Search Results (612)

A comparison of two synthesis methods for depositing Au nanoparticles onto TiO₂ was performed: (1) impregnation with HAuCl₄ followed by thermal treatment in argon, and (2) magnetron sputtering from a Au disc. The obtained materials were used for acetaldehyde decomposition in a high temperature reaction chamber and ch aracterised by UV-Vis/DR, XPS, XRD, SEM, and photoluminescence measurements. The process was carried out using an air/acetaldehyde gas flow under UV or UV-Vis LED irradiation. The mechanism of acetaldehyde decomposition and conversion was elaborated by in situ FTIR measurements of the photocatalyst surface during the reaction. Simultaneously, concentration of acetaldehyde in the outlet gas was monitored using gas chromatography. All the Au/TiO₂ samples showed absorption in the visible region, with a maximum around 550 nm. The plasmonic effect of Au nanoparticles was observed under UV-Vis light irradiation, especially at elevated temperatures such as 100 °C, for Au/TiO₂ prepared by the magnetron sputtering method. This resulted in a significant increase in the conversion of acetaldehyde at the beginning, followed by gradual decrease over time. The collected FTIR spectra indicated that, under UV-Vis light, acetaldehyde was strongly adsorbed onto Au/TiO₂ surface and formed crotonaldehyde or aldol. Under UV, acetaldehyde was mainly adsorbed in the form of acetate species. The plasmonic effect of Au nanoparticles increased the adsorption of acetaldehyde molecules onto TiO₂ surface, while reducing their decomposition rate. The increased temperature of the process enhanced the decomposition of the acetaldehyde. Full article

100 nm thick TiO₂/TiN bilayers with varying thickness ratios were deposited via reactive sputtering of a Ti target in controlled oxygen and nitrogen atmospheres. Post-deposition annealing in air at 600 °C was performed to induce nitrogen diffusion through the oxygen-deficient TiO₂ layer. The resulting changes in morphology and chemical environment were investigated in detail using transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and UV-Vis spectroscopy. Detailed TEM and XPS analyses have confirmed nitrogen diffusion across the TiO₂ layer, with surface nitrogen concentration and the ratio of interstitial to substitutional nitrogen dependent on the TiO₂/TiN mass ratio. Optical studies demonstrated modifications in optical constants and a reduction of the effective bandgap from 3.2 eV to 2.6 eV due to new energy states introduced by nitrogen doping. Changes in surface free energy induced by nitrogen incorporation showed a correlation to nitrogen doping sites on the surface, which had positive effects on overall photocatalytic activity. Photocatalytic activity, assessed through methylene blue degradation, showed enhancement attributed to nitrogen doping. Additionally, deposition of a 5 nm gold layer on the annealed sample enabled investigation of synergistic effects between nitrogen doping and gold incorporation, resulting in further improved photocatalytic performance. These findings establish the TiO₂/TiN bilayer as a versatile platform for supporting thin gold films with enhanced photocatalytic properties. Full article

The development of non-noble metal catalysts for gas-phase propylene epoxidation with H₂/O₂ remains challenging due to their inadequate activity and stability. Herein, we report a Cs⁺-modified Ni/TS-1 catalyst (9%Ni-Cs/TS-1), which exhibits unprecedented catalytic performance, giving a state-of-the-art PO formation rate of 382.9 g_PO·kg_cat⁻¹·h⁻¹ with 87.8% selectivity at 200 °C. The catalyst stability was sustainable for 150 h, far surpassing reported Ni-based catalysts. Ni/TS-1 exhibited low catalytic activity. However, the Cs modification significantly enhanced the performance of Ni/TS-1. Furthermore, the intrinsic reason for the enhanced performance was elucidated by multiple techniques such as XPS, N₂ physisorption, TEM, ²⁹Si NMR, NH₃-TPD-MS, UV–vis, and so on. The findings indicated that the incorporation of Cs⁺ markedly boosted the reduction of Ni, enhanced Ni⁰ formation, strengthened Ni-Ti interactions, reduced acid sites to inhibit PO isomerization, improved the dispersion of Ni nanoparticles, reduced particle size, and improved the hydrophobicity of Ni/TS-1 to facilitate propylene adsorption/PO desorption. The 9%Ni-Cs/TS-1 catalyst demonstrated exceptional performance characterized by a low cost, high activity, and long-term stability, offering a viable alternative to Au-based systems. Full article

