Search Results (2,441)

By using the Ekeland variational principle and Nehari manifold, we study the following fractional p-Laplacian Kirchhoff equations: $M\left({\left[u\right]}_{s,p}^p+{\int }_{{\mathbb{R}}^N}V\left(x\right){\left|u\right|}^{p}dx\right)[{(-\Delta )}_p^{s}u+$${V\left(x\right)\left|u\right|}^{p-2}u]={\lambda \left|u\right|}^{q-2}uln\left|u\right|,x\in {\mathbb{R}}^N,\left(\mathrm{P}\right)$. In these equations, $\lambda \in \mathbb{R}\setminus \left\{0\right\},$$p\in (1,+\infty )$, $s\in (0,1),sp<N,$$p_s^{*}={\displaystyle \frac{Np}{N-sp}}$, $M\left(\tau \right)=a+b{\tau }^{\theta -1}$, $a,b\in {\mathbb{R}}^{+},$$1<\theta <{\displaystyle \frac{p_s^{*}}{p}}$, $V\left(x\right)\in C({\mathbb{R}}^N,\mathbb{R})$ is a potential function and ${(-\Delta )}_p^s$ is the fractional p-Laplacian operator. The existence of solutions is deeply influenced by the positive and negative signs of $\lambda$. More precisely, (i) Equation (P) has one ground state solution for $\lambda >0$ and $p\theta <q<p_s^{*}$, with a positive corresponding energy value; and (ii) Equation (P) has at least two nontrivial solutions for $\lambda <0$ and $p<q<p_s^{*}$, with positive and negative corresponding energy values, respectively. Full article

A compact electrochemical sensor module for pH detection was developed for potential integration into specialized devices used for live cell or tissue incubation, for applications in highly parallelized cell culture analysis, by incorporating Organ-on-Chip devices. This research focuses on the deposition, structural and chemical analysis, and functional characterization of different titanium-oxide layers with various compositions as potentially sensitive materials for pH sensing applications. The titanium-oxide layers were deposited using vacuum sputtering and atomic layer deposition at 100 °C and 300 °C, respectively. Transmission electron microscopy and X-ray photoelectron spectroscopy were utilized to determine the specific composition and structure of different titanium-oxide layers. These TiO_x-functionalized electrodes were connected to the application-specific analog front-end chip of the low-power readout circuit for precise evaluation. The pH sensitivity of the differently modified electrodes, employing various TiO_x materials, was evaluated using pH calibration solutions ranging from pH 6 to 8. Among the various deposition solutions, such as sputtering or high-temperature atomic layer deposition, the TiO_x layer deposited using low-temperature atomic layer deposition proved more suitable for pH sensing applications, with a sensitivity of 54.8–56.7 mV/pH, which closely approximates the Nernstian response. Full article

With the rapid advancement of energy storage technologies, there is a growing demand for affordable, efficient, and environmentally benign battery systems. Sodium-ion batteries (SIBs) present a promising alternative to lithium-ion systems due to sodium’s high abundance and similar electrochemical properties. Particular attention is given to developing NASICON -sodium (Na) super ionic conductor, type cathode materials, especially Na3V2(PO4)3, which exhibits high thermal and structural stability. This study focuses on the sol–gel synthesis of Na₃V₂(PO₄)₃ using citric acid and ethylene glycol, as well as investigating the effect of annealing temperature (400–1000 °C) on its structural and electrochemical properties. Phase composition, morphology, textural characteristics, and electrochemical performance were systematically analyzed. Above 700 °C, a highly crystalline NASICON phase free of secondary impurities was formed, as confirmed by X-ray diffraction (XRD). Microstructural evolution revealed a transition from a loose amorphous structure to a dense granular morphology, accompanied by changes in specific surface area and porosity. The highest surface area (67.40 m²/g) was achieved at 700 °C, while increasing the temperature to 1000 °C caused pore collapse due to sintering. X-ray photoelectron spectroscopy (XPS) confirmed the predominant presence of V³⁺ ions and the formation of V⁴⁺ at the highest temperature. The optimal balance of high crystallinity, uniform elemental distribution, and stable texture was achieved at 900 °C. Electrochemical testing in a Na/NVP half-cell configuration delivered an initial capacity of 70 mAh/g, which decayed to 55 mAh/g by the 100th cycle, attributed to solid-electrolyte interphase (SEI) formation and irreversible Na⁺ trapping. These results demonstrate that the proposed approach yields high-quality Na₃V₂(PO₄)₃ cathode materials with promising potential for sodium-ion battery applications. Full article

