Search Results (4,693)

Poly(3-thienylboronic acid) (PThBA) has recently been suggested as a conducting polymer with affinity for saccharides. In this study, thin films of this compound were deposited onto gold electrodes. The system obtained was studied as a possible chemical sensor. The measurements were performed by impedance spectroscopy using potassium ferro/ferricyanide as a redox mediator. The thickness of the polymer and the deposition of the adhesive sublayer were optimized to achieve a compromise between the blocking of defects in the polymer layer and the unnecessary increase in the internal resistance of this conductometric sensor. A comparative study of the influence of fructose, glucose, and sorbitol on transversal polymer resistance was conducted. The binding constants for these saccharides were extracted from the concentration dependencies of sensor conductance. Among them, sorbitol showed the highest affinity with a binding constant up to ~15,000 L·mol⁻¹, followed by fructose (~8700 L·mol⁻¹) and glucose (~4500 L·mol⁻¹). In order to exclude the contribution of the analyte tautomers on the obtained binding constants, measurements of ethylene glycol were also performed. The effects of pH and the redox state of PThBA on its affinity properties were studied, revealing higher affinities at alkaline pH and in oxidized state of the chemosensitive polymer. The developed system has the capacity to be applied in chemical sensors and virtual sensor arrays with electrical affinity control. Full article

Poly(5-indolylboronic acid) was synthesized electrochemically via cyclic voltammetry using various electrodes, including screen-printed carbon electrodes, glassy carbon electrodes, highly oriented pyrolytic graphite, and 304 stainless steel. This study provides a thorough analysis of the resulting conducting polymer’s electrochemical behavior, morphological and structural characteristics, and potential applications. The following techniques were employed: cyclic voltammetry, electrochemical impedance spectroscopy, Fourier-transform infrared spectroscopy, Raman spectroscopy, and field-emission scanning electron microscopy. The polymer exhibits pH-dependent redox activity within the pH range of 4–10, displaying Nernstian behavior and achieving a specific areal capacitance of 0.234 mF∙cm⁻² on an SPCE electrode. This result highlights the electrode’s efficiency in terms of charge storage. Impedance data indicate that the modified electrodes demonstrate a substantial decrease in charge transfer resistance and improved interfacial conductivity compared to bare electrodes. Contact angle measurements show that the presence of boronic acid groups makes the polymer hydrophilic. However, when 5PIBA was incubated in the presence of molecules containing hydroxyl groups or certain proteins, such as casein, no adsorption was observed. This suggests limited interaction with functional groups such as amino, hydroxide, and carboxyl groups present in these molecules, indicating the potential application of the polymer in biocorrosion. 5PIBA forms homogeneous, stable, and electroactive coatings on various substrates, making it a promising and versatile material for electrochemical technologies, and paving the way for future functionalization strategies. Full article

Molecularly imprinted polymer (MIP) biosensors offer an attractive strategy for selective biomolecule detection, yet imprinting proteins with structural fidelity remains a major challenge. In this work, we present a rationally designed electrochemical biosensor for matrix metal-loproteinase-8 (MMP-8), a key salivary biomarker of periodontal disease. By integrating graphene oxide (GO) with electropolymerized poly(eriochrome black T, EBT) films on screen-printed carbon electrodes, the partially reduced GO interface enhanced electrical conductivity and facilitated the formation of well-defined poly(EBT) films with re-designed polymerization route, while template extraction generated artificial antibody-like sites capable of specific protein binding. The MIP-based electrodes were comprehensively validated through morphological, spectroscopic, and electrochemical analyses, demonstrating stable and selective recognition of MMP-8 against structurally similar interferents. Complementary density functional theory (DFT) modeling revealed energetically favorable interactions between the EBT monomer and catalytic residues of MMP-8, providing molecular-level insights into imprinting specificity. These experimental and computational findings highlight the importance of rational monomer selection and nanomaterial-assisted polymerization in achieving selective protein imprinting. This work presents a systematic approach that integrates electrochemical engineering, nanomaterial interfaces, and computational validation to address long-standing challenges in protein-based MIP biosensors. By bridging molecular design with practical sensing performance, this study advances the translational potential of MIP-based electrochemical biosensors for point-of-care applications. Full article

