Search Results (115)

Nanomaterials’ special features enable their extensive application in chemical and biochemical nanosensors for food assays; food packaging; environmental, medicinal, and pharmaceutical applications; and photoelectronics. The analytical strategies based on novel nanomaterials have proved their pivotal role and increasing interest in the assay of key food components. The choice of transducer is pivotal for promoting the performance of electrochemical sensors. Electrochemical nano-transducers provide a large active surface area, enabling improved sensitivity, specificity, fast assay, precision, accuracy, and reproducibility, over the analytical range of interest, when compared to traditional sensors. Synthetic routes encompass physical techniques in general based on top–down approaches, chemical methods mainly relying on bottom–up approaches, or green technologies. Hybrid techniques such as electrochemical pathways or photochemical reduction are also applied. Electrochemical nanocomposite sensors relying on conducting polymers are amenable to performance improvement, achieved by integrating redox mediators, conductive hydrogels, and molecular imprinting polymers. Carbon-based or metal-based nanoparticles are used in combination with ionic liquids, enhancing conductivity and electron transfer. The composites may be prepared using a plethora of combinations of carbon-based, metal-based, or organic-based nanomaterials, promoting a high electrocatalytic response, and can accommodate biorecognition elements for increased specificity. Nanomaterials can function as pivotal components in electrochemical (bio)sensors applied to food assays, aiming at the analysis of bioactives, nutrients, food additives, and contaminants. Given the broad range of transducer types, detection modes, and targeted analytes, it is important to discuss the analytical performance and applicability of such nanosensors. Full article

This work introduces an original approach to the manufacturing of ionizing radiation-sensitive systems for radiotherapy applications—dosimetry. They are based on the Fricke dosimetric solution and the formation of macro-gels and capsules, and nano- and micro-gels. The reaction of ionic polymers, such as sodium alginate, with Fe and Ca metal ions is employed. Critical polymer concentration (c*) is taken as the criterion. Reaction of ionic polymers with metal ions leads to products related to c*. Well below c*, nano- and micro-gels may form. Above c*, macro-gels and capsules can be prepared. Nano- and micro-gels containing Fe in the composition can be used for infusion of a physical gel matrix to prepare 2D or 3D dosimeters. In turn, macro-gels can be formed with Fe ions crosslinking polymer chains to obtain radiation-sensitive hydrogels, so-called from wall-to-wall, serving as 3D dosimeters. The encapsulation process can lead to capsules with Fe ions serving as 1D dosimeters. This work presents the concept of manufacturing various gel structures, their main features and manufacturing challenges. It proposes new directions of research towards novel dosimeters. Full article

Adaptive vehicle control systems are crucial for enhancing safety, performance, and efficiency in modern transportation, particularly as vehicles become increasingly automated and responsive to dynamic environments. This review explores the advancements in bio-inspired actuators and their potential applications in adaptive vehicle control systems. Bio-inspired actuators, which mimic natural mechanisms such as muscle movement and plant tropism, offer unique advantages, including flexibility, adaptability, and energy efficiency. This paper categorizes these actuators based on their mechanisms, focusing on shape memory alloys, dielectric elastomers, ionic polymer–metal composites, polyvinylidene fluoride-based electrostrictive actuators, and soft pneumatic actuators. The review highlights the properties, operating principles, and potential applications for each mechanism in automotive systems. Additionally, it investigates the current uses of these actuators in adaptive suspension, active steering, braking systems, and human–machine interfaces for autonomous vehicles. The review further outlines the advantages of bio-inspired actuators, including their energy efficiency and adaptability to road conditions, while addressing key challenges like material limitations, response times, and integration with existing automotive control systems. Finally, this paper discusses future directions, including the integration of bio-inspired actuators with machine learning and advancements in material science, to enable more efficient and responsive adaptive vehicle control systems. Full article

