Light Stability Research Articles

Feasible estimation of weathering stability for free film acrylic coatings via dynamic mechanical analysis as the sole characterization method

AbstractWeathering stability is a highly relevant materials property, especially for exterior coatings. Assessment of artificially or naturally weathered coatings is however still mostly subjective without distinct correlation between the formulation of a coating and its weathering stability. An aggravating issue in the industrial context is the often very sparse information on the exact chemical composition of materials by the manufacturers. In this study, a quantitative method to examine weathering-induced changes in coatings with limited chemical information is described, which is based solely on dynamic mechanical analysis (DMA). This approach is applied to free films to eliminate possible influences of the substrate during the measurement. The effects of artificial weathering on three exemplary acrylic waterborne wood coatings are then examined and compared to the results of state of the art artificial weathering. Precisely, the impact of additional light stabilizer on mechanical properties, molecular weight, and Tg is monitored. For the exemplary systems, it could be shown that the molecular weight of the polymers decreases during artificial weathering, where the most prominent decrease was observed in the first 300 h. In the same time frame, E′ and E″ also decrease, while the glass transition temperature increased dependent of the formulation by 6–15°C. Remarkably, for coatings without light stabilizer an apparent two-staged degradation mechanism is observed, which leads to an increase of E′ and E″ after 600 h of artificial weathering, accompanied with an increased brittleness of the free film. The primary goal of this approach is to offer a tool for quick and systematic investigation of new coating formulations in the industrial context.

Self‐reduction triggered color tuning of Eu3+‐doped aluminosilicate glass for solid‐state white illumination

AbstractRare earth‐doped transparent glass, boasting high transmittance and excellent luminescent properties, holds great potential in the field of all‐inorganic solid‐state white illumination. Currently reported single‐structure solid‐state white lighting usually has the problems of low color rendering index (CRI) and high correlated color temperature (CCT) due to the lacking of red light emission. In this work, a novel single‐structure MgO–Al2O3–SiO2–Eu2O3 (MAS: Eu) glass with color tuning was prepared by the simple glass melting process. Interestingly, the prepared Eu3+‐doped aluminosilicate glass possessed a unique capability to achieve color emission under different excitation wavelengths. The reason for this was attributed to the good self‐reduction capability of the MAS glass, which effectively reduced Eu3+ to Eu2+ under an air atmosphere. Meanwhile, only by regulating the Eu3+ doping concentration, the MAS glass also achieved a tunable emission from blue to white to red light under 380 nm excitation. The acquisition of white light was realized through the multispectral emission of blue–green light emitted by Eu2+ and orange–red light emitted by Eu3+. Remarkably, the single‐structure MAS glass doped with 8 wt.% Eu3+ successfully achieved high‐quality white light and high thermal stability, exhibiting a high CRI of 86, a low CCT of 2761 K, good chromaticity parameters of (0.407 and 0.3192), and the emission intensity at 423 K remains above 86.35% that of room temperature. Meanwhile, the doped Eu3+ exceeded 12 wt.%, without any observable concentration quenching. Moreover, the MAS: Eu glass showed a high transmittance of 90 and a moderate thermal conductivity of 1.45 W/mK (epoxy resin ∼0.17 W/mK). These results would dramatically inspire the development of high‐quality solid‐state white lighting applications.

Stable Organic‐Inorganic Hybrid Sb(III) Halide Scintillator for Nonplanar Ultra‐Flexible X‐Ray Imaging