The development of high-performance supercapacitor electrodes is crucial to meet the increasing demand for efficient and sustainable energy storage systems. Cobalt oxide (Co₃O₄), with its high theoretical capacitance, is a promising electrode material, but its practical application is hindered by poor conductivity limitations and structural instability during cycling. In this work, lanthanum La³⁺-doped Co₃O₄ nanocubes were synthesized via a hydrothermal approach to tailor their structural and electrochemical properties. Different doping concentrations (1, 3, and 5%) were introduced to investigate their influence systematically. X-ray diffraction confirmed the retention of the spinel phase with clear evidence of La³⁺ incorporation into the Co₃O₄ lattice. Also, Raman spectroscopy validated the structural integrity through characteristic Co-O vibrational modes. Scanning electron microscopy analysis revealed uniform cubic morphologies across all samples. The formation of the cubic spinel structure of 1% La³⁺-doped Co₃O₄ are confirmed from XPS and TEM studies. Electrochemical evaluation in a 3 M KOH electrolyte demonstrated that 1% La³⁺-doped Co₃O₄ nanocubes delivered the highest performance, achieving a specific capacitance of 1312 F g⁻¹ at 1 A g⁻¹ and maintaining a 79.8% capacitance retention and a 97.12% Coulombic efficiency over 10,000 cycles at 5 Ag⁻¹. It can be demonstrated that La³⁺ doping is an effective strategy to enhance the charge storage capability and cycling stability of Co₃O₄, offering valuable insights for the rational design of next-generation supercapacitor electrodes. Full article

Traditional liquid electrolyte batteries face safety concerns such as leakage and flammability, while further optimization has reached a bottleneck. Solid electrolytes are therefore considered a promising solution. Here, a PEO–LiTFSI–LATP (PELT) composite electrolyte was developed by incorporating nanosized Li_1.3Al_0.3Ti_1.7(PO₄)₃ fillers into a polyethylene oxide matrix, effectively reducing crystallinity, enhancing mechanical robustness, and providing additional Li⁺ transport channels. The PELT electrolyte exhibited an electrochemical stability window of 4.9 V, an ionic conductivity of 1.2 × 10⁻⁴ S·cm⁻¹ at 60 °C, and a Li⁺ transference number (tLi+) of 0.46, supporting stable Li plating/stripping for over 600 h in symmetric batteries. More importantly, to address poor electrode–electrolyte contact in conventional layered cells, we proposed an integrated electrode–electrolyte architecture by in situ coating the PELT precursor directly onto LiFePO₄ cathodes. This design minimized interfacial impedance, improved ion transport, and enhanced electrochemical stability. The integrated PELT/LFP battery retained 74% of its capacity after 200 cycles at 1 A·g⁻¹ and showed superior rate capability compared with sandwich-type batteries. These results highlight that coupling LATP-enhanced polymer electrolytes with an integrated architecture is a promising pathway toward high-safety, high-performance solid-state lithium-ion batteries. Full article

This article presents studies of surface layers produced by electro-spark deposition (ESD) on cast iron using a W-Ni-Co sintered electrode. To minimize the number of required experiments, a two-factor, five-level Hartley experimental design was chosen. The assessment involved observing the effect of voltage and capacitor capacity during the ESD process (on layer thickness and wear of the sample and counter-sample under technically dry friction conditions). Microscopic and tomographic observations were performed to analyze the thickness and structure of the layers. Image analysis methods were employed to examine the cross-section of the layers. ESD diffusion analyses were performed on the produced layer. Scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX) were performed to characterize the microstructure and composition of the coating. In addition, in order to evaluate the performance properties of tungsten coatings, the tribological tests were also conducted on a TRB³ Ball-on-Disc testing device. Hardness tests confirm an increase in the hardness of cast iron with a tungsten layer by over 400 µHV. The tests showed that higher voltages during the ESD process result in thicker layers and reduced wear of the sample with a tungsten layer at the expense of increased wear of the counter-sample (ball). Full article

