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Tea waste contains various substances with phenolic hydroxyl groups, including lignin, tannins, tea polyphenols, etc., which are rarely utilized. In this study, tea waste was directly dispersed with graphene oxide to prepare tea waste/reduced graphene oxide (TW/rGO) hydrogel through a one-step hydrothermal method. The prepared hydrogel presented a continuous three-dimensional porous structure and exhibited good mechanical properties with a compressive strength of 53.4 ± 4.0 kPa. It also showed excellent electrochemical performance as an electrode material. Its specific capacitance reached 434.7 F g−1 at a current density of 1 A g−1, and its capacitance retention was 55.8% when the current density was increased to 100 A g−1. In addition, an TW/rGO assembled all-solid-state supercapacitor demonstrated a superior specific capacitance of 372.8 F g−1 and a competitive energy density of 12.9 Wh kg−1 at 1 A g−1. [ABSTRACT FROM AUTHOR]

A comprehensive investigation into the design and electrochemical optimization of composite electrodes consisting of poly(3,4-ethylenedioxythiophene) (PEDOT)/graphene oxide (GO)/Methanococcus deltae and reduced graphene oxide (rGO)/Methanococcus deltae hybrids, anchored onto stainless-steel (SS) substrates, has been conducted. The GO and rGO materials were synthesized using a modified Hummer method. The resulting SS/PEDOT/GO and SS/PEDOT/rGO composite electrodes were subjected to systematic electrochemical characterization, focusing on the PEDOT p-type and n-type doping/undoping processes within diverse solvent environments (CH3CN and H2O) and electrolyte compositions (LiClO4 and KCl). Raman spectroscopy analysis confirmed the successful integration of graphene derivatives into the electrode structures, while field-emission scanning electron microscopy (FESEM) and atomic force microscopy (AFM) revealed increased surface roughness upon GO and rGO incorporation. This increase in surface roughness is believed to enhance the adhesion of Methanococcus deltae microorganisms and facilitate efficient electron transport. Electrochemical measurements showed that the resulting SS/PEDOT/GO and SS/PEDOT/rGO anodes exhibit remarkable electrocatalytic activity. The SS/PEDOT/GO electrode achieved a maximum power density of 1014.420 mW/cm2, while the SS/PEDOT/rGO electrode reached 632.019 mW/cm2. [ABSTRACT FROM AUTHOR]

Background/Objectives: This study aims to develop a screen-printed carbon electrode (SPCE) modified with silver nanoparticles (AgNPs) and gold nanoparticles (AuNPs) for the detection of human serum albumin (HSA). The objectives include utilizing green synthesis methods for nanoparticle production and evaluating the electrochemical performance of the modified electrodes. Methods: AgNPs and AuNPs were synthesized using Phulae pineapple peel extract (PPA) as a reducing agent. The nanoparticles were characterized using UV-visible spectrophotometry (UV-vis), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and transmission electron microscopy (TEM). The electrochemical performance of AgNP/SPCE and AuNP/SPCE was assessed by cyclic voltammetry (CV) studies, and the electrodes were functionalized with anti-HSA antibodies for HSA detection. Results: Characterization revealed spherical nanoparticles ranging from 10 to 30 nm. Both AgNP/SPCE and AuNP/SPCE demonstrated improved electrochemical performance compared to bare SPCEs. The modified sensors could detect serum albumin concentrations from 10 to 400 μg/mL, with high correlation values of 0.97 and 0.99 for AgNPs and AuNPs, respectively. Conclusions: This research demonstrates the potential of using agricultural waste for green synthesis of nanoparticles and highlights the application of AgNPs and AuNPs in developing sensitive biosensing platforms for the detection of human serum albumin. [ABSTRACT FROM AUTHOR]

Through system identification for robust control methods and utilizing real-time experimental field data, a comprehensive mathematical model is derived that represents the dynamic performance of a single electrode positioning system (EPS) in an industrial electric arc melting furnace (EAF). This EPS is characterized by large, time-varying dynamic parameters, which fluctuate based on operating conditions, specifically as the electrode weight changes within its operational range. The system identification methodology for robust control is developed in four main steps, progressing from experimental design to model validation. This approach yields a nominal model of the actual system and provides a trustworthy estimate of the region of uncertainty of the model, bounded by models of the real system under maximum and minimum electrode weight conditions (limit operating models). The methodology generates three fourth-order time-delay models using an ARMAX structure. The results are promising, as system identification for robust control enables the derivation of mathematical models specifically tailored for designing robust controllers. These controllers significantly enhance the EPS control system's performance and substantially reduce energy consumption and environmental emissions. [ABSTRACT FROM AUTHOR]

Solar saline water splitting is a promising approach to sustainable hydrogen production, harnessing abundant solar energy and the availability of brine resources, especially in the Atacama Desert. Bischofite salt (MgCl2·6H2O) has garnered significant attention due to its wide range of industrial applications. Efficient hydrogen production in arid or hyper arid locations using bischofite solutions is a novel and revolutionary idea. This work studied the electrochemical performance of Mn2O3 electrodes using a superposition model based on mixed potential theory and evaluated the superficial performance of this electrode in contact with a 0.5 M bischofite salt solution focusing on the hydrogen evolution reaction (HER) and oxygen reduction reaction (ORR) that occur during saline water splitting. The application of the non-linear superposition model provides valuable electrochemical kinetic parameters that complement the understanding of Mn2O3, this being one of the novelties of this work. [ABSTRACT FROM AUTHOR]

Polyanionic structures, (MO4)n−, can be beneficial to the transport of lithium ions by virtue of the open three-dimensional frame structure. However, an unstable interface suppresses the life of the (MO4)n−-based anode. In this study, MnWO4@C nanorods with dense nanocavities have been synthesized through a hydrothermal route, followed by a chemical deposition method. As a result, the MnWO4@C anode exhibits better cycle and rate performance than MnWO4 as a Li-ion battery; the capacity is maintained at 718 mAh g−1 at 1000 mA g−1 after 400 cycles because the transport of lithium ions and the contribution of pseudo-capacitance are increased. Generally, benefiting from the carbon shell and electrolyte additive (e.g., FEC), the cycle performance of the MnWO4@C electrode is also effectively improved for lithium storage. [ABSTRACT FROM AUTHOR]

As modern civilization's energy demands continue to rise, the need for efficient renewable energy solutions becomes increasingly critical. In addressing this challenge, our research explores the potential of newly developed iron (Fe)-doped molybdenum disulfide (MoS2) thin-film electrodes, synthesized through a simple hydrothermal method, as a promising energy storage device. By systematically varying the Fe doping levels, we aim to elucidate the relationship between Fe content and the structural, morphological, and electrochemical properties of the MoS2 electrodes. The optimized FM-3 electrode exhibited a remarkable areal capacitance of 8.25 F/cm2 at a current density of 10 mA/cm2 with an energy density of 0.22 mWh/cm2 and a power density of 2.2 mW/cm2. Furthermore, the FM-3 demonstrated impressive long-term cycling stability, retaining 85.58% of its initial capacitance after 10,000 charge–discharge cycles. To further explore practical applicability, an asymmetric pouch-type supercapacitor device was assembled using an FM-3 electrode and activated carbon. The device achieved an impressive areal capacitance of 0.43 F/cm2 at a current density of 20 mA/cm2, delivering an energy density of 0.133 mWh/cm2 and a power density of 7.5 mW/cm2. The exceptional performance of the FM-3 electrode can be attributed to the enhanced diffusion rate, charge transfer efficiency, and better carrier mobility induced by Fe doping. This work not only highlights the significant electrochemical performance improvements of Fe-doped MoS2 electrodes but also demonstrates their potential for scalable energy storage solutions, making a valuable contribution to the field of next-generation energy storage technologies. [ABSTRACT FROM AUTHOR]