Nanocrystals of Eu-doped GaN powders are produced via pyrolysis of a viscous compound made from europium and gallium nitrates. Furthermore, carbohydrazide is used as a fuel and toluene as a solvent; subsequently, a crucial nitridation process is carried out at 1000 °C for one hour. A slight shift of 0.04 degrees toward larger angles was observed for the X-ray diffraction patterns in the Eu-doped GaN powders regarding the undoped GaN powders, while Raman scattering also displayed a slight shift of 10.03 cm⁻¹ toward lower frequencies regarding the undoped GaN powders for the vibration mode, E₂(H), in both cases indicating the incorporation of europium atoms into the GaN crystal lattice. A scanning electron microscope micrograph demonstrated a surface morphology for the Eu-doped GaN with a shape similar to elongated platelets with a size of 3.77 µm in length. Energy-dispersive spectroscopy and X-ray photoelectron spectroscopy studies demonstrated the europium elemental contribution in the GaN. The X-ray photoelectron spectroscopy spectrum for gallium demonstrated the binding energies for Ga 2P_3/2, Ga 2P_1/2, and Eu 3d_5/2, which could indicate the incorporation of europium into the GaN and the bonding between gallium and europium atoms. The transmission electron microscope micrograph showed the presence of nanocrystals with an average size of 9.03 nm in length. The photoluminescence spectrum showed the main Eu³⁺ transition at 2.02 eV (611.69 nm) for europium emission energy, corresponding to the ⁵D₀ ⟶ ⁷F₂ transition of the f shell, which is known as a laser transition. Full article

Zinc oxide (ZnO) is a wide bandgap semiconductor with optoelectronic and photocatalytic properties, which depend on its optical, structural, and morphological characteristics. In this study, we synthesized ZnO thin films by chemical bath deposition (CBD) and then thermally annealed them at 400 °C and 600 °C to evaluate the effect of thermal treatments. We characterized their structural, optical, morphological, and chemical properties using X-ray diffraction (XRD), UV–Vis spectroscopy, scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). The optical bandgap values were 3.20 eV for the as-grown thin films, and 3.23 eV and 3.21 eV after annealing at 400 °C and 600 °C, respectively. SEM micrographs revealed a change from elongated agglomerates in the as-grown thin films to uniform flower-like structures after annealing at 600 °C. XPS analysis confirmed ZnO formation in all samples, and we detected residual precursor species only in the as-grown thin films, which were completely removed by annealing at 600 °C. These results demonstrate that the CBD synthesis of ZnO can tune its optical and morphological properties through thermal annealing, making it suitable for optoelectronic, sensing, and photocatalytic applications. Full article

NASICON-type Li_1+XFe_XTi_2-X(PO₄)₃ (x = 0.1, 0.3, 0.4) solid electrolytes for all-solid-state Li-ion batteries were synthesized using a sol–gel method. This study investigated the impact of substituting Fe³⁺ (0.645 Å), a trivalent cation, for Ti⁴⁺ (0.605 Å) on ionic conductivity. Li_1+XFe_XTi_2-X(PO₄)₃ samples, subjected to various sintering temperatures, were characterized using TG-DTA, XRD with Rietveld refinement, XPS, FE-SEM, and AC impedance to evaluate composition, crystal structure, fracture-surface morphology, densification, and ionic conductivity. XRD analysis confirmed the formation of single-crystalline NASICON-type Li_1+XFe_XTi_2-X(PO₄)₃ at all sintering temperatures. However, impurities in the secondary phase emerged owing to the high sintering temperature above 1000 °C and increased Fe content. Sintered density increased with the densification of Li_1+XFe_XTi_2-X(PO₄)₃, as evidenced by FE-SEM observations of sharper edges of larger quasi-cubic grains at elevated sintering temperatures. At 1000 °C, with Fe content exceeding 0.4, grain coarsening resulted in additional grain boundaries and internal cracks, thereby reducing the sintered density. Li_1.3Fe_0.3Ti_1.7(PO₄)₃ sintered at 900 °C exhibited the highest density among the other conditions and achieved the maximum total ionic conductivity of 1.51 × 10⁻⁴ S/cm at room temperature, with the lowest activation energy for Li-ion transport at 0.37 eV. In contrast, Li_1.4Fe_0.4Ti_1.6(PO₄)₃ sintered at 1000 °C demonstrated reduced ionic conductivity owing to increased complex impedance associated with secondary phases and grain crack formation. Full article

