Search Results (260)

Electro-oxidation of urea (UOR) in alkaline medium is one of the most effective alternative ways of producing green hydrogen, as the oxidation potential in UOR is less and thermodynamically more favorable than conventional water oxidation. The development of cost-effective materials in catalyzing UOR is recently seeking more attention in the research hotspot. Suitably modifying the Ni-based catalysts towards active site creation and preventing surface passivation is much important in this context, following which we reported the synthesis of Ni₃S₂ (NS) supported with CuCo (CC) bimetallic (NSCC). A simple hydrothermal route for NS synthesis and the electrodeposition method for CuCo (CC) deposition is adapted in a self-supported manner. The NS and CC catalysts exhibited sheet-like morphology, as confirmed by SEM and TEM analysis. The bimetallic CC deposition prevented the surface passivation of nickel sulfide (NS) over oxygen evolution reaction (OER) and improved the charge-transfer kinetics. The NSCC catalyst catalyzed UOR in an alkaline medium, which required a lower potential of 1.335 V vs. RHE to attain the current density of 10 mAcm⁻², with a lower Tafel slope value of 131 mVdec⁻¹. In addition, a two-electrode cell setup is constructed with an operating cell voltage of 1.512 V for delivering 10 mAcm⁻² current density. This study illustrates the new strategy of designing heterostructure catalysts for electrocatalytic UOR. Full article

An electrochemical immunosensor for the quantification of prostate-specific antigens (PSAs) using silver nanocrystals (AgNCs) is reported. The silver nanocrystals were synthesized using a conventional citrate reduction protocol. The silver nanocrystals were characterized using scanning electron microscopy (SEM) and field effect scanning electron microscopy (FESEM), X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), Fourier-transform infrared spectroscopy (FTIR), UV-Vis spectroscopy, and small-angle X-ray scattering (SAXS). The proposed immunosensor was fabricated on a glassy carbon electrode (GCE), sequentially, by drop-coating AgNCs, the electro-deposition of EDC-NHS, the immobilization of anti-PSA antibody (Ab), and dropping of bovine serum albumin (BSA) to prevent non-specific binding sites. Each stage of the fabrication process was characterized by cyclic voltammetry (CV). Using square wave voltammetry (SWV), the proposed immunosensor displayed high sensitivity in detecting PSA over a concentration range of 1 to 10 ng/mL with a detection limit of 1.14 ng/mL and R² of 0.99%. The immunosensor was selective in the presence of interfering substances like glucose, urea, L-cysteine, and alpha-methylacyl-CoA racemase (AMACR) and it showed good stability and repeatability. These results compare favourably with some previously reported results on similar or related technologies for PSA detection. Full article

This work presents the improvement of the electro-optical response of n-type crystalline silicon via dip-coated graphene oxide (GO) thin films. GO was deposited on Si/SiO₂ by immersion, and the resulting heterostructures were characterized by cyclic voltammetry measurements and Raman spectroscopy. Raman analysis revealed a slight but measurable broadening (~0.7 cm⁻¹) of the Si TO phonon mode at 514 cm⁻¹, indicating local interfacial strain. Cyclic voltammetry measurements showed a substantial increase in photocurrent in comparison to pristine silicon substrates. These effects are attributed to a GO-induced p-type inversion layer and enhanced interfacial charge transfer. The results suggest that GO can serve as a functional interfacial layer for improving silicon-based optoelectronic and photoelectrochemical devices. Full article

