Search Results (962)

The development of flexible and self-powered electronic systems requires triboelectric materials that combine high charge retention, mechanical compliance, and stable dielectric properties. Here, we report a redox reaction approach to prepare liquid metal particle-reduced graphene oxide (LMP@rGO) core–shell structures and introduce into a poly(acrylic acid) (PAA) hydrogel to create a high-performance triboelectric layer. The spontaneous interfacial reaction between gallium oxide of LMP and graphene oxide produces a conformal rGO shell while simultaneously removing the native insulating oxide layer onto the LMP surface, resulting in enhanced colloidal stability and a controllable semiconductive bandgap of 2.7 (0.01 wt%), 2.9 (0.005 wt%) and 3.2 eV (0.001 wt%). Increasing the GO content promotes more complete core–shell formation, leading to higher zeta potentials, stronger interfacial polarization, and higher electrical performance. After embedding in PAA, the LMP@rGO structures form hydrogen-bonding networks with the hydrogel nature, improving both dielectric constant and charge retention while notably preserving soft mechanical compliance. The resulting LMP@rGO/PAA hydrogels show enhanced triboelectric output, with the 2.0 wt/vol% composite generating sufficient power to illuminate more than half of 504 series-connected LEDs. All the results demonstrate the potential of LMP@rGO hydrogel composites as promising triboelectric layer materials for next-generation wearable and self-powered electronic systems. Full article

Pt-rare earth metal (Pt-RE) alloys are considered to be one of the most promising electrocatalysts for producing oxygen reduction reactions (ORRs) due to their compressively strained Pt overlayer and their exceptional negative-alloy formation energies, which result in excellent activity and stability. However, there are still great challenges in the chemical synthesis of Pt-RE nanoalloys. Herein, we report a simple method employing the nanopores of porous carbon as nanoreactors to synthesize a Pt₅La nanoalloy. The Pt₅La alloy nanoparticles are embedded in porous carbon (Pt₅La@C) with a particle size of around 1–3 nm and also exhibit a very narrow size distribution because of the confined-space effect. The as-prepared Pt₅La@C nanoalloy exhibits highly efficient ORR performance with a half-wave potential of 0.912 V in 0.1 M HClO₄, which is 56 mV higher than that of a commercial Pt/C catalyst. Moreover, it achieves an improved intrinsic activity of 0.69 mA cm⁻² and, a mass activity of 0.42 A mg_Pt⁻¹ at 0.90 V. In addition, it also delivers a very stable lifespan performance, with negligible decay in half-wave potential after accelerated stress testing for 10,000 cycles. This work also provides a new method for the development of promising Pt-RE nanoalloys with ultrasmall nanoparticles with a very narrow size distribution for various efficient energy-conversion devices. Full article

A first-principles investigation was conducted to characterize the novel Cr₂ZnC MAX phase and its exfoliated MXene nanosheet, Cr₂C. The study critically examines the effect of electron correlations on the bulk phase, revealing that the PBE+U framework, unlike standard PBE, yields a dramatically enhanced magnetic moment of 12.80 μ_B (vs. 1.88 μ_B), confirming the necessity of this approach for Cr-based carbides. The phase stability is confirmed through rigorous analysis of its thermodynamic, dynamic, and mechanical properties. For the derived 2D Cr₂C, results confirm a robust half-metallic state with a total magnetic moment of 8.00 μ_B, characterized by a metallic spin-majority channel and a semiconducting spin-minority channel with a 2.41 eV direct gap, leading to near-ideal spin polarization. These combined features establish Cr₂C as a highly promising candidate for next-generation spintronic applications and 2D magnetic devices requiring room-temperature stability. Full article

