Search Results (2,612)

A pyranochromene-based ligand, 2-amino-4-(4-chlorophenyl)-5-oxo-4H,5H-pyrano[3,2-c]chromene-3-carbonitrile (ACLPh-PC-3-CN), was employed as a chelating modifier for the electrochemical determination of Cd(II) in water samples. ACLPh-PC-3-CN was co-immobilized with Nafion on a glassy carbon electrode to form a stable ACLPh-PC-3-CN/Nafion film that combines ligand-based coordination with cation-exchange-assisted preconcentration of Cd²⁺ at the electrode surface. The Cd(II) response at the modified electrode was characterized by cyclic voltammetry and differential pulse anodic stripping voltammetry, and the data support a predominantly 1:1 Cd(II)–ligand interaction at the interface under the selected conditions. At an optimized pH of 6.0, the sensor provided a linear calibration range from 16.21 to 56.72 μM, with a detection limit of 0.60 μM and a quantification limit of 2.0 μM, and showed good precision (repeatability 2.3% RSD, reproducibility 3.1% RSD) and short-term stability (94% of the initial response after 14 days). The ACLPh-PC-3-CN/Nafion-modified electrode tolerated common inorganic ions and surfactant species (≤5% signal change) and was successfully applied to the determination of Cd(II) in tap water and Red Sea water, affording recoveries between 98.7% and 101%. While the current detection limit is higher than typical guideline values for Cd in drinking water, the proposed sensor compares favorably with several reported electrochemical Cd(II) sensors in terms of simplicity, precision, and matrix tolerance, and represents a useful platform for coordination-based electrochemical sensing of cadmium in environmental water samples. Full article

Liquid electrolytes in conventional lithium-ion batteries pose safety risks associated with flammability, leakage, and explosion, whereas solid polymer electrolytes are generally limited by insufficient ionic conductivity at ambient temperature, restricting the development of high-energy lithium batteries. To address these issues, flexible poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)-based gel polymer electrolyte membranes (GPEs) were prepared via a slit-coating process combined with UV curing. NASICON-type lithium aluminum titanium phosphate (Li_1.3Al_0.3Ti_1.7P₃O₁₂, LATP) and garnet-type tantalum-doped lithium lanthanum zirconate (Li_6.4La₃Zr_1.4Ta_0.6O₁₂, LLZTO) were introduced as inorganic ceramic fillers to improve the ion-transport and interfacial properties of the GPE. Among the investigated samples, the PVDF-HFP-based GPE containing 10 wt% LLZTO exhibited the best overall performance, with an ionic conductivity of 3.40 × 10⁻⁴ S·cm⁻¹ at ambient temperature and a Li⁺ transference number of 0.77. Cyclic voltammetry results showed that the LLZTO-modified electrolyte membrane exhibited sharper and more symmetric redox peaks, higher peak current response, and better curve overlap during repeated cycles, indicating improved electrochemical reversibility and interfacial stability. In addition, LLZTO incorporation enhanced the mechanical strength, broadened the electrochemical stability window, and improved the flame-retardant behavior of the membrane. The LiFePO₄/GPE/Li cell assembled with the optimized membrane delivered an initial discharge capacity of 160 mAh·g⁻¹ at 0.1 C and maintained 80 mAh·g⁻¹ at 1 C, demonstrating good rate capability. Moreover, a capacity retention of 96% was maintained after 100 cycles at 0.1 C, confirming excellent cycling stability. Therefore, this work provides an effective strategy for the structural optimization and scalable preparation of high-performance gel polymer electrolyte membranes for lithium battery applications. Full article

Traditional solid-contact ion-selective electrodes (SC-ISEs) are severely constrained by a long-standing thermodynamic bottleneck, which requires hours of pre-conditioning and stabilization to establish a stable phase-boundary potential. To fundamentally bypass this limitation, we present a paradigm shift in electrochemical ion sensing that exploits dynamic kinetics rather than waiting for thermodynamic equilibrium. In this paper, we report a transient potential profiling method that eliminates the need for equilibration by analyzing the open-circuit voltage decay during the first 60 s of polarization. A discharge step on indicator electrode returns the membrane to a reproducible initial state, allowing for the extraction of a concentration correlated coefficient. Using a calcium ISE with an optimized membrane, the early-stage polarization dynamics were fitted to a single exponential saturation model, predicting the steady state response with an average error of 1.6%. The method achieved high repeatability (intra-day RSD 3.22%), batch to batch reproducibility (4.57%), and recovery rates from 90.7% to 115.0% in real water samples. Validation against ion chromatography showed high agreement (R² = 0.997). This strategy enabled conditioning free, disposable ISEs for point of care and environmental monitoring. Full article

