Search Results (251)

Current liquid-phase resonant biosensors, such as Quartz Crystal Microbalance, Surface Acoustic Wave, or Surface Plasmon Resonance, typically rely on specialized piezoelectric substrates or complex optical setups. These requirements often necessitate cleanroom fabrication, thereby limiting cost-effective scalability. This study presents a high-integration sensing platform based on standard Printed Circuit Board (PCB) technology, incorporating an embedded inductor within a fluidic system for real-time monitoring. This design leverages industrial manufacturing standards to achieve a compact, low-cost, and scalable architecture. Detection is governed by shifts in the resonance frequency of an LC tank circuit; specifically, increases in bulk ionic strength induce a frequency decrease, whereas biomolecular adsorption at the sensor surface leads to a frequency increase. This phenomenon can be explained by the modulation of the inter-turn capacitance, which is modeled as a combination of capacitive elements accounting for contributions from the bulk electrolyte and the surface-bound dielectric layer. Such divergent responses provide an intrinsic self-discriminating capability, allowing for the analytical differentiation between surface interactions and bulk effects. To the best of our knowledge, this is the first demonstration of an inductor-based resonant sensor fully embedded in a PCB fluidic architecture for continuous liquid-phase analyte monitoring. Validated through a protein-antibody model (Bovine Serum Albumin-anti-Bovine Serum Albumin), the sensor demonstrated a limit of detection of 1.7 ppm (0.026 mM) and a linear dynamic range of 31–211 ppm (0.47–3.2 mM). These performance metrics, combined with a reproducibility of 4 ± 3%, indicate that the platform meets the requirements for robust analytical applications. Its inherent simplicity and potential for miniaturization position this technology as a viable candidate for point-of-care diagnostics in diverse environments. Full article

Perovskite solar cells (PSCs) have achieved remarkable efficiencies, yet further progress is limited by defect-induced nonradiative recombination and instability associated with uncontrolled crystallization. Here, we develop a protic ionic-liquid precursor engineering strategy based on methylammonium acetate (MAAc) for high-performance inverted (p–i–n) triple-cation perovskite solar cells. Systematic variation of the MAAc content reveals that a moderate concentration yields perovskite films with enlarged grains, suppressed pinholes, and strongly reduced residual PbI₂. Steady-state and time-resolved photoluminescence measurements, together with electrochemical impedance spectroscopy and light-intensity-dependent analysis, demonstrate that MAAc effectively suppresses trap-assisted nonradiative recombination, prolongs carrier lifetime, and increases recombination resistance without introducing additional transport losses. As a result, optimized inverted devices deliver a champion power conversion efficiency of 23.68% with a high open-circuit voltage of 1.21 V, a fill factor of ~0.83, negligible J–V hysteresis, and excellent device-to-device reproducibility. Moreover, the MAAc-2M devices exhibit markedly improved operational and shelf stability, retaining 73.2% of their initial efficiency after 30 days, compared to 53.2% for the control. This work establishes MAAc as an effective ionic-liquid additive that simultaneously governs crystallization and defect chemistry, offering a general route to efficient and stable inverted perovskite solar cells via protic ionic-liquid-assisted precursor engineering. Full article

This work reports on novel acid–base conjugate pairs of monocationic allyldiamidinium and dicationic diamidinium salts, some of which are ionic liquids (ILs) at ambient temperatures. A series of allyldiamidinium salts of the general formula [C₃H(NRMe)₄]X (R = Me, Et, Pr, allyl, CH₂CH₂OMe; X = Cl, bistriflimide, dicyanamide) were prepared from C₃Cl₄ or C₃Cl₅H and the appropriate secondary amine, RNMeH. Alkylated ethylenediamines similarly yield bicyclic allyldiamidinium salts, whereas longer diamines (H₂N(CH₂)_nNH₂ (n = 3, 4, 5)) were isolated as their conjugate acids, the diamidinium dicationic salts [C₃H₂(HN(CH₂)_nNH)₂]X₂. The salts were characterized by NMR, ES-MS, DSC, TGA, and miscibility or solubility studies. Additionally, the ILs were characterized by their viscosities. The conductivities of the diamidinium ILs were also measured, and this allowed for an investigation of their Walden parameters. In contrast to expectations, since the ion pairing and clustering were expected to be significant, this showed them to be “superionic”. Previous reports of Walden plots of dicationic ILs were found to be erroneous, and a reanalysis of the literature data found that all reported dicationic and even tetracationic ILs can be classified as superionic. The salts [C₃H(NMe₂)₄]Cl, [C₃H(EtN(CH₂)₂NEt)₂]OTf, and [C₃H₂(HN(CH₂)_nNH)₂]Cl₂ (n = 3, 4, 5) were also characterized by single-crystal X-ray diffraction. Full article

