Luminous Properties Research Articles

Preparation and Photophysical Properties of Znq2 Metallic Nanomaterials

AbstractBis(8‐hydroxyquinolates) Zinc (Znq2) can be used as a light‐emitting layer material in OLED devices to achieve its efficient electroluminescence effect. In this paper, Znq2 powder has been successfully synthesized and modified by the physical vapor deposition (PVD) method. Precursors and nano‐materials are characterized by XRD, SEM, PL, and so on. The performance of the modified material has been significantly improved. The emission intensity and absorption intensity in the deposited products increased with the increase in PVD temperature. At 453 K, luminous properties such as luminous intensity reach the optimal value including its fluorescence lifetime. Fluorescence lifetime values vary from 13 to 17 ns with the increase in temperature. The luminescence mechanism is also discussed. The energy gap and absorption spectrum of HOM‐LUMO are calculated by the DFT/UB3LYP method. The experimental values agree well with the theoretical values. The nanomaterial crystals modified by PVD technology are more orderly, impurities are reduced, and the luminous stability of the material is improved, which may be one of the reasons for the relatively slow decline in product life. The research combined with theoretical simulation is expected to be helpful to the research and promotion of such materials.

Color-tunable luminescence and energy transfer of Ba2YZrO6:R (R = Dy3+, Sm3+, Dy3+/Sm3+)

Abstract Rare earth ions (Dy3+ and Sm3+) doped luminescence materials have been attracted more interest owing to their excellent luminous properties. Here, Ba2YZrO6:R (R = Dy3+, Sm3+, Dy3+/Sm3+) are prepared in air by using high-temperature solid-state method. The crystal phase and purity are investigated by X-ray diffraction (XRD). The luminous properties are studied by using optical spectrometer. Green emission of Ba2YZrO6:Dy3+ with excitation at 260 nm is observed. Ba2YZrO6:Sm3+ with excitation 271 and 407 nm shows yellow and red-orange emission, respectively. Under excitation 271 nm, Ba2YZrO6:Dy3+, Sm3+ show emission from green to yellow with increasing Sm3+ concentration from 2 to 10 mol%. Ba2YZrO6:Dy3+, Sm3+ with excitation 407 nm glow yellow light. We investigate the concentration dependent spectra and confirm the optimal Dy3+ and Sm3+ concentrations. We estimate the concentration quenching mechanism in Ba2YZrO6:R (R = Dy3+, Sm3+) and Ba2YZrO6:Dy3+, Sm3+. The luminous mechanism and energy transfer process are analyzed by using the energy level transitions of Dy3+ and Sm3+ ions.

Study on the properties of Sm3+-Doped CaTbAl3O7 phosphors

New single phase and adjustable emission phosphors have attracted a lot of attention because of the good luminous properties. In this work, Sm3+ doped CaTbAl3O7 phosphors are prepared in air by solid-state method. The crystal structure, concentration dependent spectra, lifetimes, and luminescence properties are investigated. Because of the 4f8 → 4f75d1 and 4f → 4f transitions of Tb3+ ion, host (CaTbAl3O7) shows an excitation spectrum in the range of 220–520 nm under monitored at 544 nm and emits yellow-green light under excitation 248, 284, and 368 nm due to the 5D4 → 7FJ (J = 0, 1, 2, 3, 4, 5, and 6) transitions of Tb3+ ion. CaTbAl3O7:Sm3+ under monitored 598 nm contains the excitation spectral peaks of both CaTbAl3O7 and Sm3+ ion. With excitation at 368 nm, CaTbAl3O7:Sm3+ glows orange-red light, its PL spectrum has both host (CaTbAl3O7) and Sm3+ ion contributing, and the chromaticity coordinates are about (0.5499, 0.4351). Under excitation 402 nm, the red-orange emission of CaTbAl3O7:Sm3+ is only the contribution of Sm3+ ion and the chromaticity coordinates are about (0.5823, 0.4168). The energy transfer process from Tb3+ in host (CaTbAl3O7) to Sm3+ ions can be confirmed via the spectral properties. We explain the luminous mechanism of CaTbAl3O7:Sm3+ by the energy level diagrams of Tb3+ and Sm3+.

