Search Results (850)

The development of simulated-solar-light photocatalysts for methyl orange (MO) removal is limited by insufficient light utilization, rapid photogenerated charge recombination, and restricted interfacial reaction sites. Here, vertically aligned ZnO nanorods on a conductive nanoporous Cu (NPCu) scaffold were modified with low-abundance RE-containing surface species (RE = Ce, Sm, Er, Tm, and Yb). The notation RE(OH)₃@ZnO/NPCu is retained solely as an operational sample identifier and does not constitute a crystallographic or stoichiometric phase assignment. XRD resolves the ZnO/NPCu framework, EDS confirms the local presence of RE, and XPS identifies RE-dependent oxidation state and surface oxygen environments; collectively, these measurements do not uniquely establish RE(OH)₃ or distinguish hydroxide from oxide, oxyhydroxide, and other hydroxylated/adsorbed surface configurations. The distinguishing feature is a controlled five-RE comparison on one common ZnO/NPCu architecture, together with separate evaluation of NPCu under H₂O₂-free and H₂O₂-assisted conditions. Across three independent H₂O₂-free runs, the Er-modified sample achieved 96.61 ± 0.30% MO degradation within 9 min with k_obs = 0.3930 ± 0.0071 min⁻¹. Dosage screening identified 20 μL of 40 wt% H₂O₂ in 20 mL MO solution (approximately 13.5 mM) as a practical plateau dosage. Photolysis, dark, NPCu/H₂O₂, and catalyst-removal controls support an additional solid-catalyst-dependent Cu-associated peroxide contribution while not excluding trace homogeneous reactions. Three independent cycling experiments and post-cycle SEM/XRD/EDS support operational durability, although quantitative metal leaching was not measured. Tauc, Mott–Schottky, EIS, temperature-dependent kinetic, and scavenger results are interpreted as comparative descriptors or indirect evidence rather than direct proof of intrinsic band gaps, atom-specific carrier densities, or a unique microscopic mechanism. The AI-assisted component is restricted to exploratory contextualization because reference-grouped validation shows poor out-of-reference generalization. The conclusions are confined to the tested MO system. Full article

In this work, we aim to enhance the photocatalytic performance of SrTiO₃ by constructing a heterojunction with photoactive BiOBr. The novelty of this study lies in demonstrating the dual functionality of the SrTiO₃/BiOBr heterojunction in both photocatalytic tetracycline degradation and antibacterial applications and correlating its performance with its interfacial electronic properties. A SrTiO₃/BiOBr (50STO) heterojunction was successfully synthesized by combining microwave-assisted sol–gel-derived SrTiO₃ with co-precipitated BiOBr via solid-state calcination. XRD analysis revealed that the synthesized composite consisted of crystalline cubic SrTiO₃ and tetragonal BiOBr, confirming the successful formation of a 50STO heterojunction while preserving the crystal structures of both components. PL and EIS analyses revealed modified charge-carrier behavior, further supporting the successful formation of the 50STO heterojunction. XPS confirmed the chemical states of the constituent elements and revealed changes in the surface chemical environment following the coupling of SrTiO₃ with BiOBr. SEM, elemental mapping, and UV–Vis DRS analyses demonstrated uniform elemental distribution, enhanced visible-light absorption, suppressed electron–hole recombination, and improved interfacial charge transfer. Consequently, the optimized 50STO composite achieved 45% tetracycline degradation under visible-light irradiation within 150 min, whereas pristine SrTiO₃ degraded only 2%. The apparent reaction rate constant increased from 6.11 × 10⁻⁷ to 3.2 × 10⁻³ min⁻¹, while the heterojunction remained stable over five reuse cycles. Radical scavenging and LC–MS analyses identified h⁺ and •OH as the dominant reactive species and revealed successive tetracycline degradation. The composite also exhibited excellent antibacterial activity against E. coli under white-light irradiation. Full article

