Search Results (191)

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

Batteries are used as energy storage devices in various equipment. Today, research is focused on solid-state batteries (SSBs), replacing the liquid electrolyte with a solid separator. The solid separators provide electrolyte stability, no leakage, and provide mechanical strength to the battery. Separators are mostly manufactured by either traditional processes or 3D printing technologies. These processes involve making a slurry of plastic, active and conductive material and usually adding a plasticizer when making thin films or filaments for 3D printing. This study investigates the additive manufacturing of solid-state electrolytes (SSEs) by employing fused deposition modeling (FDM) with recyclable, bio-derived polylactic acid (PLA) filaments. Precise control of macro-porosity is achieved by systematically varying key process parameters, including raster orientation, infill percentage, and interlayer adhesion conditions, thereby enabling the formation of tunable, interconnected pore networks within the polymer matrix. Following 3D printing, these engineered porous frameworks are infiltrated with lithium hexafluorophosphate (LiPF₆), which functions as the active ionic conductor. A tailored thermal sintering protocol is then applied to promote solid-phase fusion of the embedded salt throughout the macro-porous PLA scaffold, resulting in a mechanically robust and ionically conductive composite separator. The electrochemical ionic conductivity and structural integrity of the sintered SSEs are characterized through electrochemical impedance spectroscopy (EIS) and standardized mechanical testing to assess their suitability for integration into advanced solid-state battery architectures. The solid-state separator achieved an average ionic conductivity of 2.529 × 10⁻⁵ S·cm⁻¹. The integrated FDM-sintering process enhances ion exchange at the electrode–electrolyte interface, minimizes material waste, and supports cost-efficient, fully recyclable component fabrication. 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

The application of graphene nanoplatelets (GNPs) in polymer composites is a challenge due to their high tendency to agglomerate and restack during processing. In this work, alkyl phosphonium-based ionic liquid was used to assist the dispersion of GNP in an ethylene-vinyl acetate (EVA) matrix, through a melt-mixing procedure. The mechanical properties and creep resistance of the films prepared by the film extrusion process were evaluated. The results demonstrated that the noncovalent treatment of GNP with the ionic liquid (IL) enhanced the electrical conductivity and creep stability of the EVA composites. The microwave absorbing properties were studied in the X-band and Ku-band. A reflection loss (RL) of −15 dB for EVA containing 0.5 wt% of GNP and 1:1 wt% of GNP/IL was achieved. The use of a multi-layered structure containing thin film layers was efficient for enhancing the microwave absorbing performance, with a minimum RL of −24.6 dB and effective absorption bandwidth of 4.3 GHz. This result is attributed to the internal reflection and scattering of the radiation between layers. The use of simple, low-cost materials and procedures, combined with the system’s excellent mechanical and electrical properties, makes it a promising candidate for multifunctional applications as electrostatic dissipative and microwave absorbing materials for electronic packaging and other electronic devices. Full article

Fractured vuggy reservoirs exhibit intricate fracture networks, where large fractures impose significant shielding effects on smaller ones, posing formidable challenges for efficient exploitation. A systematic evaluation of foaming volume, drainage half-life, decay behavior, and viscosity under varying temperatures and salinities was conducted for conventional foam, polymer-enhanced foam, and gel foam. The results yield the following conclusions: Compared to conventional foam, polymer-enhanced foam exhibits markedly improved stability. In contrast, gel foam, cross-linked with chemical agents, maintains stability for over one week at elevated temperatures, albeit at the expense of reduced foaming capacity. The three-dimensional network structure formed post-gelation enables gel foam to retain a thicker liquid film, exhibiting exceptional foam stability. As salinity increases, the base liquid viscosity of conventional foam remains largely unaffected, whereas polymer foam shows marked viscosity reduction. Gel foam displays a non-monotonic viscosity response—initially increasing due to ionic cross-linking and subsequently declining from excessive charge screening. All three systems exhibit significant viscosity decreases under high-temperature conditions. Visualized plate fracture model experiments revealed distinct flow patterns and mobility control performance; narrow fractures exacerbate bubble coalescence under shear stress, leading to enlarged bubble sizes and diminished plugging efficiency. Among the three systems, gel foam exhibited superior mobility control characteristics, with uniform bubble size distribution and enhanced stability. Integrating the findings from the foam mobility control experiments in parallel fracture systems with the diversion outcomes of mobility control and flooding, distinct performance trends emerge. It can be seen that the stronger the foam stability, the stronger the mobility control ability, and the easier it is to start the shielding effect. Combined with the stability of different foam systems, understanding the mobility control ability of a foam system is the key to increasing the sweep coefficient of a complex fracture network and improve oil-washing efficiency. Full article