Silicon carbide (SiC)-coated carbon nanowalls (CNWs) have been proposed for use as implantable scaffold electrodes. Therefore, we investigated the effects of the SiC coating on CNWs and assessed the effects of the application of electrical stimulation (ES) on human mesenchymal stem cells cultured on SiC-coated CNWs. Measurements were conducted using immunofluorescence staining, proliferation assays, and quantitative reverse transcription polymerase chain reaction. Our results showed that the SiC coating increased the cell adhesion area, and the combination of the SiC coating and ES promoted cell proliferation. Furthermore, ES enhanced osteogenic differentiation on CNWs, both with and without the SiC coating. In SiC-coated samples, the increase in wall thickness of CNWs by the SiC coating promoted neural differentiation. These findings indicate that scaffold electrodes composed of SiC-coated CNWs enhance cell adhesion and proliferation; the application of ES to such electrodes promotes osteogenic differentiation, while the SiC coating itself promotes neural differentiation. Full article

Background: Passive brain–computer interface (pBCI) systems use a combination of electroencephalography (EEG) and machine learning (ML) to evaluate a user’s cognitive and physiological state, with increasing applications in both clinical and non-clinical scenarios. pBCI systems have been limited by their traditional reliance on sensor technologies that cannot easily be integrated into non-laboratory settings where pBCIs are most needed. Advances in textile-electrode-based EEG show promise in overcoming the operational limitations; however, no study has demonstrated their use in pBCIs. This study presents the first application of fully textile-based EEG for pBCIs in differentiating cognitive states. Methods: Cognitive state comparisons between eyes-open (EO) and eyes-closed (EC) conditions were conducted using publicly available data for both novel textile and traditional dry-electrode EEG. EO vs. EC differences across both EEG sensor technologies were assessed in delta, theta, alpha, and beta EEG power bands, followed by the application of a Support Vector Machine (SVM) classifier. The SVM was applied to each EEG system separately and in a combined setting, where the classifier was trained on dry EEG data and tested on textile EEG data. Results: The textile EEG system accurately captured the characteristic increase in alpha power from EO to EC (p < 0.01), but power values were lower than those of dry EEG across all frequency bands. Classification accuracies for the standalone dry and textile systems were 96% and 92%, respectively. The cross-sensor generalizability assessment resulted in a 91% classification accuracy. Conclusions: This study presents the first use of textile-based EEG for pBCI applications. Our results indicate that textile-based EEG can reliably capture changes in EEG power bands between EO and EC, and that a pBCI system utilizing non-traditional textile electrodes is both accurate and generalizable. Full article

This study reports a binder-free, catalyst-free method for fabricating vertically aligned carbon nanotubes (VACNTs) directly on copper (Cu) foil using plasma-enhanced chemical vapor deposition (PECVD) for electrochemical double-layer capacitor (EDLC) applications. This approach eliminates the need for catalyst layers, polymeric binders, or substrate pre-treatments, simplifying electrode design and enhancing electrical integration. The resulting VACNTs form a dense, uniform, and porous array with strong adhesion to the Cu substrate, minimizing contact resistance and improving conductivity. Electrochemical analysis shows gravimetric specific capacitance (C_grav) and areal specific capacitance (C_areal) of 8 F g⁻¹ and 3.5 mF cm⁻² at a scan rate of 5 mV/s, with low equivalent series resistance (3.70 Ω) and charge transfer resistance (0.48 Ω), enabling efficient electron transport and rapid ion diffusion. The electrode demonstrates excellent rate capability and retains 92% of its initial specific capacitance after 3000 charge–discharge cycles, indicating strong cycling stability. These results demonstrate the potential of directly grown VACNT-based electrodes for high-performance EDLCs, particularly in applications requiring rapid charge–discharge cycles and sustained energy delivery. Full article

This study reviews the scientific use of chest-strap wearables, analyzing their advantages and limitations, following PRISMA guidelines. Eligible studies assessed chest-strap devices in adults and reported physiological outcomes such as heart rate, heart rate variability, R–R intervals, or electrocardiographic waveform morphology. Studies involving implanted devices, wrist-worn wearables, or lacking validation against reference standards were excluded. Searches were conducted in PubMed, Scopus, Web of Science, and ScienceDirect for studies published in the last 10 years. The quality of the studies was assessed using the Mixed Methods Appraisal Tool, and results were synthesized narratively. Thirty-two studies were included. The most frequently evaluated devices were the Polar H10 and Zephyr BioHarness 3.0, which showed strong correlations with electrocardiography at rest and during light-to-moderate activity. Reported limitations included motion artefacts, poor strap placement, sweating, and degradation of the skin–electrode interface. None of the devices had CE or FDA approval for clinical use, and most studies were conducted in controlled settings, limiting generalizability. Ergonomic concerns such as discomfort during prolonged wear and restricted mobility were also noted. Overall, chest-strap sensors showed good validity and were widely used in validation studies. However, technical refinements and large-scale field trials are needed for broader clinical and occupational application. This review is registered in PROSPERO and is part of the SIREN project. Full article