Hydrogen sulfide (H₂S) is a contaminant for water quality, which can affect the eyes, respiratory system, and central nervous system, and may also cause damage to multiple organs such as the heart. Therefore, rapid and sensitive detection of trace H₂S is of great importance. In this work, a novel gold nanoparticle/2D porphyrin metal–organic framework nanocomposite (Au NPs/2D Cu-TCPP MOF) was prepared, and a novel electrochemical sensing method was established for the rapid determination of H₂S by differential pulse voltammetry (DPV). In 0.1 M PBS (pH 7.0), the detection limit of H₂S is as low as 0.03 μM, the linear range is 0.1–10 μM, and the response time is about 7 s. In addition, this method exhibits good stability and reproducibility, which can be applied to the rapid detection of H₂S in mine water samples. This study provides a reference for the development of new detection methods for H₂S in various complex environments. Full article

Hydrogel-based sensors have emerged as transformative soft-sensing platforms, featuring tissue-matched compliance, high water content, stimuli responsiveness, and chemical tunability, properties which are unachievable with conventional rigid sensors. Despite substantial advances, the existing reviews focus on individual polymer categories, discrete transduction mechanisms, or targeted standalone applications, failing to establish an integrated pipeline from material design to final sensing performance. This review fills these crucial gaps by systematically correlating polymer chemistry, crosslinking tactics, and fabrication protocols with the selection of transduction mechanisms and resultant sensing performance across biomedical and environmental fields. We conduct a critical assessment of natural and synthetic polymers together with chemical, physical, and hybrid composite crosslinking methodologies. Multiple sensing modalities, including piezoresistive, capacitive, thermogalvanic, electrochemical, colorimetric, ratiometric fluorescence, and piezoionic sensing are elaborated alongside representative quantitative performance parameters. Emerging platforms, including self-powered thermogalvanic sensors, SERS-integrated biosensors, and MXene/MOF composites, are highlighted as underexplored frontiers. In addition, persistent bottlenecks including dehydration-derived signal drift, inferior long-term operational stability, unsatisfactory target selectivity, and obstacles toward large-scale manufacturability are rigorously analyzed. Ultimately, this review constructs a holistic unified framework bridging polymer molecular design, fabrication engineering, signal transduction, and practical end-use applications, laying a clear developmental roadmap for next-generation flexible and smart hydrogel-based sensing systems. Full article

The present study addresses the fabrication of porous gyroid architectures by additive manufacturing from preceramic polymer feedstocks. Photocurable emulsions were engineered by combining a silicone powder with acrylate monomers and dispersing an emulsified secondary phase of calcium nitrate. The formulations showed light-curing behaviour compatible with digital light processing vat photopolymerization (DLP-VPP), enabling high-fidelity replication of triply periodic minimal surface (TPMS) gyroids (designed porosity: 85 vol.%). After pyrolysis in nitrogen at 700 °C, the lattices converted into CaO–SiO₂-derived amorphous matrices embedding an in situ turbostratic/pyrolytic carbon fraction, as suggested by the photothermal response and preliminary impedance behaviour, although the latter was measured in liquid electrolyte and therefore does not isolate electronic transport. To improve robustness during polymer-to-ceramic conversion, pharmaceutical borosilicate waste glass (BASG) was added as a passive filler (30–70 wt.%). The waste-glass phase acts as a passive filler that improves processing robustness and can mitigate shrinkage-induced damage during pyrolysis, while remaining electrically insulating (dielectric) and therefore not directly contributing to electronic conduction. The resulting structures combine high surface-to-volume ratio, controlled open porosity, and structural integrity with electrochemical responsiveness under the adopted test conditions, making them promising architected platforms for electrochemical components where interconnected porosity is advantageous. Full article

