Photoluminescence Characteristics Research Articles

Spectral studies of thermally stable Dy3+/Sm3+ co-doped Li2Ba5W3O15 phosphors for warm white LEDs

In the current study, a series of Li2Ba5W3O15: RE3+ (RE = Dy, Sm) [LBW:Dy3+/Sm3+] phosphors were prepared using a high-temperature solid-state method. X-ray diffraction, Scanning electron microscopy with energy-dispersive x-ray analysis scans showed that the crystal form was consistent with the standard LBW and comprised small irregularly shaped particles. Diffuse reflectance spectral (DRS) data was utilized to calculate the band gaps. Fluorescence study shows that LBW material doped with Dy3+ and Sm3+ yield distinct colors at 496 nm (blue) for Dy3+ and 582 nm (green-yellow), 612 nm (yellow), and 669 nm (red) for Sm3+ when excited by near-ultraviolet (336 nm) light. The observation of energy transfer between Dy3+ and Sm3+ ions play a role in modifying the luminescence of LBW:Dy3+/Sm3+ co-doped phosphors. With a constant excitation wavelength (λ Ex), different levels of activator doping lead to a change in the emission colors from their neutral white light to a deep orange-red region for LBW:Dy3+/Sm3+ phosphors. The decay curves demonstrate a decrease in lifetime with an increase in the concentration of activator ions (Sm3+). For D3S5 phosphor, the temperature-dependent photoluminescence characteristics were analyzed under λ Ex = 336 nm excitation. The results indicate excellent luminescence thermal stability with an activation energy of 0.16 eV at λ Ex = 336 nm. With its low color-correlated temperature and good thermal stability, the prepared phosphor sample shows potential as a solid-state emitting phosphor that can be used with UV chip stimulation for warm white LED applications.

Polyvinylalcohol Composite Filled with Carbon Dots Produced by Laser Ablation in Liquids

Carbon dots (CDs), owing to their excellent photoluminescent features, have been extensively studied for physics preparation methods and for biomedical and optoelectronic device applications. The assessment of the applicability of CDs in the production of luminescent polymeric composites used in LEDs, displays, sensors, and wearable devices is being pursued. The present study reports on an original, environmentally friendly, and low-cost route for the production of carbon dots with an average size of 4 nm by laser ablation in liquid. Jointly, to prove the significance of the study for a wide range of applications, a free-standing flexible polyvinyl alcohol (PVA) composite containing photoluminescent carbon dots was manufactured. CDs were prepared using targets of porose charcoal with a density of 0.271 g/cm3 placed in phosphate-buffered saline (PBS) liquid solution and irradiated for 30 min by pulsed IR diode laser. The optical properties of the obtained suspension containing carbon dots were studied with UV-ViS and FTIR spectroscopies. The photoluminescence of the produced carbon dots was confirmed by the emission peak at 480 nm in the luminescence spectrum. A narrow luminescence band with a full width at half-maximum (FWHM) of less than 40 nm could be an asset in spectral emission analysis in different applications. Atomic force microscopy confirms the feasibility of manufacturing CDs in clean and biocompatible environments, paving the way for an easier and faster production route, crucial for their wider applicability.

Printable Light-Emitting Metasurfaces with Enhanced Directional Photoluminescence.

Nanoimprint lithography is gaining popularity as a cost-efficient way to reproduce nanostructures in large quantities. Recent advances in nanoimprinting lithography using high-index nanoparticles have demonstrated replication of photonic devices, but it is difficult to confer special properties on nanostructures beyond general metasurfaces. Here, we introduce a novel method for fabricating light-emitting metasurfaces using nanoimprinting lithography. By utilizing quantum dots embedded in resin, we successfully imprint dielectric metasurfaces that function simultaneously as both emitters and resonators. This approach to incorporating quantum dots into metasurfaces demonstrates an improvement in photoluminescence characteristics compared to the situation where quantum dots and metasurfaces are independently incorporated. Design of the metasurface is specifically tailored to support photonic modes within the emission band of quantum dots with a large enhancement of photoluminescence. This study indicates that nanoimprinting lithography has the capability to construct nanostructures using functionalized nanoparticles and could be used in various fields of nanophotonic applications.