Perovskite solar cells (PSCs) leverage the exceptional photoelectric properties of perovskite materials, yet interfacial energy level mismatches limit carrier extraction efficiency. In this work, energy level alignment was exploited to reduce the charge transport barrier, which can be conducive to the transmission of photo-generated carriers and reduce the probability of electron–hole recombination. We designed a dual-transition perovskite solar cell (PSC) with the structure of FTO/TiO₂/Nb₂O₅/CH₃NH₃PbI₃/MoO₃/Spiro-OMeTAD/Au by finite element analysis methods. Compared with the pristine device (FTO/TiO₂/CH₃NH₃PbI₃/Spiro-OMeTAD/Au), the open-circuit voltage of the optimized cell increases from 0.98 V to 1.06 V. Furthermore, the design of a circular platform light-trapping structure makes up for the light loss caused by the transition at the interface. The short-circuit current density of the optimized device increases from 19.81 mA/cm² to 20.36 mA/cm², and the champion device’s power conversion efficiency (PCE) reaches 17.83%, which is an 18.47% improvement over the planar device. This model provides new insight for the optimization of perovskite devices. Full article

The Tuztaşı low-sulfidation epithermal Au–Ag deposit (Biga Peninsula, Türkiye) records a multi-stage hydrothermal history that can be interpreted through the trace and rare-earth-element (REE) chemistry of quartz. High-precision LA-ICP-MS analyses of five representative quartz samples (23 ablation spots; 10 analytically robust) reveal two fluid stages. Early fluids were cold, dilute meteoric waters (δ¹⁸O₍H₂O₎ ≈ −6.8 to +0.7‰), whereas later fluids circulated deeper, interacted with felsic basement rocks, and evolved in composition. Mineralized quartz displays marked enrichment in As (raw mean = 2854 ± 6821 ppm; filtered mean = 70 ± 93 ppm; one spot 16,775 ppm), K (498 ± 179 ppm), and Sb (57.8 ± 113 ppm), coupled with low Ti/Al (<0.005) and elevated Ge/Si (0.14–0.65 µmol mol⁻¹). Chondrite-normalized REE patterns show pronounced but variable LREE enrichment ((La/Yb)_n ≤ 45.3; ΣLREE/ΣHREE up to 10.8) and strongly positive Eu anomalies (δEu ≤ 9.3) with slightly negative Ce anomalies (δCe ≈ 0.29); negligible Ce–Eu covariance (r² ≈ 0.05) indicates discrete redox pulses. These signatures indicate chemically evolved, reducing fluids conducive to Au–Ag deposition. By contrast, barren quartz is characterized by lower pathfinder-element contents, less fractionated REE profiles, higher Ti/Al, and weaker Eu anomalies. A composite exploration toolkit emerges: As > 700 ppm, As/Sb > 25, Ti/Al < 0.005, Ge/Si > 0.15 µmol mol⁻¹, and δEu ≫ 1 reliably identify ore-bearing zones when integrated with δ¹⁸O data and fluid-inclusion microthermometry from earlier studies on the same vein system. This study provides one of the first systematic applications of integrated trace-element and REE analysis of quartz to a Turkish low-sulfidation epithermal system, offering an applicable model for vectoring mineralization in analogous settings worldwide. Full article

