UV Light Exposure Research Articles

Analysis of the Skin and Brain Transcriptome of Normally Pigmented and Pseudo-Albino Southern Flounder (Paralichthys lethostigma) Juveniles to Study the Molecular Mechanisms of Hypopigmentation and Its Implications for Species Survival in the Natural Environment.

Southern flounder skin pigmentation is a critical phenotypic characteristic for this species' survival in the natural environment. Normal pigmentation allows rapid changes of color for concealment to capture prey and UV light protection. In contrast, highly visible hypopigmented pseudo-albinos exhibit a compromised immune system and are vulnerable to predation, sensitive to UV exposure, and likely have poor survival in the wild. Skin and brain tissue samples from normally pigmented and hypopigmented individuals were analyzed with next-generation RNA sequencing. A total of 1,589,613 transcripts were used to identify 952,825 genes to assemble a de novo transcriptome, with 99.43% of genes mapped to the assembly. Differential gene expression and gene enrichment analysis of contrasting tissues and phenotypes revealed that pseudo-albino individuals appeared more susceptible to environmental stress, UV light exposure, hypoxia, and osmotic stress. The pseudo-albinos' restricted immune response showed upregulated genes linked to cancer development, signaling and response, skin tissue formation, regeneration, and healing. The data indicate that a modified skin collagen structure likely affects melanocyte differentiation and distribution, generating the pseudo-albino phenotype. In addition, the comparison of the brain transcriptome revealed changes in myelination and melanocyte stem cell activity, which may indicate modified brain function, reduced melanocyte migration, and impaired vision.

Enhanced photodegradation of textile dye wastewater using silane/polymer doped ZnO nanocomposites and antibacterial activity

Accumulation of textile dye wastewater is major global issue that causes negative impact to the ecosystem. This study focuses on industrial textile dye effluent treatment by photodegradation, and degradation of Malachite green dye under sunlight, visible and UV light. ZnO demonstrated hexagonal wurtzite structure with average crystallite size 38 nm for ZnO/PEG, 21 nm for ZnO/PEG/VTES and 17 nm for ZnO/PEG/VTMS. Field Emission Scanning Electron Microscopy and Energy Dispersive Spectroscopy revealed nanometer sized particles and purity. Bandgap energy and particle size of ZnO/PEG/VTMS is 102 nm and 3.134 eV is lesser than ZnO/PEG (147 nm, 3.181 eV) and ZnO/PEG/VTES (109 nm, 3.151 eV). Photoluminescence analysis revealed reduced recombination rate of ZnO/PEG/VTMS. Antibacterial efficacy of ZnO/PEG/VTMS was tested against Staphylococcus aureus (35 mm) and Escherichia coli (29 mm). Photodegradation of textile dye wastewater by ZnO/PEG/VTMS under visible and UV light exposure revealed an effective way for textile dye effluent treatment, which maintained its efficiency even after five photodegradation cycles.

Influence of rapid heat treatment on the photocatalytic activity and stability of calcium titanates against a broad range of pollutants

Calcium titanate (CTO) photocatalysts were synthesized using a sol–gel method by adopting a cost-efficient, rapid calcination technique. The CTOs were characterized by X-ray diffractometry, X-ray photoelectron spectroscopy, infrared spectroscopy, nitrogen adsorption, porosimetry measurements, scanning/transmission electron microscopy, and diffuse reflectance spectroscopy. Their photocatalytic activity was assessed through the photocatalytic degradation of phenol, oxalic acid, and chlorophenol under UV light exposure, using a commercial CTO as a reference. The stability of the samples was evaluated using compounds with –OH, –COOH, and –Cl functional groups. Characterization results showed that CTO composites containing anatase, rutile, and brookite titania were obtained. Increasing the calcination temperature led to various crystalline compositions, higher crystallinity, larger primary crystallite sizes, and smaller specific surface areas. The photocatalytic activity of all CTO/TiO2 composites was superior compared to the commercial CTO we used as a reference. The high photocatalytic activity of the best-performing composites was attributed to their higher specific surface areas and the synergistic effect between the crystal phases. A cost comparison was also made between our unique calcination technique and conventional calcination, and it was found that our method is approximately 35% more cost-effective, while retaining the photocatalytic activity.

