Search Results (246)

The report presents the electrical, structural, and microstructural properties of high-pressure–high-temperature-treated (HPHT) composites composed of δ-like Bi₂O₃ nanograins embedded in an aluminosilicate glassy matrix. Nanocomposites were obtained by heat treatment of the Bi₂O₃-Al₂O₃-SiO₂ ternary glass system, followed by high-pressure molding (above 750 MPa). The total oxygen conductivity σ_t of the studied nanocomposites was high and approached a value of 4.5 × 10⁻⁴ S/cm at 600 °C. Due to HPHT treatment, we could also determine the intragrain conductivity of δ-Bi₂O₃ nanocrystallites. In this case, the value of σ_δ was even higher and was equal to 1.3 × 10⁻³ S/cm at 600 °C. It was also possible to study the temperature dependence of intragrain conductivity, showing two activation energies, which probably reflect the order–disorder transition within the sublattice of mobile O²⁻ ions. The obtained nanocomposites exhibited promising properties for applications in electrochemical devices operating in the intermediate temperature range from 300 to 600 °C. Full article

Pyrrolidinyl-substituted silacyclopentane (CH₂)₄Si(Pyr)₂ and α-amino isobutyric acid (H₂Aib) react with the release of one equivalent pyrrolidine (HPyr) and the formation of the pentacoordinate silicon bis-chelate (Aib)Si(CH₂)₄(HPyr), which features the di-anion of the amino acid as an (O,N)-chelator and one equivalent of pyrrolidine as an additional lone-pair donor. Crystallographic analyses of the chloroform solvate (Aib)Si(CH₂)₄(HPyr)·(CHCl₃), which undergoes a phase transition at 200 K, and a solvent-free modification (Aib)Si(CH₂)₄(HPyr), which features two crystallographically independent molecules of the complex, revealed that the N atom of the HPyr ligand, as well as the carboxylate of Aib, occupy the axial positions in the trigonal bipyramidal Si coordination sphere; the Si–C bonds of the silacyclopentane rest on equatorial sites. For the isolated molecule in a solvent environment, computational analyses revealed that the energy difference between this configuration and the related isomer with an equatorial HPyr and equatorial–axial positioning of the silacyclopentane motif is marginal. In DMSO solution, the adduct (Aib)Si(CH₂)₄(HPyr) decomposed, forming the hexacoordinate Si complex (HAib)₂Si(CH₂)₄ as one of the decomposition products. In a deliberate manner, this compound was accessible from the diethylamino-substituted silacyclopentane (CH₂)₄Si(NEt₂)₂ and H₂Aib with the liberation of diethylamine. (HAib)₂Si(CH₂)₄ features two mono-anions of the α-amino acid as (O,N)-chelators, their carboxylate O atoms are trans-disposed to silacyclopentane, and their NH₂ groups are mutually trans. Full article

For agricultural films, spectral matching, UV protection, and environmental durability are essential for efficient crop production. A self-cleaning silane-crosslinked red/blue dual-emission carbon dot/polyvinyl alcohol composite film (KH/RB-CQDs/PVA) was fabricated via a covalent anchoring strategy. RB-CQDs were synthesized by a two-step hydrothermal method using o-phenylenediamine: initial blue-emitting carbon cores formed, then phosphoric acid-assisted secondary treatment covalently bridged residual precursor-derived red fluorophores onto cores through pyrophosphate bonds, as evidenced by TEM, XPS, ³¹P NMR, HPLC-MS and DFT. This rigid bridging suppressed excessive core growth and energy transfer while spatially separating dual emission, endowing excellent photostability (>95% fluorescence retention after 50 min UV and 30 d storage). Subsequently, KH-560 was employed to construct a robust covalent crosslinked network anchoring RB-CQDs in PVA and forming rough Si-O-Si surface structures, confirmed by SEM and XPS. The resulting film exhibited 16.16% quantum yield, 291% tensile strength enhancement, 95% UV shielding, and <1% contaminant residue. Chlorophyll fluorescence kinetics, gas-exchange analyses, and photosynthetic response curves demonstrated that KH/RB-CQDs/PVA increased the potato net photosynthetic rate by 55.46% and tuber yield by 76% through synergistic optimization of photosystem II electron transport and RuBisCO-mediated carbon assimilation. This work provides a molecular design principle for high-performance intelligent agricultural films. Full article

