Search Results (292)

Polyampholytes combine cationic and anionic groups in one macromolecular platform and are emerging as versatile components for energy storage and conversion. This review synthesizes how their charge balance, hydration, and architecture can be engineered to address ionic transport, interfacial stability, and safety across batteries, supercapacitors, solar cells, and fuel cells. We classify annealed, quenched, and zwitterionic systems, outline molecular design strategies that tune charge ratio, distribution, and crosslinking, and compare device roles as gel or solid electrolytes, eutectogels, ionogels, binders, separator coatings, and interlayers. Comparative tables summarize ionic conductivity, cation transference number, electrochemical window, mechanical robustness, and temperature tolerance. Across Li and Zn batteries, polyampholytes promote ion dissociation, homogenize interfacial fields, suppress dendrites, and stabilize interphases. In supercapacitors, antifreeze hydrogels and poly(ionic liquid) networks maintain conductivity and elasticity under strain and at subzero temperature. In solar cells, zwitterionic interlayers improve work function alignment and charge extraction, while ordered networks in fuel cell membranes enable selective ion transport with reduced crossover. Design rules emerge that couple charge neutrality with controlled hydration and dynamic crosslinking to balance conductivity and mechanics. Key gaps include brittleness, ion pairing with multivalent salts, and scale-up. Opportunities include soft segment copolymerization, ionic liquid and DES plasticization, side-chain engineering, and operando studies to guide translation. Full article

Conductive hydrogels are ideal for flexible strain sensors, yet their practical use is often limited by water evaporation, signal hysteresis, and structural instability, which impair linearity, durability, and long-term reliability. To overcome these challenges, we developed a robust multiple-network hydrogel composed of poly(vinyl alcohol) (PVA), polyacrylic acid (PAA), in situ polymerized polyaniline (PANi), and the ionic liquid [EMIM][TFSI]. The resulting composite exhibits an exceptional linear piezoresistive response across its entire working range—from rest to fracture strain of 290%—together with high conductivity (0.68 S/cm), fast response/recovery (0.34 s/0.35 s), and a maximum gauge factor of 2.78. Mechanically robust (tensile strength ≈ 3.7 MPa, modulus ≈ 1.3 MPa), the hydrogel also demonstrates outstanding cyclic durability, withstanding over 12,000 stretching–relaxation cycles, and markedly improved dehydration resistance, retaining about 60% of its mass after 3 days at room temperature. This work provides a holistic material solution for developing high-performance, reliable strain sensors suitable for wearable electronics and soft robotics. Full article

Polylactic acid (PLA) is considered as an attractive polymer due to its renewable origin, biodegradability, and promising tensile strength and modulus. However, its inherent brittleness, characterized by a low impact resistance and elongation at break, can significantly restrict its application. This work proposes a new insight to improve the toughness of PLA while keeping its biocompatibility by incorporating two biocompatible ionic liquids (ILs), 1-ethyl-3-methylimidazolium ethyl sulfate ([emim][EtSO₄]), and tris(2-hydroxyethyl) methylammonium methylsulfate ([Tris][MeSO₄]). The modified PLA systems were thoroughly characterized to evaluate their mechanical and thermal behavior. Results demonstrated that the addition of 1 wt% of either IL resulted in significant improvement in modulus. Increasing the amount of IL resulted in an increase in the toughness while maintaining the material’s original stiffness and also the thermal stability. Furthermore, the foaming potential of the modified PLA using supercritical CO₂ was investigated as an environmentally friendly processing method. The ionic liquids contributed positively to the foamability of the material, suggesting improved gas solubility and cell nucleation during the foaming process. The addition of both IL decreased the cell size and resulted in narrower cell size distribution. These findings highlight the potential of ionic liquid-modified PLA systems for the processing of lightweight, and high-performance packaging materials. Full article

Solid polymer and composite polymer electrolytes have been investigated as a replacement for liquid electrolytes in lithium batteries and have shown promising conductivities at room temperature. However, the literature reports often do not fully investigate the effects of residual solvent or testing apparatus conditions, leading to discrepancies in reported performance and possible conflation of conductivity values. Using combinations of poly (vinylidene fluoride-co-hexafluoropropylene), succinonitrile, and lithium lanthanum zirconium tantalum oxide, this work aims to develop an understanding of how polymer electrolyte composition, including solvent retention, affects conductivity. A custom-designed controllable pressure test fixture was utilized to determine ionic conductivity of the composite polymer electrolyte films at a wide range of pressures (1.5–18.7 psi) and temperatures 10–90 °C. Applied pressure during testing greatly influences apparent conductivities, with optimal composite film conductivity values ranging from 1.2 × 10⁻⁵ to 4.1 × 10⁻⁵ S cm⁻¹ at room temperature. At elevated temperatures, the composite films achieved greater than 1 mS cm⁻¹. The ideal pressure was found to be dependent on the polymer electrolyte additives. Symmetric cell testing showed over 99% Coulombic efficiency for over one hundred cycles at 0.1 mA cm⁻². The results of this work highlight the importance of careful characterization of electrolyte films and controlled test fixture pressure when developing polymer electrolytes. 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