Visible light communication (VLC) has emerged as a transformative optical wireless technology for sixth-generation (6G) networks, offering license-free spectrum access, inherent electromagnetic-interference immunity, high spatial confinement, and the unique ability to combine high-speed wireless connectivity with solid-state lighting infrastructure. However, the transition from conventional VLC links to practical 6G optical wireless systems requires far more than advanced modulation and signal processing. Future VLC performance will be strongly determined by the co-design of photonic front-ends, including high-speed transmitters, spectrally engineered emitters, reconfigurable optical interfaces, intelligent receivers, and energy-autonomous detection units. This article provides a comprehensive, device-centered review of photonic hardware and artificial intelligence (AI) enablers for next-generation 6G VLC systems. Particular attention is given to micro-LEDs, laser diodes, color-conversion materials, including perovskite quantum dots, advanced photodetectors, imaging receivers, wavelength-shifting fiber receivers, solar-cell-based receivers, optical reconfigurable intelligent surfaces (RISs), metasurfaces, beam-steering components, and optical wireless power transfer. This review discusses how AI can support inverse photonic design, transmitter and receiver calibration, nonlinear impairment mitigation, channel-aware beam control, and energy-aware resource management. Unlike broader VLC surveys that mainly emphasize network architecture, this article provides a device-centered perspective on AI-enabled photonic integration for 6G VLC, supported by a comprehensive survey of recent experimental demonstrations. Key challenges related to bandwidth, optical efficiency, receiver field of view, mobility, safety, standardization, and practical deployment are summarized, followed by a research roadmap for 2025–2032. Full article

Garnet-structured compounds have long been recognized as versatile host platforms for luminescent phosphors, owing to their robust chemical stability and highly tunable cationic sublattices. Conventional aluminate and gallate garnets, however, generally face intrinsic limitations, including severe concentration quenching at high dopant levels, relatively high phonon energy, and unsatisfactory efficiency for long-wavelength near-infrared (NIR) emission. In recent years, sodium-based germanate garnets, constructed by introducing aliovalent Na⁺ into dodecahedral sites combined with Ge⁴⁺ substitution in tetrahedral frameworks, have emerged as a promising branch of garnet phosphors. The aliovalent Na+ incorporation brings unique structural effects, including energy migration blocking, coordination environment distortion, and defect level modulation, which endow the materials with advantages in mitigating concentration quenching, boosting energy transfer efficiency, and enhancing thermal stability. This review systematically summarizes the crystal structure classification and luminescence fundamentals of sodium-based germanate garnet systems, and introduces mainstream synthesis techniques represented by the high-temperature solid-state method. Focusing on representative host systems, the luminescence characteristics and energy transfer mechanisms of both rare earth- and transition metal-doped systems are elaborated in detail, followed by a summary of four representative performance regulation strategies: cationic disorder engineering, crystal field engineering, defect engineering and dual-site cooperative regulation. The multifunctional applications of these materials in white light-emitting diodes, plant growth lighting, fluorescence temperature sensing, NIR imaging, and information encryption are also presented. Finally, existing challenges and future research perspectives are proposed to provide guidance for the development of high-performance garnet phosphors. Full article

The ubiquitous use of the plant hormone indole-3-acetic acid (IAA) or auxin in modern agriculture has led to its emergence as a water contaminant, necessitating efficient removal technologies. Addressing the need for high-performance sorbent materials, this study reports the synthesis and characterization of four novel nanocomposites based on halloysite (Hal), bentonite (Ben), sepiolite (Sep), and diatomaceous earth (DE) functionalized with silver nanoparticles (AgNPs). Successful immobilization and morphological features were confirmed via XRD and SEM-EDS. Crucially, post-adsorption EDS analysis provided direct solid-state evidence of pollutant capture through the distinct quantification of organic carbon. High-Performance Liquid Chromatography (HPLC) tests demonstrated that all functionalized materials exhibited a drastically enhanced IAA adsorption capacity over their pristine counterparts during a 96-h kinetic monitoring window. Kinetic profiling revealed a biphasic adsorption pathway characterized by a rapid initial sequestration within the first 10 h followed by a diffusion-limited equilibration, while thermodynamic modeling converged excellently with Langmuir and Sips equations, confirming a surface-confined chemisorption mechanism governed by uniform monolayer deposition. Notably, the performance ranking was found to be primarily governed by the architectural accessibility of the silicate frameworks rather than the absolute magnitude of their specific surface area. Furthermore, solution-phase spectroscopic studies coupled with Dynamic Light Scattering (DLS) and Zeta Potential measurements unraveled a robust, surface-confined ligand exchange mechanism. Rather than triggering colloidal aggregation, IAA coordination induced a controlled, systematic development of an organic molecular shell around the individual silver cores. This work underscores the potential of these engineered AgNPs@silicate platforms as sustainable, high-efficiency materials for the environmental remediation of emerging phytohormone contaminants. Full article