Green Synthesis of Various Heteroatom‐doped Carbon Quantum Dots from Urine, Whey, and Their Mixture: The Optimization of Synthesis and Potential Applications

AbstractThe employment of biomass waste for the fabrication of carbon quantum dots (CQDs), as a novel fluorescent material with high photoluminescence (PL) activity, has gained intense interest for the last decade. However, the fabrication of CQD from biomass waste encounters challenges including low fluorescence yield, reproducibility, and stability. Therefore, the novel, simple, flexible fabrication routes for CQDs using biomass waste as a precursor are still essential for practical applications. In this study, we reported the employment of human urine (U), sour whey (W), and their mixture (U/W) as precursors for the hydrothermal green synthesis approach. For all cases, CQDs with an excitation‐dependent emission nature were obtained with a quantum yield (QY) value of 48 %, 28 %, and 39 % for U, W, and U/W, respectively. For each case, doping of various heteroatoms such as N, P, S, etc., in the structure of CQDs contributed PL characteristics with high QY, reasonably low cytotoxicity, and, robust pH and storage stability which indicate their high potential in various biomedical applications such as bioimaging and pH sensors. This study proves the utilization of human urine and whey as the precursors for the fabrication of CQDs through a low‐cost, flexible, and eco‐friendly green synthesis procedure.

Non-amphoteric N-type doping with Sn of GaAs(631) layers grown by molecular beam epitaxy

The Sn-doping effects on the electrical conduction and optical properties of GaAs(631)A epilayers grown by molecular beam epitaxy were investigated. We found that the conduction type conversion, frequently observed in the doping of layers grown on high-index substrates, is avoided when tin-doping is implemented. The maximum free-carrier concentration (n) obtained in GaAs(631):Sn was 2 × 1019 cm−3, an order of magnitude higher than previously reported for GaAs(631):Si, and within the same order of magnitude for the growth of GaAs(100):Si. The electron mobility was suitable for many optoelectronic applications. Raman spectroscopy showed low lattice disorder in (631) oriented samples, compared with singular (100) samples. The photoluminescence characterization of the samples revealed the blueshift of the optical transitions close to E0 associated with the Moss–Burstein effect for Sn doping. Photoreflectance spectroscopy was used to study the doping properties at the critical points E1 and E1 + Δ1, where the major affectation with n was perceived in the broadening parameter Γ.

Photoluminescence and transport properties of fluorinated graphene via a weak fluorination strategy

The zero-bandgap properties of graphene (Gr) limit its various applications. Fluorination is an alternative strategy to open the bandgap to broaden its applications. However, traditional fluorination methods are detrimental to human health and contribute extensively to environmental pollution. Here, we develop a simple and safe process of weak fluorination that introduces fluorine atoms into Gr, breaking its zero-bandgap structure. This strategy is more environmentally friendly, risk-free, and harmless to humans, making it suitable for large-scale production. Through this highly controllable weak fluorination process, micro-area selective fluorination is achieved and induces excellent photoluminescence characteristics but maintains a high mobility, compared to the pristine Gr with zero bandgap. The degree of fluorination determines the photoelectric and transport properties of Gr. This work provides an experimental foundation for developing materials based on fluorinated graphene and designing high-performance functional devices.

Electropositive Citric Acid-Polyethyleneimine Carbon Dots Carrying the PINK1 Gene Regulate ATP-Related Metabolic Dysfunction in APP/PS1-N2a Cells.

