Search Results (1,633)

Microphysiological systems (MPSs) have emerged as alternatives to animal testing in drug development, following the FDA Modernization Act 2.0. Double-layer channel-type MPS chips with porous membranes are widely used for modeling various organs, including the intestines, blood–brain barrier, renal tubules, and lungs. However, these chips faced challenges owing to optical interference caused by light scattering from the porous membrane, which hinders cell observation. Trans-epithelial electrical resistance (TEER) measurement offers a non-invasive method for assessing barrier integrity in these chips. However, existing electrode-integrated MPS chips for TEER measurement have non-uniform current densities, leading to compromised measurement accuracy. Additionally, chips made from polydimethylsiloxane have been associated with drug absorption issues. This study developed an electrode-integrated MPS chip for TEER measurement with a uniform current distribution and minimal drug absorption. Through a finite element method simulation, electrode patterns were optimized and incorporated into a polyethylene terephthalate (PET)-based chip. The device was fabricated by laminating PET films, porous membranes, and patterned gold electrodes. The chip’s performance was evaluated using a perfused Caco-2 intestinal model. TEER levels increased and peaked on day 5 when cells formed a monolayer, and then they decreased with the development of villi-like structures. Concurrently, capacitance increased, indicating microvilli formation. Exposure to staurosporine resulted in a dose-dependent reduction in TEER, which was validated by immunostaining, indicating a disruption of the tight junction. This study presents a TEER measurement MPS platform with a uniform current density and reduced drug absorption, thereby enhancing TEER measurement reliability. This system effectively monitors barrier integrity and drug responses, demonstrating its potential for non-animal drug-testing applications. Full article

All inorganic CsPbBr₃ possesses ideal stability in halide perovskites, but its wide bandgap and relatively poor film quality seriously limit the performance enhancement and possible applications of perovskite solar cells (PSCs). In this work, a triple-functional poly(3-Hexylthiophene) (P3HT) modifier was introduced to realize color-tunable semi-transparent CsPbBr₃ PSCs. From the optical perspective, the P3HT acted as the assistant photoactive layer, enhanced the light absorption capacity of the CsPbBr₃ film, and broadened the spectrum response range of devices. In view of the hole transport layer, P3HT modified the energy level matching between the CsPbBr₃/anode interface and facilitated the hole transport. Simultaneously, the S⁻ in P3HT formed a more stable Pb-S bond with the uncoordinated Pb²⁺ on the surface of CsPbBr₃ and played the role of a defect passivator. As the P3HT concentration increased from 0 to 15 mg/mL, the color of CsPbBr₃ devices gradually changed from light yellow to reddish brown. The PSC treated by an optimal P3HT concentration of 10 mg/mL achieved a champion power conversion efficiency (PCE) of 8.71%, with a V_OC of 1.30 V and a J_SC of 8.54 mA/cm², which are remarkably higher than those of control devices (6.86%, 1.22 V, and 8.21 mA/cm²), as well its non-degrading stability and repeatability. Here, the constructed CsPbBr₃/P3HT heterostructure revealed effective paths for enhancing the photovoltaic performance of CsPbBr₃ PSCs and boosted their semi-transparent applications in building integrated photovoltaics (BIPVs). Full article

Bismuth vanadate (BiVO₄) has attracted significant attention as a photoanode material for photoelectrochemical (PEC) water splitting due to its suitable bandgap (~2.4 eV), strong visible light absorption, chemical stability, and cost-effectiveness. Despite these advantages, its practical application remains constrained by intrinsic limitations, including poor charge carrier mobility, short diffusion length, and sluggish oxygen evolution reaction (OER) kinetics. This review critically summarizes recent advancements aimed at enhancing BiVO₄ PEC performance, encompassing synthesis strategies, defect engineering, heterojunction formation, cocatalyst integration, light-harvesting optimization, and stability improvements. Key fabrication methods—such as solution-based, vapor-phase, and electrochemical approaches—along with targeted modifications, including metal/nonmetal doping, surface passivation, and incorporation of electron transport layers, are discussed. Emphasis is placed on strategies to improve light absorption, charge separation efficiency (η_sep), and charge transfer efficiency (η_trans) through bandgap engineering, optical structure design, and catalytic interface optimization. Approaches to enhance stability via protective overlayers and electrolyte tuning are also reviewed, alongside emerging applications of BiVO₄ in tandem PEC systems and selective solar-driven production of value-added chemicals, such as H₂O₂. Finally, critical challenges, including the scale-up of electrode fabrication and the elucidation of fundamental reaction mechanisms, are highlighted, providing perspectives for bridging the gap between laboratory performance and practical implementation. Full article