Insight into the structure, spectroscopic, Raman, photo luminance and electrical properties Cd substituted Ba–Zn R-type hexaferrites

The impact of cadmium (Cd) substitution on structural, spectral, and dielectric properties of R-type hexagonal ferrites BaZn2-xCdxFe4O11 has been investigated. These were synthesized by auto-combustion sol-gel route. The single phase of R-type hexaferrites confirmed using X-ray diffraction analysis. This spectroscopy predicted the specific absorption bands belonging to hexagonal ferrites. There was a decline in dielectric loss and dielectric constant. This is due to electric polarization and little grain growth. Ac-conductivity shows an increasing behavior with frequency. The value of the slope extracted from the curve of log (ac) and log (ω) was found in the range 0.2–0.8 GHz. The variation in dielectric parameters of all samples with an increment of dopant (cadmium) and frequency suggests that these materials are important in high-frequency applications. Two distinct modes were observed in Raman analysis at 235 cm−1 and 330 cm−1. P.L. spectra explain the mechanism of absorption and emission.

Phosphor-in-glass film sintered on sapphire lens for laser welding hermetic packaging of high-power white LEDs

White light-emitting diodes (WLEDs) represent a revolutionary type of energy-saving and environmentally friendly light source, which has been extensively employed in a multitude of lighting and display applications. Nevertheless, traditional organic packaging is unable to fulfill the requirements of highly reliable high-power WLEDs, including hemertic property, heat resistance, and excellent luminous properties. Herein, an all-inorganic hermetic packaging based on laser-localized welding and phosphor-in-glass film sintered on a sapphire lens (PiGF-SL) has been developed for high-power WLEDs. The PiGF-SL with a Kovar frame was welded to a three-dimensional direct-plated ceramic (3D-DPC). The high-strength and crack-free welded joint with a shear strength of 258.83 MPa and packaging cavity with excellent gas tightness (leakage rate 8.6 × 10−10 Pa m3/s) were simultaneously obtained, resulting in the high-power WLED capable of maintaining its excellent optical properties for an extended period in harsh environments. Furthermore, the optical performance of welded WLEDs was optimized by adjusting the PiGF-SL film thickness and red CaAlSiN3:Eu2+ (CASN) phosphor content. The welded WLED emits a cool white light by improving the PiGF thickness to 91 μm and exhibits high color quality with red CASN phosphor content of 8 wt%, which simultaneously presents outstanding color rendering index (CRI) of 91, luminous efficacy (LE) of 44.8 lm/W, and correlated color temperature (CCT) of 4322 K. Following a 200-h aging process, the laser-welded PiGF-SL-based WLED exhibited a slightly reduced efficiency loss and a stable color quality in comparison to reflow-soldered and epoxy-bonded WLEDs. Our work provides valuable guidance and solutions for the highly reliable and board-level packaging of WLEDs.

The dual role of Dy3+ in a novel Sr2Al2SiO7:Eu2+, Dy3+ long-persistent luminescence glass–ceramic

A novel Sr2Al2SiO7:Eu[Formula: see text], Dy[Formula: see text] long-persistent luminescence (LPL) glass–ceramic has been successfully synthesized by the recrystallization-melting method in the SrO-Al2O3-SiO2-B2O3-Li2O glass system. The glass–ceramic form enhances the plasticity of the material compared to traditional Sr2Al2SiO7:Eu[Formula: see text], Dy[Formula: see text] phosphorescence powders. Additionally, the Dy[Formula: see text] ions serve a dual role as fluorescence emission centers and sensitizers for afterglow. By controlling the concentration of Dy[Formula: see text], the characteristic fluorescence intensity can be adjusted to achieve color-tunable photoluminescence. Besides, Dy[Formula: see text] ions, as trap centers, capture the electrons, resulting in a longer afterglow than the Eu[Formula: see text] singly doped sample. After exposure to ultraviolet light, the initial brightness intensity of the Dy:Eu = 16:1 sample increases to 1525 mcd/m2, and the emission lasts for 30 min. These optimized bulk materials, with unique luminous properties, have potential applications in future optoelectronic devices.

