Search Results (229)

Over the past few decades, lithium-ion batteries (LIBs) have gained significant attention due to their inherent potential for environmental sustainability and unparalleled energy storage efficiency. Meanwhile, polymer electrolytes have gained popularity in several fields due to their ability to adapt to various battery geometries, enhanced safety features, greater thermal stability, and effectiveness in reducing dendrite growth on the anode. However, their relatively low ionic conductivity compared to liquid electrolytes has limited their application in high-performance devices. This limitation has led to recent studies revolving around the development of poly(ionic liquids) (PILs), particularly imidazolium-mediated polymer backbones as novel electrolyte materials, which can increase the conductivity with fine-tuning structural benefits, while maintaining the advantages of both solid and gel electrolytes. In this study, a curated dataset of 120 data points representing eight different polymers was used to predict ionic conductivity in imidazolium-based PILs as well as the emerging ionene substructures. For this purpose, four ML models: CatBoost, Random Forest, XGBoost, and LightGBM were employed by incorporating chemical structure and temperature as the models’ inputs. The best-performing model was further employed to estimate the conductivity of novel ionenes, offering insights into the potential of advanced polymer architectures for next-generation LIB electrolytes. This approach provides a cost-effective and intelligent pathway to accelerate the design of high-performance electrolyte materials. Full article

Electrochromic (EC) devices are gaining increasing attention for next-generation smart windows and low-power displays due to their reversible color modulation, low operating voltage, and flexible form factors. Recently, electrochromic energy storage devices (EESDs) have emerged as a promising class of multifunctional systems, enabling simultaneous energy storage and real-time visual monitoring. In this study, we report a flexible dual-functional EESD constructed using polyaniline (PANI) films doped with anthraquinone-1-sulfonic acid sodium salt (AQS), coupled with a redox-active PVA-based gel electrolyte also incorporating AQS. The incorporation of AQS into both the polymer matrix and the gel electrolyte introduces synergistic redox activity, facilitating bidirectional Faradaic reactions at the film–electrolyte interface and within the bulk gel phase. The resulting vertically aligned PANI-AQS nanoneedle films provide high surface area and efficient ion pathways, while the AQS-doped gel electrolyte contributes to enhanced ionic conductivity and electrochemical stability. The device exhibits rapid and reversible color switching from light green to deep black (within 2 s), along with a high areal capacitance of 194.2 mF·cm⁻² at 1 mA·cm⁻² and 72.1% capacitance retention over 5000 cycles—representing a 31.5% improvement over undoped systems. These results highlight the critical role of redox-functionalized gel electrolytes in enhancing both the energy storage and optical performance of EESDs, offering a scalable strategy for multifunctional, gel-based electrochemical systems in wearable and smart electronics. Full article

Solid-state electrolytes (SSEs) have emerged as a promising solution for next-generation lithium-ion batteries due to their excellent safety and high energy density. However, their practical application is still hindered by critical challenges such as their low ionic conductivity and high interfacial resistance at room temperature. The innovative application of 3D printing in the field of electrochemistry, particularly in solid-state electrolytes, endows energy storage devices with attractive characteristics. In this study, ceramic-in-gel polymer electrolytes (GPEs) based on PVDF-HFP/PAN@LLZTO were fabricated using a direct ink writing (DIW) 3D printing technique. Under the optimal printing conditions (printing speed of 40 mm/s and fill density of 70%), the printed electrolyte exhibited a uniform and dense sponge-like porous structure, achieving a high ionic conductivity of 5.77 × 10⁻⁴ S·cm⁻¹, which effectively facilitated lithium-ion transport. A structural analysis indicated that the LLZTO fillers were uniformly dispersed within the polymer matrix, significantly enhancing the electrochemical stability of the electrolyte. When applied in a LiFePO₄|GPEs|Li cell configuration, the electrolyte delivered excellent electrochemical performance, with high initial discharge capacities of 168 mAh·g⁻¹ at 0.1 C and 166 mAh·g⁻¹ at 0.2 C, and retained 92.8% of its capacity after 100 cycles at 0.2 C. This work demonstrates the great potential of 3D printing technology in fabricating high-performance GPEs. It provides a novel strategy for the structural design and industrial scalability of lithium-ion batteries. Full article