Vehicle damage detection is an important task in intelligent transportation systems and insurance assessment, yet it remains challenging due to the subtle appearance, irregular shapes, and spatial dispersion of damage regions in complex environments. We propose a specialized structural synergy that organically integrates a GSConv-based Slim-Neck, a dynamic Bi-Level Routing Attention mechanism, and an orientation-aware SIoU loss. Rather than a superficial architectural combination, this cooperative design introduces a novel methodological framework engineered specifically to resolve the fundamental conflict between edge-deployment efficiency and fine-grained feature preservation in vehicle inspection. The method is evaluated on the publicly available Car Damage Detection dataset and compared with representative two-stage and one-stage detectors, including DETR, Faster R-CNN, YOLOv5n, YOLOv8n, and YOLO11n. Experimental results show that the proposed approach achieves a mAP50 of 67.9% and mAP50–95 of 53.8%, outperforming the baseline YOLO11n and other lightweight YOLO variants with only a moderate increase in computational cost. These results indicate that the proposed framework offers a favorable trade-off between detection accuracy and efficiency, showing potential for vehicle damage inspection under resource-constrained conditions. Full article

The solidification process is crucial for preparing high-performance superconductors and is strongly dependent on the characteristics of the starting powder, including particle size, morphology, and phase purity. This review concisely examines the study on four key superconductors: REBCO, Bi-2212, FeSeTe, and MgB₂. In REBCO, additives such as CeO₂, Pt, or BaO₂ powder can refine the RE-211 phase. In Bi-2212, Pb doping stabilizes the high-T_c phase. For FeSeTe, doping with F or Co modifies phase separation and introduces Δκ pinning. Meanwhile, in MgB₂, the incorporation of SiC nanoparticles powder generates effective pinning centers. Concurrently, processing conditions exert a decisive influence on the final microstructure, as demonstrated by the TSMG/TSIG route in REBCO, partial melting parameters for Bi-2212, specific cooling protocols and thermal treatments for FeSeTe, and optimized sintering and post-annealing processes for MgB₂. Future research directions should prioritize fundamental understanding of phase separation mechanisms during powder processing, development of multi-component doping strategies for powder modification, and advancement of scalable powder processing routes for practical conductor architectures. Full article

Conventional flexible substrates for strain sensors generally exhibit good flexibility and processability; however, their limited heat resistance restricts their long-term application in high-temperature environments. Aiming at the problem of insufficient heat resistance of high-temperature flexible strain sensing matrix, triphenyltetramethylcyclotrisiloxane (P₃), trimethyltrivinylcyclotrisiloxane (V₃) and octamethylcyclotetrasiloxane (D₄) were used as raw materials in this paper. Methyl vinyl phenyl silica gel (MVMPS) with high phenyl and vinyl content was prepared by anionic ring-opening polymerization, and condensed with KH-570 (3-Methacryloxypropyltrimethoxysilane) to obtain a condensed modified gel (C-MVMPS). Subsequently, a methyl vinyl phenyl silicone rubber composite was fabricated using fumed silica as the reinforcing filler and Si69 as the coupling agent and vulcanization assistant. In addition, flake silver powder was incorporated to prepare an Ag/MVMPS conductive adhesive, and a sandwich-structured strain sensor with a silicone rubber/Ag-MVMPS conductive adhesive/silicone rubber configuration was fabricated. The synthesized methyl vinyl monophenyl silicone gum exhibited a number-average molecular weight of 170,449, a phenyl content of 25.19%, and a vinyl content of 24.44%. The composite showed the best overall performance at 3 phr (parts per hundred of rubber) Si69 (Bis(gamma-triethoxysilylpropyl) tetrasulfide) and 30 phr SiO₂ (Fumed silica), with a 5% weight-loss temperature (T_5%) of 367.14 °C and a 10% weight-loss temperature (T_10%) of 529.6 °C. The prepared sandwich-structured sensor exhibited clear and stable resistance responses within the strain range of 10–80%. The sensitivity increased with increasing strain, and good reproducibility was maintained under different loading rates. Moreover, the sensor still exhibited continuous and distinguishable cyclic responses after 1000 cycles at 20% strain. These results provide an experimental basis and a feasible design strategy for the application of methyl vinyl phenyl silicone rubber in high-temperature flexible strain sensors. Full article