Introduction: Hospital-acquired infections remain a significant healthcare concern due to the persistence of pathogens such as Staphylococcus aureus and Escherichia coli on frequently touched surfaces. Conventional TiO₂ coatings are limited to UV activation, which restricts their application under normal indoor light. Combining TiO₂ with ZnO and employing green synthesis methods may overcome these limitations. Methodology: Biogenic TiO₂ and ZnO nanoparticles were synthesized using Bacillus subtilis under mild aqueous conditions. The nanoparticles were characterized by SEM, XRD, UV-Vis, and FTIR, confirming nanoscale size, crystalline phases, and organic capping. A multilayer TiO₂/ZnO coating was fabricated on glass substrates through layer-by-layer deposition. Antibacterial activity was tested against S. aureus and E. coli using disk diffusion, direct contact assays, ROS quantification (FOX assay), and scavenger experiments. Statistical significance was evaluated using ANOVA. Results: The TiO₂/ZnO multilayer exhibited superior antibacterial activity under visible light, with inhibition zones of ~15 mm (S. aureus) and ~12 mm (E. coli), significantly outperforming single-component coatings. Direct contact assays confirmed strong bactericidal effects, while scavenger tests verified ROS-mediated mechanisms. FOX assays detected elevated H₂O₂ generation, correlating with antibacterial performance. Discussion: Synergistic effects of band-gap narrowing, Zn²⁺ release, and ROS generation enhanced visible-light photocatalysis. The multilayer structure improved light absorption and charge separation, providing higher antimicrobial efficacy than individual oxides. Conclusion: Biogenic TiO₂/ZnO multilayers represent a sustainable, visible-light-activated antimicrobial strategy with strong potential for reducing nosocomial infections on hospital surfaces and surgical instruments. Future studies should assess long-term durability and clinical safety. Full article

The efficient degradation of antibiotics in pharmaceutical wastewater remains a critical challenge against environmental contaminants. Conventional photocatalysts face potential limitations such as narrow visible-light absorption, rapid carrier recombination, and reliance on precious metal cocatalysts. This review investigates the coordination structure of MXene as a cocatalyst to synergistically enhance photocatalytic antibiotic degradation efficiency and the coordination structure modification mechanisms. MXene’s tunable bandgap (0.92–1.75 eV), exceptional conductivity (100–20,000 S/cm), and abundant surface terminations (-O, -OH, -F) enable the construction of Schottky or Z-scheme heterojunctions with semiconductors (Cu₂O, TiO₂, g-C₃N₄), achieving 50–70% efficiency improvement compared to pristine semiconductors. The “electron sponge” effect of MXene suppresses electron-hole recombination by 3–5 times, while its surface functional groups dynamically optimize pollutant adsorption. Notably, MXene’s localized surface plasmon resonance extends light harvesting from visible (400–800 nm) to near-infrared regions (800–2000 nm), tripling photon utilization efficiency. Theoretical simulations demonstrate that d-orbital electronic configurations and terminal groups cooperatively regulate catalytic active sites at atomic scales. The MXene composites demonstrate remarkable environmental stability, maintaining over 90% degradation efficiency of antibiotic under high salinity (2 M NaCl) and broad pH range (4–10). Future research should prioritize green synthesis protocols and mechanistic investigations of interfacial dynamics in multicomponent wastewater systems to facilitate engineering applications. This work provides fundamental insights into designing MXene-based photocatalysts for sustainable water purification. Full article

