Search Results (124)

Microbial Fuel Cell (MFC) is a novel bioelectrochemical system that catalyzes the oxidation of chemical energy in organic waste and converts it directly into electrical energy through the attachment and growth of electroactive microorganisms on the electrode surface. This technology realizes the synergistic effect of waste treatment and renewable energy production. A CF-NiO-PANI capacitor composite anode was prepared by loading polyaniline on a CF-NiO electrode to improve the capacitance of a CF electrode. The electrochemical characteristics of the composite anode were evaluated using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), and the electrode materials were analyzed comprehensively by scanning electron microscopy (SEM), energy diffusion spectrometer (EDS), and Fourier transform infrared spectroscopy (FTIR). MFC system based on CF-NiO-PANI composite anode showed excellent energy conversion efficiency in potato starch wastewater treatment, and its maximum power density increased to 0.4 W/m³, which was 300% higher than that of the traditional CF anode. In the standard charge–discharge test (C1000/D1000), the charge storage capacity of the composite anode reached 2607.06 C/m², which was higher than that of the CF anode (348.77 C/m²). Microbial community analysis revealed that the CF-NiO-PANI anode surface formed a highly efficient electroactive biofilm dominated by electrogenic bacteria (accounting for 47.01%), confirming its excellent electron transfer ability. The development of this innovative capacitance-catalytic dual-function anode material provides a new technical path for the synergistic optimization of wastewater treatment and energy recovery in MFC systems. Full article

The transition toward sustainable and decentralized energy solutions necessitates the development of innovative bioelectronic systems capable of harvesting and converting renewable energy. Here, we present a novel photo-bioelectrochemical fuel cell architecture based on a biohybrid anode integrating laser-induced graphene (LIG), poly(3,4-ethylenedioxythiophene) (PEDOT), and isolated thylakoid membranes. LIG provided a porous, conductive scaffold, while PEDOT enhanced electrode compatibility, electrical conductivity, and operational stability. Compared to MXene-based systems that involve complex, multi-step synthesis, PEDOT offers a cost-effective and scalable alternative for bioelectrode fabrication. Thylakoid membranes were immobilized onto the PEDOT-modified LIG surface to enable light-driven electron generation. Electrochemical characterization revealed enhanced redox activity following PEDOT modification and stable photocurrent generation under light illumination, achieving a photocurrent density of approximately 18 µA cm⁻². The assembled photo-bioelectrochemical fuel cell employing a gas diffusion platinum cathode demonstrated an open-circuit voltage of 0.57 V and a peak power density of 36 µW cm⁻² in 0.1 M citrate buffer (pH 5.5) under light conditions. Furthermore, the integration of a charge pump circuit successfully boosted the harvested voltage to drive a low-power light-emitting diode, showcasing the practical viability of the system. This work highlights the potential of combining biological photosystems with conductive nanomaterials for the development of self-powered, light-driven bioelectronic devices. Full article

The accelerating global demand for sustainable and efficient energy storage has driven substantial interest in supercapacitor technology due to its superior power density, fast charge–discharge capability, and long cycle life. However, the low energy density of supercapacitors remains a key bottleneck, limiting their broader application. This review provides a comprehensive and focused overview of the latest breakthroughs in supercapacitor research, emphasizing strategies to overcome this limitation through advanced material engineering and device design. We explore cutting-edge developments in electrode materials, including carbon-based nanostructures, metal oxides, redox-active polymers, and emerging frameworks such as metal–organic frameworks (MOFs) and covalent organic frameworks (COFs). These materials offer high surface area, tunable porosity, and enhanced conductivity, which collectively improve the electrochemical performance. Additionally, recent advances in electrolyte systems—ranging from aqueous to ionic liquids and organic electrolytes—are critically assessed for their role in expanding the operating voltage window and enhancing device stability. The review also highlights innovations in device architectures, such as hybrid, asymmetric, and flexible supercapacitor configurations, that contribute to the simultaneous improvement of energy and power densities. We identify persistent challenges in scaling up nanomaterial synthesis, maintaining long-term operational stability, and integrating materials into practical energy systems. By synthesizing these state-of-the-art advancements, this review outlines a roadmap for next-generation supercapacitors and presents novel perspectives on the synergistic integration of materials, electrolytes, and device engineering. These insights aim to guide future research toward realizing high-energy, high-efficiency, and scalable supercapacitor systems suitable for applications in electric vehicles, renewable energy storage, and next-generation portable electronics. Full article

