Search Results (85)

In this work, biodegradable poly(vinyl alcohol) (PVA) and ferroelectric poly(vinylidene fluoride-co-hexafluoropropylene) (P(VDF-HFP)) nanofibers were successfully fabricated via co-electrospinning. The morphology and microstructure of co-electrospun PVA/P(VDF-HFP) nanofibers were analyzed, demonstrating that P(VDF-HFP) incorporation significantly affected fiber diameter and phase distribution. These structural features altered the fiber diameter and surface area of the co-electrospun system, thereby affecting interfacial polarization and the resulting dielectric and energy storage performance. As a result, the dielectric constant of the PVA/P(VDF-HFP) nanofibers (M1) was enhanced by up to 1.8 times compared with pure PVA nanofibers (M0), owing to interfacial polarization arising from increased surface charge accumulation at the PVA/P(VDF-HFP) interfaces. Meanwhile, dielectric loss and electrical conductivity were effectively controlled, indicating improved electrical stability of the co-electrospun system. Furthermore, ferroelectric and energy storage analyses revealed that appropriate incorporation of P(VDF-HFP) and phase distribution significantly enhanced polarization and energy storage performance. The energy storage density increased from 0.83 to 3.21 mJ cm⁻³ at 20 MV m⁻¹, corresponding to an improvement of 287% while maintaining a high energy efficiency of approximately 90%. Owing to their favorable dielectric properties, mechanical flexibility, and environmental compatibility, the co-electrospun PVA/P(VDF-HFP) nanofibers demonstrate great potential for low-field wearable and biomedical energy storage devices. Full article

This review focuses on the use of metal–organic frameworks (MOFs) for environmental remediation through adsorption processes in both liquid and gas phases. Due to their high surface areas and chemical tunability, MOFs offer promising performance in adsorbing environmental pollutants compared to traditional materials. In this work, we discuss advanced synthesis techniques, including solvothermal, room temperature, and mechanochemical techniques, and how each technique influences the resulting MOF’s structural properties. Furthermore, we analyze the use of MOFs as adsorbents for CO₂ and volatile organic compounds (VOCs) in the gas phase, as well as their role in removing heavy metals, fluorides, dyes, and emerging pharmaceutical contaminants. Although MOFs possess intrinsic limitations, such as instability in the presence of water and challenges in cyclic regeneration, their combination with other materials has aimed to overcome these drawbacks by leveraging the best properties of each component in new hybrid materials. Finally, we evaluate various challenges, such as large-scale implementation, toxicity, and long-term stability, proposing sustainable solutions for environmental remediation. Full article

The widespread occurrence of fluoride pollution in water bodies and its toxic effects on aquatic organisms have raised significant environmental concerns; however, studies on water quality criteria for fluoride remain relatively limited. This study aimed to derive such criteria and assess the ecological risks of fluoride in China’s surface waters, for the reference of readers. Acute and chronic toxicity data were collected globally, covering 34 species (14 families, 4 phyla) and 7 species (5 families, 3 phyla), respectively. Using species sensitivity distribution (SSD) methods, the short-term water quality criterion (SWQC) and long-term water quality criterion (LWQC) were derived as 17.47 mg/L and 3.334 mg/L. Ecological risk assessment based on the risk quotient (RQ) identified several high-risk areas among 32 major river and lake basins, with RQ values of 6.326 (Xihe River), 1.953 (Ebinur Lake), 1.368 (Chagan Lake), and 1.158 (Shahe River). At the provincial level, Guangxi Zhuang Autonomous Region showed as no risk (RQ = 0.0001140), while other regions were classified as moderate or low risk. This study achieved its objectives of deriving water quality criteria for fluoride and conducting an ecological risk assessment for surface waters in China. It also highlights current limitations, including insufficient fluoride toxicity data and the frequent oversight of key indicators in existing assessments. Future research could focus on improving water quality criteria derivation and risk assessment methods through integrated predictive modeling and expanded toxicity datasets. Full article