(1) Background: Alzheimer's disease (AD) is characterized by β-amyloid (Aβ) peptide accumulation and mitochondrial dysfunction during the early stage of disease. PINK1 regulates the balance between mitochondrial homeostasis and bioenergy supply and demand via the PINK1/Parkin pathway, Na+/Ca2+ exchange, and other pathways. (2) Methods: In this study, we synthesized positively charged carbon dots (CA-PEI CDs) using citric acid (CA) and polyethyleneimine (PEI) and used them as vectors to express PINK1 genes in the APP/PS1-N2a cell line to determine mitochondrial function, electron transport chain (ETC) activity, and ATP-related metabolomics. (3) Results: Our findings showed that the CA-PEI CDs exhibit the characteristics of photoluminescence, low toxicity, and concentrated DNA. They are ideal biological carriers for gene delivery. PINK1 overexpression significantly increased the mitochondrial membrane potential in APP/PS1-N2a cells and reduced reactive-oxygen-species generation and Aβ1-40 and Aβ1-42 levels. An increase in the activity of NADH ubiquinone oxidoreductase (complex I, CI) and cytochrome C oxidase (complex IV, CIV) induces the oxidative phosphorylation of mitochondria, increasing ATP generation. (4) Conclusions: These findings indicate that the PINK gene can alleviate AD by increasing bioenergetic metabolism, reducing Aβ1-40 and Aβ1-42, and increasing ATP production.

Structural and photoluminescence investigation of Y2O3:Sm3+ nano‐powders: Organic agent's effect

AbstractIn this article, the authors delve into the synthesis of Y2O3:Sm3+ nanopowders using the sol–gel method, employing organic agents such as ethylene glycol (EG) and polyethylene glycol (PEG). This thorough investigation focuses on the structural, morphological, and photoluminescence characteristics of these nanopowders, with particular consideration for their potential applications in the field of optical devices. X‐ray diffraction patterns indicate that all powders crystallize in pure cubic phases (Ia‐3). Transmission electron microscopy (TEM) analysis reveals the presence of particles with dimensions less than 70 nm. Specifically, morphological and structural data suggest that the crystallite size of nanopowders prepared with PEG exceeds that of nanopowders prepared with EG. In exploring the photoluminescence properties, the emission spectra of the powders, recorded at λem = 600 nm, exhibit two absorption bands attributed to the charge transfer state (CTS) from O2− → Sm3+, with a maximum absorption at 223 nm, and to the intraconfigurational transition 4f5‐4f5 of Sm3+. A red/orange emission, attributed to the 4G5/2 → 6H7/2 transition, predominates under these conditions. A significant improvement in the intensity of photoluminescence is notably observed in samples prepared with organic agents compared to those prepared without agents. Finally, chromatic coordinates underscore the strong potential of Y2O3:Sm3+ nanopowders as promising phosphors for lighting applications.

Revealing photoluminescence and nonlinear optical absorption characteristics of PbMo0.75W0.25O4 single crystal for optical limiting applications

Nonlinear absorption properties of PbMo0.75W0.25O4 single crystal fabricated by the Czochralski method were studied. The band gap energy of the crystal was determined as 3.12 eV. Urbach energy which represents the defect states inside the band gap was found to be 0.106 eV. PbMo0.75W0.25O4 single crystal has a broad photoluminescence emission band between 376 and 700 nm, with the highest emission intensity occurring at 486 nm and the lowest intensity peak at 547 nm, depending on the defect states. Femtosecond transient absorption measurements reveal that the lifetime of localized defect states is found to be higher than the 4 ns pulse duration. Open aperture (OA) Z-scan results demonstrate that the PbMo0.75W0.25O4 single crystal exhibits nonlinear absorption (NA) that includes two-photon absorption (TPA) as the dominant mechanism at the 532 nm excitations corresponding to 2.32 eV energy. NA coefficient (β eff ) increased from 7.24 × 10−10 m W−1 to 8.81 × 10−10 m W−1 with increasing pump intensity. At higher intensities β eff tends to decrease with intensity increase. This decrease is an indication that saturable absorption (SA) occurred along with the TPA, called saturation of TPA. The lifetime of the defect states was measured by femtosecond transient absorption spectroscopy. Saturable absorption behavior was observed due to the long lifetime of the localized defect states. Closed aperture (CA) Z-scan trace shows the sign of a nonlinear refractive index. The optical limiting threshold of PbMo0.75W0.25O4 single crystal at the lowest intensity was determined as 3.45 mJ/cm2. Results show that the PbMo0.75W0.25O4 single crystal can be a suitable semiconductor material for optical limiting applications in the visible region.

