Search Results (1,393)

The development of high-performance supercapacitor electrodes is crucial to meet the increasing demand for efficient and sustainable energy storage systems. Cobalt oxide (Co₃O₄), with its high theoretical capacitance, is a promising electrode material, but its practical application is hindered by poor conductivity limitations and structural instability during cycling. In this work, lanthanum La³⁺-doped Co₃O₄ nanocubes were synthesized via a hydrothermal approach to tailor their structural and electrochemical properties. Different doping concentrations (1, 3, and 5%) were introduced to investigate their influence systematically. X-ray diffraction confirmed the retention of the spinel phase with clear evidence of La³⁺ incorporation into the Co₃O₄ lattice. Also, Raman spectroscopy validated the structural integrity through characteristic Co-O vibrational modes. Scanning electron microscopy analysis revealed uniform cubic morphologies across all samples. The formation of the cubic spinel structure of 1% La³⁺-doped Co₃O₄ are confirmed from XPS and TEM studies. Electrochemical evaluation in a 3 M KOH electrolyte demonstrated that 1% La³⁺-doped Co₃O₄ nanocubes delivered the highest performance, achieving a specific capacitance of 1312 F g⁻¹ at 1 A g⁻¹ and maintaining a 79.8% capacitance retention and a 97.12% Coulombic efficiency over 10,000 cycles at 5 Ag⁻¹. It can be demonstrated that La³⁺ doping is an effective strategy to enhance the charge storage capability and cycling stability of Co₃O₄, offering valuable insights for the rational design of next-generation supercapacitor electrodes. Full article

In the shift toward sustainable energy, there is a strong demand for efficient and durable energy storage solutions. Supercapacitors, in particular, are a promising technology, but they require high-performance materials that can be produced using simple, eco-friendly methods. This has led researchers to investigate new materials and composites that can deliver high energy and power densities, along with long-term stability. Herein, we report a green synthesis approach to create a composite material consisting of reduced graphene oxide and silver nanoparticles (rGO/Ag). The method uses ascorbic acid, a natural compound found in fruits and vegetables, as a non-toxic agent to simultaneously reduce graphene oxide and silver nitrate. To enhance electrochemical performance, the incorporation of silver nanoparticles into the rGO structures is optimized. In this study, different molar concentrations of silver nitrate (1.0, 0.10, and 0.01 M) are used to control silver nanoparticle loading during the synthesis and reduction process. A correlation between silver concentration, defect density in rGO, and the resulting capacitive behavior was assessed by systematically varying the silver molarity. The synthesized materials exhibited excellent performance as supercapacitor electrodes in a three-electrode configuration, with the rGO/Ag 1.0 M composite showing the best performance, reaching a maximum specific capacitance of 392 Fg⁻¹ at 5 mVs⁻¹. Furthermore, the performance of this optimized electrode material was investigated in a two-electrode configuration as a coin cell device, which demonstrates a maximum areal-specific capacitance of 22.63 mFcm⁻² and a gravimetric capacitance of 19.00 Fg⁻¹, which is within the range of commercially viable devices and a significant enhancement, outperforming low-level graphene-based devices. Full article

The global transition toward renewable energy sources has intensified in response to escalating environmental challenges. Nevertheless, the inherent intermittency and instability of renewable energy necessitate the development of reliable energy storage technologies. Supercapacitors are particularly notable for their high specific capacitance, rapid charge and discharge capability, and exceptional cycling stability. Concurrently, the increasing demand for efficient and sustainable energy storage systems has stimulated interest in multifunctional electrode materials that integrate electrocatalytic activity with electrochemical energy storage. Two-dimensional transition metal dichalcogenides (TMDs), owing to their distinctive layered structures, large surface areas, phase state, energy band structure, and intrinsic electrocatalytic properties, have emerged as promising candidates to achieve dual functionality in electrocatalysis and electrochemical energy storage for asymmetric supercapacitors (ASCs). Specifically, their unique electronic properties and catalytic characteristics promote reversible Faradaic reactions and accelerate charge transfer kinetics, thus markedly enhancing charge storage efficiency and energy density. This review highlights recent advances in TMD-based multifunctional electrodes. It elucidates mechanistic correlations between intrinsic electronic properties and electrocatalytic reactions that influence charge storage processes, guiding the rational design of high-performance ASC systems. Full article