Soil electrical conductivity (EC) and water content are key indicators of soil health, influencing nutrient availability, salinity stress, and crop productivity. Monitoring these parameters is critical for precision agriculture. However, most existing measurement systems are costly, which restricts their use in practical field conditions. The aim of this study was to develop and validate a low-cost, portable system for simultaneous measurement of soil EC, water content, and temperature, while maintaining accuracy comparable to laboratory-grade instruments. The system was designed with four electrodes arranged in two pairs and employed an AC bipolar pulse method with a constant-current circuit, precision rectifier, and peak detector to minimize electrode polarization. Experiments were carried out in sandy loam soil at water contents of 13%, 18%, and 22% and KNO₃ concentrations of 0, 0.1, 0.2, and 0.4 M. Measurements from the developed system were benchmarked against a professional impedance analyzer (E4990A). The findings demonstrated that EC increased with both frequency and water content. At 100 Hz, the mean error compared with the analyzer was 8.95%, rising slightly to 9.98% at 10 kHz. A strong linear relationship was observed between EC and KNO₃ concentration at 100 Hz (R² = 0.9898), and for the same salt concentration (0.1 M KNO₃) at 100 Hz, EC increased from ~0.26 mS/cm at 13% water content to ~0.43 mS/cm at 22%. In conclusion, the developed system consistently achieved <10% error while maintaining a cost of ~€55, significantly lower than commercial devices. These results confirm its potential as an affordable and reliable tool for soil salinity and water content monitoring in precision agriculture. Full article

Conductive polymer hydrogels have attracted extensive attention in wearable devices, soft machinery, and energy storage due to their excellent mechanical and conductive properties. However, their preparation is often complex, expensive, and time-consuming. Herein, we report a facile precipitation method to prepare conductive polymer composite hydrogels composed of poly(acrylic acid) (PAA), poly(vinyl alcohol) (PVA), and poly(3,4-ethylenedioxythiophene) (PEDOT) via straightforward solution blending and centrifugation. During the preparation, PEDOT, grown along the PAA template, is uniformly dispersed in the hydrogel matrix. After shaping and rinsing, the PEDOT/PAA/PVA hydrogel shows good mechanical and electrical properties, with a conductivity of 4.065 S/m and a Young’s modulus of 311.6 kPa. As a strain sensor, it has a sensitivity of 1.86 within 0–100% strain and a response time of 400 ms. As a bioelectrode, it exhibits lower contact impedance than commercially available electrodes and showed no signs of skin irritation in the test. The method’s versatility is confirmed by the observation of similar performance of hydrogels with different compositions (e.g., polyaniline (PANI)/PAA/PVA). These results demonstrate the broad applicability of the method. Full article

In this study, high-conductivity W-doped Ga₂O₃ thin films were successfully fabricated by directly depositing a composition of Ga₂O₃ with 10.7 at% WO₃ (W:Ga = 12:100) using electron beam evaporation. The resulting thin films were found to be amorphous. Due to the ohmic contact behavior observed between the W-doped Ga₂O₃ film and platinum (Pt), Pt was used as the contact electrode. Current-voltage (J-V) measurements of the W-doped Ga₂O₃ thin films demonstrated that the samples exhibited significant current density even without any post-deposition annealing treatment. To further validate the excellent charge transport characteristics, Hall effect measurements were conducted. Compared to undoped Ga₂O₃ thin films, which showed non-conductive characteristics, the W-doped thin films showed an increased carrier concentration and enhanced electron mobility, along with a substantial decrease in resistivity. The measured Hall coefficient of the W-doped Ga₂O₃ thin films was negative, indicating that these thin films were n-type semiconductors. Energy-Dispersive X-ray Spectroscopy was employed to verify the elemental ratios of Ga, O, and W in the W-doped Ga₂O₃ thin films, while X-ray photoelectron spectroscopy analysis further confirmed these ratios and demonstrated their variation with the depth of the deposited thin films. Furthermore, the W-doped Ga₂O₃ thin films were deposited onto both p-type and heavily doped p⁺-type silicon (Si) substrates to fabricate heterojunction diodes. All resulting devices exhibited good rectifying behavior, highlighting the promising potential of W-doped Ga₂O₃ thin films for use in rectifying electronic components. Full article

