Search Results (155)

:The growing demand for smart electronic devices in daily life requires sustainable, renewable energy sources that reliably power portable and wearable systems. Triboelectric nanogenerators (TENGs) have emerged as a promising platform for smart textile-based energy harvesting due to their material versatility and mechanical compliance. In this work, electrospun poly (vinylidene fluoride) (PVDF) fiber mats incorporating boron nitride (BN) nanoparticles and reduced graphene oxide (rGO) were investigated to elucidate the roles of insulating and conductive nanofillers in governing the structural and electroactive properties of PVDF-based triboelectric materials. Electrospun PVDF mats containing 5 wt.% BN exhibited enhanced β-phase content (82%), attributed to the nucleating effect of BN and strong interfacial interactions between the nanofiller and the PVDF matrix. In contrast, 7 wt.% rGO demonstrated a high electroactive β-phase fraction (81%), arising from filler-induced dipole alignment and enhanced charge transport within the fibrous network. A comparative analysis of BN and rGO highlights filler-driven mechanisms influencing the electroactive phase formation and triboelectric charge generation in PVDF mats. The corresponding triboelectric power density reached 231 μWcm⁻² for the 7 wt.% rGO/PVDF and 281 μWcm⁻² for the 5 wt.% BN/PVDF-based TENGs, providing valuable insights for the rational design of high-performance, flexible triboelectric materials for wearable energy-harvesting applications. Full article

The growing demand for portable and wireless electronic devices, along with the necessity to reduce reliance on non-renewable energy sources, has driven the need for energy harvesting materials. Nanocomposites, combining a polymeric matrix and a high-performance dielectric ceramic phase, are a promising solution. In such systems, the design of a hybrid matrix–filler interface is critical for achieving desired properties. Here, nanocomposites (NCs) were prepared by adding various amounts of hydrothermally synthesized BaTiO₃ (BT) nanoparticles (NPs) to polydimethysiloxane (PDMS). To investigate hybrid interfaces, NPs were used either bare or surface-functionalized with two silanes, 3-glycidyloxypropyltrimethoxysilane (GPTMS) or 2-[acetoxy(polyethyleneoxy)propyl]triethoxysilane (APEOPTES). NC films (80–100 μm thick) were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDXS), and thermogravimetric analysis (TGA). Dielectric properties and breakdown strength (E_BD) were measured, and the theoretical volumetric energy density was calculated as a function of the filler loading and functionalization. The results demonstrate that hybrid interface design is pivotal for enhancing dielectric performance in NCs. APEOPTES-functionalized NPs significantly improved the dielectric response at a low filler loading (3.5%vol.), increasing permittivity from 2.8 to 7.5, E_BD from 33.8 to 42.1 kV/mm and energy density from 30 to >100 mJ/cm³. These findings underscore that designing hybrid interfaces through NP functionalization provides an effective strategy to achieve superior dielectric performance in PDMS-based NCs, retaining the advantages of the elastomeric matrix by reducing the amount of ceramic fillers. Full article

A carbon nanotube (CNT)-integrated microfluidic electrochemical sensor was developed for sensitive nanoparticle detection using gold nanoparticles (AuNPs) as the model analyte. The device incorporated screen-printed polyethylene terephthalate (PET) electrodes, a polydimethylsiloxane (PDMS) microchannel, and a CNT membrane that simultaneously served as a filtration layer and working electrode. This configuration enhanced analyte trapping, increased the electroactive surface area, and accelerated electron transfer under convective flow. The CNT membrane was fabricated by vacuum filtration and torch-assisted bonding, ensuring strong adhesion without adhesives or plasma treatment. Electrochemical analysis showed that the filter-integrated CNT sensor exhibited an oxidation current of 63 µA compared to 11 µA for the non-filter sensor, representing a fifteen-fold sensitivity enhancement. The detection limit improved from 1.0 × 10⁻³ to 7.5 × 10⁻⁴ mol·L⁻¹ with excellent reproducibility (RSD < 5%) and ∼90% accuracy. These findings validated the filtration-assisted accumulation mechanism and demonstrated the effectiveness of CNT-integrated microfluidic sensors for enhanced nanoparticle detection, while highlighting their potential for future adaptation to biosensing applications. Full article