Bi3+ doped Ti/Sb-SnO2/PbO2 electrode materials were fabricated by electrodeposition to improve their electrochemical performance in zinc electrowinning. The surface morphology, chemical composition, and hydrophilicity of the as-prepared electrodes were characterized using scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and contact angle. An electrochemical measurement and an accelerated lifetime experiment were also conducted to investigate the electrocatalytic performance and stability of the electrodes. The results show that the Bi3+ modification electrode has an important effect on the coating morphology, the crystal structure, the surface hydrophilicity, the electrocatalytic activity, and the stability. The electrode prepared from the solution containing 2 mmol·L−1 Bi(NO3)3 (marked as the Ti/Sb-SnO2/2Bi-PbO2 electrode) exhibits the best hydrophilicity performance (θ = 21.6°) and the longest service life (1196 h). During the electrochemical characterization analysis, the Ti/Sb-SnO2/2Bi-PbO2 electrode showed the highest oxygen evolution activity, which can be attributed to it having the highest electroactive surface (qT* = 21.20 C·cm−2) and the best charge-transfer efficiency. The DFT calculation demonstrated that the doping of Bi3+ leads to a decrease in the OER reaction barrier and an increase in the DOS of the electrode, which further enhances the catalytic activity and the conductivity of the electrode. Moreover, the simulated zinc electrowinning experiment demonstrated that the Ti/Sb-SnO2/2Bi-PbO2 electrode consumes less energy than other electrodes. Therefore, it is expected that the Bi3+ modified electrode will become a very promising electrode material for zinc electrowinning in the future. [ABSTRACT FROM AUTHOR]

Silicon (Si) as the anode material for lithium-ion batteries (LIBs) has attracted much attention due to its high theoretical specific capacity (4200 mAh/g). However, the specific capacity and cycle stability of the LIBs are reduced due to the pulverization caused by the expansion of Si coated on Cu (copper) foil during cycles. In order to solve this problem, researchers have used an ultra-thin Si deposition layer as the electrode, which improves cyclic stability and obtains high initial coulomb efficiency of LIBs. However, suitable substrate selection is crucial to fabricate an ultrathin Si deposition layer electrode with excellent performance, and a substrate with a three-dimensional porous structure is desirable to ensure the deposition of an ultrathin Si layer on the whole surface of the substrate. In this paper, the Si thin layer has been deposited on a binder-free hybrid film of carbon nanotubes (CNTs) and carbon nanocoils (CNCs) by magnetron sputtering. Compared with densely packed CNT film and flat Cu foil, the loose and porous film provides a large surface area and space for Si deposition, and Si can be deposited not only on the surface but also in the interior part of the film. The film provides a large number of channels for the diffusion and transmission of Li+, resulting in the rapid diffusion rate of Li+, which improves the effective lithium storage utilization of Si. Furthermore, the CNC itself is super elastic, and film provides an elastic skeleton for the Si deposition layer, which eases its volume expansion during charge and discharge processes. Electrochemical tests have showed that the Si/CNT–CNC film electrode has excellent performance as anode for LIBs. After 200 cycles, the Si/CNT–CNC film electrode still had possessed a specific capacity of 2500 mAh/g, a capacity retention of 92.8% and a coulomb efficiency of 99%. This paper provides an effective way to fabricate high performance Si-nanocarbon composite electrodes for LIBs. [ABSTRACT FROM AUTHOR]

Despite the numerous ongoing research studies in the area of conducting polymer-based electrode materials for supercapacitors, the implementation has been inadequate for commercialization. Further understanding is required for the design and synthesis of suitable materials like conducting polymer-based gels as electrode materials for supercapacitor applications. Among the polymers, conductive polymer gels (CPGs) have generated great curiosity for their use as supercapacitors, owing to their attractive qualities like integrated 3D porous nanostructures, softness features, very good conductivity, greater pseudo capacitance, and environmental friendliness. In this review, we describe the current progress on the synthesis of CPGs for supercapacitor applications along with their morphological behaviors and thermal properties. We clearly explain the synthesis approaches and related phenomena, including electrochemical approaches for supercapacitors, especially their potential applications as supercapacitors based on these materials. Focus is also given to the recent advances of CPG-based electrodes for supercapacitors, and the electrochemical performances of CP-based promising composites with CNT, graphene oxides, and metal oxides is discussed. This review may provide an extensive reference for forthcoming insights into CPG-based supercapacitors for large-scale applications. [ABSTRACT FROM AUTHOR]

The need for alternative energy storage options beyond lithium-ion batteries is critical due to their high costs, resource scarcity, and environmental concerns. Zinc-ion batteries offer a promising solution, given zinc's abundance, cost effectiveness, and safety, particularly its compatibility with non-flammable aqueous electrolytes. In this study, the potential of laser-ablation-based titanium oxide as a novel cathode material for zinc-ion batteries was investigated. The ultra-short laser pulses for in situ nanostructure generation (ULPING) technique was employed to generate nanostructured titanium oxide. This laser ablation process produced highly porous nanostructures, enhancing the electrochemical performance of the electrodes. Zinc and titanium oxide samples were evaluated using two-electrode and three-electrode setups, with cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge–discharge (GCD) techniques. Optimal cathode materials were identified in the Ti-5W (laser ablated twice) and Ti-10W (laser ablated ten times) samples, which demonstrated excellent charge capacity and energy density. The Ti-10W sample exhibited superior long-term performance due to its highly porous nanostructures, improving ion diffusion and electron transport. The potential of laser-ablated titanium oxide as a high-performance cathode material for zinc-ion batteries was highlighted, emphasizing the importance of further research to optimize laser parameters and enhance the stability and scalability of these electrodes. [ABSTRACT FROM AUTHOR]

Increasing the energy density and power of supercapacitors through hybrids of carbonaceous materials and metal oxides continues to be the subject of numerous research works. The correlation between specific capacitance and the properties of materials used as electrodes attracts great interest. In the present study, we investigated composites (GO/Mn3O4) prepared by the hydrothermal method with a variable ratio of GO/Mn3O4 and tested them as supercapacitor electrode materials in three- and two-electrode cells. The chemical characterization carried out by X-ray photoelectron spectroscopy and the adsorption techniques used allowed the determination of the surface carbon and oxygen content, as well as its textural properties. In this work, we analyzed the contribution of the double layer and the Faradaic reactions to the value of the final capacitance of the synthesized materials. Beyond empirically obtaining the electrochemical properties, these have been related to the physicochemical characteristics of the hybrids to help design materials with the best performance for supercapacitor electrodes. [ABSTRACT FROM AUTHOR]

We introduce a novel dual redox mediator synthesized by covalently linking ferrocene dicarboxylic acid (FcDA) and thionine (TH) onto a pre-treated glassy carbon electrode. This unique structure significantly enhances the electro-oxidation of dopamine (DA) and the reduction of hydrogen peroxide (H2O2), offering a sensitive detection method for both analytes. The electrode exhibits exceptional sensitivity, selectivity, and stability, demonstrating potential for practical applications in biosensing. It facilitates rapid electron transfer between the analyte and the electrode surface, detecting H2O2 concentrations ranging from 1.5 to 60 µM with a limit of detection (LoD) of 0.49 µM and DA concentrations from 0.3 to 230 µM with an LoD of 0.07 µM. The electrode's performance was validated through real-sample analyses, yielding satisfactory results. [ABSTRACT FROM AUTHOR]