Femtosecond laser has been widely utilized in functional microstructural surfaces for applications such as anti-reflection, radiative cooling, and self-cleaning. However, achieving high-efficiency manufacturing of high-consistency functional microstructures (with feature sizes ~1 μm) over large areas remains a challenge. Here, we report a femtosecond laser temporal and spatial modulation technique for fabricating large-area anti-reflective microholes on magnesium fluoride (MgF₂) windows. The beam was transformed into a Bessel beam to extend the Rayleigh length, enabling the fabrication of microhole arrays with sub-micron precision and surface roughness variations within 10 nm over a 6 μm focal position shift range (5–11 μm). By modulating MHz burst pulses, the aspect ratio of the microholes was increased from 0.3 to 0.7 without compromising a processing speed of 10,000 holes per second. As a proof of concept, large-area anti-reflective microholes were fabricated on a 20 mm × 20 mm surface of the MgF₂ window, forming a nanoscale refractive index gradient layer and achieving a transmittance increase to over 98%. This method provides a feasible solution for the efficient and high-consistency manufacturing of functional microstructures over large areas. Full article

High-fluoride hot springs serve as a natural laboratory for investigating microbial adaptation and variations in community structure under extreme environments. This study utilized water chemistry analysis and 16S rRNA gene sequencing to investigate the correlation between high-fluoride hot springs and microbial community structure and diversity. The results show that the five hot springs exhibited an average F⁻ content of 15.04 mg/L, with weakly alkaline pH, high total dissolved solids, and Na⁺ as the dominant cation. The hydrochemical type was classified as HCO₃⋅SO₄-Na, consistent with the chemical characteristics of high-fluorine water. Microbial abundance and diversity were significantly reduced in the hot springs as compared to the surface water and groundwater samples. The dominant phyla in the study area included Pseudomonadota, Cyanobacteriota, Bacteroidota, and Actinomycetota. The genus-level composition varied significantly across samples, with no dominant genus observed universally. The specific genera present in different samples exhibit unique functional attributes, such as Tepidimonas, Rhodobacter, Hyphomonas, Parvibaculum, Polynucleobacter and Limnohabitans. Cluster analysis confirmed that dissimilarity coefficients highlight the significant influence of microbial abundance on inter-sample differences among hot springs. Redundancy analysis of the top 11 phyla by abundance in water samples revealed that the presence of F⁻ exerts inhibitory effects on microbial growth. Full article

Fluoride contamination in groundwater is a pressing environmental and public health issue, with chronic exposure linked to skeletal and dental fluorosis. Here, we report the synthesis of magnesium oxide nanoparticles via a controlled co-precipitation method employing dimethylformamide (DMF) as solvent and either ammonium hydroxide (MgO-1) or ammonium carbonate (MgO-2) as precipitating agents. The resulting materials were comprehensively characterized using thermogravimetric analysis (TGA/DSC), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and scanning electron microscopy coupled with energy dispersive spectroscopy (SEM/EDS). Additionally, BET surface area and porosity analyses revealed mesoporous structures, with MgO-1 showing a slightly higher surface area (14.12 m² g⁻¹) than MgO-2 (13.87 m² g⁻¹). Both MgO-1 and MgO-2 exhibited high crystallinity, nanoscale particle sizes (81.6 nm and 128.1 nm, respectively), and distinct morphological features. Batch adsorption studies revealed maximum fluoride uptake capacities of 117.6 mg/g (MgO-1) and 94.5 mg/g (MgO-2) at neutral pH, with MgO-1 exhibiting superior performance due to its smaller particle size and higher specific surface area. Fluoride removal remained above 98% between pH 3–9, confirming stability across a wide pH range, with a minor decline at pH 11 due to OH⁻ competition. Adsorption equilibrium data were best described by the Temkin isotherm model, suggesting heterogeneous surface interactions and an exothermic process, while kinetic analyses indicated pseudo-second-order behavior for MgO-1 and pseudo-first-order for MgO-2. Both materials maintained high fluoride selectivity in the presence of competing anions and successfully reduced fluoride in tap water from 2.11 mg/L to below the WHO limits without altering water hardness. These findings underscore the potential of engineered MgO nanomaterials as efficient, selective, and sustainable adsorbents for water defluoridation, offering a promising pathway toward scalable remediation technologies in fluoride-affected regions. Full article