Novel bilayer 2D V2O5 as a potential catalyst for fast photodegradation of organic dyes

Two-dimensional (2D) materials have recently drawn interest in various applications due to their superior electronic properties, high specific surface area, and surface activity. However, studies on the catalytic properties of the 2D counterpart of V2O5 are scarce. In the present study, the catalytic properties of 2D V2O5 vis-à-vis bulk V2O5 for the degradation of methylene blue dye are discussed for the first time. The 2D V2O5 catalyst was synthesized using a modified chemical exfoliation technique. A massive increase in the electrochemically active surface area of 2D V2O5 by one order of magnitude greater than that of bulk V2O5 was observed in this study. Simultaneously, ~ 7 times increase in the optical absorption coefficient of 2D V2O5 significantly increases the number of photogenerated electrons involved in the catalytic performance. In addition, the surface activity of the 2D V2O5 catalyst is enhanced by generating surface oxygen vacancy defects. In the current study, we have achieved ~ 99% degradation of 16 ppm dye using the 2D V2O5 nanosheet catalysts under UV light exposure with a remarkable degradation rate constant of 2.31 min−1, which is an increase of the order of 102 from previous studies using V2O5 nanostructures and nanocomposites as catalysts. Since the enhanced photocatalytic activity emerged from the surface and optical properties of the catalyst, the current study shows great promise for the future application of 2D V2O5 in photo- and electrocatalysis.

Optimizing Ultraviolet Illumination for Detecting Fluorescent Orthodontic Adhesive Residues during Debonding Procedures.

Fluorescence-aided identification technique (FIT) studies for orthodontic resins are relatively new, using an arbitrary selection of resins, lights, and work parameters. In order to provide FIT guidelines for optimal visualization, the objectives of this study were to describe the electromagnetic characteristics of fluorescent orthodontic resins, determine appropriate light specification, and describe light and work parameter effects on resin fluorescence. This in vitro study assessed five fluorescent orthodontic resins and a non-fluorescent control resin using spectrophotometry, a scaled image analysis of 25 μm thick resins to compare intensities, and a visual assessment. Light sources varied by flashlight lens (narrow [N], average [X], and magnified [Z]) and UV intensity (X and X High). Work parameters included distance (20-300 mm) and angulation (15-70°). Visual scores were assigned to determine discernibility. The average excitation maxima was 384 nm. Fluorescence increased with more direct UV light exposure. The highest intensity was recorded with Light X High at 50 mm and 70°. Visual assessment followed image analysis trends, and fluorescence was clinically discernable for all 25 μm thick samples. Excitation wavelength range of 395-405 nm is appropriate for FIT illumination. All resins were anisotropic and showed greater fluorescence with greater angle, higher UV intensity, and closer proximity.

Engineering S-scheme heterojunction MgO/WO3-integrated Graphene photocatalyst for robust detoxification of tetracycline: Mechanistic insight and actual matrix remediation

The widespread usage of pharmaceutical compounds for treating humans and animals has led to substantial environmental harm to living organisms globally. Herein, the engineering of step-scheme (S-scheme) heterojunction composite incorporating a co-adsorbent agent is garnering attention as a promising approach for environmental remediation, owing to its improved redox potential and expanded active surface area. This study is the first to employ a graphene-integrated MgO/WO3 S-scheme heterostructure (denoted as MWG) as a ternary photocatalyst for the disintegration of tetracycline (TCY) under UV light exposure. The results confirmed that the MWG nanocatalyst exhibited a significantly improved photocatalytic activity in the degradation of TCY when contrasted with pure MgO, WO3, and graphene (GRP) nanomaterials. Kinetic investigation elucidated that the detoxification of TCY under optimized circumstances was best described by a pseudo first-order kinetic model with regression coefficients higher than 0.97. The scavenging tests revealed that HO● species are the primary agents involved in the TCY degradation during the photocatalytic process. Trapping experiments, photoelectrochemical techniques, and band structure analysis were conducted to propose the plausible detoxification mechanism via the MWG/UV process. A notable enhancement in the biodegradability of actual wastewater was attained following treatment with the MWG/UV process, resulting in 79.6% and 64.8% COD and TOC elimination, respectively, over a 200 min of reaction time. To sum up, the employment of a graphene-integrated MgO/WO3 S-scheme heterojunction composite under UV light illumination can be considered a novel and effective approach for the remediation of real pharmaceutical effluents in real-world scenarios, attributable to its robust redox capacity, significant stability, economic viability, and heightened efficacy in degradation/mineralization processes.

