Search Results (355)

The Dongga Au deposit is located in the giant Xiongcun porphyry Cu-Au ore district within the Southern Lhasa terrane; however, the evolution of ore-forming fluids and the mechanisms of gold precipitation during the main mineralization stage remain poorly constrained. This study integrates geological observations and in situ LA-ICP-MS trace element analyses of pyrite to address the above issues. Three generations of pyrite are identified: Py1 occurring in quartz–sulfide veins, Py2 in chlorite–sulfide veins, and Py3 in pyrite veins. Trace element data show that Au and As contents are relatively low in all three pyrite generations and mainly occur as lattice-bound elements, whereas Pb, Ag, Bi, Cu, and Zn are predominantly hosted in micro- to nano-scale mineral inclusions. Ore-forming temperatures estimated from Se concentrations in pyrite indicate progressive cooling from ~400 °C to ~270 °C (Py1 to Py3). Combined with thermodynamic modeling and mineral assemblage constraints, this suggests that the ore-forming fluid experienced significant meteoric water input, accompanied by decreasing temperature, sulfur fugacity, and oxygen fugacity, as well as increasing pH. The principal gold mineralization stage occurred at approximately 340 °C, where temperature and pH conditions jointly stabilized Au transport primarily as Au(HS)₂⁻. We propose the mixing between meteoric water and mineralized magmatic fluid caused a decrease in sulfur fugacity, oxygen fugacity and temperature, thereby limiting the availability of HS⁻ required for stabilizing Au(HS)₂⁻ complexes and thus resulting in the decoupling of Au(HS)₂⁻, which triggered gold precipitation. Full article

Proton exchange membranes (PEMs) are essential for PEM fuel cells, with proton conductivity arising from the hydration-induced ionic channel network. PEM performance can be enhanced through pretreatments, such as annealing, which reconstruct the ionic channels. This study investigates the ionic channel network variation in Nafion 212 under continuous annealing at 90 °C using current-sensing atomic force microscopy (CSAFM). A nanoscale PEM fuel cell was formed with a Pt-coated CSAFM tip and Pt-coated Nafion surface. Topography and surface roughness analyses revealed geometrical changes from annealing. Current-sensing images and histograms qualitatively assessed local conductance and ionic channel distribution. The ionic channel network density was quantitatively evaluated using the number of protons moving through the ionic channel network (NPMI), derived from CSAFM and electrodynamics principles. NPMI directly reflects ionic channel density. From the unannealed state to 60 h, NPMI increased linearly at 1 × 10⁴ h⁻¹, indicating enhanced channel formation. Beyond 60 h, NPMI decreased linearly at 1.9 × 10⁵ h⁻¹, reflecting progressive network degradation. As the ionic channel network increases, the number of protons reaching the membrane surface also increases, whereas in the opposite case it decreases. Thus, NPMI becomes evaluation criterion for ionic channel network density. These findings systematically link nanoscale structural changes to ionic channel reconstruction and proton transport in Nafion 212, providing insight into PEM performance evolution under thermal treatment. Full article

Multijunction solar cells employing a GaInP/GaAs/Ge triple-junction configuration are the dominant technology for space photovoltaic applications. The choice of an efficient electrode is crucial in solar cells, as it enables effective charge carrier collection and transport while allowing maximum light to reach the active layer. Indium tin oxide (ITO)/graphene hybrid electrodes have emerged as smart transparent conductors offering significant advantages over conventional brittle ITO films. Graphene electrodes were prepared by cold-wall chemical vapor deposition and ITO electrodes were commercially obtained and used as a base for hybrid ITO/graphene electrodes. Raman spectroscopy confirmed the successful integration and characteristic G and 2D bands on the ITO surface. Nanoscale current mapping via Tunneling Atomic Force Microscopy (TUNA-AFM) verified continuous conductive pathways throughout the film with ~60% increase in nanoscale tunneling current at graphene/ITO interfaces, indicating improved local charge transport pathways. These results demonstrate the suitability of ITO/graphene hybrid electrodes a promising material for multijunction solar cells and other aerospace technologies. Full article