With the growing demand for strategic metals and the gradual depletion of traditional metal ore deposits, coal and coal-bearing strata are regarded as potential sources of rare metals; consequently, research into the characteristics of associated elements in coal-bearing strata has become one of the primary avenues of searching for new alternative resources. To investigate the sedimentary environmental characteristics and controlling factors of the coal-bearing strata along the southern margin of the Junggar Basin, coal seams 9–15 of the Xishanyao Formation in Sulphur Gully (Early Middle Jurassic) were selected as the subject of this study. This study employed analytical techniques including industrial analysis, total sulphur analysis, X-ray powder diffraction (XRD), X-ray fluorescence spectroscopy (XRF) and inductively coupled plasma mass spectrometry (ICP-MS) to determine the mineralogical and elemental geochemical characteristics of coal samples from Seylangou mining area, specifically from coal seams 9–15 and their overlying and underlying strata. Based on analyses of elemental ratios such as Al₂O₃/TiO₂, Sr/Ba, Rb/Sr, Ni/Co and V/(Ni + V), the source of material during the deposition of this deposit was identified, and the characteristics of the depositional environment, as indicated by palaeosalinity, palaeoclimate and redox conditions, were revealed. The results indicate that the macroscopic coal-rock types of coal seams 9–15 at the Sulphur Gully Coal Mine on the southern margin of the Junggar Basin are predominantly semi-dull to dull, with small amounts of filamentous coal and lustrous coal. The average proportion of the vitrinite group in the coal is 42.75%, the inertinite group is 51.40%, and the liptinite is 2.25%. The average content of inorganic matter in the coal is 3.60%, and the average maximum reflectance of the vitrinite group is 0.651%. The coal represents a transitional stage from low-rank to medium-rank coal, corresponding to a metamorphic stage of Grade I–II. The coal is classified as a bituminous coal with medium total moisture, very low ash, medium-volatile matter, medium-to-high fixed carbon and very low sulphur. The minerals in the coal seam are predominantly kaolinite, calcite and quartz. The major elements in the ceiling of the coal seam are dominated by SiO₂, followed by Al₂O₃; the coal itself is dominated by CaO, SiO₂ and Al₂O₃; and the base plate of the coal seam is dominated by Al₂O₃. The trace elements Cs and Bi are relatively enriched in the coal seam ceiling; Sr is relatively enriched in the coal; whilst Li, Cr and other elements are highly enriched in the coal seam base plate. The source rocks of the coal and the roof consist of deposits of felsic igneous rock (dacite), whilst the source rocks of the floor consist of deposits of intermediate igneous rock (andesite). The depositional environment ranges from marine brackish water at the base to transitional slightly brackish water and then to terrestrial freshwater at the top; the depositional climate was cold and arid, and the depositional environment was oxidising. This study provides valuable insights for further research into the elemental geochemical characteristics, sediment sources and depositional environments of the Xishanyao Formation coal seams in Liuhuangou, Xinjiang. Full article

This paper presents an analysis of the physicochemical and biological properties of the developed composite zinc phosphate cement modified with bismuth oxide and phosphorus slag additives. The powder phase was synthesized by sintering a frit with an optimal composition (ZnO, MgO, SiO₂, Bi₂O₃) using phosphorus slag as the active component. The study included an assessment of the microstructure, chemical resistance in aggressive environments (5% NaCl solution, 10% lactic acid, carbonated water), solubility in artificial saliva, and cytotoxicity in human fibroblasts. The addition of phosphorus slag was found to promote the formation of low-melting eutectics, which reduces the sintering temperature by 100 °C and increases the material’s whiteness to 97.8%. X-ray diffraction analysis confirmed the presence of zincite, quartz, and periclase phases, forming a dense microstructure without pronounced pores or cracks. The experimental cement demonstrated high acid resistance: the maximum weight loss in lactic acid was 8%, while the leaching of toxic elements (Pb, As, Cr, etc.) remained extremely low (10–67 ppm), confirming the material’s environmental safety. Testing of the composite zinc phosphate cement in artificial saliva revealed minimal weight loss compared to similar products. Biological testing showed that the cement’s cytotoxicity is dose-dependent; at a 0.3 g dose and a 1:4 dilution, the material loses its toxic properties and becomes safe for living tissue. The developed zinc phosphate composite cement composition offers improved aesthetic and mechanical properties, high chemical stability, and biocompatibility at working concentrations, making it promising for use in clinical dentistry. Full article

