Zinc Metal Research Articles

Numerical study of P3HT-based hybrid solid-state qantum dot solar cells with CdS quantum dots employing different metal oxides using SCAPS-1D

This study presents a comprehensive numerical investigation into solid-state quantum dot solar cells (SSQDSCs) utilizing P3HT poly(3-hexylthiophene) as both a hole transport and absorber layer employing SCAPS-1D simulation software, the research explores the performance of cells composed of FTO (Fluorine-doped Tin Oxide) as the front contact, integrated with different metal oxides (Titanium dioxide (TiO2), zinc oxide (ZnO), and tin dioxide (SnO2), CdS (Cadmium sulfide )quantum dots, P3HT, and Pt (platinum )as the back contact namely Hybrid solar cell. The thickness of each layer is systematically optimized, and the influence of various CdS quantum dots sizes is thoroughly examined. The study also dived into the characterization of interface defects at the P3HT/CdS junction, involving modifications to the electron affinity of P3HT. Additionally, the impact of metal work function variations was also investigated analyzing at each case critical parameters such as open-circuit voltage (VOC), short-circuit current density (JSC), fill factor (FF), power conversion efficiency (PCE) and quantum efficiency. The results demonstrate that optimization of these parameters has the potential to elevate solar cell efficiency to 18%. These simulation findings offer valuable insights for comparative analysis and a deeper understanding of the challenges encountered in experimental research.

High-viscoelasticity alginate-based coatings for reversible zinc metal anodes

High-safety aqueous zinc (Zn) ion batteries are troubled by dendrite growth and hydrogen evolution reaction on Zn anode, which can be well solved via the construction of surface protective layer. The recent researches mainly focus on the bulk property of the protective layer, but its separation from Zn anode is ignored. In this work, high-viscoelasticity alginate-based (HVAA) layer was in-situ constructed on Zn anodes by the cross-linking of sodium alginate with formaldehyde and the plastifying of glycerin. HVAA layer can combine with H2O and coordinate with Zn2+ ions in aqueous electrolyte to achieve viscoelasticity on Zn anode, which can accommodate volume change of Zn anode during plating/stripping processes to continuously protect Zn anodes under the real battery system. Physical block effect of HVAA layer impedes hydrogen evolution corrosion reaction by avoiding the immediate contact of Zn anodes with aqueous electrolyte. Ionic conductive ability of HVAA layer by coordinating oxygen-containing groups with Zn2+ can uniform ion flux to induce the homogeneous deposition of Zn2+ on Zn anode. Zn anode with HVAA endows ZnZn symmetric battery with stably cycle of 4000 h and Zn-iodide full batteries with better electrochemical performance of 8000 cycles comparing with bare Zn anode. This work opens a novel route to continuously protect Zn anode through the high-viscoelasticity films to closely fit with Zn surface and implement the high-value application of renewable sources.

Breath inspired multifunctional low-cost inorganic colloidal electrolyte for stable zinc metal anode

The practical application of aqueous zinc-ion batteries (AZIBs) is primarily constrained by issues such as corrosion, zinc dendrite formation, and the hydrogen evolution reaction occurring at the zinc metal anode. To overcome these challenges, strategies for optimizing the electrolyte are crucial for enhancing the stability of the zinc anode. Inspired by the role of hemoglobin in blood cells, which facilitates oxygen transport during human respiration, an innovative inorganic colloidal electrolyte has been developed: calcium silicate-ZnSO4 (denoted as CS-ZSO). This electrolyte operates in weak acidic environment and releases calcium ions, which participate in homotopic substitution with zinc ions, while the solvation environment of hydrated zinc ions in the electrolyte is regulated. The reduced energy barrier for the transfer of zinc ions and the energy barrier for the desolvation of hydrated ions imply faster ion transfer kinetics and accelerated desolvation processes, thus favoring the mass transfer process. Furthermore, the silicate colloidal particles act as lubricants, improving the transfer of zinc ions. Together, these factors contribute to the more uniform concentration of zinc ions at the electrode/electrolyte interface, effectively inhibiting zinc dendrite formation and reducing by-product accumulation. The Zn//CS-ZSO//Zn symmetric cell demonstrates stable operation for over 5000 h at 1 mA cm−2, representing 29-fold improvement compared to the Zn//ZSO//Zn symmetric cell, which lasts only 170 h. Additionally, the Zn//CS-ZSO//Cu asymmetric cell shows stable average Coulombic efficiency (CE) exceeding 99.6% over 2400 cycles, significantly surpassing the performance of the ZSO electrolyte. This modification strategy for electrolytes not only addresses key limitations associated with zinc anodes but also provides valuable insights into stabilizing anodes for the advancement of high-performance aqueous zinc-ion energy storage systems.