A variety of factors, such as absorption, reflection, and attenuation by atmospheric elements, influence the quantity of solar energy that reaches the surface of the Earth. This, in turn, impacts photovoltaic (PV) power generation. In light of this, a digital assessment of solar energy variability through short-term measurements was conducted to enhance PV power output. The clear-sky index $\left(K_t^{*}\right)$ methodology was employed, effectively eliminating any indications of solar energy obstruction and comparing the measured radiation to the theoretical clear-sky radiation. The solar energy data were gathered in Mozambique, specifically in the southern region at Maputo–1, Massangena, Ndindiza, and Pembe, in the mid-region at Chipera, Nhamadzi, Barue–1, and Barue–2, as well as in the northern region at Nipepe-1, Nipepe-2, Nanhupo-1, Nanhupo-2, and Chomba, over the period from 2005 to 2024, with measurement intervals ranging from 1 to 10 min and 1 h during the measurement campaigns conducted by FUNAE and INAM, with additional data sourced from the PVGIS, Meteonorm, NOAA, and NASA solar databases. The analysis indicates a $K_t^{*}$ value with a density approaching 1 for clear days, while intermediate-sky days exhibit characteristics that lie between those of clear and cloudy days. It can be inferred that there exists a robust correlation among sky types, with values ranging from 0.95 to 0.89 per station, alongside correlated energies, which experience a regression with coefficients between 0.79 and 0.95. Based on the analysis of the sample, the region demonstrates significant potential for solar energy utilization, and similar sampling methodologies can be applied in other locations to optimize PV output and other solar energy projects. Full article

This study reports on green-synthesized zinc oxide nanoparticles (ZnONPs), focusing on their physicochemical characterization, photocatalytic properties, and agricultural applications. Dynamic light scattering (DLS) analysis revealed a mean hydrodynamic diameter of 337.3 nm and a polydispersity index (PDI) of 0.400, indicating moderate polydispersity and nanoparticle aggregation, typical of biologically synthesized systems. High-resolution transmission electron microscopy (HR-TEM) showed predominantly spherical particles with an average diameter of ~28 nm, exhibiting slight agglomeration. Energy-dispersive X-ray spectroscopy (EDX) confirmed the elemental composition of zinc and oxygen, while X-ray diffraction (XRD) analysis identified a hexagonal wurtzite crystal structure with a dominant (002) plane and an average crystallite size of ~29 nm. Photoluminescence (PL) spectroscopy displayed a distinct near-band-edge emission at ~462 nm and a broad blue–green emission band (430–600 nm) with relatively low intensity. The ultraviolet–visible spectroscopy (UV–Vis) absorption spectrum of the synthesized ZnONPs exhibited a strong absorption peak at 372 nm, and the optical band gap was calculated as 2.67 eV using the Tauc method. Fourier-transform infrared spectroscopy (FTIR) analysis revealed both similarities and distinct differences to the pigeon extract, confirming the successful formation of nanoparticles. A prominent absorption band observed at 455 cm⁻¹ was assigned to Zn–O stretching vibrations. X-ray photoelectron spectroscopy (XPS) analysis showed that raw pigeon droppings contained no Zn signals, while their extract provided organic biomolecules for reduction and stabilization, and it confirmed Zn²⁺ species and Zn–O bonding in the synthesized ZnONPs. Photocatalytic degradation assays demonstrated the efficient removal of pollutants from sewage water, leading to significant reductions in total dissolved solids (TDS), chemical oxygen demand (COD), and total suspended solids (TSS). These results are consistent with reported values for ZnO-based photocatalytic systems, which achieve biochemical oxygen demand (BOD) levels below 2 mg/L and COD values around 11.8 mg/L. Subsequent reuse of treated water for irrigation yielded promising agronomic outcomes. Wheat and barley seeds exhibited 100% germination rates with ZnO NP-treated water, which were markedly higher than those obtained using chlorine-treated effluent (65–68%) and even the control (89–91%). After 21 days, root and shoot lengths under ZnO NP irrigation exceeded those of the control group by 30–50%, indicating enhanced seedling vigor. These findings demonstrate that biosynthesized ZnONPs represent a sustainable and multifunctional solution for wastewater remediation and agricultural enhancement, positioning them as a promising candidate for integration into green technologies that support sustainable urban development. Full article