Effect of Ce<sup>3+</sup> Concentration and YAG Crystal Particles Size on Photoluminescence

Purpose of research. Determine the effect on the photoluminescence of phosphors from yttrium-aluminum garnet activated by cerium ions Ce3+, the size of its particles and the concentration of cerium ions in them.Methods. Structural electron and confocal microscopic, fluorescent, microspectral studies using a laser lex = 473 nm as an excitation source, energy dispersive, X-ray diffraction studies, as well as goniophotometric measurements on the radial distribution of light intensity excited by the LED matrix were carried out.Results. A detailed granulometric analysis of the particle sizes of phosphors was carried out for two samples from different manufacturers, cumulative distributions M(d) were constructed and their quantiles were established. Based on the results of measuring photoluminescence from individual particles in the compositions of phosphors based on YAG:Ce3+, a Stokes shift was detected in these samples: short-wavelength – for particles with sizes less than 10 μm and with low concentration and long-wavelength – with sizes greater than 10 μm with an increased concentration of over ~0.2% . The obtained microspectral size-emission dependences lem(d) and energy Imax(d) were consistent with the description based on the proposed physical mechanism of their formation by the 5d → 2F5/2 and 5d → 2F7/2 transitions.Conclusion. A short-wavelength shift of photoluminescence intensity maxima for particles smaller than 10 μm was discovered, due to a significant increase in the influence of surface stresses due to a reduction in the number of atoms. For larger particle sizes, the characteristic photoluminescence intensity maxima cease to depend on the wavelength. The radial distribution of luminous intensity determined by the goniophotometric method made it possible to calculate the value of the luminous flux equal to 1350 lm and 1140 lm, respectively, for LED matrices containing 8 LEDs with the studied phosphors.

Observation of broad triangular Frank-type stacking faults and characterization of stacking faults with emission wavelengths below 430 nm in 4H–SiC epitaxial layers

Frank-type stacking faults in 4H–SiC epitaxial layers were investigated using room-temperature photoluminescence mapping and high-angle annular dark-field high-resolution scanning transmission electron microscopy. Remarkably, the intrinsic Frank-type stacking fault (5,2) and intrinsic multilayer Frank-type stacking fault (4,2), which have been reported to have elongated triangular shapes to date, were found to have broader triangular shape, which was typical shape of Shockley-type stacking faults. The shaping of stacking faults could be explained based on the directions of the partial dislocations bounding the stacking faults. Formation models for the intrinsic (5,2) and (4,2) stacking faults were proposed. In addition, we observed Frank-type stacking faults (3,2,2,3) and (3,3) and Shockley-type stacking faults (3,3,3,2,3,2) and (3,2,3,3,3,2), which were not reported before. All of these stacking faults were composed with the stacking numbers 2 and 3 in the Zhdanov notation and showed very close characteristic photoluminescence emission wavelengths of 427–428 nm. Formation models for the stacking faults of (3,2,2,3), (3,3), (3,3,3,2,3,2), and (3,2,3,3,3,2) were proposed, also. Based on the proposed formation models of (4,2) and (3,3) stacking faults, formation models for the Frank-type stacking faults (4,1) and (3,2) were discussed. Finally, we pointed out that the (4,1) Frank-type stacking fault should be the intrinsic not the extrinsic fault, and the (3,2) Frank-type stacking fault is the extrinsic fault.

High-Performance Broadband Image Sensing Photodetector Based on MnTe/WS2 van der Waals Epitaxial Heterostructures.

