Search Results (6,187)

Biomass-derived hard carbon (BHC) has attracted considerable attention as a sustainable and cost-effective anode material for sodium-ion batteries (SIBs), owing to its natural abundance, environmental friendliness, and promising electrochemical performance. This review provides a detailed overview of recent progress in the synthesis, structural design, and performance optimization of BHC materials. It encompasses key fabrication routes, such as high-temperature pyrolysis, hydrothermal pretreatment, chemical and physical activation, heteroatom doping, and templating techniques, that have been employed to control pore architecture, defect density, and interlayer spacing. Among these strategies, activation-assisted pyrolysis and heteroatom doping have shown the most significant improvements in sodium (Na) storage capacity and long-term cycling stability. The review further explores the correlations between microstructure and electrochemical behavior, outlines the main challenges limiting large-scale application, and proposes future research directions toward scalable production and integration of BHC anodes in practical SIB systems. Overall, these advancements highlight the strong potential of BHC as a next-generation anode for grid-level and renewable energy storage technologies. Full article

Herein, we propose an ultrasensitive electrochemical immunosensor based on glucose oxidase labeling and enzyme-catalyzed Au staining. In brief, the primary antibody (Ab₁), bovine serum albumin, an antigen and then a bionanocomposite that contains a second antibody (Ab₂), poly(3-anilineboronic acid) (PABA), Au nanoparticles (AuNPs) and glucose oxidase (GOx) are modified on a glassy carbon electrode coated with multiwalled carbon nanotubes, yielding a corresponding sandwich-type immunoelectrode. In the presence of glucose, a chemical reduction of NaAuCl₄ by enzymatically generated H₂O₂ can precipitate a lot of gold on the Ab₂-PABA-AuNPs-GOx immobilized immunoelectrode. In situ anodic stripping voltammetry (ASV) detection of gold in 8 μL 1.0 M aqueous HBr-Br₂ is conducted for the antigen assay, and the ASV detection process takes approximately 6 min. This method is employed for the assay of human immunoglobulin G (IgG) and human carbohydrate antigen 125 (CA125), which demonstrates exceptional sensitivity, high selectivity and fewer required reagents/samples. The achieved limits of detection (S/N = 3) by the method are 0.25 fg mL⁻¹ for IgG (approximately equivalent to containing 1 IgG molecule in the 1 microlitre of the analytical solution) and 0.1 nU mL⁻¹ for CA125, which outperforms many previously reported results. Full article

Inkjet printing enables contactless deposition onto fragile substrates for printed energy-storage devices and supports flexible batteries and supercapacitors with reduced material use. This review examines multilayer and interdigital architectures and analyzes how ink rheology, droplet formation, colloidal interactions, and the printability window govern performance. For batteries, reported inkjet-printed electrodes commonly deliver capacities of ~110–150 mAh g⁻¹ for oxide cathodes at C/2–1 C, with coulombic efficiency ≥98% and stability over 10²–10³ cycles; silicon anodes reach ~1.0–2.0 Ah g⁻¹ with efficiency approaching 99% under stepwise formation. Typical current densities are ~0.5–5 mA cm⁻² depending on areal loading, and multilayer designs with optimized drying and parameter tuning can yield rate and discharge behavior comparable to cast films. For supercapacitors, inkjet-printed microdevices report volumetric capacitances in the mid-hundreds of F cm⁻³, translating to ~9–34 mWh cm⁻³ and ~0.25–0.41 W cm⁻³, with 80–95% retention after 10,000 cycles and coulombic efficiency near 99%. In solid-state configurations, stability is enhanced, although often accompanied by reduced areal capacitance. Although solids loading is lower than in screen printing, precise material placement together with thermal or photonic sintering enables competitive capacity, rate capability, and cycle life while minimizing waste. The review consolidates practical guidance on ink formulation, printability, and defect control and outlines opportunities in greener chemistries, oxidation-resistant metallic systems, and scalable high-throughput printing. Full article