High-manganese steel has emerged as a potential alternative material to austenitic stainless steel for liquid hydrogen storage and transportation environments, owing to its superior mechanical characteristics and limited hydrogen diffusivity. However, its hydrogen embrittlement (HE) susceptibility limits its engineering applications. This study investigates the effect of microstructural regulation through trace titanium (Ti, 0.021 wt%) addition on HE resistance in high-manganese steel. By means of Electron Backscatter Diffraction (EBSD), TEM, SEM, and Slow Strain Rate Tensile (SSRT) tests, the effects of Ti on the microstructure, mechanical properties, and HE susceptibility of high-manganese steel are systematically investigated. The results show that the addition of Ti did not significantly alter the average austenite grain size or phase composition, but it generated a large number of Ti(C,N) nanoscale precipitates with sizes ranging from 20 to 70 nm within the matrix. The elongation loss of the 25Mn-Ti specimen was significantly lower than that of the 25Mn specimen when hydrogen-charged for 72 h, decreasing from 18.4% to 9.3%. The fracture surfaces consistently exhibited ductile dimple morphology, whereas 25Mn steel demonstrated significant cleavage-induced brittle fracture. EBSD analysis revealed that hydrogen-charged 25Mn-Ti steel exhibited higher Kernel Average Misorientation (KAM) value retention rate and more uniform grain strain distribution, indicating enhanced microstructural deformation compatibility. The main mechanism was that Ti pre-formed nanoscale Ti(C,N) precipitates during the preparation of 25Mn high-manganese steel, which played a key role in inhibiting HE. These precipitates altered hydrogen diffusion behavior and distribution patterns, reduced stress concentration levels, and inhibited hydrogen-induced crack initiation. This work is of great significance for improving the HE resistance of high-manganese steels. Full article

Understanding the atomic-scale ionic motion and transport in layered transition-metal oxides is essential for elucidating structural stability and electronic behaviour in complex systems. Here, we investigate nanoscale Na dynamics in Na₁RuO₃ and Na_1.5RuO₃ using room-temperature ab initiomolecular dynamics at the r²SCAN + U level. While Na mobility plays a key role in local coordination, its nanoscale mechanism remains nuanced and unexplored. Our simulations show that Na ions undergo pervasive rattling, with Na_1.5RuO₃ enabling exploration of larger volumes and exhibiting incipient migration compared to the more confined behaviour in Na₁RuO₃. In addition, oxygen’s contribution to redox capacity decreases from $43\%$ to $24\%$ with increasing Na content. These nanoscale insights demonstrate that tuning the local ionic environment governs charge compensation and dynamical response in ruthenate frameworks, with direct implications for the design of Na-ion battery cathodes. Full article

Molecular-scale detection based on quantum tunnelling is promising for molecular electronics and high-sensitivity analysis, owing to its sensitivity to molecular structure and energy levels. However, conventional two-electrode tunnelling measurements suffer from overlapping conductivity of different molecules, limiting molecular discrimination in complex systems. To address this, we propose an electrochemical-gate-controlled nanoscale tunnelling strategy that expands the two-electrode system to a three-electrode configuration via a tunable gate potential, enabling the differentiation of distinct molecules at near-single-molecule sensitivity. Scanning the gate potential under constant tunnelling bias modulates the alignment between molecular orbitals and the electrode Fermi level, altering the statistical characteristics of molecular tunnelling transport. Experimental results show that target molecules induce a bimodal distribution of tunnelling current (background and molecule-correlated channels), with the second peak exhibiting distinct gate potential dependence. Comparative analysis of ascorbic acid (AA), acetylcholine (ACh), and uric acid (UA) reveals unique trajectories of characteristic peaks with gate potential, forming an electrochemical gate response fingerprint. This gate-dependent conductance trajectory provides a novel statistical dimension for molecular recognition, enabling differentiation of distinct molecules. Full article

