Search Results (2,163)

The fabrication of high-resolution and mechanically robust copper patterns remain a critical challenge in flexible electronics. Here, we present a universal metallization strategy that combines sequential two-step laser transfer, including laser-induced backward transfer and laser-induced forward transfer, with subsequent electroless copper plating. In this approach, laser-induced backward transfer first generates a transferable copper particle donor layer; subsequently, laser-induced forward transfer selectively embeds these catalytic copper particles into the surface of target substrates, constructing spatially confined activation networks while minimizing direct thermal exposure. These embedded seeds are then amplified into continuous copper conductors via electroless copper plating, achieving a high-resolution pattern (average minimum linewidth of approximately 20 μm) with robust interfacial integrity. Benefiting from laser-induced mechanical interlocking, the resulting copper patterns exhibit a low electrical resistivity of ~2.0 × 10⁻⁸ Ω·m (comparable to bulk copper) and maintain stable electromechanical performance even after 8000 bending cycles across a radius range of 3 to 6 mm. Furthermore, the fabricated versatile electrodes are successfully integrated into a triboelectric nanogenerator for tactile sensing and Morse code transmission. With its inherent substrate universality (e.g., polyimide, wood, fabric, and paper) and process scalability, this strategy provides a versatile route for manufacturing reliable copper electrodes in next-generation flexible electronic systems. 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

Crop fungal and viral diseases cause annual economic losses exceeding USD 150 billion globally, demanding rapid, sensitive, and field-deployable diagnostic technologies. This review critically evaluates recent advances in electrochemical biosensing platforms for early crop pathogen detection, focusing on immunosensors, genosensors, aptasensors, and VOC-based systems. Reported analytical performances demonstrate ultralow detection capabilities, including 0.3 fg mL⁻¹ for viral coat proteins, 15 DNA copies for bacterial pathogens, 0.5 fg µL⁻¹ RNA detection for viroids, and nanomolar-level VOC sensing (35–62 nM), with response times ranging from 2 to 60 min. Comparative analysis reveals that genosensors and aptasensors generally achieve the lowest LODs due to nucleic acid amplification or high-affinity recognition, while immunosensors provide robust protein-level specificity validated against ELISA. Volatile organic compound (VOC) sensors enable non-invasive, pre-symptomatic monitoring but face specificity challenges. Despite strong laboratory performance, practical adoption is limited by matrix-derived electrochemical interference, environmental instability of biorecognition elements, workflow complexity, and insufficient standardization across studies. Emerging innovations, including magnetic bead enrichment, nanoporous and graphene-based electrodes, microfluidic integration, AI-assisted impedance interpretation, and biodegradable substrates, are progressively addressing these bottlenecks. This review emphasizes that successful field translation requires holistic workflow engineering, matrix-matched validation, and harmonized performance metrics rather than incremental sensitivity improvements alone. By integrating analytical chemistry, nanomaterials engineering, and agricultural decision-support frameworks, electrochemical biosensing platforms hold significant potential to enable decentralized, rapid, and sustainable crop disease management. Full article

Electrochemical sensors for oxyanion detection are widely reported across environmental, industrial, and biological contexts, with recent literature often emphasising material innovation and increasingly low detection limits. Despite this activity, translation beyond laboratory demonstrations remains limited, raising questions about how electrochemical signals are interpreted and validated. In this review, recent electrochemical oxyanion sensors are examined from a measurement-centred perspective, focusing on how signals are generated, conditioned, and calibrated across major sensing strategies, including direct faradaic detection, modified-electrode and electrocatalytic systems, accumulation-based approaches, and enzyme- or mediator-assisted architectures. Rather than cataloguing sensor materials or device configurations, the analysis examines the assumptions underlying commonly reported performance metrics. Across sensing strategies, signal behaviour is frequently governed by interfacial chemistry, surface history, and experimental constraints rather than by invariant properties of the target oxyanion. Consequently, sensitivity, selectivity, and detection limits often reflect context-dependent behaviour within narrowly defined laboratory regimes. By synthesising these patterns, the review identifies recurring interpretive limitations in how electrochemical responses are linked to analyte determination. The resulting framework clarifies the analytical basis of the existing literature and highlights design-relevant constraints and validation practices that must be addressed for electrochemical oxyanion sensors to progress from feasibility demonstrations to robust analytical tools. Full article