In this study, we present a cost-effective approach for fabricating nanopores on single-crystal silicon using a silver–alumina–silver (Ag/AAO/Ag) metal–insulator–metal (MIM) structured mask. Self-ordered porous anodic aluminum oxide (AAO) films were prepared via two-step anodization and coated with silver layers on both sides to form the MIM structure. When irradiated with a 532 nm nanosecond laser, the MIM mask excites surface plasmon polaritons (SPPs), resulting in a localized field enhancement that enables the etching of nanopores into the silicon substrate. This method successfully produced nanopores with diameters as small as 50 nm and depths up to 28 nm. The laser-induced SPP-assisted machining significantly enhances the specific surface area of the processed surface, making it promising for applications in catalysis, biosensing, and microcantilever-based devices. For instance, an increased surface area can improve catalytic efficiency by providing more active sites, and enhance sensor sensitivity by amplifying response signals. Compared to conventional lithographic or focused ion beam techniques, this method offers simplicity, low cost, and scalability. The proposed technique demonstrates a practical and efficient route for the large-area subwavelength nanostructuring of silicon surfaces. Full article

Plant Microbial Fuel Cells (PMFCs) represent a promising technology that uses electroactive bacteria to convert the chemical energy in organic matter into electrical energy. The addition of carbon pellet on electrodes may increase the specific surface area for colonization via bacteria. Use of nutrients such as urea could enhance plant growth. Our study aims to address the following questions: (1) Does carbon pellet layering affect the electrical performance of PMFCs? (2) Does urea treatment of the plants used to feed the PMFCs affect the electrical performance? A new prototype of PMFC has been tested: the plant pot is on the top, drainage water percolates to the tub below, containing the Microbial Fuel Cells (MFCs). To evaluate the best layering setup, two groups of MFCs were constructed: a “Double layer” group (with carbon pellet both on the cathode and on the anode), and a “Single layer” group (with graphite only on the cathode). All MFCs were plant-fed by Spathiphyllum lanceifolium L leachate. After one year, each of the previous two sets has been divided into two subsets: one wetted with percolate from plants fertilized with urea, and the other with percolate from unfertilized plants. Open circuit voltage (mV), short circuit peak current, and short circuit current after 5 s (mA) produced values that were measured on a weekly basis. PMFCs characterized by a “Single layer” group performed better than the “Double layer” group most times, in terms of higher and steadier values for voltage and calculated power. Undesirable results regarding urea treatment suggest the use of less concentrated urea solution. The treatment may provide consistency but appears to limit voltage and peak values, particularly in the “Double layer” configuration. Full article

Vigilance refers to a sustained attentional state enabling the detection of specific but unpredictable changes in the external environment. This state typically declines rapidly over time. A deterioration in vigilance can lead to serious errors or accidents in both occupational and special scenarios, rendering vigilance intervention a critical area of interest for researchers. Transcranial direct current stimulation (tDCS) has shown promise in mitigating vigilance decrement. However, the timing of such interventions may yield differential effects, a question that remains unresolved in the literature. The present study examines the possibility of using the average power in the low alpha frequency band (alpha-1) as an Electroencephalography-based index of vigilance to identify a candidate entry point for tDCS application that may enhance efficacy, and further explores how the timing of tDCS influences vigilance outcomes. In the pilot experiment, we determined the timing for guiding tDCS based on the average power of the low alpha frequency band (alpha-1) from five participants, which was identified as the third stage of the experiment. The validity of this timing has been verified in subsequent independent samples with a larger size. In the formal experiment, ninety-nine participants were randomly assigned to three groups, receiving early intervention, late intervention, or a no-stimulus control, and completed a 20 min visual modification of the Bakan Task. The early-stimulated group (n = 33) received anodal stimulation (2 mA) on the right posterior parietal cortex during the first 8 min of the test (0–8 min), the late-stimulated group (n = 33) received stimulation on the same location during the middle 8 min of the test (8–16 min), while the blank control group (n = 33) received no stimulation. Results indicated that the late-stimulated group (8–16 min of stimulation), for which alpha-1 power guided the tDCS onset timing, was associated with a greater attenuation of vigilance decrement compared to the early-stimulated group (0–8 min of stimulation). Both groups demonstrated significant differences in vigilance during the first stage following stimulation. Full article

