Search Results (9)

The oxygen-evolving IrO₂-Ta₂O₅/Ti anode (OEA), primarily used in electrolyzers for plating, metal powder production, electrowinning (EW), and water electrolysis, is analyzed. This study focuses on the distribution of oxygen evolution reaction (OER) activity and the associated operational loss over the randomized OEA texture. The OER activity and its distribution across the IrO₂-Ta₂O₅ coating surface are key factors that influence EW operational challenges and the lifecycle of OEA in EW processes. To understand the OER activity distribution over the coating’s randomized texture, we performed analyses using anode polarization in acid solution at both low and high (EW operation relevant) overpotentials and electrochemical impedance spectroscopy (EIS) during the OER. These measurements were conducted on anodes in both their as-prepared and deactivated states. The as-prepared anode was deactivated using an accelerated stability test in an acid solution, the EW simulating electrolyte. The obtained data are correlated with fundamental electrochemical properties of OEA, such as structure-related pseudocapacitive responses at open circuit potential in the same operating environment. OER and Ir dissolution kinetics, along with the physicochemical anode state upon deactivation, are clearly characterized based on current and potential dependent charge transfer resistances and associated double layer capacitances obtained by EIS. This approach presents a useful tool for elucidating, and consequently tailoring and predicting, anode OER activity and electrolytic operational stability in industrial electrochemical applications. Full article

Ordered mesoporous carbon materials (OMCMs) are widely used as high-performance electrode materials due to their uniform pore structure, excellent electrical conductivity, and good stability. In this paper, three OMCMs with controllable N content were prepared by a nanocasting method using Fe₃O₄ nanocrystals as the template and organic ligands as the carbon source. By adopting a ligand exchange strategy, oleic acid, oleic amine, and octyl amine were successfully capped onto the Fe₃O₄ nanocrystals, respectively, which allowed the rational control of the elemental composition of OMCMs at the molecular level. Further characterizations revealed that the nitrogen content of the resulting OMCMs increased as the proportion of nitrogen atoms in the ligand increased, while the order of the porous structure decreased as the hydrocarbon chain length decreased. This study demonstrates that both the N-doping content and the order of the OMCMs are influenced by the N-containing ligand. This finding will provide a fundamental aspect for their further applications as high-performance electrode and catalytic materials in the field of electrochemistry. Full article

The electrochemical performances of an oxygen-evolving anode produced by the reactivation of waste Ti substrate by a typical IrO₂-Ta₂O₅ coating are correlated to the textural (non)uniformities of the coating and its exhaustion state. Coating degradation is considered operational loss of the activity in a metal electrowinning process. It was found that (pseudo)capacitive performances can vary over the coating surface by 20–30% and depend on the type of dynamics of the input perturbation: constant through cyclic voltammetry (CV) or discontinuous time-dependent through electrochemical impedance spectroscopy (EIS). CV-EIS data correlation enabled profiling of the capacitive properties through the depth of a coating and over its surface. The correlation was confirmed by the findings for the analysis of coating activity for an oxygen evolution reaction, finally resulting in the reliable proposition of a mechanism for the operational loss of the anode. It was found that the less compact and thicker coating parts performed better and operated more efficiently, especially at lower operational current densities. Full article

Activated carbon (AC) compounds derived from biomass precursors have garnered significant attention as electrode materials in electric double-layer capacitors (EDLCs) due to their ready availability, cost-effectiveness, and potential for mass production. However, the accessibility of their active sites in electrochemistry has not been investigated in detail. In this study, we synthesized two novel macro/micro-porous carbon structures prepared from a chitosan precursor using an acid/potassium hydroxide activation process and then examined the relationship between their textural characteristics and capacitance as EDLCs. The material characterizations showed that the ACs, prepared through different activation processes, differed in porosity, with distinctive variations in particle shape. The sample activated at 800 °C (Act-chitosan) was characterized by plate-shaped particles, a specific surface area of 4128 m²/g, and a pore volume of 1.87 cm³/g. Assessment of the electrochemical characteristics of Act-chitosan showed its remarkable capacitance of 183.5 F/g at a scan rate of 5 mV/s, and it maintained exceptional cyclic stability even after 10,000 cycles. The improved electrochemical performance of both chitosan-derived carbon structures could thus be attributed to their large, well-developed active sites within pores < 2 nm, despite the fact that interconnected macro-porous particles can enhance ion accessibility on electrodes. Our findings provide a basis for the fabrication of biomass-based materials with promising applications in electrochemical energy storage systems. Full article

High mass loading (ca. 30 mg/cm²) electrodes were prepared with carbon recovered from catalytic methane cracking (MC). As-fabricated supercapacitors displayed 74% of capacitance retention from 6 mA/cm² to 60 mA/cm² and a Ragone plot’s slope of −7 Wh/kW (compared to 42% and −31 Wh/kW, respectively, for high mass loading devices fabricated with commercial carbon). The high-rate capability of the MC-recovered carbon is attributed to the presence of carbon black and carbon nanotubes produced during the reaction, which likely increased the electronic and ionic conductivity within the electrode. These results suggest that the by-product of this hydrogen generation route might be a suitable active material for supercapacitors. Full article

