Search Results (513)

Organic-rich shales in China’s deep-water shelf environments possess significant shale gas resource potential. To investigate the reservoir development characteristics of deep-water shelf shale, 143 shale samples were collected from the low-maturity Xiamaling Formation in the Zhangjiakou area and the high to over-mature Wufeng–Longmaxi Formations in the southeastern margin of the Sichuan Basin. Basic analytical methods, including X-ray diffraction (XRD), total organic carbon (TOC) analysis, rock pyrolysis, and solid bitumen reflectance measurements, were employed alongside advanced reservoir characterization techniques such as field-emission scanning electron microscopy (FE-SEM), low-pressure CO₂/N₂ physisorption, mercury intrusion porosimetry (MIP), and focused ion beam scanning electron microscopy (FIB-SEM). This study focuses on the petrographical, geochemical, and microscopic pore structure characteristics of these marine shales. The results indicate that the mineral composition of deep-water shelf sedimentary shale is dominated by quartz, clay minerals, feldspar, calcite, dolomite, apatite, and pyrite, with quartz being the most abundant. The Xiamaling Formation shales, at low maturity, are relatively rich in siliceous components, while the high to over-mature Wufeng and Longmaxi Formation shales are richer in carbonate components. The kerogen type of organic matter in the Xiamaling Formation is primarily Types II₁ and II₂, whereas the Wufeng–Longmaxi shales are predominantly Types I and II₁. TOC content is highest in the Wufeng Formation, followed by the Longmaxi Formation, with the Xiamaling Formation exhibiting the lowest TOC levels. Pore development in the Wufeng and Longmaxi shales is significantly superior to that in the Xiamaling shales. Overall, the Wufeng and Longmaxi Formations demonstrate more favorable pore characteristics and hydrocarbon generation potential compared to the Xiamaling Formation. The Wufeng and Longmaxi Formations’ shales will be the key targets for shale gas exploration in the future. The findings of this study contribute to the understanding and development of theories of marine shale gas accumulation in China and hold both theoretical and practical significance for the efficient and rational exploitation of shale oil and gas resources. Full article

Organic–inorganic hybrid halide perovskites have attracted extensive attention due to their excellent optoelectronic properties and potential applications in field-effect transistors (FET), light-emitting diodes (LEDs), and photodetectors. However, conventional three-dimensional (3D) perovskites are limited by intrinsic instability and ion migration. Two-dimensional Ruddlesden-Popper (2D RP) perovskites offer improved structural stability, but many systems still suffer from modest photoluminescence efficiency and limited charge-transport performance. In this work, a novel 2D RP perovskite, (C₆H₅NH₃)₂CsPb₂Cl₇, was designed and synthesized, where the anilinium ion (C₆H₅NH₃⁺) serves as the organic spacer. Structural characterization indicates that the material possesses high crystallinity and a smooth surface morphology. Optical measurements reveal a violet emission peak at 411 nm with a single-peak feature and a full width at half maximum (FWHM) of 10 nm. The bandgap is determined to be 3.1 eV. Time-resolved photoluminescence (TRPL) measurements show an average lifetime of 4 ns, and the photoluminescence quantum yield (PLQY) is 29.8%. Based on the measured PLQY and lifetime, the radiative and non-radiative recombination rates were estimated to be K_r ≈ 7.45 × 10⁷ s⁻¹ and K_nr ≈ 1.76 × 10⁸ s⁻¹, respectively, suggesting that radiative recombination is appreciable although non-radiative pathways remain present. FET measurements demonstrate an on/off current ratio of 10⁴ and a carrier mobility of 1.1 cm² V⁻¹ s⁻¹. Without any systematic optimization, (C₆H₅NH₃)₂CsPb₂Cl₇ exhibits relatively favorable emissive behavior and measurable field-effect charge transport performance when compared with structurally similar 2D RP perovskites reported under comparable, non-optimized conditions. This study expands the family of chloride-based 2D perovskites and provides a basis for future improvements in their recombination and field-effect transport properties. Full article