Regulating the Zn electrode/electrolyte interface with lactose additive for high performance Zn anode

The practical utilization of rechargeable aqueous zinc metal batteries (AZMBs) has been constrained by the formation of zinc dendrites and other associated issues. This article introduces lactose, a compound rich in hydroxyl groups, as an electrolyte additive into the aqueous solution of the electrolyte with the objective of suppressing the harmful growth of zinc dendrites. The lactose additive, with its strong zincophilicity, robust intermolecular hydrogen bonding, and a large number of exposed high electronegativity hydroxyl groups, enables lactose to effectively modulate the electrode/electrolyte interface in a dynamic manner, thereby achieving the stability and reversibility of the zinc anode. The findings presented in this work demonstrate the uniform deposition and stripping of zinc in a 2 M ZnSO4 electrolyte with the addition of lactose, thereby enhancing the cycling performance of Zn||Zn batteries. The alteration of the zinc ion environment on the surface of the zinc electrode, in conjunction with the dynamic modulation of the Gouy-Chapman-Stern (GCS) layer by lactose, increases the nucleation overpotential, thereby facilitating to a uniform deposition morphology in lieu of the formation of large-scale dendrites. Furthermore, the formation of hydrogen bonds serves to prevent the occurrence of side reactions. These factors act in concert to enhance the electrochemical performance of AZMBs. The addition of lactose to the electrolyte has resulted in a significant enhancement in the Coulombic efficiency of the card-type Zn||Cu asymmetric battery, reaching 99.7 %. The biodegradability of lactose and the sustainability of its source make this research conducive to the development of environmentally friendly battery electrolyte additives.

Voltage-driven Molecular Switch of Highly Periodically N‒heterocyclic Adlayer Enabled Deep Cycled Zinc Metal Battery

Voltage-driven Molecular Switch of Highly Periodically N‒heterocyclic Adlayer Enabled Deep Cycled Zinc Metal Battery

Antioxidant and antidiabetic potential of Cystoseira myrica-mediated green metallic zinc nanoparticles using the algal extract: synthesis and characterization

Abstract Cystoseira myrica marine macroalgae (CSR) were used to produce metallic zinc nanoparticle composites by utilizing the phytochemicals naturally found in the algae. This involves homogenizing the residuals of CSR (10 g), zinc nitrate solution (5 M; 100 ml), and methanol liquid extract (100 ml) at 30 °C for 24 h of sonication and stirring, followed by filtration and drying. This resulted in a hybrid bio-composite (Zn/CSR), which demonstrated strong antioxidant and antidiabetic properties when compared to zinc oxide (ZnO) and CSR used separately. The Zn/CSR hybrid showed excellent antioxidant activity against common radicals such as DPPH (91.5 ± 1.66%), nitric oxide (90.4 ± 1.2%), ABTS (92.2 ± 1.9%), and O2 ·− (27.8 ± 1.12%) (p < 0.05), performing better than the standard antioxidant, ascorbic acid. Regarding its antidiabetic properties, the Zn/CSR composite significantly inhibited key enzymes involved in diabetes, including both commercial enzyme forms (α-amylase (80.3 ± 1.65%), α-glucosidase (96.6 ± 1.11%), amyloglucosidase (95.8 ± 1.3%)) and their crude intestinal forms (α-amylase (72.3 ± 1.5%), α-glucosidase (94.2 ± 1.7%)) (p < 0.05). This improvement increases the impact of the green CSR extract in reducing the agglomeration behaviors of the loaded metal and the formation of a capping layer from the phytochemicals on its surface, in addition to the beneficial effects of the CSR as substrate, which enhances the biological functions of the loaded metal and its interaction interfaces. The Zn/CSR composite also outperformed commercial miglitol drugs and slightly surpassed acarbose in effectiveness. Given the high cost and potential side effects of current medications, the Zn/CSR composite could be a cost-effective alternative for antioxidant and antidiabetic treatments. These findings also emphasize the role of CSR-derived phytochemicals and algae residues in enhancing the biological activity of the metal nanoparticles.