For the first time, single-entity electrochemistry (SEE) was demonstrated in a hydrogel matrix. SEE involves the investigation of the electrochemical characteristics of individual nanoparticles (NPs) by observing the signal generated when a single NP, suspended in an aqueous solution, collides with an electrode and triggers catalytic reactions. Challenges associated with SEE in electrolyte-containing solutions such as signal variation due to NP aggregation and noise fluctuation caused by convection phenomena can be addressed by employing a hydrogel matrix. The polymeric hydrogel matrix acts as a molecular sieve, effectively filtering out unexpected signals generated by aggregated NPs, resulting in more uniform signal observations compared to the case in a solution. Additionally, the hydrogel environment can reduce the background current fluctuations caused by natural convection and other factors such as impurities, facilitating easier signal analysis. Specifically, we performed SEE of platinum (Pt) NPs for hydrazine oxidation within the agarose hydrogel to observe the electrocatalytic reaction at a single NP level. The consistent porous structure of the agarose hydrogel leads to differential diffusion rates between individual NPs and reactants, resulting in variations in signal magnitude, shape, and frequency. The changes in the signal were analyzed in response to gel concentration variations. Full article

Delicate design and precise manipulation of electrode morphology has always been crucial in electrochemistry. Generally, porous morphology has been preferred due to the fast kinetic transport characteristics of cations. Nevertheless, more refined design details such as the granularity uniformity that usually goes along with the porosity regulation of film electrodes should be taken into consideration, especially in long-term cation insertion and extraction. Here, inorganic electrochromism as a special member of the electrochemical family and WO₃ films as the most mature electrochromic electrode material were chosen as the research background. Two kinds of WO₃ films were prepared by magnetron sputtering, one with a relatively loose morphology accompanied by nonuniform granularity and one with a compact morphology along with uniform particle size distribution, respectively. Electrochemical performances and cyclic stability of the two film electrodes were then traced and systematically compared. In the beginning, except for faster kinetic transport characters of the 50 W-deposited WO₃ film, the two electrodes showed equivalent optical and electrochemical performances. However, after 5000 CV cycles, the 50 W-deposited WO₃ film electrode cracked seriously. Strong stress distribution centered among boundaries of the nonuniform particle clusters together with the weak bonding among particles induced the mechanical damage. This discovery provides a more solid background for further delicate film electrode design. Full article

This review article emphases on the modern approaches to the types of sol-gel materials that are beneficial for electrochemistry, monitored by a report of recent advances in the numerous fields of sol-gel electrochemistry. Modified electrodes for sensors and supercapacitors as well as anti-corrosion are described. Sol-gel synthesis expands the capabilities of technologists to obtain highly porous, homogeneous, and hybrid thin-film materials for supercapacitor electrode application. The widespread materials are transition metal oxides, but due to their low conductivity, they greatly impede the rate capability of electrochemical supercapacitors. The way to optimize their properties is the production of complex oxides or different composites. Among the new materials, a special place is occupied by perovskites and materials with an olivine-type structure, which can be easily obtained by the sol-gel method. The sol-gel coating process has demonstrated excellent chemical stability to advance the corrosion resistance of the various metal alloy substrates. Furthermore, the sol-gel process is a user-friendly technique for applying a hybrid sol-gel coating to provide corrosion resistance. The hybrid sol-gel coating technique is the most attractive, easy to prepare at a lower temperature, and has shown the potential to swap Cr-based coatings. The hybrid sol-gel coating has exhibited promising properties of adherent and uses chemically inert to enhance the corrosion resistance of the metal and alloys. Hence, this review article emphases on the recent advances and approaches in the sol-gel coating processes that influence the belongings of its hybrid sol-gel coating for protecting metal substrates and their alloys from corrosion. In addition, the author discusses the current problem and challenges of hybrid anti-corrosion sol-gel coatings. Metal oxides and composites based on them are actively used to create electrochemical sensors. They synthesized, including the anhydrous and citrate sol-gel methods. Such materials are widely used as glucose biosensors and harmful gas sensors. Full article

Kraft lignin (KL) was activated using selected ionic liquids (ILs). The activated form of the biopolymer, due to the presence of carbonyl groups, can be used in electrochemical tests. To increase the application potential of the system in electrochemistry, activated lignin forms were combined with manganese dioxide, and the most important physicochemical and morphological-microstructural properties of the novel, functional hybrid systems were determined using Fourier transform infrared spectroscopy (FTIR), elemental analysis (EA), scanning electron microscopy (SEM), zeta potential analysis, thermal stability (TGA/DTG) and porous structure analysis. An investigation was also made of the practical application of the hybrid materials in the production of lithium ion batteries. The capacity of the anode (MnO₂/activated lignin), working at a low current regime of 50 mA·g⁻¹, was ca. 610 mAh·g⁻¹, while a current of 1000 mA·g⁻¹ resulted in a capacity of 570 mAh·g⁻¹. Superior cyclic stability and rate capability indicate that this may be a promising electrode material for use in high-performance lithium ion batteries. Full article