Search Results (213)

Deep eutectic solvents (DESs) have undergone a remarkable transformation over the past two decades, evolving from a laboratory curiosity into one of the most actively investigated solvent platforms in green chemistry. Yet, despite this rapid expansion, and although the field is well served by numerous topical reviews, it still lacks a corpus-wide, cross-disciplinary synthesis capable of guiding strategic research priorities, identifying critical knowledge gaps, and informing policy and industrial investment decisions. The present work addresses this need through a thorough analysis of global DES research from 2003 to 2025, based on a deduplicated corpus of 17,757 publications retrieved from the Web of Science Core Collection and Scopus following PRISMA-adapted screening guidelines. The analysis maps temporal publication dynamics, geographic and institutional contributions, thematic evolution, journal landscape, component usage patterns, international collaboration networks, market projections, and alignment with the United Nations Sustainable Development Goals. The results document an exponential growth trajectory—from a single publication in 2004 to 3954 in 2025 (CAGR > 30%)—and reveal a clear thematic transition from early electrochemistry-dominated research toward extraction, pharmaceutical, and environmental applications, with machine-learning-assisted design and hydrophobic DES formulations emerging as the most dynamic current frontiers. China leads global output with 6819 publications (38.4%), while the United States and Malaysia achieve the highest citation-per-publication ratios among the leading nations (≈46.7 and ≈38.9, respectively, versus ≈27.6 for China), and Spain pairs a comparatively modest output with a high h-index, indicating that impact is large relative to volume. Type III DESs and NADESs collectively account for approximately 69% of the literature, with choline chloride present in 72% of reported formulations. The global DES market, valued at approximately USD 166 million in 2024, is projected to reach USD 370 million by 2030. Despite this progress, critical translational barriers persist: fewer than 0.3% of publications include techno-economic or life cycle assessment analysis, standardized characterization protocols remain absent, and toxicological datasets are systematically incomplete. This panoramic analysis is intended to serve as an evidence-based reference for researchers prioritizing future directions, for funding agencies assessing the maturity and needs of the field, and for industrial stakeholders evaluating the readiness of DES technologies for scale-up. Full article

High-strength Mg alloys always contain heavy RE solutes, which leads to the high cost of Mg alloys preventing commercial use. In this work, we developed a new high-performance Mg–3Nd–1Yb–0.6Zn–0.4Zr alloy with low RE content and investigated the effects of heat treatment on the microstructure and mechanical properties. The results show that the main secondary phase in the as-cast alloy is the eutectic Mg₁₂RE phase at grain boundaries. The average grain size is measured to be 24.6 μm. After solution treatment, the grain-boundary eutectic Mg₁₂RE phase is completely dissolved into the matrix, without obvious grain growth. The alloy exhibits an obvious age-hardening effect during aging at 200 °C, and its hardness reaches a peak at 15 h, with a hardness increment of ~31 HV. A high-density prismatic β′ phase is formed in the matrix after peak aging. The peak-aged alloy presents optimal mechanical properties, with ultimate tensile strength, yield strength and elongation of 282 MPa, 202 MPa and 6.8%, respectively, which are remarkably superior to those of typical alloys such as EV31A and WE43. Quantitative calculation of strengthening mechanisms indicates that age hardening is the dominant strengthening mechanism of the peak-aged alloy, and the precipitation strengthening contribution of prismatic β′ phase is 158 MPa, accounting for approximately 78% of the yield strength. Full article

Aqueous zinc–iodine batteries (AZIBs) are emerging as highly promising candidates for next-generation, grid-scale energy storage due to the intrinsic safety of water-based electrolytes, the high theoretical capacity of the zinc anode, and the rapid conversion kinetics of the iodine cathode. However, the practical commercialization of AZIBs is severely impeded by formidable interfacial instabilities, including the uncontrollable growth of zinc dendrites, parasitic hydrogen evolution reactions (HER), and the notorious polyiodide (I₃⁻, I₅⁻) shuttle effect. These macroscopic degradation modes are fundamentally rooted in the robust [Zn(H₂O)₆]²⁺ primary solvation sheath and the immense thermodynamic driving force for polyiodide dissolution in highly polar aqueous media. To address these interconnected challenges, electrolyte engineering has evolved into the most potent, holistic strategy. This comprehensive review systematically evaluates the latest advancements in electrolyte engineering for AZIBs. We first deeply decipher the fundamental thermodynamic mechanisms governing Zn²⁺ desolvation and iodine multiphase conversion. Subsequently, we critically analyze cutting-edge regulation paradigms, including water-in-salt (WIS) and localized high-concentration electrolytes (LHCE), cosolvent networks, functional molecular additives, deep eutectic solvents (DES), and quasi-solid-state hydrogels. By integrating in situ/operando spectroscopic characterizations with multiscale theoretical computations (such as MD and DFT), we elucidate the structure–activity relationships at the atomic level. Finally, we provide strategic perspectives on the future trajectories of the field, emphasizing the stabilization of multi-electron (I⁻/I⁰/I⁺) halogen chemistry, AI-driven high-throughput screening, and the rigorous standardization of Ah-level pouch cell engineering for extreme-environment applications. Full article