Hydrometallurgy is currently the mainstream industrial process for recovering valuable components (nickel, cobalt, manganese, lithium, etc.) from spent ternary lithium-ion battery cathode materials. During the crushing of lithium batteries, cathode materials, anode materials (graphite), and electrolytes become mixed. Consequently, fluoride ions inevitably enter the leaching solution during the hydrometallurgical recycling process, with concentrations as high as 100–300 mg/L. These fluoride ions not only adversely affect the quality of the recovered precursor products but also pose environmental risks. To address this issue, this study employs a synthesized lanthanum–zirconium (La@Zr) composite material, with a specific surface area of 67.41 m²/g and a pore size of 2–50 nm, which can reduce the fluoride ion concentration in the leaching solution to below 5 mg/L, significantly lower than the 20 mg/L or higher that is typically achieved with traditional calcium salt defluorination processes, without introducing new impurities. Under optimal adsorption conditions, the lanthanum–zirconium adsorbent exhibits a fluoride ion adsorption capacity of 193.4 mg/g in the leaching solution, surpassing that of many existing metal-based adsorbents. At the same time as the valuable metals, Li, Ni, and Co, are basically not adsorbed, the selective adsorption of fluoride ions can be achieved. Adsorption isotherm studies indicate that the adsorption process follows the Langmuir model, suggesting monolayer adsorption. The secondary adsorption process is primarily governed by chemical adsorption, and elevated temperatures facilitate the removal of fluoride ions. Kinetic studies demonstrate that the adsorption process is well described by the pseudo-second-order model. After desorption and regeneration with NaOH solution, the adsorbent still has a favorable fluoride removal performance, and the adsorption rate of fluoride ions can still reach 95% after four cycles of use. With its high capacity, rapid kinetics, and excellent selectivity, the adsorbent is highly promising for large-scale implementation. Full article

The electrochemical performance of Li-ion batteries employing LiFePO₄ (LFP) cathodes supported by bio-sourced activated carbon derived from millet cob (MC) and water hyacinth (WH) were systematically investigated. Carbon activation was carried out using potassium hydroxide (KOH) at varying mass ratios of KOH to precursor material: 1:1, 2:1, and 5:1 for both WH and MC-derived carbon. The physical properties (X-ray diffraction patterns, BET surface area, micropore and mesopore volume, conductivity, etc.) and electrochemical performance (specific capacity, discharge at various current rates, electrochemical impedance measurement, etc.) were determined. Material characterization revealed that the activated carbon derived from MC exhibits an amorphous structure, whereas that obtained from WH is predominantly crystalline. High specific surface areas were achieved with activated carbons synthesized using a low KOH-to-carbon mass ratio (1:1), reaching 413.03 m²·g⁻¹ for WH and 216.34 m²·g⁻¹ for MC. However, larger average pore diameters were observed at higher activation ratios (5:1), measuring 8.38 nm for KOH/WH and 5.28 nm for KOH/MC. For both biomass-derived carbons, optimal electrical conductivity was obtained at a 2:1 activation ratio, with values of 14.7 × 10⁻³ S·cm⁻¹ for KOH/WH and 8.42 × 10⁻³ S·cm⁻¹ for KOH/MC. The electrochemical performance of coin cells based on cathodes composed of 85% LiFePO₄, 8% of these activated carbons, and 7% polyvinylidene fluoride (PVDF) as a binder, with lithium metal as the anode were studied. The LiFePO₄/C (LFP/C) cathodes exhibited specific capacities of up to 160 mAh·g⁻¹ at a current rate of C/12 and 110 mAh·g⁻¹ at 5C. Both LFP/MC and LFP/WH cathodes exhibit optimal energy density at specific values of pore size, pore volume, charge transfer resistance (R_ct), and diffusion coefficient (D_Li), reflecting a favorable balance between ionic transport, accessible surface area, and charge conduction. Maximum energy densities relative to active mass were recorded at 544 mWh·g⁻¹ for LFP/MC 2:1, 554 mWh·g⁻¹ for LFP/WH 2:1, and 568 mWh·g⁻¹ for the reference LFP/graphite system. These performance results demonstrate that the development of high-performing bio-sourced activated carbon depends on the optimization of various parameters, including chemical composition, specific surface area, pore volume and size distribution, as well as electrical conductivity. Full article

A triboelectricity-enhanced piezoelectric nanogenerator (PENG) based on pressure-processed multi-electrospun polymeric layers is herein developed for efficient vibrational energy harvesting. The hybridization of piezoelectric and triboelectric mechanisms through electrospinning has been utilized to enhance electrical output by increasing contact areas and promoting alignment within piezoelectric materials. A multi-layer structure comprising alternating poly (vinylidene fluoride) (PVDF) and poly (hexamethylene adipamide) (PA 6/6) exhibits superior electrical performance. A lateral Janus configuration, providing distinct positive and negative triboelectric polarities, has further optimized device efficiency. This approach introduces a novel operational mechanism, enabling superior performance compared to conventional methods. The fiber-based architecture ensures exceptional flexibility, low weight, and a high surface-to-volume ratio, enabling enhanced energy harvesting. Experimentally, the PENG achieved an open-circuit voltage of 14.59 V, a short-circuit current of 205.7 nA, and a power density of 7.5 mW m⁻² at a resistance of 30 MΩ with a five-layer structure subjected to post-processing under pressure. A theoretical model has mathematically elucidated the output results. Long-term durability (over 345,600 cycles) has confirmed its robustness. Demonstrations of practical applications include monitoring human joint motion and respiratory activity. These results highlight the potential of the proposed triboelectricity-enhanced PENG for vibrational energy harvesting in flexible and wearable electronic systems. Full article