Melamine, characterized by its high nitrogen content, has been illegally added to food and feed to falsely increase apparent protein levels. However, melamine and its metabolites pose serious risks to human and animal health, including kidney stones, renal failure, and even death, as well as potential carcinogenic effects. Therefore, accurate detection of trace melamine is of great importance and urgency. Electrochemical sensors based on nanomaterials have been widely used for melamine detection due to their high sensitivity, good selectivity, rapid response, and simple operation. In this work, a composite nanosheet-structured electrode was fabricated, and a dense layer of gold nanoparticles was modified on its surface to enhance electrochemical performance. Cyclic voltammetry and electrochemical impedance spectroscopy measurements indicated that this electrode exhibited highly sensitive electrochemical properties. In addition, differential pulse voltammetry was employed for melamine detection, and the results showed a wide linear range of 20–500 nM with an LOD of 4.7 nM. The proposed electrode enabled the detection of melamine in milk samples, exhibiting good anti-interference ability and long-term stability. Full article

Hydrogen peroxide fuel cells have emerged as a promising class of electrochemical energy conversion device owing to the dual redox character of H₂O₂, its liquid-phase storage, and its ability to operate in air-free environments. In this work, a dual-compartment direct H₂O₂ fuel cell using a Prussian Blue cathode and a tantalum anode, separated by a Nafion 115 proton exchange membrane, was systematically characterized and optimized with respect to electrolyte pH and ionic composition. The influence of pH on OCV was investigated independently in each compartment across the range of pH 2 to 12. In the tantalum compartment, OCV increased non-linearly with pH from 573 mV to 808 mV, driven by the enhanced electrochemical reactivity of the system under alkaline conditions. In the Prussian Blue compartment, OCV decreased from 676 mV to 199 mV with increasing pH, reflecting the instability of the material in alkaline conditions. The effect of the electrolyte ionic composition on average current density was subsequently investigated by varying the concentrations of NaCl and Dy(NO₃)₃. Increasing NaCl from 0 to 2.5 M produced an increase in current density from 0.414 mA/cm² to 0.973 mA/cm², consistent with ohmic resistance reduction through improved ionic conductivity. The addition of Dy(NO₃)₃ produced a positive response with an optimal concentration of $0.05$ M, at which current density reached 1.08 mA/cm², before declining sharply. Under the fully optimized conditions, pH 12 in the tantalum compartment, pH 2 in the Prussian Blue compartment, 0.3 M H₂O₂, 2.0 M NaCl, and 0.05 M Dy(NO₃)₃, the cell produced an OCV of 724 mV and a peak power density of 0.283 mW/cm² at a current density of 0.8 mA/cm². These results demonstrate that meaningful electrochemical performance can be achieved in a dual-compartment H₂O₂ fuel cell without the use of precious metal catalysts and highlight electrolyte engineering as an effective strategy for improving cell output in this class of device. Full article

Hormones regulate numerous physiological processes and are essential for maintaining metabolic homeostasis. Accurate hormone quantification is crucial for the diagnosis and monitoring of endocrine and metabolic disorders. Electrochemical biosensors have recently emerged as promising platforms for hormone detection, offering simplicity, rapid response, cost-effectiveness, and high sensitivity compared to conventional techniques such as chromatography and mass spectrometry. This review summarizes the advances in electrochemical biosensors for detecting clinically relevant hormones, including cortisol, estrogen, progesterone, thyroid-stimulating hormone, parathyroid hormone, prolactin, and insulin, since 2010. Particular attention has been paid to developments in electrode modification strategies, including nanomaterials, redox enzymes, and novel recognition elements, which significantly improve the sensitivity and selectivity. These advances enable hormone detection at lower concentrations in various biological and environmental matrices. Despite these promising developments, challenges related to sensor stability, fabrication costs, and regeneration procedures limit their large-scale commercialization. Future research should focus on improving robustness, optimizing immobilization strategies, and integrating innovative materials to enhance the analytical performance. Continued collaboration among researchers, engineers, and healthcare professionals is essential. With ongoing technological progress, electrochemical biosensors are expected to play an important role in clinical diagnosis, point-of-care testing, and personalized medicine. Full article