Two multifunctional Eu-MOFs with dual photochromic and luminous centers for multiple optical switches and anti-counterfeiting properties

In this work, two multifunctional Eu-MOFs with dual photochromic and luminous centers, formulated as Eu3[(ipbp)4·6H2O]·3H2O (1) and Eu[(ipbp)·(p-BDC)·H2O] (2) (ipbp = 1-(3,5-isophthalic acid)-4,4′-bipyridine chloride, p-BDC = terephthalate), were successfully constructed by solvothermal reactions. The carboxylate pyridine ligand gives the two frameworks excellent photochromic properties, while the metal europium endows the two compounds splendid luminous properties. In addition, the application of the two compounds in three kinds of optical switches is further demonstrated. Finally, the two compounds with dynamic multicolor anti-counterfeiting properties were also explored. This work not only proposed bicentric light-emitting and color-changing materials, but also provided a new strategy for studying multiple optical switches and dynamic anti-counterfeiting.

Impact of Gd-substitution on structural, dielectric, spectroscopic, Raman, and photo luminance properties of Ba0.4Sr0.6Co2Fe16O27 ceramics

This paper represents a detailed study of Gd3+ substitutions on Structural, Dielectric, Spectroscopic, Raman, and Photo luminance Properties of Ba0.4Sr0.6Co2Fe16O27 magnetic oxides were prepared using the sol-gel auto combustion method. All of these specimens were sintered at 1100 °C for 5 h. X-ray diffraction analysis (XRD) confirmed the single-phase detection and structural analysis. The lattice parameters a and c show the insignificant behavior 5.893–5.933 Å, and 32.049–32.476 Å with the concentration of gadolinium ions. The crystallite size ranged from 25 to 30 nm, demonstrating a growing tendency as Gd-substitution was enhanced. The discrepancy in the ionic radii of iron (Fe3+) and substituent elements (Gd3+) is the cause of the variation in cell volume and lattice constants. FTIR spectroscopy confirmed the presence of absorption bands (590 and 3000 cm−1) for prepared BaSr-based W-type hexa-ferrites. The vibrational bands of metal oxide ions are responsible for the 590 and 685 cm−1 peaks. The Raman spectrum showed six discrete, brittle peaks: 320, 440, 620, 690, 1300, and 1600 of synthesized nanomaterials—the dielectric constant and dielectric loss increase by substituting the Gd3+ ion. The dielectric parameters and dielectric loss at higher frequencies suggest that the prepared material may be excellent for switching, sensing, and high-frequency applications.

Sb3+ and Er3+ co-doped Cs2NaYCl6 double perovskite with ultra-high sensitivity for optical thermometry

Optical thermometry has attracted great attention because it enables accurate temperature measurement in harsh environments due to non-contact temperature measurement. Three-dimensional (3D) lead-free halide perovskites have a great application potential in this field, due to its outstanding luminous properties and stability. In this work, the Sb3+ and Er3+ are introduced in Cs2NaYCl6 double perovskites (DPs). The Sb3+ doping Cs2NaYCl6 DPs exhibits bright blue emission from the Sb3+ activated self-trapped excitons (STEs) and Sb3+,Er3+ co-doped Cs2NaYCl6 has efficient green emission with excellent photoluminescence quantum yields (PLQY) of 81.1% because of the presence of energy transfer from self-trapped excitons to Er3+ ions. Excitingly, the ratio between the fluorescence intensity at 524 nm and 550 nm (FIR(I524 nm/I550 nm)) and the ratio between the fluorescence intensity at 524 and 456 nm (FIR(I524 nm/I456 nm)) both have a high correlation with temperature in the range of 298–473 K. The maximum of relative sensitivity values reach to 1.18%/K (I524 nm/I550 nm) and 1.19%/K (I524 nm/I456 nm) at 298 K, respectively. The outstanding temperature sensitivity suggests that the Sb3+,Er3+ co-doped Cs2NaYCl6 has enormous application potential in ratiometric optical thermometry.

Fabrication and luminous properties of BaAl2O4-LuAG:Ce composite phosphor ceramics for solid-state laser lighting

