Search Results (69)

Ultra-deep lattice-like fractured carbonate reservoirs, formed by multi-period tectonic movements, feature strong heterogeneity, multi-scale fracture nesting, and anisotropic in situ stress. However, hydraulic fracture (HF) propagation behaviors within these complex formations remain poorly understood. In this study, using an unstructured fracture network approach, we simulated HF propagation in two typical fault-controlled lattice-like structures: compressive-torsion and pull-apart overlap zones. The performance of commingled, staged, and temporary plugging fracturing was evaluated, alongside sensitivity analyses of wellbore orientation, plugging timing, pump rate, and fluid viscosity. Results indicate that HFs in compressive-torsion zones exhibit long, straight geometries with local tensile activation points. Conversely, pull-apart overlap zones promote step-shaped, multi-branched fractures with superior lateral connectivity. The optimal timing for temporary plugging exhibits a delayed trend with increasing natural fracture density, ranging from 50% to 70% of the fracturing process in compressive-torsion zones, whereas an earlier implementation is preferred in pull-apart overlap zones, occurring at 33–65% of the fracturing process. Furthermore, HFs in compressive-torsion zones are less sensitive to viscosity and pump rate. To optimize stimulated volume, a moderate viscosity of 50–60 mPa·s is universally recommended. Regarding pump rates, 8–10 m³/min is ideal for balanced connectivity in pull-apart overlap zones, whereas >12 m³/min is required for compressive-torsion zones. These findings provide critical theoretical and engineering guidelines for differentiated fracturing strategies in ultra-deep reservoirs. Full article

This study investigates the effect of equal channel angular pressing (ECAP) temperature and pass number on the microstructural evolution and hardness response of a CuAg0.1 alloy. ECAP was performed by using route B_c at room temperature and 100 °C for up to six passes. X-ray diffraction results showed that no additional crystalline phase was detected after ECAP, while peak broadening and relative intensity changes indicated deformation-induced lattice distortion, defect accumulation, and a tendency toward preferred orientation. Optical microscopy revealed progressive microstructural subdivision with increasing pass number, particularly under room-temperature processing. Vickers microhardness increased sharply after the first ECAP pass and approached a saturation-like regime after approximately four passes. Room-temperature ECAP produced higher hardness and hardness-derived estimated strength values than processing at 100 °C, indicating more effective defect storage and suppressed recovery. In contrast, the lower hardening response at 100 °C is attributed mainly to thermally assisted recovery and dislocation rearrangement. The section-dependent hardness response suggests ECAP-induced anisotropy was associated with the imposed shear deformation and preferred crystallographic orientation. Within the investigated processing, four-pass room-temperature ECAP provided the most effective hardness-based strengthening response. Full article

Powder X-ray diffraction was used to validate the crystal structure of iron metal powder and to demonstrate a transparent workflow for extracting crystallographic and microstructural information from a simple laboratory dataset. The diffraction profile collected over the angular range of approximately 36° to 95° contains three dominant reflections located at 2θ = 44.850°, 65.218°, and 82.540°. Conversion of the peak positions into d-spacings using Bragg’s law gives values of approximately 2.020 Å, 1.430 Å, and 1.170 Å. The squared-sine ratios, when referenced to the first reflection, follow the sequence of 1:2:3, which is characteristic of the allowed reflections of a body-centered cubic lattice when multiplied by the first allowed value of N = h² + k² + l² = 2. Therefore, the peaks are assigned to the (110), (200), and (211) reflections of α-Fe. The extracted lattice constants are 2.853, 2.860, and 2.865 Å, yielding an average value of 2.859 Å, which is close to the accepted room-temperature value of approximately 2.866 Å for α-Fe. Peak-width calculations based on the observed, instrument-uncorrected FWHM values are included only as illustrative apparent line-broadening indicators. Because an external instrumental standard was not measured under identical conditions, no quantitative coherent-domain size or microstrain is claimed. The Williamson–Hall treatment is therefore used only to demonstrate the sensitivity of size-strain interpretation to peak breadth, profile selection, and the limited number of available reflections. The intensity hierarchy was analyzed using the body-centered cubic-structure factor, reflection multiplicity, Fe atomic form factor, and Lorentz polarization correction. The comparison between calculated and experimental intensities shows stronger disagreement than the lattice-parameter analysis, illustrating the greater sensitivity of intensity analysis to preferred orientation, specimen preparation, peak-profile selection, and background treatment. The work provides a publication-style reconstruction of an iron powder XRD experiment, connecting peak fitting, indexing, lattice-parameter determination, crystallite size estimation, size-strain analysis, and intensity interpretation in a single critical framework. Full article