Calcareous soil modified with metallic and organic ZnO nanoparticles limits photosynthetic pigment accumulation and macronutrient uptake in Swiss chard (Beta vulgaris var. cicla)

Previous studies on the effects of zinc oxide nanoparticles have mainly examined controlled agricultural settings, failing to consider their behavior in real agricultural soil. As a result, our knowledge of their environmental impact remains incomplete. This study was specifically developed to observe the comparative effects of metallic zinc oxide nanoparticles, zinc sulfate, and zinc oxide green nanoparticles at different concentrations (25, 50, 75 and 100mg of Zn kg-1 of soil) on growth parameters, the mineral content (N, P, K and Zn) in root and leaf, the content of chlorophyll a (CHLa), b (CHLb), and total (CHLt), and carotenoids in Swiss chard plants grown in calcareous soil. Leaf area and dry root weight increased by 23.27% and 46.20%, respectively, in zinc sulfate modified soil. Total chlorophyll and carotenoids also increased by 40.12% and 32.59%. The concentration of N, P, K and Zn in roots was 2.89, 1.74, 1.70 and 1.52 times higher, while in leaves, the concentration was 1.48, 1.44, 1.76 and 2.22 times higher in plants grown with zinc sulfate. The effects on plant growth can be attributed to the type of fertilizer used and its influence on macronutrient absorption in the soil. The utilization of zinc sulfate as a soil treatment led to elevated absorption of macronutrients and zinc, suggesting a connection between the fertilizer type and the crop’s agronomic and physiological reactions.

Assessment of Heavy Metal (Zinc, Copper, Lead and Cadmium) Contamination in Common Edible Shellfish Species of the Hooghly River and Sunderbans, India

The content of four heavy metals (Zinc, Copper, Lead and Cadmium) in muscles of three shell fish species - prawns -Penaeus monodon and Penaeus indicus and crabs-Scylla serrata, the most prime shellfish food resources of human in the domestic and international market were studied at four stations in the estuarine belt near Bay-of-Bengal which receives wastes of various types from industries and various anthropogenic activities. The samples were digested by acid digestion. The metal contents were quantified using an AAS (Atomic absorption spectrophotometer). The distribution of trace metals accumulated in the muscle tissues of the above mentioned species was in the order- Zn > Cu> Pb> Cd. In the present study, levels of Zinc in the shell fishes ranged from 07.44±0.65 to 128.10 ±2.96 ; Cu ranged from 5 ±0.15 to 99.14 ±1.31; Pb varied from 1.67± 0.14 to 23.99 ± 0.79 and Cd ranged from 1.29± 0.35 to 7.09 ± 0.80.The concentration of the four metals exhibited spatial variation as station 1 >station 2 > station 3 > station 4, which could be a reflection of different bioavailability of metal concentrations in the water body at different stations. The results obtained showed that the metal concentrations in most of the cases were above the threshold value recommended by WHO. Metals such as Cu, Zn, Pb, Cd, can affect various aquatic organisms as well as human being either directly or indirectly as they can enter into the food chain and may be biomagnified at higher trophic levels which is one of the top concerns for human health. Essential heavy metals such as Zinc and Copper are relatively less harmful at low concentration while non-essential metals such as Cd and Pb are highly toxic even at low concentrations.