In laser wireless power transmission systems, the powersphere serves as a spherical enclosed receiver that performs photoelectric conversion, achieving uniform light distribution within the cavity through infinite internal light reflection. However, in practical applications, the high level of light absorption displayed by photovoltaic cells leads to significant disparities in light intensity between directly irradiated regions and reflected regions on the inner surface of the powersphere, resulting in poor light uniformity. One approach aimed at addressing this issue uses a spectroscope to split the incident beam into multiple paths, allowing the direct illumination of all inner surfaces of the powersphere and reducing the light intensity difference between direct and reflected regions. However, experimental results indicate that light transmission through lenses introduces power losses, leading to improved uniformity but reduced output power. To address this limitation, this study proposes a method that utilizes multiple incident laser beams combined with a centrally positioned spherical reflector within the powersphere. A wireless power transmission system model was developed using optical simulation software, and the uniformity of the intracavity light field in the system was analyzed through simulation. To validate the design and simulation accuracy, an experimental system incorporating semiconductor lasers, spherical mirrors, and a powersphere was constructed. The data from the experiments aligned with the simulation results, jointly confirming that integrating a spherical reflector and distributed incident lasers enhances the uniformity of the internal light field within the powersphere and improves the system’s efficiency. Full article

Zinc oxide (ZnO), a wide-bandgap semiconductor, has garnered significant interest for photocatalytic applications due to its excellent chemical stability, non-toxicity, and strong oxidative capability. In this study, density functional theory (DFT) calculations were employed to explore the impact of ruthenium (Ru) doping on the structural, electronic, and magnetic properties of wurtzite ZnO. The introduction of Ru leads to bandgap narrowing and the emergence of impurity states, thereby enhancing visible light absorption. Charge density analysis reveals enhanced electron delocalization, while the projected density of states (PDOS) indicates strong hybridization between the Ru 4d orbitals and the ZnO electronic states. The density of states at the Fermi level, N(EF), exhibits a notable dependence on doping concentration and magnetic configuration. For non-magnetic states, N(EF) reaches 11 states/eV and 9.5 states/eV at 12.5% and 25% Ru concentrations, respectively. In ferromagnetic configurations, these values decrease to 0.65 states/eV and 1.955 states/eV, while antiferromagnetic states yield 4.945 states/eV and 0.65 states/eV. These variations highlight Ru’s crucial role in regulating electronic density, thereby affecting electrical conductivity, magnetic properties, and photocatalytic efficiency. The results offer theoretical guidance for designing high-performance Ru-doped ZnO photocatalysts. Full article

Excessive copper ions in the human body can cause a variety of diseases, such as gastrointestinal disorders, cirrhosis, and Alzheimer’s disease. Techniques like Inductively Coupled Plasma–Mass Spectroscopy and Atomic Absorption Spectroscopy are available for copper detection, but the associated cost issues for sample preparation and labor limit their application for on-site detection. Herein, we are reporting a versatile method for detecting copper ions using a peptide-functionalized gold nanoparticle sensor in combination with various optical spectroscopic techniques. The peptide (CW) exhibited selective sensing ability for Cu(II) with visual colorimetric and optical spectroscopic changes compared to other metal ions tested. CW showed a visual colorimetric response from colorless to light brown color after interaction with Cu(II). Converting CW to a gold nanoparticle appended (CW-AuNPs) nanoplatform enabled a multimodal detection platform for Cu (II), which utilizes colorimetric and optical spectrum changes and surface-enhanced Raman spectroscopy (SERS) to enable highly sensitive sensing of Cu(II), even at extremely low concentrations (76 nms.). CW-AuNPs exhibit a controlled aggregation property in the presence of Cu(II), resulting in the creation of hot spots for SERS-based detection. Moreover, the peptide unit attached to the gold nanoparticles serves both as a binding motif for Cu(II) and as a Raman reporter for Cu(II) sensing. Our comprehensive analysis, including solution-state and dry-mapping Raman spectroscopic studies, demonstrates remarkable picomolar sensitivity of the peptide–gold nanoparticle system for Cu(II) detection. Moreover, we prepared a paper test strip from CW-AuNPs and used it as a visual colorimetric platform for sensitive detection of copper ions. Full article