Physics-based simulations are increasingly used to improve understanding of electrosurgical processes and to enable model-based estimation of tissue state when direct sensing is limited. The performance of such simulation-based virtual sensing approaches strongly depends on an accurate representation of the electrode–tissue interface. Despite its central role in electrical and thermal coupling, the influence of the electrode–tissue contact area has received limited attention in existing simulation studies. In this work, the influence of the electrode–tissue contact area on the sensitivity of key temperature-dependent tissue parameters was investigated for electrosurgical monopolar soft coagulation. Using a multiphysics finite element model under controlled boundary conditions, the sensitivity of maximum temperature development and necrotic tissue volume formation was analyzed with respect to varying contact areas and initial values of electrical conductivity, thermal conductivity, and effective heat capacity. The results demonstrate that parameter sensitivities are strongly contact-area-dependent. Electrical conductivity exhibits the most pronounced influence, particularly at larger contact areas, while thermal conductivity remains of minor relevance. In contrast, effective heat capacity significantly affects necrotic tissue volume formation, with increasing sensitivity for larger contact areas. These findings emphasize the importance of accurately accounting for electrode–tissue contact conditions in simulation-based analyses and clarify how contact-area-dependent sensitivities influence model-based tissue state estimation in electrosurgical coagulation. Full article

In recent years, two-dimensional (2D) materials have attracted growing attention for their application in chemoresistive gas sensors. Among these materials, graphene stands out due to its exceptional electrical, mechanical, and chemical properties. A simple and low-cost method for producing graphene involves the use of a laser to induce its formation on carbon-rich substrates, such as polyimides. This technique, first introduced in 2014, has been successfully applied in the fabrication of various types of sensors, including pressure sensors, temperature sensors, biosensors, and gas sensors. For chemoresistive gas sensors, laser-induced graphene (LIG) has been used either as an electrode or as part of the nanocomposite forming the active sensing layer. Moreover, this technology has allowed the use of heating elements. Sensing performance, including sensitivity and selectivity, can be tailored by incorporating different materials into the nanocomposite, such as metallic nanoparticles, metal oxides, or conductive polymers. These modifications can be implemented using low-cost and scalable fabrication methods, making this approach highly suitable for the development of affordable and efficient gas sensors. In this contribution, we present a comprehensive overview of the contributions, reported from the proposal of LIG technology in 2014 to 2025, about the use of this fabrication process in the development of chemoresistive gas sensors. Full article

Hybrid nanomaterials that integrate surface functionality, colloidal stability, and efficient electron-transfer pathways are highly attractive for improving electrochemical sensing performance. Herein, we report the fabrication and evaluation of polyethyleneimine-functionalized gallium nitride nanoparticles (GaN) decorated with gold nanoparticles (GaN-PEI-Au) as a tunable electrode modifier for enhanced differential pulse voltammetry (DPV) detection of erythromycin. Branched polyethyleneimine was employed as a multifunctional interfacial layer to stabilize GaN dispersions, introduce amine-rich surface chemistry, and enable in situ gold nanoparticle formation at the GaN-PEI. The optimized GaN-PEI-Au material exhibited high colloidal stability, a characteristic Au localized surface plasmon resonance in the ~520–525 nm range, and well-defined Au nanoparticles attached to the GaN surface. When applied as an electrode coating, GaN-PEI-Au significantly enhanced the erythromycin oxidation response compared to bare Au and GaN-PEI interfaces, consistent with synergistic increases in electroactive surface area and interfacial charge-transfer efficiency. Under optimized DPV conditions, GaN-PEI-Au-modified electrodes enabled quantitative erythromycin determination with a linear range of 5 nM–2 µM (R² = 0.990), sensitivity of 1.32 × 10⁻³ µA nM⁻¹, and a limit of detection of 52.5 nM, while maintaining stable baseline behavior during repeated scans. The reported GaN-PEI-Au nanocomposites represent a robust platform for sensitive electrochemical detection of pharmaceutical compounds. Full article