Sensors and biosensors designed for biomarker detection in biological samples often suffer from performance loss caused by surface fouling, interface blocking, and matrix interference. Although these effects are frequently discussed separately, in real sensing systems they are strongly interconnected and they determine analytical reliability, especially in body fluids like serum, plasma, whole blood, sweat, and other complex media. This review provides a practical and mechanism-oriented overview of how these processes originate, how they differ, and how they ultimately lead to signal drift, reduced sensitivity, false-positive responses, and shortened sensor lifetime. We first discuss the molecular origins of interface failure, including protein adsorption, conditioning film formation, nonspecific binding, ionic strength effects, pH fluctuations, viscosity-related diffusion changes, and electroactive interferents. The impact of these phenomena is then compared across major sensing platforms, including electrochemical, potentiometric, optical, capacitive sensors, field-effect transistors and wearable biosensors. A central part of this review focuses on practical prevention strategies already employed in real biomarker sensing platforms. These include hydration-driven antifouling coatings, zwitterionic and hydrogel interfaces, post-immobilization blocking with bovine serum albumin, mercaptohexanol and ethanolamine, ionophore and membrane engineering in ion-selective electrodes, hydrophobic solid-contact layers for water-layer suppression, regeneration workflows, membrane and microfluidic pre-treatment, and AI-assisted drift correction. By combining advances in materials engineering, surface chemistry, sample handling, and algorithmic correction, this review highlights strategies to improve sensor stability in complex biological fluids. Overall, it offers a practical guide for developing next-generation low-fouling, drift-resistant, and self-correcting sensing systems for reliable biomarker analysis at the point of care. Full article

Artificial muscles are an emerging class of actuators designed to mimic the compliant, efficient, and versatile behavior of biological muscles for fields including the following: soft robotics, prosthetics, wearable enhancements, haptic interfaces, and biomedical devices. These systems encompass various actuation mechanisms, including pneumatic, hydraulic, thermal, ionic, electrochemical, and electrostatic. Each with distinct tradeoffs in voltage, strain, output force, bandwidth, efficiency, and manufacturability. Among them, electrostatic actuators have attracted increased attention due to their fast response times, high energy densities, strong compatibility with soft materials, and scalability from microscale devices to large-area and stacked actuators. However, challenges such as dielectric breakdown, material fatigue, and fabrication complexity continue to limit widespread deployment. This review presents a structured classification of various artificial muscle technologies and an in-depth examination of electrostatic actuators including dielectric elastomers, electrostrictive and ferroelectric polymers, liquid crystal elastomers, electrostatic film motors, stacked architectures, and microscale/milliscale devices. In this review the operating principles, materials, architectures, performance characteristics, and failure modes of electrostatic actuators will be discussed. Additionally, a comparison will highlight tradeoffs across actuator families based on metrics such as voltage, force, strain, bandwidth, and manufacturability. Lastly, we outline future research directions in materials, physics-informed modeling, system integration, and scalable fabrication necessary to advance electrostatic artificial muscles toward practical, real-world deployment. Full article

Poly(3,4-ethylenedioxythiophene) (PEDOT)-based gels have emerged as a prominent class of functional conductive materials, owing to their unique electromechanical coupling characteristics that integrate electrical functionality and mechanical adaptability. This review systematically elucidates the electromechanical properties of PEDOT-derived gels—defined as the synergistic response of electrical behaviors (conductivity, carrier mobility, electrochemical stability) and mechanical performances (flexibility, stretchability, tensile strength, bending resistance)—under mechanical deformation, as well as their mutual regulatory mechanisms. Focusing on how preparation processes and structural regulation modulate these electromechanical properties, this work first introduces the development history, intrinsic conductive mechanisms, and inherent electromechanical characteristics of PEDOT. It then systematically summarizes mainstream synthesis methods, analyzing their effects on balancing mechanical flexibility and electrical conductivity. Addressing the brittleness and poor electromechanical stability of pure PEDOT, this review further explores composite synergistic mechanisms with conductive/non-conductive polymers, metallic materials, inorganic nanoparticles, and biomaterials, clarifying how interfacial interactions optimize mechanical deformability while preserving or enhancing electrical performance. Finally, it summarizes the applications of PEDOT-based composites in electromechanically compatible fields including flexible sensing, micro/nano patterning, implantable biomedicine, anti-corrosion protection, and energy storage. This review aims to clarify the connotation of PEDOT’s electromechanical properties, refine the focus of relevant research, and provide a theoretical basis for designing high-performance PEDOT-based gels with balanced electromechanical properties. Full article