AbstractFlexible scintillator screens with excellent stability and low detection limits are crucial for X‐ray imaging applications. 0D organic metal halide materials have emerged as a strong contender in the scintillator fields, owing to their excellent optical characteristics and simple maneuverability. Herein, high‐quality and large quantities of C38H36P2Sb2Cl8 single crystals are synthesized through a simple solution approach. The prepared single crystals with dimer‐structure [Sb2Cl8]2− exhibit yellow emission with a near‐unity high photoluminescence quantum yield (PLQY) of 99.8%, and possess an exceptional light yield of 41300 photons MeV−1, and a detection limit as low as 45.6 nGyair s−1. On this basis, a large‐size and ultra‐flexible C38H36P2Sb2Cl8 scintillator utilized for X‐ray imaging is prepared by template assembled method, demonstrating a high spatial resolution of 8.15 lp mm−1. The prepared ultra‐flexible scintillator screen can achieve excellent X‐ray imaging even after multiple bending and stretching, which can also provide clear non‐planar X‐ray imaging for irregular objects. In addition, the scintillator shows excellent stability in light, heat, X‐ray irradiation, and water. These results not only expand the optoelectronic application field of organic‐inorganic hybrid antimony halides but also promote the rapid development of efficient ultra‐flexible scintillators.

White Light Generation and Stability Analysis of High-Power Blue LDs with Remote YAG Phosphors

This paper presents a comprehensive analysis of white light generation and the associated aging dynamics using high-power blue laser diodes (LDs) combined with transmissive single crystal remote YAG phosphors. By systematically varying input currents (ranging from 0.6 A to 3 A) and phosphor thicknesses (250 μm and 500 μm), this study elucidates the optical and electrical characteristics of LD-phosphor systems under diverse operating conditions. The results highlight the system’s potential for stable and efficient white light generation, making it suitable for high-power lighting applications. Experimental setups included both single LDs and a 4 × 2 LD array. For the single LD, a peak optical output of 4.16 W was achieved at 3 A, corresponding to an initial luminous flux of approximately 700 Lm and a correlated color temperature (CCT) of 4653 K, with minimal color temperature shift observed during a 60 min aging process. The 4 × 2 LD array demonstrated consistent white light output across varying phosphor thicknesses, with maximum luminous fluxes of 1857 Lm at 1.4 A and 2622 Lm at 1.6 A for phosphor thicknesses of 250 μm and 500 μm, respectively. Importantly, the phosphor exhibited excellent thermal stability throughout the aging process, with the CCT maintained within a range of 4600 K to 5500 K. These findings underscore the reliability and applicability of LD-based white light systems in demanding high-power lighting environments, offering a promising alternative to conventional light sources for automotive, industrial, and specialized lighting applications.

Utilization of soybean protein isolate hydrolysates as carriers: Improved encapsulation efficiency and stability of curcumin

This study aimed to explore the potential of soybean protein isolate hydrolysates (SPIH) prepared via Alcalase as delivery carriers and develop novel SPIH-Cur nanoparticles. Hydrolysis caused the varying degrees degradation in the 7S and 11S subunits, significantly enhancing SPI's antioxidant activity. The reduction in particle size and the exposure of hydrophobic groups in SPIH contributed to the formation of stable SPIH-Cur nanoparticles, due to their well binding capacity to curcumin (Cur). The 30 min SPIH-Cur sample exhibited the highest encapsulation efficiency (83.09 %), owing to its high binding affinity (Ka = 9.56 × 103 M−1). Encapsulation by SPIH also significantly improved Cur's thermal and light stability. Moreover, FTIR, fluorescence spectra, and molecular docking analyses revealed that the formation of SPIH-Cur were primarily driven by hydrophobic forces and hydrogen bonds. Above results provide a foundation for fabricating nanoparticles that deliver lipophilic bioactive compounds with high encapsulation efficiency and stability derived from SPIH.

7-(Diethylamino) coumarin-3-carboxylic acid as a novel antibrowning agent: Activity and mechanism