Electron transfer (ET) is a foundational biogeochemical process in paddy soils, distinctively molded by alternating anaerobic-aerobic conditions from flooding-drainage cycles. Despite extensive research on heavy metal(loid) (denoted as “HM”, e.g., As, Cd, Cr, Hg) dynamics in paddies, ET has not been systematically synthesized as a unifying regulatory mechanism, and the trade-offs of ET-based mitigation strategies remain unclear. These critical gaps have drastically controlled HMs’ mobility, which further modulates bioavailability and subsequent accumulation in rice (Oryza sativa L., a staple sustaining half the global population), posing substantial food safety risks. Alongside progress in electroactive microorganism (EAM) research, extracellular electron transfer (EET) mechanism delineation, and soil electrochemical monitoring, ET’s role in orchestrating paddy soil HM dynamics has garnered unparalleled attention. This review explicitly focuses on the linkage between ET processes and HM biogeochemistry in paddy ecosystems: (1) elucidates core ET mechanisms in paddy soils (microbial EET, Fe/Mn/S redox cycling, organic matter-mediated electron shuttling, rice root-associated electron exchange) and their acclimation to flooded conditions; (2) systematically unravels how ET drives HM valence transformation (e.g., As(V) to As(III), Cr(VI) to Cr(III)), speciation shifts (e.g., exchangeable Cd to oxide-bound Cd), and mobility changes; (3) expounds on ET-regulated HM bioavailability by modulating soil retention capacity and iron plaque formation; (4) synopsizes ET-modulated HM accumulation pathways in rice (root uptake, xylem/phloem translocation, grain sequestration); (5) evaluates key factors (water management, fertilization, straw return) impacting ET efficiency and associated HM risks. Ultimately, we put forward future avenues for ET-based mitigation strategies to uphold rice safety and paddy soil sustainability. Full article

Background/Objectives: Leishmaniasis constitutes one of the most fatal parasitic diseases globally, adversely impacting the health of individuals residing in both intertropical and temperate zones. In these geographical areas, the administration of treatment is often inconsistent and largely ineffective with the available pharmaceuticals, as these exhibit more pronounced side effects than the therapeutic advantages they purport to provide. Methods: Consequently, the current investigation seeks to engage in molecular modeling of novel pharmacological candidates incorporating 1,2,3 disubstituted triazole moieties, coordinated with Cu^II metal centers, in pursuit of promising bioactive properties. Results: Two complexes were prepared and X-ray analysis revealed a comparable structural configuration surrounding the copper (II) atom. The planar square coordination geometry was elucidated through the assessment of the ${\tau }_4=0$ (tau four) parameters. The comprehensive characterization encompasses HRMS-ESI (+), NMR, elemental analyses, mid-infrared, and UV-vis spectroscopic techniques. Time-dependent density functional theory (TD-DFT) analyses will substantiate the findings obtained through UV-vis spectroscopy. Crucially, the biological assays against Leishmania (L.) amazonensis revealed that Complex 1 exhibited outstanding potency against the intracellular amastigote form, demonstrating a half-maximal inhibitory concentration (IC₅₀) of 0.4 µM. This activity was 6-fold higher than that of amphotericin B (IC₅₀ = 2.5 µM) and 33-fold higher than pentamidine (IC₅₀ = 13.3 µM). Furthermore, Complex 1 showed a promising selectivity index (SI = 9.7) against amastigotes, surpassing the reference drugs and meeting the criteria for a lead compound. While less active on promastigotes, both complexes demonstrated high stability in DMSO solution, a prerequisite for biological testing. Conclusions: These results unequivocally identify Complex 1 as a highly promising candidate for the development of new antileishmanial therapies, warranting further in vivo studies. Full article

Medicinal and aromatic plants contain valuable natural compounds widely used in health, food, and cosmetics. This study compares the antioxidant capacities and phenolic compositions of tea and ethanol extracts from eight species naturally growing in Fethiye, Muğla, Türkiye. Antioxidant activity was assessed using the β-carotene bleaching method, 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS⁺), cupric reducing antioxidant capacity (CUPRAC), and metal chelating activity. Herbal teas generally showed stronger antioxidant activity than ethanol extracts. Rosemary tea had the highest activity (2.90 µg/mL), followed by lavender (11.30 µg/mL). In metal chelating, rosemary tea exhibited a half-maximal inhibitory concentration (IC₅₀) of 9.22 µg/mL, close to ethylenediaminetetraacetic acid (EDTA). Phenolic profiling showed rosemary tea contained 30.74 mg/g rosmarinic acid and 0.74 mg/g quercetin. These results support the traditional use of southwestern Türkiye’s medicinal plants and emphasize the antioxidant potential of herbal teas. Integrating ethnobotanical knowledge with phytochemical data provides a basis for functional food development, crop improvement, and conservation of local plant genetic resources. Unlike previous studies focusing on single species or limited solvent comparisons, this research simultaneously evaluates both herbal tea and ethanol extracts of eight locally grown medicinal plants, offering a unique perspective on their comparative antioxidant and phenolic diversity. Full article