Silicon-based electrodes offer a high theoretical capacity and a low cost, making them a promising option for next-generation lithium-ion batteries. However, their practical use is limited due to significant volume changes during charge/discharge cycles, which negatively impact electrochemical performance. This study proposes a practical method to increase silicon content in lithium-ion batteries with minimal changes to the manufacturing process by using dual-layer electrodes (DLEs). These DLEs are fabricated with two slurries containing silicon and graphite as active materials. Notably, the electrode with the silicon as the outermost layer on top of the graphite layer (Si-on-top) demonstrated a superior initial capacity of 935 mAh/g and retained 70% of its capacity (537 mAh/g) after 100 cycles at 0.5 C. In contrast, a single-layered electrode (SLE) with a silicon–graphite mixture retained only 50.3% of its capacity (370 mAh/g) under the same conditions. These findings suggest that DLEs, particularly with the silicon layer located on top, effectively increase silicon content in the negative electrode while remaining compatible with existing manufacturing processes. This approach offers a realistic strategy for enhancing the performance of lithium-ion batteries without significant process modifications. [ABSTRACT FROM AUTHOR]

Because current collectors (CCs), Binders (BDs), and conductive additives (CAs) in cathodes and anodes do not directly contribute to charging and discharging, they decrease the energy density of the battery. Improvement of battery energy density is essential for future batteries. If it were possible to pack electrode active materials into the empty space without using CCs, BDs, and CAs, the energy density of the battery would increase. Therefore, attempts to avoid using these materials in batteries are being investigated. In this review article, methods for manufacturing electrodes without using these materials, as well as the performance and durability of the electrodes, are summarized and discussed. After explaining the function and necessity of the CCs, BDs, and CAs, methods for manufacturing electrodes without using CCs, BDs, and CAs, as well as the performance and durability of the electrodes, were summarized and discussed. In addition to battery performance, the mechanical durability of the electrodes is also explained since not using CCs, BDs, and CAs will cause problems with the electrodes' mechanical durability. [ABSTRACT FROM AUTHOR]

Silicon (Si) is recognized as a promising candidate for next-generation lithium-ion batteries (LIBs) owing to its high theoretical specific capacity (~4200 mAh g−1), low working potential (<0.4 V vs. Li/Li+), and abundant reserves. However, several challenges, such as severe volumetric changes (>300%) during lithiation/delithiation, unstable solid–electrolyte interphase (SEI) formation, and inherently low electrical and ionic conductivity, impede its practical application. To mitigate these challenges, direct contact between the surface of the Si particle and the electrolyte must be prevented. In this review, we elucidated the surface coating strategies to enhance the electro–chemical performance of Si-based materials. We identified the impact of various coating methods and materials on the performance of Si electrodes. Furthermore, the integration of coating strategies with nanostructure design can effectively buffer Si electrode volume expansion and prevent direct contact with the electrolyte, thereby synergistically enhancing electrochemical performance. We highlight opportunities and perspectives for future research on Si-negative electrodes in LIBs, drawing on insights from previous studies. [ABSTRACT FROM AUTHOR]

Miniaturized energy storage devices, such as electrostatic nanocapacitors and electrochemical micro-supercapacitors (MSCs), are important components in on-chip energy supply systems, facilitating the development of autonomous microelectronic devices with enhanced performance and efficiency. The performance of the on-chip energy storage devices heavily relies on the electrode materials, necessitating continuous advancements in material design and synthesis. This review provides an overview of recent developments in electrode materials for on-chip MSCs and electrostatic (micro-/nano-) capacitors, focusing on enhancing energy density, power density, and device stability. The review begins by discussing the fundamental requirements for electrode materials in MSCs, including high specific surface area, good conductivity, and excellent electrochemical stability. Subsequently, various categories of electrode materials are evaluated in terms of their charge storage mechanisms, electrochemical performance, and compatibility with on-chip fabrication processes. Furthermore, recent strategies to enhance the performance of electrode materials are discussed, including nanostructuring, doping, heteroatom incorporation, hybridization with other capacitive materials, and electrode configurations. [ABSTRACT FROM AUTHOR]

Lithium iron phosphate (LiFePO4 or LFP) is a promising cathode material for lithium-ion batteries (LIBs), but side reactions between the electrolyte and the LFP electrode can degrade battery performance. This study introduces an innovative coating strategy, using atomic layer deposition (ALD) to apply a thin (5 nm and 10 nm) Al2O3 layer onto high-mass loading LFP electrodes. Galvanostatic charge–discharge cycling and electrochemical impedance spectroscopy (EIS) were used to assess the electrochemical performance of coated and uncoated LFP electrodes. The results show that Al2O3 coatings enhance the cycling performance at room temperature (RT) and 40 °C by suppressing side reactions and stabilizing the cathode–electrolyte interface (CEI). The coated LFP retained 67% of its capacity after 100 cycles at 1C and RT, compared to 57% for the uncoated sample. Post-mortem analyses, including scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS), were conducted to investigate the mechanisms behind the improved performance. These analyses reveal that Al2O3 coatings are highly effective in reducing LFP electrode degradation during cycling, demonstrating the potential of ALD Al2O3 coatings to enhance the durability and performance of LFP electrodes in LIBs. [ABSTRACT FROM AUTHOR]

Piezoelectric microactuators have been widely used for actuation, sensing, and energy harvesting. While out-of-plane piezoelectric configurations are well established, both in-plane deflection and asymmetric electrode placement have been underexplored in terms of actuation efficiency. This study explores the impact of asymmetric electrode geometry on the performance of slender unimorph actuators that deflect in-plane, where actuator length is much larger than width or thickness. After validating the finite element modeling method against experimental data, the geometric parameters of the proposed unimorph model are manipulated to explore the effect of different electrode geometries and layer thicknesses on actuation efficiency. Four key findings were that (1) the fringing field within the piezoelectric material plays a measurable role in performance, (2) symmetry in electrode placement is generally nonoptimal, (3) optimal electrode geometry is independent of scale, and (4) the smaller the ratio of width to thickness, the larger the deflection. The findings contribute to the development of efficient design strategies that optimize the performance of planar actuators for potential implications for microelectromechanical systems (MEMS). To aid designers of piezoelectric unimorph actuators in determining the optimal electrode geometry, three types of parameterized figures and two types of simulation apps are provided. [ABSTRACT FROM AUTHOR]

Despite over two decades of intense research into bioelectrochemical systems (BESs), their practical implementation remains unrealized, partly due to the low performance of bioelectrodes. With the introduction of additive manufacturing techniques, the development of a new generation of bioelectrodes with custom-shaped geometries using conductive composites has become feasible. This study examines the potential of using two conductive composites, Poly-lactic acid (PLA) and thermoplastic polyurethane (TPU), for 3D-printed electrodes. Electrochemical characterization reveals that TPU has a charge transfer resistance approximately two orders of magnitude higher than PLA, rendering it unsuitable for bioelectrodes. The presence of triangular patterns enhances the performance of planar electrodes, with optimal results observed for PLA-based electrodes with surface pattern depths between 0.6 and 1.4 mm. Additionally, electrodeposition (ED) of graphene oxide (GO) further improves performance across all cases. During the subsequent biotic start-up, patterned PLA electrodes with a depth of 1.4 mm exhibit higher current. However, these 3D-printed electrodes exhibit degradation after 56 days of operation. [ABSTRACT FROM AUTHOR]

To obtain highly efficient yet easily produced water-splitting cathodes, Ni-MoO2 composite coatings were electrodeposited at a Ni foam substrate with an open-pore structure, pore size of 450 µm, in a Watts-type bath. The concentration of MoO2 particles (about 100 nm) was varied, while the intensive mixing of the solution was provided by air bubbling with 0.5 L min−1. Electrodeposition was performed at different constant current densities at room temperature. The morphology and composition of the coatings were investigated by SEM and EDS. The hydrogen evolution reaction (HER) was tested in KOH of different concentrations, at several temperatures, in a three-electrode H-cell by recording polarization curves and EIS measurements. The lowest achieved HER overpotential was −158 mV at −0.5 A cm−2. Up-scaled samples, 3 × 3.3 cm2, were tested in a single zero-gap cell showing decreasing cell voltage (from 2.18 V to 2.11 V) at 0.5 A cm−2 over 5 h in 30% KOH at 70 °C with electrolyte flow rate of 58 mL min−1. Compared to pure Ni foams used as both cathode and anode under the same conditions, the cell voltage is decreased by 200 mV, showing improved electrode performance. [ABSTRACT FROM AUTHOR]