Multidentate Chelating Ligands Enable High-Performance Zinc-Bromine Flow Batteries.

Zinc bromine flow battery (ZBFB) is a promising battery technology for stationary energy storage. However, challenges specific to zinc anodes must be resolved, including zinc dendritic growth, hydrogen evolution reaction, and the occurrence of "dead zinc". Traditional additives suppress side reactions and zinc dendrite formation by altering the solvation structure of Zn2+ and adsorbing onto the zinc surface through only a limited number of zincophilic sites, resulting in weak adsorption on zinc metal and potential inability to simultaneously optimize the solvation structure of zinc ions. Obviously, increasing the number of potential zincophilic sites in the additive can significantly enhance the interaction with zinc. Herein, we propose a strong chelate, ethylenediamine tetramethylene phosphonic acid (EDTMPA) as the additive, which boasts six potent zincophilic sites, not only promotes the formation of the water-deficient inner Helmholtz plane but also plays a crucial role in restructuring the solvation environment of Zn2+. As a result, the zinc symmetric flow battery with EDTMPA exhibited exceptional coulombic efficiency of 99.4% over 800 cycles, surpassing the previous studies by a significant margin. Furthermore, the assembled ZBFB has showcased a dendrite-free and enduring cycling over 400 cycles at 80 mA cm-2.

Multidentate Chelating Ligands Enable High‐Performance Zinc‐Bromine Flow Batteries

Zinc bromine flow battery (ZBFB) is a promising battery technology for stationary energy storage. However, challenges specific to zinc anodes must be resolved, including zinc dendritic growth, hydrogen evolution reaction, and the occurrence of "dead zinc". Traditional additives suppress side reactions and zinc dendrite formation by altering the solvation structure of Zn2+ and adsorbing onto the zinc surface through only a limited number of zincophilic sites, resulting in weak adsorption on zinc metal and potential inability to simultaneously optimize the solvation structure of zinc ions. Obviously, increasing the number of potential zincophilic sites in the additive can significantly enhance the interaction with zinc. Herein, we propose a strong chelate, ethylenediamine tetramethylene phosphonic acid (EDTMPA) as the additive, which boasts six potent zincophilic sites, not only promotes the formation of the water‐deficient inner Helmholtz plane but also plays a crucial role in restructuring the solvation environment of Zn2+. As a result, the zinc symmetric flow battery with EDTMPA exhibited exceptional coulombic efficiency of 99.4% over 800 cycles, surpassing the previous studies by a significant margin. Furthermore, the assembled ZBFB has showcased a dendrite‐free and enduring cycling over 400 cycles at 80 mA cm−2.

Measurements of Heavy Elements and Radioactivity Concentration Levels in Types of Fertilizers and Pesticides Commonly Used in Sana’a Yemen

This study aims to measure heavy metals (HMs) concentration and radioactivity concentration levels in fertilizer and pesticide samples collected from local markets in Sana’a, Yemen. Gamma spectroscopy employing a Survey Sodium Iodide NaI (TI) RIIDEYM-G detector was used for radiation and dose assessments. As for heavy metal analyses, this study used Inductively Coupled Optical Emission Spectroscopy (ICP-OES). Thirty samples were collected from local markets in Sana’a, Yemen. Radioactivity measurements show low levels of radioactivity concentration. The average dose rates due to fertilizer and pesticide samples were 1.14 and 1.07 mSv/y, respectively. These values are nearly equal to the recommended annual radiation dose rate limit (1mSv/y) recommended by the International Commission on Radiological Protection (ICRP). For heavy metal analysis, it was found that the average concentrations of heavy metals (HMs) (cadmium (Cd), chromium (Cr), copper (Cu), iron (Fe), nickel (Ni), lead (Pb), and zinc (Zn)) in the fertilizer samples were 1.08 mg/kg, 4.944 mg/kg, 13.8495 mg/kg, 274.371 mg/kg, 3.30446 mg/kg, 15.35686 mg/kg, and 24.4547 mg/kg, respectively. Heavy metal concentrations in fertilizer samples were mainly less than European (EU) guideline limits, with the exception of a few samples. The average concentrations of heavy metals (Cd, Cr, Cu, Fe, Ni, Pb, and Zn) in the pesticide samples were 0.8 mg/kg, 0.5784 mg/kg, 52.280 mg/kg, 73.4651 mg/kg, 2.4482 mg/kg, 3.199 mg/kg, and 1.1309 mg/kg, respectively. The heavy metal concentrations in pesticide samples were less than the corresponding values in fertilizer samples.