Plant microbial fuel cells (PMFCs) represent an eco-friendly solution for generating clean energy by converting biological processes into electricity. This work presents the first integration of tin sulfide (SnS)-coated 304 stainless steel (SS304) electrodes into Aloe vera-based PMFCs for enhanced energy harvesting. SnS thin films were obtained via chemical bath deposition and screen printing, followed by thermal treatment. X-ray diffraction (XRD) revealed a crystal size of 15 nm, while scanning electron microscopy (SEM) confirmed film thicknesses ranging from 3 to 13.75 µm. Over a 17-week period, SnS-coated SS304 electrodes demonstrated stable performance, with open circuit voltages of 0.6–0.7 V and current densities between 30 and 92 mA/m², significantly improving power generation compared to uncoated electrodes. Polarization analysis indicated an internal resistance of 150 Ω and a power output of 5.8 mW/m². Notably, the system successfully charged a 15 F supercapacitor with 8.8 J of stored energy, demonstrating a practical proof-of-concept for powering low-power IoT devices and advancing PMFC applications beyond power generation. Microbial biofilm formation, observed via SEM, contributed to enhanced electron transfer and system stability. These findings highlight the potential of PMFCs as a scalable, cost-effective, and sustainable energy solution suitable for industrial and commercial applications, contributing to the transition toward greener energy systems. These incremental advances demonstrate the potential of combining low-cost electrode materials and energy storage systems for future scalable and sustainable bioenergy solutions. Full article

The practical application of transparent supercapacitors (TSCs) is limited by the inherent trade-off between transparency and conductivity, as well as the environmental and economic drawbacks of electrode materials. This study presents a novel and scalable method for fabricating porous carbon-modified silk-derived carbon fiber meshes as electrode materials for transparent supercapacitors. The process involves the in situ growth of a cobalt organic complex on a silk mesh, followed by carbonization to produce a flexible, transparent carbon fiber mesh with a hierarchical porous structure (specific surface area: 570 m²/g). The resulting material exhibits good mechanical properties and electrical conductivity due to the nanographene-like structure formed during the cobalt-catalyzed carbonization process. This TSC achieves an optical transparency of up to 65% and an aerial capacitance of 9.65 mF/cm² at a scan rate of 0.01 V/s, surpassing many existing transparent electrodes. Additionally, the device demonstrates outstanding electrochemical stability, retaining 89% of its initial capacitance after 2000 cycles at a scan rate of 0.5 V/s, showcasing superior durability. This study presents a pioneering method for developing TSCs by utilizing sustainable silk-derived carbon materials and a cost-effective fabrication process. Full article

Polybenzoxazines (PBZs) have garnered significant attention as a versatile class of precursors for the development of advanced carbon-based materials, particularly in the field of electrochemical energy storage. This review comprehensively examines recent progress in the synthesis, structural design, and application of polybenzoxazine-derived materials for supercapacitor electrodes. Owing to their intrinsic nitrogen content, tunable functionality, and excellent thermal and mechanical stability, polybenzoxazines serve as ideal precursors for producing nitrogen-doped porous carbons with high surface areas and desirable electrochemical properties. This review discusses the influence of molecular design, polymerization conditions, and carbonization parameters on the resulting microstructure and performance of the materials. Furthermore, the electrochemical behavior of these materials in both electric double-layer capacitors (EDLCs) and pseudocapacitors is analyzed in detail. Challenges such as optimizing pore architecture, improving conductivity, and achieving scalable synthesis are also addressed. This article highlights emerging trends and offers perspectives on the future development of polybenzoxazine-derived materials for next-generation high-performance supercapacitors. Full article

