Search Results (886)

Nephrite is a significant jade resource, and systematic investigation of its deposits contributes to regional metallogenic synthesis and exploration targeting. The recently discovered white nephrite deposit in the Dikou area, Fujian Province, remains inadequately characterized. This study presents a comprehensive mineralogical investigation employing polarizing microscopy, scanning electron microscopy, electron probe microanalysis, X-ray powder diffraction and laser Raman spectroscopy to elucidate the mineralogical and petrochemical characteristics of Dikou nephrite and constrain its genesis. The results demonstrate that tremolite constitutes the predominant mineral phase, accompanied by abundant diopside and quartz, with minor dolomite, prehnite, and apatite. Based on subtle compositional variations, tremolite can be categorized into two generations: early metasomatic Tr-I and late-stage Tr-II. All tremolite samples exhibit Fe-depleted, Mg-enriched composition with Mg# > 0.99. The mineral assemblage and textural relationships record multiple episodes of hydrothermal metasomatism. Integrated with the regional geological constraints, the deposit formation is genetically linked to the Neoproterozoic–Early Paleozoic ocean–continent transition of the South China Plate and is classified as D-type nephrite. The Dikou nephrite exhibits the mineral assemblage typical of dolomite-related deposits, displaying a distinctive felt-like fibrous texture that yields a homogeneous structure and superior aesthetic quality. Its Fe-depleted composition imparts a notably lighter coloration relative to D-type nephrite from other deposits. This study advances understanding of Dikou nephrite genesis, highlights the diversity of metallogenic environments in Fujian Province, and provides a theoretical framework for exploration of analogous deposits. Full article

Two-dimensional (2D) materials exhibit electronic and collective excitation properties that are highly sensitive to surface chemistry and thickness, requiring surface-sensitive characterization at low electron energies. Here, we investigate graphene, hexagonal boron nitride (h-BN), molybdenum disulfide (MoS₂), and titanium carbide (Ti₃C₂) MXene using an advanced home-built scanning low-energy electron microscopy system combined with time-of-flight electron spectroscopy (SLEEM/ToF). The system uniquely records electron energy-loss spectra (EELS) from transmitted electrons rather than from the reflected electrons used in conventional SLEEM. Compared with high-energy EELS, our low-energy ToF-EELS approach offers enhanced surface sensitivity and reduced beam-induced damage, enabling direct probing of π and π + σ plasmon excitations. Additionally, complementary techniques, including scanning transmission electron microscopy (STEM), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS), were employed to characterize structural and chemical properties. EELS were acquired for all investigated 2D materials at electron landing energies of 500–1500 eV, and in the 5–50 eV range for selected materials, including graphene and MoS₂. Analysis of these spectra enabled determination of the average plasmon positions across the measured energy range for all studied materials. Furthermore, a quantitative determination of the inelastic mean free path (IMFP) was achieved for graphene in the 10–50 eV range, yielding a value of 1.9 ± 0.2 nm. These results demonstrate the potential of SLEEM–ToF for surface-sensitive analysis of 2D materials. Full article

Titanium and its alloys are widely used in orthopedic and dental implantology for their corrosion resistance and biocompatibility supporting osseointegration; however, their usage is accompanied by release of wear debris that may induce inflammatory responses. The necessity of formation of multifunctional coatings that accelerate osseointegration and provide long-term mechanical stability of titanium implants remains highly relevant. We propose a new simple and scalable coating method based on the laser shock processing technique, with TiO₂ and SrCO₃ powder mix used as an absorption layer. Our results show that this treatment created an approximately 158.3 ± 35.8 μm thick coating consisting of a mixed SrTiO₃-TiO₂ phase. The hardness of this coating evaluated by Vickers microhardness measurements showed a hardness increase of 3.3 times compared to the initial titanium substrate. Piezoelectric force microscopy (PFM) analysis revealed the presence of a reverse piezoelectric effect in the obtained structure confirming the highly likely successful synthesis of coating impregnated with SrTiO₃. This piezoelectric coating can be readily deposited onto titanium substrates using the proposed method, enabling exploration of potential biomedical applications in future research. Full article