Zincophilic Sites Enriched Hydrogen‐Bonded Organic Framework as Multifunctional Regulating Interfacial Layers for Stable Zinc Metal Batteries

AbstractTo construct an efficient regulating layer for Zn anodes that can simultaneously address the issues of dendritic growth and side reactions is highly demanded for stable zinc metal batteries (ZMBs). Herein, we fabricate a hydrogen‐bonded organic framework (HOF) enriched with zincophilic sites as a multifunctional layer to regulate Zn anodes with controlled spatial ion flux and stable interfacial chemistry (MA‐BTA@Zn). The framework with abundant H‐bonds helps capture H2O and remove the solvated shells on [Zn(H2O)6]2+, leading to suppressed side reactions. The HOF layer also helps form electrolyte‐philic surfaces and expose Zn (002) crystal planes which benefit for rapid conduction and uniform deposition of Zn2+, and weakened sides reactions. Additionally, the electrochemically active zincophilic sites (C=O, −NH2 and triazine groups) favor the targeted guidance and penetration of Zn2+ and provide advantageous sites for uniform Zn deposition. High Young's modulus of the HOF layer further contributes to a high interfacial flexibility and stability against Zn plating‐associated stress. The MA‐BTA@Zn symmetric cells thereby obtain a substantially extended battery life over 1000 h at 4 mA cm−2. The MA‐BTA@Zn||Cu half‐cell demonstrates a highly reversible Zn stripping/plating process over 1500 cycles with impressive average Coulombic efficiency (CE) of 99.5 % at 10 mA cm−2.

Enhanced Polyaniline Cathode in Capacity and Cyclability of Zinc Metal Batteries by Natural Glycyrrhizic Acid Self-Doping

Enhanced Polyaniline Cathode in Capacity and Cyclability of Zinc Metal Batteries by Natural Glycyrrhizic Acid Self-Doping

Stable Zinc Metal Battery Development: Using Fibrous Zirconia for Rapid Surface Conduction of Zinc Ions With Modified Water Solvation Structure.

The two most critical technical issues in Zn-based batteries, dendrite formation, and hydrogen evolution reaction, can be simultaneously addressed by introducing negatively charged fibrous ZrO2 as a separator. Electron redistribution between ZrO2 and Zn2+ ions renders the ZrO2 surface a preferred adsorption site for Zn2+ ions, making surface conduction the primary ion-transport mode. Surface conduction enables fibrous ZrO2 to exhibit a 6.54 times higher single-Zn-ion conductivity than that of conventional glass fiber, minimizing the concentration gradient of Zn2+ and suppressing dendrite formation. Additionally, strong Zr─O─Zn bonding stabilizes the Zn2+ ions with fewer solvated H2O molecules (≈2), preventing water molecules from approaching the electrode surface, as evidenced by a 58.8% decrease in the hydrogen evolution rate. Consequently, the cycling stability of a fibrous-ZrO2-based Zn/Zn symmetric cell (3000h at 1mAhcm-2 and 5mAcm-2) is approximately ten times greater than that of the conventional variant. Furthermore, a fibrous-ZrO2-based Zn-I2 full cell exhibits a notably high energy density (271.4Whkg-1) as well as a long lifespan (≈5000 cycles) at an ultrahigh current density (4Ag-1).

