Search Results (491)

A series of Er³⁺–Tm³⁺–Yb³⁺ tri-doped fluorophosphate glasses with different molar compositions were synthesized using the conventional melt-quenching technique, and their optical properties were measured and analyzed. Under laser excitation at 980 nm, blue, green and red upconverted emissions were observed at around 475, 545 and 660 nm, respectively. Based on the results and the energy level diagrams, energy transfer processes were proposed to explain the population mechanisms of the emitting levels. A final characterization was developed within the framework of the CIE 1931 chromaticity coordinate diagram. Varying the doping concentrations of the optically active rare-earth ions, as well as the laser pumping power, enabled modulation of the three primary colors, resulting in blue, green and relatively close to white light emissions. This tunability of the upconverted emissions highlights the potential of these fluorophosphate glasses as tunable optical devices, laser systems and visual show effects. Full article

Cyanotypes, known as photographs and architectural plans made by photo-reproduction from the 19th and 20th centuries, are subjects for conservation. Wet cleaning for conservation treatment has been reported to be unsuitable for cyanotypes because Prussian blue on cyanotypes is thought to move physically with the application of water. The manner in which Prussian blue is fixed onto the paper substrate is important for determining the treatment method. This study is the first step toward clarifying this mechanism. The presence of Prussian blue in cyanotypes was first confirmed using X-ray diffraction analysis (XRD). Then, the location of Prussian blue in the fibre was confirmed using optical microscopy and micro-Raman spectroscopy analysis, by observing the blue colour and by detecting its cyanide bond. With field-emission scanning electron microscopy (FE-SEM), particles approximately 20–100 nm in size were observed on the surface of cyanotype paper fibres, and particles approximately 20–50 nm in size were observed from the cross-section of the paper fibres. The location where the particles were observed agreed with the location where the blue colour was observed and cyanide bond was detected. The fact that the sensitiser solution soaked into the paper fibres and formed Prussian blue within the paper fibres when exposed to light is thought to be important for the blue fixation of cyanotypes. Full article

White-light-emitting diodes (wLEDs) are central to next-generation lighting technologies, yet their reliance on critical raw materials (CRMs), such as rare-earth elements, raises concerns regarding sustainability and supply security. In this work, we present a simple, low-cost method to produce photoluminescent carbon-based nanostructures—known as oxidative debris (OD)—via alkaline treatment of graphene oxide (GO) using KOH solutions ranging from 0.04 M to 1.78 M. The resulting OD, isolated from the supernatant after acid precipitation, exhibits strong and tunable photoluminescence (PL) across the visible spectrum. Emission peaks shift from blue (~440 nm) to green (~500 nm) and yellow (~565 nm) as a function of treatment conditions, with excitation wavelengths between 300 and 390 nm. Optical, morphological. and compositional analyses were performed using UV-Vis, AFM, FTIR, and Raman spectroscopy, confirming the presence of highly oxidized aromatic domains. The blue-emitting (S2) and green/yellow-emitting (R2) fractions were successfully separated and characterized, demonstrating potential color tuning by adjusting KOH concentration and treatment time. This study highlights the feasibility of reusing GO-derived byproducts as sustainable phosphor alternatives in wLEDs, reducing reliance on CRMs and aligning with green chemistry principles. Full article

This study investigates near-infrared (NIR)-induced, Phyto-enhanced, second harmonic generation-mediated photodynamic therapy (Phyto-SHG-PDT) using barium titanate (BT)/rhein/polyethylene glycol 100 (PEG100) and BT/Yemenite “Etrog” leaf extract/PEG100 nanoconjugates. We compare continuous-wave (CW), multi-line Argon-ion laser illumination in the NIR range with high-peak-power femtosecond (fs) 800 nm pulses. Under CW NIR light, BT/rhein nanoconjugates reduced PC3 prostate cancer cell viability by 18% versus non-irradiated controls (p < 0.05), while BT/extract nanoconjugates exhibited 15% dark toxicity. The observed SHG signal matched theoretical predictions and previous CW laser studies. Reactive Oxygen Species (ROS) scavenger 1,3-diphenyl-isobenzofuran (DPBF) showed reduced absorbance at 410 nm upon NIR illumination, indirectly supporting SHG emission at 400 nm from nanoconjugates. Under fs-pulsed laser exposure, pronounced two-photon absorption (TPA) and SHG effects were observed in both nanoconjugate types. Our results demonstrate the effectiveness of BT/rhein nanoconjugates under both laser conditions, while the BT/extract nanoconjugates benefited from high-power pulsed excitation. These results highlight the potential of BT-based Phyto-SHG-PDT nanoconjugates for NIR and blue light applications, leveraging nonlinear optical effects for advanced photochemical cancer therapies. Full article