This study systematically investigates the formulation–property relationships of epoxy-based silver conductive adhesives by varying silver filler architecture, total filler loading, and organic carrier design. Rotational viscometry, four-point probe measurements, thermal conductivity analysis, and scanning electron microscopy (SEM) were employed to elucidate the correlations among rheological behavior, conductive network formation, and electrical–thermal transport properties. All formulations incorporate dicyandiamide (DICY) as a latent curing agent, in combination with a thermally activated accelerator and silane coupling agents, to stabilize filler–matrix interfaces and suppress moisture-assisted side reactions. This latent curing chemistry enables effective low temperature curing at approximately 155 °C, providing compatibility with temperature-sensitive flexible polymer substrates. After sealed storage at 25 °C and 60% relative humidity for two weeks, all formulations exhibited viscosity variations within ≤16%, demonstrating extended pot life and good storage stability under ambient conditions. Meanwhile, the normalized volume resistivity and thermal conductivity remained close to their initial values, with maximum relative deviations of approximately 12% and 7%, respectively, from the initial (Day 0) values across all formulations, indicating stable electrical and thermal transport properties during storage. Differences in conductive network formation and filler packing characteristics were reflected in the observed electrical and thermal transport behaviors. Balanced electrical–thermal performance was achieved without the need for high-temperature sintering or post-annealing, underscoring the effectiveness of the low temperature curing strategy. Overall, this work defines a practical formulation design window that simultaneously achieves low temperature curability, long pot life, stable rheology, and robust electrical–thermal performance. The results provide useful material-level guidelines for the development of epoxy-based silver conductive adhesives intended for conductive interconnects on flexible polymer substrates and related flexible electronic applications. Full article

In this study, Ti-Co-Ce getter films were deposited via magnetron sputtering to investigate their activation mechanism—the thermal removal of surface passivation layers to restore gas sorption capability. The morphology before and after film activation was characterized using scanning electron microscopy (SEM) and atomic force microscopy (AFM). The oxygen content on the film surface before and after activation was measured using an energy-dispersive X-ray spectrometer (EDS), and gas desorption during activation was monitored with a quadrupole mass spectrometer (QMS). The combined results confirmed the absence of O₂ desorption during activation, suggesting oxygen migration into the film bulk. Crucially, in situ X-ray photoelectron spectroscopy (XPS) combined with controlled Ar⁺ ion sputtering depth profiling (0–30 nm) was employed to directly probe the chemical-state evolution within the thin film before and after thermal activation at 400 °C, thereby providing direct evidence of the activation dynamics. The data reveal that within the 0–10 nm near-surface region, a strong oxygen chemical potential gradient drives rapid oxide reduction and inward migration of lattice oxygen. At depths of 20–30 nm, moderate reduction coupled with oxygen enrichment induces phase separation, while around 30 nm, a dynamic equilibrium between oxygen inflow and outflow is established. These findings provide a theoretical basis for optimizing activation processes and guiding the development of low-temperature getter materials. This work is particularly relevant for MEMS, vacuum electronics, and other applications with stringent thermal budgets, expanding the design possibilities for heat-sensitive device integration. Full article

This study investigated sulphide textures and trace element chemistry from the Tomingley Gold Project (TGP) region of Central-West NSW, eastern Australia, using in situ techniques. In particular, the study focused on pyrite and arsenopyrite to gain insights into ore-forming processes and determine which trace elements within these minerals can be used as potential pathfinder elements for mineral exploration in the TGP. A total of 41 drill core samples from a variety of lithologies (volcaniclastic, monzodiorite, graphitic siltstone, dacite, andesite) were described and analysed using reflected light microscopy, high-resolution microscopy (via Scanning Electron Microscope or SEM), elemental mapping (via Electron Probe Micro Analysis or EPMA) and targeted trace element analysis of sulphide grains (via Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry or LA-ICP-MS). Findings show that pyrite and arsenopyrite are the major sulphides that host fracture-fill/inclusions of native gold and ‘invisible gold’. Pyrite rich in groundmass inclusions should be evaluated due to their characteristic high concentrations of both As and Au. Pyrite trace element chemistry (Sn, Bi, W, Sb, Au and Se) was able to delineate mineralised from unmineralised samples in volcaniclastics, graphitic siltstones and andesites but was much more challenging for lithologies like dacites and monzodiorites. The study also found that Au may have been introduced into the system earlier and existed as ‘invisible gold’ in earlier generations of pyrite. This study highlighted the utility of in situ techniques to discriminate mineralised signatures from unmineralised samples, and this has proven to be far more effective compared to whole-rock techniques, emphasising the benefits of such datasets in mineral exploration. Full article