Groundwater in the Qingshui River Plain of southern Ningxia is one of the main water sources for local domestic and agricultural use. However, due to the geological background of the area, 33.94% of the groundwater samples had fluoride concentrations that exceeded the WHO drinking water standards. To examine the spatial patterns and formation processes of fluoride in groundwater, researchers gathered 79 rock samples, 2618 soil samples, 21 sediment samples, 138 groundwater samples, and 82 surface water samples across the southern Qingshui River Plain. The collected data were analyzed using statistical approaches and hydrogeochemical diagrams. The findings reveal that fluoride levels in groundwater exhibit a gradual increase from the eastern, western, and southern peripheral sloping plains toward the central valley plain. Vertically, higher fluoride concentrations are found within 100 m of depth. Over a ten-year period, fluoride concentrations have shown minimal variation. Fluoride-rich rocks, unconsolidated sediments, and soils are the primary sources of fluoride in groundwater. The primary mechanisms governing high-fluoride groundwater formation are rock weathering and evaporative concentration, whereas cation exchange adsorption promotes fluoride (F⁻) mobilization into the aquifer. Additional sources of fluoride ions include leaching of fluoride-rich sediments during atmospheric precipitation infiltration and recharge from fluoride-rich surface water. Full article

The plateaus of north-central Mexico have an arid to semiarid climate and groundwater naturally contaminated with inorganic arsenic (iAs) and fluoride (F). Like other arid and semiarid areas, this region faces great challenges to maintain a safe supply of drinking and irrigation water. Studies conducted in the past few decades on various locations within this region have reported groundwater iAs, F, and nitrate-nitrogen (NO₃-N), and either their source, enrichment processes, health risks, and/or potential water treatments. The relevant findings are analyzed and condensed here to provide an overview of the groundwater situation of the region. Studies identify volcanic rocks (rhyolite) and their weathering products (clays) as the main sources of iAs and F and report that these solutes become enriched through evaporation and residence time. In contrast, NO₃-N is reported as anthropogenic, with the highest concentrations found in large urban centers and in agricultural and livestock farm areas. Health risks are high since the hot spots of contamination correspond to populated areas. Health problems associated with NO₃-N in drinking water may be underestimated. Removal technologies of the contaminants remain at the laboratory or pilot stage, except for the reverse osmosis filtration units fitted to selected wells within the state of Chihuahua. A recent approach to supplying drinking water free of iAs and F to two urban centers consisted of switching from groundwater to surface water. Incipient research currently focuses on the potential repercussions of irrigating crops with As-rich water. The groundwater predicaments concerning contamination, public health impact, and irrigation suitability depicted here can be applied to semiarid areas worldwide. Full article

Li/graphite fluoride (Li/CF_x) batteries display the highest energy densities among those of commercially available primary Li batteries but fail to satisfy the high-performance requirements of advanced applications. To address this drawback, two liquid organic dinitrates, namely, 1,4-butanediol dinitrate (BDE) and 2,2,3,3-tetrafluoro-1,4-butanediol dinitrate (TBD), were employed as high-energy energetic materials, and they were highly compatible with the electrolytes of Li/CF_x batteries. The use of Super P electrodes confirmed that the reduction reaction mechanisms of both nitrate ester-based compounds delivered considerable specific capacities, associated with discharge potentials matching that of the Li/CF_x battery. When considering the combined mass of the electrolyte and cathode as the active material, the overall energy densities of the Li/CF_x batteries increased by 25.3% (TBD) and 20.8% (BDE), reaching 1005.50 and 969.1 Wh/kg, respectively. The superior performance of TBD was due to the synergistic effects of the high electronegativities and levels of steric hindrance of the F atoms. Moreover, the nanocrystal LiF particles generated by TBD induced crack formation within the fluorinated graphite, increasing the lithium-ion accessible surface area and enhancing its utilization efficiency. These combined factors enhanced the reactivity of TBD and facilitated its involvement in electrochemical reactions, thus improving the capacity of the battery. The developed strategy enables the facile, cost-effective enhancement of the capacities of Li/CF_x batteries, paving the way for their practical use in energy-demanding devices. Full article