To address the lack of suitable glass systems for silicon nitride (Si₃N₄) surface metallization, which requires high wettability and thermal stability, and robust bonding between the copper layer and the ceramic substrate, a novel Bi₂O₃-TeO₂-B₂O₃-CuO glass system was developed. This study systematically investigated the influence of Bi₂O₃ concentration, glass properties, optimized paste composition, and brazing mechanism using phase analysis, microstructural characterization, particle size statistics, thermal analysis, and tensile testing. An optimal glass composition containing 20 mol% Bi₂O₃ was identified, exhibiting high thermal stability (ΔT = 224 °C) and a coefficient of thermal expansion of 9.63 × 10⁻⁶ °C⁻¹. At a brazing temperature of 750 °C, the glass demonstrated excellent wettability with a contact angle of 27°. A conductive paste comprising 94 wt% Cu and 6 wt% glass yielded a thick film with a minimum resistivity of 6.25 μΩ·cm and a maximum tensile strength of 25.2 MPa. Mechanism analysis revealed that the superior wettability drives the liquid glass phase to form a thin intermediate layer that significantly reinforces adhesion. These findings contribute to the research and development of subsequent novel glass systems with superior performance. Full article

To overcome the limitations imposed by the intermittent nature of sunlight in photocatalytic applications, this research constructs a round-the-clock purification system. We integrated an optimized S-scheme CoFe₂O₄/BiVO₄ (CFO/BV) heterojunction (synthesized via ultrasonic self-assembly at a 0.5:0.5 ratio) with a thermal energy storage (TES) unit consisting of SiO₂-encapsulated Na₂SO₄·10H₂O phase change materials (PCMs). Comprehensive characterization techniques, including XRD, HRTEM, UV-Vis DRS, EPR, and DSC, confirmed the successful formation of the interface, a broadened visible-light response (λ > 650 nm), efficient radical production, and a high latent heat storage capacity (>200 J/g). Under simulated solar irradiation, the composite exhibited superior performance, degrading 98% of the Rhodamine B within 6 h (k = 0.00994 min⁻¹), significantly surpassing single-component counterparts. More importantly, during the subsequent 12 h dark period, the heat released from the PCM maintained the reaction temperature above 35 °C, driving a 64% degradation efficiency via a thermocatalytic pathway. The system demonstrated robust stability (>90% efficiency after five cycles), excellent magnetic recoverability (98%), and high tolerance to saline textile wastewater (<10% activity loss). Furthermore, Life Cycle Assessment (LCA) indicated a 40% reduction in energy consumption compared to conventional UV/TiO₂ processes, highlighting a sustainable strategy for continuous wastewater remediation through synergistic photocatalysis and thermocatalysis. Full article

Thermally grown amorphous SiO₂ (a-SiO₂) on Si is widely used in microfluidic and biointerface devices, where surface charge governs capillary flows. We used amplitude-modulation Kelvin probe force microscopy (AM-KPFM) in air to test whether low-power visible light modulates a-SiO₂ surface potential and to derive mathematical charging-discharging models. Single-point contact potential difference (CPD) was recorded on ~0.6 µm p-type a-SiO₂ on p-type monocrystalline Si during repeated illumination cycles with continuous-wave diode lasers at 405, 505, and 685 nm delivered by optical fiber. The 405 and 505 nm wavelengths produced reproducible negative CPD shifts with steady-state values of ~−28 mV and ~−16 mV, while 685 nm stayed within noise (±2.5 mV). The 405 nm response followed bi-exponential kinetics with fast (tens of seconds) and slow (hundreds of seconds) components dominated by the slow process; after switch-off, CPD relaxed only from ~−28 to ~−23 mV over ~10³ s, indicating retention for ≥10³–10⁴ s. The 505 nm charging trace fit a single slower xponential, whereas discharging could not be fit robustly. These results demonstrate wavelength-dependent optical tuning of a-SiO₂ surface potential and provide compact kinetic descriptors for comparing charging, discharging, and retention. Full article