To address the high-salinity and hyper-humid thermal environment of tropical oceans and meet industrial demands for high strength and lightweight, austenitic low-density steel was developed as a novel corrosion-resistant steel. A 3.5 wt.% NaCl solution was used to simulate the marine environment to study the effect of Si on the corrosion behavior of this steel. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and electron probe microanalysis (EPMA) were employed to characterize the microstructures and corrosion behaviors of two test steels, as well as the phase compositions and element distributions of corrosion products after polarization and cyclic immersion accelerated corrosion tests. The results show that a dense oxide film initially forms on the steel surface in 3.5 wt.% NaCl solution at the early corrosion stage. Si addition induces SiO₂ formation and promotes Al conversion to Al₂O₃, enhancing oxide film compactness and inhibiting matrix atom outward diffusion and Cl⁻ inward penetration. With prolonged corrosion, the oxide film is dissolved or broken, forming a dense rust layer dominated by Fe₃O₄, Fe₂O₃ and FeOOH. Si enriches in the inner rust layer adjacent to the matrix and pitting cavities, inhibiting pitting deepening and promoting γ-FeOOH to α-FeOOH transformation, thus improving the steel’s corrosion resistance. Full article

The newly identified greisen-hosted Nb-Ta mineralization in the Qidashan iron deposit, Liaoning Province, China, offers a unique opportunity to explore how hydrothermal processes contribute to the enrichment of critical metals. In this study, an integrated analytical approach of petrographic observation and scanning electron microscopy–energy-dispersive spectrometer (SEM-EDS), electron probe microanalyzer (EPMA), and laser ablation inductively coupled plasma mass spectrometer (LA-ICP-MS) U-Pb dating of columbite-group minerals (CGMs) were employed to systematically decipher the paragenetic sequence, micro-structure, elemental composition and mineralization age of CGMs, aiming at the genesis of greisen-hosted Nb-Ta mineralization. The mineralization is characterized by the abundant occurrence of CGMs. Three generations of CGMs and two mineralization stages are distinguished: stage I contains CGM Is and CGM IIs, with Nb₂O₅ ranging from 25.7 to 69.56 wt.% and Ta₂O₅ from 5.8 to 52.5 wt.%; stage II contains CGM IIIs, with Nb₂O₅ between 59.5 and 71.5 wt.% and Ta₂O₅ between 3.5 and 16.2 wt.%. CGM Is consist of euhedral, homogeneous crystals of more than 100 μm, exhibit low Ta/(Nb + Ta) ratios (0.05–0.06) and high Mn/(Fe + Mn) ratios (0.19–0.26), and belong to columbite-Fe. CGM IIs generally overgrow on CGM Is with hydrothermal overprinting textures, and show significant compositional gaps compared to CGM Is, exhibiting higher Ta/(Nb + Ta) ratios (0.13–0.55) and restricted Mn/(Fe + Mn) ratios (0.15–0.18), with some belonging to columbite-Fe and others to tantalite-Fe, which reveals a transition from magma to “hydrosilicate fluid”. CGM IIIs are mainly anhedral and homogeneous, with a grain size of less than 50 μm. However, some CGM IIIs overgrow on CGM IIs and/or CGM Is with patchy textures indicative of subsequent hydrothermal overprinting of hydrosilicate fluid, forming a coarse-grain size over 100 μm. CGM IIIs are characterized by lower Ta/(Nb + Ta) ratios (0.03–0.14) and variable Mn/(Fe + Mn) ratios (0.08–0.26), and they belong to columbite-Fe. LA-ICP-MS U-Pb dating yields weighted mean ²⁰⁶Pb/²³⁸U ages of 2646 ± 15 Ma for stage I and 2500 ± 28 Ma for stage II, indicating two-stage Nb-Ta mineralization. The early mineralization may correlate with the partial melting of volcanic–sedimentary rocks due to the geothermal anomalies associated with ~2.7 Ga submarine volcanism, and the late mineralization formed by the magmatic hydrothermal activities related to emplacement of the Qidashan granite in 2.5 Ga. We therefore propose that the two-stage greisen-hosted Nb-Ta mineralization probably widely occurred in these sedimentary–metamorphic iron deposits in the Anshan–Benxi area and even in the northern edge of the North China Craton, and it may provide new insights for evaluating the Nb-Ta resource potential in similar Algoma-type iron deposits globally. Full article

