Concentration-dependent luminescence characterization of terbium-doped strontium aluminate nanophosphors.

The present investigation describes the synthesis of luminescent terbium-doped strontium aluminate nanoparticles emitting bright green light, which were synthesized through a solid-state reaction method assisted by microwave radiation. Various samples containing different concentrations of Tb were synthesized, and an analysis of their structural and morphological features was conducted using powder x-ray diffraction, Fourier transform infrared spectroscopy and field emission scanning electron microscopy. The band gaps of the samples were determined utilizing the Kubelka-Munk method. The quenching mechanism observed was identified to be due to dipole-dipole interaction using the Dexter theory. The optimized sample with a terbium concentration of 4 at.% has a luminescence lifetime of 1.05 ms with 20.62% quantum efficiency. The results of this study indicate that the terbium-doped strontium aluminate fluorescent nanoparticles exhibit promising potential for a wide range of applications, including bioimaging, sensing and solid-state lighting.

Synthesis and Characterisation of SrAl2O4: Eu3+ Orange-Red Emitting Nanoparticles.

The current study involves the synthesis and characterisation of europium doped strontium aluminate nanophosphors using the solid-state reaction method with varying concentrations of europium. The existence of the SrAl2O4 phase in all samples was verified using X-ray diffraction and FTIR analysis. The lattice parameters as well as phase fractions were determined using Rietveld refinement. Surface morphology was studied using field emission scanning electron microscope. Using the Tauc plot method acquired from the diffuse reflectance spectra, the band gaps of the samples were determined and it was found that the doped samples possess lower band gaps compared to the host. Our findings demonstrate that these nanophosphors exhibiting bright orange-red emission under UV excitation with quantum efficiency 70.68%, can be applied for display and fluorescence imaging.

Development of hydrophobic, mechanically reliable, and glow-in-the-dark glue using Arabic gum.

A smart nanocomposite adhesive was created to facilitate a simple production of long-persistent photoluminescent and hydrophobic commercial products. Even after being left in the dark for up to 90 min, the created photoluminescent adhesive agent continued to generate light. A surface-specific nanocomposite adhesive agent consisting of lanthanide-activated strontium aluminate (LSA) nanoparticles (NPs; 5-14 nm) immobilized in the environmentally friendly Arabic gum (AG) was developed. A light-transmitting nanocomposite adhesive agent was manufactured by dispersing LSA nanoparticles evenly across the AG matrix without agglomeration. An excitation peak at 365 nm and an emission wavelength at 519 nm were observed for the prepared adhesives at different concentrations of LSA NPs. The emission spectra showed either fluorescence or afterglow phosphorescence, depending on the LSA ratio. The photochromic transition from colourless to green beneath an ultraviolet (UV) lamp and greenish yellow in a dark room was tracked. The LSA NPs in the Arabic gum matrix imparted enhanced hydrophobicity and scratch resistance to the LSA@AG nanocomposite. The LSA@AG nanocomposite demonstrated excellent durability and photostability. This study confirmed that the mass production of smart adhesives for applications such as smart windows, smart packaging, and safety directional signs in buildings is possible.

Possibility to Apply Strontium Aluminate to Produce Light-Emitting Plants: Efficiency and Safety.

Light-emitting plants (LEPs) provides light in areas without electricity. The phosphorescent compound was used as a lighting material for LEP development. However, using the phosphorescent compound for LEPs development required optimization and phytotoxicity evaluation. Strontium aluminate (SrAl2 O4 ) is a phosphorescent compound that can glow for a long time and is easily recharged by visible light. In this study, using SrAl2 O4 to develop LEPs was evaluated. Additionally, plant stress under SrAl2 O4 was investigated. Metabolomic analysis can explain the possible mechanism of plants' stress under SrAl2 O4 . After, injecting 3 mL of 5 % (w/v) SrAl2 O4 products 1, 2, and 3 into the stem of Ipomoea aquatica, the result showed that SrAl2 O4 products 2 and 3 caused oxidative stress. The metabolomic analysis also indicated that I. aquatica responded to SrAl2 O4 product 1 by increasing pipecolic acid and salicylic acid, while I. aquatica injected with SrAl2 O4 products 2 and 3 showed a decrease in salicylic acid around 0.005 and 0.061-fold, respectively, compared to control plants. and an excess accumulation of MDA around 10.00-12.00 µmol g-1 FW. A 15 % concentration of SrAl2 O4 can be used for LEPs development, enabling photoemission 18-fold for 50 min. SrAl2 O4 product 1 has the potential to be a material for LEPs.