We develop an analytical framework to describe the impact of in-plane strain on the electronic and transport properties of graphene. Starting from a strain-modified nearest-neighbor tight-binding model, we derive the energy spectrum and group velocities, explicitly incorporating bond-dependent hopping renormalization. A dimensionless anisotropy parameter, derived from velocity fluctuations, is introduced to quantify directional transport imbalance. We show that this parameter admits a closed-form expression entirely determined by the strain tensor, linking lattice deformation directly to measurable transport quantities. In the small-strain regime, a compact expression is obtained, $\eta \approx ϵ\left(1+\nu \right)\cos \left(2\theta \right)$, revealing an angular dependence controlled solely by the orientation of the applied deformation. This establishes that strain acts as a purely geometric control parameter, separating magnitude and orientation effects. Within the semiclassical Boltzmann framework, the same parameter fully determines the conductivity tensor, leading to simple expressions for the longitudinal components ${\sigma }_{x,y}={\sigma }_0\left(1\mp \eta \right)$ and a clear identification of the preferred transport direction. Importantly, the total conductivity remains constant, while strain redistributes transport between orthogonal directions. These results provide a transparent and predictive description of strain-induced transport anisotropy, demonstrating that the directional electronic response can be tuned without modifying the material composition, offering a practical route to control electronic response in graphene through purely mechanical means. Full article

The structure and composition of a refractory Ni-containing CrMoNbTaVW high-entropy-alloy (HEA) thin film were investigated. The HEA thin film with a thickness of 5 μm was grown via conventional direct current magnetron sputtering from a multiple-elemental compound target. The Ni-containing HEA thin film with a Ni concentration of 3.6 at. % exhibits a single-phase body-centered cubic (BCC) crystal structure with a lattice parameter of a = 0.316 nm. The grains in the HEA thin film are columns, extended in the growth direction. They are not aligned exactly perpendicular to the substrate surface. The thin film grows in a polycrystalline structure with a tendency to preferred orientation or texture. Energy-dispersive X-ray analyses of the HEA thin film show near-equal atomic concentrations of Cr, Mo, Nb, Ta, V, and W elements in the range 15–17 at. % with almost uniform distribution. In contrast, Ni is not uniformly distributed in the film, and grains with a different Ni concentrations were observed. The defects observed in the HEA thin film are mainly single dislocations or an assembly of dislocations, which could be caused by residual stresses in the layer forming during the growth of the HEA thin film. Full article

Scandium (Sc)-doped aluminum nitride (AlN) thin films are critical for high-frequency, high-power surface acoustic wave (SAW) devices. A composite Sc doping strategy for AlN thin films is proposed, which combines magnetron sputtering pre-doping with post-doping via ion implantation to achieve gradient doping and tailor microstructural characteristics. The crystal structure, surface composition, and microstructural defects of the films were characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), energy-dispersive X-ray spectroscopy (EDS) and transmission electron microscopy (TEM). Results indicate that the Sc content in pre-doped ScAlN films was optimized from below 10 at.% to above 30 at.%, while the films maintained a stable (002) preferred orientation. XPS analysis confirmed the formation of Sc-N bonds, and EDS mapping revealed a gradient distribution of Sc within the subsurface region, extending to a depth of approximately 200 nm. High-resolution TEM revealed localized lattice distortions and surface amorphization induced by ion implantation. This work demonstrates the feasibility of ion implantation as a supplementary doping technique, offering theoretical insights for developing AlN films with high Sc doping concentrations and structural stability. These findings hold significant potential for optimizing the performance of high-frequency, high-power SAW devices. Full article