This study presents the development of a low-cost H₂ gas sensor made from a titanium dioxide–zinc oxide composite by means of a simple, cost-effective screen-printing method. The sensing material was created by mixing titanium dioxide and zinc oxide nanoparticles with an organic binder, which was screen-printed onto a glass substrate containing silver electrodes. These samples were then characterized using X-ray diffraction (XRD) and field-emission scanning electron microscopy (FESEM). The XRD results confirmed that the films boasted well-defined crystallinity, with predominant anatase and hexagonal ZnO phases, as well as uniformity of grains. Sensor performance was evaluated in a custom-built chamber at hydrogen concentrations of 100 to 1000 ppm and at operating temperatures of 100 °C, 200 °C, and 300 °C. The results indicate improved sensor performance as the operating temperature increased to 300 °C, with the best sensitivity values of 0.99, 1.17, and 1.31 at hydrogen concentrations of 100, 500, and 1000 ppm, respectively. The sensor showed stable and reproducible response characteristics, and its responses were retimed after a few hundred seconds. Low-cost fabrication, ease of processing, and reliable sensor performance make titanium oxide–zinc oxide composites promising candidates for hydrogen detection. Full article

This study investigates the combined effect of electrodeposited gold nanoparticles (AuNPs) and AuNP–polypyrrole (PPy)-modified Saccharomyces cerevisiae on electrochemical glucose sensing. AuNPs were deposited onto electrode surfaces by cyclic voltammetry, and the resulting interfaces were characterized using atomic force microscopy, cyclic voltammetry, and electrochemical impedance spectroscopy. AFM analysis confirmed increased surface roughness and height variability after deposition, indicating substantial restructuring of the electrode interface. Electrochemical measurements showed that AuNP deposition altered interfacial charge storage and transfer and increased the measured charge-transfer resistance. Glucose sensing was evaluated in a ferricyanide-mediated system using yeast layers with or without AuNP and PPy modification over a 0–60 mM concentration range. All configurations exhibited saturating, non-linear glucose responses described by Hill fitting. Among the evaluated yeast-modified electrodes, the AuNP–PPy modified yeast produced the strongest glucose-induced current increase and the best low-concentration performance, achieving a limit of detection of 0.540 mM, compared with 1.016 mM and 1.330 mM for single-modified layers and 3.360 mM for unmodified yeast. These results show that combining AuNP electrodeposition with AuNP–PPy yeast modification improves interfacial properties and enhances mediator-assisted electrochemical glucose sensing. Full article

This paper presents the design, modeling, and experimental validation of a capacitive tactile sensor specifically conceived to sense shear-driven contact dynamics in robotic manipulation. The proposed device is a layered flexible capacitive structure, in which controlled tangential interactions are induced. The electrode design maximizes sensitivity to shear motion and promotes an isotropic response with respect to slip direction, thereby addressing two key limitations that affect the majority of existing slip-sensing technologies. An analytical model was developed to describe the essential relationship between shear-induced displacements and the electrical response, providing insight into the design parameters and supporting the selection of geometry and materials. To test the sensor in real conditions, a dedicated capacitive readout circuit based on high-frequency excitation and synchronous demodulation was developed to robustly acquire capacitance variations while rejecting static offsets and parasitic effects. Several formulations for the interposed dielectric layer material were investigated, including viscous fluids and composite mixtures with high-permittivity nanoparticles, with the aim of improving electrical sensitivity while preserving mechanical stability. Experimental results obtained under controlled loading and sliding conditions demonstrate that the sensor is highly sensitive to changes in contact state and tangential interaction dynamics. The sensor responded consistently to both load-induced shear and slip-related phenomena, enabling the reliable monitoring of contact dynamics rather than binary slip detection. A proof-of-concept integration into a robotic finger confirms the suitability of the proposed approach for grasp monitoring. Full article