Developing efficient and durable oxygen reduction reaction (ORR) catalysts is crucial for advancing fuel cell technology and sustainable energy conversion. In this study, a scalable strategy was employed to synthesize ZIF-derived nitrogen-sulfur co-doped carbon nanosheets embedded with in situ generated ZnS and Co₉S₈ nanoparticles. The synergistic effect of heteroatom doping and metal sulfide modification effectively modulated the electronic structure, optimized charge transfer pathways, and enhanced structural stability. The optimized catalyst exhibited a half-wave potential of 0.83 V vs. RHE, close to that of commercial 20 wt% Pt/C (0.85 V), excellent 4e⁻ ORR selectivity, and exceptional stability, with only a ~15 mV degradation after 10,000 cycles. These results demonstrate that the combination of nitrogen sulfur co-doping and in situ metal sulfide addition pro-vides an effective approach for designing highly active and durable non-precious metal catalysts for the ORR. This synthetic concept provides practical guidance for the scalable preparation of multifunctional nanomaterial-based catalysts for electrochemical energy applications. Full article

The uptake and accumulation of heavy metals by wild-grown mushrooms is raising health concerns for consumers worldwide with respect to variability conditioned by species and harvesting site specificity. This study aims to evaluate the concentration of elements (Zn) and heavy metals (Cd, Pb, Hg) in wild-growing edible mushroom samples (n = 200) collected from industrial and non-industrial areas in Poland. Over half of the analyzed mushroom samples (51%) exceeded EU limits for Cd, Pb, or Hg. Xerocomellus chrysenteron and X. subtomentosus (XCS) showed the highest accumulation, with median Cd and Pb concentrations of 3.53 mg/kg and 0.63 mg/kg fresh mass, respectively, in industrial areas. Spatial factors, including distance from emission sources and wind direction, significantly influenced element accumulation, with Cd levels in XCS up to 20 times higher than in Suillus species. A high-consumption scenario (96 g/day) indicated a substantial non-carcinogenic risk (HQ > 1) from Cd exposure via XCS consumption, both in industrial (HQ up to 9.01) and non-industrial areas (HQ max = 1.80), with cumulative hazard index (HI) ranging from 1.21 to 11.01. It is imperative to select the optimal regions for mushroom harvesting and to refrain from consuming species that accumulate elements to the greatest extent. Full article

Background: In this study, 28 caffeic acid phenethyl ester (CAPE) derivatives were designed and synthesized, and their anti-proliferative activities were evaluated against two representative human hepatocellular carcinoma (HCC) cell lines. The half-maximal inhibitory concentration (IC₅₀) was used as the activity metric. Among these derivatives, compound WX006 displayed the most potent anti-proliferative effect, with IC₅₀ values of 3.332 μM and 3.764 μM after 48 h of treatment, significantly lower than those of the parent compound CAPE. Consequently, WX006 was selected for further investigation into its antitumor efficacy and underlying mechanisms. Methods: To investigate the pharmacological mechanism of WX006, we employed a combination of high-throughput transcriptomics, metabolomics, and mitochondrial function analysis to elucidate its intracellular mechanisms of action. Results: WX006 disrupts cytoplasmic-mitochondrial metal ion homeostasis, triggering ferroptosis and cuproptosis through iron-copper dysregulation. Computational modeling revealed that WX006 selectively inhibits mitochondrial NDUFS2 subunit of respiratory chain complex I, which may induce NAD⁺ exhaustion and consequent energy metabolism collapse in tumor cells. These “metabolism & metal homeostasis” dual mechanisms collectively underpin its robust anti-tumor effects. Therapeutic efficacy of WX006 was further validated in murine H22 ectopic xenograft and Hepa1-6-Luc orthotopic xenograft models, where WX006 exhibited superior tumor suppression compared to sorafenib, alongside favorable safety profiles. Conclusions: Our findings establish a foundational rationale for further pharmaceutical development of CAPE derivates as a promising therapeutic candidate for hepatocellular carcinoma. Full article