Organic pollutant degradation demands photocatalysts that couple efficient charge separation with strong redox capability. Direct Z-scheme heterojunction architectures fulfill these requirements and are consequently considered promising candidates. However, the rational design of such systems continues to present a major obstacle. Herein, a CdSe/amorphous MoSe_x (CdSe/a-MoSe_x) direct Z-scheme heterojunction was successfully synthesized via a simple solid-state grinding and low-temperature hydrothermal method. Within 120 min under visible-light irradiation, methylene blue (MB, 40 mg/L) was degraded to 97.3% efficiency by the CdSe/a-MoSe_x heterojunction, whose photocatalytic activity markedly exceeded that of pristine CdSe and a-MoSe_x. Intimate interfacial contact between CdSe and a-MoSe_x enables photogenerated carriers to separate and migrate more efficiently, underpinning the observed performance enhancement. Moreover, the suitable band alignment derived from valence-band (VB) XPS and Mott-Schottky measurements supports the formation of a direct Z-scheme charge-transfer pathway. The Z-scheme mechanism effectively inhibits electron-hole recombination while maintaining the robust oxidation and reduction capabilities of the photogenerated carriers. This study offers a straightforward approach for fabricating CdSe/a-MoSe_x direct Z-scheme heterojunctions for the efficient photocatalytic degradation of organic pollutants. Full article

Developing white organic light-emitting diodes (WOLEDs) with high exciton utilization, balanced charge transport, and stable complementary emission remains a challenge for solid-state lighting and display applications. Herein, a triplet reverse intersystem crossing (RISC)-assisted strategy is proposed to enhance triplet exciton harvesting to construct efficient hybrid WOLEDs. The increased RISC channels promote the up-conversion of triplet excitons into radiative singlet excitons, thereby improving the overall exciton utilization efficiency. By further introducing an ultrathin PO-01 layer as an orange orange-emitting component, a hybrid WOLED with a current efficiency of 49.1 cd/A and 34.8 lm/W is realized. Moreover, suppressed efficiency roll-offs and stable spectra are achieved due to balanced charge transport. This work provides a practical route toward high-performance WOLEDs. Full article

Traditional enzyme immobilization strategies often rely on chemical crosslinkers or solid carriers, thereby increasing processing complexity and potentially compromising catalytic efficiency. Here, we present a carrier-free approach for generating stable biocatalytic particles by exploiting the intrinsic aggregation behavior of four phylogenetically distinct AA10 LPMO homologues (Kpap_p40, Kari_p40, Alip_p40, and Psuf_p40) as scaffolds for catalytically active inclusion bodies (CatIBs) in Escherichia coli. Each AA10 variant was genetically fused to either mCherry or a thermostable Bacillus α-amylase (BacAmy) and expressed in E. coli BL21(DE3), resulting in the predominant formation of insoluble protein inclusion bodies (IBs). Protein partitioning was quantified by SDS–PAGE densitometry, intracellular localization by confocal microscopy, particle size and morphology by dynamic light scattering and FESEM, and secondary structure by FTIR spectroscopy. All variants assembled into submicron, structured aggregates with hydrodynamic diameters ranging from 620 to 824 nm and were enriched in α-helical and β-sheet secondary structure, consistent with the formation of structured aggregates rather than extensive amorphous misfolding. mCherry IBs retained fluorescence and displayed polar localization in vivo, while BacAmy CatIBs exhibited maximal catalytic activity at 80 °C, maintained substantial activity up to 95 °C, and demonstrated broad pH tolerance with pronounced pH stability from a slightly acidic to a mild alkaline range. FTIR analysis showed that BacAmy CatIBs contained 47–54% α-helical structure, while mCherry IBs contained 42–45% α-helical structure, indicating the preservation of partially native protein conformations within the aggregated state. Differences among variants influenced particle size, dispersity, and aggregate morphology. These findings demonstrate the potential of AA10 LPMO domains as versatile structural modules for engineering thermostable, carrier-free biocatalysts and provide a foundation for expanding their application beyond oxidative polysaccharide cleavage toward sustainable enzyme material design. Full article