Co²⁺-doped CsPbI₃ nanocrystals (NCs) (CsPbI₃:xCo, x = 0, 5, and 10 mol%) were synthesized in situ within a borosilicate glass matrix by the fusion method followed by controlled thermal treatment at 500 °C for 6–24 h. Transmission electron microscopy images showed quasi-spherical NCs with mean diameters of 4.9–7.1 nm. Energy-dispersive X-ray spectroscopy suggested cobalt incorporation within the nanocrystalline regions. X-ray diffraction patterns confirmed the exclusive stabilization of the cubic α-phase across all compositions, with systematic lattice contraction from a = 6.321 Å to a = 6.301 Å with increasing Co content, consistent with preferential B-site substitution of Pb²⁺ by Co²⁺. Transmittance measurements confirmed macroscopic optical transparency of all glass-NC composites after thermal treatment. The crystal field theory and Tanabe–Sugano analysis for d⁷ ions in tetrahedral (Td) symmetry yielded Δ = 5032 cm⁻¹ and B = 725 cm⁻¹ in the as-prepared state, evolving to Δ = 4428 cm⁻¹ and B = 805 cm⁻¹ after thermal treatment, confirming Td Co²⁺ coordination and significant metal–iodide covalency. CIE 1931 chromaticity analysis revealed tunable emission from deep-red coordinates to near-white-light regions, demonstrating potential for LED and single-material WLED phosphor applications. Long-term photoluminescence measurements demonstrated full preservation of α-phase excitonic emission after approximately 365 days under ambient conditions, establishing the robust phase stability of CsPbI₃:xCo NCs embedded in borosilicate glass. Full article

A hybrid DC–RF inductively coupled plasma (ICP) driven by a single-turn internal antenna was experimentally investigated to quantify magnetic confinement effects in low-pressure argon discharges. Superposition of a dc current on the RF antenna generated an azimuthal magnetic field that modified electron transport and reduced cross-field diffusion in the near-antenna region. Spatially resolved measurements of plasma density, electron temperature, plasma potential, and magnetic-field components were obtained using Langmuir, emissive, and B-dot probes. Increasing the dc current enhanced electron confinement and increased the plasma density by up to an order of magnitude at low RF power, together with improved radial and axial uniformity. A semi-empirical diffusion model incorporating electron-temperature-dependent ambipolar transport reproduced the measured ion-density distributions, ni(R,Z), within ±15%. The results support the interpretation that the discharge behaviour is governed by the coupled effects of localized magnetic confinement and inductive power deposition, and show that hybrid DC–RF excitation provides an effective route to denser and more spatially extended plasmas under low-pressure conditions. Full article

This study investigates subauroral phenomena during the main phase of the 10 May 2024 geomagnetic storm using a combination of ground-based observations from the WD IZMIRAN observatory (magnetometer, ionosonde, and all-sky imager) and Global Self-consistent Model of the Thermosphere, Ionosphere, Protonosphere (GSM TIP) simulations. During 18:00–20:00 UT, we identified the simultaneous occurrence of ionospheric signatures of Polarization Jets (PJ)/Sub-Auroral Ion Drifts (SAID) and Strong Thermal Emission Velocity Enhancement (STEVE) over Kaliningrad, consistent with previously reported PJ/SAID identification from DMSP drift velocity measurements. This identification is supported by: (1) characteristic purple emissions (clearly visible in all three channels) moving rapidly westward; (2) U-shaped structures in ionogram sequences; (3) the reproduction of supersonic westward plasma drifts within a narrow latitudinal band by the first-principles model; and (4) observed and simulated significant Ne depletion. The estimated ion drift velocity from all-sky imaging (assuming an emission altitude of 200 km) is consistent with GSM TIP simulations, which predicted PJ/SAID velocities of ~750 m/s driven by a latitudinally narrow (~3°) but longitudinally extended (>50°) poleward electric field (40 mV/m). Simulations reveal that this PJ/SAID phenomenon causes a reversal of the zonal thermospheric wind at 250 km and induces Ne disturbances across the 200–700 km altitude range. The electron temperature enhancement (up to 1500 K) exhibits a “falling drop” shape, peaking at 350 km, while ion heating exceeds 150 K. The neutral temperature shows a dual response: frictional heating at 120–160 km and localized cooling at 175–250 km due to drop in electron density. Additionally, an increase in atomic oxygen concentration was predicted within the 90–200 km range across the PJ/SAID longitudinal sector. Full article