The long-term conservation of Prunus persica (peach), a crop of significant agronomic and genetic value, remains challenging due to its recalcitrance to conventional cryopreservation methods. Low tolerance to dehydration and cryoprotectant toxicity often results in poor survival and regrowth, thereby limiting the reliability of germplasm storage. This study evaluated whether combining an alginate hydrogel matrix with Pluronic F-68 improves vitrification efficiency and post-thaw regeneration of peach shoot tips by enhancing dehydration dynamics and reducing cryo-injury. Shoot tips were immobilized in thin sodium alginate layers on aluminum foil strips, with the hydrogel providing mechanical stabilization and moderating water loss during exposure to PVS3 and subsequent liquid nitrogen immersion. To further mitigate cryoinjury, Pluronic F-68, a non-ionic surfactant with membrane-stabilizing properties, was incorporated into the system. Differential scanning calorimetry revealed that the hydrogel reached complete vitrification after 120 min in PVS3, whereas encapsulated shoot tips required 150 min for full suppression of crystallization. The optimized system achieved 71% post-cryopreservation survival and 40% regrowth, compared with 25% and 9% in non-encapsulated controls. PF-68 accelerated vitrification kinetics, lowered crystallization enthalpies, and improved post-thaw viability. These findings demonstrate that engineered hydrogel–surfactant matrices can stabilize the microenvironment during vitrification and offer a promising approach for the long-term cryopreservation of peach germplasm. Full article

Tungsten is a critical raw material with increasingly important industrial applications. It is primarily found in minerals such as scheelite and wolframite (0.5% W), which are extracted and processed at the mine site to produce a high-grade scheelite concentrate (60% W). This process results in significant tungsten losses in the form of tailings, currently not utilized at the EU level. Deep eutectic solvents and imidazolium-based ionic liquids have been shown to possess excellent utility for recovering tungsten from low-grade concentrates, achieving tungsten oxide (96% purity) at high global yields (80%). In this study, an optimized ionic liquid-based process (involving leaching, solvent extraction, crystallization, and calcination) was developed at the laboratory scale. Important issues such as solvent flammability or the commercial availability of ionic liquids were addressed to ensure the safety and industrial feasibility of the process. Furthermore, a pilot plant was designed, constructed, and operated for a significant period (3 days). Tungsten oxide was produced with improved purity (>99%) and global yield (91.6%) in continuous operation. Full article

The development of new types of nanocomposites capable of manipulating light is critical for various modern photonics applications. Recently, we proposed the use of overlooked glass-forming ionic liquid crystals made of cadmium octanoate containing gold, carbon, or both carbon and gold nanoparticles as promising optical and nonlinear optical materials. These were characterized using nanosecond laser pulses at a wavelength of 532 nm. In this paper, femtosecond radiation at different wavelengths (600 nm and 800 nm) is employed to study ultrafast electronic nonlinear optical processes in mesomorphic glass nanocomposites. The observed nonlinear optical response probed at the femtosecond time scale dramatically differs from that at the nanosecond time scale reported previously. The intensity-dependent effective nonlinear absorption coefficient of all studied samples remains positive due to the dominant reverse saturable absorption effect, while the nonlinear refractive index exhibits a sign reversal depending on the intensity and wavelength of laser pulses. The strategy for producing glass-forming ionic liquid crystal gold–carbon nanocomposites with an ultrafast nonlinear optical response is of high interest for modern applications in advanced photonics, and it can also be applied to other types of glass-forming metal alkanoates and nanomaterials. Full article

The motivation for increasing the efficiency of renewable energy sources is the basic problem of ongoing research. Currently, intensive research is underway in technology based on the use of dye-sensitized solar cells (DSSCs). The aim of this work is to investigate the effect of modifying the iodide electrolyte with liquid crystals (LCs) known for the self-organization of molecules into specific mesophases. The current–voltage (I-V) and power–voltage (P-V) characteristics were determined for the ruthenium-based dyes N3, Z907, and N719 to investigate the influence of their structure and concentration on the efficiency of DSSCs. The addition of a nematic LC of 4-n-pentyl-4-cyanobiphenyl (5CB) to the iodide electrolyte influences the I-V and P-V characteristics. A modification of the I-V characteristics was found, especially a change in the values of short circuit current (I_SC) and open circuit voltage (V_OC). The conversion efficiency for cells with modified electrolyte shows a complex dependence that first increases and then decreases with increasing LC concentration. It may be caused by the orientational interaction of LC molecules with the titanium dioxide (TiO₂) layer on the photoanode. A too high concentration of LC may lead to a reduction in total ionic conductivity due to the insulating effect of the elongated polar molecules. Full article

