Search Results (830)

The global transition towards a low-carbon energy system urgently demands efficient and safe energy storage solutions. Aqueous zinc-ion batteries (AZIBs) are considered a promising alternative to lithium-ion batteries due to their inherent safety and environmental friendliness. However, conventional manufacturing methods are costly and labor-intensive, hindering their large-scale production. Recent advances in 3D printing technology offer innovative pathways to address these challenges. By combining design flexibility with material optimization, 3D printing holds the potential to enhance battery performance and enable customized structures. This review systematically examines the application of 3D printing technology in fabricating key AZIB components, including electrodes, electrolytes, and integrated battery designs. We critically compare the advantages and disadvantages of different 3D printing techniques for these components, discuss the potential and mechanisms by which 3D-printed structures enhance ion transport and electrochemical stability, highlight critical existing scientific questions and research gaps, and explore potential strategies for optimizing the manufacturing process. Full article

Silica-modified electrodes possess physicochemical properties that make them valuable in electrochemical sensing and energy-related applications. Although intrinsically insulating, silica thin films can selectively interact with redox species, producing sieving effects that enhance electrochemical responses. We synthesized Class I hybrid silica matrices incorporating either negatively charged poly(4-styrene sulfonic acid) or positively charged poly(diallyl dimethylammonium chloride). These hybrid films were deposited onto ITO electrodes and evaluated via cyclic voltammetry in aqueous ferrocenium solutions. The polyelectrolyte charge played a key role in the electroassisted incorporation of ferrocene: silica-PSS films promoted accumulation, while silica-PDADMAC films hindered it due to electrostatic repulsion. In situ UV-vis spectroscopy confirmed that only a fraction of the embedded ferrocene was electroactive. Nevertheless, this fraction enabled effective mediated detection of cytochrome c in solution. These findings highlight the crucial role of ionic interactions and hybrid composition in electron transfer to redox proteins, providing valuable insights for the development of advanced bioelectronic sensors. Full article

The anodic behavior of zinc electrodes is important for energy storage, corrosion protection, electrochemical processing, and other practical applications. This study investigates the anodic galvanostatic polarization of zinc foil and bulk electrodes in aqueous oxalic acid solutions, revealing significant differences in their electrochemical behavior, particularly in induction period durations. The induction period’s duration depended on electrolyte concentration, current density, and temperature. Notably, the temperature dependence of the kinetics exhibited contrasting trends: the induction period for foil electrodes increased with temperature, while that of bulk electrodes decreased. Chemical analysis and polishing treatment comparisons showed no significant differences between the foil and bulk electrodes. However, Scanning Electron Microscopy (SEM) observations of samples anodized at different temperatures, combined with Inductively Coupled Plasma–Optical Emission Spectroscopy (ICP-OES) analysis of dissolved electrode material, provided insights into the distinct anodic behaviors. X-ray Diffraction (XRD) studies further confirmed these findings, revealing a crystallographic orientation dependence of the anodic behavior. These results provide detailed information about the electrochemical properties of zinc electrodes, with implications for optimizing their performance in various applications. Full article

Myocardial infarction (MI) remains one of the most common cardiovascular diseases and a leading cause of morbidity and mortality worldwide. In recent years, natural polymeric patches have attracted increasing attention as a promising therapeutic platform for myocardial tissue repair. This study explored the fabrication and evaluation of screen-printed electrodes (SPEs) on chitosan film as a novel platform for cardiac patch applications. Chitosan is a biodegradable and biocompatible natural polymer that provides an ideal substrate for SPEs, providing mechanical stability and promoting cell adhesion. Silver ink was employed to enhance electrochemical performance, and the electrodes exhibited strong adhesion and structural integrity under wet conditions. Mechanical testing and swelling ratio analysis were conducted to assess the patch’s physical robustness and aqueous stability. Silver ink was employed to enhance electrochemical performance, which was evaluated using cyclic voltammetry. In vitro, electrical stimulation through the chitosan–SPE patch significantly increased the expression of cardiac-specific genes (GATA-4, β-MHC, troponin I) in bone marrow mesenchymal stem cells (BMSCs), indicating early cardiogenic differentiation potential. In vivo, the implantation of the chitosan–SPE patch in a rat MI model demonstrated good tissue integration, preserved myocardial structure, and enhanced ventricular wall thickness, indicating that the patch has the potential to serve as a functional cardiac scaffold. These findings support the feasibility of screen-printed electrodes fabricated on chitosan film substrates as a cost-effective and scalable platform for cardiac repair, offering a foundation for future applications in cardiac tissue engineering. Full article