Photoluminescent and photochromic smart window from recycled polyester reinforced with cellulose nanocrystals.

Smart windows with long-persistent phosphorescence, ultraviolet (UV) light protection, high transparency, and high rigidity were developed by easily immobilizing varying ratios of lanthanide-activated aluminate phosphor nanoscale particles within a composite of recycled polyester/cellulose nanocrystals (RPET/CNC). Cellulose nanocrystals were prepared from rice straw waste. Cellulose nanocrystals were used at low concentration as both crosslinker and drier to improve both transparency and hardness. The phosphor nanoscale particles must be distributed into the recycled polyester/cellulose nanocrystals composite bulk without agglomeration to produce transparent RPET/CNC substrates. Photoluminescence characteristics were also studied using spectroscopic profiles of excitation/emission and decay/lifetime. The hardness efficiency was also examined. This transparent recycled polyester waste/cellulose nanocrystals nanocomposite smart window has been shown to change colour under UV light to strong green and to greenish-yellow when it is dark, as proved by Commission Internationale de l'éclairage (CIE) laboratory colour parameters. It was found that the afterglow RPET/CNC smart window had phosphorescence intensities of 428, 493, and 523 nm upon excitation at 368 nm. There was evidence of improved UV shielding, photostability, and hydrophobic activity. In the presence of a low phosphor ratio, the luminescent RPET/CNC substrates showed quick and reversible fluorescence photochromic activity when exposed to UV radiation.

Synthesis of lanthanide-doped strontium aluminate nanoparticles encapsulated in polyacrylonitrile nanofibres: photoluminescence properties for anticounterfeiting applications.

Photochromism has been applied as an interesting technique in order to improve the anticounterfeiting of commercial commodities. To build up a mechanically reliable anticounterfeiting nanocomposite, it has been vital to enhance the engineering process of the anticounterfeiting material. In the current study, we developed mechanically reliable and highly photoluminescent lanthanide-doped strontium aluminate nanoparticles (LSAN)/polyacrylonitrile (PAN) hybrid nanofibres successfully fabricated using an electrospinning technique for anticounterfeiting applications. The produced nanocomposite films exhibited ultraviolet-induced photochromic anticounterfeiting properties. To guarantee the transparency of the LSAN-PAN film, LSAN must be immobilized onto the nanoparticle size to allow better dispersion without aggregation in the polyacrylonitrile matrix. The LSAN-PAN nanofibrous film demonstrated absorbance intensity that exhibited at 354 nm and associated with an emission intensity at 424 nm. The produced LSAN-PAN films demonstrated an enhanced hydrophobicity when increasing the ratio of LSAN, without adversely influencing their native appearance and mechanical performance. Upon excitation with ultraviolet light, the translucent nanofibrous substrates exhibited fast and reversible photochromic activity to greenish-yellow without exhaustion. The nanofibrous films exhibited stretchability, transparency, flexibility, and ultraviolet light-induced photochromism at low cost. The current strategy can be considered as an efficient technique towards the development of various anticounterfeiting materials for a better market with economic and social values.

Simple preparation of novel photochromic polyvinyl alcohol/carboxymethyl cellulose security barcode incorporated with lanthanide-doped aluminate for anticounterfeiting applications.