Achieving selective cleavage of specific chemical bonds using ultrafast laser pulses remains a central challenge in ultrafast strong-field molecular physics. Here, we theoretically investigate the coherent control of strong-field dissociation of the heteronuclear molecular ion HD⁺ initially prepared in vibrationally excited states driven by an ultrashort pulse with a quadratic spectral phase. Our results reveal a pronounced sensitivity of both the total dissociation probability and the branching ratio (H⁺ + D vs. H + D⁺) to the chirp rate of the laser pulse. To uncover the underlying physical mechanism, we analyze the population dynamics in the coupled $1s\sigma$ and $2p\sigma$ electronic states and identify pronounced Rabi oscillations arising from the coherent interplay between multiphoton excitation and field-induced stimulated emission. By tuning the laser chirp rate, these oscillations can be suppressed via quantum interference, thereby reshaping the dissociation dynamics and significantly enhancing the dissociation probability of the H + D⁺ channel. These findings demonstrate that spectral-phase engineering provides a robust and versatile strategy for selective control of branching ratios in strong-field molecular dissociation. Full article

The rational design of electrode materials with tailored composition and architecture is crucial for advancing high-capability electrochemical energy storage systems. This study reports that gadolinium-modified NiFe₂O₄ nanosheet electrodes were effectively synthesized on nickel foam via a hydrothermal approach followed by thermal treatment. A series of compositions (NiFe, NiFe–Gd1, NiFe–Gd2, and NiFe–Gd3) were prepared to systematically examine the effect of Gd incorporation on structural features and electrochemical properties. X-ray diffraction (XRD) analysis confirmed the formation of the cubic spinel NiFe₂O₄ phase without detectable secondary phases, indicating that the crystal structure remains intact after Gd introduction. X-ray photoelectron spectroscopy (XPS) further verified the presence of Ni²⁺, Fe³⁺, and Gd³⁺ species within the lattice environment. Morphological analysis using field-emission scanning electron microscopy (FESEM) revealed a nanosheet-based architecture, where the optimized NiFe–Gd2 electrode exhibited a porous and interconnected nanosheet framework with abundant exposed edges. This structural configuration improves electrolyte penetration and facilitates efficient ion transport during charge storage processes. Electrochemical measurements demonstrated that the NiFe–Gd2 electrode delivers an areal capacitance of 5235 mF cm⁻² at 10 mA cm⁻², along with improved reaction kinetics and low internal resistance. An asymmetric supercapacitor assembled using NiFe–Gd2 as the positive electrode and activated carbon as the negative electrode operated stably within a 0–1.5 V potential window, achieving an energy density of 0.136 mWh cm⁻² and a power density of 3.14 mW cm⁻², while retaining 86.55% of its initial capacitance after 7000 cycles. These results highlight the potential of rare-earth engineering as a viable strategy for designing advanced spinel ferrite electrodes and pave the way for the development of high-performance, durable, and scalable supercapacitor systems for practical energy storage applications. Full article

In order to achieve rapid and qualitative detection of soluble heavy metal ions, nitrogen-doped fluorescent carbon quantum dots (N-CQDs) were synthesized using chitin extracted from shrimp and crab shells as the carbon source. The structural, morphological, and optical properties of the synthesized N-CQDs were systematically characterized using transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FTIR), Raman, X-ray photoelectron spectroscopies (XPS), ultraviolet-visible (UV-Vis) absorption spectroscopy and fluorescence spectroscopy. The resulting N-CQDs exhibited a carbonization yield of 54.46% and a fluorescence quantum yield of 34.33%. Their morphology, structure and optical properties were thoroughly characterized using a range of analytical techniques. The synthesized N-CQDs exhibited excellent fluorescence properties, and remarkable stability. When applied for metal ion detection, the N-CQDs displayed a distinct and selective fluorescence quenching response exclusively toward Fe³⁺ ions. The detection limit for Fe³⁺ at room temperature was 4.04 μmol/L. Furthermore, due to the inherent nitrogen present in the acetyl amino groups of chitin, nitrogen doping was achieved without the need for external dopants during the hydrothermal synthesis process. Owing to their high stability, low cost and low toxicity, the N-CQDs synthesized in this study provide a promising fluorescence sensing platform with excellent selectivity for Fe³⁺ detection, achieved through precise control of surface functional groups. Full article

