Search Results (3,665)

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

The development of cost-effective and highly sensitive hydrogen peroxide (H₂O₂) biosensors with robust stability is critical due to the pivotal role of H₂O₂ in biological processes and its broad utility across various applications. In this work, porous ceria hollow microspheres (CeO₂-phm) were synthesized using a solvothermal synthesis method and employed in the construction of an electrochemical biosensor for H₂O₂ detection. The resulting CeO₂-phm featured a uniform pore size centered at 3.4 nm and a high specific surface area of 168.6 m²/g. These structural attributes contribute to an increased number of active catalytic sites and promote efficient electrolyte penetration and charge transport, thereby enhancing its electrochemical sensing performance. When integrated into screen-printed carbon electrodes (CeO₂-phm/cMWCNTs/SPCE), the CeO₂-phm/cMWCNTs/SPCE-based biosensor exhibited a wide linear detection range from 0.5 to 450 μM, a low detection limit of 0.017 μM, and a high sensitivity of 2070.9 and 2161.6 μA·mM⁻¹·cm⁻²—surpassing the performance of many previously reported H₂O₂ sensors. In addition, the CeO₂-phm/cMWCNTs/SPCE-based biosensor possesses excellent anti-interference performance, repeatability, reproducibility, and stability. Its effectiveness was further validated through successful application in real sample analysis. Hence, CeO₂-phm with solvothermal synthesis has great potential applications as a sensing material for the quantitative determination of H₂O₂. Full article

Traditional liquid electrolyte batteries face safety concerns such as leakage and flammability, while further optimization has reached a bottleneck. Solid electrolytes are therefore considered a promising solution. Here, a PEO–LiTFSI–LATP (PELT) composite electrolyte was developed by incorporating nanosized Li_1.3Al_0.3Ti_1.7(PO₄)₃ fillers into a polyethylene oxide matrix, effectively reducing crystallinity, enhancing mechanical robustness, and providing additional Li⁺ transport channels. The PELT electrolyte exhibited an electrochemical stability window of 4.9 V, an ionic conductivity of 1.2 × 10⁻⁴ S·cm⁻¹ at 60 °C, and a Li⁺ transference number (tLi+) of 0.46, supporting stable Li plating/stripping for over 600 h in symmetric batteries. More importantly, to address poor electrode–electrolyte contact in conventional layered cells, we proposed an integrated electrode–electrolyte architecture by in situ coating the PELT precursor directly onto LiFePO₄ cathodes. This design minimized interfacial impedance, improved ion transport, and enhanced electrochemical stability. The integrated PELT/LFP battery retained 74% of its capacity after 200 cycles at 1 A·g⁻¹ and showed superior rate capability compared with sandwich-type batteries. These results highlight that coupling LATP-enhanced polymer electrolytes with an integrated architecture is a promising pathway toward high-safety, high-performance solid-state lithium-ion batteries. Full article

Microbial electrolysis cells (MECs) present a viable platform for sustainable hydrogen generation from organic waste, but their scalability is limited by cathode performance, cost, and durability. This study evaluates three hybrid carbon nanotube (CNT) cathodes—acid-washed CNT (AW-CNT), thin layer non-acid-washed CNT (TN-NAW-CNT), and thick layer non-acid-washed CNT (TK-NAW-CNT)—each composed of stainless-steel-supported CNTs coated with molybdenum phosphide (MoP). These were benchmarked against woven carbon cloth (WCC) under varied operational conditions. A custom multi-channel reactor operated for 341 days, testing cathode performance across applied voltages (0.7–1.2 V), buffer types (phosphate vs. bicarbonate), pH (7.0 and 8.5), buffer concentrations (10–200 mM), and substrates including acetate, lactate, and treated acid whey. CNT-based cathodes consistently showed higher current densities than WCC across most conditions with significant difference found at higher applied voltages. TK-NAW-CNT achieved peak current densities of 259 A m⁻² at 1.2 V and maintained >41 A m⁻² in real-waste conditions with no added buffer. Long-term performance losses were minimal: 4.5% (TN-NAW-CNT), 0.1% (TK-NAW-CNT), 10.8% (AW-CNT), and 6.8% (WCC). CNT cathodes showed improved performance from reduced resistance and greater electrochemical stability, while proton transfer improvements benefited all materials due to buffer type and pH conditions. These results highlight CNT-based cathodes as promising, scalable alternatives to WCC for energy-positive wastewater treatment. Full article