Poly(vinylidene fluoride) (PVDF) nanofibers have emerged as promising materials for flexible piezoelectric sensors, yet their performance is fundamentally constrained by the limited formation and alignment of the electroactive β-phase. In this study, we report a phase-engineering strategy that integrates ionic functionalization, inorganic nanofiller incorporation, and post-fabrication corona poling to achieve enhanced crystalline ordering and electromechanical coupling in electrospun PVDF nanofibers. Tetrabutylammonium perchlorate increases solution conductivity, enabling uniform, bead-free fiber formation, while barium titanate nanoparticles act as nucleation centers that promote β-phase crystallization at the expense of the non-polar α-phase. Subsequent corona poling further aligns molecular dipoles and strengthens remnant polarization within both the PVDF matrix and embedded nanoparticles. Structural analyses confirm the synergistic evolution of crystalline phases, and piezoelectric measurements demonstrate a substantial increase in peak-to-peak output voltage under dynamic loading conditions. This combined phase-engineering approach provides a simple and scalable route to high-performance PVDF-based piezoelectric sensors and highlights the importance of coupling crystallization control with dipole alignment in designing next-generation wearable electromechanical materials. Full article

Deep eutectic solvents (DES) have emerged as a versatile and sustainable medium for the green synthesis of nanomaterials, offering a viable alternative to conventional organic solvents and ionic liquids. Nanomaterials can be synthesised in DESs via multiple routes, including chemical reduction, solvothermal, and electrochemical methods. Among the different pathways, this review focuses on the electrochemical synthesis of nanomaterials in DESs, as it offers several advantages: low cost, scalability for large-scale production, and low-temperature processing. The size, shape, and morphology (e.g., nanoparticles, nanoflowers, nanowires) of the resulting nanostructures can be tuned by adjusting the concentration of the electroactive species, the applied potential, the current density, mechanical agitation, and the electrolyte temperature. The use of DES as an electrolytic medium represents an environmentally friendly alternative. From an electrochemical perspective, it exhibits high electrochemical stability, good solubility for a wide range of precursors, and a broad electrochemical window. Furthermore, their low surface tensions promote high nucleation rates, and their high ionic strengths induce structural effects such as templating, capping and stabilisation, that play a crucial role in controlling particle morphology, size distribution and aggregation. Despite significant progress, key challenges persist, including incomplete mechanistic understanding, limited recyclability, and difficulties in scaling up synthesis while maintaining structural precision. This review highlights recent advances in the development of metal, alloy, oxide, and carbon-based composite nanomaterials obtained by electrochemical routes from DESs, along with their applications. Full article

A water-soluble hydroxypropyl cellulose (HPC) polymer matrix has been filled with different weight percentages (wt.%) of multiwalled carbon nanotubes (MWCNTs), fullerenes C₆₀, fullerenols C₆₀(OH)_24, and their combinations. We study the potential of the 0D nanoparticles for improving electrical properties of the conductive MWCNT network in a biocompatible matrix. Physicochemical effects of fillers content, both individually and in combinations (MWCNTs/C₆₀ and MWCNTs/C₆₀(OH)₂₄), for these composite systems, have been investigated. The performed SAXS analysis shows improved nanofiller dispersion for films with two fillers. The electrical percolation threshold (P_c) in MWCNTs composites occurs at ≈1.0 wt.%. A synergistic effect for binary filler composites on the electrical conductivity has been evaluated by keeping a constant amount of 0.5 wt.% MWCNTs (σ ≈ 3 × 10⁻⁹ S·m⁻¹) and increasing the amount of C₆₀ or C₆₀(OH)₂₄. A large increase in the electrical conductivity is obtained for the bifiller composites with 0.5 wt.% MWCNTs and 1.5 wt.% of C₆₀(OH)₂₄, reaching σ ≈ 0.008 S·m⁻¹. Further, the sensing properties of 4.0/1.0 MWCNT/C₆₀ nanocomposites were demonstrated by measuring both piezoresistive (PR) and thermoresistive (TR) responses. The combination of semiconductive fullerene/fullerenols combined with MWCNTs allows obtaining more homogeneous composites in comparison to single MWCNTs composites and also gives possibilities for tuning the electrical conductivity of the system. Overall, it is demonstrated that the use of bifillers with a water soluble biopolymeric matrix allows the development of eco-friendly high-performance electroactive materials for sustainable digitalization. Full article