Clinical, dermoscopic and histopathological features of multiple cutaneous tumours ascribed to sun damage in a Chinese crested dog

AbstractThis case report describes the clinical, dermoscopic and histopathological findings of three different neoplastic lesions (angiokeratoma, squamous cell carcinoma and multiple melanocytomas) and non‐tumoral skin in a hairless Chinese crested dog following chronic sun exposure. The non‐tumoral skin was characterized by “sunburn cells”, collagen degeneration, dermal elastosis and fibrosis, described in most species as caused by UV light exposure. Cutaneous angiokeratomas have been rarely reported in the canine literature. In this particular case we consider a possible correlation with UV damage.

Application of Bi0.5Na0.5TiO3 −based catalysts for piezocatalytic, photocatalytic and piezo-photocatalytic degradation of organic pollutants in wastewater remediation

In order to attain visible light driven piezo-photocatalyst for treatment of organic pollutants, Ag doped Bi0.5Na0.5TiO3 particles (Bi0.5Na0.5-x AgxTiO3 particles with x = 0, 0.01, 0.03, and 0.05) have been synthesised via sol–gel route. X-ray diffraction (XRD) study confirmed the monoclinic phase structure with Cc space group for all compositions. The Rietveld refinement using FullPROF program was performed to ensure the phase purity of the samples. The structure is reconfirmed by matching vibrational modes in Raman spectra as well. Morphological and elemental analysis were done using scanning electron microscopy (SEM) equipped energy dispersive x-ray spectra (EDX) and found the particle size ranging from 300-400 nm. UV–vis absorbance spectra were employed to find the optical bandgap for all synthesised particles, found in the range of 3.65–2.63 eV. The best piezo-photocatalytic activity found for sample x = 0.01 tested for rhodamine B dye, which is ∼ 82 % in 80 min under the exposure of UV light and mechanical disturbances, whereas degradation was ∼ 52.4 % and ∼ 22.7 % for photo- and piezocatalysis, respectively. Kinetics study and rate constant values were found using first order rate kinetics equation. Trapping experiment and stability test for the catalysts were done systematically, finding that hydroxyl and superoxide radicals are major active species and ∼ 9 % decrement in degradation capacity over three cycles were found due to loss of catalyst amount. The improvement in degradation is attributed to least recombination rate, greater oxygen vacancies, high degradation yield, high absorption capacity and optimum bandgap values over the other compositions. Therefore, 1 % Ag doped BNT sample can be novel efficient piezo-photocatalyst for treatment of organic dyes.

Shape Dependence of Photoresponsive Molecular Crystals Composed of Naphthyl Acrylic Acid Stimulated by Solid-State [2 + 2] Photocycloaddition

Photomechanical molecular crystals, actuated by solid-state photochemical reactions, manifest a spectrum of mechanical motions upon light exposure, underscoring their prospective integration into the next generation of intelligent materials and devices. Utilizing the solid-state photodimerization of naphthyl acrylic acid as a paradigm, this study delved into the interplay between crystal morphology and reaction dynamics on the photomechanical responses of molecular crystals. Distinct crystal forms—bulk, microrods, and microplates—were cultivated through tailored crystallization conditions. While bulk crystals of naphthyl acrylic acid (NA) underwent shattering and splintering upon UV light exposure, the microplate counterparts displayed unique cracking patterns with fissures yet retained their overall structural integrity. In contrast, NA microrods underwent pronounced bending under identical irradiation conditions. These phenomena are attributed to the efficient lattice reconfiguration stemming from the [2 + 2] cycloaddition photochemical reaction within the crystals. An intermediate fluorescence enhancement was observed across all crystal types upon light exposure. Collectively, our results underscore the pivotal role of crystal shape in dictating photomechanical behavior, thereby heralding novel strategies for developing advanced photomechanical materials.