Browning caused by polyphenol oxidase (PPO) and microorganisms significantly impacts the nutritional quality of fruits and vegetables. This study identified 7-(Diethylamino) coumarin-3-carboxylic acid (7-DCCA) as an effective inhibitor of both PPO and bacteria. Enzyme assays revealed that 7-DCCA competitively inhibits PPO activity with an IC50 value of 0.275 ± 0.002 mM. Fluorescence and molecular simulation methods demonstrated that 7-DCCA forms a complex with PPO through hydrogen bonding and hydrophobic interactions, altering the enzyme's structure and reducing its activity. Thermogravimetric and differential scanning calorimetry (DSC) assays showed that 7-DCCA stabilizes PPO, delaying its thermal decomposition. Antibacterial tests proved that 7-DCCA inhibits Staphylococcus aureus and Escherichia coli by disrupting cell membranes. Additionally, 7-DCCA suppressed PPO and peroxidase activities, delaying phenolic oxidation and preventing browning in fruits and vegetables. Cytotoxicity assays confirmed its safety, with over 85 % cell viability at concentrations up to 0.1 mM. Stability experiments verified that 7-DCCA had greatly light and thermal stability. This study highlighted 7-DCCA as a promising antibrowning agent with potential application in food preservation.

Fabrication and characterization of curcumin-encapsulated composite nanoparticles based on soybean protein isolate hydrolysate/soybean polysaccharides: Interaction mechanism, stability and controlled release properties

This study developed a stable nanoparticle (CUR-SPIH/SSPS) using soybean protein isolate hydrolysate (SPIH) and soybean polysaccharides (SPSS) to protect curcumin (CUR) from degradation during storage and exposure to light and heat conditions, achieving controlled release. The SPIH to SPSS mass ratio of 5:1 gave the CUR-SPIH/SPSS nanoparticles with the highest CUR encapsulation efficiency (95.60 ± 3.00 %) and the strongest antioxidant capacity (90.26 ± 2.42 % and 66.78 ± 1.89 % for ABTS•+ and DPPH radical scavenging ability, respectively), and CUR was successfully encapsulated within the CUR-SPIH/SPSS as evidenced by X-ray diffraction. FTIR and fluorescence spectroscopy analysis confirmed that the interactions in CUR-SPIH/SPSS are primarily driven by electrostatic, hydrogen bonding, and hydrophobic interactions. Moreover, the CUR-SPIH/SPSS nanoparticles significantly enhanced CUR's thermal and UV light stability. The UV degradation kinetics showed that the half-life of CUR-SPIH/SPSS (247.55 min) was 1.61 times longer than that of free CUR (154.03 min). The release rate of CUR incorporated into CUR-SPIH/SPSS was significantly delayed during in vitro gastrointestinal digestion. This study introduces an innovative nanoparticle strategy for the stable delivery of lipophilic compounds.

Erbium chloride‐mediated nucleation/crystallization control for high‐performance tin‐based perovskite solar cells

AbstractTin‐halide perovskite solar cells (THPSCs), while offering low toxicity and high theoretical power conversion efficiency, suffer from inferior device performance compared to lead‐based counterparts. The primary limitations arise from challenges in fabricating high‐quality perovskite films and mitigating the oxidation of Sn2+ ions, which leads to severe non‐radiative voltage losses. To address these issues, we incorporate the rare‐earth element erbium chloride (ErCl3) into PEA0.15FA0.70EA0.15SnI2.70Br0.30 perovskite to effectively control the nucleation and crystal growth, significantly influencing the morphology of the perovskite films. As a result, the ErCl3‐processed THPSC exhibits an impressive open‐circuit voltage (VOC) of 0.83 V and power conversion efficiency (PCE) of 14.0% with the superior light and air stability, compared to the control device (VOC = 0.77 V and PCE = 12.8%). This ErCl3‐strategy provides a feasible solution for high‐performance THPSCs by regulating nucleation/crystallization kinetics and mitigating excessive crystal defects during the preparation process of lead‐free perovskites.image

Solid‐phase synthesis of grafted carbon black for superior aging resistance in biodegradable poly(butylene adipate‐co‐butylene terephthalate) composite films