Forgery and low-quality products pose a danger to society. Therefore, there are increasing demands for the production of easy-to-recognize and difficult-to-copy anticounterfeiting materials. Products with smart photochromic and fluorescence properties can change colour and emission spectra responding to a light source. In this context, we devised a straightforward preparation of a luminescent polyvinyl alcohol/carboxymethyl cellulose (PVA/CMC) nanocomposite to function as a transparent labelling film. The lanthanide-doped aluminate (LdA) was prepared in the nanoparticle form to indicate diameters of 35-115 nm. Different ratios of the LdA were physically dispersed in the PVA/CMC nanocomposite label film to provide photochromic, ultraviolet protection, antimicrobial activity, and hydrophobic properties. Fluorescence peaks were detected at 365 and 519 nm to indicate a colour change to green. As a result of increasing the phosphor ratio, improved superhydrophobic activity was achieved as the contact angle was increased from 126.1° to 146.0° without affecting the film's original physical and mechanical properties. Both ultraviolet (UV) light protection and antibacterial activity were also investigated. The films showed a quick and reversible photochromic response without fatigue. The current strategy reported the development of a photochromic smart label that is transparent, cost effective, and flexible. As a result, numerous anticounterfeiting products can benefit from the current label for a better market. LdA-loaded PVA/CMC films demonstrated antibacterial activity between poor, good, very good, and outstanding as the percentage of LdA in the film matrix increased. The current film can be applied as a transparent photochromic security barcode for anticounterfeiting applications and smart packaging.

Photochromic and fluorescent ink using photoluminescent strontium aluminate pigment and screen printing towards anticounterfeiting documents.

Novel inorganic-organic hybrid photochromic and fluorescent ink for anticounterfeiting documents was developed using a pigment/resin ink formula enclosing a long-lived luminescent inorganic pigment with good thermal photostability. The produced ink exhibited an optimal excitation wavelength at 360 nm with an absorption colour and fluorescence changes in the printed document. To develop a transparent printed film from pigment/resin ink, the phosphorescent pigment has to be well dispersed physically without agglomeration. The pigment/resin hybrid was applied effectively onto commercial cellulose paper sheets using screen-printing technology. An homogeneous photochromic layer was deposited on cellulose paper document surface to afford a considerable greenish-yellow colour as demonstrated by CIE coloration measurements under a UV lamp, even at a pigment concentration as low as 0.1 wt% of the ink formulation. The printed paper sheets exhibited three excitation bands at 235, 274 and 378 nm and three emission bands at 416, 418 and 436 nm. Fluorescence optical microscopy, Fourier-transform infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and wavelength-dispersive X-ray fluorescence spectrometry of the printed paper sheet were explored. The screen-printed paper sheets displayed a reversible and fast photochromism during ultraviolet irradiation without fatigue. The rheological properties, stability, and printability of the ink were studied.

Preparation of flame-retardant, hydrophobic, ultraviolet protective, and luminescent transparent wood.

Transparent wood with multifunctional properties has recently attracted more attention as an efficient building product. Here, we describe the development of transparent wood with long-persistent phosphorescence, tough surface, high durability, photostability, and reversibility without fatigue, and with ultraviolet shielding, superhydrophobicity, and flame-retardant activity. This long-persistent phosphorescent, or glow-in-the-dark, smart wood exhibited an ability to continue emitting light for prolonged periods of time. The photoluminescent translucent wooden substrate was prepared by immobilizing lignin-modulated wooden bulk with an admixture of methylmethacrylate (MMA), ammonium polyphosphate (APP), and lanthanide-doped strontium aluminate (LSA; SrAl2 O4 :Eu2+ ,Dy3+ ) phosphor nanoparticles. The photoluminescent transparent wood displayed a colour switch from colourless to bright white beneath ultraviolet (UV) light and greenish-yellow in the dark as reported by Commission Internationale de l'Éclairage laboratory colorimetric space coordinates. The generated phosphorescent wooden substrates demonstrated an absorbance band at 365 nm and an emission band at 516 nm. The phosphorescent transparent wood was improved flame-retardant properties, ultraviolet shielding, and superhydrophobic properties, as well as a reversible long-persistent phosphorescent responsiveness to UV light without fatigue. The current approach demonstrated a potential large-scale production strategy for multifunctional transparent wooden substrates for a range of applications such as smart windows, gentle indoor and outdoor lighting, and safety directional signs in buildings.

Simple production of photoluminescent polyester coating using lanthanide-doped pigment.

