Search Results (40)

The electrochemical water splitting method is widely regarded as an efficient and sustainable approach for producing high-purity hydrogen in an environmentally friendly manner. Cost-effective and efficient electrocatalysts are essential for augmenting the electrocatalytic water oxidation reaction. Herein, the PEG-WO₃-NiO electrocatalyst is acknowledged for attaining efficient oxygen evolution reaction (OER) performances in alkaline conditions. The NiO nanoparticles anchored themselves to the PEG-WO₃‘s surface and produced an effective interfacial contact between the electrocatalyst materials. Among various compositions, the optimized ratio of the PEG-WO₃-NiO electrocatalyst exhibits a low overpotential of 349.7 mV at a current density of 10 mA cm⁻² and a Tafel slope of 71.22 mV dec⁻¹ for the OER in 1 M KOH. Additionally, the electrocatalyst demonstrates excellent stability, maintaining its performance even after 5000 cyclic voltammetry (CV) cycles and chronopotentiometry analysis. Given its durability and high electrochemically active surface area, the PEG-WO₃-NiO electrocatalyst contributes to the advancement of cost-effective and scalable solutions for water oxidation applications. Full article

Cobalt electrochemical deposition, with its bottom–up growth properties, is a core technology for creating metal interconnects. Additives are crucial during electrodeposition to control the quality of deposits by adsorbing onto the Co surface. The functional groups of additive molecules are the key to tailoring the adsorption behavior. This study focuses on heteroaromatic thiol additives, including 2-mercaptobenzimidazole (MBI), 2-mercapto-5-benzimidazolesulfonic acid sodium salt dehydrate (MBIS), and 2-mercaptobenzoxazole (MBO). Cyclic voltammetry, chronopotentiometry, quantum chemical calculations, and characterization tests were employed to investigate the adsorption behavior of additive molecules with different functional groups on cobalt. The results indicate that the inhibitory strength of the three additives on electrodeposition follows the following order: MBI > MBIS > MBO. The strong inhibitory effect of MBI primarily stems from the adsorption of the thiol group, the pyridine-like nitrogen in the heterocycle, and the benzene ring. MBIS exhibits reduced inhibitory capability due to the combined effects of the sulfonic acid group and hydrolysis ionization. MBO, with the introduction of an oxygen atom in the heterocycle, shows the weakest adsorption and inhibitory capability among the three. Full article

Water electrolysis for hydrogen production is of great importance for the reliable use of renewable energy sources to have a clean environment. Electrolyzers play a key role in achieving the carbon-neutral target of 2050. Among the different types of water electrolyzers, proton exchange membrane water electrolyzers (PEMWEs) represent a well-developed technology that can be easily integrated into the smart grid for efficient energy management. In this study, a discrete dynamic mathematical model of a PEMWE was developed in MATLAB/Simulink to simulate cell performance under various operating conditions such as temperature, inlet flow rate, and current density loads. A lab-scale test bench was designed and set up, and a 5 cm² PEMWE was tested at different temperatures (40–80 °C) and flow rates (3–12 mL/min), obtaining Linear Sweep Voltammetry (LSV), Cyclic Voltammetry (CV), Chrono-potentiometry (CP), and Electrochemical Impedance Spectroscopy (EIS) results for comparison and adjustment of the dynamic model. Sensitivity analysis of different operating variables confirmed that current density and temperature are the most influential factors affecting cell voltage. The parametric sensitivity of various chemical–physical and electrochemical parameters was also investigated. The most significant ones were estimated via non-linear least squares optimization to fine-tune the model. Additionally, strong correlations between these parameters and temperature were identified through regression analysis, enabling accurate performance prediction across the studied temperature range. Full article