The influence of Zn²⁺, Ca²⁺ and Co²⁺ doping on the thermal, structural, morphological, and magnetic characteristics of CdBi_0.1Fe_1.9O₄ nanoparticles synthetized via the sol–gel technique and calcined at 300, 600, 900 and 1200 °C was investigated. Thermal analysis revealed the initial formation of metallic glyoxylates up to 300 °C, followed by their decomposition into metal oxides and subsequent ferrite formation. X-ray diffraction revealed that the ferrites were poorly crystallized at lower temperatures, whereas at higher calcination temperatures all nanocomposites exhibited well-crystalized ferrites coexisting with the SiO₂ matrix, except for the Co_0.1Cd_0.9Bi_0.1Fe_1.9O₄@SiO₂ nanocomposite, which formed a single, well-defined crystalline phase. Atomic force microscopy images revealed spherical ferrite particles encapsulated within an amorphous layer, with particle size, surface area, and coating thickness influenced by both the type of dopant ion and the calcination temperature. The structural parameters estimated by X-ray diffraction, as well as the magnetic characteristics, were strongly influenced by the dopant type and thermal treatment. These results demonstrate that the structural and magnetic characteristics of CdBi₀.₁Fe₁.₉O₄ ferrites can be effectively tuned through controlled doping and calcination, providing insights for the design of tailored functional applications. Full article

Stretchable semiconductors capable of maintaining electrical performance under large mechanical deformation are essential for reliable wearable electronic devices. However, polymer semiconductors often suffer from electrical degradation when subjected to tensile strain. In this study, electrical stability under strain was achieved by using a rubber-blended poly(2,5-bis(2-octyldodecyl)-3,6-di(thiophen-2-yl)diketopyrrolo[3,4-c]pyrrole-1,4-dione-alt-thieno[3,2-b]thiophene) (DPPT-TT) polymer semiconductor based on a conjugated polymer/elastomer phase separation-induced elasticity (CONPHINE) structure. Unlike most previous studies on fully stretchable thin-film transistors (TFTs), which primarily report overall performance changes under mechanical strain, this work systematically identifies the dominant origin of electrical performance degradation through a stepwise electrical analysis encompassing the gate insulating layer, the semiconductor layer, and complete devices. Bottom-gate top-contact (BGTC) and bottom-gate bottom-contact (BGBC) devices were fabricated on rigid Si/SiO₂ substrates to examine the intrinsic properties of the DPPT-TT/styrene-ethylene-butylene-styrene (SEBS) CONPHINE film. As a result, the device exhibits 90% mobility retention even at 100% tensile strain applied parallel to the charge transport direction. Quantitative resistance analysis using the Y-function method reveals that variations in channel resistance play a dominant role in strain-induced performance degradation, whereas changes in contact resistance contribute only marginally. These findings demonstrate that stabilizing channel resistance, rather than contact resistance, is important for achieving high mobility retention under large mechanical deformation, thereby providing concrete and quantitative design guidelines for reliable stretchable TFTs. Full article

To address the problem of insufficient detection accuracy, high false negative rate of small targets, and large positioning errors of ships in complex marine environments and foggy conditions, an improved DBL-YOLO method based on YOLOv11 is proposed. This method customizes and optimizes modules according to the characteristics of foggy scenes—the C3k2-MDSC module is designed to efficiently extract and fuse multi-scale spatial features, and a dynamic weight allocation mechanism is adopted to balance the contributions of features at different scales in the foggy and blurred environment; a lightweight BiFPN structure is introduced to enhance the efficiency of cross-scale feature transmission and solve the problem of feature attenuation in foggy conditions; a novel fusion of the Deformable-LKA attention mechanism is innovated, which combines a large receptive field and spatial adaptive adjustment capabilities to focus on the key contour features of blurred ships in foggy conditions; an Inner-SIoU regression loss function is proposed, which optimizes the positioning accuracy of dense and small targets through an auxiliary bounding box dynamic scaling strategy. Experimental results show that in foggy scenes, the recall rate is increased by 3.4%, the F1 score is increased by 1%, and mAP@0.5 and mAP@0.5:0.95 are increased by 1.4% and 3.1%, respectively. The final average precision reaches 98.6%, demonstrating excellent detection accuracy and robustness. Full article