Enhancing the safety of lithium-ion batteries (LIBs) by replacing flammable electrolytes is a key challenge. Ionic liquid (IL)-based electrolytes are considered an interesting alternative due to their thermal and chemical stability, high voltage stability window, and tunable properties. This study investigates the electrochemical behavior of two newly synthesized ILs, comparing them to conventional alkyl carbonate-based electrolytes. Nitrogen-doped carbon silicon oxycarbide (NC-SiOC), used as the active material in negative electrodes, was combined with two polymeric binders: poly(acrylic acid) (PAA) and poly(acrylonitrile) (PAN). NC-SiOC/PAN electrodes exhibited a significantly higher initial charge capacity—approximately 25–30% greater than their PAA-based counterparts in the first cycle at 0.1 A g⁻¹ (850–990 mAh g⁻¹ vs. 600–700 mAh g⁻¹), and demonstrated an improved initial Coulombic efficiency (67% vs. 62%). Long-term cycling stability over 1000 cycles at 1.6 A g⁻¹ retained 75–80% of the initial 0.1 A g⁻¹ capacity. This outstanding performance is attributed to the synergistic effects of nitrogen-rich carbonaceous phases within the NC-SiOC material and the cyclized-PAN binder, which facilitate structural stability by accommodating volumetric changes and enhancing solid electrolyte interphase (SEI) stability. Notably, despite the lower ionic transport properties of the IL electrolytes, their incorporation did not compromise performance, supporting their feasibility as safer electrolyte alternatives. These findings offer one of the most promising electrochemical performances reported for SiOC materials to date. Full article

Poly(ionic liquids) (PILs) show great promise as a new class of solid electrolytes for energy applications, including high-temperature polymer electrolyte fuel cells, owing to their combination of the unique electrochemical properties of ionic liquids and macromolecular architecture. In this study, we prepared and characterized PIL-based composite polymer electrolyte membranes containing silica nanofibers (SiO₂NFs). The SiO₂NFs were prepared via electrospinning, followed by calcination, and were used as a thermally and mechanically stable, porous substrate. The crosslinked protic PIL was synthesized via in situ radical polymerization of imidazolium hydrogensulfate-based reagents (one monomer and one crosslinker). It was then used as the membrane matrix. The prepared freestanding PIL membranes remained thermally stable at temperatures of up to 180 °C. Furthermore, the PIL/SiO₂NF composite electrolyte membranes demonstrated improved mechanical properties due to reinforcement by the NF framework. These composite membranes also exhibited relatively high proton conductivity (approximately 0.1 to 1 mS/cm) in the 100–150 °C temperature range. Full article

The rising concentration of atmospheric carbon dioxide (CO₂), driven largely by fossil fuel combustion, is a major contributor to global climate change and ocean acidification. As conventional CO₂ capture technologies, primarily amine-based solvents, face challenges such as high energy requirements, volatility, and degradation, there is an urgent need for alternative materials that are both efficient and sustainable. Ionic liquids (ILs) and poly (ionic liquids) (PILs) have emerged as promising candidates due to their unique physicochemical properties, including negligible vapor pressure, high thermal and chemical stability, structural tunability, and strong CO₂ affinity. This review provides a comprehensive overview of recent advancements in the design, synthesis, and application of ILs and PILs for CO₂ capture. We examine the mechanisms of CO₂ absorption in IL and PIL systems, analyze the structure-property relationships influencing capture performance, and compare their advantages and limitations relative to conventional solvents. Special attention is given to the role of functional groups, anion/cation selection, and polymeric architectures in enhancing CO₂ uptake and reducing regeneration energy. Finally, the review highlights current challenges and future research directions for scaling up IL and PIL-based technologies in industrial carbon capture and sequestration systems. Full article

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

To address the challenge of ultra-deep desulfurization in fuels, a series of heteropolyacid-based poly(ionic liquid) catalysts (C4-PIL@PW, C8-PIL@PW, and C16-PIL@PW) were synthesized via radical polymerization and anion exchange methods. The prepared catalysts were characterized via FT-IR, XRD pattern, and Raman spectroscopy. Optimal reaction parameters (e.g., temperature, catalyst dosage, and O/S molar ratio) were systematically investigated, as well as the catalytic mechanism. The typical sample C8-PIL@PW exhibited exceptional oxidative desulfurization (ODS) performance, achieving a sulfur removal of 99.2% for dibenzothiophene (DBT) without any organic solvent as extractant. Remarkably, the sulfur removal could still retain 89% after recycling five times without regeneration. This study provides a sustainable and high-efficiency catalyst for ODS, offering insights into fuel purification strategies. Full article