This study investigates the mechanism behind the heat-induced color change (brown to yellowish green) in Mn- and Fe-rich elbaite tourmaline under reducing atmosphere at 500 °C. A combination of analytical techniques including gemological characterization, electron microprobe analysis (EMPA), laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, and ultraviolet–visible (UV-Vis) spectroscopy was employed. Chemical analysis confirmed the samples as intermediate members of the elbaite–fluorelbaite series, with an average formula of ^X(Na₀.₆₆ □₀.₂₆ Ca₀.₀₈) _Σ1.₀₀^Y(Li₁.₂₉Al₁.₁₀Mn₀.₃₁ Fe²⁺₀.₁₅Ti₀.₀₁Zn₀.₀₁) _Σ2.₈₇ ^ZAl₆^T[Si₆O₁₈] (BO₃)₃^V(OH)₃.₀₀^W(OH₀.₅₁F₀.₄₉) _Σ1.₀₀, enriched in Mn (17,346–20,669 μg/g) and Fe (8396–10,750 μg/g). Heat treatment enhanced transparency and induced strong pleochroism (yellowish green parallel c-axis, brown perpendicular c-axis). UV-Vis spectroscopy identified the brown color origin in the parallel c-axis direction: absorption bands at 730 nm (Fe²⁺ d–d transition, ⁵T_2g → ⁵E_g), 540 nm (Fe²⁺→Fe³⁺ intervalence charge transfer, IVCT), and 415 nm (Fe²⁺→Ti⁴⁺ IVCT + possible Mn²⁺ contribution). Post-treatment, the 540 nm band vanished, creating a green transmission window and causing the color shift parallel the c-axis. The spectra perpendicular to the c-axis remained largely unchanged. The disappearance of the 540 nm band, attributed to the reduction of Fe³⁺ to Fe²⁺ eliminating the Fe²⁺–Fe³⁺ pair interaction required for IVCT, is the primary color change mechanism. The parallel c-axis section of the samples shows brown and yellow-green dichroism after heat treatment. A decrease in the IR intensity at 4170 cm⁻¹ indicates a reduced Fe³⁺ concentration. The weakening or disappearance of the 4721 cm⁻¹ absorption band of the infrared spectrum and the near-infrared 976 nm absorption band of the ultraviolet–visible spectrum provides diagnostic indicators for identifying heat treatment in similar brown elbaite–fluorelbaite. Full article

This study aimed to determine the optimal application sequence of cold atmospheric helium plasma (CAP) with fluoride varnish to enhance enamel protection and fluoride uptake. A total of 91 bovine incisor teeth were randomly assigned into seven groups (n = 13 each): negative control (C, no treatment), comparative controls [helium gas (He, gas only)], helium plasma (P, plasma only)], positive control [fluoride varnish (V)], and three experimental groups: plasma followed by varnish (PV), varnish followed by plasma (VP), and plasma before and after varnish (PVP). Specimens were analyzed using scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX), and microhardness testing at 0, 24, and 48 h post-treatment. SEM revealed that helium plasma treatment enhanced the even dispersion of fluoride and reduced imperfections on the enamel surface. EDX analysis indicated significant alterations in the elemental composition, particularly with respect to the amount of fluoride (F) and the calcium-to-phosphorus (Ca/P) ratios. In the PVP group (CAP before and after varnish), the fluoride atomic percentage increased notably from 1.21% (varnish group) to 7.31% at 48h. Concurrently, the Ca/P ratio increased from 1.95 to 2.39 corresponding with a statistically significant 24% improvement in enamel hardness (repeated-measures ANOVA with Bonferroni correction, p < 0.05). The timing of CAP application critically affects fluoride absorption and enamel hardening. This study clearly demonstrates how sequential CAP treatment maximizes fluoride effectiveness, offering a promising route for non-invasive caries prevention. Full article