Recently, the world's first plasma-propelled drone was successfully flown, demonstrating that plasma propulsion technology is suitable for drone flight. The research on plasma propulsion drones has sparked a surge of interest. This study utilized a proxy model and the NSGA-II multi-objective genetic algorithm to optimize the geometric parameters based on staggered thrusters that affect the performance of electroaerodynamics (EAD) thrusters used for solid-state plasma aircraft. This can help address key issues, such as the thrust density and the thrust-to-power ratio of solid-state plasma aircraft, promoting the widespread application of plasma propulsion drones. An appropriate sample set was established using Latin hypercube sampling, and the thrust and current data were collected using a customized experimental setup. The proxy model employed a genetically optimized Bayesian regularization backpropagation neural network, which was trained to predict the effects of variations in the geometric parameters of the electrode assembly on the performance parameters of the plasma aircraft. Based on this information, the maximum achievable value for a given performance parameter and its corresponding geometric parameters were determined, showing a significant increase compared to the sample data. Finally, the optimal parameter combination was determined by using the NSGA-II multi-objective genetic algorithm and the Analytic Hierarchy Process. These findings can serve as a basis for future researchers in the design of EAD thrusters, helping them produce plasma propulsion drones that better meet specific requirements. [ABSTRACT FROM AUTHOR]

As modern society continues to advance, the depletion of non-renewable energy sources (such as natural gas and petroleum) exacerbates environmental and energy issues. The development of green, environmentally friendly energy storage and conversion systems is imperative. The energy density of commercial lithium-ion batteries is approaching its theoretical limit, and even so, it struggles to meet the rapidly growing market demand. Lithium–oxygen batteries have garnered significant attention from researchers due to their exceptionally high theoretical energy density. However, challenges such as poor electrolyte stability, short cycle life, low discharge capacity, and high overpotential arise from the sluggish kinetics of the oxygen reduction reaction (ORR) during discharge and the oxygen evolution reaction (OER) during charging. This article elucidates the fundamental principles of lithium–oxygen batteries, analyzes the primary issues currently faced, and summarizes recent research advancements in air cathodes and anodes. Additionally, it proposes future directions and efforts for the development of lithium–air batteries. [ABSTRACT FROM AUTHOR]

Supercapacitors hold promise for energy storage due to their exceptional power density and fast charge/discharge cycles. However, their performance hinges on the electrode material. Zeolitic imidazolate frameworks (ZIFs) are attractive options due to their tailorable structure and high surface area. But traditional ZIF synthesis relies on toxic solvents derived from fossil fuels, hindering their envisioned environmental benefit. This study explores using bio-derived solvents for a greener and potentially superior approach. The researchers employed anodic electrodeposition to synthesise cobalt-based ZIFs (Co-ZIFs) as supercapacitor electrode materials. Two linkers (2-methylimidazole and benzimidazole) and two bio-derived solvents (CyreneTM and γ-valerolactone (GVL)) were investigated. X-ray diffraction analysis revealed that bio-derived solvents enhanced the crystallinity of Co-ZIFs compared to traditional solvents. Notably, CyreneTM promoted better crystallinity for Co-bIM/Co-mIM structures. The Full Width at Half Maximum (FWHM) analysis suggests CyreneTM promotes Co-bIM/Co-mIM crystallinity (lower FWHM). Co-mIM in CyreneTM exhibits the best crystallinity (FWHM = 0.233) compared to other ZIF samples. Scanning electron microscopy confirmed these findings, showing larger and well-defined crystals for bio-derived solvent-synthesised ZIFs. The choice of solvent significantly impacted the final ZIF structure. While 2-methylimidazole consistently formed ZIF-67 regardless of the solvent, benzimidazole exhibited solvent-dependent behaviour. GVL yielded the highly porous Co-ZIF-12 structure, whereas DMF (N,N-dimethylformamide) and CyreneTM produced the less porous ZIF-9. This work reports the first-ever instance of ZIF-12 synthesis via an electrochemical method, highlighting the crucial interplay between solvent and precursor molecule in determining the final ZIF product. The synthesised binder-free Co-ZIF electrodes were evaluated for supercapacitor performance. The capacitance data revealed GVL as the most effective solvent, followed by DMF and then CyreneTM. This suggests GVL is the preferred choice for this reaction due to its superior performance. The ZIF-12-based electrode exhibits an impressive specific capacitance (Csp) of 44 F g⁻1, significantly higher than those achieved by ZIF-9-Cyrene (1.2 F g⁻1), ZIF-9-DMF (2.5 F g⁻1), ZIF-67-GVL (35 F g⁻1), ZIF-67-Cyrene (6 F g⁻1), and ZIF-67-DMF (16 F g⁻1) at 1 A g−1. This surpasses the Csp of all other ZIFs studied, including high-performing ZIF-67(GVL). ZIF-12(GVL) maintained superior Csp even at higher current densities, demonstrating exceptional rate capability. Among the bio-derived solvents, GVL outperformed CyreneTM. Notably, the Co-bIM in the GVL sample exhibited a ZIF-12-like structure, offering potential advantages due to its larger pores and potentially higher surface area compared to traditional ZIF-67 and ZIF-9 structures. This work presents a significant advancement in Co-ZIF synthesis. By utilising bio-derived solvents, it offers a more sustainable and potentially superior alternative. This paves the way for the eco-friendly production of Co-ZIFs with improved properties for supercapacitors, gas separation, catalysis, and other applications. [ABSTRACT FROM AUTHOR]

Poly(3,4-ethylenedioxythiophene) (PEDOT) and PEDOT-functionalized carbon nanoparticles (f-CNPs) were synthesized by in situ chemical oxidative polymerization and pyrolysis methods. f-CNP-PEDOT nanocomposites were prepared by varying the concentration of PEDOT from 1 to 20% by weight (i.e., 1, 2.5, 5, 10, and 20 wt%). Several characterization techniques, such as field-emission scanning electron microscopy (FESEM), attenuated total reflectance-Fourier transform infrared (ATR-FTIR), X-ray diffraction (XRD), N2 Brunauer–Emmett–Teller (BET) and Barrett–Joyner–Halenda (BJH) analyses, as well as cyclic voltammetry (CV), galvanostatic charge discharge (GCD), and electrochemical impedance spectroscopy (EIS), were applied to investigate the morphology, the crystalline structure, the N2 adsorption/desorption capability, as well as the electrochemical properties of these new synthesized nanocomposite materials. FESEM analysis showed that these nanocomposites have defined porous structures, and BET surface area analysis showed that the standalone f-CNP exhibited the largest surface area of 801.6 m2/g, whereas the f-CNP-PEDOT with 20 wt% exhibited the smallest surface area of 116 m2/g. The BJH method showed that the nanocomposites were predominantly mesoporous. CV, GCD, and EIS measurements showed that f-CNP functionalized with 5 wt% PEDOT had a higher capacitive performance compared to the individual f-CNPs and PEDOT constituents, exhibiting an extraordinary specific capacitance of 258.7 F/g, at a current density of 0.25 A/g, due to the combined advantage of enhanced electrochemical activity induced by PEDOT doping, and highly developed porosity of f-CNPs. Symmetric aqueous supercapacitor devices were fabricated using the optimized f-CNP-PEDOT doped with 5 wt% of PEDOT as active material, exhibiting a high capacitance of 96.7 F/g at 1.4 V, holding practically their full charge, after 10,000 charge–discharge cycles at 2 A/g, thus providing the highest electrical electrodes performance. Hereafter, this work paves the way for the potential use of f-CNP-PEDOT nanocomposites in the development of high-energy-density supercapacitors. [ABSTRACT FROM AUTHOR]