AbstractBiodegradable films mitigate plastic pollution but often lack UV‐aging resistance, shortening their lifespan. While anti‐aging additives can boost the films' durability, small molecule migration constrains the extension of their service life. This study introduces a straightforward solid‐phase reaction for producing carbon black (CB) grafted with the UV absorber UV531, termed CB‐UV531. This material was then blended with the biodegradable polymer PBAT and transformed into a film via blow molding, yielding a durable UV‐resistant biodegradable film (PBAT/CB‐UV531). This solid‐phase grafting reaction does not require any solvents, thereby reducing solvent contamination and waste, and it is simple to operate, allowing for scalable production. Compared to the unmodified CB, the obtained CB‐UV531 exhibits significantly improved thermal stability, which can effectively reduce the loss of UV531 during the subsequent high‐temperature film‐blowing process. Furthermore, the chemically bonded UV absorber on the surface of CB‐UV531, coupled with its reduced particle size, promotes enhanced dispersibility and consistent stability within the PBAT/CB‐UV531 film, markedly improving its long‐term resistance to UV aging. This method is expected to enhance the anti‐aging effects of various commercial light stabilizer additives and can be used to extend the lifespan of different biodegradable materials.Highlights A simple solid‐phase reaction method was developed to prepare CB‐UV531. CB‐UV531 reveals smaller size and superior dispersibility. Biodegradable PBAT/CB‐UV531 film was prepared via a blowing process. UV531 migration loss in PBAT/CB‐UV531 film is significantly reduced. PBAT/CB‐UV531 film shows enhanced thermal stability and aging resistance.

Anion regulation for surface passivation enables ultrahigh-stability perovskite nanocrystals.

All-inorganic perovskite CsPbBr3 nanocrystals (NCs) display high photoluminescence quantum yield and narrow emission, which show great potential application in optoelectronic devices. However, the poor environment stability of NCs will hinder their practical application. Herein, a series of ionic liquids with different anions (BF4-, Br-, and NO3-) were used as a sole capping ligand to synthesize NCs. Among the three samples, 1-hexadecyl-3-methylimidazolium tetrafluoroborate ([C16MIM]BF4) capped NCs have the highest stability in light, thermal, and water, possibly attributing to the in situ passivation of bromine vacancy via pseudohalogen BF4- and tight binding of ionic liquid ligands and lead atoms. In addition, green-emission [C16MIM]BF4 NCs were used to assemble a white light-emitting diode device, and it possessed a wide National Television System Committee color gamut of 124.5% and a stable emission peak at high driving currents of 380 mA. This work paves the way for resurfacing perovskite NCs with ultrahigh stability, thereby driving the perovskite NC display industry closer to real-world application.

Colloidal Synthesis of Blue-Emitting Cs3TmCl6 Nanocrystals via Localized Excitonic Recombination for Down-Conversion White Light-Emitting Diodes.

Lead-halide perovskite nanocrystals (NCs) have gained significant attention for their promising applications in lighting and display technologies. However, blue-emitting NCs have struggled to match the high efficiency of their red and green counterparts. Moreover, many reported blue-emitting perovskite NCs contain heavy metal lead (Pb), which poses risks to human health and the environment. In this study, we synthesized rare-earth-based Cs3TmCl6 NCs via the hot injection method, which exhibit a broadband blue emission at 440 nm. Combined experimental and theoretical studies indicate that the broadband emission in Cs3TmCl6 arises from self-trapped excitons due to the excited-state structural distortion of the [TmCl6]3- cluster. Furthermore, the ultrafast dynamics of charge carriers were analyzed using time-resolved photoluminescence and transient absorption measurements. Encouraged by the remarkable thermal, light, and water stabilities of Cs3TmCl6 NCs, as evidenced by experimental and theoretical results, a white light-emitting diode was further designed and fabricated using the Cs3TmCl6 NCs as the color converter. The device exhibits outstanding performance, achieving a long half-lifetime of 336 h and a large color-rendering index of 87.0. Combining eco-friendly features and a facile synthesis method, the rare-earth-based Cs3TmCl6 NCs mark a significant breakthrough as a reliable blue emitter, showcasing their future potential in lighting and display applications.

Separation and purification of antimicrobial substances from Paenibacillus polymyxa KH-19 and analysis of its physicochemical characterization.