The six platinum group elements (PGE) are among the rarest elements in the upper continental crust of the earth. Higher values of PGE have been detected in the upper mantle and in chondrite meteorites. The PGE are siderophile and chalcophile elements and are divided into the following: (1) the Ir subgroup (IPGE) = Os, Ir, and Ru and (2) the Pd subgroup (PPGE) = Rh, Pt, and Pd. The IPGE are more refractory and less chalcophile than the PPGE. High concentrations of PGE led, in rare cases, to the formation of mineral deposits. The PGE are carried in discrete phases, the platinum group minerals (PGM), and are included as trace elements into the structure of base metal sulphides (BM), such as pentlandite, chalcopyrite, pyrite, and pyrrhotite. Similarly to PGE, the PGM are also divided into two main groups, i.e., IPGM composed of Os, Ir, and Ru and PPGM containing Rh, Pt, and Pd. The PGM occur both in mafic and ultramafic rocks and are mainly hosted in stratiform reefs, sulphide-rich lenses, and placer deposits. Presently, there are only 169 valid PGM that represent about 2.7% of all 6176 minerals discovered so far. However, 496 PGM are listed among the valid species that have not yet been officially accepted, while a further 641 are considered as invalid or discredited species. The main reason for the incomplete characterization of PGM resides in their mode of occurrence, i.e., as grains in composite aggregates of a few microns in size, which makes it difficult to determine their crystallography. Among the PGM officially accepted by the IMA, only 13 (8%) were discovered before 1958, the year when the IMA was established. The highest number of PGM was discovered between 1970 and 1979, and 99 PGM have been accepted from 1980 until now. Of the 169 PGM accepted by the IMA, 44% are named in honour of a person, typically a scientist or geologist, and 31% are named after their discovery localities. The nomenclature of 25% of the PGM is based on their chemical composition and/or their physical properties. PGM have been discovered in 25 countries throughout the world, with 64 from Russia, 17 from Canada and South Africa (each), 15 from China, 12 from the USA, 8 from Brazil, 6 from Japan, 5 from Congo, 3 from Finland and Germany (each), 2 from the Dominican Republic, Greenland, Malaysia, and Papua New Guinea each, and only 1 from Argentine, Australia, Bulgaria, Colombia, Czech Republic, England, Ethiopia, Guyana, Mexico, Serbia, and Tanzania each. Most PGM phases contain Pd (82 phases, 48% of all accepted PGM), followed, in decreasing order of abundances, by those of Pt 35 phases (21%), Rh 23 phases (14%), Ir 18 phases (11%), Ru 7 phases (4%), and Os 4 phases (2%). The six PGE forming the PGM are bonded to other elements such as Fe, Ni, Cu, S, As, Te, Bi, Sb, Se, Sn, Hg, Ag, Zn, Si, Pb, Ge, In, Mo, and O. Thirty-two percent of the 169 valid PGM crystallize in the cubic system, 17% are orthorhombic, 16% hexagonal, 14% tetragonal, 11% trigonal, 3% monoclinic, and only 1% triclinic. Some PGM are members of a solid-solution series, which may be complete or contain a miscibility gap, providing information concerning the chemical and physical environment in which the mineral was formed. The refractory IPGM precipitate principally in primitive, high-temperature, mantle-hosted rocks such as podiform and layered chromitites. Being more chalcophile, PPGE are preferentially collected and concentrated in an immiscible sulphide liquid, and, under appropriate conditions, the PPGM can precipitate in a thermal range of about 900–300 °C in the presence of fluids and a progressive increase of oxygen fugacity (fO₂). Thus, a great number of Pt and Pd minerals have been described in Ni-Cu sulphide deposits. Two main genetic models have been proposed for the formation of PGM nuggets: (1) Detrital PGM represent magmatic grains that were mechanically liberated from their primary source by weathering and erosion with or without minor alteration processes, and (2) PGM reprecipitated in the supergene environment through a complex process that comprises solubility, the leaching of PGE from the primary PGM, and variation in Eh-pH and microbial activity. These two models do not exclude each other, and alluvial deposits may contain contributions from both processes. Full article