This study explores the development of aluminum-doped MgV₂O₄ spinel cathodes for aqueous zinc-ion batteries (AZIBs), addressing the challenges of poor Zn²⁺ ion diffusion and structural instability. Al³⁺ ions were pre-inserted into the spinel structure using a sol-gel method, which enhanced the material’s structural stability and electrical conductivity. The doping of Al³⁺ mitigates the electrostatic interactions between Zn²⁺ ions and the cathode, thereby improving ion diffusion and facilitating efficient charge/discharge processes. While pseudocapacitive behavior plays a dominant role in fast charge storage, the diffusion of Zn²⁺ within the bulk material remains crucial for long-term performance and stability. Our findings demonstrate that Al-MgV₂O₄ exhibits enhanced Zn²⁺ diffusion kinetics and robust structural integrity under high-rate cycling conditions, contributing to its high electrochemical performance. The Al-MgVO cathode retains a capacity of 254.3 mAh g⁻¹ at a high current density of 10 A g⁻¹ after 1000 cycles (93.6% retention), and 186.8 mAh g⁻¹ at 20 A g⁻¹ after 2000 cycles (90.2% retention). These improvements, driven by enhanced bulk diffusion and the stabilization of the crystal framework through Al³⁺ doping, make it a promising candidate for high-rate energy storage applications. Full article

Gel-polymer electrolytes offer a promising route toward safer and more stable sodium-ion batteries, but conventional polymer systems often suffer from low ionic conductivity and limited voltage stability. In this study, we developed composite GPEs by embedding methylammonium lead chloride (CH₃NH₃PbCl₃, MPCl) into a UV-crosslinked ethoxylated trimethylolpropane triacrylate (ETPTA) matrix, with sodium alginate (SA) as an ionic conduction enhancer. Three types of membranes—GPE-P, GPE-El, and GPE-Eh—were synthesized and systematically compared. Among them, the high-MPCl formulation (GPE-Eh) exhibited the best performance, achieving a high ionic conductivity of 2.14 × 10⁻³ S·cm⁻¹, a sodium-ion transference number of 0.66, and a wide electrochemical window of approximately 4.9 V vs. Na⁺/Na. In symmetric Na|GPE|Na cells, GPE-Eh enabled stable sodium plating/stripping for over 600 h with low polarization. In Na|GPE|NVP cells, it delivered a high capacity retention of ~79% after 500 cycles and recovered ~89% of its initial capacity after high-rate cycling. These findings demonstrate that the perovskite–polymer composite structure significantly improves ion transport, interfacial stability, and electrochemical durability, offering a viable path for the development of next-generation quasi-solid-state sodium-ion batteries. Full article

In polymer-based lithium batteries, polymer electrolytes (PEs) exhibit limited ionic conductivity at room temperature (25 °C). To address this issue, this paper describes a hexagonal-structure-based single-ion conducting gel polymer electrolyte (h-SICGPE) framework with a robust and efficient cross-linked polymer network, applicable to polymer-based batteries even at 25 °C. The proposed cross-linked polymer network backbone of the h-SICGPE, as a semisolid-state thin film type, has the homogeneous honeycomb structure incorporating anion receptor(s) inside each of its hexagonal closed cells and is obtained by cross-linking between trimethylolpropane tris(3-mercaptopropionate) and poly(ethylene glycol) diacrylate in a newly synthesized anion–receptor solution. The excellent structural capability of the h-SICGPE incorporating Li⁺/TFSI⁻ can enhance ionic conductivity and electrochemical stability by suppressing crystallinity and expanding free volume. Further, the anion receptor in its free volume helps to effectively increase the lithium-ion transference number by immobilizing counter-anions. Experimental results demonstrate dramatically superior performance at 25 °C, such as ionic conductivity (2.46 mS cm⁻¹), oxidative stability (4.9 V vs. Li/Li⁺), coulombic efficiency (97.65%), and capacity retention (88.3%). These results confirm the developed h-SICGPE as a promising polymer electrolyte for high-performance polymer-based lithium batteries operable at 25 °C. Full article

Controlled porosity with precise pore sizes in carbon monoliths (CMs) is crucial for optimizing performance in electrochemical energy storage and adsorption applications. This study explores the influence of porosity in CMs, developed from polymer precursors via the sol–gel route, employing soft templating, in situ graphene growth, and post-activation. The effects on CO₂ and H₂ sorption and electrochemical capacitor (EC) performance are analyzed. Graphene is successfully grown in situ from graphene oxide (GO), as confirmed by several characterization analyses. The amount of GO incorporated influences the crosslink density of the polymer gel, generating various pore structures at both micro- and mesoscales, which impacts performance. For instance, CO₂ capture peaks at 5.01 mmol g⁻¹ (0 °C, 101 kPa) with 10 wt % GO, due to the presence of wider micropores that allow access to ultramicropores. For H₂ storage, the best performance is achieved with 5 wt % GO, reaching 12.8 mmol g⁻¹ (−196 °C, 101 kPa); this is attributed to the enlarged micropore volumes between 0.75 and 2 nm that are accessible by mesopores of 2 to 3 nm. In contrast, for the ECs, lower GO loadings (0.5 to 2 wt %) improve ion accessibility via mesopores (4 to 6 nm), enhancing rate capability through better conduction. Full article