Electrolytic capacitors store larger amounts of energy thanks to their thin dielectric layers and enlarged surface area. However, the benefits of using a liquid electrolyte are at the expense of the possibility of leakage, evaporation, or rupture of the device over time. As a solution, solid electrolytes, such as conductive polymers, substitute the liquid ones decreasing the internal resistance and enlarging the lifetime of these devices. PEDOT:PSS is a widely used conductive polymer in the formation of solid electrolytic capacitors. However, using the enlarged surface of the porous electrodes efficiently requires industrial processes, the efficacy of which has not been explored. In this work, porous aluminium electrodes with dielectric layers of different thicknesses were coated with PEDOT:PSS at different levels of doping in order to study the efficiency of the production of solid electrolytic capacitors in industry. The combination of odd random phase electrochemical impedance spectroscopy (ORP-EIS) with surface characterization techniques (SEM-EDX, GDOES) formed a methodology that allowed the study of both the electrical properties and the level of impregnation for these model systems. All samples consisting of a porous aluminium electrode with an amount of PEDOT:PSS deposited on top resulted in an inefficient degree of penetration between the two electrodes. However, the electrochemical analysis proved that the use of dopants produces systems with the highest capacitive properties. Consequently, the evolution towards better solid electrolytic capacitors does not rely solely on the proper coverage of the porous electrodes, but on the proper electrical properties of the PEDOT:PSS within the pores. [ABSTRACT FROM AUTHOR]

In this study, the effects of electrode porosity on nerve regeneration and functional recovery after sciatic nerve transection in rats was investigated. A sieve-type neural electrode with 70% porosity was designed and compared with an electrode with 30% porosity. Electrodes were fabricated from photosensitive polyimide and implanted into the transected sciatic nerves. Motor function recovery was evaluated using the Sciatic Function Index. The number of active channels and their signal quality were recorded and analyzed to assess the sensory neural signal acquisition. Electrical impedance spectroscopy was used to evaluate the electrode performance. The group implanted with the 70% porosity electrode demonstrated significantly enhanced nerve regeneration and motor function recovery, approaching control group levels by the fifth week. In contrast, the group with the 30% porosity electrode exhibited limited improvement. Immunohistochemical analysis confirmed extensive nerve fiber growth within the 70% porous structure. Moreover, the 70% porosity electrode consistently acquired neural signals from more channels compared to the 30% porosity electrode, demonstrating its superior performance in sensory signal detection. These findings emphasize the importance of optimizing electrode porosity in the development of advanced neural interfaces, with the potential to enhance clinical outcomes in peripheral nerve repair and neuroprosthetic applications. [ABSTRACT FROM AUTHOR]

Dopamine (DA), ascorbic acid (AA), and uric acid (UA) are crucial neurochemicals, and their abnormal levels are involved in various neurological disorders. While electrodes for their detection have been developed, achieving the sensitivity required for in vivo applications remains a challenge. In this study, we proposed a synthetic Au24Cd nanoenzyme (ACNE) that significantly enhanced the electrochemical performance of metal electrodes. ACNE-modified electrodes demonstrated a remarkable 10-fold reduction in impedance compared to silver microelectrodes. Furthermore, we validated their excellent electrocatalytic activity and sensitivity using five electrochemical detection methods, including cyclic voltammetry, differential pulse voltammetry, square-wave pulse voltammetry, normal pulse voltammetry, and linear scanning voltammetry. Importantly, the stability of gold microelectrodes (Au MEs) modified with ACNEs was significantly improved, exhibiting a 30-fold enhancement compared to Au MEs. This improved performance suggests that ACNE functionalization holds great promise for developing micro-biosensors with enhanced sensitivity and stability for detecting small molecules. [ABSTRACT FROM AUTHOR]

Aluminum–air (Al–air) batteries are considered one of the most promising next-generation energy storage devices. In this paper, we carry out an orthogonal experimental study on the SLM printing process parameters in 3D-printed Al–air battery anodes. The surface roughness, densification, and discharge performance of the electrodes under different process parameters are observed to reveal the effects of different process parameters on the forming quality and discharge performance of aluminum–air battery anodes. The results show that the laser power is the most important factor affecting the surface roughness of the porous aluminum anode, and the scanning spacing is the most important factor affecting the densification. The best printing parameters for the porous aluminum anode can be obtained when the laser power is 325 W, the scanning speed is 1000 mm/s, the scanning spacing is 0.12 mm, and the thickness of the powder spread is 0.03 mm. At this time, the surface roughness of the porous aluminum anode obtained by this process parameter is 15.01 μm, the densification is 94.97%, and the discharge is stable with a high value. In addition, we also carry out data validation to ensure that the data we obtain are optimal and valid. [ABSTRACT FROM AUTHOR]

The current study focused on the design of an extremely sensitive electrochemical sensor of ascorbic acid based on a mixture of NiAl2O4-NiO nanoparticles that, produced in a single step using the sol–gel method, on an ITO electrode. This new sensing platform is useful for the detection of ascorbic acid with a wide range of concentrations extending from the attomolar to the molar. SEM micrographs show the porous structure of the NiAl2O4-NiO sample, with a high specific surface area, which is beneficial for the catalytic performance of the nanocomposite. An XRD diffractogram confirmed the existence of two phases, NiAl2O4 and NiO, both corresponding to the face-centred cubic crystal structure. The performances of the modified electrode, as a biomolecule, in the detection of ascorbic acid was evaluated electrochemically by cyclic voltammetry and chronoamperometry. The sensor exhibited a sensitive electrocatalytic response at a working potential of E = +0.3 V vs. Ag/Ag Cl, reaching a steady-state current within 30 s after each addition of ascorbic acid solution with a wide dynamic range of concentrations extending from attolevels (10−18 M) to molar (10 mM) and limits of detection and quantification of 1.2 × 10−18 M and 3.96 × 10−18 M, respectively. This detection device was tested for the quantification of ascorbic acid in a 500 mg vitamin C commercialized tablet that was not pre-treated. [ABSTRACT FROM AUTHOR]

The electrode is a key component in a microbial electrolysis cell (MEC) that needs significant improvement for practical implementation. Accurate and reproducible analytical methods are substantial for the effective development of electrode technology. Linear sweep voltammetry (LSV) is an essential analytical method for evaluating electrode performance. In this study, inoculated carbon brush (IB), abiotic brush (AB), Pt wire (PtW), stainless steel wire (SSW), and mesh (SSM) were tested to find the most suitable counter electrode under different medium conditions. The coefficient of variation (Cv) of maximum current (Imax) was the most decisive indicator of the reproducibility test. This study shows that (i) the electrode used in operation is an appropriate counter electrode in an acetate-added condition, (ii) the anode LSV test should avoid the use of Pt wire as counter electrodes, and (iii) PtW is an appropriate counter electrode in cathode LSV in all conditions. [ABSTRACT FROM AUTHOR]