Two-dimensional transition metal dichalcogenide (TMDC) heterostructure is receiving considerable attention due to its novel electronic, optoelectronic, and spintronic devices with design-oriented and functional features. However, direct design and synthesis of high-quality TMDC/MnTe heterostructures remain difficult, which severely impede further investigations of semiconductor/magnetic semiconductor devices. Herein, the synthesis of high-quality vertically stacked WS2/MnTe heterostructures is realized via a two-step chemical vapor deposition method. Raman, photoluminescence, and scanning transmission electron microscopy characterizations reveal the high-quality and atomically sharp interfaces of the WS2/MnTe heterostructure. WS2/MnTe-based van der Waals field effect transistors demonstrate high rectification behavior with rectification ratio up to 106, as well as a typical p-n electrical transport characteristic. Notably, the fabricated WS2/MnTe photodetector exhibits sensitive and broadband photoresponse ranging from UV to NIR with a maximum responsivity of 1.2 × 103 A/W, a high external quantum efficiency of 2.7 × 105%, and fast photoresponse time of ∼50 ms. Moreover, WS2/MnTe heterostructure photodetectors possess a broadband image sensing capability at room temperature, suggesting potential applications in next-generation high-performance and broadband image sensing photodetectors.

Halide Engineering in Mixed Halide Perovskite-Inspired Cu2AgBiI6 for Solar Cells with Enhanced Performance.

Cu2AgBiI6 (CABI) is a promising perovskite-inspired absorber for solar cells due to its direct band gap and high absorption coefficient. However, the nonradiative recombination caused by the high extrinsic trap density limits the performance of CABI-based solar cells. In this work, we employ halide engineering by doping bromide anions (Br-) in CABI thin films, in turn significantly improving the power conversion efficiency (PCE). By introducing Br- in the synthetic route of CABI thin films, we identify the optimum composition as CABI-10Br (with 10% Br at the halide site). The tailored composition appears to reduce the deep trap density as shown by time-resolved photoluminescence and transient absorption spectroscopy characterizations. This leads to a dramatic increase in the lifetime of charge carriers, which therefore improves both the external quantum efficiency and the integrated short-circuit current. The photovoltaic performance shows a significant boost since the PCE under standard 1 sun illumination increases from 1.32 to 1.69% (∼30% relative enhancement). Systematic theoretical and experimental characterizations were employed to investigate the effect of Br- incorporation on the optoelectronic properties of CABI. Our results highlight the importance of mitigating trap states in lead-free perovskite-inspired materials and that Br- incorporation at the halide site is an effective strategy for improving the device performance.

Probing multifunctional applications of LiCa2Mg2V3O12: Sm3+ phosphor using Judd-Ofelt analysis and dual mode non-contact optical thermometry

LiCa2Mg2V3O12:Sm3+ phosphors have been prepared by solid state method and analysed by X-ray diffraction, EDX-elemental mapping, UV–VIS-NIR spectroscopy, photoluminescence (PL) and temperature dependent photoluminescence (TDPL). The absorption spectra analysis using Judd-Ofelt theory provides the intensity parameters and manifest the covalent nature of Sm-O bond. The PL spectra monitored at 338 nm excitation exhibits emission peaks of Sm3+ at 567, 617 and 651 nm in addition to the broad band emission of LiCa2Mg2V3O12 host. The Commision Internationale deL’Eclairage (CIE) coordinates, correlated color temperature (CCT) and color rendering index (CRI) values elucidate the efficient yellow emission of phosphors. The radiative parameters are evaluated and have outrageous branching ratio and cross section that aids in visible laser applications. The optical thermometry of phosphor is carried out by utilizing FIR method through selecting spectral modes 6H5/2/VO43-, 6H7/2/VO43- and 6H9/2/ VO43-. The mode 6H9/2/ VO43- have higher absolute sensitivity (Sa) and relative sensitivity (Sr) values of 0.4418 K−1 and 1.6079 % K−1. The temperature resolution of modes are 0.1633, 0.1677 and 0.1563 K respectively. The thermochromic study reveals the high chromaticity shift (Δs = 0.1869) of phosphor and the Sa(x) and Sr(x) values evaluated based on CIE coordinates are 0.0011 K−1 and 0.2407 % K−1 respectively. The PL and TDPL characteristics of prepared phosphor suggest that it have multifunctional application in the fields of lasers, thermo-sensors, thermochromic displays and LEDs.