On the diverse utility of Cu doped ZnS/Fe3O4 nanocomposites.

The global water crisis is a growing concern, with water pollution from organic dyes being a significant issue. Photocatalysis has emerged as a sustainable and renewable method for removing organic pollutants from wastewater. The study synthesized innovative (2.5, 5 and 10 wt%) Cu doped zinc sulfide/iron oxide nanocomposites using a sonochemical method, which have versatile applications in adsorption and photocatalytic degradation of organic pollutants in wastewater. The nanocomposites underwent comprehensive characterization using powder X-ray diffraction, fourier-transform infrared spectroscopy, photoluminescence spectroscopy, Ultraviolet-Visible spectrophotometer, field emission scanning electron microscopy combined with energy dispersive X-ray spectroscopy and Mott-Schottky analysis. The synthesized samples demonstrate strong adsorption ability to remove RhB and MB dyes. Afterward, we evaluated their capability to degrade Rhodamine B (RhB) dye under UV light exposure. The greatest photocatalytic efficiency was noticed when employing a UV-C lamp in combination with the 10 wt% Cu doped ZnS/Fe3O4 nanocomposite as photocatalyst (98.8% degradation after 60 min irradiation). The Langmuir-Hinshelwood model can be used to describe the pseudo first order kinetics of RhB dye photodegradation. The calculated ban gap values are 4.77, 4.67, and 4.55 eV, for (2.5, 5 and 10 wt%) Cu doped ZnS/Fe3O4, respectively. Furthermore, 10 wt% Cu doped ZnS/Fe3O4 showed good recyclability, with a degradation rate of 89% even after five cycles. Consequently, prepared samples have outstanding photocatalytic activity and can be used as useful adsorbents in water purification.

Photo-Healable Fabrics: Achieving Structural Control via Photochemical Solid-Liquid Transitions of Polystyrene/Azobenzene-Containing Polymer Blends.

While polymer fabrics are integral to a wide range of applications, their vulnerability to mechanical damage limits their sustainability and practicality. Addressing this challenge, our study introduces a versatile strategy to develop photohealable fabrics, utilizing a composite of polystyrene (PS) and an azobenzene-containing polymer (PAzo). This combination leverages the structural stability of PS to compensate for the mechanical weaknesses of PAzo, forming the fiber structures. Key to our approach is the reversible trans-cis photoisomerization of azobenzene groups within the PAzo under UV light exposure, enabling controlled morphological alterations in the PS/PAzo blend fibers. The transition of PAzo sections from a solid to a liquid state at a low glass transition temperature (Tg ∼ 13.7 °C) is followed by solidification under visible light, thus stabilizing the altered fiber structures. In this study, we explore various PS/PAzo blend ratios to optimize surface roughness and mechanical properties. Additionally, we demonstrate the capability of these fibers for photoinduced self-healing. When damaged fabrics are clamped and subjected to UV irradiation for 20 min and pressed for 24 h, the mobility of the cis-form PAzo sections facilitates healing while retaining the overall fabric structure. This innovative approach not only addresses the critical issue of durability in polymer fabrics but also offers a sustainable and practical solution, paving the way for its application in smart clothing and advanced fabric-based materials.

Extraction and characterization of carotenoid pigments with antioxidant and antibacterial potential from marine yeast Rhodotorula sp. KSB1.