Early and accurate detection of pneumonia from chest X-ray images is essential for improving treatment and clinical outcomes. Medical imaging datasets often exhibit class imbalance and uncertainty in feature extraction, which complicates conventional classification methods and motivates the use of advanced approaches combining deep learning and fuzzy logic. This study proposes a hybrid approach that combines deep learning architectures (VGG16, EfficientNetV2, MobileNetV2, ResNet50) for feature extraction with fuzzy logic-based classifiers, including Fuzzy C-Means, Fuzzy Decision Tree, Fuzzy KNN, Fuzzy SVM, and ANFIS (Adaptive Neuro-Fuzzy Inference System). Feature selection techniques were also applied to enhance the discriminative power of the extracted features. The best-performing model, ANFIS with MobileNetV2 features and Gaussian membership functions, achieved an overall accuracy of 98.52%, with Normal class precision of 97.07%, recall of 97.48%, and F1-score of 97.27%, and Pneumonia class precision of 99.06%, recall of 98.91%, and F1-score of 98.99%. Among the fuzzy classifiers, Fuzzy SVM and Fuzzy KNN also showed strong performance with accuracy above 96%, while Fuzzy Decision Tree and Fuzzy C-Means achieved moderate results. These findings demonstrate that integrating deep feature extraction with neuro-fuzzy reasoning significantly improves diagnostic accuracy and robustness, providing a reliable tool for clinical decision support. Future research will focus on optimizing model efficiency, interpretability, and real-time applicability. Full article

This study investigates how the inclusion of refuse-derived fuel (RDF) alters the surface chemistry and electrostatic behavior of oak-based biochar. Biochars were produced using downdraft gasification at 850 °C from 100% oak (HW) and a ternary blend comprising 50% oak, 30% pine, and 20% RDF (HW/SW/RDF). Characterization using Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), zeta potential, pH, and electrophoretic mobility was conducted to assess surface functionality and colloidal behavior. The RDF-containing biochar exhibited a 43.3% increase in surface nitrogen content (from 0.24% to 0.90%) and a 6.6% rise in calcium content (from 2.07% to 2.27%) alongside the introduction of chlorine (0.20%) and elevated silicon levels (0.69%) compared to RDF-free counterparts. A concurrent reduction in oxygen-containing functional groups was observed, as O1s decreased from 15.75% in HW to 13.37% in HW/SW/RDF. Electrokinetic measurements revealed a notable decrease in zeta potential magnitude from −31.5 mV in HW to −24.2 mV in HW/SW/RDF, indicating diminished surface charge and colloidal stability. Moreover, the pH declined from 10.25 to 7.76, suggesting a loss of alkalinity and buffering capacity. These compositional and electrostatic shifts demonstrate that RDF inclusion significantly modifies the surface reactivity of biochar, influencing its performance in catalysis, ion exchange, and nutrient retention. The findings underscore the need for tailored post-treatment strategies to enhance the functionality of RDF-modified biochars in environmental applications. Full article

This study examines the effects of laser pulse duration on the structural, morphological, optical, and gas-sensing characteristics of ${\mathrm{Al}}_2{\mathrm{O}}_3$/AgO thin films deposited on glass substrates using pulsed laser deposition (PLD). Pulse durations of 10, 8, and 6 nanoseconds were achieved through optical lens modifications to control both energy density and laser spot size. X-ray diffraction (XRD) and atomic force microscopy (AFM) analyses showed a distinct reduction in both crystallite and grain sizes with decreasing pulse width, along with significant improvements in surface morphology refinement and film compactness. Hall effect measurements revealed a transition from n-type to p-type conductivity with decreasing pulse width, demonstrating increased hole concentration and reduced carrier mobility attributed to grain boundary scattering. Furthermore, current-voltage (I-V) characteristics demonstrated improved photoconductivity under illumination, with the most pronounced enhancement observed in samples prepared using longer pulse durations. Gas sensing measurements for ${\mathrm{NO}}_2$ and ${\mathrm{H}}_2$S revealed enhanced sensitivity, improved response/recovery characteristics at 250 °C, with optimal performance achieved in films deposited using shorter pulse durations. This improvement is attributed to their larger surface area and higher density of active adsorption sites. Our results demonstrate a clear relationship between laser pulse parameters and the functional properties of ${\mathrm{Al}}_2{\mathrm{O}}_3$/AgO films, providing valuable insights for optimizing deposition processes to develop advanced gas sensors. Full article