This study develops a one-pot anodic templating electrodeposition strategy using dual-cation-crosslinking and interpenetrating networks, coupled with pulsed electrical signals, to fabricate a vessel-mimetic multilayered tubular hydrogel. Typically, the anodic electrodeposition is performed in a mixture of sodium alginate (SA) and carboxymethyl chitosan (CMC), with the ethylenediaminetetraacetic acid calcium disodium salt hydrate (EDTA·Na₂Ca) incorporated to provide a secondary ionic crosslinker (i.e., Ca²⁺) and modulate the cascade reaction diffusion process. The copper wire electrodes serve as templates for electrochemical oxidation and enable a copper ion (i.e., Cu²⁺)-induced tubular hydrogel coating formation, while pulsed electric fields regulate layer-by-layer deposition. The dual-cation-crosslinked interpenetrating hydrogels (CMC/SA-Cu/Ca) exhibit rapid growth rates and tailored mechanical strength, along with excellent antibacterial performance. By integrating the unique pulsed electro-fabrication with biomimetic self-assembly, this study addresses challenges in vessel-mimicking structural complexity and mechanical compatibility. The approach enables scalable production of customizable multilayered hydrogels for artificial vessel grafts, smart wound dressings, and bioengineered organ interfaces, demonstrating broad biomedical potential. Full article

This study presents the development and comprehensive characterization of biopolymer-based nanofibrous composites composed of polyvinyl alcohol (PVA), chitosan (CS), boric acid (BA), and a natural antifungal agent natamycin (NAT), designed for therapeutic applications. A dual-layer 3D-fiber composite (PVA/CS/BA_PVA/NAT) was successfully fabricated using a layer-by-layer 3D bioprinting technique and electro-spinning, integrating BA into the core matrix and NAT into the outer layer. Mechanical tests revealed a significantly improved elastic modulus of 763.04 ± 14.54 MPa and the highest ultimate tensile stress (50.45 ± 2.58 MPa) among all samples. Despite a moderate strain at break (11.77 ± 0.49%), the composite preserved sufficient elasticity suitable for biological interfaces. Morphological assessment via SEM confirmed the successful deposition of continuous and bead-free nanofibers, with controlled fiber alignment and reduced average fiber diameters, especially in the BA-incorporated structure. The dual-layered system displayed enhanced uniformity and structural coherence. The drug release analysis demonstrated sustained NAT delivery over a 90 min period. Kinetic modeling showed a high correlation with the Korsmeyer–Peppas model (R² > 0.99), suggesting diffusion-controlled release, supported by the Korsmeyer–Peppas model’s Fickian diffusion exponent. In contrast, zero- and first-order models exhibited weaker fits, underscoring the relevance of a matrix-based release mechanism governed by the layered configuration. Crucially, antifungal assays against Candida albicans revealed substantial bioactivity. The PVA/CS/BA_PVA/NAT formulation achieved the largest inhibition zone (1.64 ± 0.13 cm), significantly outperforming single-layer controls such as PVA/CS/BA (1.25 ± 0.08 cm) and PVA/CS_PVA/NAT (1.43 ± 0.08 cm), while neat PVA exhibited no inhibition. These results confirm the synergistic antifungal efficacy of BA and NAT within the dual-layer structure. Together, these findings highlight the potential of the 3D-printed PVA/CS/BA_PVA/NAT composite as a mechanically robust, morphologically optimized, and bioactive platform for antifungal therapy and wound-healing applications. Full article

Noble metals are widely recognized for their ability to catalyze the electro-oxidation of organic compounds, with smaller particle sizes significantly enhancing electrocatalytic activity. In this study, catalytic electrodes decorated with atomic-level platinum and Pt-Au clusters were fabricated using cyclic atomic-metal electrodeposition. The interactions between the iminium (protonated imine) groups in emeraldine salt polyaniline (PANI) and metal chloride complexes in the electrolyte enabled precise control over the cluster size and composition. The electrocatalytic activity of these electrodes for propanol oxidation was systematically evaluated using cyclic voltammetry (CV). Notably, PANI electrodes decorated with odd-numbered atomic-level Pt clusters exhibited higher peak oxidation currents compared to even-numbered clusters, revealing a unique even–odd effect. For atomic-level Pt-Au clusters, the catalytic activity was significantly influenced by the sequence of Pt and Au deposition, with PANI-Au₁Pt₃ achieving the highest catalytic activity (35.34 mA/cm²). Bi-metallic clusters consistently outperformed mono-metallic clusters, and clusters containing only one Pt atom demonstrated superior catalytic activity. These findings provide valuable insights into the design of high-performance catalytic electrodes by leveraging atomic-level control of the cluster size, composition, and deposition sequence, paving the way for advanced applications in electrochemical sensors. Full article