In this article, the mechanism of relaxation polarization currents occurring at a constant temperature (isothermal process) in crystals with ionic-molecular chemical bonds (CIMBs) in an alternating electric field was investigated. Methods of the quasi-classical kinetic theory of dielectric relaxation, based on solutions of the nonlinear system of Fokker–Planck and Poisson equations (for the blocking electrode model) and perturbation theory (by expanding into an infinite series in powers of a dimensionless small parameter) were used. Generalized nonlinear mathematical expressions for calculating the complex amplitudes of relaxation modes of the volume-charge distribution of the main charge carriers (ions, protons, water molecules, etc.) were obtained. On this basis, formulas for the current density of relaxation polarization (for transient processes in a dielectric) in the k-th approximation of perturbation theory were constructed. The isothermal polarization currents are investigated in detail in the first four approximations (k = 1, 2, 3, 4) of perturbation theory. These expressions will be applied in the future to compare the results of theory and experiment, in analytical studies of the kinetics of isothermal ion-relaxation (in crystals with hydrogen bonds (HBC), proton-relaxation) polarization and in calculating the parameters of relaxers (molecular characteristics of charge carriers and crystal lattice parameters) in a wide range of field parameters (0.1–1000 MV/m) and temperatures (1–1550 K). Asymptotic (far from transient processes) recurrent formulas are constructed for complex amplitudes of relaxation modes and for the polarization current density in an arbitrary approximation k of perturbation theory with a multiplicity r by the polarizing field (a multiple of the fundamental frequency of the field). The high degree of reliability of the theoretical results obtained is justified by the complete agreement of the equations of the mathematical model for transient and stationary processes in the system with a harmonic external disturbance. This work is of a theoretical nature and is focused on the construction and analysis of nonlinear properties of a physical and mathematical model of isothermal ion-relaxation polarization in CIMB crystals under various parameters of electrical and temperature effects. The theoretical foundations for research (construction of equations and working formulas, algorithms, and computer programs for numerical calculations) of nonlinear kinetic phenomena during thermally stimulated relaxation polarization have been laid. This allows, with a higher degree of resolution of measuring instruments, to reveal the physical mechanisms of dielectric relaxation and conductivity and to calculate the parameters of a wide class of relaxators in dielectrics in a wide experimental temperature range (25–550 K). Full article

This study explores the use of a pre-acclimated Geobacter-enriched inoculum as a novel strategy to accelerate the start-up of biocathodes. Unlike conventional inoculation with broad-spectrum communities, the proposed inoculum combines a long-term electroactive consortium, previously adapted to anaerobic bioelectrochemical conditions, with digestate produced under controlled laboratory conditions. This prior acclimation ensures the presence of Geobacter strains already conditioned to electrode-associated growth, promoting rapid colonization and early electrochemical activity. Experiments were conducted in a dual-chamber electrochemical cell equipped with a three-electrode setup polarized at −1 V vs. Ag/AgCl. The enriched biocathode reached current densities exceeding 1.4 A/m² within 24 h, whereas the control exhibited significantly lower, less stable, and inconsistent performance. Unlike previously reported approaches based on broad-spectrum co-inoculation, this work presents a tailor-made inoculum in which the electroactive community is not only dominated by Geobacter, but also selectively preconditioned under functional bioelectrochemical conditions. This prior adaptation is a key differentiator that markedly enhances start-up efficiency. The results demonstrate that strategic enrichment with pre-acclimated Geobacter significantly accelerates start-up and improves electrochemical performance, offering a promising pathway toward more efficient and scalable bioelectrochemical systems for wastewater treatment and renewable energy generation. Full article