Search Results (3,486)

Diesel-powered equipment is widely used in underground coal mines for auxiliary transportation, material handling, and equipment relocation because of its long operating endurance, convenient refueling, and strong adaptability to complex operating conditions. However, carbon monoxide (CO) emissions from such equipment can accumulate locally under restricted ventilation, idling, and frequent start–stop operation, thereby threatening occupational health and mine safety. This review focuses on CO purification technologies for diesel-powered mining equipment. The operating characteristics and influencing factors are analyzed, and different technical routes are compared, including in-cylinder control, wet scrubbing, adsorption, non-thermal plasma (NTP), and catalytic oxidation. Recent advances in noble-metal catalysts, transition-metal and CeO₂-based reducible oxide catalysts, and single-atom catalyst (SAC) design strategies are summarized. Research progress in exhaust aftertreatment systems is also discussed. Overall, CO purification for diesel-powered mining equipment requires coordinated optimization of low-temperature activity, safety-oriented thermal management, flow resistance, and long-term operational stability. Future research should focus on structured catalytic units, durability under coupled exhaust conditions, online monitoring, and field validation to improve the compatibility of CO purification systems with underground mining conditions. Full article

Carbon-based materials, including graphene, carbon nanotubes, laser-induced graphene, and pyrolyzed glassy carbon, are widely used in sensing applications due to their high conductivity, large surface area, and tunable surface chemistry. Meanwhile, microfluidic systems enable precise fluid handling, reduced sample consumption, and enhanced analytical performance through improved mass transport and device miniaturization. The integration of carbon-based materials with microfluidic platforms has enabled the development of compact, portable, and highly sensitive devices for water monitoring. This review summarizes recent advances in carbon-based microfluidic sensors for water monitoring applications. Key carbon materials and their sensing mechanisms, particularly electrochemical transduction, are discussed. Various microfluidic integration strategies, including paper-based devices, polymer-based devices, MEMS-based systems, and flexible platforms, are highlighted, with emphasis on mass transport enhancement and overall system performance. Representative recent advances in carbon-based microfluidic sensors for water monitoring, including the detection of heavy metal ions, nutrients, and emerging contaminants, are reviewed. Finally, challenges related to scalable manufacturing, long-term operational stability, biofouling/surface fouling, and reproducible system integration are discussed, together with future perspectives on intelligent carbon-based microfluidic platforms featuring AI-assisted analytics, sense-response functionality, and self-healing and dynamic antifouling capabilities for water monitoring. These advances are expected to enable real-time, low-cost, and field-deployable water monitoring systems for environmental protection and public health management. Overall, this review highlights the critical role of integrating carbon-based sensing materials with microfluidic engineering in advancing next-generation water monitoring technologies. Full article

The growing demand for high-performance electromagnetic interference (EMI) shielding materials in modern communication and integrated electronics has stimulated interest in materials with tunable dielectric responses. In this study, a series of A-site-doped perovskite oxides—LaCoO₃, (La_0.5Sr_0.5)CoO₃, and (La₁/₃Sr₁/₃Ba₁/₃)CoO₃—were synthesized via a sol–gel method to investigate their dielectric behavior in the radio-frequency (RF) range. Dielectric spectroscopy reveals that LaCoO₃ exhibits a positive permittivity characteristic of semiconductors, whereas Sr substitution induces a metallic state in (La_0.5Sr_0.5)CoO₃, whose dielectric response exhibits a Drude-like dispersion behavior within the measured RF frequency range. Further incorporation of Ba into the A-site results in ternary co-doping, suggesting a reduction in effective carrier transport and a shift in the characteristic dispersion frequency toward the low-frequency region. Consequently, (La₁/₃Sr₁/₃Ba₁/₃)CoO₃ displays a near-zero permittivity at approximately 2.5 kHz, indicating a transition in the dominant reactive response from inductive-like to capacitive-like behavior, which is consistent with the impedance spectroscopy results. This work demonstrates that cation engineering at the A-site enables precise control over the RF dielectric response in perovskite oxides, offering a potential pathway for the design of tunable electromagnetic functional materials relevant to EMI shielding applications with tailored permittivity characteristics. Full article