With the growing global emphasis on nuclear reactor decommissioning, reliable thermal neutron detection has become increasingly important for ensuring critical safety and for the identification of fuel debris and radioactive waste. In this context, this study developed and characterized a Ce-doped CaF₂/⁶LiF (Ce:CaF₂/LiF) eutectic scintillator for thermal neutron detection with Ce concentrations ranging from 0.5 to 10 mol%. The eutectic samples were grown by the melt-solidification method, and their crystalline properties were evaluated using inductively coupled plasma mass spectrometry, X-ray diffraction, scanning electron microscopy, and field-emission electron probe microanalysis. Radioluminescence, photoluminescence, transmittance, scintillation decay, and pulse-height measurements were conducted to assess their scintillation performance. Structural characterization revealed a well-defined eutectic microstructure together with several Ce-rich phases. The results of the effective neutron sensitivity demonstrated that the Ce concentration was effectively optimized based on the effective neutron sensitivity: the sample with 1 mol% Ce exhibited the highest neutron sensitivity (approximately 1.5 times that of a Ce:LiCaAlF₆ single crystal) and a 1.6-times higher neutron-induced light yield, while maintaining a fast effective decay time of 400 ns. These findings suggest that the Ce:CaF₂/LiF eutectic is a promising candidate for high-performance thermal-neutron scintillators for applications in nuclear decommissioning. Full article

The fabrication of sustainable packaging films based on chitosan/starch (CTS/Starch) blends, reinforced with Chitosan Nanoparticles (CNPs), was achieved via the casting blend technique. This research explored the impact of varying CNPs loading on critical physicochemical properties, including water vapor permeation (WVP), thermal stability, and mechanical strength. To elucidate the structural and chemical complexities of the blend films, surface morphology was investigated via Scanning Electron Microscopy (SEM), internal architecture was visualized using Transmission Electron Microscopy (TEM), and molecular interactions were probed through Fourier Transform Infrared (FTIR) spectroscopy. The reduction in WVP from 6.18 ± 0.54 to 5.38 ± 0.93 g.m⁻¹.s⁻¹.pa⁻¹, equilibrium moisture content (EMC) from 16.52 ± 1.03% to 12.5 ± 1.05%, and water absorbency (WA) from 340 ± 1.63% to 88.65 ± 1.12% in CTS/Starch blend films demonstrated loaded with (0–8 wt%) CNPs loading. Concurrently, films with 2–8 wt% CNP loading exhibited an increase in opacity from 2.38 ± 1.01 mm⁻¹ to 4.83 ± 0.83 mm⁻¹, accompanied by a decrease in transmittance from 89.20 ± 0.50% to 79.70 ± 1.20%. These findings collectively indicated that the CNP-incorporated chitosan/starch composites offer enhanced ultraviolet light shielding and improved water barrier capabilities compared to the non-reinforced chitosan/starch films, underscoring their promising utility in food and pharmaceutical packaging applications. Full article

Mitochondria play a crucial role in cellular bioenergetics, signaling, and metabolism; yet, many fundamental mechanisms such as the proton transfer along the membranes, the link between membrane curvature and oxidative phosphorylation, and the nanoscale organization of enzyme supercomplexes remain poorly understood due to the limitations of classical biochemical approaches. This review addresses this gap by systematically analyzing the contemporary physical methods used to investigate the mitochondrial structure and function from the micro to nano scale. It covers advanced fluorescence and super-resolution microscopy, electron and volume electron microscopy, and scanning probe techniques, as well as cryo-electron tomography for resolving supramolecular assemblies in near-native conditions. The review highlights the applications of the modern fluorescent probes, expansion and phase microscopy, and machine-learning-based image analysis for a quantitative assessment of the mitochondrial morphology, membrane potential, and dynamics in living cells and tissues. Complementary spectroscopic and scattering methods, including Raman spectroscopy, NMR, and X-ray and neutron scattering, are discussed as tools for probing the redox state, metabolite composition, and membrane organization. Emphasis is placed on integrating high-resolution experimental data with advanced computational frameworks to test competing models of mitochondrial function and pathology, and to guide the development of biomimetic and biomedical technologies. Full article

“Heijin” (the literal translation from Chinese being “Black Gold”) seal stone represents a unique variety of sulfur-rich, dickite-dominant jade, yet its mineralogical genesis and structural properties remain insufficiently characterized. This study utilizes a multi-analytical approach comprising polarized light microscopy, X-Ray diffraction (XRD), Raman spectroscopy, Fourier-transform infrared spectroscopy (FTIR), Scanning Electron Microscopy coupled with Energy-Dispersive X-Ray Spectroscopy (SEM-EDS), Electron Probe Microanalysis (EPMA), and Thermogravimetry and Differential Scanning Calorimetry (TG-DSC) to investigate the phase composition, crystalline order, and thermal evolution of this material. The results demonstrate that “Heijin” stone is primarily composed of highly ordered 2M₁ dickite with a Hinckley index (HI) ranging from 0.92 to 1.50. Its distinctive black appearance originates from the disseminated distribution of micrometer-scale pyrite, which is accompanied by trace amounts of svanbergite. This aluminum phosphate–sulfate (APS) mineral serves as a critical indicator of high sulfur fugacity and acidic hydrothermal alteration environments. Furthermore, a significant correlation exists between the crystalline order of dickite, its micro-morphology, and its thermal stability. Samples characterized by high crystallinity (HI ≈ 1.50) exhibit well-developed, euhedral book-like aggregates and elevated dehydroxylation temperatures (T_m ≈ 665 °C), whereas samples with lower crystalline order correspond to fragmented microstructures and reduced thermal stability. This research defines the mineralogical identity of “Heijin” stone and provides a scientific basis for employing thermal analysis to evaluate the crystalline quality of dickite-based jade materials. Full article