The nucleation and growth mechanisms of copper electrodeposition from Cu(I)-containing-reline, a deep eutectic solvent, were investigated through a combination of electrochemical techniques and surface characterization. Cyclic voltammetry revealed the characteristic nucleation loop associated with an overpotential-driven electrocrystallization process, from which the equilibrium potential of the Cu(I)/Cu(0) redox couple was determined to be −0.35 V vs. a Ag quasi-reference electrode. Experimental potentiostatic current density transients were analyzed using nucleation models capable of accounting for both adsorption and three-dimensional (3D) diffusion-controlled growth, thereby allowing deconvolution of the individual contributions to the overall current response. The kinetic parameters, including the nucleation frequency and the number density of active sites, exhibited an exponential dependence on the applied overpotential, thus indicating enhanced nucleation kinetics at greater driving forces, while determining a Cu(I) diffusion coefficient of (3.39 + 0.09) × 10⁻⁷ cm² s⁻¹. Thermodynamic analysis showed that the Gibbs free energy of the formation of the critical nucleus decreases with increasing overpotential and follows the expected dependence on the inverse square of the overpotential, in agreement with classical nucleation theory. The estimated critical nucleus size was found to be smaller than one atom, suggesting that nucleation occurs at highly active surface sites. Furthermore, an exchange current density of (3 ± 1) μA cm⁻² was estimated for the Cu(I) electrochemical reduction. Scanning electron microscopy revealed a high density of copper nanoparticles (~20 nm) distributed across the electrode surface, along with larger aggregates (~100 nm) formed by coalescence and growth, consistent with a progressive nucleation mechanism. X-ray photoelectron spectroscopy confirmed that the deposits consist exclusively of metallic copper, with no evidence of oxidized species. These results demonstrate that copper electrodeposition in reline is governed by a complex interplay between the thermodynamic driving force, the interfacial kinetics, and mass transport, comprehensively providing fundamental insight into the electrocrystallization processes in deep eutectic solvents. Full article

This study systematically investigates the synergistic effects of Sr and La-Ce mixed rare earth (RE) additions on the microstructure and mechanical properties of AlSi9Cu3 alloy. The results show that adding 0.02 wt.% Sr and 0.10 wt.% RE together produces the most pronounced refinement, reducing the secondary dendrite arm spacing (SDAS) from 40.12 μm to 26.98 μm and decreasing the aspect ratio of eutectic Si from 12.3 to 7.8. Sr modifies eutectic Si by inducing twin formation and suppressing anisotropic growth, while RE promotes the dispersion distribution of Al₄Ce phases and enhances constitutional undercooling. The synergistic effect leads to a more uniform appearance of dendrites and secondary phases. Consequently, the tensile strength reaches 258.6 MPa, accompanied by a transition in fracture mode from brittle cleavage to ductile dimple fracture. This work provides experimental support for microstructural control and the strengthening–toughening design of AlSi9Cu3 alloys. Full article

To address the demand for lightweight, high-performance Al-Si-Mg alloys in aerospace and automotive industries, this work proposes a novel synergistic strengthening strategy by combining rare-earth Y microalloying and in situ synthesized ZrB₂ nanoparticles to construct a hybrid reinforcement architecture. The effects of Y-ZrB₂ additions on the microstructure, crystallographic orientation evolution, and mechanical properties of Al-Si-Mg alloys were systematically investigated via XRD, SEM, EBSD, and tensile/hardness tests. Results show that compared with the base alloy and single-modified alloys, the co-addition of Y and ZrB₂ simultaneously enhances mechanical properties and optimizes grain structure. The optimal comprehensive performance is achieved at 0.3 wt.% Y + 2 wt.% ZrB₂ after T6 heat treatment, with ultimate tensile strength of 332.87 MPa, yield strength of 271.35 MPa, elongation of 16.24%, and Vickers hardness of 153.9 HV. Phase analysis and SEM-EDS confirm a synergistic coupling relationship between Y-rich phases and ZrB₂ nanoparticles. EBSD characterization reveals that Y-ZrB₂ modification has negligible effect on the morphology and crystallographic orientation stability of primary α-Al grains, but effectively regulates the lattice rotation, texture redistribution, and growth behavior of eutectic Si. At the optimal composition, the fraction of high-angle grain boundaries (HAGBs) reaches a maximum of 34.3%. Furthermore, the synergistic effect significantly increases the geometrically necessary dislocation (GND) density and reduces the Schmid factor of the dominant {111}⟨110⟩ slip system, thus enhancing dislocation strengthening and plastic deformation resistance. This work clarifies the intrinsic strength-ductility synergy mechanism of Y-ZrB₂ co-modified Al-Si-Mg alloys, paving a new pathway for the development of advanced lightweight aluminum alloys. Full article