This study evaluated and compared two encapsulation techniques—co-crystallization and ionic gelation—for stabilizing bioactive components derived from lavender distillation residues. Utilizing aqueous ethanol extraction (solid residues) and concentration (liquid residues), phenolic-rich extracts were incorporated into encapsulation matrices and processed under controlled conditions. Comprehensive characterization included encapsulation efficiency (Ef), antioxidant activity (AA), moisture content, hygroscopicity, dissolution time, bulk density, and color parameters (L*, a*, b*). Co-crystallization outperformed ionic gelation across most criteria, achieving significantly higher Ef (>150%) and superior functional properties such as lower moisture content (<0.5%), negative hygroscopicity (−6%), and faster dissolution (<60 s). These features suggested enhanced physicochemical stability and suitability for applications requiring long shelf life and rapid solubility. In contrast, extruded beads exhibited high moisture levels (94.0–95.4%) but allowed better control over morphological features. The work introduced a mild-processing approach applied innovatively to the valorization of lavender distillation waste through structurally stable phenolic delivery systems. By systematically benchmarking two distinct encapsulation strategies under equivalent formulation conditions, this study advanced current understanding in bioactive microencapsulation and offers new tools for developing functional ingredients from aromatic plant by-products. Full article

Microwave-assisted ionothermal strategies offer an effective pathway for rapid zeolite crystallization under mild conditions, while conventional ionothermal approaches are still constrained by prolonged crystallization cycles that limit their industrial applicability. Herein, we report a microwave-activated, ionic liquid-mediated synthesis strategy that enables the precise modulation of crystallization kinetics and composite assembly. By introducing ZSM-5 seeds into the ionic liquid system, the nucleation and growth of AlPO₄-5 were significantly accelerated, reducing crystallization time by up to 75% (optimal condition: 60 min). Among various imidazolium-based ionic liquids, [BMMIm]Br demonstrated an optimal balance of hydrophilic and hydrophobic interactions, yielding composite zeolites with high surface area (350 m²·g⁻¹) and large pore volume (0.28 cm³·g⁻¹). Comprehensive characterization (XRD, SEM-EDX, NH₃-TPD) confirmed the formation of well-defined ZSM-5/AlPO₄-5 core–shell structures and revealed tunable acid site distributions depending on the ionic liquid used. In methanol to olefins (MTO) reactions, the composite catalyst exhibited outstanding selectivity towards light olefins (C₂=–C₄=: 72.84%), markedly outperforming the individual ZSM-5 and AlPO₄-5 components. The superior catalytic behavior is primarily attributed to the synergistic effect of hierarchical acid site tuning and the integrated core–shell architecture, which together optimize reaction selectivity. This strategy provides a promising route for the rational design of high-performance zeolites with significant industrial applicability. Full article

Piezoelectric polymer composites, particularly polyvinylidene fluoride (PVDF) blended with barium titanate (BT), show promise for wearable technologies as both energy harvesters and haptic actuators. However, these composites typically exhibit limited electromechanical coupling and insufficient β-phase formation. This study presents a novel approach using ionic liquids (ILs) to enhance PVDF-based piezoelectric composite performance. Through solution-casting methods, we examined the effect of IL concentration on the structural, mechanical, and piezoelectric properties of PVDF/BT composites. Results demonstrate that the use of IL significantly improves β-phase crystallization in PVDF while enhancing electrical properties and mechanical flexibility, which are key requirements for effective energy harvesting and haptic feedback applications. The optimized composites show a 25% increase in β-phase content, enhanced flexibility, and a 100% improvement in piezoelectric voltage output compared to other more conventional PVDF/BT systems. The IL-modified composite exhibits superior piezoelectric response, generating an output voltage of 9 V and an output power of 40.1 µW under mechanical excitation and a displacement of 138 nm when subjected to 13 V peak-to-peak voltage, making it particularly suitable for haptic interfaces. These findings establish a pathway toward high-performance, flexible piezoelectric materials for multifunctional wearable applications in human–machine interfaces. Full article

Black, needle-like single crystals of [Pd@Bi₁₀][AlCl₄]₄ were synthesized in a one-pot reaction between PdCl₂, Bi, and BiCl₃ at 180 °C in the Lewis acidic ionic liquid (LAIL) medium [BMIm]Cl∙4.2AlCl₄ (BMIm = 1-n-butyl-3-methylimidazolium). Single-crystal X-ray diffraction revealed that the compound crystallizes in the triclinic space group P$\overline{1}$ with the unit cell parameters a = 11.0233(5) Å, b = 26.1892(14) Å, c = 26.2687(14) Å, α = 90.842(2)°, β = 92.1940(10)°, γ = 91.164(2)°, closely matching its platinum-containing analog. The structure features pentagonal antiprismatic [Pd@Bi₁₀]⁴⁺ cluster cations charge-balanced by tetrahedral [AlCl₄]⁻ anions. Bonding and charge analysis reveal unoptimized Pd–Bi and strong Bi–Bi covalent interactions consistent with electronegativity trends and the previously reported host–guest model. Electronic structure calculations performed with the TB-LMTO-ASA program show that [Pd@Bi₁₀][AlCl₄]₄ exhibits semiconducting behavior, suggesting a bandgap opening of 0.71 eV. Full article