Aiming to contribute to environmental remediation strategies, this work proposes a novel fabrication of photoelectrocatalytic electrodes containing a BiOI coating deposited onto non-conductive glass (NCG) for CO₂ conversion applications. When BiOI electrodes are not deposited onto fluorine-doped tin oxide (FTO) or indium tin oxide (ITO) conductive supports, the electrochemical measurements enable the registration of the (photo)electrochemical response for bare BiOI, thereby excluding remnant signals from the conductive supports and reporting an exclusive and proper photoelectrocatalytic BiOI response. A systematic procedure was carried out to improve the physicochemical properties of BiOI through a simple variation in the amount of reagents employed in a solvothermal synthesis, thus increasing the crystallite size and surface area of the resulting material (BiOI-X3-20wt.%). The tailored BiOI coating on a non-conductive support showed activity in performing CO₂ photoelectroreduction under UV–Vis irradiation in aqueous media. Finally, the BiOI-X3-20wt.% sample was evaluated for photocatalytic CO₂ conversion in gaseous media, producing CO as the primary reaction product. This study confirms that BiOI is a suitable and easily synthesized material, with potential applications for CO₂ capture and conversion when employed as a photoactive coating for environmental remediation. Full article

Rechargeable aqueous zinc-ion batteries (AZIBs) have garnered significant research attention in the energy storage field owing to their inherent safety, cost-effectiveness, and environmental sustainability. Nevertheless, critical challenges associated with zinc anodes—including dendrite formation, hydrogen evolution corrosion, and mechanical degradation—substantially impede their practical implementation. Grain boundary engineering (GBE) emerges as an innovative solution for zinc anode optimization through the precise regulation of grain boundary density, crystallographic orientation, and chemical states in metallic materials. This study comprehensively investigates the fundamental mechanisms and application prospects of GBE in zinc-based anodes, providing pivotal theoretical insights and technical methodologies for designing highly stable electrode architectures. The findings are expected to promote the development of aqueous zinc batteries toward a high energy density and long cycle life. Full article

In this study, sugarcane bagasse (SCB), an abundant agricultural byproduct, was transformed into activated carbon via a controlled thermochemical pyrolysis route for high-performance energy storage applications. Herein, we utilized the activated carbon derived from pure sugarcane bagasse (SCB-AC) and further activated using KOH (SCB-KOH-AC) as an electrode material in aqueous symmetric supercapacitor configurations. The synthesized activated carbon was subjected to analysis using a range of characteristics including FT-Raman spectroscopy, which was employed to confirm the functional groups present in the carbon materials. The XPS analysis provided insights into the elemental composition and ionic states. The SEM analysis revealed that both activated carbon and KOH/activated carbon materials exhibited a layered or stacked, albeit slightly random, orientation. Electrochemical studies demonstrated that the synthesized carbon electrodes exhibited impressive specific capacitance values of (SCB) activated carbon (132.20 F/g) and KOH-activated, pure SCB AC (SCB-A) 253.41 F/g at 0.5 A/g. Furthermore, the SCB KOH-activated carbon (AC) electrode revealed a higher specific capacitance value and A//SCB-A symmetric devices delivered energy density reaching 17.91 Wh/kg and power density up to 2990 W/kg. The KOH-activated carbon electrode demonstrated remarkable cycling stability retaining 93.89%, even after 10,000 cycles. These results suggest that the sugarcane bagasse-derived activated carbon is a sustainable and low-cost candidate for next-generation supercapacitor electrodes. The results demonstrate enhanced capacitance, stability, and pore structure tailored for energy storage applications. The KOH-activated carbon SCB carbon symmetric device with symmetric electrodes exhibited a suitable bio-mass carbon for future energy storage applications. Full article