Current tumor diagnostics rely on fluorodeoxyglucose (FDG)-PET imaging, but FDG’s short half-life and high cost limit its widespread use. Infrared (IR) probes are emerging as non-radioactive alternatives to conventional tracers for tissue section and other in vitro imaging applications. Because cells and tissues are relatively free of absorption peaks between 1800 and 2200 cm⁻¹, metal-carbonyl complexes, especially cyclopentadienylrhenium(I) tricarbonyl (Cp[Re(CO)₃]) derivatives, absorb strongly in this window and provide robust platforms for bioconjugation. Furthermore, Cp[Re(CO)₃] fragments can be introduced into organic substrates via an elegant three-component reaction that simultaneously forges the cyclopentadienyl-metal and cyclopentadienyl-substituent bonds. As a result, the functionalized half-sandwich complex is obtained in a single step without any special handling issues. We have therefore properly modified a glucose molecule with that complex and developed a novel glucoconjugated Cp[Re(CO)₃] probe that enables IR-based visualization of diseased cells at 2100 cm⁻¹, offering a non-invasive, non-radioactive histological tool and a promising basis for future medical imaging devices. Full article

As metal-containing resists attract increasing research interest in high-resolution lithography, gaining insights into the photochemical mechanisms, particularly in relation to the ligand functionality, is actively demanded. In this work, a controlled pair of organotin carboxylates with analogous structures but different functional groups has been designed and synthesized as deep-ultraviolet (DUV) resists. Both resists demonstrate 90 nm half-pitch resolution and the capability of pattern transfer on carbon-based hard-mask layers. Through various characterizations and comparison of the controlled pair, we propose two competitive reaction paths for the organotin system with olefin groups, which regulate the lithographic sensitivity and dissolution contrast. Our findings highlight the structural adjustability of organotin carboxylates and their potential application as high-resolution and etch-durable DUV resists. Full article

In recent years, polymer-based hybrid nanocomposites have emerged as promising alternatives to traditional heavy metal shields due to their low density, flexibility, and environmental safety. In this study, the synthesis of PS-PEG copolymers and the gamma radiation-shielding properties of PS-PEG/As₂O₃, PS-PEG/BN, and PS-PEG/As₂O₃/BN nanocomposites with different compositions are investigated. The goal is to find the optimal nanocomposite composition for gamma radiation shielding and dosimetry. Therefore, the mass attenuation coefficient (MAC), linear attenuation coefficient (LAC), half-value layer (HVL), tenth-value layer (TVL), effective atomic number, mean free path (MFP), radiation shielding efficiency (RPE), electron density, and specific gamma-ray constant were presented. Gamma rays emitted by the Eu source were detected by a high-purity germanium (HPGe) detector device. GammaVision was used to analyze the given data. Photon energy was in the vicinity of 121.8–1408.0 keV. The MAC values in XCOM simulation tools were used to compute. Gamma-shielding efficiency was increased by an increased number of NPs at a smaller photon energy. At 121.8 keV, the HVL of a composite with 70 wt% As₂O₃ NPs is 2.00 cm, which is comparable to the HVL of lead (0.56 cm) at the same energy level. Due to the increasing need for lightweight, flexible, and lead-free shielding materials, PS-b-PEG copolymer-based nanocomposites reinforced with arsenic oxide and BN NPs will be materials of significant interest for next-generation radiation protection applications. Full article