Practical consideration on Racah parameter and Tanabe−Sugano diagram analyses for Mn4+ and Cr3+-activated phosphors

The Racah parameters and Tanabe−Sugano (T−S) diagram are widely used as describing the electron−electron repulsion effects within the metal complexes in coordination chemistry. The present study discusses the Racah and related parameters for the Mn4+ and Cr3+-activated phosphors. The main subjects are two-fold: (i) to clarify how different input parameters of the excited-state energies make a difference in the Racah parameters derived from the general model and (ii) to further clarify the differences between the general and our newly proposed models. The three different excited-state energies of (1) the zero-phonon line energy, (2) the photoluminescence (PL) and/or PL excitation (PLE) peak energies, and (3) the Stokes shift-corrected PLE peak energy are considered in (ii). It is shown that the choice of such excited-state energies is of crucial importance for obtaining reliable Racah parameters and T−S diagram. The present analysis of (ii) also suggests our newly proposed model to promise the Racah parameters being satisfied the requirements of B and C to be smaller than and their ratio of C/B being not largely changed from the free-ion values. The lattice temperature effects on the PL and PLE spectral features of the 3d3 ion-activated phosphors are also discussed in detail.

Up-converted white light emission in Er3+ doped MgAl2O4 nanocrystals

This work presents the influence of host defect centers on the photoluminescence characteristics of Mg1−xErxAl2O4 (x = 0.005, 0.01, and 0.03) nanocrystals under UV and near-infrared (NIR) excitations. The spinel-structured nanocrystals are synthesized through the combustion method. The Rietveld refinement and nuclear magnetic resonance analyses estimated the Er3+ ion occupancy at octahedral and other random sites of the MgAl2O4 lattice, and the existence of various lattice defects. Diffuse reflectance spectra showed broad bands attributed to oxygen vacancies as well as antisite defects and sharp peaks attributed to f–f transitions of Er3+ ions. The upconversion luminescence spectra consisted of sharp emission lines, ascribed to Er3+ ions, in the green and red wavelength regions, which overlapped over the broad curve attributed to intrinsic defects. Further, the UV excited downconversion luminescence spectra showed two broad emission bands in blue–violet and red-NIR regions with a very weak Er3+ ion emission feature. This up- and downconversion emission revealed energy transfer between host and Er3+ ions via intrinsic defects. As a result, the emission color changes from bluish purple to white by varying the excitation wavelength from UV to NIR. This rare earth activated luminescence from MgAl2O4 nanocrystals would exhibit potential applications in display devices and solid-state lighting.

Structural and Photoluminescence Characteristics of a Novel Single‐Phase White‐Emitting Phosphor SrBi2Nb2O9:Dy3+

A group of white light‐emitting phosphors SrBi2Nb2O9:xDy3+ (SBN:xDy3+) are prepared by high‐temperature solid reaction. The crystal phase, morphology, and photoluminescence (PL) characteristics of the prepared SBN:xDy3+ are analyzed. The X‐ray diffraction results prove that the synthesized samples are pure phase, in which the shift of the main peak depicted that crystal interplanar distance decreases after Dy3+ replacing Bi3+. The scanning electron microscope results show that the average crystal size of the sample is ≈1–10 μm. Energy dispersive X‐ray spectroscopy shows that the ratio of element composition of the SBN:xDy3+ is similar to the theoretical calculation. The PL excitation illustrates the excitation peaks mainly exist at 389, 399, 426, and 450 nm due to the transitions of Dy3+. For PL, the emission peaks of samples with different doping concentrations are centered at 479 and 573 nm. The ratio of yellow intensity to blue intensity indicates that Dy3+ is located at a high symmetry site, which has the possibility to produce suitable white light. The Commission Internationale de l’Eclairage coordinates of the SBN:xDy3+ are located near the standard white light coordinate. All these results prove that SrBi2Nb2O9:xDy3+ can be a potential material in the white light application.