This work reports on the synthesis and electrochemical investigation of sustainable carbon–TiO₂ nanocomposites derived from marine biowaste, designed to elucidate light-assisted charge storage mechanisms in non-aqueous electrolytes. Porous carbons obtained from prawn chitin and blue shark gelatin were decorated in situ with TiO₂ nanoparticles using a deep eutectic solvent (DES) as a green synthesis medium. Structural and morphological characterisation revealed that TiO₂ incorporation induces significant nanoscale reorganisation of the carbon framework, resulting in hierarchical porosity, increased surface area, and intimate semiconductor–carbon interfaces. Electrochemical evaluation in a three-electrode configuration using an ethaline-based DES electrolyte demonstrated that TiO₂ decoration substantially enhances capacitive performance and cycling stability, with the prawn chitin-derived composite achieving a specific capacitance of 54 ± 3 F g⁻¹ and 91% retention after 10,000 cycles. Under illumination, all TiO₂-containing composites exhibited a pronounced increase in anodic current response and discharge time, indicating photo-assisted surface charge accumulation. Although the absolute capacitance values are modest compared to those of aqueous supercapacitor systems, the results provide mechanistic insight into the interplay among nanostructure, semiconductor photoactivity, and ion transport in viscous, hydrogen-bonded DES electrolytes. By combining waste-derived carbons, green synthesis routes, and photo-responsive nanostructures, this study highlights a sustainable strategy for developing multifunctional carbon-based nanomaterials with light-modulated electrochemical behaviour. Full article

In this work, we present a numerical proof-of-concept study of a device for nanoparticle sorting, targeting size ranges relevant to exosome-like dimensions (typically 40–200 nm), which remains challenging for passive sorting techniques. The system consists of three silicon waveguides embedded in a CYTOP layer and arranged in a two-step directional-coupler configuration, integrated with a microchannel that carries a water-based buffer as the carrier fluid, transporting the suspended nanoparticles. Three-dimensional Finite Element Method (3D-FEM) simulations were performed, incorporating both optical and hydrodynamic forces to track particle dynamics within the microchannel and demonstrate controlled, size-selective particle deflection. First, numerical simulations show that nanospheres with diameters ranging from 500 nm to 700 nm can be effectively separated by the transverse trapping force at a 4:1 power-splitting ratio. Then, to extend the concept toward smaller size ranges, a bifurcated microchannel is introduced, enabling fluid-assisted transport in low-optical-field regions and allowing reliable separation of particles with smaller diameters (between 200 nm and 400 nm), accompanied by an 8:1 power-splitting ratio. These results demonstrate, within a numerical framework, the feasibility of an integrated photonic–microfluidic approach for size-selective nanoparticle sorting. The proposed strategy may support future pre-processing steps in liquid biopsy workflows, particularly for enriching nanoscale components such as exosome-sized vesicles, rather than constituting a direct diagnostic tool. Full article

Sol–gel processing provides an unusually controllable route to nanoporous solids, making silica aerogels the leading reference systems for extremely low thermal conductivity due to their high porosity, nanoscale pore sizes, and tunable solid frameworks. Under near-ambient conditions, thermal transport is multi-scale and multiphase, arising primarily from coupled solid conduction through the skeletal network and gas conduction within the pore space. Accordingly, aerogel design has emphasized suppressing solid-phase transport by reducing network connectivity, increasing tortuosity, and enhancing boundary scattering, while also limiting gaseous conduction through the control of pore size and gas pressure. This critical review provides an integrated overview of these mechanisms and the theory-to-experiment toolbox used to quantify the separate and combined contributions of the solid and gas phases to the effective thermal conductivity. We link key structural and environmental parameters (porosity, pore size distribution, density, backbone morphology, and pressure) to dominant transport regimes and the assumptions embedded in common models. Classical approaches, including effective-medium and percolation-based models, are assessed alongside phonon-scaling descriptions that incorporate characteristic length scales. Particular attention is given to the Knudsen effect and pressure-sensitive gas-conduction models, which are central to interpreting performance at atmospheric conditions and under vacuum or low-pressure operation. This review highlights inconsistencies across datasets and modeling practices, identifies persistent knowledge gaps, and outlines practical directions toward processable structure–property guidelines for manufacturing aerogels with targeted thermal performance, with regard to conduction-dominated heat transport mechanisms. Full article