The molecular structure and mechanical resilience of the binder are crucial for mitigating volume expansion, maintaining electrode structural integrity, and enhancing the cycling stability of silicon-based anode materials in lithium-ion batteries. In this study, from the perspective of binder molecular structural design, commercial carboxymethyl cellulose (CMC) was modified with silk protein (SF), which has good mechanical properties and abundant surface functional groups, to address issues such as high brittleness, poor compliance and easy cracking of the electrode structure during charge and discharge cycles, and to enhance the mechanical properties of the CMC-based binder and its interaction with silicon particles, so as to improve the cycle stability of silicon-based materials. The mechanical properties of the CMC binder were significantly improved and the interaction between the binder and the surface of the silicon particles was enhanced by the addition of SF. When the SF content was optimized at 6 wt%, the electrode exhibited the best electrochemical performance, delivering a specific capacity of 1182 mAh/g at a high current density of 5000 mA/g, and retaining a capacity of 1138 mAh/g after 50 cycles at 1000 mA/g, demonstrating excellent electrochemical durability. Full article

This study reports a binder-free, catalyst-free method for fabricating vertically aligned carbon nanotubes (VACNTs) directly on copper (Cu) foil using plasma-enhanced chemical vapor deposition (PECVD) for electrochemical double-layer capacitor (EDLC) applications. This approach eliminates the need for catalyst layers, polymeric binders, or substrate pre-treatments, simplifying electrode design and enhancing electrical integration. The resulting VACNTs form a dense, uniform, and porous array with strong adhesion to the Cu substrate, minimizing contact resistance and improving conductivity. Electrochemical analysis shows gravimetric specific capacitance (C_grav) and areal specific capacitance (C_areal) of 8 F g⁻¹ and 3.5 mF cm⁻² at a scan rate of 5 mV/s, with low equivalent series resistance (3.70 Ω) and charge transfer resistance (0.48 Ω), enabling efficient electron transport and rapid ion diffusion. The electrode demonstrates excellent rate capability and retains 92% of its initial specific capacitance after 3000 charge–discharge cycles, indicating strong cycling stability. These results demonstrate the potential of directly grown VACNT-based electrodes for high-performance EDLCs, particularly in applications requiring rapid charge–discharge cycles and sustained energy delivery. Full article

We explore a plasmonic interface for perovskite solar cells (PSCs) by integrating inkjet-printed TiO₂-AuNP microdot arrays (MDA) into the electron transport layer. This systematic study examines how the TiO₂ blocking layer (BL) surface conditioning, AuNP layer positioning, and nanoparticle loading collectively influence device performance. Pre-annealing the BL increases its hydrophobicity, yielding smaller and denser AuNP microdots with an enhanced localized surface plasmon resonance (LSPR). Positioning the AuNP MDA at the BL/perovskite interface (above the BL) maximizes near-field plasmonic coupling to the absorber, resulting in higher photocurrent and power conversion devices; these trends are corroborated by finite-difference time-domain (FDTD) simulations. Moreover, these devices demonstrate better stability over time compared to those with AuNPs at the transparent electrode (under BL). Although higher AuNP concentrations improve dispersion stability, preserve MAPI crystallinity, and yield more uniform nanoparticle sizes, device measurements showed no performance gains. After annealing, the samples with the Au content of 23 wt% relative to TiO₂ achieved optimal PSC efficiency by balancing plasmonic enhancement and charge transport without the increased resistance and recombination losses seen at higher loadings. Importantly, X-ray diffraction (XRD) confirms that introducing the TiO₂-AuNP MDA at the interface does not disrupt the perovskite’s crystal structure, underscoring the structural compatibility of this plasmonic enhancement. Overall, our findings highlight a scalable strategy to boost PSC efficiency via engineered light-matter interactions at the nanoscale without compromising the perovskite’s structural integrity. 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