Bovine rotavirus (BRV) is one of the leading causes of neonatal diarrhea in calves and remains a major concern in veterinary medicine due to its high morbidity and economic impact. Rapid, sensitive, and cost-effective diagnostic approaches are therefore required for early detection and disease control. In this study, electrochemical immunosensors were developed for the detection of BRV with the aim of improving existing multiplex diagnostic strategies. Screen-printed carbon electrodes (SPEs) were employed as the sensing platform and modified with molybdenum disulfide nanoparticles (MoS₂ NPs) to enhance electrochemical performance. Mouse monoclonal antibodies against the BRV VP6 protein were immobilized onto the electrode surface, followed by blocking with bovine serum albumin. BRV detection was carried out using differential pulse voltammetry, cyclic voltammetry, and electrochemical impedance spectroscopy. To further improve sensitivity, a sandwich immunoassay format was constructed using gold nanoparticle-labeled secondary antibodies. The MoS₂-modified sandwich immunosensor exhibited superior analytical performance, achieving a limit of detection of 1.11 ng/mL, a limit of quantification of 3.72 ng/mL, a relative standard deviation of 1.89% (n = 5), and a linear response with R² = 0.99. The developed immunosensors demonstrated reliable performance in real sample analysis, with a selectivity rate of 100 ± 2.95%. These findings suggest that MoS₂-based electrochemical immunosensors offer a promising platform for rapid and sensitive BRV detection and have potential applications in veterinary diagnostics. 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

Electrochemical vibration sensors offer high sensitivity, low mechanical noise, and superior low-frequency performance, making them attractive for applications such as seismic detection and underwater acoustic sensing. However, existing electrochemical seismometers, angular accelerometers, and vector hydrophones primarily focus on sensitivity and noise, while sensor linearity—especially across wide frequency ranges—remains insufficiently investigated. In practice, linearity degradation frequently occurs at low and high frequencies due to diffusion limitations of electroactive species in the electrolyte. In this study, the linearity mechanism of electrochemical vibration sensors is analyzed, and two key structural parameters affecting linearity are identified: one is the anode–cathode spacing and the other is the effective cathode length. To improve linearity, an electrochemical sensing electrode incorporating an ultra-narrow insulating ring and a tapered micro-orifice is proposed. Finite element simulations are performed to evaluate the effects of electrode spacing, orifice geometry and excitation frequency. The sensor is fabricated using MEMS fabrication technology and experimentally characterized. Results show a peak sensitivity of 1242 V/(m/s) and excellent linearity within an input velocity range of 0.0002–0.012 m/s at 5 Hz, 10 Hz, 40 Hz and 100 Hz, with correlation coefficients exceeding 0.998. The proposed design provides an effective approach for linearity enhancement in electrochemical vibration sensors. Full article

Drought stress induces the excessive accumulation of hydrogen peroxide (H₂O₂), leading to oxidative damage and reduced crop productivity. This study presents a dual-function nanotechnology-based strategy for monitoring and mitigating drought-induced oxidative stress in cereal crops. Hierarchical CuO nanostructures were grown directly on copper substrates by hydrothermal oxidation, and the influence of growth time on morphology and hydrogen peroxide sensing performance was systematically evaluated. An optimal growth time of 3 h produced CuO nanoflower architectures with high surface area, yielding superior electrocatalytic activity toward H₂O₂ detection, with a low detection limit of 1.9 µM and high sensitivity of 11.92 mA·mM⁻¹·cm⁻². The optimized sensor enabled reliable quantification of H₂O₂ in oat (Avena sativa) and rye (Secale cereale) under drought stress, revealing species-dependent oxidative responses. In parallel, magnesium oxide (MgO) nanoparticles effectively alleviated drought-induced oxidative damage, reducing H₂O₂ accumulation by up to 63% in oat and 61% in rye and significantly improving plant growth and chlorophyll content. The integration of CuO-based sensing with MgO nanoparticle-assisted stress mitigation provides a robust framework for plant stress diagnostics and intervention, highlighting the potential of nanotechnology-enabled strategies for crop stress diagnostics and precision agriculture. Full article