A novel Dy³⁺-doped self-activated Sr₂NaMg₂V₃O₁₂ (SNMVO) phosphor was synthesized via a high-temperature solid-state reaction method. Its microstructure, surface morphology, valence state, and luminescence properties were investigated. The results showed that the prepared phosphor exhibited bright green emission at 521 nm and yellow emission at 575 nm under 345 nm excitation. The luminescence intensity showed a strong concentration dependence, with an optimal Dy³⁺ ion doping concentration of 0.05 mol, and the concentration quenching (CQ) mechanism was dipole–dipole (d-d) interaction. Energy transfer between vanadate and Dy³⁺ was observed, with a maximum transfer efficiency of 63.5%. The thermal activation energy (0.1859 eV) indicated good thermal stability. Furthermore, this phosphor can be used as a yellow phosphor for white light-emitting diodes (wLEDs) and for anti-counterfeiting patterns. Full article

Against the backdrop of energy conservation and environmental protection, developing more stable and efficient phosphors has become an urgent challenge. In this study, we have synthesized a series of Ca_2.5Hf_2.5Ga₃O₁₂:Eu³⁺ (CHGO:Eu³⁺) red phosphors via a high-temperature solid-state method, which exhibit strong red emission at 610 nm under 394 nm excitation, corresponding to the ⁵D₀→⁷F₂ transition of Eu³⁺. To improve the lattice vacancies caused by charge imbalance when Eu³⁺ is doped into the CHGO lattice to replace Ca²⁺, we introduce the charge compensator M⁺ (M = Li, Na, K). The results of the emission spectrum show that the introduction of charge compensators can effectively improve the luminescence intensity. Among them, K⁺ has the most significant effect on increasing the emission intensity of Eu³⁺, making the emission intensity of the phosphor more than twice that when there are no charge compensation ions. Additionally, the quantum efficiency and thermal stability of these phosphors are significantly improved compared to the CHGO:0.075Eu³⁺ sample before substitution. At 423 K, the emission intensity of the CHGO:0.075Eu³⁺, 0.075K⁺ sample still remains at 88.7% of that at 298 K. The color rendering index of the prepared white LED is 81.2, and its CIE chromaticity coordinates are (0.3212, 0.3065). This indicates that the prepared CHGO:0.075Eu³⁺, 0.075K⁺ red phosphor has broad application prospects in solid-state lighting. Full article

Copper complexes have recently emerged as key materials for advancing dye-sensitized solar cells (DSSCs) toward more sustainable and high-performance photovoltaic technologies. This minireview summarizes the most significant achievements reported from 2024 onwards, highlighting the multifaceted role of copper in DSSCs as sensitizers, redox mediators, and functional components in innovative device architectures. Significant progress has been achieved in all these roles; however, the most remarkable advances concern copper-based redox mediators, where fine-tuning of ligand environments, additives, and electrolyte formulations has enabled excellent efficiencies, exceeding 10%, together with outstanding long-term stability. Developments in aqueous and quasi-solid-state systems further enhance the environmental compatibility and durability of these devices. In addition, novel concepts, including retro cells and copper-based “zombie” DSSCs, demonstrate the versatility of copper chemistry in simplifying device design and enabling new applications. Overall, these findings confirm copper complexes as highly promising earth-abundant alternatives to noble-metal-based systems although further work is still required to optimize light absorption, suppress charge recombination, and improve large-scale device stability. Full article