Searching anode materials is an important task for the development of sodium-ion batteries. In this regard, bronze-phase titanium dioxide, TiO₂(B), has been considered as one of the promising materials, owing to its crystal structure with open channels and voids facilitating Na⁺ diffusion and storage. However, the electrochemical de-/sodiation mechanism of TiO₂(B) has not been clearly comprehended, and further experiments are required. Herein, in situ and ex situ observations by a combination of X-ray photoelectron spectroscopy, X-ray diffraction, Raman spectroscopy, gas chromatography–mass spectrometry was used to provide additional insights into the electrochemical reaction scenario of bronze-phase TiO₂ in Na-ion batteries. The findings reveal that de-/sodiation of TiO₂(B) occurs through a reversible intercalation reaction and without the involvement of the conversion reaction (no metallic titanium is formed and no oxygen is released). At the same time, upon the first Na⁺ uptake process, crystalline TiO₂(B) becomes partially amorphous, but is still driven by the Ti⁴⁺/Ti³⁺ redox couple. Importantly, TiO₂(B) has pseudocapacitive electrochemical behavior during de-/sodiation based on a quantitative analysis of the cyclic voltammetry data. The results obtained in this study complement existing insights into the sodium storage mechanisms of TiO₂(B) and provide useful knowledge for further improving its anode performance for SIBs application. Full article

We have developed a new bioanode based on a cascade of reactions catalyzed by two enzymes. A glassy carbon electrode is modified with β-glucosidase and glucose oxidase enzymes entrapped within an osmium redox polymer. Cellobiose, the fuel for the anode, is hydrolyzed by β-glucosidase (TxGH116), yielding two molecules of D-glucose. Glucose is then oxidized by glucose oxidase (GOx) into δ-gluconolactone and produces electrons that are transferred to the electrode mediated by osmium redox polymer. We investigated the kinetic parameters of both enzymes at different temperatures. For GOx, the effect of enzyme loading and enzyme/polymer ratio were also optimized. The proposed bioanode is coupled to a biocathode based on horseradish peroxidase (HRP) in which H₂O₂, the oxidant, is reduced. We investigated the performance of the biofuel cell on cellobiose and sugarcane hydrolysates subjected to different pretreatments. Alkaline pretreatments of biomass were found to be more effective than phosphoric acid pretreatment. Adding TxGH116 β-glucosidase further enhanced current generation, even when commercial cellulase was used. Full article

Recycling of lithium-ion batteries (LIBs) requires efficient separation of active material from current collectors to enable high-quality recovery of both the coating and the metal foil. In this study, a water-based delamination process for anode foils was systematically investigated under variations in temperature, particle size, ultrasonic power, and prior mechanical stressing of the particles. Mechanically cut and pre-folded foil pieces were treated in a batch setup at different temperatures (room temperature to 100 °C) and ultrasonic power levels (50 and 100%). Results show that higher temperatures strongly promote delamination, with 100% removal of the active layer achieved on the smooth foil side at 80 °C without ultrasonic treatment. Ultrasonic treatment at moderate power (50%) yielded greater delamination than at full power (100%), likely due to more effective cavitation dynamics at moderate intensity. Mechanical pre-stressing by folding significantly reduced delamination, with three folds effectively preventing separation. In comparison, mechanically comminuted particles from a granulator achieved similar delamination to three-folded particles after 5 min treatment, and higher delamination after 30 min. These findings highlight the importance of process parameters in achieving efficient aqueous delamination, providing insights for scaling low-energy recycling processes for LIB production scrap. Full article

