Zinc Research Articles

Efficiency of Reverse Osmosis Usage in Drinking Water Depots to Reduce Iron (Fe3+), Copper (Cu2+) and Zinc (Zn2+) Ion Levels

Research on the efficiency of reverse-osmosis drinking water depot to decreased levels of iron (Fe3+), Copper (Cu2+) and Zinc (Zn2+) ions have been done. The raw, the treated, and waste water are filtered using reverse osmosis (RO) three times a week. HNO3 then was added to the sample until it reached 15 mL. The determination of the concentration of the three ions was performed using atomic absorption spectrophotometer (AAS). The results showed a decrease of Fe3+ concentration of 73.21%, for Cu2+ decrease by 80.25%, while Zn2+ decrease by 82.08%. For waste water obtained iron ion concentration of 0.1794 mg/L, for Cu2+ by 0.0239 mg/L, while Zn2+ by 0.0962 mg/L.

Modulating Fibrotic Mechanical Microenvironment for Idiopathic Pulmonary Fibrosis Therapy

AbstractIdiopathic pulmonary fibrosis (IPF) is exacerbated by injurious mechanical forces that destabilize the pulmonary mechanical microenvironment homeostasis, leading to alveolar dysfunction and exacerbating disease severity. However, given the inherent mechanosensitivity of fibrotic lungs, where type II alveolar epithelial cells (AEC IIs) are subjected to persistent stretching and overactivated myofibroblasts experience malignant interactions during mechanotransduction, it becomes imperative to develop effective strategies to modulate the pulmonary mechanical microenvironment. Herein, cyclo (RGDfC) peptide‐decorated zeolitic imidazolate framework‐8 nanoparticles (named ZDFPR NPs) are constructed to target and repair the aberrant mechanical force levels in pathological lungs. Specifically, reduces mechanical tension in AEC IIs by pH‐responsive ZDFPR NPs that release zinc ions and 7, 8‐dihydroxyflavone to promote alveolar repair and differentiation. Meanwhile, malignant interactions between myofibroblast contractility and extracellular matrix stiffness during mechanotransduction are disrupted by the fasudil inhibition ROCK signaling pathway. The results show that ZDFPR NPs successfully restored pulmonary mechanical homeostasis and terminated the fibrosis process in bleomycin‐induced fibrotic mice. This study not only presents a promising strategy for modulating pulmonary mechanical microenvironment but also pioneers a novel avenue for IPF treatment.

(Fe, Co) oxide nanowires on gold nanoparticles modified MOF-derived carbon nanoflakes for high-efficiency sodium-ion batteries and supercapacitors across electrolytes

The three-dimensional conductive porous carbon nanosheets (CPCN) are from the bimetallic metal-organic framework (MOFs) consisting of organic ligating groups that incorporate zinc and cobalt ions deposited onto a flexible carbon cloth (CC). Utilizing a hydrothermal approach, iron-cobalt oxide (FCO) nanowires are intricately embedded onto CPCN modified with gold (Au), forming a flexible FCO/Au/CPCN@CC electrode. The electrochemical characteristics of electrodes are evaluated in 1 M Na2SO4, supercapacitor's storage capacity is tested at 4 V using 1 M NaPF6 electrolyte. Among its remarkable attributes are a peak energy density of 291.5 W h kg−1 achieved at a power density of 153.85 W kg−1, and even at the maximum power density of 1749.9 W kg−1, it maintains 144.78 W h kg−1. Undergoing 10,000 rounds of GCD, the equipment sustains a capacitance retention of 84.27 %. Moreover, the performance of the FCO/Au/CPCN@CC anode in sodium-ion batteries (SIBs) is assessed. At 0.1C, the discharge capacity reaches 958 mAh g−1, and there is almost no loss after the rate cycle. The Coulomb efficiency surpasses 98 % during 500 cycles at a large C-rate. The integration of Au nanoparticles onto the CPNC surface enhances the energy storage characteristic of the FCO/Au/CPCN@CC composite material in both battery and supercapacitor applications.