Microlasers are innovative photonics devices that have recently attracted attention for their unique characteristics, including compactness, broad spectral emission, and low lasing threshold. These properties are beneficial in biophotonics as these lasers can interact with biological materials without causing damage, especially for optical biosensing applications. Among the optical materials recently used as gain media in microlasers are organic dyes, rare-earth ions, fluorescent proteins, and semiconductors, including quantum dots and perovskites. Moreover, different optical cavities and current laser configurations have increased the versatility of microlasers. Recently, digital sensing methods based on novel algorithms, machine learning, and neural networks have been combined with microlaser systems to enhance their accuracy and expand their applications. This work provides a comprehensive review of recent progress in microlasers, covering gain media, microcavity types, and their applications in biophotonics, including conventional spectral-based sensing and new digital approaches for the biomedical field. Full article

The corrosion behavior of hot-press-formed (HPF) B-pillar components fabricated from Al–Si-coated boron steel was investigated with an emphasis on the forming-induced crack morphology. The specimens were extracted from the inner and outer surfaces of the top, flat, and radius regions. Microstructural characteristics and coating cracks were examined using optical microscopy, as well as field-emission scanning electron microscopy (FE-SEM) in combination with energy-dispersive spectroscopy (EDS), and corrosion behavior was evaluated using cyclic corrosion immersion and potentiodynamic polarization tests in a 3.5 wt.% NaCl aqueous solution. The Al–Si coating exhibited a multilayered structure composed of alternating Al- and Fe-rich layers. The crack morphology strongly depended on the local stress state: wide macrocracks were mainly formed on the outer surface of the radius region under tensile deformation, whereas the narrow microcracks predominated on the inner surface subjected to compressive deformation. Cyclic corrosion immersion tests showed that the corrosion propagated preferentially along the coating cracks and was more severe on the inner surfaces, where narrow microcracks promoted aggressive crevice corrosion owing to chloride ion accumulation and local acidification. By contrast, wider macrocracks on the outer surface mitigated crevice corrosion by allowing electrolyte exchange. Potentiodynamic polarization tests indicated similar corrosion rates for all regions; however, the outer radius region exhibited a relatively noble corrosion potential owing to oxide film formation on the locally exposed substrate areas. These results demonstrate that the crack morphology induced by curved forming is a key factor governing the corrosion behavior of HPF B-pillar components. Full article

As the global transportation sector accelerates toward net-zero targets, the rapid deployment of alternative fuels like hydrogen, ammonia, and batteries introduces complex and novel safety challenges. This study systematically maps the intellectual structure of safety and risk research on zero-emission transportation systems to evaluate field maturity and identify critical knowledge gaps. We conducted a comprehensive bibliometric analysis of 151 core publications retrieved from the Web of Science from 2000 to 2025. By integrating quantitative performance analysis with qualitative science mapping techniques, the results identify that the domain is nascent and rapidly expanding, and a distinct inflection in publication occurred in 2020. However, science mapping reveals a fragmented intellectual structure. Among the four identified research clusters, two dominant streams emerge as the primary drivers of the field. The first is a “motor theme” focused on lithium-ion battery reliability and thermal runaway, while the second is a “basic theme” focused on hydrogen dispersion and toxicity risks. The analysis exposes a blind spot regarding the lack of cross-modal research addressing the physical safety interactions between different fuel systems operating in the shared infrastructure. Finally, this study proposes a future research agenda focusing on gathering real-world accident data and using system-theoretic approaches to manage integrated alternative fuel risks. Full article

To investigate the seasonal characteristics, sources, and regional transport patterns of precipitation components in the high-elevation mountainous regions, field sampling was conducted at Mt. Heng (Hunan, South China) from June 2021 to May 2022. In total, 114 precipitation samples were collected and subjected to chemical analysis, including pH, major inorganic ions, and heavy metals. During the study period, the precipitation at Mt. Heng was generally weakly acidic. The concentrations of metals and acidic anions (NO₃⁻ and SO₄²⁻) were higher in the winter and lower in the summer, whereas the concentration of the primary neutralizing cation, NH₄⁺, peaked during the summer. An association was observed between precipitation pH and metal concentrations, whereby acidic precipitation samples exhibited marginally elevated metal concentrations overall. An additional analysis of winter precipitation chemistry at Mt. Heng revealed an increasing trend of ions from 2015 to 2018, followed by a decrease from 2019 to 2021. This trend coincided with the concentrations of NO₂ and SO₂ in the surrounding cities, reflecting the results of clean air actions. The results of the source analysis revealed five major sources: secondary sources (41.5%), coal combustion (24.7%), a mixed source of biomass burning and aged sea salt (11.6%), dust (10.8%), and industrial emissions (11.4%). Backward trajectory cluster analysis revealed that air masses originating from the northern regions were generally more polluted than those from the southern regions. This study provides fundamental data and scientific support for regional atmospheric pollution control and ecological protection in South China. Full article