Macroporous silica thin films were synthesized via the sol–gel method to elucidate the relationship between pore structure and the degree of polarization of light (DoP). The films were characterized by scanning electron microscopy (SEM) to determine their mean pore size and surface porosity, while polarization-resolved speckle imaging was employed to evaluate the degree of polarization and its distribution on the Poincaré sphere. The results show that surface porosity is a key structural parameter governing the DoP, with increasing values leading to enhanced scattering and a progressive isotropization of the polarization-state distributions. Poincaré sphere mapping further reveals distinct scattering regimes and polarization-conversion pathways, providing insights that are not accessible with conventional optical measurements. Overall, these findings show that speckle imaging is a rapid, cost-effective, and non-destructive approach to probing structural and optical anisotropies in porous materials, with direct relevance to systems where pore accessibility dictates performance, including liquid-crystal devices, photochromic coatings, and other nanostructured photonic platforms. Full article

This study aims to develop an innovative electrochemical genosensor based on activated biochar (ABC) derived from the biomass of the seaweed Sargassum spp. The synthesis process begins with the pyrolysis of Sargassum spp. at 500 °C to obtain biochar (BC), which is chemically activated with nitric acid (HNO₃). The physicochemical properties of the resulting material, such as morphology and surface area, were characterized using techniques including scanning electron microscopy (SEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and the Brunauer–Emmett–Teller (BET) method for surface area. BET results showed an increase in surface area from 22.9367 ± 0.0879 m²/g (BC) to 159.2915 ± 2.2641 m²/g (ABC). For the development of the genosensor, a hydrolyzed collagen gel matrix enriched with ABC is created. This nanostructured, biocompatible mixture is used to immobilize a DNA probe on a graphite electrode, employing the large surface area of ABC and the formation of a functional HC-based coating. The system’s viability was evaluated by cyclic voltammetry (CV), which showed changes in the maximum anodic peak current (Ipa) during fabrication: 27.78 ± 1.87 μA for the bare electrode, 35.25 ± 1.24 μA for ABC 30%, and 39.25 ± 1.84 μA for HC + ABC 30%. After ssDNA immobilization and hybridization to dsDNA, Ipa decreased to 28.81 ± 1.565 μA and 23.10 ± 1.25 μA, respectively. Finally, hematoxylin (Hx) was used as an intercalating indicator from hybridization, reducing the maximum anodic peak current to 15.51 ± 1.13 μA, consistent with additional interfacial limitations associated with dsDNA formation. Overall, the developed system demonstrates a sustainable, promising platform for molecular diagnostics in electrochemical DNA biosensor development. Full article

Near-field scanning microwave microscopy (NSMM) offers the ability to probe local electromagnetic properties beyond the classical Abbe diffraction limit, but achieving high resolution over practical scan areas remains challenging. In this work, we introduce a novel three-dimensional (3D) NSMM probe consisting of a split-ring resonator (SRR) coupled to a microstrip line and loaded with vertically extended metallic bars. The 3D loading enhances electric-field localization in the sensing region by introducing field singularities. Full-wave numerical simulations are used to extract the field-spread function ($FSF$) of the probe and to quantify how probe geometry, stand-off distance, and bar dimensions control the $FSF$ and its spatial-frequency (k-space) content. An imaging model is then developed in which the NSMM image is represented as a convolution between the object and $FSF$ in one and two dimensions. This framework demonstrates that progressively localized $FSFs$, obtained through 3D loading and resonator miniaturization, systematically improve image fidelity and preserve higher spatial frequencies. The probe is fabricated using printed circuit board technology (PCB) with vertically attached metallic bars, and its performance is validated by imaging a dielectric slab containing a cylindrical air-filled void. The measured line profiles and two-dimensional images are in good agreement in general characteristics with the convolution-based model, confirming that the proposed 3D SRR-based probe operates as a spatial filter whose engineered near-field distribution governs the achievable resolution in NSMM imaging. Full article