Metal Contamination and Human Health Risk Assessment of Soils from Parks of Industrialized Town (Galati, Romania)

The aim of the present study was to evaluate the contamination state of the surface soil from 10 parks from Galati, Romania, and the health hazards of the soil. The soil samples, collected in each site from the playing ground and from the edge of the park, were analyzed by using combined Wavelength- (WDXRF) and Energy-Dispersive (EDXRF) X-ray fluorescence techniques. A total number of 27 chemical elements (Ag, Al, As, Ba, Ca, Cd, Cr, Co, Cu, Fe, Hg, K, Mg, Mn, Na, Ni, P, Pb, Rb, Sb, Sc, Sn, Sr, Ti, V, Zn and Zr) were quantified in the urban soils, and the results were compared to the normal and alert values from Romanian legislation for toxic trace elements, as well as with European and world average values of element concentrations. The mineralogical analyses were performed by Scanning Electron Microscopy with Energy-Dispersive X-ray Analysis (SEM-EDX) and the Attenuated Total Reflectance–Fourier Transform Infrared technique (ATR-FTIR). To assess the soil contamination and the impact on human health of the presence of potential toxic elements and heavy metals in the soil, a series of pollution and health risk indices were used. All the results indicated an unpolluted to moderately polluted soil. The soil samples collected from the edge of the parks presented higher values for the specific pollutants, which originated from heavy traffic, such as Cu, Cr, Zn and Pb. The non-carcinogenic and carcinogenic risk to children was assessed using estimated daily intake (EDI) in relation to the pathways whereby pollutants can enter the human body, such as ingestion, dermal contact, inhalation and vaporization. Using the obtained values for EDI, the hazard quotient and hazard index were determined, which strengthen the formerly issued presumption that soil pollution is moderate and, by itself, does not present any threat to children’s health.

Simultaneous Modulation on Solvation Shell and Electrode Interface for Reversible Zinc Anode Realized by a Mutiplefunctional Additive

AbstractThe inferior reversibility of Zn metal anode caused by undesired Zn dendrite and severe interfacial side reactions has to be addressed for the commercial application of Zinc ion batteries (ZIBs). Here, a multiple functional sodium benzaldehyde 2,4‐disulfonate(B24DADS) additives with various blocks of polar sulfonate group, Lewis basic aldehyde groups, and hydrophobic benzene ring is proposed to regulate the solvation structure of Zn2+, construct an H2O‐poor and zincophilic dual electric layer structure, and create a passive SEI on the Zn anode surface, thus restaining dendrite growth and interfacial side reactions. Furthermore, uniform deposition mechanics of the Zn are revealed by the synergistic effect of induced deposition, additive‐derived SEI formation, and texture regulation. In addition, Na+ can also limit the growth of zinc dendrites based on electrostatic shielding mechanisms. Therefore, the multifunctional B24DADS additive grants the anode to deliver remarkable electrochemical performance. Under critical test conditions (20 mA cm−2/20 mAh cm−2), the zinc provides superior long cycling (3700 h) with a low polarization voltage (0.02 V). B24DADS containing electrolyte is well matched with manganese dioxide cathode. This effort renders a promising way to explore advanced additives with unique molecular structures for addressing zinc dendrite growth and rampant side effects.

A sustainable route: from wasted alkaline manganese batteries to high-performance cathode for aqueous zinc ion batteries

A sustainable route: from wasted alkaline manganese batteries to high-performance cathode for aqueous zinc ion batteries

Distribution of Pb, Zn, Fe, As, Sn, Sb, Bi, and Ni Between Oxide Liquid and Metal in the ‘CuO0.5’-CaO-AlO1.5 System in Equilibrium with Cu Metal at 1400 °C