Although disubstituted imidazolium cation is sterically crowded, hundreds of ionic liquids based on this cation have been reported as electrolytes for energy storage devices. In contrast to disubstituted imidazolium, non-substituted imidazolium is uncrowded sterically and has not yet been investigated as an electrolyte, to the best of our knowledge. Hence, imidazolium hydrogen sulfate [Imi][HSO4], in mixture with water, was studied as an electrolyte for PANI-based electrode materials. For comparison, pyrrolidinium with hydrogen sulfate or p-toluene sulfonate ([Pyrr][HSO4] or [Pyrr][PTS]), in mixture with water, were also investigated as alternatives to the conventional electrolyte (i.e., aqueous H2SO4) for PANI electrodes. Walden plots of binary mixture ionic liquid–water weight ratios with the optimal ionic conductivity (i.e., [Imi][HSO4]/water 48/52 wt% (195.1 mS/cm), [Pyrr][HSO4]/water 41/59 wt% (186.6 mS/cm), and [Pyrr][PTS]/water 48/52 wt% (43.4 mS/cm) along with the electrochemical performances of PANI in these binary mixtures showed that [Pyrr][HSO4]aq or [Imi][HSO4]aq are convenient electrolytes for PANI/PIL, as opposed to [Pyrr][PTS]aq. Furthermore, replacing the conventional aqueous electrolyte H2SO4 with [Imi][HSO4] aq increased the specific capacitance of PANI/PIL from 249.8 to 268.5 F/g at 15 mV/s. Moreover, PANI/PIL electrodes displayed a quasi-ideal capacitive behavior in [Imi][HSO4]aq (the correction factor of CPE4 was 0.99). This primary study has shown that non-substituted imidazolium as an electrolyte could enhance the electrochemical performances of PANI electrodes and could be a good alternative to the conventional electrolyte. [ABSTRACT FROM AUTHOR]

Microbial fuel cells (MFCs) are sustainable energy recovery systems because they use organic waste as biofuel. Using critical raw materials (CRMs), like platinum-group metals, at the cathode side threatens MFC technology's sustainability and raises costs. By developing an efficient electrode design for MFC performance enhancement, CRM-based cathodic catalysts should be replaced with CRM-free materials. This work proposes developing and optimizing iron-based air cathodes for enhancing oxygen reduction in MFCs. By subjecting iron phthalocyanine and carbon black pearls to controlled thermal treatments, we obtained Fe-based electrocatalysts combining high surface area (628 m2 g−1) and catalytic activity for O2 reduction at near-neutral pH. The electrocatalysts were integrated on carbon cloth and carbon paper to obtain gas diffusion electrodes whose architecture was optimized to maximize MFC performance. Excellent cell performance was achieved with the carbon-paper-based cathode modified with the Fe-based electrocatalysts (maximum power density-PDmax = 1028 mWm−2) compared to a traditional electrode design based on carbon cloth (619 mWm−2), indicating the optimized cathodes as promising electrodes for energy recovery in an MFC application. [ABSTRACT FROM AUTHOR]

Graphene oxide (GO) was used as an ion-to-electron transducer for all-solid-state nitrate electrodes based on an alkyl ammonium salt as the sensing element. Commercially available carbon screen-printed electrodes modified with GO were used as conductive substrates, whose morphology and distribution along the surface were evaluated by scanning electron microscopy and Raman spectroscopy. The potentiometric performance of the GO-based electrodes revealed a Nernstian slope of −53.5 ± 2.0 mV decade−1 (R2 = 0.9976 ± 0.0015) in the range from 3.0 × 10−6 to 10−2 M and a lower limit of detection of 1.9 × 10−6 M. An impressive reproducibility between equally prepared electrodes (n = 15) was demonstrated by a variation of <6% for the calibration parameters. Constant current chronopotentiometry and water layer tests were used to evaluate the potential signal stability, providing similar performance to previously published works with graphene-based ion-selective electrodes. Notably, the GO-based sensors showed the absence of a water layer, a long-term drift of 0.3 mV h−1, and a stable performance (LOD and sensitivity) over 3 months. The applicability of the proposed sensors was demonstrated in determining nitrate levels in water samples with great accuracy, yielding recovery values from 87.8 to 107.9%, and comparable (p > 0.05) results to a commercial nitrate probe. These findings demonstrate the use of GO as an alternative ion-to-electron transducer for the fabrication of all-solid-state potentiometric electrodes. [ABSTRACT FROM AUTHOR]

This research focuses on the rational design of porous enzymatic electrodes, using horseradish peroxidase (HRP) as a model biocatalyst. Our goal was to identify the main obstacles to maximizing biocatalyst utilization within complex porous structures and to assess the impact of various carbon nanomaterials on electrode performance. We evaluated as-synthesized carbon nanomaterials, such as Carbon Aerogel, Coral Carbon, and Carbon Hollow Spheres, against the commercially available Vulcan XC72 carbon nanomaterial. The 3D electrodes were constructed using gelatin as a binder, which was cross-linked with glutaraldehyde. The bioelectrodes were characterized electrochemically in the absence and presence of 3 mM of hydrogen peroxide. The capacitive behavior observed was in accordance with the BET surface area of the materials under study. The catalytic activity towards hydrogen peroxide reduction was partially linked to the capacitive behavior trend in the absence of hydrogen peroxide. Notably, the Coral Carbon electrode demonstrated large capacitive currents but low catalytic currents, an exception to the observed trend. Microscopic analysis of the electrodes indicated suboptimal gelatin distribution in the Coral Carbon electrode. This study also highlighted the challenges in transferring the preparation procedure from one carbon nanomaterial to another, emphasizing the importance of binder quantity, which appears to depend on particle size and quantity and warrants further studies. Under conditions of the present study, Vulcan XC72 with a catalytic current of ca. 300 µA cm−2 in the presence of 3 mM of hydrogen peroxide was found to be the most optimal biocatalyst support. [ABSTRACT FROM AUTHOR]

Liquid metal (LM) is widely used in flexible electronic devices due to its excellent metallic conductivity and ductility. However, the fabrication of LM flexible strain sensors with high sensitivity and linearity is still a huge challenge, since the resistance of LM does not change much with strain. Here, a highly sensitive and linear fully flexible strain sensor with a resistive sensing function is proposed. The sensor comprises an Fe-doped liquid metal (Fe-LM) electrode for enhanced performance. The design and manufacturing of flexible strain sensors are based on the technology of controlling surface wettability by femtosecond laser micro/nano-processing. A supermetalphobic microstructure is constructed on a polydimethylsiloxane (PDMS) substrate to achieve the selection adhesion of Fe-LM on the PDMS substrate. The Fe-LM-based flexible strain sensor has high sensitivity and linearity, a gauge factor (GF) up to 1.18 in the strain range of 0–100%, excellent linearity with an R2 of 0.9978, a fast response time of 358 ms, and an excellent durability of more than 2400 load cycles. Additionally, the successful monitoring of human body signals demonstrates the potential of our developed flexible strain sensor in wearable monitoring applications. [ABSTRACT FROM AUTHOR]

Heavy metal poisoning has a life-threatening impact on the human body to aquatic ecosystems. This necessitates designing a convenient green methodology for the fabrication of an electrochemical sensor that can detect heavy metal ions efficiently. In this study, boron (B) and nitrogen (N) co-doped laser-induced porous graphene (LIGBN) nanostructured electrodes were fabricated using a direct laser writing technique. The fabricated electrodes were utilised for the individual and simultaneous electrochemical detection of lead (Pb2+) and cadmium (Cd2+) ions using a square wave voltammetry technique (SWV). The synergistic effect of B and N co-doping results in an improved sensing performance of the electrode with better sensitivity of 0.725 µA/µM for Pb2+ and 0.661 µA/µM for Cd2+ ions, respectively. Moreover, the sensing electrode shows a low limit of detection of 0.21 µM and 0.25 µM for Pb2+ and Cd2+ ions, with wide linear ranges from 8.0 to 80 µM for Pb2+ and Cd2+ ions and high linearity of R2 = 0.99 in case of simultaneous detection. This rapid and facile method of fabricating heteroatom-doped porous graphene opens a new avenue in electrochemical sensing studies to detect various hazardous metal ions. [ABSTRACT FROM AUTHOR]