We present a systematic study of the fundamental optical properties of indium selenide (InSe) single crystals over a temperature range of 17 K to 300 K. The high structural quality of the β-polytype crystals was confirmed through X-ray diffraction, Raman spectroscopy, and high-resolution transmission electron microscopy, demonstrating excellent crystallinity and a nearly stoichiometric In:Se ratio. The temperature-dependent absorption and photoluminescence (PL) spectra are characterized by a prominent free exciton (FX) resonance. At 17 K, the photoluminescence spectrum exhibits a distinct fine-structure splitting of the Wannier–Mott exciton, yielding a triplet state at 1.333 eV and a singlet state at 1.336 eV. Additionally, a biexciton (XX) is localized at an energy of 1.322 eV as confirmed by the nonlinear dependence of intensity on excitation power density. At low temperatures, the absorption spectrum exhibits the free exciton ground state (n = 1) at 1.338 eV together with the first excited state (n = 2) at 1.350 eV. We systematically tracked and analyzed the temperature evolution of these quasiparticle energies. These findings enhance our understanding of the intrinsic many-body interactions in high-quality InSe, providing essential parameters for advancing its applications in innovative optoelectronic and quantum light-emitting devices. Full article

Indoor air quality management has become increasingly critical for public health, particularly after the global COVID-19 respiratory disease outbreaks that highlighted airborne pathogen transmission risks. This review investigates an advanced air and surface purification method that is used in devices utilising heterogeneous photocatalysis with tungsten oxide (W₁₈O₄₉) and zinc oxide (ZnO) catalyst systems to generate controlled concentrations of hydrogen peroxide for continuous indoor sanitisation. The photocatalytic system converts ambient water vapour into aerosolised hydrogen peroxide at concentrations of 0.04–0.05 ppm, significantly below established safety thresholds, while maintaining effective antimicrobial activity. The W₁₈O₄₉ catalyst demonstrates superior visible-light absorption compared to conventional titanium dioxide (TiO₂) systems, with ZnO serving as an effective cocatalyst to reduce electron–hole recombination and enhance reactive oxygen species generation. Safety analysis based on OSHA, WHO, and ACGIH guidelines confirms that continuous exposure to these low hydrogen peroxide concentrations poses no health risks to occupants. Real-world applications demonstrate up to 90% reduction in airborne pathogens and a 20–30% decrease in sick leave rates in office environments. The technology offers significant economic benefits through reduced healthcare costs and improved productivity while providing environmentally sustainable air purification without harmful residues. This photocatalytic approach represents a scientifically validated, safe, and economically viable solution for next-generation indoor air quality management across healthcare, educational, commercial, and residential sectors. Full article