FeCoCrNiNb_xN (x = 0, 0.25, 0.5, 0.75, 1 molar) high-entropy nitride (HEN) films were fabricated on 304 stainless steel and Si wafers using magnetron sputtering to investigate the influence of Nb content on the microstructure, mechanical properties, and tribological performance. X-ray diffraction (XRD) analysis reveals a face-centered cubic (FCC) structure with a preferred orientation in the (200) plane, which transfers to the (111) plane as the Nb content increases. The lattice distortion induced by Nb incorporation enhanced crystallinity, with the Nb_0.5N film exhibiting the highest diffraction peak intensity and interplanar distance. Cross-sectional SEM images displayed columnar crystal structures, while the surface morphology evolved from “cauliflower-like” to smoother clusters with increasing Nb content, reducing average roughness from 7.54 nm (Nb₀) to 4.89 nm (Nb₁). The hardness and elastic modulus initially decrease, then peak at 25.56 GPa and 265.36 GPa, respectively, for the Nb₁ film, attributed to solid solution strengthening and high-entropy effects. Tribological tests demonstrated that Nb₁ achieved the lowest coefficient of friction (0.46), wear volume (1.23 × 10⁻³ mm³), and wear rate (5.11 × 10⁻⁸ mm³·N⁻¹·m⁻¹), owing to NbN phase formation, refined grains, and reduced surface roughness. The wear mechanisms are abrasive and oxidative wear. Full article

Japanese swords have a history of more than one thousand years and are recognized as metallic art objects. The sword-making process is not clearly understood, especially for old swords made before about 1600 A.D. Knowledge of structural information such as crystallite sizes and anisotropy is important to understand the sword characteristics and the sword-making process. Bragg-edge transmission imaging is a useful noninvasive method that can extract this structural information continuously over a wide area of the sword. Neutron CT is powerful enough to detect quenched areas, voids, and precipitates. Using both methods, we measured more than 10 swords and obtained information on the two-dimensional crystallite size distribution, anisotropy parameter, lattice plane spacing, and quenched regions. Comparison of the results indicated the following features: the crystallite size distributions showed two patterns: an almost uniform distribution of small-sized crystallites, and mixed distributions of large- and small-sized crystallites. The patterns were observed in different eras and places. The preferred orientation showed different patterns, and strain areas due to quenching were observed in many swords. The quenched area showed a trend that the quenching was weaker for old swords than newer ones. CT images showed the boundaries of the quenched regions and a void in the layered structure for one sword, for which a layered structure was confirmed. Full article

We developed dye-sensitized solar cells based on anatase–titanium dioxide (A-TiO₂) nanotubes (TiNTs) and nanocubes (TiNcs) with {001} crystal facets generated using simple and facile electrochemical anodization. We also demonstrated a simple way of developing one-dimensional, two-dimensional, and three-dimensional self-assembled TiO₂ nanostructures via electrochemical anodization, using them as an electron-transporting layer in DSSCs. TiNTs maintain tubular arrays for a limited time before becoming nanocrystals with {001} facets. Using FESEM and TEM, we observed that the TiO₂ nanobundles were transformed into nanocubes with {001} facets and lower fluorine concentrations. Optimizing the reaction approach resulted in better-ordered, crystalline anatase TiNTs/Ncs being formed on the Ti metal foil. The anatase phase of as-grown TiO₂ was confirmed by XRD, with (101) being the predominant intensity and preferred orientation. The nanostructured TiO₂ had lattice values of a = 3.77–3.82 and c = 9.42–9.58. The structure and morphology of these as-grown materials were studied to understand the growth process. The photoconversion efficiency and impedance spectra were explored to analyze the performance of the designed DSSCs, employing N719 dye as a sensitizer and the I⁻/I³⁻ redox pair as electrolytes, sandwiched with a Pt counter-electrode. As a result, we found that self-assembled TiNTs/Ncs presented a more effective photoanode in DSSCs than standard TiO₂ (P25). TiNcs (0.5 and 0.25 NH₄F) and P25 achieved the highest power conversion efficiencies of 3.47, 3.41, and 3.25%, respectively. TiNcs photoanodes have lower charge recombination capability and longer electron lifetimes, leading to higher voltage, photocurrent, and photovoltaic performance. These findings show that electrochemical anodization is an effective method for preparing TiNTs/Ncs and developing low-cost, highly efficient DSSCs by fine-tuning photoanode structures and components. Full article