AbstractThe increasing complexity of ore resources and recycled materials in the feed of pyrometallurgical processes present a technical challenge to the metallurgical engineers working on maximizing the recovery of the valuable elements and minimizing the environmental impact of the processes. To address this challenge, the availability of computational tools that can predict the mass and energy balance in complex systems is required. Then, the accurate description of phase equilibria in the complex multicomponent systems describing the chemistry of the pyrometallurgical processes becomes critical for the correct implementation of the indicated tools and facing the outlined industrial challenges. In the present study, the distribution of selected elements (Pb, Zn, Fe, As, Sn, Sb, Bi, and Ni) between oxide liquid and metal in the ‘CuO0.5’–CaO–AlO1.5 system in equilibrium with Cu metal at 1400 °C (liquidus of CaAl2O4) was experimentally studied using the equilibration and quenching technique followed by the electron probe X-ray microanalysis of the resulted samples. The study covered a wide range of effective p(O2) over the system from 10−11 to 10−3.5 (corresponding to formation of immiscible CuO0.5-rich slag). To avoid loss of volatile elements (Pb, Zn, As, Sn, Sb, and Bi), a correlation between ‘CuO0.5’ in oxide liquid and p(O2) in open system was obtained first, followed by studying the volatile elements distribution in closed conditions (Al2O3 crucible sealed in SiO2 ampoule), where ‘CuO0.5’ concentration was used as a marker to evaluate the effective p(O2) over the system. The experimental results were then used for the optimization of the thermodynamic model parameters of the system as part of the integrated experimental and self-consisting thermodynamic modeling research program of phase equilibria in the Cu–Pb–Zn–Fe–Ca–Si–Al–Mg–O–S–(As, Sn, Sb, Bi, Ag, Au, Ni, Cr, Co, and Na) gas/oxide liquid/matte/speiss/metal/solids system. Graphical Abstract

Hair and Blood Trace Elements (Cadmium, Zinc, Chrome, Lead, Iron and Copper) Biomonitoring in the Athletic Horse: The Potential Role of Haematological Parameters as Biomarkers

The aim of the present study was the evaluation of the bioaccumulation of cadmium (Cd), Zinc (Zn), Chrome (Cr), Lead (Pb), Iron (Fe) and Copper (Cu), in the blood, serum, tail and mane of horses from the industrialized area of Milazzo (Messina, Sicily), to understand the relationships between haematological parameters: Red Blood Cells (RBCs), White Blood Cells (WBCs), Haemoglobin (Hb), Haematocrit (Hct), Mean Corpuscular Volume (MCV), Mean Corpuscular Haemoglobin (MCH), Mean Corpuscular Haemoglobin Concentration (MCHC), Platelets (PLTs) and the concentrations of trace elements. Blood and hair samples from 20 healthy Italian Saddle horses and water, hay and concentrates samples were obtained to determine the haemogram and mineral concentration using a Thermo Scientific iCAP-Q ICP-MS spectrometer. Descriptive analysis showed a higher concentration of Zn, Cr, Pb, Fe, and Cu in the blood and a higher concentration of Cd in the tail than other substrates. A positive correlation was found for Cr (p < 0.0001) and Zn (p < 0.01) between blood and serum substrates, for Zn (p < 0.001) between mane and tail and for Pb (p < 0.01) between blood and mane, while a negative correlation was observed for Cr (p < 0.01) between blood and tail. Results showed a close relationship between the bioaccumulation of certain trace elements in biological substrates and haematological parameters, which represent useful biomarkers suggesting further studies, given the role of haematological parameters in athletic horses.

Evaluating health risks of PM2.5-bound heavy elements in Faridabad, Haryana (India): an industrial perspective.