The paper presents experimental results for a modified pulsed plasma thruster (PPT) with solid propellant, using a coaxial anode–cathode design. Graphite from pencil leads served as propellant, and a tungsten trigger electrode was tested to reduce carbonization effects. Experiments were performed in a vacuum chamber at 0.001 Pa, employing diagnostics such as discharge current/voltage recording, power measurement, ballistic pendulum, time-of-flight (TOF) method, and a Faraday cup. Current and voltage waveforms matched an oscillatory RLC circuit with variable plasma channel resistance. Key discharge parameters were measured, including current pulse duration/amplitude and plasma channel formation/decay dynamics. Impulse bit values, obtained with a ballistic pendulum, reached up to 8.5 μN·s. Increasing trigger capacitor capacitance reduced thrust due to unstable “pre-plasma” formation and partial pre-discharge energy loss. Using TOF and Faraday cup diagnostics, plasma front velocity, ion current amplitude, current density, and ion concentration were determined. Tungsten electrodes produced lower charged particle concentrations than graphite but offered better adhesion resistance, minimal carbonization, and stable long-term performance. The findings support optimizing trigger electrode materials and PPT operating modes to extend lifetime and stabilize thrust output. Full article

Thallium is a soft metal with a grey or silvery hue. It commonly occurs in two oxidation states in chemical compounds: Tl⁺ and Tl³⁺. Thermodynamically, Tl⁺ is significantly more stable and typically represents the dominant form of thallium in environmental systems. However, in this chemical form, thallium remains highly toxic. This study focuses on the modification of a glassy carbon electrode (GCE) with silver nanostructures stabilised by potato starch derivatives. The modified electrode (GCE/AgNPs-E1451) was used for the determination of trace amounts of thallium ions using anodic stripping voltammetry. Emphasis was placed on assessing the effect of surface modification on key electrochemical performance parameters of the electrode. Measurements were carried out in a base electrolyte (EDTA) and in a real soil sample collected from Bali. The stripping peak current of thallium exhibited linearity over the concentration range from 19 to 410 ppb (9.31 × 10⁻⁸ to 2.009 × 10⁻⁶ mol/dm³). The calculated limit of detection (LOD) was 18.8 ppb (9.21 × 10⁻⁸ mol/dm³), while the limit of quantification (LOQ), corresponded to 56.4 ppb (2.76 × 10⁻⁷ mol/dm³). The GCE/AgNPs-E1451 electrode demonstrates several significant advantages, including a wide detection range, reduced analysis time due to the elimination of time-consuming pre-concentration steps, and non-toxic operation compared to mercury-based electrodes. Full article

All inorganic CsPbBr₃ possesses ideal stability in halide perovskites, but its wide bandgap and relatively poor film quality seriously limit the performance enhancement and possible applications of perovskite solar cells (PSCs). In this work, a triple-functional poly(3-Hexylthiophene) (P3HT) modifier was introduced to realize color-tunable semi-transparent CsPbBr₃ PSCs. From the optical perspective, the P3HT acted as the assistant photoactive layer, enhanced the light absorption capacity of the CsPbBr₃ film, and broadened the spectrum response range of devices. In view of the hole transport layer, P3HT modified the energy level matching between the CsPbBr₃/anode interface and facilitated the hole transport. Simultaneously, the S⁻ in P3HT formed a more stable Pb-S bond with the uncoordinated Pb²⁺ on the surface of CsPbBr₃ and played the role of a defect passivator. As the P3HT concentration increased from 0 to 15 mg/mL, the color of CsPbBr₃ devices gradually changed from light yellow to reddish brown. The PSC treated by an optimal P3HT concentration of 10 mg/mL achieved a champion power conversion efficiency (PCE) of 8.71%, with a V_OC of 1.30 V and a J_SC of 8.54 mA/cm², which are remarkably higher than those of control devices (6.86%, 1.22 V, and 8.21 mA/cm²), as well its non-degrading stability and repeatability. Here, the constructed CsPbBr₃/P3HT heterostructure revealed effective paths for enhancing the photovoltaic performance of CsPbBr₃ PSCs and boosted their semi-transparent applications in building integrated photovoltaics (BIPVs). Full article