This work demonstrates the use of SUS316L stainless steel as a new material for the fabrication of quasi-reference electrodes (QREs) intended to replace conventional reference electrodes (REs) in electrochemical sensors. The present study examined the potentials generated by SUS316L specimens annealed in air at 400 °C and above for 1 h or more. Annealing above 500 °C increased the proportion of Cr in surface oxide films, hence reducing the stability of the potential. Samples annealed at 400 °C for 5 h produced the most stable electrode potential, which was attributed to a higher concentration of Fe in the oxide layer. The potential of such specimens increased by only 28.3 mV between test durations of 24 and 168 h, and potential data acquired at 30 s intervals had a standard deviation of less than 2 µV. Applying a surface treatment prior to immersion in the simulated tap water evidently stabilized the electrode potential, as a consequence of the formation of an inner oxide layer together with an outer layer consisting primarily of iron oxides. 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

Cu₂S has wide-ranging applications in the energy field, particularly as electrode materials and components of energy storage devices. However, the migration of copper ions is prone to component segregation and copper precipitation, impairing long-term thermal stability and service performance. Ce₂S₃ not only possesses the unique 4f electron layer structure of Ce but also has high thermal stability and chemical inertness. Here, we report for the first time that the thermal stability and mechanical properties of Cu₂S can be significantly enhanced by introducing the dispersed phase Ce₂S₃. Thermogravimetry—differential scanning calorimetry (TG-DSC) results show that the addition of 6 wt% Ce₂S₃ improves the thermal stability of Cu₂S sintered at 400 °C. X-ray diffraction (XRD) results indicate that the crystal structure of Cu₂S gradually transforms to tetragonal Cu_1.96S and orthorhombic Cu_1.8S phase at 400 °C with the increase of Ce₂S₃ addition. Scanning electron microscopy (SEM) results show that the particle size gradually decreased with the increase of Ce₂S₃ amount, indicating that the Ce₂S₃ addition increased the reactivity. The Ce content in Cu₂S increased gradually with the increase of Ce₂S₃ amount at 400–600 °C. The 7 wt% Ce₂S₃-Cu₂S exhibits paramagnetic behavior with a saturation magnetization of 1.2 µ_B/Ce. UV-Vis analysis indicates that the addition of Ce₂S₃ can reduce the optical energy gap and enrich the band structure of Cu₂S. With increasing addition of Ce₂S₃ and rising sintering temperature, the density of Ce₂S₃-Cu₂S gradually increases, and the hardness of Ce₂S₃-Cu₂S increases by 52.5% at 400 °C and by 34.2% at 600 °C. The friction test results show that an appropriate addition amount of Ce₂S₃ can increase the friction coefficients of Cu₂S. Ce₂S₃ modification offers a novel strategy to simultaneously enhance the structural and service stability of Cu₂S by regulating Cu ion diffusion and suppressing compositional fluctuations. Full article

Bismuth vanadate (BiVO₄) has attracted significant attention as a photoanode material for photoelectrochemical (PEC) water splitting due to its suitable bandgap (~2.4 eV), strong visible light absorption, chemical stability, and cost-effectiveness. Despite these advantages, its practical application remains constrained by intrinsic limitations, including poor charge carrier mobility, short diffusion length, and sluggish oxygen evolution reaction (OER) kinetics. This review critically summarizes recent advancements aimed at enhancing BiVO₄ PEC performance, encompassing synthesis strategies, defect engineering, heterojunction formation, cocatalyst integration, light-harvesting optimization, and stability improvements. Key fabrication methods—such as solution-based, vapor-phase, and electrochemical approaches—along with targeted modifications, including metal/nonmetal doping, surface passivation, and incorporation of electron transport layers, are discussed. Emphasis is placed on strategies to improve light absorption, charge separation efficiency (η_sep), and charge transfer efficiency (η_trans) through bandgap engineering, optical structure design, and catalytic interface optimization. Approaches to enhance stability via protective overlayers and electrolyte tuning are also reviewed, alongside emerging applications of BiVO₄ in tandem PEC systems and selective solar-driven production of value-added chemicals, such as H₂O₂. Finally, critical challenges, including the scale-up of electrode fabrication and the elucidation of fundamental reaction mechanisms, are highlighted, providing perspectives for bridging the gap between laboratory performance and practical implementation. Full article