Nanostructured Co₃O₄ was synthesized via a sol–gel approach employing the ionic liquid 1-ethyl-3-methylimidazolium trifluoromethylsulfonate ([EMIm]TfO) and subsequently evaluated as a high-performance anode material for lithium-ion batteries. Ionic liquids, distinguished by their low volatility, high thermal stability, and tunable chemical properties, represent a greener alternative to conventional organic solvents for the synthesis of functional nanomaterials. The electrochemical performance of the as-prepared material was systematically assessed through galvanostatic charge–discharge cycling, cyclic voltammetry, and rate capability tests. The Co₃O₄ electrode exhibited a high reversible capacity of approximately 1100 mAh g⁻¹ after 50 cycles at a current density of 200 mA g⁻¹, along with excellent coulombic efficiency approaching ~100% after the initial cycles. Furthermore, the material demonstrated strong rate capability, delivering about 600 mAh g⁻¹ at 1 C, and recovering its capacity upon returning to lower current densities. The improved electrochemical performance is primarily attributed to the nanoscale architecture induced by the ionic liquid-assisted synthesis, which facilitates rapid lithium-ion transport and effectively buffers volume variations during repeated cycling. Notably, the ionic liquid serves a dual function as both a green reaction medium and a structure-directing agent, enabling precise control over the material’s morphology and properties. This study demonstrates a versatile strategy for the rational design of potential transition-metal oxide anodes, paving the way for high-performance electrode materials. The findings contribute to the development of next-generation lithium-ion batteries tailored for clean and sustainable energy storage applications. Full article

Two-dimensional transient electroluminescent devices have attracted considerable attention owing to their simple device architecture and reduced contact-barrier dependence. However, the influence of semiconductor transport polarity on transient electroluminescence (EL) remains unclear. Here, we compare four representative transition metal dichalcogenide (TMDC) semiconductors with different transport polarities and find that ambipolar WSe₂ exhibits a stronger transient EL signal under identical driving conditions, a trend that cannot be explained by relative photoluminescence quantum yield (PLQY) alone. Transfer characteristics and gate-modulated photoluminescence (PL) measurements were further used to analyze the gate-dependent carrier doping states and the local spectral response associated with interfacial carrier modulation near the metal/TMDC interface during abrupt gate-voltage switching. Based on these results, we propose a possible physical picture in which ambipolar WSe₂ is more likely to form a transient interfacial electron–hole distribution favorable for electron–hole radiative recombination, whereas predominantly n-type materials tend to form electron-rich interfacial carrier states. These findings suggest that semiconductor transport polarity is an important material factor for designing low-dimensional transient electroluminescent devices. Full article