The present study isfocused on investigating the heavy/toxic metals (Al, Ni, Cr, Pb, Cu, As,Mn, and Zn) of PM2.5 and assessing their associated human health risks. During the study period (July 2022 to July 2023), the PM2.5 samples were collected from two distinct sites in Faridabad (92 samples from site 1 and 85 samples from site 2). In this study, the US EPA's Risk Assessment Guidance for Superfund (RAGS) was followed to evaluate the human health risk associated with PM2.5-bound heavy elements. The annual average of PM2.5 concentrations was 108 ± 16µgm⁻3 at site 1 and 154 ± 11µgm⁻3 at site 2, approximately three to fourtimes higher than the national ambient air quality standards (annual, 40µgm-3). The analysis of enrichment factors (EFs) for the elements Cr, As, Zn, Cu, Mn, Pb, and Ni indicates that the heavy elements associated with PM2.5 primarily originate from anthropogenic sources. The application of the conditional bivariate probability function (CBPF) model for Faridabad revealed local pollution sources contributing to elevated mass concentrations at the receptor site from the southern (S), northwestern (NW), northeastern (NE), southwestern (SW), and southeastern (SE) regions. Furthermore, positive matrix factorization (PMF) analysis identified the predominant sources of PM2.5-bound heavy elements as industrial emissions (41%), vehicular emissions (34%), and combustion processes (25%). After a thorough assessment of health hazards, Cr appeared as a significant carcinogenic risk factor. Children with elevated hazard quotient (HQ) values for Mn and Cr indicated non-carcinogenic health problems. Ultimately, this analysis reinforces the necessity for rigorous monitoring and intervention to safeguard public health from the potentially harmful effects of heavy elements.

Sn Penetrated Zincophilic Interface Design in Porous Zn Substrate for High Performance Zn-Ion Battery.

Rechargeable zinc-ion batteries are considered an ideal energy storage system due to their low cost and nonflammable aqueous electrolyte. However, dendrite growth, hydrogen evolution reaction, and self-corrosion of zinc anode brought about serious safety risks including short circuits and electrode expansion. Therefore, a modified host-design strategy with a 3D porous structure and bulk-phase penetrated zincophilic interface is proposed to boost the stability and lifetime of the Zn anode. The porous Zn substrate is constructed by universal HCl etching and the uniform and tight Sn-penetrated zincophilic interface is formed by effective electron beam evaporation (EBE). The porous substrate can uniform zinc ion flux and the Sn coating could effectively improve zinc ion deposition behavior, thus inhibiting the risk of dendrites growth and side reaction. As a result, the 3D Zn substrate with Sn interface (3D Zn@Sn) exhibits prolonged galvanostatic cycling performance up to 4500h with a low polarization of ≈25mV (1mAcm-2, 1mAhcm-2) in the symmetric cell. The full cell assembled with KVOH@Ti could maintain a high specific capacity of 148.6mAhg-1 after 500 galvanostatic cycles (10Ag-1). This work proposed an improved electrode design to realize the high performance of zinc ion batteries.

LC3B-Regulated Autophagy Mitigates Zinc Oxide Nanoparticle-Induced Epithelial Cell Dysfunction and Acute Lung Injury.

Zinc oxide nanoparticles (ZnONPs) are widely utilized across various industries, raising concerns about their potential toxicity, especially in the respiratory system. This study explores the role of autophagy, regulated by microtubule-associated protein 1A/1B-light chain 3B (LC3B), in ZnONPs-induced toxicity using both in vivo (LC3B knockout mice) and in vitro (BEAS-2B cells) models. Our findings demonstrate that LC3B-regulated autophagy mitigates ZnONPs-induced epithelial cell dysfunction and acute lung injury. In the absence of LC3B, oxidative stress, inflammation, and intracellular zinc accumulation are exacerbated, resulting in mitochondrial dysfunction and epithelial cell death. In vitro, LC3B knockdown disrupted zinc ion transporter expression and impaired mitophagic flux in BEAS-2B cells. Treatment with zinc ion chelators alleviated these toxic effects, confirming that free zinc ions play a critical role in driving ZnONPs toxicity. These findings highlight that targeting autophagy and maintaining zinc homeostasis could offer therapeutic strategies to reduce ZnONPs-induced lung damage.