A long-persistent phosphorescent surface coating was developed from a simple inorganic/organic nanocomposite towards the simple industrial manufacture of glow-in-the-dark products. This glow-in-the-dark smart coating is able to continue to emit light for proloned time periods. The organic/inorganic nanocomposite consisted of an organic polyester resin and inorganic europium- and dysprosium-doped strontium aluminate oxide nanoparticles. The phosphorescent lanthanide-doped strontium aluminate oxide pigment nanoparticles were added to the synthetic polyester resin in a generated pigment-loaded viscous solution that could then be harden in a few minutes using a cross-linking process in the presence of methylethyl ketone peroxide as a catalyst. The transparency of the produced glow-in-the-dark coating was accomplished simply by homogenous dispersion of the phosphorescent lanthanide-doped strontium aluminate nanoparticles into the sticky polyester resin before adding the catalyst to prevent pigment accumulation. This translucent long-persistent phosphorescent polyester nanocomposite can be simply applied under ambient conditions onto different surfaces such walls, textiles, tiles and glasses, ceramics, paper sheets, metals, and wood. The photoluminescent film displayed durable long-persistence emission with high reversibility. An optimum excitation wavelength was monitored at 360 nm, while the emission was monitored at 525 nm. Both the blank and the luminescent coating exhibited a transparent white colour in normal visible light. Conversely, the photoluminescent coating generated a bright green colour under an ultraviolet light lamp, a bright white colour after maintaining the sample for 10 sec in the dark, and a green phosphor after maintaining the sample for 100 min in the dark. The coloration parameters were explored using Commission Internationale de l'éclairage CIELAB colour coordinates. The hardness, as well as photophysical properties including emission, excitation, and life-time were studied. The surface morphology and elemental content were investigated using scanning electron microscopy, wavelength dispersive X-ray fluorescence, elemental mapping, and energy-dispersive X-ray spectroscopy. The films displayed an enhanced superhydrophobic activity without negatively influencing its native physico-mechanical properties.

Immobilization of silver and strontium oxide aluminate nanoparticles integrated into plasma-activated cotton fabric: luminescence, superhydrophobicity, and antimicrobial activity.

Smart textiles with a multifunctional surface, such as with photoluminescence, antimicrobial, and superhydrophobic properties, are highly desirable. Silver nanoparticles (Ag NPs) were prepared and immobilized onto a cotton surface using a facile pad-dry-curing technique to introduce long-lasting antimicrobial properties. The morphology of the silver immobilized cotton fibres was explored using scanning electron microscopic images and energy-dispersive X-ray spectra. The morphology of the formed Ag NPs was determined using a transmission electron microscope. Ag NPs exhibited uniform spreading and a high deposition density with a particle diameter in the range 25-55 nm. Both photoluminescence and superhydrophobic properties were explored by studying the cotton samples treated with hexadecyltrimethoxysilane nanocomposite containing lanthanide-doped strontium oxide aluminate NPs. Ultraviolet-visible light absorption, phosphorescence, and lifetime spectra were measured. The produced transparent superhydrophobic and photoluminescent film showed two absorbance bands at 273 and 367 nm and emission bands at 415 and 437 nm, as recognized by both absorption and emission spectra. Excellent antibacterial activities towards E. coli and S. aureus were monitored for the coated samples. Both fastness and colorimetric properties of Ag NPs-coated fabrics were explored.

Development of photoluminescent, superhydrophobic, and electrically conductive cotton fibres.