This study systematically investigates the effects of heat treatment at 800–1000 °C on the microstructure and mechanical properties of 10 wt.% TiB₂@Ti/AlCoCrFeNi_2.1 eutectic high-entropy alloy matrix composites (EHEAMCs) prepared by vacuum hot-pressing sintering. The results show that the materials consist of FCC, BCC, TiB₂, and Ti phases, with a preferred orientation of the (111) crystal plane of the FCC phase. As the temperature increases, the diffraction peak of the BCC phase separates from the main FCC peak and its intensity increases, while the diffraction peak positions of the FCC and BCC phases shift at small angles. This is attributed to the diffusion of TiB₂@Ti from the grain boundaries into the matrix, where the Ti solid solution increases the lattice constant of the FCC phase. Microstructural observations reveal that the eutectic region transforms from lamellar to island-like structures, and the solid solution zone narrows. With increasing temperature, the Ti concentration in the solid solution zone increases, while the contents of elements such as Ni decrease. Element diffusion is influenced by binary mixing enthalpy, with Ti and B tending to solidify in the FCC and BCC phase regions, respectively. The mechanical properties improve with increasing temperature. At 1000 °C, the average hardness is 579.2 HV, the yield strength is 1294 MPa, the fracture strength is 2385 MPa, and the fracture strain is 19.4%, representing improvements of 35.5% and 24.9% compared to the as-sintered state, respectively, without loss of plasticity. The strengthening mechanisms include enhanced solid solution strengthening due to the diffusion of Ti and TiB₂, improved grain boundary strength due to the diffusion of alloy elements to the grain boundaries, and synergistic optimization of strength and plasticity. Full article

A study of the azimuthal variation in the surface wave fundamental-mode phase velocity is performed for the Philippine Sea Plate (PSP). This azimuthal variation has been anisotropically inverted for the PSP to determine the isotropic and anisotropic structure of this plate from 0 to 260 km. This azimuthal variation is due to anisotropy in the upper mantle. The crust is found in an isotropic structure, but the lithosphere and asthenosphere exhibit anisotropic structures. For the lithosphere, the main cause of anisotropy is the alignment of anisotropic crystals approximately parallel to the direction of seafloor spreading, and the fast axis of the seismic velocity is in the direction of ~163° of azimuth. For the asthenosphere, the seismic anisotropy can be derived from the lattice-preferred orientation (LPO) in response to the shear strains induced by mantle flow, and the fast axis of the seismic velocity is also the direction of ~163° of azimuth. This result suggests that a mantle flow pattern may occur in the asthenosphere and seems to be approximately parallel to the direction of seafloor spreading observed for the lithosphere. Finally, the changes in the parameter ξ with depth are studied to estimate the depth of the lithosphere–asthenosphere boundary (LAB), observing a clear change in this parameter at 80 km depth. Full article

Molybdenum disulfide is a 2D material with excellent lubricant properties, resulting from weak van der Waals forces between lattice layers and shear-induced crystal orientation. The low forces needed to shear the MoS₂ crystal layers grant the tribological system low coefficients of friction (COF). However, film oxidation harms its efficacy in humid atmospheres, leading to an increased COF and poor surface adhesion, making its use preferable in dry or vacuum conditions. To overcome these challenges, doping MoS₂ with elements such as Nb, Ti, C, and N emerges as a promising solution. Nevertheless, the adhesion of these coatings to a steel substrate presents challenges and strategies involving the reduction in residual stresses and increased chemical affinity to the substrate by using niobium-based materials as interlayers. In this study, Nb-doped MoS₂ films were deposited on H13 steel and silicon wafers using the pulsed direct current balanced magnetron sputtering technique. Different niobium-based interlayers (pure Nb and NbN) were deposited to evaluate the adhesion properties of Nb-doped MoS₂ coatings. Unlubricated scratch tests, conducted at room temperature and relative humidity under a progressive load, were performed to analyze the COF and adhesion of the coating. Instrumented indentation tests were conducted to assess the hardness and elastic modulus of the coatings. The microstructure of the coatings was obtained by Scanning Electron Microscopy (SEM), Scanning Transmission Electron Microscopy (STEM), and Transmission Electron Microscopy (TEM), with Energy-Dispersive X-Ray Spectroscopy (EDS). Results indicated that niobium doping on MoS₂ coatings changes the structure from crystalline to amorphous. Additionally, the Nb concentration of the Nb:MoS₂ coating changed the mechanical properties, leading to different cohesive failures by different loads during the scratch tests. Results have also indicated that an NbN interlayer optimally promoted the adhesion of the film. This result is justified by the increase in hardness led by higher Nb concentrations, enhancing the load-bearing capacity of the coating. It is concluded that niobium-based materials can be used to enhance the adhesion properties of Nb-doped MoS₂ films and improve their tribological performance. Full article