Layered transition metal dichalcogenides (TMDs) have gained considerable attention as promising cathodes for aqueous zinc-ion batteries (AZIBs) because of their tunable interlayer architecture and rich active sites for Zn²⁺ storage. However, unmodified TMDs face significant challenges, including limited redox activity, sluggish kinetics, and insufficient structural stability during cycling. These limitations are primarily attributed to their narrow interlayer spacing, strong electrostatic interactions, the large ionic hydration radius, and their high binding energy of Zn²⁺ ions. To address these restrictions, an in situ organic polyaniline (PANI) intercalation strategy is proposed to construct molybdenum disulfide (MoS₂)-based cathodes with extended layer spacing, thereby improving the zinc storage capabilities. The intercalation of PANI effectively enhances interplanar spacing of MoS₂ from 0.63 nm to 0.98 nm, significantly facilitating rapid Zn²⁺ diffusion. Additionally, the π-conjugated electron structure introduced by PANI effectively shields the electrostatic interaction between Zn²⁺ ions and the MoS₂ host, thereby promoting Zn²⁺ diffusion kinetics. Furthermore, PANI also serves as a structural stabilizer, maintaining the integrity of the MoS₂ layers during Zn-ion insertion/extraction processes. Furthermore, the conductive conjugated PANI boosts the ionic and electronic conductivity of the electrodes. As expected, the PANI–MoS₂ electrodes exhibit exceptional electrochemical performance, delivering a high specific capacity of 150.1 mA h g⁻¹ at 0.1 A g⁻¹ and retaining 113.3 mA h g⁻¹ at 1 A g⁻¹, with high capacity retention of 81.2% after 500 cycles. Ex situ characterization techniques confirm the efficient and reversible intercalation/deintercalation of Zn²⁺ ions within the PANI–MoS₂ layers. This work supplies a rational interlayer engineering strategy to optimize the electrochemical performance of MoS₂-based electrodes. By addressing the structural and kinetic limitations of TMDs, this approach offers new insights into the development of high-performance AZIBs for energy storage applications. Full article

Vanadium-based cathodes are promising for aqueous zinc-ion batteries (ZIBs) due to the large interlayer distance. However, the poor stability of electrode materials due to the dissolution effects has severely hindered the commercial development. To address this challenge, we propose an in situ NH₄⁺ pre-intercalation strategy to enhance the electrochemical performance of Na_0.76V₆O₁₅ (NaVO), thereby optimizing its structural stability and ionic conductivity. Moreover, NH₄⁺ pre-intercalation introduced a large number of oxygen vacancies and defects into the material, causing the reduction of V⁵⁺ to V⁴⁺. This transformation suppresses the dissolution and enhances its conductivity, thereby significantly improving the electrochemical performance. This modified NaNVO cathodes deliver a higher capacity of 456 mAh g⁻¹ at 0.1 A g⁻¹, with a capacity retention of 88% after 140 cycles and a long lifespan, maintaining 99% of its initial capacity after 2300 cycles. This work provided a new way to optimize the cathode for aqueous zinc-ion batteries. Full article

The release of synthetic dyes like Basic Red 46 (BR46) from industrial wastewater has raised growing concerns due to their toxicity, long-term persistence, and resistance to standard biological treatment methods. In this work, we developed and tested a pilot-scale electrocoagulation–ozonation (EC–O) hybrid system aimed at removing BR46 from aqueous solutions. The system integrates electrocoagulation, using iron electrodes, with ozone-based advanced oxidation processes, facilitating a combination of coagulation, adsorption, and oxidative breakdown of dye molecules. The response surface methodology (RSM) with a central composite design (CCD) was applied to optimize the treatment process, focusing on five variables: current density, flow rate, ozone dosage, ozonation time, and initial dye concentration. The quadratic model exhibited strong predictive power, with an adjusted R² of 0.9897 and a predicted R² of 0.9812. The optimal conditions identified included a current density of 70 A/m², flow rate of 1.6 L/min, ozone dose of 2.0 g/h, and an ozonation time of 20 min, achieving a predicted removal efficiency of 91.67% for a solution with BR46 at an initial concentration of 300 mg/L. Experiments conducted under these conditions confirmed the model’s reliability, with observed removal rates exceeding 90% and deviations under 2%. The EC–O system had a treatment capability of 26.19 L/h and an energy consumption of 3.04 kWh/m³. These findings suggest that the EC–O system is an effective and scalable option for treating dye-contaminated wastewater, offering faster and more efficient results than conventional techniques. 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 rapid development of energy storage technologies has led to an increasing demand for high-performance electrode materials that can enhance both the energy density and the cycling stability of batteries. In this study, polypyrrole (PPy) nanorods with partial hollow features are utilized as a conductive and flexible framework for the in situ growth of VO₂ nanospheres via a simple hydrothermal method, forming a well-defined core–shell PPy/VO₂ nanocomposite. This hierarchical nanostructure combines the excellent electrical conductivity and mechanical flexibility of PPy with the high theoretical capacity of VO₂, creating a synergistic effect that significantly enhances the electrochemical performance. The well-integrated interface between PPy and VO₂ reduces interfacial resistance, promotes efficient electron and ion transport, and improves the overall energy conversion efficiency. Electrochemical testing reveals that the PPy/VO₂ nanocomposite delivers a high specific capacity of 413 mAh g⁻¹ at 100 mA g⁻¹ and retains 87.2% of its initial capacity after 1200 cycles, demonstrating exceptional rate capability and long-term cycling stability. This work provides a versatile strategy for designing high-performance cathode materials and highlights the promising potential of PPy/VO₂ nanocomposites for next-generation high-energy-density aqueous zinc-ion batteries. Full article