Soft rot is one of the top ten most dangerous plant pathogens in agricultural production, storage, and transport, and the use of microorganisms and their metabolites to control soft rot is a current research hotspot. In this study, we identified the antimicrobial substance in the metabolite of Paenibacillus polymyxa KH-19, and determined that the antimicrobial substance of this strain was an active protein. The protein was completely precipitated at 40-60% ammonium sulphate saturation and showed good inhibitory effects against seven pathogenic bacteria including Pectobacterium carotovorum BC2 and seven pathogenic fungi including Pyricularia oryzae. The MIC of the protein was 51.563µg/mL, temperature acid-base UV and light stability insensitive to protease, with high-temperature resistance. The antimicrobial protein was isolated and purified by DEAE-anion exchange column and Sephadex G-75 gel filtration chromatography, and the LC-MS/MS assay identified the protein as lysophosphatidyl esterase with a molecular weight of 25.255kDa. The purified antimicrobial protein increased the inhibitory effect against P. carotovorum BC2, with the diameter of the circle of inhibition being 26.50 ± 0.915mm. Bioinformatics analysis showed that the protein has the molecular formula of C1117H1732N316O338S5, encodes 224 amino acids, has an aliphatic index of 88.39, and belongs to the category of hydrophilic unstable proteins. The present study is the first report of an active protein with extreme thermoplastic and resistance to P. carotovorum BC2, which provides a reference for the preparation and application of the antimicrobial substances of P. polymyxa KH-19, as well as a theoretical basis for the study of the function of lysophosphodiesterase protein and its use as a microbial preparation.

Dopant-Free Hole Transport Material Based on Non-Covalent Interaction for Efficient Perovskite Solar Cells.

Hole transport materials (HTMs) have a critical impact on the performance of perovskite solar cells (PSCs). Especially, the dopant-free HTMs could avoid the usage of hygroscopic dopants and reduce costs, which are important for device stability. Most of the current organic dopant-free HTMs are polycyclic aromatic hydrocarbons-based planar conjugated structures. Yet, the synthesis of conjugated fused heterocycles is often complicated. In this work, intramolecular non-covalent interaction is introduced to construct two organic HTMs (DCT and DTC), which can be facilely obtained through simple reactions. Compared to DTC with hexyl chain on the central benzene ring, DCT with hexyloxy chains shows better planarity in the core structure, as a result of the intramolecular non-covalent interactions between oxygen on hexyloxy and sulfur atom on the adjacent thiophene, as reflected from its single crystal structure. Moreover, DCT in a pristine state shows a decent hole mobility comparable to the doped Spiro-OMeTAD. Ultimately, conventional devices using dopant-free DCT as HTM show a high efficiency of 22.50%, with excellent long-term stability, and light and thermal stability. The results show that the noncovalent interaction is a useful and simple design strategy for dopant-free HTMs, that can effectively improve the efficiency and stability of PSCs.

Multidentate Polymer-Stabilized Buried Interface for Efficient Planar Perovskite Solar Cells.

Buried interface engineering is crucial to improve the performance and stability of perovskite solar cells (PSCs). Although coordination materials have been widely used for buried interface modification, they are generally engineered on one surface of the interface through monodentate or bidentate molecules. Here, we propose that a multidentate polymer, sodium alginate (SA), acts with both surfaces via numerous C═O groups to reinforce buried interfaces. SA effectively reduces buried interface defects, adjusts the energy level alignment, and refines carrier dynamics. Notably, it also induces the growth of a perovskite film that is less tensile stressed and free of voids. Consequently, the champion device efficiency after SA treatment increased from 23.05% to 24.98%, along with significant improvements in both light and thermal stability. This work offers insights into efficiency and stability improvement from the perspective of multidentate polymer anchoring.