Perovskite solar cells (PSCs) have already been reported as a promising alternative to traditional energy sources due to their excellent power conversion efficiency, affordability, and versatility, which is particularly relevant considering the growing worldwide demand for energy and increasing scarcity of natural resources. However, operational concerns under environmental stresses hinder its economic feasibility. Through the addition of cesium (Cs), this study investigates how to optimize perovskite solar cells (PSCs) based on methylammonium lead-iodide (MAPbI₃) by creating mixed-cation compositions of MA_1−xCs_xPbI₃ (x = 0, 0.25, 0.5, 0.75, 1) for devices A to E, respectively. The impact of cesium content on the following factors, such as open-circuit voltage (V_oc), short-circuit current density (J_sc), fill factor (FF), and power conversion efficiency (PCE), was investigated using simulation software, with ITO/TiO₂/MA_1−xCs_xPbI₃/Spiro-OMeTAD/Au as a device architecture. Due to diminished defect density, the device with x = 0.5 (MA_0.5Cs_0.5PbI₃) attains a maximum power conversion efficiency of 18.53%, with a V_oc of 0.9238 V, J_sc of 24.22 mA/cm², and a fill factor of 82.81%. The optimal doping density of TiO₂ is approximately 10²⁰ cm⁻³, while the optimal thicknesses of the electron transport layer (TiO₂, 10–30 nm), the hole-transport layer (Spiro-OMeTAD, about 10–20 nm), and the perovskite absorber (750 nm) were identified to maximize efficiency. The inclusion of a small amount of Cs may improve photovoltaic responses; however, at elevated concentrations (x > 0.5), power conversion efficiency (PCE) diminished due to the presence of trap states. The results show that mixed-cation perovskite solar cells can be a great commercially viable option because they strike a good balance between efficiency and performance. Full article

Titanium dioxide (TiO₂) is a benchmark photocatalyst for environmental applications, but its limited visible-light activity due to a wide band gap and fast charge recombination restricts its practical efficiency. This study presents the development of heterostructured Ag (Au)/MoS₂-TiO₂ inverse opal (IO) films that synergistically integrate photonic, plasmonic, and semiconducting functionalities to overcome these limitations. The materials were synthesized via a one-step evaporation-induced co-assembly approach, embedding MoS₂ nanosheets and plasmonic nanoparticles (Ag or Au) within a nanocrystalline TiO₂ photonic framework. The inverse opal architecture enhances light harvesting through slow-photon effects, while MoS₂ and plasmonic nanoparticles improve visible-light absorption and charge separation. By tuning the template sphere size, the photonic band gap was aligned with the TiO₂-MoS₂ absorption edge and the localized surface plasmon resonance of Ag, enabling optimal spectral overlap. The corresponding Ag/MoS₂-TiO₂ photonic films exhibited superior photocatalytic and photoelectrocatalytic degradation of tetracycline under visible light. Ultraviolet photoelectron spectroscopy and Mott–Schottky analysis confirmed favorable band alignment and Fermi level shifts that facilitate interfacial charge transfer. These results highlight the potential of integrated photonic–plasmonic-semiconductor architectures for efficient solar-driven water treatment. Full article

Body-centered cubic (BCC) refractory high-entropy alloys (RHEAs) demonstrate significant potential as nuclear structural materials due to their exceptional mechanical properties and radiation tolerance. While Zr-containing RHEAs often develop multiphase structures through Zr-rich phase precipitation to enhance high-temperature mechanical performance, their irradiation response mechanisms remain poorly understood. This study investigated the microstructure evolution and radiation damage behavior in equiatomic MoNbTiVZr RHEA under Au-ion irradiation at fluences of 2 × 10¹⁵, 4 × 10¹⁵, and 1 × 10¹⁶ ions/cm². Microstructural characterization revealed that the annealed alloy primarily consisted of near-equiatomic BCC1 phase, Zr-rich BCC2 phase, (Mo,V)Zr Laves phase, and ordered Zr₂C phase. Post-irradiation analysis showed distinct defect evolution patterns: the BCC1 phase developed fine dislocation loops, while the Zr-rich BCC2 and Zr₂C phases exhibited dislocation clusters and dense dislocation networks, respectively. BCC1 phase exhibited the most pronounced irradiation hardening corresponding to its fine, dispersed dislocation loop characteristics. Phase separation induced by Zr precipitation reduced chemical complexity, accelerating irradiation defect evolution. These findings demonstrated that Zr-rich phase precipitation detrimentally impacted the radiation resistance of BCC-structured RHEAs, suggesting that single-phase stability should be prioritized in nuclear material design. Full article