Transition metals such as nickel and cobalt as an alternative to Pt and Pd can be used for oxygen evolution reactions (OERs) and hydrogen production reactions (HERs) in alkaline environments, facilitating green hydrogen production as a sustainable alternative to fossil fuels. In this study, an NiCo₂O₄ catalyst was produced by a sono-hydrothermal method using urea as a hydrolysis agent. The electrochemical performance of the catalyst-coated NiFelt electrode was evaluated at different KOH concentrations (0.25, 0.5, and 1 M) and four operating temperatures in the interval of 20–80 °C. The electrode characteristics were investigated via electrochemical spectroscopy (cyclic voltammetry, EIS, multistep chronopotentiometry, multistep chronoamperometry) using two different reference electrodes (Ag/AgCl and Hg/HgO), to obtain insight into the anodic and cathodic peaks. XRD, SEM, EDS, and TEM analyses confirmed the purity, structure, and nanoscale particle size (20–45 nm) of the NiCo₂O₄ catalyst. The electrode showed symmetric CV with Ag/AgCl, making this reference electrode more appropriate for capacitance measurements, while Hg/HgO proved advantageous for EIS in alkaline solutions due to reduced noise. The overpotential of the catalyst-coated NiFelt decreased by 108 mV at 10 mA/cm² compared to bare NiFelt, showing a good potential for its application in anion exchange membranes and alkaline electrolyzers at an industrial scale. Full article

This study explores the stability of electrodeposited copper catalysts utilized in electrochemical CO₂ reduction (ECR) across various amine media. The focus is on understanding the influence of different amine types, corrosion ramifications, and the efficacy of pulse ECR methodologies. Employing a suite of electrochemical techniques including potentiodynamic polarization, linear resistance polarization, cyclic voltammetry, and chronopotentiometry, the investigation reveals useful insights. The findings show that among the tested amines, CO₂-rich monoethanolamine (MEA) exhibits the highest corrosion rate. However, in most cases, the rates remain within tolerable limits for ECR operations. Primary amines, notably monoethanolamine (MEA), show enhanced compatibility with ECR processes, attributable to their resistance against carbonate salt precipitation and sustained stability over extended durations. Conversely, tertiary amines such as methyldiethanolamine (MDEA) present challenges due to the formation of carbonate salts during ECR, impeding their effective utilization. This study highlights the effectiveness of pulse ECR strategies in stabilizing ECR. A noticeable shift in cathodic potential and reduced deposit formation on the catalyst surface through periodic oxidation underscores the efficacy of such strategies. These findings offer insights for optimizing ECR in amine media, thereby providing promising pathways for advancements in CO₂ emission reduction technologies. Full article

This investigation addresses increasing interest in advanced composite materials, combining capacitive properties and spontaneous magnetization for energy storage applications in supercapacitors. The capacitive properties of ferrimagnetic NiFe₂O₄ (NFO) spinel nanoparticles with magnetization of 30 emu g⁻¹ were enhanced using high-energy ball-milling and the use of advanced dispersant, which facilitated charge transfer. NFO electrodes with an active mass of 40 mg cm⁻² showed a capacitance of 1.46 F cm⁻² in 0.5 M Na₂SO₄ electrolyte in a negative potential range. The charging mechanism in the negative potential range in Na₂SO₄ electrolyte was proposed. NFO was combined with conductive polypyrrole polymer for the fabrication of composites. The analysis of the capacitive behavior of the composites using cyclic voltammetry, chronopotentiometry and impedance spectroscopy at different electrode potentials revealed synergy of contributions of NFO and PPy. The highest capacitance of 6.64 F cm⁻² was obtained from cyclic voltammetry data. The capacitance, impedance, and magnetic properties can be varied by variation of electrode composition. Composite electrodes are promising for application in anodes of asymmetric magnetic supercapacitors for energy storage and magnetically enhanced capacitive water purification devices. Full article