Multidimensional Exploration of Wood Extractives: A Review of Compositional Analysis, Decay Resistance, Light Stability, and Staining Applications

Extractives, which naturally evolve as fundamental defense mechanisms in wood against environmental stresses, hold an essential place in the field of wood conservation science. Despite their low content in woody substrates, extractives are chemically complex and can be extracted accurately by solvents with different polarities, covering key components such as aliphatic, terpenoid, and phenolic compounds. The application of solvent extraction allows for the effective recovery of these extracts from forestry waste, thereby creating new opportunities for their reuse in wood modification and enhancing the economic value and potential applications of forestry waste. In the wood industry, extractives not only act as efficient preservatives and photo-stabilizers, significantly improving the decay resistance and photodegradation resistance of wood, but also serve as ideal dyes for fast-growing wood due to their abundant natural colors, which lend the product a distinct aesthetic appeal. The aim of this paper is to provide a comprehensive review of the origin and distribution characteristics of wood extractives and to examine the impact of solvent selection on extraction efficiency. At the same time, the mechanism of extractives in enhancing wood decay resistance and slowing down photodegradation is deeply analyzed. In addition, specific examples are presented to illustrate their wide utilization in the wood industry. This is intended to provide references for research and practice in related fields.

Bi2O2.33/Bi4O5I2-heterojunction photocatalysts for adsorption and visible light-driven degradation of pharmaceutical pollutants

This study introduces the innovative Bi4O5I2/Bi2O2.33 heterojunction for diclofenac (DF) degradation. Pharmaceutical pollutants, especially DF, pose significant threats to water sources, necessitating efficient treatment methods. Bi2O2.33, renowned for its unique ferromagnetic properties, emerges as a promising photocatalyst for pollutant degradation. Bi4O5I2, known for strong visible light absorption and stability, holds potential for environmental applications. Interestingly, the inclusion of titanium dioxide (TiO2) in the composite catalysts significantly influences their observed ferromagnetic properties, as revealed by Electron Paramagnetic Resonance (EPR) spectroscopy, by influencing the interactions within the Bi4O5I2/Bi2O2.33 heterojunction and influencing its structure, morphology, and spin behavior. This interaction results in enhanced EPR and Ferromagnetic Resonance (FMR) signals, indicating intriguing spin interactions, polarization effects, charge transfers, surface dynamics, and stabilized magnetic domains. While the enhanced ferromagnetism holds promise for efficient charge separation and potential applications in environmental remediation, the expected boost in visible light-driven activity was not fully realized. This limitation is attributed to TiO2 inherent inability to directly absorb visible light, hindering its utilization for enhanced photocatalysis within the heterojunction. Nevertheless, these findings elucidate the multifaceted role of TiO2 in modulating the magnetic properties of these catalysts, offering valuable insights for future advancements in the design of advanced photocatalysts for effective environmental remediation.

Physico‐chemical characterisation and light stability of dyes and pigments found in cultural heritage objects: Insights from microfading testing for assessing light fastness

AbstractUnderstanding the chemistry of dyes and pigments found in cultural heritage objects and their permanence is central for their preservation. Heritage science research has generally focused on either identification of materials present on actual objects or accelerated and natural ageing of mock‐up samples prepared using historically accurate methods to simulate the materiality of cultural heritage objects. A more recent strategy is the integration of these two research areas, which provides a holistic approach to assess both the chemical composition and stability of materials. Over the last 30 years, microfading testing (MFT) has notably contributed to understanding materials' responsiveness to light, minimising damage to objects from museum lighting and revealing insights into molecular structures of dyes and pigments, when employed in conjunction with other techniques. By combining MFT with diverse analytical methods, including imaging, spectroscopy, microscopy and chromatography, a more comprehensive approach is achieved. This joined‐up strategy contributes to improved decision‐making processes in the conservation and preservation of cultural heritage objects.

Evaluation of the Thermal and Light Stability of β-Carotene Extracted from Mauritia flexuosa Using Ionic Liquid

The growing concern over the adverse effects of synthetic dyes has generated interest in the use of natural pigments by the food industry. β-carotene, a carotenoid found in various plant sources, is recognized for its antioxidant properties and provitamin A activity. The fruit of the buriti palm (Mauritia flexuosa), which is particularly rich in β-carotene, serves as a significant natural source of this pigment. This study aimed to extract β-carotene from buriti fruit using ionic liquids as an alternative to conventional organic solvents like acetone. β-carotene content was determined by HPLC and showed that extraction with [C4mim] [BF4] not only improved β-carotene extraction efficiency compared to acetone (19.21 and 13.13 mg/100 g, respectively) but also provided greater pigment stability during light, thermal and color stability tests. Moreover, ionic liquids are aligned with the principles of green chemistry and offer a sustainable and safe alternative for the food industry. Its favorable characteristics not only reduce environmental impacts associated with conventional solvents, but also ensure an increase in the shelf life of natural dyes, thus promoting the safety and quality of food products.