Barium stannate (BaSnO₃) has emerged as a promising alternative electron transport material owing to its superior electron mobility, resistance to UV degradation, and energy bandgap tunability, yet BaSnO₃-based perovskite solar cells have not reached the efficiency levels of TiO₂-based designs. This theoretical study presents a design-driven evaluation of BaSnO₃-based perovskite solar cell architectures, incorporating MAPbI₃ or FAMAPbI₃ perovskite materials, Spiro-OMeTAD, or Cu₂O hole transport materials as well as hole-free configurations, under varying light intensity. Using a systematic device modelling approach, we explore the influence of key design variables—such as layer thickness, donor density, and interface defect concentration—of BaSnO₃ and operating temperature on the power conversion efficiency (PCE). Among the proposed designs, the FTO/BaSnO₃/FAMAPbI₃/Cu₂O/Au heterostructure exhibits an exceptionally effective arrangement with PCE of 38.2% under concentrated light (10,000 W/m², or 10 Sun). The structure also demonstrates strong thermal robustness up to 400 K, with a low temperature coefficient of −0.078% K⁻¹. These results underscore the importance of material and structural optimisation in PSC design and highlight the role of high-mobility, thermally stable inorganic transport layers—BaSnO₃ as the electron transport material (ETM) and Cu₂O as the hole transport material (HTM)—in enabling efficient and stable photovoltaic performance under high irradiance. The study contributes valuable insights into the rational design of high-performance PSCs for emerging solar technologies. Full article

The recent focus on wide-bandgap absorbers for tandem solar cell configurations and photovoltaic materials with high absorption coefficients for indoor photovoltaics has prompted a renewed interest in selenium. Over the past few years, the efficiency of Se solar cells has improved significantly, bringing the prospect of industrial production closer to reality. This study presents an innovative vapor transport deposition (VTD) technique for the scalable and cost-effective fabrication of Se thin films. The prepared Se thin films were characterized, and the results show that the VTD method is capable of producing dense and well-crystallized Se thin films. Se solar cells with a structure of glass/FTO/TiO₂/Se/Au were fabricated to evaluate the impact of substrate temperature on device performance. The optimal performance was achieved on the hot side of the substrate during deposition, with a power conversion efficiency (PCE) of 2.56%. This study provides a promising pathway for the low-cost, high-throughput manufacturing of high-performance Se solar cells, facilitating their potential industrial implementation. Full article

The growing demand for reliable micropower sources in extreme environments has accelerated the development of betavoltaic cells (BV cells) with high energy conversion efficiency and superior radiation resistance. This study demonstrates an advanced BV cell architecture utilizing three-dimensional TiO₂ nanorod arrays (TNRAs) integrated with a NiO_x hole transport layer (HTL). Monte Carlo simulations were employed to optimize the cell design and determine the fabrication parameters for growing TNRAs on FTO substrates via hydrothermal synthesis. The performance evaluation employed both electron beam (2.36 × 10⁹ e/cm²·s) and ⁶³Ni (3.4 mCi/cm²) irradiation methods. The simulation results revealed optimal energy deposition characteristics, with ~96% of β-particle energy effectively absorbed within the 2 μm thick FTO/TNRA/NiO_x/Au structure. The NiO_x-incorporated device achieved an energy conversion efficiency of 4.84%, with a short-circuit current of 119.9 nA, an open-circuit voltage of 324.2 mV, and a maximum power output of 24.0 nW, representing a 3.76-fold enhancement over HTL-free devices. Radioactive source testing confirmed stable power generation and linear efficiency scaling, validating electron beam irradiation as an effective accelerated testing methodology for BV cell research. Full article

(1) Background: Asomate, as a dithiocarbamate compound, is moderately toxic to the human body; thus, it is necessary to develop a rapid and efficient method for detection. To meet this need, this study introduced a rapid, non-destructive, and efficient method for detecting asomate residues on the surface of apples based on surface-enhanced Raman spectroscopy (SERS) combined with flexible substrates. (2) Methods: Concave Au nanorods (AuCNAs) were synthesized in advance. Then, the AuCNAs were loaded on an electrostatically spun film to generate a flexible TiO₂/ZrO₂/AuCNAs substrate for detection. (3) Results: The flexible substrate exhibited strong SERS activity, with an enhancement factor (EF) up to 9.40 × 10⁷ for 4-MBA. Meanwhile, the finite-difference time-domain (FDTD) simulation showed that the localized surface plasmon resonance (LSPR) effects related to the enhancement of the SERS signal are mainly generated from the ‘hot spots’ in AuCNAs. The density functional theory (DFT) simulation detailedly revealed that the SERS peaks could be generated by the interaction among asomate molecules, disassociated Au atoms, and Au facets. Moreover, the asomate in apple peel was analyzed with the limit of detection (LOD) as low as below 10 nM, allowing for the rapid detection of asomate directly on apple peels. (4) Conclusions: The flexible TiO₂/ZrO₂/AuCNAs film can be used for the in situ detection of asomate in apple peel at low concentrations. Moreover, the simulation methods, including FDTD and DFT, explained the mechanism of SERS from the flexible substrates. Full article