The electrochemical behavior of dysprosium ions, as well as dysprosium and nickel ion co-reduction, on inert tungsten electrodes and active nickel electrodes were studied in the eutectic KCl-NaCl-CsCl melt at a temperature of 823 K using the methods of cyclic and square-wave voltammetry and open circuit chronopotentiometry. The process of Dy³⁺ ions electroreduction was found to be reversible and to proceed within a single three-electron stage up to the polarization rate of 0.1 V/s. The increase in the polarization rate indicates a slower rate of the charge transfer, which causes the quasi-reversible character of the charge transfer. It is shown that when the KCl-NaCl-CsCl eutectic melt contains both nickel and dysprosium ions, the voltammetry curves at 823 K have a wave of nickel ion reduction at the potentials of −(0.22–0.28) V and a dysprosium ion reduction at the potentials of −(2.175–2.250) V relative to a chlorine-silver reference electrode. Apart from these waves, the voltammograms have two reduction waves at the potentials of −(1.9–1.95) V and −(2.05–2.1) V. These waves are associated with the reduction of dysprosium ions and their depolarization on metallic nickel, which was preliminary deposited on the tungsten electrode, as well as the formation of the intermetallic phases of dysprosium and nickel of various Dy_xNi_y compositions. The (E-t) dependencies of the open circuit chronopotentiometry elucidate plateaus of the potential delay, which correspond to the dissolution of separate dysprosium and nickel intermetallic phases. Based on the results of the voltammetry changes and the chronopotentiometry of the open circuit, a series of electrochemical syntheses were performed in the potentiostatic regime at the potentials of −(1.7–2.1) V. The intermetallic phases of DyNi₅, DyNi₃ and DyNi₂ were obtained at a definite ratio of the dysprosium and nickel chloride concentrations in the KCl-NaCl-CsCl eutectic melt and at a temperature of 823 K. The synthesized intermetallic samples were characterized by X-ray diffraction and scanning electron microscopy. Full article

Electrophysiological mapping (EM) using acute electrode probes is a common procedure performed during functional neurosurgery. Due to their constructive specificities, the EM probes are lagging in innovative enhancements. This work addressed complementing a clinically employed EM probe with carbonic and circumferentially segmented macrocontacts that are operable both for neurophysiological sensing (“recording”) of local field potentials (LFP) and for test stimulation. This paper illustrates in-depth the development that is based on the direct writing of functional materials. The unconventional fabrication processes were optimized on planar geometry and then transferred to the cylindrically thin probe body. We report and discuss the constructive concept and architecture of the probe, characteristics of the electrochemical interface deduced from voltammetry and chronopotentiometry, and the results of in vitro and in vivo recording and pulse stimulation tests. Two- and three-directional macrocontacts were added on probes having shanks of 550 and 770 μm diameters and 10–23 cm lengths. The graphitic material presents a ~2.7 V wide, almost symmetric water electrolysis window, and an ultra-capacitive charge transfer. When tested with clinically relevant 150 μs biphasic current pulses, the interfacial polarization stayed safely away from the water window for pulse amplitudes up to 9 mA (135 μC/cm²). The in vivo experiments on adult rat models confirmed the high-quality sensing of LFPs. Additionally, the in vivo-prevailing increase in the electrode impedance and overpotential are discussed and modeled by an ionic mobility-reducing spongiform structure; this restricted diffusion model gives new applicative insight into the in vivo-uprisen stimulation overpotential. Full article

Thin layers (up to 1 µm) of Pd-Ir alloys were electrodeposited from aqueous, galvanic baths of PdCl₂ and IrCl₃ mixtures. The morphology of the electrodeposits was examined by means of scanning electron microscopy. The composition of alloys was determined with the use of energy-dispersive spectroscopy, atomic absorption spectrometry, X-ray photoelectron spectroscopy, and Auger electron spectroscopy. For the studies of the electrochemical properties of alloys, cyclic voltammetry, chronoamperometry, and chronopotentiometry were used. It was found that Pd-Ir alloy electrodes were surface-enriched with Pd. Pd-Ir alloys subjected to different electrochemical treatment involving hydrogen sorption changed their surface state. The continuous hydrogen sorption enhanced the Ir ions’ dissolution. The values of thermodynamic functions of hydrogen sorption in strong alkaline electrolytes were comparable with those in acidic electrolytes, whereas the kinetics of the process in alkaline medium was hindered. The miscibility gap in the Pd-Ir-H system vanished for the electrode containing ca. 93.7 at.% Pd. Full article