Chitin-derived biomass carbon materials are promising supercapacitor electrode materials due to their wide availability, low cost, high specific surface area, and nitrogen doping capability. However, their practical application is limited by insufficient conductivity and cyclic stability, often requiring functional modification or integration with complementary materials. In this study, we present a novel strategy by incorporating copper sulfide (Cu₂S) into a chitin-based carbon matrix. Cu₂S, known for its high intrinsic conductivity, excellent electroactivity, and theoretical specific capacity (~335 mAh·g⁻¹), was uniformly doped into the three-dimensional carbon aerogel framework derived from chitin nanofibers (ChNF) through sol–gel, freeze-drying, and high-temperature carbonization processes. The resulting chitin-based carbon/Cu₂S composite aerogel (CChNF/Cu₂S) exhibited a hierarchical porous structure with Cu₂S nanoparticles (20–30 nm) uniformly distributed on the carbon fiber surface. Electrochemical tests demonstrated its excellent performance, achieving a specific capacitance of 852 F·g⁻¹ at 1 A·g⁻¹, highlighting the synergistic effects of the conductive Cu₂S and nitrogen-doped carbon framework for high-performance supercapacitor applications. Full article

Poly(amino acids) and gold nanoparticles are stable and biocompatible materials with distinguishing features which can be used to build nanocomposite electrochemical platforms for sensing applications. This paper presents the optimization of the building steps of these nanocomposite platforms using cyclic voltammetry. Screen-printed graphite electrodes were first modified by electropolymerizing various l-amino acids and then by electrodepositing gold nanoparticles. The electroactive surface area was calculated for all platforms, which were then applied in the electrochemical oxidation of 1-naphthol as a model analyte: oxidation peaks were observed in all cases, with the current peak height increasing with increasing analyte concentration, thus demonstrating the potential of nanocomposite platforms for developing electrochemical sensors and biosensors. Full article

This study presents the design and application of an electrochemical sensor for selective detection of lead ions (Pb²⁺) based on ionophore-modified raspberry-like Fe₃O₄–Au nanostructures. The material was engineered with a magnetic Fe₃O₄ core, coated with polyethyleneimine (PEI) to facilitate nucleation, and subsequently decorated with Au nanoparticles, providing a raspberry-like (Fe₃O₄@PEI@AuNPs) nanostructure with high surface area and excellent electrochemical conductivity. Surface functionalization with Lead Ionophore IV (ionophore thiol) introduced Pb²⁺-selective binding sites, whose presence and structural evolution were verified by TEM and Raman spectroscopy. The Fe₃O₄ core endowed strong magnetic properties, enabling facile manipulation and immobilization onto screen-printed carbon electrodes (SPCEs) via physical adsorption, while the Au nanoparticles enhanced electron transfer, supplied thiol-binding sites for stable ionophore anchoring, and increased the effective electroactive surface area. Operational conditions were systematically optimized, with acetate buffer (HAc/NaAc, pH 5.7) and chronoamperometric preconcentration (CA) at −1.0 V for 175 s identified as optimal for differential pulse voltammetry (DPV) measurements. Under these conditions, the sensor exhibited a linear response toward Pb²⁺ from 0.025 mM to 2.00 mM with superior sensitivity and reproducibility compared to conventional AuNP-modified SPCEs. Furthermore, the ionophore-modified Fe₃O₄–Au nanostructure-based sensor demonstrated outstanding selectivity for Pb²⁺ over competing heavy metal ions (Cd²⁺, Hg²⁺, Cr³⁺), owing to the specific coordination interaction of Lead Ionophore IV with target ions. These findings highlight the potential of raspberry-like Fe₃O₄@PEI@AuNP nanostructures as a robust and efficient electrochemical platform for the sensitive and selective detection of toxic heavy metal ions. Full article