Persistent microplastics contaminate wastewater systems and pose significant environmental and human health risks due to their small size, buoyancy, persistence, and diverse physicochemical properties, which reduce the effectiveness of conventional treatment technologies. Freeze crystallization, indirect freeze crystallization, eutectic freeze crystallization, and ice-templated separation have emerged as promising long-term technologies for microplastic removal. Particle rejection at the solid–liquid interface, heterogeneous ice nucleation, brine channel formation, and particle entrapment within advancing ice fronts are key crystallization mechanisms governing microplastic separation. Microplastics can adhere to or nucleate growing ice crystals, according to lab and field research. These interactions influence crystal growth kinetics and ice structure formation. Indirect freeze crystallization (IFC) and related chemical-free crystallization systems offer lower energy requirements and improved scalability. Crystallization processes concentrate microplastics for downstream treatment, may connect with photochemical or oxidative degradation at ice interfaces, and are useful in cold areas or low-temperature industrial streams. Despite these advances, several challenges remain, including freezing rate, salinity, particle size distribution, and surface weathering, which are difficult to control. Integrating crystallization into wastewater treatment systems is also difficult. This review covers the latest advances in microplastic–ice interactions, crystallization engineering, and freeze-based separation technologies. It also highlights major knowledge gaps and suggests future research to use crystallization to remove microplastics from wastewater in a sustainable, scalable, and energy-efficient manner. Full article

Non-indigenous or alien macroalgae are increasingly recognized as ecological threats, sources of raw material, and reservoirs of bioactive compounds for industry and agriculture. This review analyses the valorization potential of this biomass, focusing on their antifungal and elicitor activities against phytopathogenic fungi, particularly Mediterranean (De Bary) Whetzel, 1945. The literature published since 2020 was retrieved from Scopus using targeted keyword combinations. Three major topics were examined: (i) invasive and beach-cast macroalgal and their ecological context, (ii) antifungal and elicitor properties of macroalgal extracts, and (iii) the use of deep eutectic solvents (DES) for the green extraction of bioactive compounds. Species such as Asparagopsis armata, Rugulopteryx okamurae, and Sargassum muticum have shown promising antifungal and elicitor effects, frequently associated with phenolic compounds and polysaccharides. Extracts from these algae can inhibit the growth of fungi or activate plant defense pathways, providing environmentally friendly alternatives to synthetic pesticides. Moreover, DES and natural DES (NADES) offer tunable, biodegradable solvents capable of efficiently extracting these bioactive molecules while reducing the environmental impact associated with conventional organic solvents. Overall, the valorization of this biomass represents a sustainable strategy that simultaneously mitigates ecological and economic impacts and contributes to the development of sustainable inputs in agriculture. Full article

Saprolegnia parasitica (Oomycota) causes saprolegniosis and poses significant ecological and economic challenges in aquaculture. Experimental research on this pathogen is constrained by the lack of reliable long-term preservation methods, as routine maintenance by serial subculturing is labor-intensive and may result in genetic and phenotypic instability. Deep eutectic solvents (DESs), tunable low-melting mixtures, have recently gained attention as alternative cryoprotectants. However, their application has not been evaluated in oomycetes. Here, twelve glycerol-based two- and multicomponent DESs were assessed for cryopreservation of S. parasitica at −80 °C and compared with glycerol as a conventional cryoprotectant. Cryopreservation efficiency was assessed based on post-thaw survival and mycelial regeneration. Several two-component DESs, particularly glycerol-trehalose, supported 100% survival and high post-thaw mycelial regeneration, performing comparably to glycerol under the tested conditions. Shorter pre-incubation (30 min vs. 1 h and 3 h) and controlled-rate freezing (vs. direct freezing) significantly improved post-thaw growth. Although survival remained 100% under optimized conditions, extending storage from 7 to 32 days significantly reduced mycelial regeneration in the glycerol–trehalose treatment, indicating that survival alone, as done in existing literature, does not reflect physiological recovery. Overall, our results support the use of selected DESs as alternative cryoprotectants in oomycetes and contribute to the development of cryopreservation strategies for S. parasitica. Full article