The lateral organization of the plasma membrane (PM) is vital for cellular signaling, yet the specific mechanisms by which the internal cortical actin meshwork templates the organization of the external lipid leaflet remain poorly understood. While established models like the ‘picket-fence’ emphasize physical barriers to diffusion, recent observations of fiber-like “ghost” structures in the distribution of glycosylphosphatidylinositol-anchored proteins (GPI-APs) suggest a more intricate mode of spatial coordination. In this study, we utilize imaging total internal reflection fluorescence correlation spectroscopy (ITIR-FCS) and variable-angle TIRF to resolve whether these filamentous patterns represent genuine membrane-proximal features or optical artifacts of cytosolic transport. Our results demonstrate that these fiber-like tracks are strictly confined to the immediate PM interface and disappear as the evanescent field probes deeper into the cytosol. While the spatial distribution of GPI-APs is templated by the underlying actin meshwork, quantitative diffusion mapping shows that the lateral dynamics of the probe remains largely uniform and is not significantly modulated by these filamentous patterns. By pharmacologically perturbing the actin scaffold and membrane cholesterol, we show that this transbilayer coupling is contingent upon a cholesterol-dependent cytoskeletal pinning mechanism. These findings demonstrate a decoupling of spatial organization and molecular dynamics, providing evidence for how the actin scaffold patterns nanoscale membrane organization without imposing long-range barriers to diffusion. Full article

Heavy metal contamination of drinking water remains a persistent global challenge, exacerbated by salinity, industrial discharge, and the limitations of existing membrane technologies that are constrained by permeability–selectivity trade-offs. In this study, we develop a hybrid thin film nanocomposite (TFN) forward osmosis (FO) membrane by incorporating a zirconium-based metal–organic framework (UiO-66) and its conductive polymer-functionalized analogue (PANI@UiO-66) into the polyamide active layer via interfacial polymerization. The incorporation of UiO-66 enhances water transport through the introduction of hydrophilic microporous domains, while the polyaniline coating modulates nanoscale transport pathways and interfacial interactions. Systematic variation in filler type and loading reveals distinct functional roles of the two fillers. Membranes incorporating bare UiO-66 exhibit increased water flux, attributed to facilitated transport through MOF-derived nanochannels, but show a moderate increase in reverse solute flux. In contrast, PANI@UiO-66 incorporation results in reduced water flux but significantly suppresses reverse solute flux and enhances chromium rejection, indicating improved control over selective transport. At an optimal loading of 0.15 wt% (TFN-PU3), the membrane demonstrates an improved balance between water permeability and solute selectivity compared to the pristine thin film composite (TFC) membrane under FO conditions. The observed performance is attributed to the combined effects of modified transport pathways and interfacial interactions introduced by the hybrid filler system. The results highlight the potential of conductive polymer–MOF hybridization as a strategy for tuning membrane performance. This work provides a practical framework for designing TFN membranes for selective heavy-metal removal in saline and complex water environments. Full article

Experimental results suggest a feasible strategy for tuning the superconducting properties of MgB₂ through the incorporation of an electroluminescent inhomogeneous phase. By introducing GaP electroluminescent inhomogeneous phases into MgB₂, the effects of emission intensity variation on the sample structure, superconducting transition temperature, electrical transport behavior, and magnetic properties were systematically investigated. The results show that, at a fixed GaP addition level, the superconducting transition temperature T_c increases steadily from 38.2 K to 39.6 K with increasing emission intensity of the inhomogeneous phase, corresponding to a maximum enhancement of approximately 1.4 K. Meanwhile, the zero-resistance temperature shifts upward synchronously, indicating that the entire superconducting transition region moves toward higher temperatures. Raman measurements show that the peak position and linewidth of the E_2g phonon mode evolve systematically with emission intensity, while the electron–phonon coupling parameter λ exhibits a trend consistent with that of T_c. In addition, the nanoscale dispersed distribution of the GaP inhomogeneous phase, together with the interface/defect structures it introduces, appears to promote sample densification and enhance flux pinning, resulting in an increase in the critical current density J_c by approximately 69% at 20 K in self-field and an enhancement of the irreversibility field H_irr by about 31.5%. These results suggest that, beyond the effect of static inhomogeneous-phase incorporation, the luminescence-activated state under bias excitation is likely involved in modulating the superconducting response of MgB₂. This work provides a new experimental perspective for synergistically regulating the properties of conventional superconductors through the combined effects of inhomogeneous phases and excited states. Full article