The widespread, worldwide utilisation of alkaline batteries requires development of proper recycling methods for used batteries, which are considered both as a secondary source of valuable metals and as a threat to the environment (may contain toxic substances). As many separation methods of metal ions from battery leachates are based on the use of substances that require complex synthesis or are not eco-safe, new materials suitable for this purpose are systematically sought. Therefore, in this study, the results of the separation of Ni(II), Zn(II) and Mn(II) ions from alkaline battery leachates using polymer materials (PMs) impregnated with easily synthesised, “green” deep eutectic solvents (DESs) or with ionic liquids (ILs) were presented. Additionally, PMs surface wettability were determined and their chemical compositions were analysed using the Fourier transform infrared spectroscopy–attenuated total reflectance (FTIR–ATR) method. Among all PMs synthesised, materials containing DESs (composed of Aliquat 336 or Cyphos IL 101 and diacetamide) performed best in the separation of Ni(II) ions (removal of 93.42% and 80.86%). The application of DES-based PMs for the separation of metal ions from battery leachates is in line with green chemistry principles, and such materials can potentially be used in the processing of e-waste. 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

Ionic porous polymers have been widely utilized efficiently to anchor various metal atoms for the preparation of metal-embedded heteroatom-doped porous carbon composites as the active materials for electrocatalytic applications. However, the rational design of the heteroatom and metal elements in HPC-based composites remains a significant challenge, due to the tendency of the aggregation of metal nanoparticles during pyrolysis. In this study, a nitrogen (N)- and sulfur (S)-enriched ionic covalent organic framework (iCOF) incorporating viologen and thieno[3,4-b] thiophene (TbT) was constructed via Zincke-type polycondensation. The synthesized iCOF possesses a crystalline porous structure with a pore size of 3.05 nm, a low optical band gap of 1.88 eV, and superior ionic conductivity of 10^−2.672 S cm⁻¹ at 333 K, confirming the ionic and conjugated nature of our novel iCOF. By applying the iCOF as the precursor, a ruthenium and ruthenium(IV) oxide (Ru/RuO₂) nanoparticle-embedded N/S-co-doped porous carbon composite (NSPC-Ru) was prepared by using a two-step sequence of anion-exchange and pyrolysis processes. In the electrochemical nitrogen reduction reaction (eNRR) application, the NSPC-Ru achieves an impressive NH₃ yield rate of 32.0 μg h⁻¹ mg⁻¹ and a Faradaic efficiency of 13.2% at −0.34 V vs. RHE. Thus, this innovative approach proposes a new route for the design of iCOF-derived metal-embedded porous carbon composites for enhanced NRR performance. Full article

The impetus to study and develop polymer electrolytes for metal-ion batteries is due to their enhanced safety compared to flammable organic liquid electrolytes, promising ionic conductivity, and broad electrochemical stability window, making them to viable candidates for battery application. In the current work, we present a simple fabrication procedure and a comprehensive physico–chemical study of various PVDF-HFP-based electrolyte formulations with a sufficient addition of PEO polymer, LiTFSI conducting salt, and EMIMTFSI ionic liquid. The ionic conductivity, activation energy for ionic movement and thickness of the resulting polymer electrolyte show a non-linear dependency on the PVDF-HFP/PEO ratio. The electrolyte composition with a 0.35PEO-0.65PVDF-HFP/1LiTFSI/1EMIMTFSI mass fraction exhibits the highest ionic conductivity among the compositions, revealing $7.7\times {10}^{-5} \mathrm{S} {\mathrm{c}\mathrm{m}}^{-1}$ at 30 °C. Electrochemical tests in half full and full Li-ion batteries with a LiFePO₄ cathode and Li₄Ti₅O₁₂ anode also emphasized this composition as the most promising one, providing an initial capacity in full cells of 120 mAh g⁻¹ and a capacity retention of about 75% after 50 charge/discharge cycles at a 0.1 C current rate. In the PEO/PVDF-HFP polymer blend with EMIMTFSI as a plasticizer, the amount of crystalline parts, which are detrimental to a fast ionic diffusion, is significantly reduced. Full article