Hydrogen represents a promising clean and renewable energy source. Therefore, improving the efficiency of electrocatalysts is essential for effective hydrogen production. In this work, Ni electrocatalysts were synthesized via the electrodeposition method from ethaline deep eutectic solvent (DES) at 45 °C, 55 °C, and 65 °C under perpendicular (B_⊥) and parallel (B_‖) magnetic field directions relative to the electrode surface. Scanning electron microscopy (SEM) was employed to investigate the morphological study, which shows that Ni deposits under B_⊥ promote columnar grain growth, while B_‖ favors lateral, compact structures. Furthermore, moderate temperature (55 °C) in the case of using B_⊥ produced finer grains and smoother surfaces compared to other temperatures in the same direction, enhancing the catalytic performance for HER. Electrochemical techniques, including linear sweep voltammetry (LSV) and chronoamperometry, were employed to evaluate the catalytic performance for HER in 1 M NaOH and the adsorption–desorption process, respectively. The results suggest that efficient HER performance is associated with balanced hydrogen adsorption and desorption behavior. The Ni deposit at 55 °C under (B_⊥) exhibited the lowest overpotential (−215 mV) compared to the deposits at 45 °C and 65 °C under the same magnetic field direction, indicating superior overall HER performance. This performance is attributed to balanced hydrogen adsorption–desorption behavior despite the relatively high Tafel slope value (298 mV·dec⁻¹). However, the lowest Tafel slope among the whole samples prepared under both (B_⊥) and (B_‖) was found to be (219 mV·dec⁻¹), reflecting faster kinetics, which was obtained for the sample deposited at 45 °C under (B_‖). Full article

This study investigates the 55%Al-Zn-Si coating system. Using microstructural characterization and thermodynamic simulation, we systematically analyzed its microstructure formation, solidification behavior, and the regulatory effects of Cr, Nb, and V micro-alloying elements. The results show that the typical coating consists of a primary α-Al dendritic skeleton and an interdendritic Zn-rich eutectic phase, exhibiting a characteristic spangle morphology. The addition of Si is crucial. By participating in the formation of a Fe-Al-Si ternary compound layer, it effectively suppresses the intense reaction at the Fe/Al interface, providing essential conditions for the sufficient growth of the outer Al-rich dendrites and the formation of a continuous transition layer. Thermodynamic analysis further clarifies that the coating solidification follows three distinct stages: precipitation of the primary α-Al phase, an Al-Si binary eutectic reaction, and a final Al-Zn-Si ternary eutectic transformation. Regarding micro-alloying, this study reveals the specific roles of different elements: Cr significantly refines the transition layer structure, promoting its transformation from coarse lamellae into a fine and uniform morphology; V tends to combine with Al to form high-melting-point enriched regions, inhibiting the growth of Fe-Al intermetallics and reducing the thickness of the brittle transition layer by approximately 50%; conversely, the addition of Nb disrupts the normal solidification sequence, inducing abnormal segregation of Al-rich and Si-rich phases, which compromises the homogeneity and integrity of the coating structure. Through an in-depth analysis of the fundamental solidification mechanism and micro-alloying effects, this research provides an important theoretical basis for optimizing the microstructure of hot-dip Al-Zn sheets via precise composition design and micro-alloying strategies. Full article

In this study, potential fungicides were prepared following the principles of green chemistry. The compounds were synthesized in deep eutectic solvents as an alternative medium and compared with syntheses in traditional solvents such as ethanol. The efficiency of the reaction was improved by ultrasonic synthesis in both eutectic solvents and ethanol, resulting in higher yields while reducing reaction energy and time. For the first time, deep eutectic solvents (DES) were used for quaternisation reactions, with choline chloride as a hydrogen bond acceptor and urea, glycerol, malic acid, malonic acid, and levulinic acid as donors. DES, composed of biodegradable, non-toxic, and renewable components, represented a greener alternative to conventional solvents. However, reactions in DES by the conventional method generally resulted in lower yields, probably due to solubility and viscosity limitations inherent in the eutectic medium. The combination of ultrasound and deep eutectic solvents proved to be a good alternative to organic solvents for the quaternisation reaction, as higher yields were achieved in a shorter time compared to conventional methods. The antifungal activity of all 18 synthesized compounds was tested. The compounds exhibited significant antifungal activity against all four pathogens, with varying levels of mycelial growth inhibition. B. cinerea was the most sensitive species (up to 70.7% inhibition), while F. culmorum was the least sensitive (≤32%). Full article