Ionic polymer–metal composites (IPMC) have the advantages of a large driving mass ratio, low driving voltage, and high current sensitivity, but their low electrode continuity, low energy storage, and unclear driving response mechanisms limit further application and development. In this study, Nafion is used as the base film and metallic silver is used as the electrode material to modify IPMC electrodes. The physical and electrochemical properties of silver-based IPMC with three electrode preparation processes are tested, and the effects of different electrode preparation processes and structures on the energy storage performance and driving performance of IPMC are analyzed. The results show that the electrode coating effect of the Hot Press Chemical Plating method (HPCP) is good and maintains better continuity, and the formed layer electrode can improve the energy storage performance of IPMC, and the enhancement of energy storage performance can improve the driving performance of IPMC. This study enhances the energy storage performance and driving performance of IPMC from the perspective of electrode process and structure and provides a basis for the study of the enhancement of energy storage performance of IPMC by the HPCP electrode preparation process. Full article

Coordination polymers are attractive materials for various fields of practical application. The high degree of freedom of choice of metal ions and organic ligands plays a critical role in functional diversification. In the present study, we report the liquid–liquid interfacial synthesis of a 2D bis(terpyridine)copper(II) polymer thin film, Cu-tpy. The synthesized Cu-tpy was characterized by various microscopic observations such as TEM, SEM, and AFM, and spectroscopic measurements such as XPS, Raman spectroscopy, SEM/EDS, and UV–Vis spectroscopy. Synchrotron-radiated X-ray scattering confirmed that Cu-tpy was oriented crystalline films. Moreover, Cu-tpy showed electrochemical micro-supercapacitor behavior in the solid-state owing to its ionic nature. This study expands the potential of bis(terpyridine)metal(II) polymers as electro-functional materials. Full article

Polyphenylene sulfide (PPS)-based separators have garnered significant attention as high-performance components for next-generation lithium-ion batteries (LIBs), driven by their exceptional thermal stability (>260 °C), chemical inertness, and mechanical durability. This review comprehensively examines advances in PPS separator design, focusing on two structurally distinct categories: porous separators engineered via wet-chemical methods (e.g., melt-blown spinning, electrospinning, thermally induced phase separation) and nonporous solid-state separators fabricated through solvent-free dry-film processes. Porous variants, typified by submicron pore architectures (<1 μm), enable electrolyte-mediated ion transport with ionic conductivities up to >1 mS·cm⁻¹ at >55% porosity, while their nonporous counterparts leverage crystalline sulfur-atom alignment and trace electrolyte infiltration to establish solid–liquid biphasic conduction pathways, achieving ion transference numbers >0.8 and homogenized lithium flux. Dry-processed solid-state PPS separators demonstrate unparalleled thermal dimensional stability (<2% shrinkage at 280 °C) and mitigate dendrite propagation through uniform electric field distribution, as evidenced by COMSOL simulations showing stable Li deposition under Cu particle contamination. Despite these advancements, challenges persist in reconciling thickness constraints (<25 μm) with mechanical robustness, scaling solvent-free manufacturing, and reducing costs. Innovations in ultra-thin formats (<20 μm) with self-healing polymer networks, coupled with compatibility extensions to sodium/zinc-ion systems, are identified as critical pathways for advancing PPS separators. By addressing these challenges, PPS-based architectures hold transformative potential for enabling high-energy-density (>500 Wh·kg⁻¹), intrinsically safe energy storage systems, particularly in applications demanding extreme operational reliability such as electric vehicles and grid-scale storage. Full article

The growing burden of degenerative, cardiovascular, neurodegenerative, and cancerous diseases necessitates innovative approaches to improve our pathophysiological understanding and ability to modulate biological processes. Organic bioelectronics has emerged as a powerful tool in this pursuit, offering a unique ability to interact with biology due to the mixed ionic–electronic conduction and tissue-mimetic mechanical properties of conducting polymers (CPs). These materials enable seamless integration with biological systems across different levels of complexity, from monolayers to complex 3D models, microfluidic chips, and even clinical applications. CPs can be processed into diverse formats, including thin films, hydrogels, 3D scaffolds, and electrospun fibers, allowing the fabrication of advanced bioelectronic devices such as multi-electrode arrays, transistors (EGOFETs, OECTs), ion pumps, and photoactuators. This review examines the integration of CP-based bioelectronics in vivo and in in vitro microphysiological systems, focusing on their ability to monitor key biological events, including electrical activity, metabolic changes, and biomarker concentrations, as well as their potential for electrical, mechanical, and chemical stimulation. We highlight the versatility and biocompatibility of CPs and their role in advancing personalized medicine and regenerative therapies and discuss future directions for organic bioelectronics to bridge the gap between biological systems and electronic technologies. 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

Solid polymer electrolytes (SPEs) are gaining attention as viable alternatives to traditional aqueous electrolytes in zinc–air batteries (ZABs), owing to their enhanced performance and stability. In this study, anion-exchange solid polymer electrolytes (A-SPEs) were synthesized via electrophilic aromatic substitution and substitution reactions. Thin films were prepared using the solvent casting method and characterized using proton nuclear magnetic resonance (¹H-NMR), Fourier-transform infrared spectroscopy (FT-IR), and thermogravimetric analysis (TGA). The ion-exchange capacity (IEC), KOH uptake, ionic conductivity, and battery performance were also obtained by varying the degree of functionalization of the A-SPEs (30 and 120%, denoted as PSf30/PSf120, respectively). The IEC analysis revealed that PSf120 exhibited a higher quantity of functional groups, enhancing its hydroxide conductivity, which reached a value of 22.19 mS cm⁻¹. In addition, PSf120 demonstrated a higher power density (70 vs. 50 mW cm⁻²) and rechargeability than benchmarked Fumapem FAA-3-50 A-SPE. Postmortem analysis further confirmed the lower formation of ZnO for PSf120, indicating the improved stability and reduced passivation of the zinc electrode. Therefore, this type of A-SPE could improve the performance and rechargeability of all-solid-state ZABs. Full article