Hybrid composite pile foundations face critical challenges in terms of optimizing load transfer mechanisms across variable soil densities, particularly in regions like Kano, Nigeria, characterized by loose to dense sandy deposits and fluctuating groundwater levels. This study addresses the need for sustainable, high-performance foundation systems that are adaptable to diverse geotechnical conditions. The research evaluates the mechanical behavior of steel–concrete and timber–concrete hybrid piles, quantifying skin friction dynamics, combining eight (8) classical ultimate bearing capacity (UBC) methods (Vesic, Hansen, Coyle and Castello, etc.) with numerical simulations, and assessing load distribution across sand relative densities (10%, 35%, 50%, 75%, 95%). Laboratory investigations included the geotechnical characterization of Wudil River well-graded sand (SW), direct shear tests, and interface shear tests on composite materials. Relative densities were calibrated using electro-pneumatic compaction. Increasing Dr from 10% to 95% reduced void ratios (0.886–0.476) and permeability (0.01–0.0001 cm/s) while elevating dry unit weight (14.1–18.0 kN/m³). Skin friction angles rose from 12.8° (steel–concrete) to 37.4° (timber–concrete) at Dr = 95%, with timber interfaces outperforming steel by 7.4° at Dr = 10%. UBC for steel–concrete piles spanned from 353.1 kN (Vesic, Dr = 10%) to 14,379 kN (Vesic, Dr = 95%), while timber–concrete systems achieved 9537.5 kN (Hansen, Dr = 95%). PLAXIS simulations aligned closely with Vesic’s predictions (14,202 vs. 14,379 kN). The study underscores the significance of soil density, material interfaces, and method selection in foundation design. Full article

The novel hydro-electro hybrid priming (HEHP) technique, which synergistically combines controlled hydration and electrostatic field application, represents an innovative chemical-free approach to improve seed germination synchrony. However, the regulatory mechanism of HEHP on cell wall remodeling during post-imbibition remains unclear. Here, we demonstrate that HEHP accelerates carrot (Daucus carota L.) seed germination by synchronizing cell wall hydrolysis and synthesis pathways. Comparative transcriptomics revealed 4591 differentially expressed genes (DEGs) between HEHP-treated and untreated seeds, with significant enrichment in cell wall organization (GO terms) and phenylpropanoid biosynthesis (KEGG pathway). HEHP significantly induced the expression of expansin (EXP), hydrolases (xyloglucan endotransglucosylase (XET), pectinesterase (PE), and phenylalanine ammonia lyase (PAE)), and synthases (cellulose synthase (CesA)), reducing endosperm rupture force considerably at S20 compared to hydropriming (HYD). Enzymatic assays confirmed earlier activity peaks for XET and PE in HEHP, correlating with the sustained expression of key genes. Notably, HEHP pre-activated germination-related metabolism, evidenced by fewer post-imbibition DEGs, and synchronized lignin deposition via transient phenylalanine ammonia lyase (PAL) and 4-coumarate/CoA ligase (4CL) activation. These synergies enabled faster radicle emergence than HYD. Our findings reveal that HEHP optimizes cell wall loosening–reinforcement dynamics through transcriptional priming, offering a tailored solution for mechanized sowing in Apiaceae crops. Full article

A prototype of an industrial installation for the deposition of self-restoring nitride coatings on the surface of reed switch contacts using electro-spark erosion alloying was developed, manufactured, and tested under the laboratory conditions at LLC Nitron. It was shown that the coatings are formed inside a bulb of reed switches at the final stage of their production following the impact from the spark breakdown between the contacts, stimulated via alternating magnetic and electric fields. The nitrogen concentration in the surface layers of the nitride coatings, estimated by means of X-ray microanalysis, was ca. 19 at. % and their thickness, measured by time-of-flight secondary ion mass spectrometry via sputter depth profiling, ranged between 250 and 350 nm. The novelty of the presented work consists of the development of an innovative piece of equipment, the operating principle and design of which are protected by intellectual property rights (four Russian patents). The technological approach implemented in this installation differs from the industrial galvanic technology due to its high level of environmental safety and economic efficiency, since it does not require the use of gold, ruthenium, or other high-priced metals. Full article