We present a novel disposable electrochemical biosensor for highly sensitive and selective glucose detection, employing gold-modified screen-printed electrodes combined with square wave (SWV) and linear sweep voltammetry (LSV). The sensor integrates recombinant corn-derived manganese peroxidase with glucose oxidase, bovine serum albumin, and gold nanoparticles to enhance stability and signal transduction. Glucose detection by LSV covered 0.001–6.5 mM (R² = 0.9913; LOD = 0.50 µM), while SWV achieved a broader range of 0.0006–6.5 mM (R² = 0.998; LOD = 0.29 µM). The sensor demonstrated excellent selectivity, showing minimal interference from common electroactive species including caffeine, aspartame, and ascorbic acid, and provided rapid responses, making it ideal for point-of-care and food monitoring applications. Full article

Amperometric biosensors, due to their high sensitivity, fast response time, low cost, simple control, miniaturization capabilities, and other advantages, are receiving significant attention in the field of medical diagnostics, especially in monitoring blood glucose levels in diabetic patients. In this study, an amperometric glucose biosensor based on immobilized enzyme glucose oxidase (GOx) and bimetallic platinum cobalt (PtCo) nanoparticles was developed. The PtCo nanoparticles, deposited on a graphite rod electrode, exhibited peroxidase-like catalytic properties and were able to electrocatalyze the reduction of H₂O₂. After immobilization of the GOx, an amperometric signal generated by the biosensor was directly proportional to the glucose concentration in the range of 0.04–2.18 mM. The biosensor demonstrated a sensitivity of 19.38 μA mM⁻¹ cm⁻², with a detection limit of 0.021 mM and a quantification limit of 0.064 mM. In addition to this analytical performance, the biosensor exhibited excellent repeatability (relative standard deviation (RSD) was 4.90%); operational and storage stability, retaining 98.93% and 95.33% of its initial response after 26 cycles of glucose detection and over a 14-day period, respectively; and anti-interference ability against electroactive species, as well as exceptional selectivity for glucose and satisfactory reproducibility (RSD 8.90%). Additionally, the biosensor was able to detect glucose levels in blood serum with a high accuracy (RSD 5.89%), indicating potential suitability for glucose determination in real samples. Full article

This study presents the development of a TiO₂ nanowire-based electrochemical sensor for the selective and sensitive detection of hydrogen peroxide (H₂O₂) under neutral pH conditions, with a particular focus on its application in analyzing plant stress. The sensor exhibited a linear detection range of 0–0.5 mM, a sensitivity of 0.0393 mA · mM⁻¹, and a detection limit of 2.8 μM in phosphate-buffered saline solution (PBS, pH 7.4). This work’s main novelty lies in the systematic investigation of the relationship between TiO₂ nanostructure morphology, which is controlled by hydrothermal synthesis parameters, and the resulting sensor performance. Interference studies confirmed excellent selectivity in the presence of common electroactive species found in plant samples, such as NaCl, KNO₃, glucose, citric acid, and ascorbic acid. Real sample analysis using barley plant extracts grown under salt stress and treated with Fe₃O₄ nanoparticles confirmed the sensor’s applicability in complex biological matrices, enabling accurate quantification of endogenously produced H₂O₂. Endogenous H₂O₂ concentrations were found to range from near-zero levels in control and Fe₃O₄-only treated plants, to elevated levels of up to 0.36 mM in salt-stressed samples. These levels decreased to 0.25 and 0.15 mM upon Fe₃O₄ nanoparticle treatment, indicating a dose-dependent mitigation of stress. This finding was supported by genome template stability (GTS) analysis, which revealed improved DNA integrity in Fe₃O₄-treated plants. This study takes an integrated approach, combining the development of a nanostructured sensor with physiological and molecular stress assessment. The urgent need for tools to detect stress at an early stage and manage oxidative stress in sustainable agriculture underscores its relevance. Full article