This study presents the design and implementation of a crop environmental monitoring system powered by a plant–soil bioelectrochemical energy source. The system integrates a Cu–Zn electrode power unit, a boost converter, a supercapacitor-based energy management module, and a wireless sensing node for real-time monitoring of environmental parameters. Unlike conventional plant microbial fuel cells (PMFCs), the output current originates partly from the galvanic effect of Cu–Zn electrodes and is further regulated by rhizosphere conditions and microbial activity. Under the optimal external load (900 Ω), the system achieved a maximum output power of 0.477 mW, corresponding to a power density of 0.304 mW·cm⁻². Stability tests showed that with the boost converter and supercapacitor, the system maintained a stable operating voltage sufficient to power the sensing node. Soil moisture strongly influenced performance, with higher water content increasing power by about 35%. Theoretical calculations indicated that Zn corrosion alone would limit the anode lifetime to ~66 days; however, stable output during the experimental period suggests contributions from plant–microbe interactions. Overall, this work demonstrates a feasible self-powered crop monitoring system and provides new evidence for the potential of plant–soil bioelectrochemical power sources in low-power applications. Full article

This work provides the first demonstration of FFTCCV as a dual-purpose method, serving both as a real-time diagnostic tool and as a phase- and morphology-engineering strategy. By adjusting the scan rate, FFTCCV directs the crystallographic evolution of Ni (OH)₂ on Ni foam—stabilizing α-nanoflakes at 0.7 V·s⁻¹ and β-platelets at 0.007 V·s⁻¹—while simultaneously enabling electrode-resolved ΔQ tracking and predictive state-of-health (SoH) monitoring. This approach enabled the precise regulation of electrode morphology and phase composition, yielding high areal capacitance (546.5 mF·cm⁻² at 5 mA·cm⁻²) with ~75% retention after 3000 cycles. These improvements advance the development of high-performance micro-supercapacitors, facilitating their integration into wearable and miniaturized devices where compact and durable energy storage is required. Beyond performance enhancement, FFTCCV also enabled continuous monitoring of capacitance during extended operation (up to 40,000 s). By recording both anodic and cathodic responses, the method provided time-resolved insights into device stability and revealed characteristic signatures of electrode degradation, phase transitions, and morphological changes. Such detection allows recognition of early failure pathways that are not accessible through conventional testing. This monitoring capability functions as an embedded health sensor, offering a pathway for predictive diagnosis of supercapacitor failure. Such functionality is particularly important for energy-driven actuators and smart materials, where uninterrupted operation and preventive maintenance are critical. FFTCCV therefore provides a scalable strategy for developing energy-autonomous microsystems with improved performance and real-time state-of-health monitoring. Full article

This review sheds some light on the emerging niche of the reuse of spent adsorbents in electrochemical devices. Reuse and repurposing extend the adsorbent’s life cycle, remove the need for long-term storage, and generate additional value, making it a highly eco-friendly process. Main adsorbent-type materials are overviewed, emphasising desired properties for initial adsorption and subsequent conversion to electroactive material step. The effects of the most frequent regeneration procedures are compared to highlight their strengths and shortcomings. The latest efforts of repurposing and reuse in supercapacitors, fuel cells, and batteries are analysed. Reuse in supercapacitors is dominated by materials that, after a regeneration step, lead to materials with high surface area and good pore structure and is mainly based on the conversion of organic adsorbents to some form of conductive carbon adlayer. Additionally, metal/metal-oxide and layered-double hydroxides are also being developed, but predominantly towards fuel cell and battery electrodes with respectable oxygen reduction characteristics and significant capacities, respectively. Repurposed adsorbents are being adopted for peroxide generation as well as direct methanol fuel cells. The work puts forward electrochemical devices as a valuable avenue for spent adsorbents and as a puzzle piece towards a greener and more sustainable future. Full article