Mitochondria-targeting metal complexes (MTMCs) are a mechanistically distinct class of metallopharmaceuticals. Unlike first-generation platinum drugs that form nuclear DNA adducts, MTMCs exploit organelle-specific vulnerabilities such as hyperpolarised mitochondrial membrane potential (ΔΨm), elevated reactive oxygen species (ROS), limited mitochondrial DNA (mtDNA) repair capacity, and redox-dependent enzymes such as thioredoxin reductase (TrxR). We systematically searched PubMed, Web of Science, Scopus, and Google Scholar databases for studies published between 2016 and 2026, applying predefined inclusion criteria that included subcellular localization evidence and functional bioenergetic endpoints. The search identified 147 studies covering Pt(II/IV), Ru(II/III), Au(I/III), Ir(III), Os(II), Re(I), and V(IV/V) complexes and metal–organic framework nanoplatforms. Mechanistic evidence converges on four intramitochondrial target categories: inhibition of ETC (Electron Transport Chain) Complexes I/III with consequent ATP depletion; ROS overproduction, coupled with glutathione and TrxR depletion; outer mitochondrial membrane permeabilization and intrinsic apoptotic cascade activation; and mtDNA damage within a compartment limited to base excision repair. Multi-modal cell death—the co-occurrence of apoptosis, ferroptosis, necroptosis, and autophagic cell death—was a recurrent finding across the reviewed studies. This review thoroughly surveys the latest trends in MTMC drug design (metals, ligand structures, and mechanisms of action) and summarises analytical techniques for speciation, pharmacokinetics, safe monitoring, and resistance, while critically analysing translational barriers and clinical failures. To address the field’s inconsistent terminology, we introduce an explicit localization evidence hierarchy that distinguishes mitochondria-targeting complexes (through quantitative ICP-MS fractionation or co-localization with defined Pearson/Manders coefficients) from simply mitochondria-localising or mitochondria-perturbing agents, and we apply it throughout. We also point out that the idea of selectivity being purely driven by membrane voltage (ΔΨm) and thermodynamics is constrained by membrane and protein binding, as well as the transmembrane pH gradient, kinetic limitations, and demonstrated heterogeneity of cancer-cell membrane potential, and, as such, the functional mitochondrial effects must not be equated with mitochondrial accumulation. Since elemental quantification cannot distinguish intact complex from protein adducts and decomposition products, speciation-aware pharmacokinetics emerges as a prerequisite for a credible exposure–response interpretation. The translational progress will depend less on new chemotypes than on this analytical and pharmacokinetic rigour, together with organelle-level safety monitoring and biomarker-guided patient selection. Full article

This review analyzes electrochemically deposited polyaniline (PANI) nanocomposite thin films containing metallic, semiconducting, and dielectric fillers, including Ag/PANI, Mo/MoO_x/PANI, CeO₂/PANI, Fe₂O₃/PANI, Al₂O₃/PANI, CuO/PANI, Co₃O₄/PANI, and CoFe₂O₄/PANI. The work examines how filler chemistry and loading influence optical-gap evolution, Urbach disorder, dielectric dispersion, nonlinear optical response, structural coherence, and dc conductivity under comparable electrochemical growth conditions. The comparative analysis shows that optical-gap narrowing and conductivity enhancement are not necessarily coupled. Ag/PANI exhibits simultaneous optical softening and improved conductivity, consistent with metallic bridging, dielectric screening, and enhanced charge connectivity. In contrast, Mo/MoO_x/PANI shows strong optical-gap reduction but reduced conductivity, indicating that optically active interfacial states may remain localized or mobility-limiting. Oxide fillers produce additional regimes: CeO₂/PANI can suppress Urbach disorder and microstrain through order stabilization, whereas Al₂O₃/PANI may widen higher-energy transitions and reduce transport through wide-gap barrier effects. Based on these contrasts, a unified framework is proposed that separates the interfacial electronic function from the transport-connectivity function. This approach classifies PANI nanocomposites into transport-assisted metallic, mobility-limiting interfacial, order-stabilized oxide, and barrier-dominated dielectric regimes, providing practical criteria for selecting filler type and loading windows in optoelectronic, sensing, and photonic applications. Full article