Chemical vapor deposition (CVD) is a highly adaptable manufacturing technique used to fabricate high-quality thin films, making it essential across numerous industries. As materials fabrication processes progress, CVD has advanced to enable the precise deposition of both inorganic 2D materials, such as graphene and transition metal dichalcogenides, and high-quality polymeric thin films, offering excellent conformality and precise nanostructure control on a wide range of substrates. Conjugated conducting polymers have emerged as promising materials for next-generation electronic, optoelectronic, and energy storage devices due to their unique combination of electrical conductivity, optical transparency, ionic transport, and mechanical flexibility. Oxidative CVD (oCVD) involves the spontaneous reaction of oxidant and monomer vapors upon their adsorption onto the substrate surface, resulting in step-growth polymerization that commonly produces conducting or semiconducting polymer thin films. oCVD has gained significant attention for its ability to fabricate conjugated conducting polymers under vacuum conditions, allowing precise control over film thickness, doping levels, and nanostructure engineering. The low to moderate deposition temperature in the oCVD method enables the direct integration of conducting and semiconducting polymer thin films onto thermally sensitive substrates, including plants, paper, textiles, membranes, carbon fibers, and graphene. This review explores the fundamentals of the CVD process and vacuum-based manufacturing, while also highlighting recent advancements in the oCVD method for the fabrication of conjugated conducting and semiconducting polymer thin films. Full article

The rational design of ordered chromogenic supramolecular polymeric systems is critical for the advancement of next-generation stimuli-responsive, optical, and semiconducting materials. Previously, we reported the design of a stimuli-responsive, lamellar self-assembled platform composed of an imidazole-appended perylene diimide of varying methylene spacer length (n = 3, 4, and 6) and a commercially available diacid-functionalized diacetylene monomer, 10, 12 docosadiynedioic acid, in a 1:1 molar ratio. Herein, we expound on the importance of the composition of the imidazole-appended perylene diimide of varying methylene spacer length (n = 3, 4, and 6) and 10, 12 docosadiynedioic acid in the ratio of 2:1 to the supramolecular self-assembly, final morphology, and properties. Topochemical polymerization of the drop-cast films by UV radiation yielded blue-phase polydiacetylene formation, and subsequent thermal treatment of the films produced a thermoresponsive blue-to-red phase transformation. Differential scanning calorimetry (DSC) studies revealed a dual dependence of the methylene spacer length and stimuli treatment (UV and/or heat) on the thermal transitions of the films. Furthermore, small-angle X-ray scattering (SAXS) and wide-angle X-ray scattering (WAXS) showed well-defined hierarchical semiconducting nanostructures with interconnected “chessboard”-patterned lamellar stacking. Upon doping with an ionic liquid, the 2:1 platform showed higher ionic conductivity than the previous 1:1 one. The results presented here illustrate the importance of the composition and architecture to the ionic domain connectivity and ionic conductivity, which will have far-reaching implications for the rational design of semiconducting polymers for energy applications including fuel cells, batteries, ion-exchange membranes, and mixed ionic conductors. Full article

The integration of two-dimensional (2D) nanomaterials into polymer-based packaging presents a promising avenue for sustainable, high-performance materials. This perspective explores the roles of colloidal interactions in the assembly of 2D materials into thin films for packaging applications. We begin by analyzing the types of colloidal forces present in 2D nanomaterials and their impact on dispersion and stability. We then explore how these colloidal forces can be modulated through chemical structure, ionic intercalation, and shear forces, influencing the stacking behavior and orientation of 2D materials within the films. The incorporation of these 2D materials into polymer-based packaging systems is also considered, with a focus on how surface functionalization and dispersion techniques enhance their interaction with the polymer matrix to improve barrier properties against gases and moisture, increase mechanical strength, and impart antimicrobial effects. This work underscores the critical role of colloidal interactions in optimizing the design and performance of 2D-nanomaterial-based packaging for sustainable development. Full article

This study presents the synthesis of a transparent, flexible gel polymer electrolyte (GPE) based on the protic ionic liquid BMImHSO₄ and on polyvinyl alcohol (PVA) through solution casting and electrochemical evaluation in a 2.5 V symmetrical C/C electrical double-layer solid-state capacitor (EDLC). The freestanding GPE film exhibits high thermal stability (>300 °C), wide electrochemical windows (>2.7 V), and good ionic conductivity (2.43 × 10⁻² S cm⁻¹ at 20 °C). EDLC, using this novel GPE film, shows high specific capacitance (81 F g⁻¹) as well as good retention above 90% of the initial capacitance after 4500 cycles. The engineered protic ionic liquid GPE is, hopefully, applicable to high-performance solid-state electrochemical energy storage. Full article