The need for energy storage and the rapid development of new electronic platforms have prompted intense research into small and secure energy storage devices, particularly supercapacitors (SCs). Layered double hydroxides (LDHs) are potential electrode materials for SCs because of their excellent physicochemical and electrical characteristics. They involve interlayer spacing, high oxidation states, simplicity of synthesis, and distinct morphologies. Despite their potential, several kinds of LDHs still face constraints, such as particle aggregation, moderate surface area, and high resistance, which limit their use in energy storage. To overcome these challenges and enhance the electrochemical performance of LDHs, they have used strategies such as anion intercalation, oxygen vacancy, heteroatom, surfactant, fluorine, and metal doping, which have been demonstrated as electrode materials for SCs. Therefore, this review discusses recent advances in different LDHs and studies comparing bare and modified LDH for three- and two-electrode systems, with an emphasis on their morphologies, surface areas, and electrical properties for SC applications. It was found that modified LDHs achieve enhanced electrochemical performance in comparison to their corresponding bare LDHs. Consequently, there are potential opportunities to modify the surface of the recently invented LDHs for electrochemical investigations, which could result in improving their performance. This review also presents future perspectives on LDH-based energy storage devices for supercapacitors. Full article

The development of portable and wearable electronics has promoted the advancement of fiber supercapacitors (FSCs), but their low energy density still limits their application in flexible devices. Herein, we incorporated micron-sized graphene dispersions at varying concentrations into the polyaniline (PANI) precursor solution prepared via electrochemical polymerization and subsequently electrodeposited PANI/graphene composites onto the surface of carbon nanotube (CNT) fibers, ultimately obtaining fibrous PANI/graphene@CNT composite electrodes. This electrode material not only exhibits the superior electrochemical activity characteristic of conducting polymers synthesized by electrochemical polymerization but also possesses a relatively high specific surface area. Furthermore, we fabricated coaxial fiber supercapacitors using PANI/graphene@CNT composite fibers and CNT films as the positive and negative electrode materials, respectively. The maximum energy density and power density could reach 160.5 µWh cm⁻² and 13 mW cm⁻² respectively, proving its excellent energy storage and output capabilities. More importantly, the prepared CFASC device showed remarkable mechanical and electrochemical durability. Even after 3000 bending cycles, it retained 89.77% of its original capacitance, highlighting its promising applicability in the realm of flexible electronics. The resulting devices demonstrate excellent electrochemical performance and mechanical stability. Full article

Over the last few decades, polymer composites have been rapidly making inroads in critical applications of electrical storage devices such as batteries and supercapacitors. Structural supercapacitor composites (SSCs) have emerged as multifunctional materials capable of storing energy while bearing mechanical loads, offering lightweight and compact solutions for energy systems. This study investigates the functionalization of Bisphenol A-based thermosetting polymers with ionic liquids, aiming to synthesize dual-functional structural electrolytes for SSC fabrication. A multifunctional sandwich structure was subsequently fabricated, in which the fabricated SSC served as the core layer, bonded between two structurally robust outer skins. The core layer was fabricated using carbon fibre layers coated with 10% graphene nanoplatelets (GNPs), while the skin layers contained 0.25% GNPs dispersed in the resin matrix. The developed device demonstrated stable operation up to 85 °C, achieving a specific capacitance of 57.28 mFcm⁻² and an energy density of 179 mWhm⁻² at room temperature. The performance doubled at 85 °C, maintaining excellent capacitance retentions across all experimented temperatures. The flexural strength of the developed sandwich SSC at elevated temperature (at 85 °C) was 71 MPa, which exceeds the minimum requirement for roofing sheets as specified in Australian building standard AS 4040.1 (Methods of testing sheet roof and wall cladding, Method 1: Resistance to concentrated loads). Finite element analysis (FEA) was performed using Abaqus CAE to evaluate structural integrity under mechanical loading and predict damage initiation zones under service conditions. The simulation was based on Hashin’s failure criteria and demonstrated reasonable accuracy. This research highlights the potential of multifunctional polymer composite systems in renewable energy infrastructure, offering a robust and energy-efficient material solution aligned with circular economy and sustainability goals. Full article