In the past, powder-like microwave absorbers have made notable breakthroughs in performance enhancements, but complicated processes and undesirable properties have limited their practical application. Herein, a novel poly(ionic liquid) (PIL)-based ionic gel with excellent microwave absorption properties was prepared via a facile UV-initiated polymerization method. By simply adjusting the mole ratio of the polymerizable ionic liquid (IL)monomer and the IL dispersion medium, the microwave absorption properties of the obtained ionic gels can be tuned. A maximum reflection loss (RL_max) of −45.7 dB and an effective absorption bandwidth (EAB) of 8.08 GHz were achieved, which was mainly ascribed to high ionic conduction loss induced by the high content of the dispersion medium. Furthermore, it displayed recyclable, adhesive, and self-healing properties, thus providing a new candidate for developing efficient microwave absorbers for practical applications. Full article

Lithium-ion batteries are restricted in development due to safety issues such as poor chemical stability and flammability of organic liquid electrolytes. Replacing liquid electrolytes with solid ones is crucial for improving battery safety and performance. This study aims to enhance the performance of polyethylene oxide (PEO)-based polymer via blending with poly(vinylidene fluoride-hexafluoropropylene) (P(VDF-HFP)). The experimental results showed that the addition of P(VDF-HFP) disrupted the crystalline regions of PEO by increasing the amorphous domains, thus improving lithium-ion migration capability. The electrolyte membrane with 30 wt% P(VDF-HFP) and 70 wt% PEO exhibited the highest ionic conductivity, widest electrochemical window, and enhanced thermal stability, as well as a high lithium-ion transference number (0.45). The cells assembled with this membrane electrolyte demonstrated an excellent rate of performance and cycling stability, retaining specific capacities of 122.39 mAh g⁻¹ after 200 cycles at 0.5C, and 112.77 mAh g⁻¹ after 200 cycles at 1C and 25 °C. The full cell assembled with LiFePO₄ as the positive electrode exhibits excellent rate performance and good cycling stability, indicating that prepared solid electrolytes have great potential applications in lithium batteries. Full article

Cultural Heritage is a vital socioeconomic driver that must contend with works of art continuously exposed to degradation processes, which are further exacerbated by climate change. Aged coatings, varnishes, and soil can compromise the appearance of artworks, preventing their preservation and valorization. In response, soft matter and colloidal systems, such as nanostructured cleaning fluids (NCFs), have proved to be valuable solutions for safely and effectively cleaning works of art. Here, a novel cleaning system is proposed, for the first time employing microgels of poly(N-isopropylacrylamide) (PNIPAM) with surface chains of oligoethylene glycol methyl ether methacrylate (OEGMA) to favor shear deformation by lubrication. These microgels are loaded with NCFs featuring “green” solvents and different kinds of bio-derived or petroleum-based surfactants (non-ionic, zwitterionic). Rheological characterization of the combined systems highlighted a sharp transition from solid to liquid-like state in the 21–24 °C range when the zwitterionic surfactant dodecyldimethylamine oxide was used; the system displays a solid-like behavior at rest but flows easily at intermediate strains. At slightly higher temperature (>24 °C), an inversion of the G′, G″ values was observed, leading to a system that behaves as a liquid. Such control of rheological behavior is significant for feasible and complete removal of soiled polymer coatings from textured ceramic surfaces, which are difficult to clean with conventional gels, without leaving residues. These results position the PNIPAM-OEGMA microgels as promising cleaning materials for the conservation of Cultural Heritage, with possible applications also in fields where gelled systems are of interest (pharmaceutics, cosmetics, detergency, etc.). Full article

Strategic utilization of carbon dioxide as both a carbon mitigation tool and a sustainable C1 feedstock represents a pivotal pathway toward green chemistry. Although poly(ionic liquid)s (PILs) exhibit promise in CO₂ conversion, conventional divinylbenzene (DVB) cross-linked architectures are limited by reduced ionic density and limited accessibility of active sites. Herein, we reported a binuclear imidazolium-functionalized PIL catalyst (P-BVIMCl), synthesized through a simple self-polymerization process, derived from rationally designed ionic liquid monomers formed by quaternization of 1,4-bis(chloromethyl)benzene with N-vinylimidazole. The dual active sites in P-BVIMCl-quaternary ammonium cation (N⁺) and nucleophilic chloride anion (Cl⁻) synergistically enhanced CO₂ adsorption/activation and epoxide ring-opening. Under optimal catalyst preparation conditions (100 °C, 24 h, water/ethanol = 1:3 (v/v), 10 wt% AIBN initiator) and reaction conditions (100 °C, 2.0 MPa CO₂, 10 mmol epichlorohydrin, 6.7 wt% catalyst loading, 3.0 h), P-BVIMCl catalyzed the synthesis of glycerol carbonate (GLC) with a yield of up to 93.4% and selectivity of 99.6%, maintaining activity close to 90% after five cycles. Systematic characterization and density functional theory (DFT) calculations confirmed the synergistic activation mechanism. This work established a paradigm for constructing high-ionic-density catalysts through molecular engineering, advancing the development of high-performance PILs for industrial CO₂ valorization. Full article