Micro-Electro-Mechanical System (MEMS) technology is employed to fabricate surface acoustic wave (SAW)-type and resistive-type ozone sensors on quartz glass (SiO₂) substrates. The fabrication process commences by using a photolithography technique to define interdigitated electrodes (IDEs) on the substrates. Electron-beam evaporation (EBE) followed by radio frequency (RF) magnetron sputtering is then used to deposit platinum (Pt) and chromium (Cr) electrode layers as well as a zinc oxide (ZnO) sensing layer, respectively. Finally, annealing is performed to improve the crystallinity and sensing performance of the ZnO films. The experimental results reveal that the ZnO thin films provide an excellent ozone-concentration sensing capability in both sensors. The SAW-type sensor demonstrates a peak sensitivity at a frequency of 200 kHz, with a rapid response time of just 35 s. Thus, it is suitable for applications requiring a quick response and high sensitivity, such as real-time monitoring and high-precision environmental detection. The resistive-type sensor shows optimal sensitivity at a relatively low operating temperature of 180 °C, but has a longer response time of approximately 103 s. Therefore, it is better suited for low-cost and large-scale applications such as industrial-gas-concentration monitoring. Full article

Wide-bandgap semiconductor betavoltaic batteries have a promising prospect in Micro-Electro-Mechanical Systems for high power density and long working life, but their material selection is still controversial. Specifically, the silicon carbide (SiC) betavoltaic battery was reported to have higher efficiency, although its bandgap is lower than that of gallium nitride (GaN) or diamond, which is inconsistent with general assumptions. In this work, the effects of different semiconductor characteristics on the battery energy conversion process are systematically analyzed to explain this phenomenon, including beta particle energy deposition, electron–hole pair (EHP) creation energy and EHPs collection efficiency. Device efficiencies of the betavoltaic battery using SiC, GaN, diamond, gallium oxide (Ga₂O₃), aluminum nitride (AlN) and boron nitride (BN) are compared to determine the optimum semiconductor. Results show that SiC for the betavoltaic battery has higher efficiency than GaN, Ga₂O₃ and AlN because of higher EHPs collection efficiency, less energy loss and fewer material defects, which is the optimal selection currently. SiC betavoltaic batteries were prepared, with the device efficiency having reached 14.88% under an electron beam, and the device efficiency recorded as 7.31% under an isotope source, which are consistent with the predicted results. This work provides a theoretical and experimental foundation for the material selection of betavoltaic batteries. Full article

Traditional detection methods such as atomic absorption spectroscopy offer high sensitivity and accuracy for heavy metal ion detection; however, they are often limited to laboratory environments due to bulky equipment and complex procedures. To meet the demand for rapid on-site detection, this study employs electrochemical analysis and utilizes Micro-Electro-Mechanical Systems (MEMS) technology to fabricate a microelectrode sensor chip for the electrochemical detection of heavy metal ions, Hg(II) and As(III). Nano-gold particles were electrodeposited on the sensing area of the working electrode of this chip using a constant-potential deposition method. Uniform distribution of the nanoparticles was obtained, which enhanced the effective specific surface area and electrochemical activity of the working electrode. Therefore, wide detection concentration ranges for Hg(II) of 5 to 1000 µg/L and for As(III) of 5 to 5000 µg/L were displayed, with detection limits of 1.4 µg/L and 2.4 µg/L, respectively. Moreover, the sensor exhibited satisfactory reproducibility, stability and anti-interference capability. These characteristics enable the developed microelectrode sensor chip to be utilized in the monitoring of a diverse range of pollution sources. Full article