Pigments are coloring agents used widely in different industrial sectors. There is a demand for using natural pigments rather than synthetic dyes because of the health hazards caused by synthetic dyes. Many natural pigments have different medicinal activities which can contribute to the nutritional value of the product. This study was carried forward with marine yeasts which can produce pigments. A total of 4 marine yeast isolates were recovered from the mangrove area of Sundarbans, West Bengal, India. Among them, the isolate KSB1 produced 856µg/g total concentration of carotenoid pigment and the dry mass weight was 3.56g/L. The stability of the extracted pigments was checked using temperature, pH, UV light exposure time, and different saline conditions. The pigments were characterized using HPLC and FTIR analysis. All of the extracted pigments showed good antioxidant activity in DPPH, metal chelating, and reducing power assay. The pigments were also found to have good antibacterial activity against the bacterial pathogens Staphylococcus aureus, Listeria monocytogenes, and Escherichia coli. Carotenoid pigment from KSB1 was found to have maximum activity in all the pathogens. The cytogenotoxicity using onion roots and phytotoxicity analysis indicated that the pigments were non-toxic and safe for cells. Finally, the potential marine yeast was identified using 18s rRNA sequencing and identified as Rhodotorula sp. KSB1 (Accession no. MH782232).

Photo-regulated PROTACs: A novel tool for temporal control of targeted protein degradation

PROTACs (Proteolysis targeting chimeras) are chimeric molecules designed to induce targeted protein degradation via the ubiquitin–proteasome system. These molecules catalytically degrade target proteins and sustainably inhibit their function. Therefore, PROTAC's unique mechanism of action is not only beneficial in medicine but also serves as a valuable tool for molecular biological analysis in fields like chemical biology, biochemistry, and drug discovery. This study presents a novel turn-off (ON-OFF) type PROTAC development strategy utilizing a photocleavable linker. The inclusion of this linker enables temporal control of the degradation activity targeting BRD4 protein upon UV light exposure. PROTAC-2 demonstrated the most potent degradation activity against BRD4 among the other synthesized PROTACs with varying linker lengths. The UV light-induced cleavage of PROTAC-2 was confirmed, leading to a reduction in its BRD4 degradation activity. Notably, this study introduces a novel linker capable of nullifying degradation activity of PROTACs which is activated by light irradiation. These findings offer a promising strategy for the development of turn-off type PROTACs, providing enhanced temporal control over protein degradation. The approach holds significant potential for applications in molecular function studies and drug discovery.

Diagnose und Therapie aktinischer Keratosen

Actinic keratosis (AK) is considered a chronic and recurring in situ skin neoplasia, with a possible transformation into invasive squamous cell carcinoma (SCC). Among others, predominant risk factors for development of AK are UV-light exposure and immunosuppression. Basal epidermal keratinocyte atypia (AK I) and proliferation (PRO Score) seem to drive malignant turnover, rather than clinical appearance of AK (Olsen I-III). Due to the invasiveness of punch biopsy, those histological criteria are not regularly assessed. Non-invasive imaging techniques, such as optical coherence tomography (OCT), reflectance confocal microscopy (RCM) and line-field confocal OCT (LC-OCT) are helpful to distinguish complex cases of AK, Bowen's disease and SCC. Moreover, LC-OCT can visualize the epidermis and the papillary dermis at cellular resolution, allowing real-time PRO Score assessment. The decision-making for implementation of therapy is still based on clinical risk factors, ranging from lesion- to field-targeted and ablative to non-ablative regimes, but in approximately 85% of the cases a recurrence of AK can be observed after a 1-year follow-up. The possible beneficial use of imaging techniques for a non-invasive follow-up of AK to detect recurrence or invasive progression early on should be subject to critical evaluation in further studies.

Facile green synthesis of Zn doped MoO3 nanoparticles and its photocatalytic and photoluminescence studies

In the field of nanoscience, the use of plant components for the synthesis of nanoparticles (NPs) is currently gaining popularity and has several advantages over physicochemical methods. Murraya koenigii (MK) leaf powder was used as the green fuel in the effective synthesis of the Zinc-doped molybdenum trioxide (Zn-MoO3) NPs by the green combustion method. The green synthesized NPs were characterized using XRD, FTIR, SEM, EDAX, UV–Vis and Photoluminescence (PL) spectroscopy techniques. The XRD pattern revealed the presence of an orthorhombic phase. The Tauc relation was used to calculate the energy band gap value of the samples found to be between 2.9 and 3.1 eV. The prepared NPs emit cyan light. Latent fingerprint analysis has revealed more distinct patterns in the near UV region (365 nm) and is useful in forensic investigations. The Rose Bengal (RB) dye degradation experiments are carried out under UV light exposure. Zn-MoO3 NPs have greater degradation efficiency than pure MoO3 NPs. Up to 99 % dye degradation is achieved in 150 min. After 3 photocatalysis cycles, the recycling test detects only an 8% decrease in photocatalyst efficiency. The obtained results proved that Zn-doped MoO3 NPs are the most suitable photocatalyst for RB degradation.