Nowadays, the research community envisions smart materials composed of biodegradable, biocompatible, and sustainable natural polymers, such as cellulose. Most applications of cellulose electroactive materials are developed for energy storage and sensors, while only a few are reported for linear actuators. Therefore, we introduce here cellulose-multiwall carbon nanotube composite (Cell-CNT) fibers compared with pristine multiwall carbon nanotube (CNT) fibers made by dielectrophoresis (DEP) in their linear actuation in an organic electrolyte. Electrochemical measurements (cyclic voltammetry, square wave potential steps, and chronopotentiometry) were performed with electromechanical deformation (EMD) measurements. The linear actuation of Cell-CNT outperformed the main actuation at discharging, having 7.9 kPa stress and 0.062% strain, making this composite more sustainable in smart materials, textiles, or robotics. The CNT fiber depends on scan rates switching from mixed actuation to main expansion at negative charging. The CNT fiber-specific capacitance was much enhanced with 278 F g⁻¹, and had a capacity retention of 96% after 5000 cycles, making this fiber more sustainable in energy storage than the Cell-CNT fiber. The fiber samples were characterized by scanning electron microscopy (SEM), BET (Braunauer-Emmett-Teller) measurement, energy dispersive X-ray (EDX) spectroscopy, FTIR, and Raman spectroscopy. Full article

The development of transition metal (TM) catalysts to replace precious metals has garnered increasing interest. Specifically, platinum (Pt)-based catalysts have been extensively investigated for their electrochemical performance in hydrogen evolution reaction (HER), which offer a clean means of producing hydrogen fuel without carbon emissions. However, the reliance on Pt-based catalysts has hindered the progress of HER development. Therefore, researchers have explored metal-organic frameworks (MOFs) as a substitute for noble Pt-based catalysts to address this issue. Nevertheless, the low electroconductivity of pure MOFs restricts their application in electrochemical fields. To overcome this limitation, MXenes have emerged as a promising two-dimensional (2D) material for coupling with MOFs to create an electrocatalyst with high electrical conductivity, a large surface area, and a tunable structure. In this study, we report the synthesis of a Ti₃C₂T_x (MXene) nanosheet-encapsulated MOFs catalyst (Ti₃C₂T_x@ZIF-8) with high activity and a low cost by encapsulating the precursor with ZIF-8 for HER in alkaline media. The catalyst exhibits an overpotential of only 507 mV at 20 mA/cm² and a low Tafel slope value of 77 mV/dec. Additionally, cyclic voltammetry (CV) indicates an electrochemical active surface area (ECSA) of 122.5 cm², and chronopotentiometry demonstrates the stable nature of the catalyst over 20 h without any significant changes in the overpotential value. The excellent electrochemical properties of Ti₃C₂T_x@ZIF-8 suggest its potential as a promising material for energy conversion applications. Full article

A preparation method of nanocomposites based on poly (3-octylthiophene-2,5-diyl) (POT) and carbon black (CB) as the transducer of an all-solid potassium ion selective electrode is proposed. POT is used as the dispersant of CB, and the obtained nanocomposites have unique characteristics, including high conductivity, high capacitance and high stability. The potassium ion selective electrode based on POT and CB was characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and chronopotentiometry. The results showed that the detection limit of potassium ions was 10^−6.2 M, and the slope was 57.6 ± 0.8 mV/façade. The water layer test and anti-interference test show that the electrode has high hydrophobicity, the static contact angle reaches 139.7° and is not easily affected by light, O₂ and CO₂. Full article