Polyaniline (PANI) nanofibers (NFs) were synthesized via two chemical oxidative polymerization approaches: a rapid mixing process and a conventional stirred tank method. PANI is a promising electrode material for supercapacitors due to its conductivity, stability, and pseudocapacitive redox behavior. The rapid mixing route proved especially effective, as fast polymerization promoted homogeneous nucleation and yielded thin, uniform, and interconnected NFs, whereas conventional stirring produced thicker, irregular fibers through heterogeneous nucleation. Structural characterization (FTIR, UV-Vis, XRD, XPS, TGA) confirmed that both samples retained the typical emeraldine form of PANI, but morphological analyses (SEM, BET) revealed that only the rapid process preserved nanofiber uniformity and porosity. This morphological control proved decisive for electrochemical behavior: symmetric supercapacitor devices fabricated from rapidly synthesized NFs delivered higher specific capacitances (378.8 F g⁻¹ at 1 A g⁻¹), improved rate capability, and superior cycling stability (90.33% retention after 3000 cycles) compared to devices based on conventionally prepared NFs. These findings demonstrate that rapid polymerization offers a simple and scalable route to morphology-engineered PANI electrodes with enhanced performance. Full article

We have demonstrated the fabrication of laminate composites with functional features to demonstrate energy storage capabilities. The present study investigates the surface modification of carbon fibers by coating dual materials of reduced graphene oxide (rGO) and cellulose-based activated carbon to enhance their energy storage capacitance for the development of structural supercapacitors. The dual coating on carbon fibers enabled a near 210-fold improvement in surface area, surpassing that of pristine carbon fibers. This formed a highly porous graphene network with activated carbon, resulting in a well-connected fiber–graphene-activated carbon network on carbon fibers. The electrochemical supercapacitor, fabricated from surface-functionalized carbon fibers, provides the best performance, with a specific capacitance of 172 F g⁻¹ in an aqueous electrolyte. Furthermore, the symmetrical structural supercapacitor (SSSC) device delivered a specific capacitance of 227 mF g⁻¹ across a wide potential window of 6 V. The electrochemical stability of the SSSC device was validated by a high capacitance retention of 97.3% over 10,000 cycles. Additionally, the study showcased the practical application of this technology by successfully illuminating an LED using the proof-of-concept SSSC device with G-aC/CF electrodes. Overall, the findings of this study highlight the potential of carbon fiber composites as a promising hybrid material, offering both structural integrity and a functional performance suitable for aerospace and automobile applications. Full article

Nickel-based metal–organic frameworks (Ni-MOFs) have received enormous amounts of attention from the scientific community due to their excellent porosity, larger specific surface area, tunable structure, and intrinsic redox properties. In previous years, Ni-MOFs and their hybrid composite materials have been extensively explored for electrochemical sensing applications. As per the reported literature, Ni-MOF-based hybrid materials have been used in the fabrication of electrochemical sensors for the monitoring of ascorbic acid, glucose, L-tryptophan, bisphenol A, carbendazim, catechol, hydroquinone, 4-chlorophenol, uric acid, kaempferol, adenine, _L-cysteine, etc. The presence of synergistic effects in Ni-MOF-based hybrid materials plays a crucial role in the development of highly selective electrochemical sensors. Thus, Ni-MOF-based materials exhibited enhanced sensitivity and selectivity with reasonable real sample recovery, which suggested their potential for practical applications. In addition, Ni-MOF-based hybrid composites were also adopted as electrode modifiers for the development of supercapacitors. The Ni-MOF-based materials demonstrated excellent specific capacitance at low current densities with reasonable cyclic stability. This review article provides an overview of recent advancements in the utilization of Ni-MOF-based electrode modifiers with metal oxides, carbon-based materials, MXenes, polymers, and LDH, etc., for the electrochemical detection of environmental pollutants and biomolecules and for supercapacitor applications. In addition, Ni-based bimetallic and trimetallic catalysts and their composites have been reviewed for electrochemical sensing and supercapacitor applications. The key challenges, limitations, and future perspectives of Ni-MOF-based materials are discussed. We believe that the present review article may be beneficial for the scientific community working on the development of Ni-MOF-based materials for electrochemical sensing and supercapacitor applications. Full article