With the growing global emphasis on nuclear reactor decommissioning, reliable thermal neutron detection has become increasingly important for ensuring critical safety and for the identification of fuel debris and radioactive waste. In this context, this study developed and characterized a Ce-doped CaF₂/⁶LiF (Ce:CaF₂/LiF) eutectic scintillator for thermal neutron detection with Ce concentrations ranging from 0.5 to 10 mol%. The eutectic samples were grown by the melt-solidification method, and their crystalline properties were evaluated using inductively coupled plasma mass spectrometry, X-ray diffraction, scanning electron microscopy, and field-emission electron probe microanalysis. Radioluminescence, photoluminescence, transmittance, scintillation decay, and pulse-height measurements were conducted to assess their scintillation performance. Structural characterization revealed a well-defined eutectic microstructure together with several Ce-rich phases. The results of the effective neutron sensitivity demonstrated that the Ce concentration was effectively optimized based on the effective neutron sensitivity: the sample with 1 mol% Ce exhibited the highest neutron sensitivity (approximately 1.5 times that of a Ce:LiCaAlF₆ single crystal) and a 1.6-times higher neutron-induced light yield, while maintaining a fast effective decay time of 400 ns. These findings suggest that the Ce:CaF₂/LiF eutectic is a promising candidate for high-performance thermal-neutron scintillators for applications in nuclear decommissioning. Full article

This paper reports initial experimental results related to the preparation of colored anodic titania thin layers using various deep eutectic solvent (DES)-based formulations. Electrolytes based on choline dihydrogen citrate–oxalic acid–ethylene glycol (1:1:1 molar ratio), choline chloride–oxalic acid (1:1 molar ratio) and choline chloride–lactic acid (1:2 molar ratio) eutectic mixtures were investigated. The anodization has been performed at constant voltage in a range of 10–100 V for various periods of time between 1 and 5 min at room temperature under mild stirring. A brief description of anodization procedures, as well as of some characteristics, from appearance and morphological viewpoints, is presented. A quantitative analysis of color characteristics in relation to the DES-based electrolyte and applied voltage using the CIELAB system is also discussed. The achieved chromatic scale follows this order of colors: golden—blue—light blue—light blue/green—pink—violet. This depends on the applied potential and the DES-based electrolyte. The films present a relatively high brightness and color saturation. The hue vs. anodization voltage diagrams suggest an almost linear dependence of the oxide growth measured against the applied voltage. The corrosion performance has been assessed through continuous immersion tests in (i) 0.5 M NaCl for 240 h and (ii) Hank’s biological solution for 96 h with intermediate visual examinations and recording corrosion potential, as well as potentiodynamic polarization curves and impedance spectra at open circuit potential. Different corrosion performances are discussed considering the aggressive medium involved and the used DES-based systems. Full article

Zinc-ion batteries have garnered significant research interest owing to their inherent safety, low cost, and environmental compatibility. Nevertheless, their widespread adoption is impeded by critical challenges including uncontrollable dendrite growth, parasitic side reactions stemming from active water molecules, and the corrosion of the zinc anode in conventional aqueous electrolytes. Herein, a hydrated deep eutectic solvent (HDES) electrolyte based on ZnSO₄, MnSO₄, and ethylene is proposed for high-performance zinc-ion batteries. This electrolyte demonstrates excellent stability and simultaneously enables the formation of a protective coating on the Zn anode surface. Spectroscopic analyses and theoretical simulations reveal that this electrolyte reconfigures the primary Zn²⁺ solvation shell by replacing water molecules with HDES components. This tailored solvation structure facilitates interfacial desolvation, elevates nucleation overpotential, and promotes uniform, dendrite-free zinc deposition. Simultaneously, a robust hydrogen bond network effectively sequesters free water, significantly suppressing the hydrogen evolution reaction and anode corrosion. Benefiting from these features, the HDES-based full cell delivers exceptional long-term stability, achieving over 2000 cycles at 3 mA cm⁻² with a capacity retention exceeding 95% and a Coulombic efficiency surpassing 85%. In sharp contrast, the traditional aqueous counterpart fails within only 200 cycles. This tenfold lifespan enhancement, coupled with cost-effectiveness and non-flammability, presents a promising strategy for advanced, grid-scale zinc-based energy storage. Full article