A simple method for the preparation of multifunctional nanocomposite was developed towards the production of water-repellent, electrically conductive, and photoluminescent film onto cotton fibres. The nanocomposite was composed of lanthanide-doped strontium aluminium oxide and silicon rubber dispersed in petroleum ether. The electrically conductive fabric was woven from nickel strips twisted with cotton filaments as core yarns, which were wrapped with pure cotton yarns. The nanoparticles (NPs) of lanthanide-doped strontium aluminium oxide were mixed with environmentally friendly room-temperature vulcanizing silicon rubber (RTV-SR) dissolved in petroleum ether to give the silicon rubber/strontium aluminate nanocomposites. The produced nanocomposites were applied onto electrically conductive cotton/nickel fibres using spray-coating technology. The surface of the cotton/nickel fibres showed different hierarchical morphologies depending on the total content of the silicon rubber. Additionally, the superhydrophobic effect was found to be improved upon increasing the total content of the luminescence pigment NPs. The morphologies of the prepared phosphor NPs were determined using transmission electron microscopy (TEM). The generated transparent luminescence film demonstrated an absorbance peak at 358 nm and an emission peak at 515 nm. Photoluminescence of cotton fibres was monitored with the generation of different colours, including grey, green-yellow, bright white, and turquoise shades as recognized using CIE Laboratory colorimetric parameters. The emission, excitation, lifetime, and decay time spectra of the phosphorescent spray-coated cotton samples were studied. The surface morphologies and chemical compositions of the spray-coated cotton/nickel were investigated using wavelength-dispersive X-ray fluorescence (WD-XRF), scanning electron microscope (SEM), Fourier-transform infrared spectra (FTIR), and energy-dispersive X-ray analyzer (EDAX). The superhydrophobic effects were characterized by measuring static water contact angle. The comfort characteristics of the treated cotton/nickel substrates were assessed by investigating their air permeability and stiffness. The treated cotton/nickel fabrics also displayed an antimicrobial activity. The results displayed water repellence with high electrical conductivity and photoluminescence properties.

Evaluation of SrAl2 O4 :Eu, Dy phosphor for potential applications in thermoluminescent dosimetry.

PURPOSE: To evaluate the use of commercial-grade strontium aluminate phosphorescent powder as a thermoluminescent (TL) dosimeter for clinical radiotherapy beams. MATERIALS AND METHOD: Commercially available Eu2+ , Dy3+ co-doped strontium aluminate powder (SrAl2 O4 :Eu, Dy) was annealed and then irradiated using 20 × 20 cm2 field size, with 6-MV (PDD10  = 70.7) and 18-MV (PDD10  = 79.4) photon beams and and 9-MeV (R50  = 3.6), 15 MeV (R50  = 5.9) and 18-MeV (R50  = 7.2) electron beams. To calibrate the relationship between the TL readings and the irradiated doses, TL glow curves were acquired for doses up to 600 cGy at all beam energies. For the percentage depth dose (PDD) measurement, the SrAl2 O4 :Eu, Dy powder was sandwiched by solid water phantoms, with varying thickness of solid water placed above to determine the depth. PDDs were measured at four representative depths and compared against the commissioning depth dose data for each beam energy. RESULTS: Linear dose response models of doses up to 200 cGy were created for all beam energies. Superlinearity was observed with doses greater than 200 cGy. The PDD measurement acquired experimentally agrees well with the commissioning data of the medical linear accelerator. Trapping parameters such as order of kinetics, activation energy and frequency factor have been obtained via TL glow curve analysis. CONCLUSION: The linear dose response demonstrates that SrAl2 O4 :Eu, Dy is a potential TLD dosimeter for both electron beams and photon beams at different beam energies. The PDD measurements further support its potential use in quality assurance and radiation dosimetry.

Development of long-persistent photoluminescent epoxy resin immobilized with europium (II)-doped strontium aluminate.

A facile approach for possible industrial production of long-persistent phosphorescence, continuing to emitting light for a long time period, smart cobbles were developed toward photoluminescent hard surfaces. The inorganic strontium aluminium oxide pigment doped with rare earth elements was added to a synthetic organic epoxy in the presence of polyamine as a hardener to make a phosphor-loaded viscous fluid that can then be hardened in a few minutes. The transparency of the solid cobbles can be accomplished easily using homogeneous dispersion of the phosphor in the epoxy resin fluid before the addition of a hardener to avoid pigment aggregation. This pigment-epoxy formula can be easily applied industrially onto flagstones surfaces under ambient conditions. The photoluminescent cobblestones demonstrated an optimum excitation wavelength at 366 nm and an emission band at 521 nm with a long-persistent phosphorescence cobble surface. The development of a translucent white colour under normal daylight, bright green under ultraviolet (UV) irradiation, bright white colour after 30 sec in the dark, and phosphorescent green colour after 75 min in the dark was indicated using Commission Internationale de l'Eclairage (CIE) Laboratory coloration measurements. The luminescent hard composite cobble exhibited a highly durable and reversible long-persistent phosphorescence light. Photoluminescence, morphological, and hardness properties as well as the elemental composition of the prepared cobbles were explored.