Advanced oxidation processes (AOPs) show significant promise to degrade recalcitrant water contaminants, such as 1,4-dioxane, but slow degradation kinetics limit the energy efficiency of this technology. We realized substantial enhancements in the degradation of 1,4-dioxane (a suspected carcinogen) using gold-coated titanium dioxide (Au/TiO₂) Janus nanoparticles (JNPs) irradiated with above-bandgap ultraviolet (UV) light (peak wavelength, 254 nm). To explain this result, we combined experimental measurements quantifying 1,4-dioxane degradation at varying UV wavelengths with finite-element simulations that provided explanatory insight into the light–matter interactions at play. The enhanced photocatalytic activity at the optimal condition (254 nm light, high intensity, Au/TiO₂) resulted from a larger quantity of photogenerated holes in the TiO₂ capable of reacting with water to form hydroxyl radicals that degrade 1,4-dioxane. This increased production of holes resulted from two sources: (1) more viable electron–hole pairs were created under 254 nm light owing to increased light absorption by the TiO₂ that was localized near the surface; (2) the metal sequestered photogenerated electrons from the TiO₂, which prevented electron–hole pairs from recombining, leaving more holes available to react with water. Our results motivate the exploration of different metal coatings (especially non-precious metals) and suggest a path toward broader implementation of TiO₂-based photocatalytic AOPs, which can effectively remove many water pollutants that survive conventional treatment techniques. Full article

This research presents a novel square-shaped photonic crystal fiber (PCF)-based surface plasmon resonance (SPR) sensor, designed using the external metal deposition (EMD) technique, for highly sensitive refractive index (RI) sensing applications. The proposed sensor operates effectively over an RI range of 1.33 to 1.37 and supports both x- polarized and y-polarized modes. It achieves a wavelength sensitivity of 15,800 nm/RIU and 14,300 nm/RIU, and amplitude sensitivities of 11,584 RIU⁻¹ and 11,007 RIU⁻¹, respectively, for the x-pol. and y-pol. The sensor also reports a resolution in the order of 10⁻⁶ RIU and a strong linearity of R² ≈ 0.97 for both polarization modes, indicating its potential for precision detection in complex sensing environments. Beyond the sensor’s structural and performance innovations, this work also explores the future integration of artificial intelligence (AI) into PCF-SPR sensor design. AI techniques such as machine learning and deep learning offer new pathways for sensor calibration, material optimization, and real-time adaptability, significantly enhancing sensor performance and reliability. The convergence of AI with photonic sensing not only opens doors to smart, self-calibrating platforms but also establishes a foundation for next-generation sensors capable of operating in dynamic and remote applications. Full article

Solar glycerol photoreforming was investigated on Au-Ni/CeO₂ photocatalysts with an overall metal content equal to 1wt% and different Au/Ni weight ratios. The deposition of gold over ceria was performed by two different methods, deposition–precipitation and photoreduction. Deposition–precipitation was the best method to deposit gold on CeO₂ with the formation of small Au nanoparticles (around 4 nm). The most active sample (0.9 wt% Au-0.1 Ni wt%/CeO₂) provided a H₂ production rate of 350 µmol/gcat∙h, much higher than the corresponding monometallic samples. A higher amount of Ni led to detrimental effects in H₂ production, likely due to the covering of the gold surface active sites by Ni. On the contrary, the presence of a small amount of Ni (0.1 wt%) allowed a remarkable improvement of the Au/CeO₂ photocatalytic stability after consecutive runs of simulated solar irradiation. This finding, as well as the activation of synergistic effects, the improved charge carrier separation, and the exploitation of the localized surface plasmon resonance property of gold, led to the proposal of an alternative photocatalytic system to the most investigated TiO₂-based photocatalysts for H₂ production. The enhanced stability is promising to further foster the investigation of these photocatalysts applied to sustainable H₂ production. Full article