Based on the “effective ionic radius match effect” and the “charge balance substitution rule of ions”, mixed Ba2+, Al3+, Lu3+, and Ce3+ ions can be effectively regulated to a BaAl2O4-LuAG:Ce biphasic structure. The contribution of BaAl2O4 like as scattering centers can reduce overall reflection losses and enhance the light extraction efficiency of these composite phosphor ceramics (CPCs). In this work, a series of x wt.% BaAl2O4-LuAG:Ce (x = 0, 3, 5, 10, 15) CPCs were fabricated by vacuum sintering using co-precipitated composite powders. Homogenization at the atomic level of mixed Ba3+, Al3+, Lu3+, and Ce3+ ions in multiphase powders provides uniform distribution of BaAl2O4 and LuAG:Ce constituent phases in composite ceramics. The introduction of BaAl2O4 has an additive effect, which also consists in uniform aggregation of pores near their grains during sintering. It allows to adjust the size and amount of microstructural defects by varying the secondary phase content. Under the excitation of 10.8 W 450 nm LDs in a reflection mode, 3 wt% BaAl2O4-based CPCs show the optimum luminous flux of 2244 lm and a luminous efficiency of 208 lm·W−1. The obtained CPCs show a high application potential in solid-state laser lighting.

Enhancement of luminous properties and stability of CH3NH3PbBr3 perovskite quantum dots using a low-cost, environmentally friendly and multisite passivation strategy

CH3NH3PbBr3 perovskite quantum dots (PeQDs) have demonstrated excellent performance and are promising for optoelectronic applications. However, poor stability caused by surface defects severely limits their further development. In this work, cheap, green Tartaric acid (Ta) was introduced as a multisite passivator for the synthesis of CH3NH3PbBr3 PeQDs by ligand-assisted reprecipitation at room temperature, and the effect of Ta on the luminous properties and stability of CH3NH3PbBr3 PeQDs was investigated. The hydroxyl group of Ta can anchor Br− of PbBr64− octahedra, reducing the Br vacancy by reducing surface Br− loss, and the carboxyl group can form a coordination bond with Pb2+, all contributing to reducing surface defects, inhibit heavy metal leakage, reduce toxicity and improve luminous properties and stability. The results showed that the FWHM (full width at half maxima) of the Ta-modified PeQDs was 19 nm, PLQY reached 88.24 % and showed bright fluorescence for 100 days at room temperature. Ta-modified PeQDs-based white LED (WLED) emitted cold white light, with ultrahigh luminous efficiency of 121.57 lm/W, color gamut of 127 % of the National Television System Committee (NTSC) standard and high operate stability. Our work provides new ideas for low-cost preparation of perovskite devices with high optoelectronic performance.

Abstract B025: Luminal-to-basal phenotypic plasticity promotes invasive phenotypes in a live-imaging assay using patient-derived bladder tumor organoids

Abstract Lineage plasticity in cancer is characterized by changes in cell state that are often associated with tumor progression and treatment resistance. While nearly all non-muscle invasive bladder cancer (NMIBC) tumors have a luminal epithelial phenotype, many muscle invasive bladder cancers (MIBC) display a basal identity. NMIBC to MIBC progression may therefore be related to a phenotypic switch from luminal-to-basal subtypes, which in turn may be associated with poorer clinical outcomes. However, current understanding of the molecular processes linking cell plasticity and tumor invasion is limited, due in part to a lack of physiologically relevant in vitro models and assays. To address these questions, we are utilizing a living biobank of 82 patient-derived bladder tumor organoid lines that our group has established. These organoids represent a 3-dimensional, heterogeneous model system for studying bladder cancer, as they can be genetically manipulated and recapitulate the molecular and histopathological features of the parental tumor. Notably, in previous work, we described luminal-to-basal phenotypic plasticity in a subset of organoid lines derived from luminal tumors, which display a shift to basal/squamous identity in culture that is reversible by orthotopic xenografting. In current studies, we are investigating cell migration and invasiveness using a live-imaging assay that we have developed to examine bladder tumor organoid outgrowth in vitro. Importantly, this assay allows longitudinal visualization as well as quantitation of invasiveness over a four-day time span. Analysis of over 25 organoid lines with plastic, stable luminal, and stable basal properties has revealed a broad spectrum of organoid outgrowth phenotypes that do not correlate with cell proliferation or clinical parameters. Instead, the degree of outgrowth correlates precisely with luminal-to-basal phenotypic plasticity, as assessed by transcriptome analyses, immunofluorescence microscopy, and in vivo xenografting. Organoid lines with minimal outgrowth have stable luminal phenotypes, whereas lines that produce their own extracellular matrix to create a leading edge of migrating cells have plastic phenotypes. Furthermore, movies of the invading organoids reveal distinct cell migratory patterns, as several organoid lines display collective migration that generates an invasive front at the leading edge. This collective migration phenotype is distinct from phenotypic plasticity, is at least partially independent from organoid outgrowth, and is undergoing further analysis. Thus, our organoid outgrowth assay identifies two different parameters of invasive potential, one of which correlates with phenotypic plasticity. Our findings characterize bladder tumor invasion patterns for the first time and suggest that lineage plasticity in NMIBC represents a key mechanism that promotes tumor invasion in MIBC. Citation Format: Clementine Le Coz, John R. Christin, Talal Syed, Zejian Wang, Caroline J. Laplaca, Andrew T. Lenis, Michael M. Shen. Luminal-to-basal phenotypic plasticity promotes invasive phenotypes in a live-imaging assay using patient-derived bladder tumor organoids [abstract]. In: Proceedings of the AACR Special Conference on Bladder Cancer: Transforming the Field; 2024 May 17-20; Charlotte, NC. Philadelphia (PA): AACR; Clin Cancer Res 2024;30(10_Suppl):Abstract nr B025.