New conjugated carbazolyl-substituted azulenes, such as 1,2,3-tris(carbazolyl)azulene and 1,2,3,6-tetrakis(carbazolyl)azulene, were synthesized via cross-coupling reactions in high yields. The resulting compounds exhibit a significant ability to absorb and emit light in the visible region, in the range of 400 to 600 nanometers. Studies have shown that azulene with carbazolyl substituents at positions 1, 2, 3, and 6 possesses unique photophysical properties, manifested as intense emission in the blue photoluminescence region (λ_PL at 444 and 490 nm), which is not observed in the original azulene. This feature arises due to the donor properties of carbazolyl substituents, which have a strong effect on the electronic structure of azulene, creating the conditions for a permitted HOMO-LUMO electronic transition. Full article

Main-chain conjugated and non-conjugated polyelectrolytes are an important class of materials that have many technological applications ranging from fire-retardant materials to carbon-nanotube composites, nonlinear optical materials, electrochromic materials for smart windows, and optical sensors for biomolecules. Here, we describe a series of poly(pyridinium salt)s-fluorene containing 9,9-bis(4-aminophenyl)fluorene moieties with various organic counterions that were synthesized using ring-transmutation polymerization and metathesis reactions, which are non-conjugated polyelectrolytes. Their chemical structures were characterized by Fourier transform infrared (FTIR), proton (¹H) and fluorine 19 (¹⁹F) nuclear magnetic resonance (NMR) spectrometers, and elemental analysis. They exhibited polyelectrolytic behavior in dimethyl sulfoxide. Their lyotropic liquid-crystalline phases were examined by polarizing optical microscopy (POM) and small angle X-ray scattering (SAXS) studies. Their emission spectra exhibited a positive solvatochromism on changing the polarity of solvents. They emitted greenish-yellow lights in polar organic solvents. They formed aggregates in polar aprotic and protic solvents with the addition of water (v/v, 0–90%), whose λ_em peaks were blue shifted. Full article

Conjugated polymers (CPs) offer many attractive features for photodiodes and photovoltaics, including solution processability, ease of scale-up, light weight, low cost, and mechanical flexibility. CPs have a wide range of energy gaps; thus, the choice of the specific polymer determines the optimum operational wavelength range. However, there are relatively few CPs with a strong absorption in the blue region of the spectrum where the human eye is most sensitive (440 to 470 nm) and none with an energy gap at 2.75 eV (450 nm), which corresponds to the peak of the CIE-1931 z(λ) color-matching function and the dominant blue light emission wavelength in computer and smartphone displays. Blue-light detectors in this wavelength range are important for light hazard control, sky polarization studies, and for blue-light information devices, where 450 nm corresponds to the principal emission of GaN-based light sources. We report on a new CP called Atums Green (AG), which shows promising characteristics as a blue-light photodetection polymer optimized for exactly this range of wavelengths centered around 450 nm. We built and measured a simple photodetector made from spin-coated films of AG and showed that its photosensitivity can be improved by the addition of asphaltene, a low-cost carbonaceous waste product. Full article

Achieving global net-zero emissions by 2050 demands integrated and scalable strategies that unite decarbonization technologies across sectors. This review provides a forward-looking synthesis of carbon capture and storage and hydrogen systems, emphasizing their integration through artificial intelligence to enhance operational efficiency, reduce system costs, and accelerate large-scale deployment. While CCS can mitigate up to 95% of industrial CO₂ emissions, and hydrogen, particularly blue hydrogen, offers a versatile low-carbon energy carrier, their co-deployment unlocks synergies in infrastructure, storage, and operational management. Artificial intelligence plays a transformative role in this integration, enabling predictive modeling, anomaly detection, and intelligent control across capture, transport, and storage networks. Drawing on global case studies (e.g., Petra Nova, Northern Lights, Fukushima FH2R, and H21 North of England) and emerging policy frameworks, this study identifies key benefits, technical and regulatory challenges, and innovation trends. A novel contribution of this review lies in its AI-focused roadmap for integrating CCS and hydrogen systems, supported by a detailed analysis of implementation barriers and policy-enabling strategies. By reimagining energy systems through digital optimization and infrastructure synergy, this review outlines a resilient blueprint for the transition to a sustainable, low-carbon future. Full article