Composite solid electrolytes are gaining interest regarding their use in Li-metal solid-state batteries. Although high ceramic content improves the electrochemical stability of ceramic-rich composite separators (C-SCE), the polymeric matrix also plays a vital role. In the first generation of C-SCE separators with a PEO-based matrix, the addition of 90–95 wt% of Li_6.45Al_0.05La₃Zr_1.6Ta_0.4O₁₂ (LLZO) does not make C-SCE stable for cell cycling with high-voltage (HV) cathodes. For the next iteration, the objective was to find an HV-stable polymeric matrix for C-SCEs. Herein, we report results on optimizing C-SCE separators with different ceramics and polymers which can craft the system towards better stability with NMC622-based composite cathodes. Both LLZO and Li_1.3Al_0.3Ti_1.7(PO₄)₃ (LATP) were utilized as ceramic components in C-SCE separators. Poly(diallyldimethylammonium) bis(trifluoromethanesulfonyl)imide (PDDA-TFSI) and poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) were used as polymers in the “polymer/LiTFSI/plasticizer”-based matrix. The initial phase of the selection criteria for the separator matrix involved assessing mechanical stability and ionic conductivity. Two optimized separator formulations were then tested for their electrochemical stability with both Li metal and HV composite cathodes. The results showed that Li/NMC622 cells with LP70_PVDF_HFP and LZ70_PDDA-TFSI separators exhibited more stable cycling performance compared to those with LZ90_PEO300k-based separators. Full article

Solid-state electrolytes for lithium-ion batteries, which enable a significant increase in storage capacity, are at the forefront of alternative energy storage systems due to their attractive properties such as wide electrochemical stability window, relatively superior contact stability against Li metal, inherently dendrite inhibition, and a wide range of temperature functionality. NASICON-type solid electrolytes are an exciting candidate within ceramic electrolytes due to their high ionic conductivity and low moisture sensitivity, making them a prime candidate for pure oxidic and hybrid ceramic-in-polymer composite electrolytes. Here, we report on producing pure and Y-doped Lithium Aluminum Titanium Phosphate (LATP) nanoparticles by spray-flame synthesis. The as-synthesized samples consist of an amorphous component and anatase-TiO₂ crystalline particles. Brief annealing at 750–1000 °C for one hour was sufficient to achieve the desired phase while maintaining the material’s sub-micrometer scale. Rietveld analysis of X-Ray diffraction data demonstrated that the crystal volume increases with Y doping. At the same time, with high Y incorporation, a segregation of the YPO₄ phase was observed in addition to the desired LATP phase. Another impurity phase, LiTiOPO₄, was observed besides YPO₄ and, with higher calcination temperature (1000 °C), the phase fraction for both impurities also increased. The ionic conductivity increased with Y incorporation from 0.1 mS/cm at room temperature in the undoped sample to 0.84 mS/cm in the case of LAY0.1TP, which makes these materials—especially considering the comparatively low sintering temperature—highly interesting for applications in the field of solid-state batteries. Full article

Lithium-ion batteries are a promising technology to promote the phase-out of fossil fuel vehicles. Increasing efforts are focused on improving their energy density and safety by replacing current materials with more efficient and safer alternatives. In this context, binary composites of organic ionic plastic crystals (OIPCs) and lithium salts show promise due to their impressive mechanical properties and ionic conductivity. Taking advantage of this, the present paper substitutes the commercial non-electrochemically active binder with an OIPC component, N-ethyl-N-methylpyrrolidinium bis(fluorosulfonyl)imide ([C₂mpyr][FSI]), in combination with LiFSI. Slurry-formulation experiments revealed that varying the new binder’s composition allows the production of diverse LiFePO₄ (LFP) cathodes via the conventional fabrication process. Large amounts of OIPC−lithium salt mixtures in the composition yielded thick electrodes with expected nominal areal capacities of up to 3.74 mAh/cm², where the balanced composition with a reduced Li⁺ concentration can demonstrate >1.5 mAh/cm² at 0.1C. Lowering the amount of these ion-conductive binders enabled LFP cathodes to perform effectively under fast cycling conditions at a C-rate as high as 2C. Preliminary battery tests with a limited Li⁺ source demonstrated the feasibility of full-cell operation without using the lithium-metal anode. This work paves the way for developing advanced rechargeable batteries using OIPC-based ion-conductive binders for a wide range of applications. Full article