Improving flow dynamics and storage longevity of a low-cost phosphorescent fingerprint powder.

An inexpensive, commercially available doped strontium aluminate phosphor with long-lived afterglow was prepared as a luminescent fingerprint dusting powder suited for challenging, highly patterned substrates; however, prolonged exposure to humidity was found to reduce that powder's affinity for fingermarks. Here, an enhanced preparation for synthesizing that fingerprint dusting powder is presented that prevents powder aggregation and loss of function upon exposure to humid environments. This was achieved by introducing a flow regulator during synthesis: hydrophobic silica SIPERNAT® D10 or SIPERNAT® D17. Increasing the hydrophobicity of the powder prevents aggregation by inhibiting the uptake of water, thereby improving the material's flow dynamics and transfer behavior from brush to fingermark. The angle of repose and flow characteristics made by the modified powders were quantified, with excellent affinity for fingermarks observed, even after being stored under 85% (±5%) humidity for 4 weeks. A preliminary comparison of the performance of the modified hydrophobic powders relative to the unmodified precursor revealed that more of the SIPERNAT® treated powder typically adhered to fingermarks while simultaneously imparting less background development. In addition, fewer clumps of particulate were observed in the developed fingermarks after addition of a hydrophobic flow regulator. This technical report outlines the updated method for synthesizing the fingerprint powder, with summarized flow performance results, and a demonstration of the modified powder's affinity for simulated fingermark evidence.

Smart Mechanoluminescent Phosphors: A Review of Strontium-Aluminate-Based Materials, Properties, and Their Advanced Application Technologies.

Mechanoluminescence, a smart luminescence phenomenon in which light energy is directly produced by a mechanical force, has recently received significant attention because of its important applications in fields such as visible strain sensing and structural health monitoring. Up to present, hundreds of inorganic and organic mechanoluminescent smart materials have been discovered and studied. Among them, strontium-aluminate-based materials are an important class of inorganic mechanoluminescent materials for fundamental research and practical applications attributed to their extremely low force/pressure threshold of mechanoluminescence, efficient photoluminescence, persistent afterglow, and a relatively low synthesis cost. This paper presents a systematic and comprehensive review of strontium-aluminate-based luminescent materials' mechanoluminescence phenomena, mechanisms, material synthesis techniques, and related applications. Besides of summarizing the early and the latest research on this material system, an outlook is provided on its environmental, energy issue and future applications in smart wearable devices, advanced energy-saving lighting and displays.

Preparation of a low-cost fingerprint powder that harnesses white light to emit long-lived phosphorescence.

An inexpensive, commercially available doped strontium aluminate phosphor with long-lived afterglow has been prepared and assessed in the role of a luminescent fingerprint dusting powder. Blue, green, and aqua phosphorescence persisting for ca. 30 s was obtainable from treated fingermarks after charging the powders with the white light (400-700 nm) setting of a forensic light source. Imaging the phosphorescent afterglow enabled the elimination of background emissions encountered during latent fingermark examination. This was demonstrated by visualising fingermarks on substrates that possess inbuilt fluorescent security features and highly patterned substrate backgrounds, without any need for bespoke scientific equipment.

Preparation of photoluminescent nanocomposite ink for detection and mapping of fingermarks.