Bifunctional Ion Rectification Layer Separators Toward Superior Reversible Dendrite‐Free Zinc Metal Anodes

AbstractThe slow transport dynamics and poor dendritic growth significantly hinder the performance of zinc metal batteries. Here, a unique difunctional ion rectification strategy is developed using vacuum evaporation technology to design a coated separator for efficient ion transport. The highly conductive Cu‐coated separator acts as an ion redistributor, ensuring homogenized electric field distribution. The excellent znophilicity of the copper coating acts as an ion accelerator, promoting ion transport and facilitating face‐to‐face zinc deposition on the separator. Consequently, this synergy enables stable battery operation at high current densities (cumulative capacity up to 10 800 mAh cm−2 at 8 mA cm−2) and high depth of discharge (over 200 h at 94% DOD). The Cu‐coated separator exhibits a reversible plating/stripping life of over 2400 h with an average coulombic efficiency of 99.88%. Notably, the Cu‐coated separator significantly enhances the rate performance and cycle capacity of Zn||V6O13 and Zn||MnO2 full cells. This functional separator with a difunctional ion rectification strategy presents a promising solution to the challenge of zinc metal anodes.

Biogenic synthesis and physicochemical characterization of metal nanoparticles based on Calotropis procera as promising sustainable materials against skin cancer

The UAE harbors a rich diversity of wild medicinal plants, such as Calotropis procera (CP), that are renowned for their extensive use in traditional medicine due to their abundance of bioactive phytochemicals. Zinc and iron metals possess significant pharmacological effects including antioxidant and anticancer properties. In this study, nanoparticles (NPs) containing zinc and iron were green synthesized utilizing ethanolic and aqueous extracts of CP aerial parts. UV-Vis spectra revealed absorption peaks around 270–275 nm, while FT-IR analysis confirmed successful coating of the NPs with plant’s phytochemicals. SEM/EDX analysis indicated a more potent reducing effect of the aqueous extract, whereas the alcoholic extract demonstrated more effective coating of the NPs. DLS showed monodispersed NPs with average sizes of 32.67–202 nm. The alcoholic extract-based zinc and iron NPs exhibited the highest phenolic and flavonoid contents (51.06 ± 2.82 µg of GAE/mg of DW and 66.26 ± 1.12 µg of Qu/mg of DW, respectively) and the strongest antioxidant effect against ABTS and DPPH radicals (IC50 = 52.81 and 148.46 µg/mL, respectively). The aqueous extract-based zinc NPs demonstrated the greatest cytotoxicity against A-431 cell lines (IC50 = 188.97 µg/mL). The findings highlight promising potential of these sustainable materials for therapeutic applications, indicating a need for continued research and development in this area.

Evolution of Frustrated Coordination in Eutectic Electrolyte Driven by Ligand Asymmetry toward High-Performance Zinc Batteries.

Eutectic electrolytes hold promise for aqueous zinc metal batteries in sustainable energy storage chemistries, yet improvement from perspective of molecule configurational engineering are ambiguous. Herein, we propose design strategy of increasing asymmetric molecular geometry in organic ligands to regulate frustrated coordination and disordered structure for eutectic electrolytes toward enhanced zinc metal batteries. The introduced asymmetry in eutectic component gives rise to relatively weak coordination strength and configurational disorder interaction among cation-anion-ligand, leading to suppressed local aggregation, steady eutectic phase and improved Zn2+diffusion kinetics. Such highly frustrated coordination state also enables disruption of hydrogen bonding network and reinforcement of anion participation, which results in confined side reactions, decreased water activity and the formation of inorganic-enriched solid electrolyte interphase. In comparison to highly symmetric ligands, asymmetric ligand-involved eutectic electrolytes with configurational disorderdeliver high Coulombic efficiency of 99.4 %, stabilized Zn plating/stripping of 5000 h and impressive rate capability even under harsh conditions such as small N/P, low temperature. The rationale in this work advances the deep understanding of asymmetric molecular engineering in eutectic electrolytes and showcases suitability of frustrated coordination to achieve high-performance zinc metal batteries.