Functional and structural analyses of IMP-27 metallo-β-lactamase: evolution of IMP-type enzymes to overcome Zn(II) deprivation.

IMP-type metallo-β-lactamases are di-Zn(II) enzymes that can inactivate a wide range of bicyclic β-lactam agents used in clinical practice. IMP-27 shares 82% amino acid sequence identity with IMP-1, the first IMP-type enzyme identified. Herein, we conducted structural determination, kinetic, and chelating agent resistance analyses of IMP-27. Once determined, IMP-27 was then compared to its mutant, namely, G262S, and IMP-1. Crystallographic structural analysis of IMP-27 showed an overall structure comparable to that of IMP-1 and other IMP-type enzymes; the positions of the zinc (Zn) ions varied across enzymes. Kinetic analysis showed that IMP-27 had lower catalytic efficiency against penicillins, ceftazidime, cephalexin, and imipenem than IMP-1; however, it had higher affinity and catalytic efficiency against meropenem, especially in the presence of Zn(II). This suggests that the catalytic site of IMP-27 is optimized to hydrolyze meropenem during molecular evolution at the expense of catalytic efficiency against penicillins. However, Zn(II) content analysis after EDTA treatment revealed no significant difference between enzymes. Moreover, analysis of IMP-27 mutants indicated that the differences in kinetic properties and chelator resistance between IMP-1 and IMP-27 were mainly due to an amino acid substitution at position 262.IMPORTANCEThe residue at position 262 has been reported as a key determinant of substrate specificity in IMP-type enzymes. Among more than 80 IMP-type metallo-β-lactamase (MBL) variants, IMP-27 was the first reported IMP-type MBL isolated from Proteus mirabilis. This enzyme has a glycine residue at position 262, which is occupied by serine in IMP-1. Compared with IMP-1, IMP-27 had a significantly higher affinity and catalytic efficiency against meropenem and improved metal-binding capacity, maintaining its activity under Zn(II)-limited conditions better than IMP-1. The analysis of the IMP-27 mutants indicated that differences between IMP-27 and IMP-1 were mainly due to an amino acid substitution at position 262. In the case of IMP-27, the G262S mutation optimized the catalytic site of IMP-27 for meropenem hydrolysis, at the expense of catalytic efficiency against penicillins.

Porous V2CTx MXene as a High Stability Zinc Anode Protective Coating.

Aqueous Zn batteries exhibit significant research potential owing to their environmental friendliness and high energy density. Nevertheless, the formation of dendrites on the zinc anode and the sluggish diffusion kinetics of zinc ions adversely affect the cycle life of zinc ion batteries. In this study, we employ porous V2CTx (MVMX) as a protective layer for the zinc anode. The uniform porous structure of MVMX promotes active site exposure and facilitates the transport of zinc ions. Remarkably, the Zn@Ti half-cell demonstrated an average CE of 99.7% in 1500 cycles. Furthermore, the Zn-Zn symmetric battery exhibited stable cycling for 1600 h at current densities of 5 mA cm-2 and 1 mAh cm-2. Additionally, the MVMX@Zn||V2O5 full cell exhibited a capacity of 198 mAh g-1 and retained a capacity of 124.75 mAh g-1 after 5000 cycles at 1 A g-1, demonstrating the potential of employing alternative MXenes for fabricating stable zinc anodes.

Anion-induced optimization of non-aqueous zinc-air battery performance: Insights into OTF− selection

Rechargeable non-alkaline zinc-air batteries (ZABs) address the CO₂ incompatibility and instability issues of conventional alkaline batteries. However, the impact of solid discharge products like zinc oxide on discharge capacity at the air cathode remains unexplored. In this study, we investigate how anions influence ion pair solvation structures using Zinc trifluoromethanesulfonate (Zn(OTF)₂)-N, N-dimethylformamide (DMF) and Zinc acetate (Zn(Ac)₂)-DMF electrolytes, and how these structures affect the distribution of discharge product. Our finding shows that anions with lower donor numbers (DNs), like the weaker ligand OTF- (20.5), enhance the zinc ion activity and promote rapid Zn2⁺ reactions with oxygen during discharge, leading to a more than tenfold increase in discharge capacity. In contrast, acetate anions with higher DNs (43.3) form stable complexes, inhibiting zinc ion activity and causing the formation of film-like discharge products, which reduces ZAB performance. The Zn(OTF)₂-DMF electrolyte also enables a battery lifespan of over 200 h, more than fivefold compared to the acetate-based system.