Tritium breeding blanket is a key component of future fusion power plants, and its performance depends on the selection, fabrication, and qualification of lithium-based ceramic material. Among the proposed lithium ceramics materials, the main candidates for ceramic breeders are lithium orthosilicate (Li₄SiO₄) and lithium metatitanate (Li₂TiO₃). These advanced ceramics and their biphasic composites are the leading candidates due to their high lithium density, favorable tritium breeding ratio (TBR ≈ 1.15–1.25 with Be₁₂Ti multiplier and 90% ⁶Li enrichment), and robust thermo-mechanical behavior within the 200–900 °C operational window of helium-cooled pebble bed (HCPB) blankets. This review provides an engineering-oriented assessment covering fabrication routes (solid-state, hydrothermal, melt-based, drip casting, powder injection molding, microwave sintering, and digital light processing additive manufacturing); microstructure–property relationships and performance under neutron irradiation; and tritium generation, retention, and release as functions of chemical composition, defect structure, and operating temperature. Induced radioactivity of Li-based ceramics and key impurity elements is quantified using activation formalisms applied to WWR-K reactor conditions, providing guidance for raw-material selection and waste-management assessment. Authors’ original contributions include (i) an empirical model of pebble crush load vs. biphasic composition (R² > 0.99); (ii) two universal semi-empirical kinetic models (exponential growth and non-linear strength degradation, R² = 0.97–0.99) for nine structural and mechanical parameters of Li₂TiO₃ under He²⁺ and H⁺ irradiation; (iii) a consolidated table of Arrhenius tritium diffusion parameters from reactor experiments and DFT; and (iv) an induced radioactivity calculation for the biphasic system with two-exponential post-irradiation decay analysis. The review identifies biphasic Li₄SiO₄–Li₂TiO₃ composites with ~30 ± 5 mol.% Li₂TiO₃ as particularly promising and formulates specific data gaps and modeling needs for the reliable deployment of ceramic breeder pebbles in helium-cooled fusion blanket systems. It should be specifically noted that Li₄SiO₄ pebbles fabricated via the melt method, as an example, typically exhibit exceptionally high densities, generally exceeding 90% of the theoretical density (TD). Building on the calculation of induced radioactivity, it is crucial to consider the microstructural distribution of highly radioactive nuclides (e.g., Co, Mn) within the ceramic matrix. If these impurities segregate at grain boundaries rather than being homogeneously distributed, there is a potential pathway to develop targeted wet-chemical methods, such as selective acid leaching, to remove these impurities post-irradiation, thereby lowering the waste disposal classification. Full article

Background/Objectives: α-lipoic acid (ALA) shows therapeutic potential but faces poor aqueous solubility (BCS Class II), gastric instability, and low oral bioavailability (~30%). This work investigated the formulation of cyclodextrin (CD) inclusion complexes of ALA to overcome the aforementioned limitations and improve nutraceutical applications. Methods: Phase solubility studies in simulated gastric and intestinal fluids screened for optimal CD, followed by molecular dynamics simulations and MM-PBSA binding free energy calculations. Inclusion complexes of choice were prepared by grinding, spray-drying, and lyophilization, followed by solid-state characterization (DSC/XRPD/FTIR). Further analysis was performed using pH-shift dissolution (USP II), permeability (PermeaPad^®, Caco-2), and (photo)stability according to ICH. Results: Hydroxypropyl-β-cyclodextrin (HPβCD) emerged as the optimal host due to favorable complexation, as confirmed by phase solubility studies and supported by molecular modeling, which revealed a favorable balance between inclusion complex stability and pH-triggered drug release. Formulations based on spray-dried and lyophilized HPβCD–ALA complexes (HPβALA-sd and HPβALA-lyo), in which ALA was fully amorphized, achieved near-complete dissolution within five minutes under biorelevant pH-shift conditions. This performance markedly exceeded that of free ALA (approximately 66% dissolution at pH 7.4) while maintaining moderate permeability (Papp 8–9 × 10⁻⁶ cm/s). Storage stability was enhanced markedly (88–90% ALA retention after 6 months at 40 °C/75% RH vs. 36% for free ALA) while UV stability was not improved through CD-complexation, probably due to interaction of UV-VIS light with the exposed portion of ALA. Conclusions: Even though the permeability of ALA–CD inclusion complexes remained medium (Papp ~ 8–9 × 10⁻⁶ cm/s) and unaffected by complexation, a significantly improved dissolution profile indicates better expected bioavailability compared to pure ALA. Full article