Assessing the sustainability and safety of polyethylene terephthalate (PET) liners for lead service lines (LSL) upgrades

Polyethylene Terephthalate (PET) liners have been proposed by industry as a more cost effective and less disruptive alternative to lead service lines (LSL) replacement. However, concerns have been raised about their aging under real-use conditions and their potential health and environmental impacts. In this study, two approaches were implemented. First, bench and pilot scale experiments were carried out to investigate the aging of a PET liner under conditions that simulate normal usage. Results show early surface oxidation and leaching of potentially hazardous metals (lead, zinc and titanium). No short-term fragmentation of the PET liner into microplastics was observed. Next, a life cycle assessment (LCA) compared the health and environmental impacts of three LSL upgrade alternatives: PET liners and full LSL replacement using either copper or PEX pipes. The installation phase was shown to be the main contributor to impact scores, while the benefits of PET liners are highly dependent on their lifespan. PEX pipes installed by torpedoing lower impacts as compared to PET liners and copper pipes for equal lifespan, while the use of PET liners remains less impactful regarding human health and ecosystem quality when a complete excavation is needed. LCA derived global human health effects due to ingestion of leached metals from PET liners, copper pipes and unreplaced LSL, and showed that PET liners and copper pipes significantly reduce health impacts by 14 and 80 DALY respectively compared to unreplaced LSL. Finally, the Integrated Exposure Uptake Biokinetic (IEUBK) model was used to assess the impact of lead exposure specifically for drinking water ingestion. Estimated Blood Lead Levels (BLL) in children and infants in households with long unreplaced LSL was up to 263.7% and 207.8% greater compared to either replacement with copper pipes or rehabilitation with PET liners, showing the clear benefits of corrective action. Combining experimental results, LCA and biokinetic modeling provides actionable information for utilities to select the best upgrade options, considering environmental, health and practical constraints, whilst identifying remaining data gaps. The relative benefits of PET liners should be carefully evaluated considering their lifespan under real-life conditions, the complete replacement costs after failure, and the growing evidence of micro- and nanoplastics (MNP) risks.

Innovative Zinc Anodes: Advancing Metallurgy Methods to Battery Applications.

Aqueous zinc metal batteries (AZMBs) are emerging as a powerful contender in the realm of large-scale intermittent energy storage systems, presenting a compelling alternative to existing ion battery technologies. They harness the benefits of metal zinc's high safety, natural abundance, and favorable electrochemical potential (-0.762V vs Standard hydrogen electrode, SHE), alongside an impressive theoretical capacity (820mAhg-1 and 5655mAhcm-3). However, the electrochemical performance of ZMBs is impeded by several challenges, including poor compatibility with high-loading cathodes and persistent side reactions. These issues are intricately linked to the inherent physicochemical properties of the zinc metal anodes (ZMAs). Here, this review delves into the traditional methods of ZMAs production, encompassing extraction, electrodeposition, and rolling processes. The discussion then progresses to an exploration of cutting-edge methodologies designed to enhance the electrochemical performance of ZMAs. These methods are categorized into alloying, pre-treatment of substrate, advanced electrodeposition techniques, and the development of composite anodes utilizing zinc powder. The review offers a comparative analysis of the merits and drawbacks of various optimization strategies, highlighting the beneficial outcomes achieved. It aspires to inspire novel concepts for the advancement and innovation of next-generation zinc-based energy storage solutions.

Targeting Metals in Alzheimer's Disease: An Update.

One pathological feature of Alzheimer's disease (AD) is the dysregulated metal ions, e.g., zinc, copper, and iron in the affected brain regions. The dysregulation of metal homeostasis may cause neurotoxicity and directly addressing these dysregulated metals through metal chelation or mitigating the downstream neurotoxicity stands as a pivotal strategy for AD therapy. This review aims to provide an up-to-date comprehensive overview of the application of metal chelators and drugs targeting metal-related neurotoxicity, such as antioxidants (ferroptotic inhibitors), in the context of AD treatment. It encompasses an exploration of their pharmacological effects, clinical research progress, and potential underlying mechanisms.