Stabilization of a Photoradiated Naphthalene Diimide-Based Organic Radical Anion Inside a Peptide-Based Gel Matrix with an Improvement of Optoelectronic Properties.

An amino acid-conjugated naphthalene diimide (NDI)-based highly red fluorescent radical anion has been found in a water medium under the photoradiated condition. This molecule has failed to form the radical anion in the monomeric state; however, the J aggregation in the aqueous medium has ensured the formation of radical anion in the ambient condition after the irradiation of both sunlight and UV light exposure. Electron paramagnetic resonance (EPR) studies clearly suggest the formation of radical anions. Herein, the stability of the radical anion in the aqueous medium is only a few minutes as a small amount of shaking is enough to quench the radical anion in the solution state. Furthermore, the incorporation of this molecule into a peptide-based hydrogel matrix and the consequent photoirradiation have not only helped to develop radical anion in the gel matrix but also increased the enormous stability of the radical anion inside the hydrogel matrix even for 30 days. It is envisaged that the formation of the radical anion within the gel matrix prevents the free movement of the NDI molecules and restricts the diffusion of molecular oxygen in the system, which leads to the stability of the radical anions in the gel. Moreover, the stability of the radical anion within the gel has helped to enhance the conductivity of the hybrid gel to a great extent. Interestingly, the radical anion-containing hybrid hydrogel has shown a potential photoswitching property.

Enhanced catalytic degradation of organic dye by Sn1-xLaxO2 nanoparticles under UV light for wastewater treatment

Effectively eliminating dyes and heavy metals from wastewater, without secondary contamination and with easy recovery, is a significant challenge. To address this, SnO2-based photocatalysts were fabricated using a straightforward sol–gel method, aiming to achieve high-value reutilization and environmental protection. Utilizing XRD, FTIR, and HRTEM, the investigation has conclusively confirmed the emergence of nanoparticles (NPs) through rigorous analysis and observation techniques. Raman, XPS, and PL spectroscopy probed electronic, optical properties, and lattice defects, offering comprehensive insights into material characteristics. Specific BET surface areas were observed to be 17.72 and 39.64 m2/g for 0 % and 5 % La samples. The introduction of dopant La to the SnO2 lattice resulted in enhanced optical properties, demonstrated by a significant red shift. La-SnO2 nanoparticles demonstrated remarkable catalytic efficacy, degrading 94 % of RB dye solution under 60 min of UV light exposure. Even after four cycles, the catalytic degradation activity remained high at 87 %, showcasing excellent structural stability. Enhanced adsorption capacity and effective separation of electron-hole pairs under light contribute to this improvement. Moreover, the study delved into defect-based room temperature ferromagnetism (RTFM) by examining the formation of a novel network, such as La3+-O-Sn4+. The results highlight the potential of these composites doped photocatalysts as effective materials for degrading harmful organic pollutants in wastewater treatment and for their application in spintronic devices. The present study aims to characterize the structural, magnetic, and optical attributes of La-doped SnO2 nanoparticles.

Nanocomposite Methacrylated Silk Fibroin-Based Scaffolds for Bone Tissue Engineering.