Evaluation of uranium migration during the maturation of hydrocarbon source rocks.

The source of uranium is an important research topic related to the exploration of sandstone-type uranium deposits, and potential uranium sources in deep basins are often overlooked. Black organic-rich shale is a common uranium-bearing rock in deep sedimentary basins. However, relatively few studies have investigated the migration of uranium during hydrocarbon generation in and release from uranium-rich shale. In this study, the uranium-rich shale in the Chang 7 member of the Yanchang Formation of the Upper Triassic in the Ordos Basin was selected to investigate the migration of uranium and other trace elements during the thermal maturation of uranium-rich shale via a semiopen pyrolysis simulation system. The gas and liquid products as well as the solid residue were thoroughly analysed by means of multiple instruments. The results showed that uranium significantly migrated before hydrocarbon generation (Ro < 0.61%), with a leaching rate between 12.1% and 18.8%. The leaching rate of uranium during the hydrocarbon generation stage (0.63% < Ro < 1.35%) was relatively low, ranging from 0 to 7.2%. Cu, Pb, Zn, Mo, and other trace elements also migrated considerably during the early stage of thermal evolution, with leaching rates ranging from 2.9 ~ 11.6%. The yield of low-molecular-weight organic acids (LOAs) was the highest in the early stage of thermal maturity, and the LOA yield exhibited a good correlation with the leaching rates of Cu, Pb, Zn, Co, Mo, etc. The generation of LOAs from source rocks was conducive to the leaching and migration of trace elements. Moreover, according to a statistical analysis of published geochemical data, the total organic carbon (TOC) content, uranium content, and U/TOC ratio in shale decreased significantly with increasing burial depth, indicating that uranium migrated significantly upon kerogen hydrocarbon generation during thermal evolution. Therefore, uranium-rich shale is an important deep uranium source in sedimentary basins.

Quantum entangle in a zinc ion pair of RNA-dependent RNA polymerase of flaviviruses and its role in the polymerization reaction

Quantum entangle in a zinc ion pair of RNA-dependent RNA polymerase of flaviviruses and its role in the polymerization reaction

Nickel-mediated V4O7 as high-performance cathode material for aqueous Zn-ion batteries

Vanadium-based materials are currently favored by researchers due to their multi-structure, which can enhance the steric resistance and electrostatic repulsion during the (de)intercalation process of zinc ions. However, their low conductivity remains an inherent hindrance to their practical application. Therefore, finding a way to adjust the electronic structure of vanadium-based compounds is considered an effective strategy. Presently, we have designed a porous Ni-mediated V4O7, wherein the presence of oxygen defects and heterostructures in V4O7/NiO (Od-NVO-4) substantially improves the diffusion kinetics of ions/electrons and boosts the electrochemical performance. As anticipated, the Zn//V4O7/NiO battery exhibits a high specific capacity (348.6 mAh g−1 at 0.1 A g−1), favorable rate capability (323.8 mAh g−1 at 4 A g−1), and remarkable cycle stability (206.3 mAh g−1 at 2 A g−1 after 2000 cycles). Additionally, the underlying mechanism of electrochemical zinc storage is comprehensively described through electrochemical kinetic analysis and theoretical calculations. These results unambiguously reveal the intrinsic link between the surface/interface structure and electrochemical performance of the cathode, offering a valuable reference for designing high-performance electrode materials.

Mutant-selective AKT inhibition through lysine targeting and neo-zinc chelation.