Gel electrolytes (GEs) play a pivotal role in the advancement of lithium metal batteries by offering high energy density and enhanced rate capability. Nevertheless, their real-world application is hampered by relatively low ionic conductivity and significant interfacial resistance at room temperatures. In this work, we developed a gel electrolyte membrane (GEM) by embedding Zeolitic Imidazolate Framework-8 (ZIF-8) metal–organic frameworks (MOFs) material into a poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) matrix through UV curing. The composite membrane, with 4 wt% ZIF-8, exhibited an ionic conductivity of 1.17 × 10⁻³ S/cm, an electrochemical stability window of 4.7 V, and a lithium-ion transference number of 0.7. The test results indicate that the electrochemical performance of LFP//GEM//Li battery has an initial specific capacity of 168 mAh g⁻¹ at 0.1 C rate. At 1 C, the discharge capacity was 88 mAh g⁻¹, and at 2 C, it was 68 mAh g⁻¹. Enhanced ionic transport, improved electrochemical stability, and optimized lithium-ion migration collectively contributed to superior rate performance and prolonged cycle life. This study offers novel insights and methodological advances for next-generation lithium metal batteries technologies. Full article

Alkali-activated-slag cementitious material (AASCM) is distinguished by minimal energy consumption, reduced pollution, and superior mechanical properties; however, it is prone to issues such as susceptibility to cracking and inadequate frost resistance. To facilitate its application in cold region construction, research on AASCM modifications was conducted following freeze-thaw cycle and chloride ion corrosion coupling tests. The test results show that the AASCM made of recycled rubber and coal ash does not change much in shape or appearance after 100 freeze-thaw cycles, with a mass loss rate of less than 5% and a compressive strength loss rate of less than 25%. Furthermore, the AASCM containing recycled rubber, coal ash, and straw fiber demonstrates an effective resistance to freeze-thaw and chloride ion coupling, maintaining its appearance and shape without notable changes and exhibiting a mass loss rate of less than 25% following 100 such tests. Following 100 tests for freeze-thaw and chloride ion coupling, the appearance and morphology of AASCM exhibited no significant alterations, with a mass loss rate below 5% and a compressive strength loss rate under 25%; microscopic analysis revealed that the C-A-S-H gel maintained a relatively dense and stable structure. Adding recycled rubber to the AASCM matrix can slow the spread of cracks, make the material more flexible, and make it more resistant to frost. Straw fibers can stop cracks from getting bigger, and adding coal ash helps make more C-A-S-H gel, which improves the AASCM’s mechanical properties. Full article

Removing residual energy from end-of-life batteries prior to transportation requires some method of deactivation. While many methods have been proposed, very few have been implemented due to limitations of cost, safety, and efficacy. In this work, multiple cell and battery types (e.g., lithium-polymer pouch cells, 18650 lithium-ion cell, alkaline batteries, and lithium-ion power-tool batteries) were deactivated using a low-cost and easily applied gel consisting of borax cross-linked polyvinyl alcohol and carbon. The PVA–carbon composite creates an external short-circuit pathway of moderate resistance that enables the complete discharge of batteries. Abusive testing conducted after deactivation demonstrates that hazards are largely eliminated, including a complete avoidance of thermal runaway from lithium-ion cells and a reduction in flammable and toxic gases by several orders of magnitude. Full article

Flexible wearable electronics face critical challenges in achieving reliable physiological monitoring, particularly due to the trade-off between sensitivity and durability in flexible electrodes, compounded by mechanical modulus mismatch with biological tissues. To address these limitations, we develop an anti-freezing ionic hydrogel through a chitosan/acrylamide/LiCl system engineered via the solution post-treatment strategy. The optimized hydrogel exhibits exceptional ionic conductivity (24.1 mS/cm at 25 °C) and excellent cryogenic tolerance. Leveraging these attributes, we construct a gel-based triboelectric nanogenerator (G-TENG) that demonstrates ultrahigh sensitivity (1.56 V/kPa) under low pressure. The device enables the precise capture of subtle vibrations at a frequency of 1088 Hz with a signal-to-noise ratio of 16.27 dB and demonstrates operational stability (>16,000 cycles), successfully differentiating complex physiological activities including swallowing, coughing, and phonation. Through machine learning-assisted analysis, the system achieves 96.56% recognition accuracy for five words and demonstrates good signal recognition ability in different ambient sound scenarios. This work provides a paradigm for designing environmentally adaptive wearable sensors through interfacial modulus engineering and ion transport optimization. Full article