The treatment of bone defects is a clinical challenge. Bone tissue engineering is gaining interest as an alternative to current treatments, with the development of 3D porous structures (scaffolds) helpful in promoting bone regeneration by ensuring temporary functional support. In this work, methacrylated silk fibroin (SilMA) sponges were investigated as scaffolds for bone tissue engineering by exploiting the combination of physical (induced by NaCl salt during particulate leaching) and chemical crosslinking (induced by UV-light exposure) techniques. A biomimetic approach was adopted to better simulate the extracellular matrix of the bone by introducing either natural (mussel shell-derived) or synthetic-origin hydroxyapatite nanoparticles into the SilMA sponges. The obtained materials were characterized in terms of pore size, water absorption capability and mechanical properties to understand both the effect of the inclusion of the two different types of nanoparticles and the effect of the photocrosslinking. Moreover, the SilMA sponges were tested for their bioactivity and suitability for bone tissue engineering purposes by using osteosarcoma cells, studying their metabolism by an AlamarBlue assay and their morphology by scanning electron microscopy. Results indicate that photocrosslinking helps in obtaining more regular structures with bimodal pore size distributions and in enhancing the stability of the constructs in water. Moreover, the addition of naturally derived hydroxyapatite was observed to be more effective at activating osteosarcoma cell metabolism than synthetic hydroxyapatite, showing a statistically significant difference in the AlamarBlue measurement on day 7 after seeding. The methacrylated silk fibroin/hydroxyapatite nanocomposite sponges developed in this work were found to be promising tools for targeting bone regeneration with a sustainable approach.

Engineering Highly Emissive Tetra(t‐Butyl)rubrene/off‐Stoichiometry Thiol‐Ene Hybrids Toward Flexible Luminescent Solar Concentrator‐Integrated Photovoltaics with Excellent Stability

Luminescent solar concentrators (LSCs) are highly valued in transparent photovoltaics for their versatility and adaptability as effective large‐area sunlight collectors. However, constructing LSCs as efficient, long‐term stable, and easily malleable power‐generating units still remains a challenge. Herein, high photostability, high photoluminescence quantum yield (ΦPL), and Stokes‐shifted emission are achieved in tetra(t‐butyl)rubrene/off‐stoichiometry thiol‐ene (TBRb/OSTE) hybrids by incorporating TBRb molecules into OSTE polymers. To demonstrate their potentials in LSCs, a luminescent solar concentrator integrated photovoltaics (LSCIPV) is created using a one‐step synthesis that combines the preparation of TBRb/OSTE hybrids, coupling with the silicon solar cell, and the encapsulation of both components. The LSCIPV demonstrates remarkable flexibility and the integration of an ethylene tetrafluoroethylene film contributes to a hydrophobic surface and antireflection effect, resulting in an external photon efficiency (ηext) of 4.9% and a power conversion efficiency of 1.04% for the 100 cm2 device. The LSCIPV exhibits good photostability over 800 h of UV light exposure. Monte Carlo ray‐tracing simulations indicate that an optimized TBRb‐based LSCIPV can potentially achieve an ηext of 1.3%, even for a large device with an area of 1 m2.

Sol-Gel technique, characterization and photocatalytic degradation activity of Manganese doped ZnO nanoparticles

Photocatalysis using semiconductor metal oxide stands out as a highly effective and efficient method for eliminating organic pollutants from wastewater. This study aims to assess the photocatalytic capabilities of Mn doped ZnO nanocomposites in degrading methylene blue (MB) dye under ultra-violet light exposure. This study details the synthesis of ZnO photocatalysts through a straightforward one-step sol-gel method, incorporating varying levels of Mn-doping (0%, 2% & 4%). The structural and optical attributes were examined using techniques such as powder X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS) and UV-Vis diffuse reflectance spectra. X-ray diffraction analyses verified the presence of a hexagonal wurtzite crystal structure in all synthesized samples, exhibiting a high degree of crystallinity. In addition, an investigation into the impact of Mn impurities on the photocatalytic performance of ZnO catalysts was conducted in the context of methylene blue (MB) degradation. The experimental findings revealed that the Mn doped ZnO nanoparticles produced exhibited significantly superior photocatalytic performance compared to pure ZnO when used in breaking down methylene blue under UV-light exposure. This study proposes that these Mn doped ZnO could serve as a highly effective photocatalyst for treating water contaminated with certain chemically persistent synthetic organic dyes. The improved photocatalytic capabilities of ZnO nanostructures doped with Mn were ascribed to the synergistic impact of increased surface area in ZnO nanosphere and enhanced efficiency in charge separation resulting from optimized Mn doping. A potential explanation for the heightened photocatalytic performance of Mn-doped ZnO nanostructures is proposed tentatively.