Recent advances in energy conversion technologies, especially solar-driven photocatalytic water splitting, are vital for satisfying the increasing global need for sustainable and clean energy. Perovskite oxides have attracted considerable attention among photocatalytic materials due to their tunable electronic structures, exceptional stability, and promise for effective hydrogen generation and environmental remediation. In this study, the optoelectronic and photocatalytic (PC) characteristics of ATiO₃ (A = Ca, Mg) perovskites, undoped and codoped with Se and Zr, have been analyzed using ab initio simulations based on the density functional theory (DFT). The calculated formation energies for codoped systems range from −1.01 to −3.32 Ry/atom, confirming their thermodynamic stability. Furthermore, band structure calculations indicate that the undoped compounds CaTiO₃ and MgTiO₃ possess indirect band gaps of 2.766 eV and 2.926 eV, respectively. In contrast, codoping alters the electronic properties by changing the band gap from indirect to direct and reducing its energy, resulting in the direct band gap values 2.153 eV, 1.374 eV, 2.159 eV, and 1.726 eV for the compounds ${{\mathrm{C}\mathrm{a}}_8\mathrm{T}\mathrm{i}}_7{\mathrm{Z}\mathrm{r}}_1{\mathrm{O}}_{23}{\mathrm{S}\mathrm{e}}_1$, ${{\mathrm{C}\mathrm{a}}_8\mathrm{T}\mathrm{i}}_6{\mathrm{Z}\mathrm{r}}_2{\mathrm{O}}_{22}{\mathrm{S}\mathrm{e}}_2$, ${{\mathrm{M}\mathrm{g}}_8\mathrm{T}\mathrm{i}}_7{\mathrm{Z}\mathrm{r}}_1{\mathrm{O}}_{23}{\mathrm{S}\mathrm{e}}_1$, and ${{\mathrm{M}\mathrm{g}}_8\mathrm{T}\mathrm{i}}_6{\mathrm{Z}\mathrm{r}}_2{\mathrm{O}}_{22}{\mathrm{S}\mathrm{e}}_2$, respectively. Additionally, this codoping improves light absorption and optical conductivity in the visible and ultraviolet ranges. These enhancements become increasingly evident with elevated dopant concentrations, leading to intensified light–matter interactions. Analysis of the band edge potentials reveals that the Se-/Zr-codoped CaTiO₃ compounds satisfy the necessary criteria for the photodissociation of water, conferring on them an ability to generate H₂ and O₂ under light irradiation. However, under different pH conditions, Se-/Zr-codoped MgTiO₃ is expected to perform better at higher pH levels, while Se-/Zr-codoped CaTiO₃ is more effective at lower pH levels. These findings highlight the promise of codoped materials for renewable energy applications, such as solar-driven hydrogen production and optoelectronic devices, with pH being a critical factor in enhancing their photocatalytic performance. Full article

Elucidating the mechanisms of CO₂ photocatalytic conversion systems is crucial for tackling the challenges of carbon neutrality. In this study, a series of Ag@g-C₃N₄ photocatalysts were constructed with metal particle size modulation as the core strategy to systematically reveal the modulation mechanism of Ag nanoparticles (Ag NPs) size variation on the selectivity of CO₂ photoreduction products. Systematic characterizations revealed that increasing Ag size enhanced visible light absorption, promoted charge separation, and improved CH₄ selectivity. Photocatalytic tests showed Ag_3.0%@CN achieved optimal activity and electron utilization. Energy band analyses indicated that Ag modification preserved favorable conduction band positions while increasing donor capacity. Further density-functional theory (DFT) calculations reveal that Ag NPs size variations significantly affect the adsorption stability and conversion energy barriers of intermediates such as *COOH, CO and CHO, with small-sized Ag₇ NPs favoring the CO pathway, while large-sized Ag NPs stabilize the key intermediates and drive the reaction towards the CH₄ pathway evolution. The experimental and theoretical results corroborate each other and clarify the dominant role of Ag NPs size in regulating the reaction path between CO and CH₄. This study provides mechanistic guidance for the selective regulation of the multi-electron reduction pathway, which is of great significance for the construction of efficient and highly selective CO₂ photocatalytic systems. Full article

The fabrication of plasmonic nanostructures with precise geometries and scalable production remains a critical challenge for advancing light–matter interaction technologies in applications such as sensing, photonics, and thermal management. Here, we present a versatile, self-assembly-based strategy for metallic nanoring fabrication. We extend Hole-mask Colloidal Lithography (HCL) by employing ring-shaped holes to produce nanorings via direct current (DC) magnetron sputtering. The process relies entirely on industry-standard thin-film techniques, enabling wafer-scale integration. Using this approach, we fabricate copper (Cu) nanorings with tunable near-infrared (NIR) resonances suitable for thermoplasmonic applications. The thermoplasmonic performance of these nanorings is evaluated under direct sunlight, revealing efficient photon-to-heat conversion. Nanorings displayed enhanced heating, outperforming nanodisks of equivalent size, with maximum surface temperatures reaching approximately 37 °C, an increase of over 13 °C above ambient, in contrast to the 6 °C increase shown by disks that reached a temperature of 30 °C. This superior performance is attributed to the nanoring geometry, which promotes stronger light absorption and localized heating. Overall, our results demonstrate that Cu nanorings represent a robust and scalable plasmonic platform with significant potential for solar-driven technologies and thermal management applications. Full article