Biobased hybrid semiconducting composites are attracting significant attention as sustainable alternatives to traditional inorganic photocatalysts for environmental remediation and energy-related applications. Recent research progress in biobased hybrid photocatalytic systems is critically reviewed to outline their design strategies, photocatalytic mechanisms, and environmental applications. These composites integrate bioderived polymers with metal oxide semiconductors, forming hybrid architectures that improve interfacial contact at the molecular level, enhance charge transfer efficiency, and impart higher structural flexibility. The polymer matrix not only provides mechanical adaptability and functional surface groups, but also serves as an environmentally friendly support that can modulate surface electronic states and influence the photoinduced electron–hole dynamics in the inorganic phase. By controlling the molecular interactions between the polymer chains and metal oxide surfaces, these hybrids can mitigate key limitations of conventional metal oxides, such as rapid electron–hole recombination and restricted visible-light absorption. This review first summarizes the fundamental electronic and structural properties of widely employed metal oxide semiconductors and highlights their intrinsic limitations in photocatalytic processes. It then examines the role of biopolymers from the perspective of molecular structure, charge transport pathways, and interfacial interaction mechanisms with the inorganic component. Various synthesis strategies—including sol–gel, hydrothermal, in situ nanoparticle generation, green synthesis, and surface functionalization—are discussed, with emphasis on their ability to tune the nanoscale morphology and interfacial chemistry of the hybrids. Applications of these biohybrid systems in dye degradation, pharmaceutical pollutant removal, heavy metal reduction, and antimicrobial photocatalysis are analyzed alongside mechanistic insights into charge separation efficiency and band alignment at the molecular interface. Furthermore, challenges related to long-term stability, reproducibility, scalability, and performance in real wastewater matrices are also addressed. Overall, this review provides a thorough discussion on the design principles, photocatalytic mechanism, and environmental applications of biobased hybrid semiconductors, while emphasizing future opportunities for the development of efficient and sustainable photocatalytic systems. Full article

This study investigates the electrostatic and electrochemical behavior of polyaniline (PANI) and its composite with amine-functionalized multi-walled carbon nanotubes (PANI/MWCNT–NH₂) to elucidate the mechanisms governing ammonia (NH₃) sensing. High-resolution atomic force microscopy (AFM) coupled with electrostatic force microscopy (EFM) demonstrates that pristine PANI forms granular macroaggregates with localized charge distribution, whereas MWCNT incorporation promotes worm-like percolative networks that enhance charge delocalization and conductivity. Electrochemical characterization by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) corroborates these nanoscale observations, revealing significantly improved interfacial electron transfer kinetics in the composite. Upon exposure to NH₃, pristine PANI undergoes rapid de-doping and nonlinear signal suppression, while the composite exhibits a more progressive electrochemical modulation. Overall, the results demonstrate that NH₃ sensing in PANI-based films is governed not solely by electroactive material content but by the interplay between nanoscale morphology, electrostatic heterogeneity, and charge transport topology. The nanotube-mediated formation of delocalized and percolative conductive pathways provides structural and electrochemical robustness, enabling tunable, high-sensitivity operation suitable for next-generation, low-power ammonia sensing platforms. Full article

Additive engineering has become a critical strategy for optimizing the morphology and performance of bulk heterojunction (BHJ) organic solar cells (OSCs), while volatile solid additives have been widely employed to control nanoscale phase separation during film formation. Concerns regarding reproducibility, residual solvent effects, and long-term stability have stimulated increasing interest in non-volatile solid additives. In recent years, solid additive engineering has emerged as a promising approach for modulating molecular packing, regulating phase separation, enhancing charge transport, and improving device stability. However, a systematic analysis of its material design principles and performance impact remains limited. This review summarizes recent progress in solid additive engineering for OSCs, categorizing reported additives into non-volatile, volatile and nanomaterials. The effects of these additives on key photovoltaic parameters, including open-circuit voltage (Voc), short-circuit current density (Jsc), fill factor (FF), and power conversion efficiency (PCE), are comparatively analyzed based on the reported data. Particular emphasis is placed on morphology and structural performance relationships and stability enhancement mechanisms. Finally, current challenges, including the lack of universal molecular design rules and limited mechanistic understanding of additive host interactions, are discussed, and future research directions are proposed. This review aims to provide a comprehensive perspective on the material-level role of solid additives and to guide the rational design of next-generation high-performance and stable organic solar cells. Full article