Landfill leachate represents a long-term source of contamination that may significantly affect groundwater and receiving water bodies through the migration of organic, inorganic, and toxic pollutants. This study evaluated the long-term migration of landfill leachate and its potential environmental impacts using the LandSim Release 2 probabilistic software model applied to two municipal waste landfills in the Republic of Serbia: the regional sanitary landfill “Gigoš” in Jagodina and the sanitary landfill “Meteris” in Vranje. The modelling framework integrated laboratory leachate analyses, hydrogeological conditions, engineered barrier system characteristics, and receptor-oriented contaminant transport assessment. Model validation was performed through comparison of simulated and laboratory-measured concentrations. Two scenarios were analyzed for each site: an engineered sanitary landfill scenario with a functional containment system and a conservative barrier-failure scenario representing complete loss of engineered barrier functionality. Ten representative leachate parameters were included, covering nitrogen compounds, inorganic ions, toxic substances, and heavy metals/metalloids. The results showed that engineered protection systems significantly delay contaminant migration and reduce receptor concentrations, while barrier-failure conditions lead to earlier pollutant breakthrough and higher environmental risk. The simulations demonstrated that under the engineered sanitary landfill scenario, receptor concentrations of all analyzed contaminants remained below the corresponding maximum allowable concentrations, with contaminant migration occurring only after several centuries. In contrast, the conservative barrier-failure scenario resulted in substantially earlier contaminant breakthrough, with nitrogen compounds and phenols representing the greatest environmental concern due to their rapid migration and exceedance of regulatory thresholds, while the “Meteris” landfill generally exhibited higher receptor concentrations than the “Gigoš” landfill. These findings highlight the importance of predictive modelling and long-term monitoring for sustainable landfill management and groundwater protection. Full article

Water resources are essential for human well-being. However, water pollution is a major global problem with significant implications for the environment and public health. To address these challenges, this study presents an integrated perspective on water pollution by correlating pollution sources, transport pathways, exposure routes, and associated risks to human health. The methodology combined a systematic review conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines with a bibliometric analysis performed by using VOSviewer version 1.6.19, a software tool for constructing and visualizing bibliometric networks. A total of 332 publications published between 2015 and 2025 were retrieved from the Scopus and Google Scholar databases and met the PRISMA eligibility criteria. The findings indicate that both natural and anthropogenic sources contribute to water contamination, introducing pollutants such as heavy metals, pesticides, pharmaceutical residues, microplastics, and pathogenic microorganisms with potential human health impacts. Bibliometric analysis revealed a transition from conventional water quality assessments toward integrated approaches emphasizing health risks and environmental interactions. The study further identified important knowledge gaps regarding contaminant mixture effects and synergistic toxicity, which remain insufficiently addressed in current scientific and regulatory frameworks. These findings highlight the need for strengthened regulatory strategies, advanced treatment technologies, and evidence-based water governance to support environmental sustainability and public health protection. Full article

Gallium (Ga)-based liquid metal (LM) composites, particularly those based on eutectic gallium–indium (EGaIn) and related alloys, have emerged as a promising materials platform for soft and deformable energy storage owing to their unique combination of metallic conductivity, fluidic deformability, and adaptive interfaces. Despite rapid advances in LM-enabled devices, binders remain insufficiently understood and are still commonly regarded as passive structural components. Here, we present a comprehensive binder-centered perspective for LM composites, establishing the binder as a key regulator of electro-chemo-mechanical coupling, interfacial stability, transport behavior, and processability in soft energy systems. We show that tailored binder chemistries in Ga-based LM systems—including stretchable batteries, printable conductors, and soft electrochemical devices—govern LM droplet dispersion, suppress coalescence and leakage, and preserve conductive percolation under large deformation, while enabling room-temperature fabrication and printability through rheological regulation and interfacial wetting. Beyond mechanical confinement, emerging binder functionalities—including dynamic bonding, supramolecular interactions, ionically conductive networks, and reversible polymer architectures—enable self-healing interfaces, adaptive transport pathways, and robust adhesion in deformable devices. By integrating recent advances in stretchable batteries, flexible supercapacitors, printable electronics, and multifunctional soft energy systems, we establish a unified multiscale framework linking binder molecular design to device-level electrochemical and mechanical performance. We further discuss sustainability and manufacturing considerations, including recyclable polymer networks, low-temperature fabrication, and scalable processing strategies. Finally, we outline current challenges and future opportunities toward programmable binder systems with tunable viscoelasticity, interfacial reactivity, and adaptive functionality. This Review establishes binder-centered engineering as a key pathway for transforming LM composites from proof-of-concept materials into resilient, manufacturable, and multifunctional soft energy technologies for wearable, stretchable, and biointegrated electronics. Full article