Currently, the growing demand for sustainable hydrogen makes the oxygen evolution reaction (OER) increasingly important. To boost the performance of electrochemical cells for water electrolysis, both cathodic and anodic sides need to be optimized. Noble metal catalysts for the OER suffer from high costs and limited availability; therefore, developing efficient, low-cost alternatives is crucial. This work investigates manganese-based materials as potential noble-metal-free catalysts. Mn antimonates, Mn chlorates, and Mn bromates were synthesized using ultrasound-assisted techniques to enhance phase composition and homogeneity. Physicochemical characterizations were performed using X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM), together with energy-dispersive X-ray spectroscopy (EDX) and surface area analyses. All samples exhibited a low surface area and inter-particle porosity within mixed crystalline phases. Among the catalysts, Mn_7.5O₁₀Br₃, synthesized via ultrasound homogenization (30 min at 59 kHz) and calcined at 250 °C, showed the highest OER activity. Drop-casted on Fluorine-Doped Tin Oxide (FTO)-coated Ti mesh, it achieved an overpotential of 153 mV at 10 mA cm⁻², with Tafel slopes of 103 mV dec⁻¹ and 160 mV dec⁻¹ at 1, 2, and 4 mA cm⁻² and 6, 8, 10, and 11 mA cm⁻², respectively. It also demonstrated good short-term stability (1 h) in acidic media, with a strong signal-to-noise ratio. Its short-term stability is comparable to that of the benchmark IrO₂, with a potential drift of 15 mV h⁻¹ and a standard deviation of 3 mV for the best-performing electrode. The presence of multiple phases suggests room for further optimization. Overall, this study provides a practical route for designing noble metal-free Mn-based OER catalysts. Full article

The development of effective catalysts for the oxygen reduction reaction (ORR) is crucial for improving the performance of fuel cells. Efficient carbon-supported Pt-Co nanocatalysts were successfully prepared by a generic two-step method: (i) electroless deposition of a Co-P coating on Vulcan XC72R carbon powder and (ii) subsequent spontaneous partial galvanic replacement of Co by Pt, upon immersion of the Co/C precursor in a chloroplatinate solution. The prepared Pt-Co particles (of a core-shell structure) are dispersed on a Vulcan XC-72 support, forming agglomerates made of nanoparticles smaller than 10 nm. The composition and surface morphology of the samples were characterized by scanning electron microscopy and energy-dispersive X-ray spectroscopy (SEM/EDS) as well as transmission electron microscopy (TEM). The crystal structures of the Co-P/C precursor and Pt-Co/C catalyst were investigated by X-ray diffraction (XRD). XPS analysis was performed to study the chemical state of the surface layers of the precursor and catalyst. The electrochemical behavior of the Pt-Co/C composites was evaluated by cyclic voltammetry (CV). Linear sweep voltammetry (LSV) experiments were used to assess the catalytic activity towards the ORR and compared with that of a commercial Pt/C catalyst. The Pt-Co/C catalysts exhibit mass-specific and surface-specific activities (of j_m = 133 mA mg⁻¹ and j_esa = 0.661 mA cm⁻², respectively) at a typical overpotential value of 380 mV (+0.85 V vs. RHE); these are superior to those of similar electrodes made of a commercial Pt/C catalyst (j_m = 50.6 mA mg⁻¹; j_esa = 0.165 mA cm⁻²). The beneficial effect of even small (<1% wt.%) quantities of Co in the catalyst on Pt ORR activity may be attributed to an optimum catalyst composition and particle size resulting from the proposed preparation method. Full article