The demand for sustainable energy storage solutions has led to increased interest in biomass-derived carbon aerogels as electrode materials for supercapacitors. These materials offer a high surface area, tunable porosity, and excellent electrochemical properties while utilizing renewable and waste biomass sources. This study evaluates the electrochemical performance of various biomass-based carbon aerogels, including those derived from cellulose, lignin, chitosan, and biomass waste, to identify key factors influencing supercapacitor efficiency. Principal Component Analysis (PCA) is employed to systematically analyze the relationships between structural and electrochemical properties, such as the specific surface area, specific capacitance, capacity retention, rate capability, energy density, and power density. The PCA results indicate that the first two principal components (PC1 and PC2) explain 58.20% of the total variance, with capacity retention (26.22%), energy density (19.55%), and specific capacitance (18.48%) identified as the most critical quantitative factors influencing supercapacitor performance. Chitosan-derived carbon aerogels exhibit superior capacitance and energy density, with a specific capacitance reaching up to 1074 F/g and energy density of 40.18 Wh/kg, whereas lignin-based aerogels demonstrate a high structural stability and capacity retention (up to 97.4%). Biomass waste-derived aerogels, despite their lower performance (176–298.6 F/g capacitance, 81.6–91.7% retention), provide cost-effective and environmentally sustainable alternatives. This quantitative analysis offers valuable insights into the rational design of high-performance, biomass-based aerogels, contributing significantly to the development of sustainable energy storage technologies. Full article

The imperative for sustainable energy has driven the demand for efficient energy storage systems that can harness renewable resources and store surplus energy for off-peak usage. Among the numerous advancements in energy storage technology, polymeric nanofibers have emerged as promising nanomaterials, offering high specific surface areas that facilitate increased charge storage and enhanced energy density, thereby improving electrochemical performance. This review delves into the pivotal role of nanofibers in determining the optimal functionality of energy storage systems. Electrospinning emerged as a facile and cost-effective method for generating nanofibers with customizable nanostructures, making it attractive for energy storage applications. Our comprehensive review article examines the latest developments in electrospun nanofibers for electrochemical storage devices, highlighting their use as separators and electrode materials. We provide an in-depth analysis of their application in various battery technologies, including supercapacitors, lithium-ion batteries, sodium-ion batteries, potassium-ion batteries, lithium–sulfur batteries, and lithium–oxygen batteries, with a focus on their electrochemical performance. Furthermore, we summarize the diverse fabrication techniques, optimization of key influencing factors, and environmental implications of nanofiber production and their properties. This review aims to offer an inclusive understanding of electrospinning’s role in advancing electrochemical energy storage, providing insights into the factors that drive the performance of these critical materials. Full article

Microbial fuel cell (MFC) technology has become a novel and attractive method for generating renewable energy during wastewater treatment. In this study, researchers combined carbon felt (CF), metal oxide (NiO), and polyaniline (PANI) to prepare CF/NiO/PANI multilayer capacitive bioelectrodes. The MFC equipped with a CF/NiO/PANI bioanode has a peak power density of 1988.31 ± 50.96 mW/m², which is 3.8 times higher than that of the MFC with a bare CF electrode, having a peak power density of 518.29 ± 27.07 mW/m². Charge–discharge cycle tests show that the storage charge capacity of the CF/NiO/PANI bioanode is 3304.64 C/m², which is 10.5 times greater than that of the bare CF anode. The electrochemical, morphological, and chemical properties of the prepared anodes are characterized using techniques such as SEM, EDS, FTIR, XPS, and XRD. Notably, high-throughput sequencing reveals that electrogenic bacteria account for 79.2% of the total microbial population on the CF/NiO/PANI multilayer capacitive bioelectrode. The synergistic effects of the composite materials result in the formation of a richer biofilm on the electrode surface, providing more active sites and enhancing capacitive characteristics. This innovative approach significantly improves the output power and peak current of MFCs, while also endowing the electrode with dual functions of simultaneous power generation and energy storage. Full article

This paper presents the application of a multi-sensor with a renewable surface based on a carbon black paste modified with ruthenium dioxide hydrate for monitoring the concentration changes of four ionic compounds (nitrate, ammonium, sodium, and calcium). By combining these into one sensor body, analyses can be performed simultaneously, based on a single standard curve, on a small number of available samples. The multi-sensor electrodes were characterized by determining both their electrical parameters, using methods such as chronopotentiometry and electrochemical impedance spectroscopy, and analytical parameters, through a series of potentiometric tests. The electrodes were characterized by high electric charge capacities ranging from 80 µF for the sodium electrode to 257 µF for the nitrate electrode. The tested electrodes showed calibration curve slopes of −51.1 mV/dec for the nitrate electrode, 59.3 mV/dec for the ammonium electrode, 57.0 mV/dec for the sodium electrode, and 26.0 mV/dec for the calcium electrode. The multi-sensor parameters allow for free determination of ions of biological significance in river water samples, soil samples, and plant substrates. The multi-sensor presented in this work can be successfully used to analyze water or plant substrates at home or among commercial crops. Full article