We report a defect-selective luminescence response in calcium-deficient hydroxyapatite (HAp) induced by electron and ion irradiation. Compacted HAp pellets prepared from hydrothermally grown nanofibers were investigated to analyze defect-related luminescence using photoluminescence (PL) and cathodoluminescence (CL) techniques, both before and after compaction. Low-energy electron beam irradiation (15 keV) produced a two-stage luminescent response, an initial enhancement arising from field-assisted activation of OH-channel vacancies (V_OH and V_OH + H_i), followed by an exponential decay attributed to defect annealing. Monochromatic transient CL measurements show that this rise–decay behavior is selective to the OH-related bands at 2.57 and 2.95 eV, whereas the 3.32 and 3.67 eV emissions exhibit only a monotonic exponential decay. The corresponding decay constants further indicate that the activated OH-channel vacancies anneal more rapidly than the other centers, consistent with their higher electron-capture probability and lower structural stability. In contrast, ${\mathrm{Ga}}^{+}$ ion irradiation (30 keV, 1.4 × 10⁻¹³ A/µm²) induced progressive monotonic luminescence quenching, primarily driven by selective annealing of oxygen vacancies in $\mathrm{P}{\mathrm{O}}_4^{3-}$ groups. These complementary pathways, electron-induced activation and ion-driven suppression, demonstrate that irradiation serves as a versatile tool for defect engineering in hydroxyapatite. Beyond providing fundamental insights into vacancy stability, these results open new routes for tailoring the optical, sensing, and bioimaging functionalities of HAp through controlled irradiation. Full article

Light-controlled ion drag pumps have attracted considerable interest in soft robotics, biomedical engineering, and microelectromechanical systems (MEMS) due to their non-contact energy supply and high spatiotemporal controllability of light. However, experimental studies on their pumping performance and influencing factors remain limited. This study integrates the photoelectric effect with field emission phenomena to design and fabricate a light-controlled ion drag pump using lanthanum-modified lead zirconate titanate (PLZT) ceramic. The light-controlled pump enables non-contact energy transfer and fluid transport via high-energy laser irradiation. A series of experiments systematically investigate its pumping performance and key influencing factors. Results indicate that optimizing electrode structure and fluid channel design, along with increased light intensity, significantly enhances pumping performance. This work provides fundamental design guidelines for the application of light-controlled ion drag pumps in microfluidics, flexible robotics, and microdevice thermal management. Full article

Divalent europium complexes have attracted significant attention in various fields due to the unique electronic configuration of the Eu(II) ion. Given the high sensitivity of the 5d → 4f emission of Eu(II) ions to the ligand field, it is crucial to explore the relationship between ligands and this emission in Eu(II) complexes. However, the heavy-atom effects on the 5d → 4f emission of Eu(II) complexes coordinated with non-metal elements in the same group remain unclear. In this study, five mononuclear Eu(II)-chalcogenide complexes, Eu[H₃B·EPh-κE,H,H]₂(DME)₂ (E = S for 1 and Se for 2; DME = 1,2-Dimethoxyethane) and Eu[EPh]₂(18-C-6) (E = S for 3, Se for 4, and Te for 5; 18-C-6 = 1,4,7,10,13,16-Hexaoxacyclooctadecane), were synthesized via reduction of diphenyl disulfide chalcogenide analogs with Eu(BH₄)₂(THF)₂ or NaH. The structures of these complexes were investigated by single-crystal X-ray diffraction, and their properties were characterized by thermogravimetric analysis and photophysical property tests. Complexes 1 and 2 are isomorphous and show similar yellowish-green luminescence, while complexes 3–5 have similar structures but crystallize in different space groups with bluish-green luminescence. This research reveals the influence of chalcogenide ligands on the 5d → 4f emission of Eu(II) complexes, providing a theoretical basis and new research ideas for the application of Eu(II) complexes in various fields, including luminescent materials, cryogenic refrigerants, and magnetic materials. Full article