H₂ has become one of the most attractive alternatives to replace fossil fuels in clean energy production, but large-scale production remains a challenge. A key step toward this goal is to develop new efficient electrocatalysts for H₂ production. This work presents a new mixed metal oxides-decorated CNT paste electrode (MMO@C), which is highly electrocatalytic, for use in the hydrogen evolution reaction (HER). MMO@C is synthesized by a solvothermal method and used as an easy-to-prepare paste electrode. XPS and X-ray analysis indicate that the electrocatalyst corresponds to a mixed surface of Ga₂O₃-CuO-Cu₂O-Cu(OH)₂@C. The MMO@C electrocatalyst shows a positive E_o of 0.12 V vs. RHE at −10 mA cm⁻² towards the HER in a neutral medium. In neutral and alkaline media, the presence of Ga₂O₃ facilitates the reduction of CuO to Cu(I) species, which is followed by the formation of Cu(s) active sites. Therefore, the excellent electrocatalytic performance toward the HER in a neutral medium is attributed to the synergistic effect between gallium and copper oxides on the electrode surface. The prominent H₂ production using MMO@C electrocatalyst is 1.31 × 10⁻² mol cm⁻², with a turnover number (TON) of 39,423, a turnover frequency (TOF) of 13,141 h⁻¹, and a faradaic efficiency (FE) of 94.3%. Although the Tafel slope reveals slow reaction kinetics, the outstanding onset potential allows for the coupling of the electrocatalyst to renewable energy production systems, making it an attractive candidate for producing green H₂ and for application in membrane water electrolyzers. Full article

Water stress represents one of the most critical limiting factors affecting plant distribution, growth rate, biomass accumulation, and crop yield across diverse growth stages. Variations in species’ drought tolerance fundamentally shape global biodiversity patterns by influencing survival rates, distribution ranges, and community composition under changing environmental conditions. This study investigated the physiological responses of six plant species (Haloxylon ammodendron (H.A.), Nitraria tangutorum Bobr. (N.T.B.), Sympegma regelii Bge. (S.R.B.), Tamarix chinensis (T.C.), Potentilla fruticosa (P.F.R.), and Sabina chinensis (Linn.) Ant. (S.C.A.)) to varying water stress levels through controlled water gradient experiments. Four treatment levels were established: W1 (full water supply, >70% field water holding capacity); W2 (mild stress, 50–55%); W3 (moderate stress, 35–40%); and W4 (severe stress, 20–25%). Height growth and leaf mass per area decreased significantly with increasing water stress across all species. S.C.A. consistently exhibited the highest leaf mass per area among the six species, while H.A. showed the lowest values across all treatments. Leaf water content declined progressively with intensifying water stress, with T.C. and P.F.R. showing the most pronounced reductions (T.C.: 16.53%, 18.07%, and 33.37% under W2, W3, and W4, respectively; P.F.R.: 19.45%, 28.52%, and 36.08%), whereas N.T.B. and H.A. demonstrated superior water retention capacity (N.T.B.: 2.44%, 6.64%, and 9.76%; H.A.: 1.44%, 4.39%, and 5.52%). Water saturation deficit increased correspondingly with declining soil moisture. Diurnal leaf water potential patterns exhibited a characteristic V-shaped curve under well-watered (W1) and mildly stressed (W2) conditions, transitioning to a double-valley pattern with unstable fluctuations under moderate (W3) and severe (W4) stress. Leaf water potential showed linear relationships with air temperature and relative humidity, and a quadratic relationship with atmospheric water potential. For all six species, the relationship between pre-dawn leaf water potential and soil water content followed the curve equation y = a + b/x. Under water-deficient conditions, S.C.A. exhibited the greatest water physiological changes, followed by P.F.R. Both logarithmic and power function relationships between leaf and soil water potentials were highly significant (all F > 55.275, all p < 0.01). T.C. leaf water potential was the most sensitive to soil water potential changes, followed by S.C.A., while H.A. demonstrated the least sensitivity. These findings provide essential theoretical foundations for selecting drought-resistant plant species in arid regions of the Qaidam Basin. This study elucidates the response mechanisms of six distinct drought-tolerant plant species under water stress. It provides critical theoretical support for selecting drought-tolerant species, designing community configurations, and implementing water management strategies in vegetation restoration projects within the arid Qaidam Basin. Furthermore, it contributes empirical data at the plant physiological level to understanding the mechanisms sustaining species diversity in arid ecosystems. Full article