Attention to electrochemical energy storage (EES) devices continues to grow as the demand increases for energy storage systems in the storage and transmission of renewable energy. The expanded market requirement for mobile electronics devices and flexible electronic devices also calls for efficient energy suppliers. EES devices applying pseudocapacitive materials and generated pseudocapacitive storage are gaining increasing focus because they are capable of overcoming the capacity limitations of electrical double-layer capacitors (EDLCs) and offsetting the rate performance of batteries. The pseudocapacitive storage mechanism generally occurs on the surface or near the surface of the electrode materials, which could avoid the slow ion diffusion process. Developing materials with beneficial nanostructures and optimized phases supporting pseudocapacitive storage would efficiently improve the energy density and charging rate for EES devices, such as batteries and flexible supercapacitors. This review offers a detailed assessment of pseudocapacitance, including classification, working mechanisms, analysis methods, promotion routes and advanced applications. The future challenges facing the effective utilization of pseudocapacitive mechanisms in upcoming energy storage devices are also discussed. Full article

The pursuit of electrochemical carbon dioxide reduction reaction (CO₂RR) as a means of energy generation and mitigation of global warming is of considerable interest. In this study, a novel RuO₂-incorporated SnO₂-fabricated glassy carbon electrode (GCE) with a Nafion binder was used for the electrochemical reduction of CO₂ in an aqueous alkaline imidazole medium. The electrode fabrication process involved the drop-casting method, where RuO₂.SnO₂ was incorporated onto the surface of the GCE. Electrochemical studies demonstrated that the GCE-RuO₂.SnO₂ electrode facilitated CO₂ reduction at −0.58 V vs. the reversible hydrogen electrode (RHE) via a diffusion-controlled pathway with the transfer of two electrons. Importantly, the first electron transfer step was identified as the rate-determining step (RDS). A Tafel slope of 144 mV dec⁻¹ confirmed the association of two-electron transfer kinetics with CO₂RR. Moreover, the standard rate constant (k_o) and formal potential (E°′) were evaluated as 2.89 × 10⁻⁵ cm s⁻¹ and 0.0998 V vs. RHE, respectively. Kinetic investigations also reveal that the deprotonation and electron release steps took place simultaneously in the CO₂RR. Based on the reported results, the GCE-RuO₂.SnO₂ electrode could be a promising candidate for CO₂ reduction, applicable in renewable energy generation. Full article

With growing environmental concerns and the need for sustainable energy, multifunctional materials that can simultaneously address water treatment and clean energy production are in high demand. In this study, we developed a cost-effective method to synthesize zinc oxide (ZnO) nanowires via the anodic oxidation of zinc foil. By carefully controlling the anodization time, we optimized the Zn/ZnO-5 min electrode to achieve impressive dual-function performance in terms of effective photoelectrocatalysis for water splitting and waste water treatment. The electrode exhibited a high photocurrent density of 1.18 mA/cm² at 1.23 V vs. RHE and achieved a solar-to-hydrogen conversion efficiency of 0.55%. A key factor behind this performance is the presence of surface defects, such as oxygen vacancies (OVs), which enhanced charge separation and boosted electron transport. In tests for waste water treatment, the Zn/ZnO-5 min electrode demonstrated the highly efficient degradation of methylene blue (MB) dye, with a reaction rate constant of 0.4211 min⁻¹ when exposed to light and a 1.0 V applied voltage significantly faster than using light or voltage alone. Electrochemical analyses, including impedance spectroscopy and voltammetry, further confirmed the superior charge transfer properties of the electrode under illumination, making it an excellent candidate for both energy conversion and pollutant removal. This study highlights the potential of using simple anodic oxidation to produce scalable and efficient ZnO-based photocatalysts. The dual-function capability of this material could pave the way for large-scale applications in renewable hydrogen production and advanced waste water treatment, offering a promising solution to some of today’s most pressing environmental and energy challenges. Full article

The electrochemical cutting technique, utilizing electrolyte flushing through micro-hole arrays in the radial direction of a tube electrode, offers the potential for cost-effective and high-surface-integrity machining of large-thickness, straight-surface structures of difficult-to-cut materials. However, fabricating the array of jet micro-holes on the tube electrode sidewall remains a significant challenge, limiting the broader application of this technology. To enhance the efficiency and quality of machining these jet micro-holes on the tube sidewall, a helical electrode electrochemical drilling method assisted by anode vibration has been proposed. The influence of parameters, such as the rotational direction and speed of the helical electrode, as well as the vibration amplitude and frequency of the workpiece, on the machining results was investigated using fluid field simulation and machining experiments. It was found that these auxiliary movements could facilitate the renewal of electrolytes within the machining gap, thereby enhancing the efficiency and quality of electrochemical drilling. Using the optimized machining parameters, an array of 10 jet micro-holes with a diameter of 200 μm was machined on the metal tube sidewall. Electrochemical cutting with radial electrolyte flushing tests were then performed through these micro-holes. Full article