Solid-state electrolytes are widely expected to enhance the performance of lithium-ion batteries, providing higher energy density and improved safety. However, challenges still need to be solved in their practical application due to low ionic conductivity and high interfacial resistance at room temperature. In this study, we successfully developed a high-performance gel polymer electrolyte (GPEs) by blending poly(vinylidene fluoride-co-hexafluoropropylene)(PVDF-HFP) and polyacrylonitrile (PAN) through UV curing, cross-linking with ethoxylated trimethylolpropane triacrylate (ETPTA), and incorporating Li_6.4La₃Zr_1.4Ta_0.6O₁₂ (LLZTO). At room temperature, the ionic conductivity of the GPEs was 2.8 × 10⁻⁴ S/cm, with a lithium-ion transference number of 0.6. Moreover, during lithium plating/stripping tests, the assembled Li/PPEL/Li symmetric cell exhibited stable cycling for up to 600 h at a current density of 0.1 mA/cm². Notably, the GPEs enabled the LiFePO₄/GPEs/Li battery to achieve excellent performance, delivering high discharge capacities at room temperature (164.3 mAh g⁻¹ at 0.1 C and 88.8 mAh g⁻¹ at 1 C), with a capacity retention of 89.4% after 200 cycles at 0.5 C. Therefore, solid-state batteries using this electrolyte exhibit excellent performance, including adequate capacity and cycling stability. Full article

Gel polymer electrolyte (GPE) with a polymer matrix swollen in liquid electrolytes offers several advantages over conventional liquid electrolytes, including no leakage, lightweight properties, and high reliability. While poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)-based GPEs show promise for lithium-ion batteries, their practical application is hindered by the intrinsic trade-off between ionic conductivity and mechanical robustness in conventional PVDF systems. Typical strategies relying on excessive plasticizers (e.g., ionic liquids) compromise mechanical integrity. Here, we propose a novel hot-pressing-induced recrystallization strategy to synergistically enhance both anisotropic ionic conductivity and puncture strength in PVDF-based GPE films. By blending PVDF with controlled amounts of 1-hexyl-3-methylimidazolium chloride ([HMIM]Cl), followed by solution casting and hot pressing, we achieve microstructural reorganization that dramatically improves through-thickness ion transport and mechanical performance. Crucially, hot-pressed PVDF with only 25 wt% [HMIM]Cl exhibits a 12.5-fold increase in ionic conductivity (reaching 4.7 × 10⁻⁴ S/cm) compared to its solution-cast counterparts. Remarkably, this formulation surpasses the conductivity of PVDF-HFP composites with a higher [HMIM]Cl content (35 wt%, 1.7 × 10⁻⁴ S/cm), demonstrating performance optimization of anisotropic conductivity. What is more, the mechanical strength of the piercing strength perpendicular to the GPE film after hot pressing increased by 42% compared to the solution-cast film. This work establishes a scalable processing route to break the conductivity–strength dichotomy in GPEs, offering critical insights for designing high-performance polymer electrolytes. Full article

This paper describes the synthesis and evaluation of samarium-doped 45S5 bioactive glass in various ratios. The bioactive glass samples were prepared using the sol–gel method and subjected to a heat treatment at 700 °C in normal atmosphere. The obtained samples were analyzed by thermogravimetric analysis (TGA) before and after the heat treatment to assess their thermal stability and compositional changes. The bioactivity of the samples was tested in vitro by immersion in simulated body fluid (SBF) at 36.5 ± 0.5 °C (normal human body temperature) and pH 7.4 (the pH of the human blood plasma), for several time periods. During the test, the pH and conductivity of the SBF solutions were monitored to track ion migration. After the in vitro test, the mass loss was evaluated and the formation of hydroxycarbonate apatite (HCA) was analyzed by FTIR spectroscopy. The microstructure of the bioactive glasses was examined using scanning electron microscopy (SEM) and the density of bioactive glass was also determined using Archimedes’ principle. This study also investigated the antimicrobial and anti-biofilm properties of both undoped and samarium-doped 45S5 bioactive glass through qualitative and quantitative assays against a range of microorganisms, including Gram-negative, Gram-positive, and yeast reference strains. The results were compared with literature data on melt-derived bioactive glass to evaluate the effects of Sm doping and the sol–gel synthesis method on bioactive glass performance. Full article

Ion-conductive gels (ICGs) are essential for achieving human–machine interfaces, bioelectronic applications, or durable wearable sensors. However, traditional solvent-dependent ICGs face bottlenecks such as dehydration-induced failure and challenges in achieving a balance between conductivity and mechanical properties. Here, this work developed a novel ternary ion-conductive xerogel (PEM-Li ICXG) system based on polyethylene glycol (PEG), poly (2-methoxyethyl acrylate) (PMEA), and LiTFSI. PEM-Li ICXGs exhibit high conductivity (2.7 × 10⁻² S/m), high adhesive capability (0.34 MPa), and solvent-free characteristics. Remarkably, the incorporation of ions into ICXGs simultaneously optimizes their mechanical performance. We demonstrate the application of ICGs in flexible sensors for strain or temperature sensing. The proposed synthesis strategy is straightforward and may further inspire the design of novel high-performance ICXGs. Full article