This study has investigated the effects of different annealing temperatures on the microstructure, chemical composition, phase structure, and piezoelectric properties of ZnO films. The analysis focuses on how annealing temperature influences the oxygen content and the preferred c-axis (002) orientation of the films. It was found that annealing significantly increases the grain size and optimizes the columnar crystal structure, though excessive high-temperature annealing leads to structural degradation. This behavior is likely related to changes in oxygen content at different annealing temperatures. High resolution transmission electron microscopy (HR-TEM) reveals that the films exhibit high-resolution lattice stripes, confirming their high crystallinity. Although the films exhibit growth in multiple orientations, the c-axis (002) orientation remains the predominant crystallographic growth. Further piezoelectric property analysis demonstrates that the ZnO films annealed at 400 °C exhibit enhanced piezoelectric performance and stable linear piezoelectric behavior. These findings offer valuable support for optimizing the piezoelectric properties of ZnO films and their applications in piezoelectric sensors. Full article

The correlation between the morphology and crystal structure of zinc dendritic particles produced by electrolysis from the alkaline electrolyte has been established. Morphology and crystal structure of Zn particles electrodeposited by the potentiostatic regime of electrolysis at overpotentials inside (−100 and −160 mV) and outside (−220, −280, and −340 mV) the plateau of the limiting diffusion current density were characterized by scanning electron microscope (SEM) and by X-ray diffraction (XRD), respectively. The particle size distribution (PSD) was performed in order to determine the dependency of the size of dendritic particles on applied electrolysis overpotential. With increasing the overpotential of electrolysis, the shape of particles changed from irregular forms denoted as precursors of dendrites to various forms of dendrites, while the size of the particles simultaneously decreased. All types of Zn dendrites exhibited the strong (002) preferred orientation, while the precursors of dendrites exhibited (101)(002) preferred orientation. The development of strong (002) preferred orientation was explained and discussed by making an analogy with the electrolytic production of lead dendrites from the concentrated nitrate electrolyte. Although zinc and lead belong to different types of crystal lattice (Pb-face-centered cubic type and Zn-hexagonal close-packed type), they have a common characteristic that is manifested by the strong preferred orientation in the crystal plane with the lowest surface energy. Full article

W-doped ZnO (WZO) films were deposited on glass substrates by using RF magnetron sputtering at different substrate bias voltages, and the relationships between microstructure and optical and electrical properties were investigated. The results revealed that the deposition rate of WZO films first decreased from 8.8 to 7.1 nm/min, and then increased to 11.5 nm/min with the increase in bias voltage. After applying a bias voltage to the substrate, the bombardment effect of sputtered ions was enhanced, and the films transformed from a smooth surface into a compact and rough surface. All the films exhibited a hexagonal wurtzite structure with a strong (002) preferred orientation and grew along the c-axis direction. When the bias voltage increased, both the residual stress and lattice parameter of the films gradually increased, and the maximum grain size of 43.4 nm was achieved at −100 V. When the bias voltage was below −300 V, all the films exhibited a high average transmittance of ~90% in the visible light region. As the bias voltage increased, the sheet resistance and resistivity of the films initially decreased and then gradually increased. The highest F_OM of 5.8 × 10⁻⁴ Ω⁻¹ was achieved at −100 V, possessing the best comprehensive photoelectric properties. Full article