, and sulfide, and discusses how the morphology of these composites influences their electrochemical performance. Full article

Conductive polymers (CPs), such as polypyrrole (PPy), have shown promising properties for use as electro-responsive bioactive scaffolds for tissue regeneration. PPy can be synthesized by chemical electrosynthesis and doped with biomolecules such as hyaluronic acid (HA). Taking advantage of the electrochemical synthesis versatility, nanofibers for surface-modified indium tin oxide (ITO) electrodes can be used as templates to produce tridimensional HA-doped PPy scaffolds. In this study, polyvinyl alcohol/chitosan (PVA/CTS) electrospun nanofibers deposited on ITO electrodes were used as a 3D template for the in situ electrosynthesis of HA-doped PPy to produce a bioactive scaffold for tissue engineering. The final material gathers the advantages of each biopolymer, the porous morphology of the nanofiber, and the conductivity of the electrosynthetized polymer. Furthermore, the biological activity of the NF-PVA/CTS@PPy:HA composite was evaluated in NIH-3T3 fibroblasts by MTT, resulting in a cell viability of 146 ± 40% and wound-healing capacity of 97 ± 1.9% at 24 h of culture. Full article

This work used activated carbon material obtained by chemical activation of abundantly available agricultural sunflower waste residues to remove metol (4-(methylamino) phenol sulfate, MTL) from aqueous solutions. The adsorbent structure was characterized using SEM-EDS and FT-IR spectroscopy. A modified screen-printed carbon electrode (SPCE) with gold nanoparticles synthesized using the Laser Ablation Synthesis in Solution (LASIS) method was used to detect MTL. The successful LASIS formation of gold nanoparticles was confirmed by the specific dark burgundy–red color. TEM measurements showed uniform pseudo-spherical particles with an average diameter of 7.9 ± 0.2 nm. The modified electrode showed improved electrochemical activity, which was confirmed by comparing it with an unmodified electrode using cyclic voltammetry and electrochemical impedance spectroscopy. The modified electrode was subsequently used to optimize the MTL detection conditions. UV–Vis spectroscopy was used to optimize the adsorption conditions, with the optimal values for pH and contact time found to be 8 and 120 min, respectively. The electrochemical detection of MTL was performed using differential pulse voltammetry, and the linear calibration range was established for concentrations ranging from 0.73–49.35 µM. The obtained limits of detection (LOD) and quantification (LOQ) were 0.06 µM and 0.2 µM, respectively. The efficiency of MTL removal was 100% after a contact time of 1 min and remained at 100% after 120 min. Full article

Reliable models of the lung environment are important for research on inhalation products, drug delivery, and how aerosols interact with tissue. pH fluctuations frequently accompany real physiological processes in pulmonary environments, so monitoring pH changes in lung-on-a-chip devices is of considerable relevance. Presented here are flexible, miniaturized, inkjet-printed pH sensors that have been developed with the aim of integration into lung-on-a-chip systems. Different types of functional pH-sensitive materials were tested: hydrogen-selective plasticized PVC membranes and polyaniline (both electrodeposited and dropcast). Their deposition and performance were evaluated on different flexible conducting substrates, including screen-printed carbon electrodes (SPE) and inkjet-printed graphene electrodes (IJP-Gr). Finally, a biocompatible dropcast polyaniline-modified IJP was selected and paired with an inkjet-printed Ag/AgCl quasireference electrode. The printed potentiometric device showed Nernstian sensitivity (58.8 mV/pH) with good reproducibility, reversibility, and potential stability. The optimized system was integrated with a developed lung-on-a-chip model with an electrospun polycaprolactone membrane and alginate, simulating the alveolar barrier and the natural mucosal environment, respectively. The permeability of the system was studied by monitoring the pH changes upon the introduction of a 10 wt.% acetic acid aerosol. Overall, the presented approach shows that electrospun-hydrogel materials together with integrated microsensors can help create improved models for studying aerosol transport, diffusion, and chemically changing environments that are relevant for inhalation therapy and respiratory research. These results show that our system can combine mechanical behavior with chemical sensing in one platform, which may be useful for future development of lung-on-a-chip technologies. Full article

High-nitrogen organic chemical wastewater is characterized by high chemical oxygen demand (COD_Cr), poor biodegradability, and toxic nitrogenous organics, posing significant challenges for conventional biological treatment. In this study, a dual-electrical treatment strategy integrating an electromagnetic Fenton (EM-Fenton) pretreatment unit with a three-dimensional biofilm electrode reactor (3D-BER) is proposed. The EM-Fenton system used iron–carbon fillers under electric and magnetic fields to generate hydroxyl radicals (·OH), enabling efficient oxidation of nitro-aromatic compounds and the conversion of organic nitrogen into NO₃⁻-N, while reducing Fe²⁺ input and iron sludge generation. Subsequently, the 3D-BER, filled with Fe₃O₄/Mn₃O₄-modified polyurethane spheres, facilitated autotrophic denitrification and phosphorus removal through enhanced extracellular electron transfer and trace hydrogen (H₂) release. Experimental results demonstrated that the EM-Fenton system achieved COD_Cr and NH₄⁺ removal rates of over 40% and 14%, respectively, under optimal HRT. The 3D-BER further improved removal efficiencies, with TN and TP reductions exceeding 80% and 81%, respectively, significantly outperforming the control groups. Microbial analysis revealed the enrichment of functional genera, such as Pararhodobacter and Thauera, and the upregulation of key denitrification pathways. This coupled system demonstrated high treatment efficiency, process synergy, and microbial selectivity, offering a promising approach for the advanced treatment of high-nitrogen industrial wastewater. Full article

This article presents a review of current research on the use of molybdenum disulfide (MoS₂) and its composites as promising materials for energy storage systems and functional coatings. Various MoS₂ morphologies, including nanoflowers, nanoplatelets, and nanorods, are considered, as well as their effects on electrochemical properties and specific capacity. Particular attention is paid to strategies for modifying MoS₂ using carbon nanomaterials (graphene, carbon nanotubes, porous carbon) and conductive polymers, which improve electrical conductivity, structural stability, and durability of electrodes. The important role of chemical vapor deposition (CVD), which allows the formation of uniform coatings with high purity, controlled thickness, and improved performance characteristics, is noted. A comparative analysis of advances in the application of MoS₂ in sodium-ion batteries, supercapacitors, and microwave absorbers is provided. It has been shown that the synergy of MoS₂ with carbon and polymer components, as well as the use of advanced deposition technologies, including CVD, opens new prospects for the development of low-cost, stable, and highly efficient energy storage devices. Full article