Somatic alterations in the oncogenic kinase AKT1 have been identified in a broad spectrum of solid tumours. The most common AKT1 alteration replaces Glu17 with Lys (E17K) in the regulatory pleckstrin homology domain1, resulting in constitutive membrane localization and activation of oncogenic signalling. In clinical studies, pan-AKT inhibitors have been found to cause dose-limiting hyperglycaemia2-6, which has motivated the search for mutant-selective inhibitors. We exploited the E17K mutation to design allosteric, lysine-targeted salicylaldehyde inhibitors with selectivity for AKT1 (E17K) over wild-type AKT paralogues, a major challenge given the presence of three conserved lysines near the allosteric site. Crystallographic analysis of the covalent inhibitor complex unexpectedly revealed an adventitious tetrahedral zinc ion that coordinates two proximal cysteines in the kinase activation loop while simultaneously engaging the E17K-imine conjugate. The salicylaldimine complex with AKT1 (E17K), but not that with wild-type AKT1, recruits endogenous Zn2+ in cells, resulting in sustained inhibition. A salicylaldehyde-based inhibitor was efficacious in AKT1 (E17K) tumour xenograft models at doses that did not induce hyperglycaemia. Our study demonstrates the potential to achieve exquisite residence-time-based selectivity for AKT1 (E17K) by targeting the mutant lysine together with Zn2+ chelation by the resulting salicylaldimine adduct.

Strong Ion‐Dipole Interactions for Stable Zinc‐Ion Batteries with Wide Temperature Range

AbstractAqueous zinc‐ion batteries are widely recognized as promising alternatives to lithium batteries due to their excellent safety, environmental compatibility, and cost‐effectiveness. Nonetheless, the formation of dendrites, corrosion, and undesirable side reactions on the zinc surface pose significant challenges to the cycling stability of zinc‐ion batteries. In this study, polar propylene carbonate (PC) is paired with tetrafluoroborate anions to establish a strong ion‐dipole interaction. Strong ion‐dipole interaction can not only alter the solvation structure of zinc ions but also facilitate the formation of a dynamic double electric layer on the surface of the zinc electrode, suppressing the formation of ZnF2 interface and carbonate, thereby facilitating uniform zinc ion deposition, and consequently improving battery cycling stability over a broad temperature range. Concretely, the formulated electrolyte enhances the cycling stability of the battery over a wide temperature range of −30 to 40 °C, accompanied by a capacity retention of ≈100% even after 10 000 cycles at −30 °C. The symmetrical battery utilizing this electrolyte exhibits stable cycling performance for over 1200 h at 25 °C and 1900 h at −30 °C, respectively. The findings provide a promising direction for the development of long‐cycle batteries capable of operating over a wide temperature range.

Pollution risk assessment and spatial distribution of potentially hazardous elements in selenium-rich soils in the Menyuan Basin of the northeastern Tibetan Plateau

The scientific utilization of selenium (Se)-rich soils necessitates the evaluation of the contents of potentially hazardous elements (PHEs). The Menyuan Basin, a representative Se-rich region located on the northern periphery of the Qinghai–Tibet Plateau, was chosen as the research area. Pollution risk and spatial source analysis was conducted for eight PHEs (As, Cr, Cu, Pb, Zn, Cd, Ni and Hg) using 5297 topsoil samples and 480 deep-soil samples. The results show that more than 50% of the total area has a Se content &gt;0.24 mg kg –1 . According to both single and comprehensive pollution indices, there are extremely few sampling sites with PHEs at risk of contamination. Low ecological risk was seen in 93.34% of the topsoil samples. The results show that although the overall level of surface soil pollution in the study area may be deemed negligible, on the surface or in deeper layers, the concentration centres of As, Cr, Ni, Zn, Pb and other elements show consistency, indicating that underlying parent rocks are the primary source of these elements. The findings presented in this study establish a scientific foundation for the secure development and utilization of Se-rich soils.