Atomic vs. sub-atomic layer deposition: impact of growth rate on the optical and structural properties of MoS2 and WS2

MoS2 and WS2 mono- and multilayers were grown on SiO2/Si substrates. Growth by atomic layer deposition (ALD) at fast growth rates is compared to sub-ALD, which is a slow growth rate process with only partial precursor surface coverage per cycle. A Raman spectroscopic analysis of the intensity and frequency difference of the modes reveals different stages of growth from partial to full surface layer coverage followed by layer-by-layer formation. The initial layer thickness and structural quality strongly depend on the growth rate and monolayers only form using sub-ALD. Optical activity is demonstrated by photoluminescence (PL) characterization which shows typical excitonic emission from MoS2 and WS2 monolayers. A chemical analysis confirming the stoichiometry of MoS2 is performed by x-ray photoelectron spectroscopy. The surface morphology of layers grown with different growth rates is studied by atomic force microscopy. Plan-view transmission electron microscopy analysis of MoS2 directly grown on freestanding graphene reveals the local crystalline quality of the layers, in agreement with Raman and PL results.

Instigating the Asymmetry of Dy3+ Ions Doped in Borate Glasses for Photonic Device w-LED Applications

For usage in solid state white light emitting device applications, dysprosium-activated calcium aluminum barium sodium borate glass was synthesized. The detailed understanding of physical, optical, structural, and photo-luminescence characteristics was examined and compared. To comprehend the oscillator strength of the ligands in the prepared glasses, the Judd-Ofelt intensity characteristics were assessed. The Ω2 greater relative oscillator strength value shows highest for the prepared glasses suggesting their cause due to hypersensitive transitions. In comparison to other glasses in the research, the potential radiative transition probabilities, branching ratios, and stimulated emission cross-section for 575 nm emission all exhibited higher values. The stimulated emission cross-section shows highest for 0.3 mol% Dy2O3 content in the present glasses. The asymmetry of synthesizedglass sample ratio has been evaluated and compared using Yellow to Blue (Y/B) emission ratio. Study of the emission spectra and assessment of CCT and DUV values for the glasses reveal emission in the CIE diagram's white light zone.

A rapid room-temperature self-healing, antibacterial, photoluminescent waterborne polyurethane coating with excellent mechanical properties based on double dynamic cross-linked network used for leather finishing

Waterborne polyurethane that integrates fast room-temperature self-healable ability, high mechanical properties, antibacterial activity, and photoluminescence features is highly desirable but challenging. Herein, a novel waterborne polyurethane (ZIWPU) is synthesized with the double dynamic cross-linked networks of multiple hydrogen bonds formed by asymmetric polyurea structure and Zn2+-carboxylate coordination bonds. Profiting from the synergistic effects of double dynamic cross-linked networks, the optimized ZIWPU2 film exhibits excellent mechanical properties (tensile strength of 34.36 MPa and toughness of 107.21 MJ/m3) and rapid room-temperature self-healing ability (healing efficiency > 85 % within 10 h) with the assistant of trace alcohol, which is superior to those of the most of currently reported room-temperature self-healing waterborne polyurethane. In addition, owing to the existence of Zn2+, ZIWPU2 is simultaneously integrated with the outstanding antibacterial ability (antibacterial rate>96 %). Especially, the carbon dots (CDs) are introduced into ZIWPU2 to give it an excellent photoluminescence function that can be used for anti-counterfeiting and crack diagnosis. Finally, this versatile WPU material is successfully applied to leather finishing.