The electrocatalytic oxidation of urea has gained significant attention as a promising pathway for sustainable energy conversion and wastewater treatment that could address the dual goals of waste remediation and renewable energy generation. Phosphorous function groups-based catalysts have been introduced as potential electrode materials for enhancing the urea electrocatalytic oxidation reaction (UEOR) due to their unique structural properties, high stability, and tunable electronic characteristics. This review presents recent advancements in phosphorous-based catalysts (phosphates/phosphides) for UEOR. It highlights the development of novel phosphorous materials, synthesis approaches, and electrocatalytic insights into urea electrooxidation on phosphorous-based materials surfaces. Key topics include the role of different metal phosphates, surface modifications, and compositional optimizations to improve electrocatalytic efficiency and durability. Through a critical evaluation of current research trends and technological progress, this review underscores the potential of phosphate-based catalysts as environmentally friendly and efficient alternatives for sustainable waste-to-energy conversion via UEOR. The review concludes with a perspective on future directions for optimizing phosphate catalysts, scaling up practical applications, and integrating UEOR systems into renewable energy infrastructures. Full article

The growing demand for clean, decentralized energy has increased interest in blue energy, which generates power from water with different salt concentrations. Despite its potential as a renewable, low-cost energy source, optimizing electrode materials remains a challenge. This work presents a nanomaterial developed via microwave-assisted sol-gel methodology for blue energy applications, where ion diffusion and charge storage are critical. AX-7 carbon, designed for this study, features wide pores, enhancing ion diffusion. Compared to commercial NORIT carbon, AX-7 has a higher mesopore volume and external surface area, improving its overall performance. The synthesis process has been optimized and scaled up for evaluation in CAPMIX electrochemical cell stacks. Moreover, the lower series resistance (Rs) significantly boosts energy recovery, with AX-7 demonstrating superior performance. This advantage is especially evident during fresh-water cycles, where this material achieves significantly lower Rs compared to the commercial one. Full article

Plasma methanol synthesis from captured CO₂ and renewable H₂ is one of the most promising technologies that can drastically lower the carbon footprint in methanol production, but the associated high energy costs make it less competitive. Herein, we investigated the impact of the high-voltage electrode configuration on methanol formation. The effect of electrode materials Cu, Al, and stainless steel (SS) SUS304 on CO₂ hydrogenation to methanol using a temperature-controlled pulsed dielectric barrier discharge (DBD) plasma reactor was examined. The electrode surface area (ESA) was varied from 157 mm² to 628 mm² to determine the effect on discharge characteristics and the overall influence of plasma surface reactions on methanol production. The Cu electrode showed superior methanol synthesis performance (0.14 mmol/kWh) which was attributed to its catalytic activity function, while the Al electrode had the least production (0.08 mmol/kWh) ascribed to the excessive oxide coating on its surface, passivating its ability to promote methanol synthesis chemical reactions. In all electrode materials, the highest methanol production was achieved at 157 mm² ESA at a constant applied voltage. Lastly, the plasma charge concentration per discharge volume was determined to be an important parameter in fine-tuning the DBD reactor to enhance methanol synthesis. Full article

A key research focus at present is the exploration and innovation of electrode materials suitable for energy storage and conversion. Molybdenum-based sulfides/selenides (primarily MoS₂ and MoSe₂) have garnered attention in recent years due to their intrinsic two-dimensional structures, which are conducive to ion/electron transfer or insertion/extraction, making them promising candidates in electrocatalytic hydrogen production and sodium-ion battery applications. However, their inherently poor electronic structures have led most research efforts to concentrate on modifications aimed at enhancing their performance in hydrogen evolution reactions (HERs) and sodium-ion batteries (SIBs). Owing to their remarkable chemical inertness, expansive specific surface areas, and tunable pore architectures, carbon-based materials have garnered significant attention in research. The utilization of biomass as a renewable and environmentally sustainable precursor offers considerable benefits, including abundant availability, ecological compatibility, and cost-effectiveness. Consequently, recent scholarly endeavors have concentrated intensively on the synthesis of valuable carbon materials derived from renewable biomass sources. This review addresses the scientific challenges related to the development of electrode materials for HERs and SIBs in electrochemical energy storage and conversion. It delves into the recent focus on the two-dimensional transition-metal chalcogenides, particularly MoS₂ and MoSe₂, and the difficulties encountered in modulating their electronic structures when applied to HERs and SIBs. The review proposes the use of eco-friendly and widely sourced biomass-derived carbon (BMC) as a supporting matrix combined with MoS₂ and MoSe₂ to regulate their structures and enhance their electrocatalytic activity and sodium storage performance. Additionally, it highlights the existing challenges faced by these BMC/MoS₂ and BMC/MoSe₂ composites and offers insights into future developments. Full article