In this study, we couple precise interface engineering via alternating current electrophoretic deposition (AC–EPD) with performance-enhancing structural transformation via annealing, enabling the development of high-performance, stable, and tunable Mn-based cathodes for aqueous zinc-ion batteries (ZIBs). Using AC–EPD to fabricate Mn(BTC) (BTC = 1,3,5-benzenetricarboxylic acid) cathodes followed by thermal annealing to synthesize MOF-derived Mn₃O₄ offers a synergistic approach that addresses several key challenges in aqueous ZIB systems. The Mn₃O₄ cathode prepared via AC–EPD from Mn(BTC) exhibited a remarkable specific capacity of up to 430 mAh/g at a current density of 200 mA/g. Interestingly, the capacity continued to increase progressively with cycling, suggesting dynamic structural or interfacial changes that improved Zn²⁺ transport and utilization over time. Such capacity enhancement behavior during prolonged cycling at elevated rates has not been observed in previously reported Mn₃O₄-based ZIB systems. Kinetic analysis further revealed that the charge storage process is predominantly governed by diffusion-controlled mechanisms. This behavior can be attributed to the intrinsic characteristics of the Mn₃O₄ phase formed from the MOF precursor, where the bulk redox reactions involving Zn²⁺ insertion require ion migration into the electrode interior. Even though the electrode was processed as an ultrathin film with enhanced electrolyte contact, the charge storage remains limited by solid-state ion diffusion rather than fast surface-driven reactions, reinforcing the diffusion-dominant nature of the system. Full article

In this study, a Zn(CN)₂–V₂O₃–C composite cathode was synthesized via AC electrophoretic deposition (EPD) and evaluated for application in aqueous zinc-ion batteries (ZIBs). Here, we report for the first time a binder-free Zn(CN)₂–V₂O₃–C composite cathode, using AC-EPD to create an ultrathin architecture optimized for probing the electrode–electrolyte interface without interference from additives or bulk effects. The composite combines Zn(CN)₂ for structural support, V₂O₃ as the redox-active material, and carbon for improved conductivity. X-ray diffraction confirmed the presence of Zn(CN)₂ and V₂O₃ phases, while scanning electron microscopy revealed a uniform, ultrathin film morphology. Electrochemical analysis demonstrated a hybrid charge storage mechanism with a b-value of 0.64, indicating both capacitive and diffusion-controlled contributions. The electrode delivered a high specific capacity (~250 mAh/g at 500 mA/g) with stable cycling performance. These results highlight the potential of metal–organic framework-derived composites for high-performance ZIB cathodes. The composite is especially effective when prepared via AC-EPD, which yields ultrathin, uniform films with strong adhesion and low agglomeration. This enhances energy storage performance and provides a reliable platform for focusing on interfacial charge storage, excluding the effect of binders on electrochemical performance. Full article

Aqueous zinc–ion batteries (AZIBs) have garnered considerable attention owing to their inherent safety, cost-effectiveness, and promising electrochemical performance. However, challenges associated with Zn metal anodes, such as dendrite formation, corrosion, and hydrogen evolution, continue to impede their widespread adoption. To overcome these limitations, a flexible and self-standing composite film anode (denoted ZCN) is engineered from a synergistic combination of Zn powder, nanocellulose, and carbon fiber to serve as a high-performance alternative to conventional Zn foil. These three constituents play the roles of enhancing the active area, improving mechanical properties and electrolyte affinity, and establishing a conductive network, respectively. This innovative design effectively mitigates dendrite growth and suppresses parasitic side reactions, thereby significantly improving the cycling stability of ZCN. As a result, this electrode enables the Zn//Zn cell to offer an ultralong lifespan of 2000 h. And the Zn-MnO₂ battery with ZCN anode demonstrates remarkable performance, realizing over 80% capacity retention after 1000 cycles. This study presents a straightforward, scalable, and cost-effective strategy for the development of dendrite-free metal electrodes, paving the way for durable and high-performance AZIBs. Full article