Major depressive disorder (MDD) is a prevalent and disabling condition. Transcranial direct current stimulation (tDCS) may improve symptoms by modulating neuroplastic and inflammatory mechanisms. This randomized, double-blind, placebo-controlled trial will recruit adult outpatients with MDD showing residual symptoms despite at least four weeks of stable SSRI treatment. Participants will be randomized to active or sham add-on tDCS while continuing their antidepressant regimen. The intervention will consist of 15 sessions over 3 weeks, targeting the left dorsolateral prefrontal cortex (anode F3, cathode F4) at 2 mA for 30 min per session. The primary outcome is the reduction of depressive symptoms measured by the Hamilton Depression Rating Scale-17 (HDRS), with remission defined as HDRS-17 ≤ 7. Secondary outcomes include cognitive performance (attention, executive functioning, memory), serum biomarkers (BDNF, VEGF, NGF, NRG1, angiogenin, IGF1, IL-6, TNF-α), cortical excitability assessed by transcranial magnetic stimulation (motor threshold, silent period, intracortical inhibition/facilitation), and cerebral hemodynamics by transcranial Doppler sonography (blood flow velocity, pulsatility, resistivity). Assessments will occur at baseline, post-treatment, and 3- and 6-month follow-ups. This trial aims to evaluate the efficacy of adjunctive tDCS in MDD with residual symptoms and its biological correlates, bridging clinical improvement with electrophysiological and neurovascular mechanisms. Full article

This study presents a sustainable upcycling strategy to convert “Pit,” a carbon-rich coke oven by-product from steel manufacturing, into high-purity graphite for use as an anode material in lithium-ion batteries. Despite its high carbon content, raw Pit contains significant impurities and has irregular particle morphology, which limits its direct application in batteries. We employed a multi-step, additive-free refinement process—including jet milling, spheroidization, and high-temperature graphitization—to enhance carbon purity and structural properties. The processed Pit-derived graphite showed a much-improved particle size distribution (D50 reduced from 25.3 μm to 14.8 μm & Span reduced from 1.72 to 1.23), increased tap density (from 0.54 to 0.80 g/cm³), and reduced BET surface area, making it suitable for high-performance lithium-ion batteries anodes. Structural characterization by XRD and TEM confirmed dramatically enhanced crystallinity after graphitization (graphitization degree increasing from ~13 for raw Pit to 95.7% for graphitized Pit at 3000 °C). The fully processed graphite (denoted S_Pit3000) delivered a reversible discharge capacity of 346.7 mAh/g with an initial Coulombic efficiency of 93.5% in half-cell tests—comparable to commercial artificial graphite. Furthermore, when composited with silicon oxide to form a hybrid anode, the material achieved an even higher capacity of 418.0 mAh/g under high mass loading conditions. These results highlight the feasibility of transforming industrial coke waste into value-added electrode materials through environmentally friendly physical processes. The upcycled graphite anode meets industrial performance standards, demonstrating a promising route toward circular economy solutions in both the steel and battery industries. Full article

The molecular structure and mechanical resilience of the binder are crucial for mitigating volume expansion, maintaining electrode structural integrity, and enhancing the cycling stability of silicon-based anode materials in lithium-ion batteries. In this study, from the perspective of binder molecular structural design, commercial carboxymethyl cellulose (CMC) was modified with silk protein (SF), which has good mechanical properties and abundant surface functional groups, to address issues such as high brittleness, poor compliance and easy cracking of the electrode structure during charge and discharge cycles, and to enhance the mechanical properties of the CMC-based binder and its interaction with silicon particles, so as to improve the cycle stability of silicon-based materials. The mechanical properties of the CMC binder were significantly improved and the interaction between the binder and the surface of the silicon particles was enhanced by the addition of SF. When the SF content was optimized at 6 wt%, the electrode exhibited the best electrochemical performance, delivering a specific capacity of 1182 mAh/g at a high current density of 5000 mA/g, and retaining a capacity of 1138 mAh/g after 50 cycles at 1000 mA/g, demonstrating excellent electrochemical durability. Full article