Microbial electrosynthesis (MES) has emerged as a promising bio-electrochemical technology for sustainable CO₂ conversion into valuable organic compounds since it uses living electroactive microbes to directly convert CO₂ into value-added products. This review synthesizes advancements in MES from 2010 to 2025, focusing on the electrode materials, microbial communities, reactor engineering, performance trends, techno-economic evaluations, and future challenges, especially on the results reported between 2020 and 2025, thus highlighting that MES technology is now a technology to be reckoned with in the spectrum of biofuel technology production. While the current productivity and scalability of microbial electrochemical systems (MESs) remain limited compared to conventional CO₂ conversion technologies, MES offers distinct advantages, including process simplicity, as it operates under ambient conditions without the need for high pressures or temperatures; modularity, allowing reactors to be stacked or scaled incrementally to match varying throughput requirements; and seamless integration with circular economy strategies, enabling the direct valorization of waste streams, wastewater, or renewable electricity into valuable multi-carbon products. These features position MES as a promising platform for sustainable and adaptable CO₂ utilization, particularly in decentralized or resource-constrained settings. Recent innovations in electrode materials, such as conductive polymers and metal–organic frameworks, have enhanced electron transfer efficiency and microbial attachment, leading to improved MES performance. The development of diverse microbial consortia has expanded the range of products achievable through MES, with studies highlighting the importance of microbial interactions and metabolic pathways in product formation. Advancements in reactor design, including continuous-flow systems and membrane-less configurations, have addressed scalability issues, enhancing mass transfer and system stability. Performance metrics, such as the current densities and product yields, have improved due to exceptionally high product selectivity and surface-area-normalized production compared to abiotic systems, demonstrating the potential of MES for industrial applications. Techno-economic analyses indicate that while MES offers promising economic prospects, challenges related to cost-effective electrode materials and system integration remain. Future research should focus on optimizing microbial communities, developing advanced electrode materials, and designing scalable reactors to overcome the existing limitations. Addressing these challenges will be crucial for the commercialization of MES as a viable technology for sustainable chemical production. Microbial electrosynthesis (MES) offers a novel route to biofuels by directly converting CO₂ and renewable electricity into energy carriers, bypassing the costly biomass feedstocks required in conventional pathways. With advances in electrode materials, reactor engineering, and microbial performance, MES could achieve cost-competitive, carbon-neutral fuels, positioning it as a critical complement to future biofuel technologies. 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 pursuit of sustainable and environmentally benign energy storage solutions has propelled significant interest in organic batteries, which utilize redox-active organic compounds as electrode materials. A pivotal component in determining their electrochemical performance, safety, and long-term stability is the electrolyte. Polymer-based electrolytes (PBEs) have emerged as promising candidates owing to their intrinsic advantages, such as enhanced thermal stability, mechanical integrity, and the mitigation of leakage and flammability risks associated with conventional liquid electrolytes. Unlike previous reviews that broadly cover solid electrolytes, this review specifically focuses on the unique developments of polymer-based electrolytes tailored for organic batteries over the past few years. This review presents a comprehensive overview of the recent progress in PBEs specifically designed for organic battery systems. It systematically examines various categories, including solid polymer electrolytes (SPEs), valued for their structural simplicity and stability; gel polymer electrolytes (GPEs), noted for their high ionic conductivity and processability; and polymer-inorganic composite electrolytes, which synergistically integrate the mechanical flexibility of polymers with the ionic conductivity of inorganic fillers. Additionally, the review delves into the latest advancements in ionogels and poly(ionic liquid) electrolytes, highlighting their potential to overcome existing limitations and enable next-generation battery performance. The article concludes with a critical discussion on prevailing challenges and prospective research directions, emphasizing the importance of advanced material design, interfacial engineering, and sustainable synthesis approaches to facilitate the practical realization of high-performance organic batteries. Full article