Solid-state batteries (SSBs) have been recognized as promising energy storage devices for the future due to their high energy densities and much-improved safety compared with conventional lithium-ion batteries (LIBs), whose shortcomings are widely troubled by serious safety concerns such as flammability, leakage, and chemical instability originating from liquid electrolytes (LEs). These challenges further deteriorate lithium metal batteries (LMBs) through dendrite growth and undesirable parasitic reactions. Polymer electrolytes (PEs) have been considered among the few viable options that have attracted great interest because of their inherent non-flammability, excellent flexibility, and wide electrochemical stability window. However, practical applications are seriously limited due to the relatively low ionic conductivity, mechanical instability, and short operational life cycle. This review covers the recent developments in the field and applications of polymer electrolytes in SSBs, including solid polymer electrolytes (SPEs), gel polymer electrolytes (GPEs), and composite polymer electrolytes (CPEs). The discussion comprises the key synthesis methodologies, electrochemical evaluation, and fabrication of PEs while examining lithium-ion’s solvation and desolvation processes. Finally, this review highlights innovations in PEs for advanced technologies like lithium metal batteries and beyond, covering emerging trends in polymer materials and advancements in PE performance and stability to enhance commercial applications. Full article

A well-known soft actuator, called ionic polymer–metal composite (IPMC), is a type of electroactive polymer (EAP) that operates in bending mode. Despite its ability to exhibit large bending, its bending controllability is often poor. Therefore, identifying the key factor that allows IPMC to bend without losing its large bending capability is a natural inquiry for researchers studying IPMC for practical applications. Our study found that the sign of the immobile charge carried by the ion exchange membrane of IPMC governs its bending controllability. We also discovered that using a negatively charged ion exchange membrane, rather than a positively charged one, is highly preferable for IPMC applications. It was also found that using a doping process and an electrochemically active electrode is essential for inducing effective bending in IPMC. Full article

The effective treatment of the surface electrode is the core technology of an ionic polymer–metal composite (IPMC), and its preparation significantly affects the driving performance of the IPMC. Copper, which is inexpensive and has excellent electrical conductivity, was selected as the surface electrode material, and copper electrode IPMCs (Cu-IPMCs) were prepared via magnetron sputtering. Orthogonal experiments were performed to optimize the parameters of the preparation process. The indices of the deformation angle and surface resistance were used, and the sample electrodes’ surface morphology and elemental content were analyzed. The results showed that sputtering pressure was the major factor affecting two indices. The Cu-IPMC, prepared at a sputtering pressure of 0.9 Pa, sputtering time of 35 min, argon flow rate of 30 sccm, and sputtering power of 150 W, had a more minor surface resistance and a larger deformation angle under continuous direct current boosting. It required a sputtering time of 1.2 h, which was more than 10 times shorter than its chemically plated counterpart. It exhibited surface resistance in the 2–3 Ω/cm range, which was 23 times smaller than chemically plated platinum. Full article

The Purcell’s swimmer, consisting of three links with two one-degree-of-freedom joints as defined by Edward M. Purcell, has been studied by several authors since its introduction in 1977. Researchers have delved into its mathematical foundations, analysing and optimising its motion for efficient propulsion. However, despite these theoretical advances, the practical realisation and experimental characterisation of Purcell’s swimmers remains relatively unexplored. Critical aspects such as material selection, manufacturing techniques, and experimental validation under real conditions represent important knowledge gaps. This paper contributes to bridging this gap by presenting a prototype of such a swimmer using ionic polymer-metal composites (IPMC) as link actuators. A simulation model is developed based on physical modelling tools in MATLAB^®/Simulink^®. Both simulation and experimental results at low-Reynolds-number ($Re$) conditions are presented to demonstrate the performance of the swimmer. Full article

Thin-film composite (TFC) membranes containing various fillers and additives present an effective alternative to conventional dense polymer membranes, which often suffer from low permeance (flux) and the permeability–selectivity tradeoff. Alongside the development and utilization of numerous new polymers over the past few decades, diverse additives such as metal–organic frameworks (MOFs), graphene oxides (GOs), and ionic liquids (ILs) have been integrated into the polymer matrix to enhance performance. However, achieving desirable interfacial compatibility between these additives and the host polymer matrix, particularly in TFC structures, remains a significant challenge. This review discusses recent advancements in TFC membranes for CO₂/N₂ separation, focusing on material structure, polymer–additive interaction, interface and separation properties. Specifically, we examine membranes operating under dry conditions to clearly assess the impact of additives on membrane properties and performance. Additionally, we provide a perspective on future research directions for designing high-performance membrane materials. Full article