Pt catalysts are investigated for methanol oxidation in direct methanol fuel cells, utilizing the electrochemical quartz microbalance method (EQCM) with exceptional resolution and sensitivity. Pt catalysts were deposited onto the gas-diffusion layer of carbon using stationary potential electrodeposition. Physical characterization and electrochemical tests were performed. SEM results showed that Pt presented dendrite crystals with nanoscale facets. Cyclic voltammetry (CV) demonstrated that the current density for the methanol oxidation reaction highly reached 1020 mA·cm⁻² for the deposited Pt catalyst by EQCM. The dendrite crystal structures of deposited Pt provide much area for high catalytic activity. It found that the peak density of the Pt catalysts for the methanol oxidation reaction decreased after five cycles. Furthermore, the response frequency for the adsorption of the deposited Pt catalysts was investigated using EQCM and compared with commercial PtRu catalysts. The results showed that the response frequency of the Pt catalysts decreased more rapidly than that of the PtRu catalysts. It is possible for the adsorption of small organic molecules on Pt catalysts to occur during the methanol electro-oxidation with CO_ad intermediates. The reaction mechanism is preliminarily discussed by the electrochemical measurement combined with EQCM. Full article

In this study, silver nanoparticles (Ag NPs) were synthesized on the surface of rutile-phase titanium dioxide (R-TiO₂) using a plasma-assisted technique. Comprehensive analyses were conducted to investigate the structural, morphological, optical, and electrical properties of the synthesized nanocomposites. Transmission electron microscopy (TEM) images revealed the uniform decoration of Ag NPs (average size: 29.8 nm) on the R-TiO₂ surface. X-ray diffraction (XRD) confirmed the polycrystalline nature of the samples, with decreased diffraction peak intensity indicating reduced crystallinity due to Ag decoration. The Williamson–Hall analysis showed increased crystallite size and reduced tensile strain, suggesting grain growth and stress relief. Raman spectroscopy revealed quenching and broadening of R-TiO₂ vibrational modes, likely due to increased oxygen vacancies. X-ray photoelectron spectroscopy (XPS) confirmed successful plasma-assisted deposition and the coexistence of Ag⁰ and Ag⁺ states, enhancing surface reactivity. UV-Vis spectroscopy demonstrated enhanced light absorption across the spectral range, attributed to localized surface plasmon resonance (LSPR), and a reduced optical bandgap. Dielectric properties, including dielectric constants, loss factor, and AC conductivity, were evaluated across frequencies (4–8 MHz) and temperatures (20–240 °C). The AC conductivity results indicated correlated barrier hopping (CBH) and overlapping large polaron tunneling (OLPT) as the primary conduction mechanisms. Composition-dependent dielectric behavior was interpreted through the Coulomb blockade effect. These findings suggest the potential of plasma assisted Ag NP-decorated R-TiO₂ nanostructures for photocatalysis, sensor and specific electro electrochemical systems applications. Full article

This study investigates the mechanical and optical characteristics of silicon nitride thin films deposited with PECVD at 80 °C for tunable silicon-rich SiN_x-SiO_y-based MEMS optical cavities. Varying the deposition parameters using SiH₄ and N₂ as precursor gases for silicon-rich SiN_x thin films allows us to tune the refractive index to a value as high as 2.40 ± 0.013 at an extinction coefficient of only 0.008, an extremely low surface roughness of only 0.26 nm, and a compressive stress of about 150 MPa. We deposited 6.5-layer pairs of silicon-rich SiN_x/SiO_y-distributed Bragg reflector (DBR) micro-electro-mechanical system (MEMS) mirror that covers the whole 1300 and 1550 nm range. Cavity architectures of 6.5 top and 6 bottom layer-pairs were fabricated in the clean room providing a variety of cavity lengths between 0.615 µm and 2.85 µm. These lengths were then simulated in order to estimate the Young’s Modulus of silicon-rich SiN_x, obtaining values from 56 to 92 GPa. One of the designs was characterised electro-thermally providing a tuning range of at least 86.7 nm centred at 1585 nm. The tunable filters are well suitable for implementation as tuning element in lasers for optical coherence tomography. Full article