The detection and quantification of reactive oxygen and nitrogen species (RONS) in plasma-treated water (PTW) are essential for advancing plasma applications in biomedical and agricultural fields. However, RONS characterization remains challenging, as conventional techniques often require chemical reagents that can alter the sample. Electrochemical impedance spectroscopy (EIS) offers a non-destructive alternative by probing the electrical response of aqueous systems and providing information on ionic concentration, charge transfer, and diffusion processes. This study investigates the feasibility of EIS as a diagnostic tool for characterizing physicochemical changes in PTW. Calibration experiments were performed using saline solutions with different ionic concentrations to evaluate the sensitivity of impedance measurements. Impedance spectra were recorded over a frequency range of 0.1 Hz to 10 kHz and analyzed using Nyquist and Bode plots with equivalent circuit modeling. Deionized water was treated with cold atmospheric plasma at different discharge powers (3.53–10.15 W) and treatment times (5–30 min) to generate RONS. The results show that EIS can monitor plasma-induced changes in conductivity and interfacial properties associated with variations in ionic content. In particular, systematic changes in solution resistance and admittance were observed and were correlated with plasma-induced changes in ionic composition. These findings demonstrate that EIS is a sensitive and non-invasive diagnostic method for PTW analysis. Full article

Rock bolt corrosion can weaken support systems and affect the long-term stability of water-flooded roadways. This study investigates the symmetry evolution of roadway deformation induced by bolt deterioration in alkaline water-flooded roadways, using Sanxin Coal Mine, Xinjiang, as a case. Electrochemical accelerated corrosion tests were conducted in 10% Na₂SO₄ solutions at pH = 9, 11, and 13 for 3, 6, and 9 d, followed by uniaxial tensile tests and FLAC3D numerical simulations. Under the controlled accelerated electrochemical conditions, the mass loss rate and corrosion rate generally increased with corrosion duration, with the greatest deterioration observed in the pH = 13 group after 9 d. The tensile curves of corroded bolts still exhibited elastic deformation, yielding, strain hardening, and post-peak softening stages. However, the yield load decreased with increasing mass loss rate, with fitted slopes of −0.1842, −0.07531, and −0.04998 kN/% for pH = 9, 11, and 13, respectively. Numerical results showed that bolt deterioration intensified roadway deformation and stress redistribution. Under severe corrosion, the horizontal displacement of the two sidewalls reached approximately −153.7 mm and 155.4 mm, while the maximum roof subsidence and floor heave reached about −188.7 mm and 191.3 mm, respectively. The shallow stress release zone expanded, and the deep stress concentration became more pronounced. Moreover, bolt deterioration intensified the roadway response while largely preserving its left–right symmetry. The numerical results incorporating the experimentally derived bolt deterioration showed increased roadway deformation and stress redistribution, indicating that bolt-capacity degradation can adversely affect roadway stability. These findings provide a reference for evaluating residual support performance and designing reinforcement measures for water-flooded roadways. Full article

Porous bilayer Ni–Co and sandwiched Ni–Co–Ni electrodes were fabricated by combining aqueous electrodeposition with high-temperature molten-salt Al deposition and subsequent electrochemical dissolution in NaCl–KCl–AlF₃ melt at 750 °C. The study aimed to determine how the initial layer architecture controls phase evolution, porous structure formation, and hydrogen evolution performance in alkaline media. SEM/EDS and XRD analyses showed that the two electrode designs followed different reaction pathways during molten-salt treatment. In the Ni–Co system, Al reacted predominantly with Co, leading mainly to Co–Al intermetallic formation and, after dissolution, to a highly open coral-like porous network. In contrast, the Ni–Co–Ni architecture promoted mainly Ni–Al phase formation and produced a more compact porous surface with a Ni-rich outer layer. Despite these morphological differences, both layered porous electrodes outperformed untreated Ni and porous Ni in 1 M NaOH. At −0.6 V vs. RHE, porous Ni–Co and NiCo–Ni reached current densities of −162 and −141 mA·cm⁻², respectively, compared with −87 mA·cm for porous Ni and −45 mA·cm for flat Ni. The Ni–Co–Ni sandwiched electrode showed the most favourable HER kinetics and benchmark performance, with the lowest Tafel slope (111 mV·dec) and the lowest potentials at −10 and −100 mA·cm (−0.132 and −0.556 V, respectively). These results demonstrate that the electrocatalytic response of molten-salt-derived porous Ni-based electrodes is governed not only by porosity development but also by the spatial arrangement of metallic layers prior to Al infiltration and dealloying. Full article