This study achieved the preparation of budget-friendly stratified Ca-Al adsorbents using a simplified precipitation synthesis route with subsequent pyroprocessing, showing superior defluoridation capabilities in aqueous environments. The structural properties and defluoridation performance of the adsorbents were systematically investigated by optimizing critical synthesis parameters, including calcium-to-aluminum molar ratios, the solution pH during co-precipitation, and calcination temperature. Characterization results revealed that the optimal sample (prepared at a Ca/Al ratio of 2:3, initial pH of 10, and calcination temperature of 600 °C) exhibited a high specific surface area, ordered mesoporous structure, and abundant surface hydroxyl groups, facilitating efficient fluoride adsorption. Batch adsorption experiments demonstrated significant effects of adsorbent mass, solution pH, and initial fluoride concentration on removal efficiency. The isothermal adsorption characteristics conformed to the Langmuir model, complemented by pseudo-second-order kinetic compliance, which jointly confirmed chemisorption-dominated monolayer coverage. Notably, the maximum adsorption capacity reached 263.33 mg g⁻¹, surpassing most comparable adsorbents reported in the literature. The material maintained a superior fluoride removal performance across a wide pH range (4~12) and exhibited superior recyclability. Rapid adsorption kinetics were observed, with equilibrium achieved within 60 min. The material showed a good removal effect in actual fluoride-containing smelting wastewater, which further proved its application potential. In addition, the analysis of the adsorption mechanism showed that the removal of fluoride was mainly achieved through the coordination between fluoride and metal ions and the ion-exchange reaction with surface hydroxyl groups. These findings suggest that the adsorbent has significant prospects for practical water quality fluoride removal applications. Full article

This study investigated the impact of zinc oxide’s (ZnO’s) morphology on the piezoelectric performance of polyvinylidene fluoride (PVDF) composites for flexible sensors. Rod-like (NR) and sheet-like (NS) ZnO nanoparticles were synthesized via hydrothermal methods and incorporated into PVDF through direct ink writing (DIW). The structural analyses confirmed the successful formation of wurtzite ZnO and enhanced β-phase content in the PVDF/ZnO composites. At a degree of 15 wt% loading, the ZnO-NS nanoparticles achieved the highest β-phase fraction (81.3%) in PVDF due to their high specific surface area, facilitating dipole alignment and strain-induced crystallization. The optimized PVDF/ZnO-NS-15 sensor demonstrated superior piezoelectric outputs (4.75 V, 140 mV/N sensitivity) under a 27 N force, outperforming its ZnO-NR counterparts (3.84 V, 100 mV/N). The cyclic tests revealed exceptional durability (<5% signal attenuation after 1000 impacts) and a rapid response (<100 ms). The application trials validated their real-time motion-monitoring capabilities, including finger joint flexion detection. This work highlights the morphology-dependent interfacial polarization as a critical factor for high-performance flexible sensors, offering a scalable DIW-based strategy for wearable electronics. Full article

Sulfur hexafluoride (SF₆), the strongest greenhouse gas, has great challenges in degradation because of its stable structure, posing significant environmental concerns. Photocatalysis offers an environmentally friendly, low-energy solution, but the fluoride deposition on catalysts reduces their activity, thus limiting their large-scale application. To prevent catalyst fluoride poisoning, we report a thin-layer graphitic carbon nitride (CN) material loaded with MoO_x (CNM) that resists fluoride deposition for long-term SF₆ degradation. By combining molecular structure design and nanostructure regulation, we construct a photocatalyst with enhanced charge carrier mobility and reduced transport distances. We find that the CNM exhibits a high specific surface area, increased contact between reactants and active sites, and efficient electron–hole separation due to the Mo-N bonds, achieving an SF₆ degradation efficiency of 1.73 mmol/g after one day due to the prolonged catalytic durability of the catalyst, which is eight times higher than pristine g-C₃N₄ (0.21 mmol/g). We demonstrate the potential of CNMs for low-energy, high-efficiency SF₆ degradation, offering a new approach to mitigate the environmental impact of this potent greenhouse gas. We envision that this study will inspire further research into advanced photocatalytic materials for environmental remediation, contributing to global efforts in combating climate change. Full article