In this paper, the possibility of combining electrocoagulation (EC), ultrasound, and the addition of zeolite for wastewater treatment was investigated for the first time. The following combinations of hybrid processes were tested: electrocoagulation with zeolite (ECZ), simultaneous electrocoagulation with zeolite and ultrasound (ECZ+US), and two-stage electrocoagulation with zeolite and ultrasound (US+Z - EC), carried out with three different electrode materials. The results show that the simultaneous assistance of ultrasound in the ECZ leads to a lower increase in pH, while the temperature increase is higher. Regarding the COD, the assistance of ultrasound is only useful for Zn electrodes in the two-stage US+Z - EC, while the reduction in voltage consumption occurs for Fe and Al electrodes. Ultrasonic assistance caused more damage to the anodes, but anode consumption was reduced for Al and Zn electrodes. The total amount of zeolite that can be recovered is between 55–97%, and recovery is higher in systems with higher turbidity reduction. Good settling ability is only achieved with Al and Fe electrodes in simultaneous performance. Taguchi's orthogonal L9 array design was applied to analyze the effects of electrode material, process type, mixing speed, and time duration on COD decrease, settling velocity, electrode, and voltage consumption. The results show that the use of ultrasound does not contribute to the desired result and generally only has a favorable effect on voltage and electrode consumption, while it has no positive effect on settling ability or COD decrease. Furthermore, although longer times and higher mixing speeds negatively impact cost due to voltage and electrode consumption, it is advisable not to choose the shortest duration and lowest speed to obtain adequate wastewater treatment quality. [ABSTRACT FROM AUTHOR]

SiO2 has a much higher theoretical specific capacity (1965 mAh g−1) than graphite, making it a promising anode material for lithium-ion batteries, but its low conductivity and volume expansion problems need to be improved urgently. In this work, pompon mum-like SiO2/C nanospheres with the sandwich and porous nanostructure were obtained by using dendritic fibrous nano silica (DFNS) and glucose as matrix and carbon source, respectively, through hydrothermal, carbonization and etching operations. The influence of SiO2 content and porous structure on its electrochemical performance was discussed in detail. The final results showed that the C/DFNS-6 with a SiO2 content of 6 wt% exhibits the best electrochemical performance as a negative electrode material for lithium-ion batteries due to its optimal specific surface area, porosity, and appropriate SiO2 content. C/DFNS-6 displays a high specific reversible capacity of 986 mAh g−1 at 0.2 A g−1 after 200 cycles, and 529 mAh g−1 at a high current density (1.0 A g−1) after 300 cycles. It also has excellent rate capability, with a reversible capacity that rises from 599 mAh g−1 to 1066 mAh g−1 when the current density drops from 4.0 A g−1 to 0.2 A g−1. These SiO2/C specific pompon mum-like nanospheres with excellent electrochemical performance have great research significance in the field of lithium-ion batteries. [ABSTRACT FROM AUTHOR]

Microheaters are used in several applications, including medical diagnostics, synthesis, environmental monitoring, and actuation. Conventional microheaters rely on thin-film electrodes microfabricated in a clean-room environment. However, low-cost alternatives based on conductive paste electrodes fabricated using printing techniques have started to emerge over the years. Here, we report a surprising effect that leads to significant electrode performance improvement as confirmed by the thorough characterization of bulk, processed, and conditioned samples. Mixing silver ink and PVA results in the solubilization of performance-hindering organic compounds. These compounds evaporate during heating cycles. The new electrodes, which reach a temperature of 80 °C within 5 min using a current of 7.0 A, display an overall 42% and 35% improvement in the mechanical (hardness) and electrical (resistivity) properties compared to pristine silver ink electrodes. To validate our results, we use the composite heater to amplify and detect parasite DNA from Trypanosoma brucei, associated with African sleeping sickness. Our LAMP test compares well with commercially available systems, confirming the excellent performance of our nanocomposite heaters. Since their fabrication relies on well-established techniques, we anticipate they will find use in a range of applications. [ABSTRACT FROM AUTHOR]

Polymer electrolyte was used as a medium for testing the performance of microband electrodes under conditions of linear diffusion. Cyclic voltammetry (CV) and chronoamperometry (CA) experiments were performed in a highly viscous medium, where diffusion rates are much slower than in fluid solutions. The log i vs. log v (CV) or log i vs. log t (CA) relationships with the current equation confirmed the existence of such conditions, yielding slope values that were lower than the expected 0.5. This could indicate an impure linear diffusion profile, i.e., some contribution from radial diffusion (edge effects). However, the desired value of 0.5 was obtained when performing these tests in monomeric solvents of similar viscosities, such as glycerol or propylene glycol. These results led to the conclusion that the current equations, which are based on Fick's laws, may not be applicable for polymer electrolytes, where various obstructions to free diffusion result in a more complicated process than for monomeric solvents. [ABSTRACT FROM AUTHOR]

This paper describes a Ag/AgCl electrochemical electrode for marine electric field measurements, which was prepared by depositing silver chloride on a silver foil substrate using double-pulse electrodeposition. The impact of positive direction peak current density and deposition time on electrode performance in the preparation of Ag/AgCl electrodes through double-pulse electrodeposition was investigated. Scanning electron microscopy and voltammetry have been used to study the properties of the prepared electrodes. This work reveals the correlation between the electrochemical behavior of electrodes and the physical properties of their surfaces, especially specific surface area and porosity. The study verified the characteristics of Ag/AgCl marine electric field electrodes obtained with different pulse parameters by analyzing the potential stability and noise level of the electrode in salt water. The study's results have positive significance for improving the accuracy of marine electric field measurements. [ABSTRACT FROM AUTHOR]

Perovskite-style materials are cathode systems known for their stability in solid oxide fuel cells (SOFCs). Pr0.5Sr0.5FeO3−δ (PSF) exhibits excellent electrode performance in perovskite cathode systems at high temperatures. Via VB subgroup metals (V, Nb, and Ta) modifying the B-site, the oxidation and spin states of iron elements can be adjusted, thereby ultimately adjusting the cathode's physicochemical properties. Theoretical predictions indicate that PSF has poor stability, but the relative arrangement of the three elements on the B-site can significantly improve this material's properties. The modification of Nb has a large effect on the stability of PSF cathode materials, reaching a level of −2.746 eV. The surface structure of PSF becomes slightly more stable with an increase in the percentage of oxygen vacancy structures, but the structural instability persists. Furthermore, the differential charge density distribution and adsorption state density of the three modified cathode materials validate our adsorption energy prediction results. The initial and final states of the VB subgroup metal-doped PSF indicate that PSFN is more likely to complete the cathode surface adsorption reaction. Interestingly, XRD and EDX characterization are performed on the synthesized pure and Nb-doped PSF material, which show the orthorhombic crystal system of the composite theoretical model structure and subsequent experimental components. Although PSF exhibits strong catalytic activity, it is highly prone to decomposition and instability at high temperatures. Furthermore, PSFN, with the introduction of Nb, shows greater stability and can maintain its activity for the ORR. EIS testing clearly indicates that Nb most significantly improves the cathode. The consistency between the theoretical predictions and experimental validations indicates that Nb-doped PSF is a stable and highly active cathode electrode material with excellent catalytic activity. [ABSTRACT FROM AUTHOR]

La-CoMoO4 was prepared as the electrode material for supercapacitors using the freeze-drying method. The physical and structural properties of the prepared electrode La-CoMoO4 were characterized by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). We further investigated the electrochemical performance of La-CoMoO4 electrode materials through cyclic voltammetry, constant current charge–discharge, and electrochemical impedance spectroscopy. The research results indicate that compared with CoMoO4 material (1400 F/g), La-CoMoO4 material has a high specific capacitance of 2248 F/g at a current density of 1 A/g. In addition, La-CoMoO4 has a high stability, with a capacitance retention rate of up to 99.2% after 5500 cycles. Finally, supercapacitor devices using La-CoMoO4 material as the positive electrode have a high energy density of 55 Wh/Kg (power density of 1000 W/Kg), making them a promising electrode material. [ABSTRACT FROM AUTHOR]