Microbial Electrochemistry Technology (MET) leverages the unique process of extracellular electron transfer (EET) between electroactive bacteria (EAB) and electrodes to enable various applications, such as electricity generation, bioremediation, and wastewater treatment. This review highlights significant advancements in EET mechanisms, emphasizing both outward and inward electron transfer pathways mediated by diverse electroactive microorganisms. Notably, the role of electron shuttles, genetic modifications, and innovative electrode materials are discussed as strategies to enhance EET efficiency. Recent studies illustrate the importance of redox-active molecules, such as flavins and metal nanoparticles, in facilitating electron transfer, while genetic engineering has proven effective in optimizing microbial physiology to boost EET rates. The review also examines the impact of electrode materials on microbial attachment and performance, showcasing new composites and nanostructures that enhance power output in microbial fuel cells. By synthesizing the recent findings and proposing emerging research directions, this work provides an overview of EET enhancement strategies, aiming to inform future technological innovations in bioelectrochemical systems (BESs). Full article

Bio-nanocomposite films were prepared using chitosan, gelatin, and varying concentrations (0, 0.5, 1.0, 2.0, and 5.0 wt%) of titanium dioxide (TiO₂) nanoparticles in acetic acid via a casting method. The incorporation of TiO₂ nanoparticles into the bio-chitosan matrix enhanced ultraviolet (UV) absorption and improved the films’ physical, mechanical, and electrical properties. Additionally, the TiO₂-loaded films exhibited antimicrobial activity, contributing to the extended preservation of packaged products by inhibiting microbial growth. Notably, the bio-nanocomposite films containing 1.0 wt% TiO₂ exhibited an electroactive response, bending under relatively low electric field strength (250 V/mm), whereas the control film without TiO₂ required higher field strength (550 V/mm) to achieve bending. This indicates potential applications in electroactive actuators requiring precise movement control. Among the tested concentrations, films containing 0.5 wt% and 1.0 wt% TiO₂ (Formulas 7 and 8) demonstrated optimal performance. These films presented a visually appealing appearance with no tear marks, low bulk density (0.91 ± 0.04 and 0.85 ± 0.18 g/cm³), a satisfactory electromechanical response at 250 V/m (17.85 ± 2.58 and 61.48 ± 6.97), low shrinkage percentages (59.95 ± 3.59 and 54.17 ± 9.28), high dielectric constant (1.80 ± 0.07 and 8.10 ± 0.73), and superior UV absorption compared with pure bio-chitosan films, without and with gelatin (Formulas 1 and 6). Full article

We are reporting the development of a high-performance, non-enzymatic electrochemical biosensor for selective lactate detection, integrating laser-induced graphene (LIG), gold nanoparticles (AuNPs), and a molecularly imprinted polymer (MIP) synthesized from poly(3,4-ethylenedioxythiophene) (PEDOT). The LIG electrode offers a highly porous, conductive scaffold, while electrodeposited AuNPs enhance catalytic activity and signal amplification. The PEDOT-based MIP layer, electropolymerized via cyclic voltammetry, imparts molecular specificity by creating lactate-specific binding sites. Cyclic voltammetry confirmed successful molecular imprinting and enhanced interfacial electron transfer. The resulting LIG/AuNPs/MIP biosensor demonstrated a wide linear detection range from 0.1 µM to 2500 µM, with a sensitivity of 22.42 µA/log(µM) and a low limit of detection (0.035 µM). The sensor showed excellent selectivity against common electroactive interferents such as glucose and uric acid, long-term stability, and accurate recovery in artificial saliva (>95.7%), indicating strong potential for practical application. This enzyme-free platform offers a robust and scalable strategy for continuous lactate monitoring, particularly suited for wearable devices in sports performance monitoring and critical care diagnostics. Full article