Environmentally friendly materials with superior structural, physical, optical, and shielding capabilities are of great technological importance and are continually being investigated. In this work, novel multicomponent borate glasses with the composition xTiO₂-10BaO-5Al₂O₃-5WO₃-20Bi₂O₃-(60-x) B₂O₃, where 0 ≤ x ≤ 15 mol%, were produced via the melt-quenching technique. The increase in TiO₂ content results in a decrease in molar volume and a corresponding increase in density, indicating the formation of a compact, rigid, and mechanically hard glass network. Elastic constant measurements further confirmed this behavior. FTIR analysis confirms the transformation of BO₃ to BO₄ units, signifying improved network polymerization and structural stability. The prepared glasses exhibit an optical absorption edge in the visible region, demonstrating their strong ultraviolet light blocking capability. Incorporation of TiO₂ leads to an increase in refractive index, optical basicity, and polarizability, and a decrease in the optical band gap and metallization number; all of these suggest enhanced electron density and polarizability of the glass matrix. Radiation shielding properties were evaluated using Phy-X/PSD software. The outcomes illustrate that the Mass Attenuation Coefficient (MAC), Effective Atomic Number (Z_eff), Linear Attenuation Coefficient (LAC) increase, while Mean Free Path (MFP) and Half Value Layer (HVL) decrease with increasing TiO₂ at the expense of B₂O₃, confirming superior gamma-ray attenuation capability. Additionally, both TiO₂-doped and undoped samples show higher fast neutron removal cross sections (FNRCS) compared to several commercial glasses and concrete materials. Overall, the incorporation of TiO₂ significantly enhances the optical performance and radiation-shielding efficiency of the environmentally friendly glass system, making these potential candidates for advanced photonic devices and radiation-shielding applications. Full article

The depletion of global lithium reserves, coupled with the necessity for environmentally sustainable and economically accessible energy storage systems, has driven the development of sodium-ion batteries (SIBs) as a promising alternative to lithium-ion technologies. Among various anode materials for SIBs, hard carbon exhibits obvious advantages and significant commercial potential owing to its high energy density, low operating potential, and stable capacity retention during prolonged cycling. Biomass represents the most attractive source of non-graphitizable carbon from a practical standpoint, being readily available, renewable, and low-cost. However, the complex internal structure of biomass precursors creates significant challenges for precise control of microstructure and properties of the resulting hard carbon materials, requiring further research and optimization of synthesis methodologies. This work reports the synthesis of hard carbon from Sasa kurilensis via pyrolysis at 900 °C and investigates the effect of alkaline pretreatment on the structural and electrochemical characteristics of the anode material for SIBs. Sasa kurilensis is employed for the first time as a source for non-graphitizable carbon synthesis, whose unique natural vascular structure forms optimal hierarchical porosity for sodium-ion intercalation upon thermal treatment. The materials were characterized by X-ray diffraction, infrared and Raman spectroscopy, scanning electron microscopy, X-ray microtomography and low-temperature nitrogen adsorption–desorption. Electrochemical properties were evaluated by galvanostatic cycling in the potential range of 0.02–2 V at a current density of 25 mAhg⁻¹ in half-cells with sodium metal counter electrodes. The unmodified sample demonstrated a discharge capacity of 160 mAhg⁻¹ by the 6th cycle, with an initial capacity of 77 mAhg⁻¹. The alkaline-treated material exhibited lower discharge capacity (114 mAhg⁻¹) and initial Coulombic efficiency (40%) due to increased specific surface area, leading to excessive electrolyte decomposition. Full article

The global decarbonisation strategy has accelerated the shift toward renewable energy and electric transport, demanding advanced electrochemical energy storage systems. Conventional anodes such as graphite and silicon composites face challenges in conductivity, stability and cycling performance. MXenes, a class of two-dimensional (2D) materials, offer promising alternatives owing to their metallic conductivity, tunable surface chemistry and high theoretical capacity. Here, we synthesise and characterise Mo₂TiC₂T_x and V₂CT_x (T = O, OH, F and/or Cl) MXenes for lithium-ion battery anodes and supercapacitors. Unlike Ti₃C₂T_x, which stores charge via intercalation and surface redox reactions, Mo₂TiC₂T_x and V₂CT_x exhibit conversion-type mechanisms. We also identify novel V₂C–VO_x heterostructures, achieving a specific capacitance of 532.4 F g⁻¹ at 2 mV s⁻¹ and an initial capacity of 493.3 mAh g⁻¹ at 50 mA g⁻¹ in lithium half-cells, with a low decay rate of 0.071% per cycle over 200 cycles. Pristine Mo₂TiC₂T_x shows 391.7 mAh g⁻¹ at 50 mA g⁻¹, decaying by 0.109% per cycle. These results experimentally validate theoretical predictions, revealing how MXene structure and transition metal chemistry govern electrochemical behaviour, thus guiding electrode design for next-generation batteries and supercapacitors. Full article