Electrochemical nitrate reduction reaction (eNO₃RR) has emerged as a promising alternative to the energy-intensive and carbon-intensive Haber–Bosch process for green ammonia synthesis. However, the intrinsic complexity of the eight-electron transfer pathway and inevitable competing side reactions limit the activity and selectivity of eNO₃RR. Maximizing the utilization of active sites and ensuring structural stability in electrocatalysts are essential for promoting surface proton-coupled electron transfer and improving Faradaic efficiency. Herein, we present a copper metal–organic framework (Cu-MOF)-derived electrocatalyst synthesized via in situ electrosynthesis on copper foam, using cetyltrimethylammonium bromide (CTAB) as a structure-directing agent, followed by electroreduction to produce a self-supported, nano-dendritic structure. This three-dimensional architecture exposes abundant active sites and facilitates electron transport, enabling efficient nitrate-to-ammonia conversion. The optimized CTAB-assisted electrode achieves an ammonia yield of 14.33 ± 0.61 mg h⁻¹ cm⁻² with a Faradaic efficiency of 90.95 ± 2.28% at −1.7 V versus Ag/AgCl. This study introduces a versatile design strategy for copper-based electrocatalysts that integrates structural stability with high activity, offering a sustainable approach for both ammonia production and nitrate remediation. Full article

Dye-sensitized solar cells (DSSCs) remain promising low-cost photovoltaic technologies because of their simple fabrication, tunable optical properties, and effective operation under low-light conditions. Titanium dioxide (TiO₂) is the most widely used photoanode material in DSSCs owing to its chemical stability, suitable band alignment, low toxicity, and excellent transparency. However, the photovoltaic performance and long-term stability of TiO₂-based DSSCs are still limited by charge recombination, slow electron transport, interfacial losses, and structural degradation. This review summarizes recent advances in defect engineering, morphology engineering, and interface engineering of TiO₂ photoanodes for high-performance DSSCs. Attention is given to the role of oxygen vacancies, Ti³⁺ states, metal/non-metal doping, and heterostructure formation in tailoring the electronic structure and charge transport behavior of TiO₂. The influence of various TiO₂ nanostructures, including nanoparticles, nanotubes, nanorods, nanosheets, and hierarchical architectures, on dye adsorption, light scattering, electron mobility, and recombination dynamics is critically discussed. Furthermore, recent progress in interface engineering strategies such as passivation layers, blocking layers, MXene incorporation, composite photoanodes, and atomic layer deposition are examined in relation to interfacial charge transfer and device stability. Current challenges involving defect-induced recombination, morphology-related transport trade-offs, and long-term degradation are also analyzed. Finally, future perspectives on hierarchical nanoarchitectures, multifunctional interfaces, flexible DSSCs, and hybrid TiO₂ systems are presented. This review provides an integrated understanding of how defect, morphology, and interface engineering collectively govern the performance of TiO₂ photoanodes and offers design guidelines for next-generation high-efficiency and stable DSSCs. Full article