Herein, we study a method for developing a broad-emission emitter that can emit radiation from the visible light to NIR regions. Firstly, an NIR phosphor’s optical properties (e.g., scattering vs. weight concentration, conversion efficiency, and emission spectra under blue and red light excitation) are investigated. Then, pcW-LEDs encapsulated with NIR down-conversion phosphor samples are prepared to test these optical properties. The results show that pcW-LEDs encapsulated with the NIR phosphor at different weight concentrations of 10.0%, 12.5%, and 15.5%, respectively, emit a broadband emission from 400 nm to 900 nm. The EQE values of the pcW-LEDs encapsulated with NIR phosphor at weight concentrations of 10%, 12.5%, and 15.0% are 26%, 23%, and 19%, respectively. The correlated color temperatures of these samples are 5767 K, 5940 K, and 6068 K, respectively. The obtained radiant fluxes of the samples are 26 mW, 22 mW, and 18 mW, respectively, at an injection current of 50 mA. Full article

In this study, Mn²⁺ and Eu²⁺-codoped Sr_3−xBa_xMgSi₂O₈ (x = 0–1.5) phosphors were synthesized at 1400 °C under a reducing atmosphere composed of 5% H₂ and 95% N₂ to produce materials with blue light emission. The resulting powders were characterized using several analytical techniques: X-ray diffraction (XRD) was employed to identify the crystalline phases, scanning electron microscopy (SEM) was used to observe the microstructure, and photoluminescence excitation (PLE) and emission (PL) spectra were measured using a fluorescence spectrophotometer. The results revealed several key findings. XRD analysis showed that the Sr₃MgSi₂O₈ (Sr_3−xBa_xMgSi₂O₈) phase coexisted with secondary phases of Sr₂SiO₄ and Sr₂MgSi₂O₇. SEM observations indicated that the synthesized powders exhibited a distinctive needle-like structure anchored on the surfaces of the particles. The PL and PLE intensities increased sharply as the BaO content increased from x = 0 to x = 0.6, followed by a more gradual increase, reaching a peak at x = 1.2. Additionally, as the value of x increased, the wavelengths corresponding to maximum PL and PLE intensities exhibited a blue shift, moving to shorter wavelengths. Further investigation focused on the excitation behavior by replotting the PLE spectra using energy (eV) as the x-axis. A Gaussian fitting function was applied to deconvolute the excitation bands, enabling an in-depth analysis of how compositional variations influenced the Stokes shift. Full article

Photodynamic therapy (PDT) is a minimally invasive technique—used for the local eradication of neoplastic cells—that exploits the interaction of light, oxygen, and a photo-responsive drug called photosensitizer (PS) for the local generation of lethal ROS. Push-pull chromophores, that bear electron donor (D) and acceptor (A) groups linked through a π-electron bridge, are characterized by a non-homogeneous charge distribution in their excited state, with charge transfer from one extremity of the chain to the other one (Internal Charge Transfer—ICT). This phenomenon has a direct impact on the photophysical features of the push-pull compounds, as the bathochromic shift of the emission maxima and intersystem crossing (ISC) of the excited state are directly connected with the production of reactive oxygen species (ROS). In continuing our research regarding the synthesis and use of oligophenylene ethynylenes (OPEs) in PDT, two new push-pull glycosyl OPE-NOF and OPE-ONF—featuring electron-donor N,N-dimethylamino (N) and dimetoxyaryl (O) and acceptor tetrafluoroaryl (F) moieties on the OPE chain—have been efficiently prepared. The interchanged position of the D groups onto the conjugated skeleton was aimed to tune and optimize the push-pull effect, while the introduction of glucoside terminations was directed to give biocompatibility and bioaffinity to the chromophores. OPE-NOF, OPE-ONF, and the synthetic intermediates were fully characterized, and their photophysical properties were investigated by using UV-Vis absorption and emission spectroscopy. OPE-NOF showed a strong charge-transfer character and high PDT effect on HeLa cancer cells when irradiated with non-harmful blue light, causing massive cancer cell death. Full article

Polyaryletherketone (PAEK) materials, including polyetheretherketone (PEEK) and polyetherketoneketone (PEKK), possess excellent mechanical properties and biocompatibility; however, their inherently low surface energy limits effective bonding with resin cements. This study investigated the effects of hydrofluoric acid (HF) etching and handheld nonthermal plasma (HNP) treatment on enhancing the adhesive performance of PAEK surfaces. Disk-shaped PEEK (BP) and PEKK (PK) specimens were divided into four groups: APA (airborne-particle abrasion), PLA (nonthermal plasma treatment), LHF (5.0% HF), and HHF (9.5% HF). Surface characterization was performed using a thermal field emission scanning electron microscope (FE-SEM). Surface wettability was evaluated using contact angle goniometry. Cytotoxicity was evaluated using HGF-1 cells exposed to conditioned media and analyzed via PrestoBlue assays. Shear bond strength (SBS) was measured after three aging conditions—NT (no aging), TC (thermocycling), and HA (highly accelerated aging)—using a light-curing resin cement. Failure modes were categorized, and statistical analysis was performed using one-way and two-way ANOVA with Tukey’s HSD test (α = 0.05). Different surface treatments did not affect surface characterization. PLA treatment significantly improved surface wettability, resulting in the lowest contact angles among all groups, followed by HF etching (HHF > LHF), while APA showed the poorest hydrophilicity. Across all treatments, PK exhibited better wettability than BP. Cytotoxicity results confirmed that all surface treatments were nontoxic to HGF-1 cells, indicating favorable biocompatibility. SBS testing demonstrated that PLA-treated specimens achieved the highest and most stable bond strength across all aging conditions. Although HF-treated groups exhibited lower bond strength overall, BP samples treated with HF showed relatively less reduction following aging. Failure mode analysis revealed a shift from mixture and cohesive failures in the NT aging condition to predominantly adhesive failures after TC and HA aging conditions. Notably, the PLA-treated groups retained mixture failure patterns even after aging, suggesting improved interfacial durability. Among the tested methods, PLA treatment was the most effective strategy, enhancing surface wettability, bond strength, and aging resistance without compromising biocompatibility. In summary, the PLA demonstrated the greatest clinical potential for improving the adhesive performance of PAEK when used with light-curing resin cements. Full article