Defect passivation with spectral shift for improved efficiency and stability of quasi-2D blue perovskite light emitting diodes

Metal halide perovskites are emerging as promising materials for next-generation light-emitting diodes (LEDs), owing to their cost-effectiveness, facile manufacturing, and excellent optoelectronic properties including a narrow emission-line full width at half maximum, high photoluminescence quantum yield, and spectral stability. However, blue-emission perovskite LEDs (PeLEDs) exhibit perovskite phase segregation and halogen ion migration during operation, attributed to crystal defects, halogen vacancies, and phase instability of mixed-halide perovskites. These defects compromise the spectral stability of blue-emitting PeLEDs, resulting in an undesirable color shift toward longer wavelengths. In this study, we introduce a dynamic treatment with phenylphosphonic dichloride (PPOCl2) to address these challenges and achieve blue-emitting PeLEDs. The chloride in PPOCl2 penetrates the quasi-2D sky-blue perovskite, reducing halide defects. Meanwhile, the phosphonic group forms covalent bonds with undercoordinated Pb on the perovskites, effectively passivating defects. PPOCl2-treated perovskite exhibits a spectral blue shift toward a deep-blue wavelength (≤467 nm), enhancing electroluminescence performance. The quasi-2D PPOCl2-treated PeLEDs achieve a maximum external quantum efficiency of 2.31 % with an emission peak at 488 nm. Dynamic treatment with PPOCl2 shows the potential to improve the performance and stability of blue emission perovskite-based LEDs, providing a spectral shift mechanism to achieve deep-blue emission in PeLEDs.

Wet-chemical preparation and physicochemical characterization of nanostructured Zn-Bi2O3/CeO2 composite: A visible-light-driven catalyst for the annihilation of pharmaceutical pollutant

A modified co-precipitation technique assisted with cetyltrimethylammonium bromide (CTAB) surfactant was used to synthesize a nanostructured and zinc-doped mixed metal oxide (Zn-Bi2O3/CeO2) composite. Using X-ray diffraction (XRD), the synthesized nanocomposite was studied in terms of its crystal structure, grain size, percentage crystallinity, and percentage porosity. Energy dispersive X-ray elemental analysis (EDX) was used to ascertain the chemical composition, SEM to confirm the creation of nanostructure material, and Fourier transform infrared spectroscopy (FTIR) to extract the existing functional groups. Investigation of light harvesting properties (UV/Vis) and thermogravimetric analysis (TGA) reveals that the doped composite exhibits a band gap driven by visible light and remarkable thermal stability at high temperatures. The pH value at which a material's net charge is zero, known as pHpzc, is 7.93 for the doped mixed metal oxide composite. The Zn-Bi2O3/CeO2 nanocomposite effectively eliminates 98.4 percent of the quinolone antibiotic (levofloxacin) via a mechanism that integrates sorption and photocatalytic degradation induced by visible light. To determine the optimal circumstances for the efficient operation of a photocatalyst, we experimented with different time intervals, beginning drug concentrations, catalyst dosages, operating temperatures, and pH levels. Reusability tests and post-activity FTIR analysis were used to investigate the long-term usability and structural stability of the newly developed doped composite photocatalyst. The scavenging tests revealed a potential photocatalytic mechanism to explain the annihilation of the levofloxacin drug on the synthesized catalyst. The physicochemical and photocatalytic evaluations recommend that the assembled integrated material has excellent potential for mineralizing medicinal products in pharmaceutical wastes.