Photocatalytic CO₂ reduction into CH₄ is a promising route for solar fuel production, but its efficiency is still limited by poor charge separation, insufficient CO₂ activation, and sluggish multi-electron transfer kinetics. Herein, Cu-modified TiO₂ (Cu/TiO₂) was prepared by calcining a Cu-modified defective MIL-125(Ti) precursor, denoted as Cu-MIL-125, through a temperature-controlled calcination strategy. The effects of calcination temperature on the structural evolution, surface chemical states, interfacial charge transport, and CO₂ photoreduction performance were examined. These results indicated that the Cu/TiO₂ was successfully prepared, while the crystallinity, porous structure, and interfacial electronic properties of Cu/TiO₂ were strongly dependent on the calcination temperature. Among the obtained samples, the Cu/TiO₂ sample obtained by calcining Cu-MIL-125 at 450 °C (450 Cu/TiO₂) exhibited the highest CH₄ formation rate, reaching 15.90 μmol g⁻¹ h⁻¹, corresponding to an approximately 9.8-fold enhancement over TiO₂ calcined from defective MIL-125(Ti) at 450 °C, together with a high CH₄ selectivity of 93.05%. Control experiments and ¹³CO₂ isotope-labeling tests confirmed that the detected carbon-containing products were generated from CO₂ under photocatalytic conditions. In situ diffuse reflectance infrared Fourier transform spectroscopy measurements further revealed the formation of carbonate, bicarbonate and hydrogenated carbon-containing intermediates during the reaction. This work offers a practical route for constructing metal–organic framework-derived Cu/TiO₂ photocatalysts for selective CH₄ production from CO₂. Full article

The divalent metal transporter DMT1 (SLC11A2) is implicated in diverse human pathologies including cancers, inflammatory and degenerative diseases. Small molecules targeting this membrane protein are actively searched. Following the identification of the pyranocoumarin praeruptorin A as an inhibitor of ferroptosis that is able to bind to DMT1, we have investigated the interaction of related natural products with DMT1 using molecular modeling to determine structure-binding relationships. Two series of compounds were tested: praeruptorins A-H and qianhucoumarins A-J, all isolated previously from the roots of the Chinese medicinal plant Peucedanum praeruptorum Dunn (Bai-Hua Qian-Hu). The antitumor compound praeruptorin C was identified as the best DMT1 ligand in the series, with a binding capacity largely superior to that of praeruptorin A and also well superior to the reference organoselenium product ebselen, at least from an in silico perspective. Praeruptorin C, and to a lower extent praeruptorins F and H, can form stable complexes with DMT1 upon binding close to the ebselen binding site. Qianhucoumarins C and I were also identified as potential binders. Altogether, the analysis of the 18 natural products enabled identification of structural elements implicated in the target binding process. The curvature of the tricyclic pyranocoumarin scaffold and the angeloyl side chain at position 9 seem to contribute importantly to the protein interaction. An experimental validation is required but the docking study paves the way to the discovery and design of tricyclic coumarin derivatives targeting DMT1. Full article

Direct methanol fuel cells (DMFCs) have attracted considerable attention recently for various applications ranging from portable ones to transportation. The efficiency of DMFCs depends on the kinetics of anodic and cathodic electrocatalysts. Due to sluggish anodic methanol oxidation reaction (MOR), DMFCs require an effective and bifunctional catalyst for promoting efficient MOR. The state-of-the-art MOR catalysts, such as Pt/C and Pt-Ru/C, have been shown to exhibit reasonable MOR activity; however, the insufficient mass activity and poor stability of carbon-supported catalysts have been a major limitation, requiring an alternative, efficient, electrocatalyst that exhibits high mass and specific activities. In addition, electrocatalysts without any carbon support (self-supported electrocatalysts) further mitigate their poor stability and therefore enhance their durability. In this regard, metal aerogel catalysts, which are entirely composed of metallic networks, recently attained special interest due to their specific advantages over conventional carbon supports, such as high catalyst utilization and improved electronic conductivity and stability. In this review, we systematically reviewed various metal aerogel catalysts developed for MOR since their first discovery in 2009. The metal aerogel demonstrated superior MOR performance relative to carbon-supported commercial catalysts, with enhancements ranging from 2-fold to 22-fold of mass activity. We also statistically compared the mass activity of metal aerogels with traditional carbon-supported, non-carbon-supported, and advanced shape-controlled catalysts and found that metal aerogels exhibited high mass activities compared to other catalyst systems. Therefore, we clearly establish that metal aerogel catalysts possess great potential as efficient MOR catalysts in DMFCs. In addition, we have provided several future research directions and strategies for further development of metal aerogel-integrated DMFC devices. Full article