Photosynthetic biogas upgrading (PBU) using microalgae is a promising biological approach for converting raw biogas into biomethane while recovering nutrients and fixing part of the biogenic CO₂ into algal biomass. Unlike conventional physicochemical technologies, which mainly separate CO₂ from CH₄, PBU can combine gas upgrading with wastewater or digestate treatment, nutrient recycling, and biomass production. This review assesses the current state of PBU technology, with particular emphasis on high-rate algal ponds, absorption columns, and closed photobioreactors. It examines the main operating parameters that control gas–liquid mass transfer, carbonate buffering, and photosynthetic activity, including the liquid-to-gas ratio, pH, alkalinity, temperature, light regime, light intensity, and gas retention time. Special attention is given to the combined effects of the L/G ratio, pH, and alkalinity, as these parameters strongly influence CO₂ absorption, CH₄ enrichment, and O₂ contamination of the upgraded gas. The use of wastewater or anaerobic digestate instead of synthetic growth media is identified as an important sustainability advantage, particularly at wastewater treatment plants with existing anaerobic digestion and nutrient-rich side streams. However, digestate use may also create operational challenges related to turbidity, ammonium inhibition, solids, and variable composition. Available studies indicate that PBU may reduce operating costs and greenhouse gas emissions under favorable conditions while creating additional value from algal biomass. Nevertheless, wider deployment is still limited by high land requirements, seasonal variability, O₂ contamination, biomass harvesting, and limited evidence from large-scale systems. Future development should therefore focus on improved oxygen management, more efficient reactor designs, nanoparticle-assisted enhancement of photosynthetic activity, better integration with wastewater treatment, and AI-supported monitoring and control to improve process stability and support scale-up. Full article

Single-molecular white circularly polarized luminescence emitters show promise for use in chiral displays and solid-state lighting, but their design remains challenging because broadband emission, exciton utilization, color balance, and chiroptical activity must be integrated within one molecule. Herein, we report a chiral single-molecular white emitter, DCz-PTZ, constructed through a π-interrupted strategy by combining a rigid spiro framework, an oxygen-bridged carbazole/cyanobenzene segment, and a phenothiazine donor. The interrupted conjugation suppresses excessive charge-transfer (CT) domination and enables dual emissive channels, including short-wavelength locally excited (LE) emission and long-wavelength CT emission. DCz-PTZ exhibits near-ideal white emission in dilute toluene solution with CIE coordinates of (0.33, 0.33), and maintains balanced dual emission in 5 wt% doped films with CIE coordinates of (0.32, 0.34). Photophysical studies support the assignment of the yellow emission to a thermally activated delayed fluorescence (TADF)-active CT state. The enantiomers show mirror-image circularly polarized signals with |g_lum| up to 2.9 × 10⁻³. Optimized white organic light-emitting diodes (WOLEDs) achieve color rendering index (CRI) up to 92 and a maximum external quantum efficiency (EQE_max) of 1.3%. This work demonstrates a π-interrupted molecular strategy for integrating dual emission, TADF exciton utilization, and circularly polarized electroluminescence (CPEL) in a single chiral emitter. Full article