Both tungsten trioxide (WO₃) nanosheet arrays and tungsten trioxide/zinc oxide (WO₃/ZnO) nanocomposites were grown on fluorine-doped tin oxide (FTO) coated glass slides using a hydrothermal method to develop a visible-light-driven photocatalyst with easy reusability. Field emission scanning electron microscopy (FE-SEM) observations confirmed the formation of irregular oxide nanosheet arrays on the FTO surfaces. X-ray diffraction (XRD) analysis revealed the presence of hexagonal WO₃ and wurtzite ZnO crystal phases. UV-Vis diffuse reflectance spectroscopy showed that integrating ZnO nanostructures with WO₃ nanosheets resulted in a blue shift of the absorption edge and a reduced absorption capacity in the visible-light region. Photoluminescence (PL) spectra indicated that the WO 0.5/ZnO 2.0 sample exhibited the lowest electron-hole recombination rate among the WO₃/ZnO nanocomposite sample. Photocatalytic degradation tests demonstrated that all WO₃/ZnO nanocomposite samples had higher photodegradation rates for a 10 ppm methylene blue (MB) aqueous solution under visible-light irradiation compared to pristine WO₃ nanosheet arrays. Among them, the WO 0.5/ZnO 2.0 sample showed the highest photocatalytic efficiency. Furthermore, it exhibited excellent recyclability and high photodegradation stability over three cycles. Full article

Dy³⁺ single-doped and Dy³⁺/Eu³⁺ co-doped ZnO:B₂O₃:WO₃:Nb₂O₅ glass was successfully synthesized using the melt quenching method. The amorphous character of the prepared samples was confirmed by X-ray diffraction (XRD). The glass transition and crystallization temperatures were examined by differential scanning calorimetry (DSC). Raman spectroscopy was applied to investigate the glass microstructure. Physical properties like the density, molar volume, oxygen molar volume and oxygen packing density of the glass were also determined. The photoluminescence excitation (PLE) and emission (PL) spectra of the resultant glass types were measured. The obtained Dy³⁺ single-doped glass was characterized by strong luminescence at 482 and 574 nm, corresponding to the ⁴F_9/2 → ⁶H_15/2 (blue) and ⁴F_9/2 → ⁶H_13/2 (yellow) transitions, respectively, and weak luminescence at 663 nm and 753 nm due to the ⁴F_9/2 → ⁶H_11/2 (red) and ⁴F_9/2 → ⁶H_9/2 + ⁶F_11/2 (red) transitions. The luminescence results indicate that energy transfer from the Dy³⁺ to Eu³⁺ ions occurs in the proposed glass system. The emitted light from the Dy³⁺ single-doped glass was found to be yellow-orange. The Dy³⁺/Eu³⁺ co-doped samples emitted darker orange light. The obtained results show that the investigated types of glass have the potential to be used as orange light-emitting materials. Full article

A zinc complex bearing a pyrazolone-based azomethine ligand has been synthesized for blue-emitting organic light-emitting diodes (OLEDs). The azomethine ligand H₂L and the complex [ZnL·H₂O] were characterized by IR, 1H NMR, XRD, and TGA/DSC techniques. According to a single-crystal X-ray diffraction analysis, the complex [ZnL·H₂O] has a molecular structure. Its solid-state PL maxima appear to be at 416 nm and emit moderate blue emission with a quantum yield (QY) of 2%, with a dehydrated form of the complex showing greater efficiency with a QY of 55.5%. ZnL-based electroluminescent devices for OLED applications were fabricated. The devices exhibit blue emission with brightness up to 5300 Cd/A. Full article