Rapid industrialization has led to a substantial increase in waste salts containing Na₂SO₄/NaCl mixtures, posing significant challenges for their phase separation and resource recovery. This study pioneers an integrated process combining frozen crystallization with stepwise decompression evaporation for Na₂SO₄/NaCl separation. Through the systematic investigation of phase transition behaviors under varying ionic ratios, the optimal combined processes corresponding to mixed salts with different compositions were identified. The experimental results demonstrate that brines with NaCl > 80.0% should preferentially undergo vacuum evaporation, while those below this threshold are suitable for prioritizing frozen crystallization for Na₂SO₄ recovery. Utilizing the complementary advantages of both processes, the mixture was prepared with a mass ratio of NaCl to Na₂SO₄ of 3:1. The frozen crystallization of the brine yielded 90.0% pure Na₂SO₄ crystals while concentrating NaCl to 92.0% in the residual liquor. Subsequent stepwise evaporation yielded 98.5% pure NaCl crystals. Finally, the removal effect and lifecycle evaluation of the process for impurity ions provide new insights for the zero liquid discharge system in industrial waste salt management. Full article

Preparative protein crystallization is regarded as an economically sustainable protein purification alternative to chromatography in biotechnological downstream processing. However, protein crystallization is a not-well-understood process that is usually slow and poorly reproducible. A promising strategy for enhancing protein crystallization is exploiting the metastable liquid–liquid phase separation (LLPS) of protein solutions. Here, we report an enhancement of lysozyme-crystallization yield by using a combination of two additives under LLPS conditions. The first additive, NaCl (0.15 M), is necessary to introduce protein–protein attractive interactions and induce LLPS by lowering temperature. The second additive, 4-(2-hydroxyethyl)-1-piperazineethanesulfonate (HEPES, 0.10 M, pH 7.4), accumulates in the metastable protein-rich liquid phase and thermodynamically stabilizes lysozyme crystals. We found that this combination of additives leads to crystallization yields of higher than 90% under LLPS conditions at a lysozyme concentration of 5% by weight and a fairly low ionic strength (0.2 M) within an operational time of the order of one hour. This crystallization yield is more than three-fold larger than that obtained from samples containing NaCl without HEPES at the same pH and ionic strength. Moreover, we determined crystallization yield as a function of incubation time, and temperature below and above the LLPS boundary. As crystallization temperature intersects with LLPS temperature, a significant increase in crystallization yield is observed. This is consistent with LLPS boosting protein crystallization. Our work suggests a possible strategy for increasing the crystallization success of other proteins, with applications in protein purification. Full article

Electroactive polymers (EAPs) represent a versatile class of smart materials capable of converting electrical stimuli into mechanical motion and vice versa, positioning them as key components in the next generation of actuators and sensors. This review summarizes recent developments in both electronic and ionic EAPs, highlighting their activation mechanisms, material architectures, and multifunctional capabilities. Representative systems include dielectric elastomers, ferroelectric and conducting polymers, liquid crystal elastomers, and ionic gels. Advances in fabrication methods, such as additive manufacturing, nanocomposite engineering, and patternable electrode deposition, are discussed with emphasis on miniaturization, stretchability, and integration into soft systems. Applications span biomedical devices, wearable electronics, soft robotics, and environmental monitoring, with growing interest in platforms that combine actuation and sensing within a single structure. Finally, the review addresses critical challenges such as long-term material stability and scalability, and outlines future directions toward self-powered, AI-integrated, and sustainable EAP technologies. Full article

Free ion impurities in liquid crystals significantly impact the dynamic electro-optic performance of liquid crystal displays, leading to slow switching times, short-term flickering, and long-term image sticking. These ionic contaminants originate from various sources, including LC cell fabrication, electrode degradation, and organic alignment layers. This study demonstrates that doping LCs with a small concentration of helical carbon nanotubes effectively reduces free ion concentrations by approximately 70%. The resulting reduction in ionic impurities lowers the rotational viscosity of the LC, facilitating faster electro-optic switching. Additionally, the purified LC exhibits enhanced dielectric anisotropy, further improving its performance in display applications. These findings suggest that helical carbon nanotubes doping offers a promising approach for mitigating ion-related issues in liquid crystals without the need for additional chemical treatments, paving the way for an efficient liquid crystal display technology. Full article