Simple and efficient detection and mapping method based on a strong turn-on fluorescent pigment was developed for fingerprint analysis. We present a phosphor powder characterized by strong emission which is useful to achieve better fingerprint detection on multicolored or photoluminescent surfaces, such as currency notes characterized by optically changeable inks and highly fluorescent positions, because it offers better contrast and reduce the difficulty of background interference. Novel photochromic ink was prepared to establish a fingerprinted colorless film onto cellulose documents with green emission for anticounterfeiting applications as illustrated by photoluminescence spectra. Inorganic/organic nanoscale composite ink was prepared from rare-earth doped aluminate phosphor nanoparticles (PNPs; 27-49 nm) dispersed in a polyacrylic acid binding agent. PNPs were dispersed efficiently in polyacrylic acid to generate a colorless mark. The produced photochromic inks were spray-coated onto off-white paper sheets enclosing invisible fingermarks, and then exposed to thermofixation. Photochromic film was detected on paper surface presenting a transparent appearance under visible daylight and switchable to green under UV light. The CIE Lab parameters and photoluminescence spectra were studied under visible light and ultraviolet irradiation. The fingerprinted sheets showed fluorescence band at 517 nm upon excitation at 366 nm, showing a bathochromic shift and reversible photochromism without fatigue. The morphologies of pigment phosphor particles and fingerprinted sheets were inspected. The rheological properties of ink and mechanical behavior of the fingerprinted paper samples were explored. HIGHLIGHTS: Novel smart ink with alkaline-earth aluminate and polyacrylic acid was developed. Dual-mode fluorescent photochromism was presented for latent fingerprint analysis. Off-white fingerprinted films under daylight showed color change to green under UV. Fluorescence band monitored at 517 nm upon excitation at 366 nm. Fluorescent fingermark on paper sheets demonstrated good photostability.

Immobilization of Strontium Aluminate into Recycled Polycarbonate Plastics towards an Afterglow and Photochromic Smart Window.

A transparent smart window made of recycled polycarbonate plastic (PCP) waste was prepared and immobilized with strontium aluminate phosphor nanoparticles (SAPN). It has afterglow emission, super-hydrophobicity, durability, photostability, good mechanical properties, ultraviolet protection, and high optical transmittance. To create an afterglow emission polycarbonate smart window (SAPN@PCP), recycled polycarbonate waste was integrated with various concentrations of SAPN (15-52 nm). SAP micro-scale powder was made using the solid-state high temperature method. The SAP nanoparticles were produced using the top-down method. To create a colorless plastic bulk, recycled polycarbonate waste was inserted into a hot bath. This colorless plastic was thoroughly combined with SAPN and cast to create an afterglow luminous smart window. To investigate its photoluminescence properties, spectrum profiles of excitation and emission were measured. According to the luminescence parameters, the phosphorescent colorless polycarbonate plates displayed a change in color to strong green under UV illumination and greenish-yellow in a dark box. The afterglow polycarbonate smart window displayed two emission peaks at 496 and 526 nm, and an absorption wavelength of 373 nm. Upon increasing the SAPN ratio, the hydrophobic activity, hardness, photostability, and UV protection were improved. Luminescent polycarbonate substrates with lower SAPN ratio demonstrated rapid and reversible fluorescence under UV light, while the higher SAPN content in the luminous polycarbonate substrates showed afterglow.

Preparation of photoluminescent and anticorrosive epoxy paints immobilized with nanoscale graphene from sugarcane bagasse agricultural waste.

Sugarcane bagasse agricultural waste has been one of the most common solid pollutants worldwide. Thus, introducing a simple method to convert sugarcane bagasse into value-added materials has been highly significant. Herein, we develop a simple and green strategy to reprocess sugarcane bagasse as a starting material for the preparation of graphene oxide nanosheets toward the preparation of novel photoluminescent, hydrophobic, and anticorrosive epoxy nanocomposite coatings integrated with lanthanide-doped aluminate nanoparticles. Environmentally friendly graphene oxide (GO) nanostructures were provided by a single-step preparation procedure from sugarcane bagasse (SCB) agricultural waste using ferrocene-based oxidation under muffled conditions. The oxidized SCB nanostructures were applied as a drier, anticorrosion, and crosslinking agent for epoxy coatings. Different concentrations of pigment phosphor were applied onto the epoxy coating. The generated epoxy-graphene-aluminate (EGA) paints were then coated onto mild steel. The hydrophobic properties and hardness as well as resistance to scratch of the EGA paints were examined. The transparency and colorimetric screening of the EGA nanocomposite paints were determined by the absorption spectral analysis and CIE Lab parameters. The luminescent translucent paints demonstrated a bright green emission at 520 nm when excited at 372 nm. The anticorrosion properties of the painted steel submerged in NaCl(aq) were inspected by the electrochemical impedance spectral (EIS) method. The EGA paints with phosphor (11% w/w) exhibited the most distinct anti-corrosion properties and long-persistent luminescence. The produced paints displayed high durability and photostability.