The screen-printed carbon electrode (SPCE) is a useful technology that has been widely used in the practical application of biosensors oriented to point-of-care testing (POCT) due to its characteristics of cost-effectiveness, disposability, miniaturization, wide potential window, and simple electrode design. Compared with gold or platinum electrodes, surface modification is difficult because the carbon surface is chemically or physically stable. Oxygen plasma (O2) can easily produce carboxyl groups on the carbon surface, which act as scaffolds for covalent bonds. However, the effect of O2-plasma treatment on electrode performance remains to be investigated from an electrochemical perspective, and sensor performance can be improved by clarifying the surface conditions of plasma-treated biosensors. In this research, we compared antibody modification by plasma treatment and physical adsorption, using our novel immunosensor based on gold nanoparticles (AuNPs). Consequently, the O2-plasma treatment produced carboxyl groups on the electrode surface that changed the electrochemical properties owing to electrostatic interactions. In this study, we compared the following four cases of SPCE modification: O2-plasma-treated electrode/covalent-bonded antibody (a); O2-plasma-treated electrode/physical adsorbed antibody (b); bare electrode/covalent-bonded antibody (c); and bare electrode/physical absorbed antibody (d). The limits of detection (LOD) were 0.50 ng/mL (a), 9.7 ng/mL (b), 0.54 ng/mL (c), and 1.2 ng/mL (d). The slopes of the linear response range were 0.039, 0.029, 0.014, and 0.022. The LOD of (a) was 2.4 times higher than the conventional condition (d), The slope of (a) showed higher sensitivity than other cases (b~d). This is because the plasma treatment generated many carboxyl groups and increased the number of antibody adsorption sites. In summary, the O2-plasma treatment was found to modify the electrode surface conditions and improve the amount of antibody modifications. In the future, O2-plasma treatment could be used as a simple method for modifying various molecular recognition elements on printed carbon electrodes. [ABSTRACT FROM AUTHOR]

The preparation of composite carbon nanomaterials is one of the methods for improving the electrochemical performance of carbon-based electrode materials for supercapacitors. However, traditional preparation methods are complicated and time-consuming, and the binder also leads to an increase in impedance and a decrease in specific capacitance. Therefore, in this work, we reduced Ni-Cu nanoparticles on the surface of nitrogen-doped carbon nanofibers (CNFs) by employing an electrostatic spinning method combined with pre-oxidation and annealing treatments. At the same time, Ni-Cu nanoparticles were vulcanized to Ni–Cu–S nanoparticles without destroying the structure of the CNFs. The area-specific capacitance of the CNFs/Ni–Cu–S–300 electrode reaches 1208 mF cm−2 at a current density of 1 mA cm−2, and the electrode has a good cycling stability with a capacitance retention rate of 76.5% after 5000 cycles. As a self-supporting electrode, this electrode can avoid the problem of the poor adhesion of electrode materials and the low utilization of active materials due to the inactivity of the binder and conductive agent in conventional collector electrodes, so it has excellent potential for application. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs) are porous materials assembled using metal and organic linkers, showing a high specific surface area and a tunable pore size. Large portions of metal open sites in MOFs can be exposed to electrolyte ions, meaning they have high potential to be used as electrode materials in energy storage devices such as supercapacitors. Also, they can be easily converted into porous metal oxides by heat treatment. In this study, we obtained high energy storage performance by preparing electrode materials through applying heat treatment to manganese MOFs (Mn-MOFs) under air. The chemical and structural properties of synthesized and thermally treated Mn-MOFs were measured by Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). The surface area and porosity were investigated by nitrogen adsorption/desorption isotherms. The electrochemical properties were studied by cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) using a three-electrode cell. It was found that Mn-MOF electrodes that underwent heat treatment at 400 °C under air consisted of Mn2O3 with high specific surface area and porosity. They also showed a superior specific capacitance of 214.0 F g−1 and an energy density value of 29.7 Wh kg−1 (at 0.1 A g−1) compared to non-treated Mn-MOFs. [ABSTRACT FROM AUTHOR]

Lithium-sulphur (Li-S) batteries offer high energy density compared to lithium-ion batteries, emerging as a promising technology for the next generation of energy storage systems. The ongoing challenge is to improve their electrochemical performance, extend their useful life and mitigate some problems that persist in this technology, by the investigation in materials with diverse properties. This work seeks to elucidate the importance and repercussions associated with functionalisation of graphene-based materials through nitrogen incorporation (more than 9 wt.% N), employing different chemical agents such as ethylenediamine and ammonia. Herein, differences in both the textural properties and the chemical environment of nitrogen within the carbonaceous network are identified, resulting in distinct electrochemical behaviours. The electrochemical performance of electrodes prepared from ammonia-functionalised samples surpasses that of ethylenediamine-functionalised samples in terms of both efficiency and rate performance. Conversely, the ethylenediamine-functionalised samples excel in stability, showing exceptional values in capacity retention per cycle. The outcomes exceeded expectations in energy performance, allowing the Li-S cells to be subjected to ultra-high rate cycling while maintaining appropriate capacity values. [ABSTRACT FROM AUTHOR]

Featured Application: The application involves exploring the impact of MXene nanosheet adhesion on the performance of supercapacitor devices for potential enhancements in energy storage and overall device functionality. Supercapacitors have garnered significant interest in recent years due to their high power density, rapid charge/discharge rates, and long cycle life. MXenes, a family of two-dimensional (2D) transition metal carbides/nitrides, have emerged as promising electrode materials for supercapacitors. However, one major challenge associated with incorporating MXenes in supercapacitor structures is the occurrence of sticking, wherein individual MXene flakes agglomerate, leading to reduced electrode performance. This review paper discusses various causes of sticking and approaches to preventing it, offering insights into the design and development of high-performance MXene-based supercapacitors. The morphology and size of MXene flakes, flake surface chemistry, thickness, surface area/volume ratio, electrode processing techniques (including solvent selection, additives incorporation, and deposition technology), and environmental factors were shown to be the basic factors resulting in sticking of MXene sheets. Among the strategies to mitigate this challenge, surface functionalization and passivation, integration with polymer matrices or carbon nanomaterials, and electrode processing optimization were considered. Possible paths for optimization and future directions of study, such as novel MXene compositions, understanding of interfaces and electrode–electrolyte interactions, development of advanced electrode architectures, and integration of energy storage systems, were assumed. [ABSTRACT FROM AUTHOR]

In this study, a cationic amphiphilic self-assembling peptide (SAP) Z23 was designed, and a simple bisphenol a (BPA) sensor, based on SAP Z23/multiwalled carbon nanotubes (Z23/MWCNTs) composite, was successfully fabricated on the surface of a glassy carbon electrode (GCE). The composite material was formed by π-π stacking interaction between the aromatic group on the hydrophobic side of Z23 and the side-wall of MWCNTs, with the charged hydrophilic group of Z23 exposed. During the electrocatalytic process of BPA, a synergistic effect was observed between Z23 and MWCNTs. The current response of the sensor based on composite material was 3.24 times that of the MWCNTs-modified electrode, which was much higher than that of the peptide-based electrode. Differential pulse voltammetry (DPV) was used to optimize the experimental conditions affecting the analytical performance of the modified electrode. Under optimal conditions, the linear range of the sensor was from 10 nM to 100 μM by amperometric measurement with sensitivity and limit of detection (LOD) at 6.569 μAμM−1cm−2 and 1.28 nM (S/N = 3), respectively. Consequently, the sensor has excellent electrochemical performance and is easy to fabricate, making it a good prospect in the field of electrochemical detection in the future. [ABSTRACT FROM AUTHOR]