This paper presents the results obtained from the chemical activation of bacterial nanocellulose (BCN) using fique juice as a culture medium. BNC activation (BNCA) was carried out with H₃PO₄ and KOH at activation temperatures between 500 °C to 800 °C. The materials obtained were characterized morphologically, physicochemically, superficially, and electrochemically, using scanning electron microscopy, X-ray photoelectron spectroscopy (XPS), the physisorption of gases N₂ and CO₂ at 77 K and 273 K, respectively, cyclic voltammetry, chronopotentiometry, and electrochemical impedance spectroscopy (EIS). The samples activated with H₃PO₄ presented specific surface areas (S_BET) around 780 m² g⁻¹, while those activated with KOH values presented specific surface areas between 680 and 893 m² g⁻¹. The XPS analysis showed that the P_XPS percentage on the surface after H₃PO₄ activation was 11 wt%. The energy storage capacitance values ranged between 97.5 F g⁻¹ and 220 F g⁻¹ by EIS in 1 M H₂SO₄. The samples with the best electrochemical performance were activated with KOH at 700 °C and 800 °C, mainly due to the high S_BET available and the accessibility of the microporosity. The capacitance of BNCAs was mainly improved by electrostatic effects due to the S_BET rather than that of pseudocapacitive ones due to the presence of phosphorus heteroatoms. Full article

In this study, an asymmetric supercapacitor (ASSC) device is assembled by the deposition and annealing of silver-doped mixed metal oxides on reduced graphene oxide (rGO)/Ni foam and activated carbon (AC) on Ni foam as positive and negative electrodes, respectively. The best performing Ag:MnCoNiO active material is synthesized on rGO/Ni foam using chronopotentiometry combined with heat treatment. The XRD study clearly confirms the crystalline nature of the electrode with MnCo₂O₄ and MnNi₂O₄ phases. FT-IR and XPS studies revealed the formation of Ag:MnCoNiO/rGO on Ni foam. SEM images show a thin-film layer of fabricated material on the surface of rGO/Ni foam. The supercapacitor properties were tested in two- and three-electrode configurations, with cyclic voltammetry (CV), galvanostatic charge/discharge (GCD), and electrochemical impedance spectroscopy (EIS) experiments in a 6 M KOH aqueous electrolyte. In the three-electrode configuration, reversible faradic reactions can be observed in a potential range of 0.0 and +0.6 V vs. Hg/HgSO₄. In the two-electrode device configuration, the system exhibits a maximum energy density of 45.5 Wh kg⁻¹ and provides a maximum power density of 4.5 kW kg⁻¹. The results showed that the doping of Ag in a MnCoNiO electrode shows promising properties, achieved by a very simple fabrication process. The results showcase the synergistic effects achieved by mixed multiple-component metal oxides, leading to improved supercapacitive properties. Full article

As high-quality substitutes for conventional catalysts, the bifunctional catalytic properties of the coating of transition-metal-based materials are pivotal for improving water-splitting efficiency. Herein, cobalt-molybdenum bimetallic phosphide nanofibers (CoMoP NFs) were synthesized via a series of facile strategies, which are divided into pyrolysis electrospun PAN and metal salts, to obtain one-dimensional morphology and a gas-solid phosphating precursor. The obtained CoMoP NFs catalyst has superior catalytic activity performance in 1M KOH. Serving as an oxygen evolution reaction (OER) catalyst, the electrode of the CoMoP NFs affords different kinds of current densities at 50 mA cm⁻² and 100 mA cm⁻², with low overpotentials of 362 and 391 mV, respectively. In addition, the hydrogen evolution reaction (HER) performance of the CoMoP NFs mainly shows when under a low overpotential of 126 mV, which can deliver a current density of 10 mA cm⁻². In order to further detect the stability of the catalyst, we used multiple cyclic voltammetry and chronopotentiometry tests for OERs and HERs, which maintain performance and carry a current density of 10 mA cm⁻² for longer. As an integrated high-performance bifunctional electrode for overall water splitting, the CoMoP NFs only require 1.75 V@10 mA cm⁻² for 40 h. This work highlights a facile method to create an electrocatalyst with fiber nanostructures which possesses excellent activity as an alkaline electrolyte. Full article