Photoluminescence properties of Pb5(PO4)3Br:RE (RE = Dy3+, Eu3+ and Tb3+) phosphor synthesised using solid-state method.

This study describes the luminous properties of Pb5(PO4)3Br doped with RE3+ (RE = Dy3+, Eu3+ and Tb3+) synthesised using the solid-state method. The synthesised phosphor was characterised using Fourier-transform infrared, X-ray diffraction, scanning electron microscopy and photoluminescence measurements. Dy3+-doped Pb5(PO4)3Br phosphor exhibited blue and yellow emissions at 480 and 573 nm, respectively, on excitation at 388 nm. Eu3+-doped Pb5(PO4)3Br phosphor exhibited orange and red emissions at 591 and 614 nm, respectively, on excitation at λex = 396 nm. Pb5(PO4)3Br:Tb3+ phosphor exhibited the strongest green emission at 547 nm on excitation at λex = 380 nm. Additionally, the effect of the concentration of rare-earth ions on the emission intensity of Pb5(PO4)3Br:RE3+ (RE3+ = Dy3+, Eu3+ and Tb3+) phosphors was investigated.

NUV-excitation Dy(III) complexes: Synthesis, structural study and impact of secondary ligands on optoelectronic properties

The ternary dysprosium complexes involving 1,1,1-trifluoro 5,5-dimethyl 2,4-hexanedione (TFDH) along with 2,2ʹ-bipyridyl and its derivatives have been synthesized. Elemental, infrared and proton NMR analyses were used to evaluate the bonding patterns between dysprosium ion and organic moieties. UV–Visible and photoluminescence spectroscopy were used to examine the optical characteristics. To confirm the anhydrous nature of synthesized complexes, IR and thermogravimetric data were utilized. The band gap value lies in semi-conducting region was explained by Tauc's plot and CV curve, respectively. The photophysical characteristics of dysprosium complexes have been studied in powdered form. The appearance of yellow luminescence on irradiation under NUV-light indicates a highly efficient transfer of energy mechanism from organic ligand to the Dy(III) ion. The CCT values were found to be suitable for cold light sources. The ∆J = 2 transition dominates the overall emission spectra with branching ratio ∼70% is ideal for laser reinforcement. The synthesized Dy(III) complexes possess band gap in semi-conducting range, good thermal stability and high luminous properties, which makes them suitable for applications in displays and lighting technologies.

Microplastics in personal care products and cosmetics in Sri Lanka

In the Sri Lankan context, the lack of baseline studies to mitigate microplastic emissions through personal care and cosmetic products poses a huge problem. Hence this study serves as the first scientific investigation to analyze and characterize microplastics in selected personal care and cosmetic items available in the Sri Lankan markets. Fifteen brands representing five categories (face wash, facial scrubs, baby creams, shaving creams, and skin creams) of personal care and cosmetic items served as the basis for this investigation. Based on a questionnaire survey, from each category, three highly utilized brands were chosen and triplicates from each brand were used for the analysis. All samples were treated with the Fenton reagent to extract microplastics. Then through Nile red staining suspected microplastic were screened and characterized through FT-IR spectroscopy. The Nile Red analysis revealed seven brands of the fifteen to be stained with Nile Red and demonstrate luminance properties under UV light. However, FT-IR analysis proved only six brands contained actual microplastics. Low-density polyethylene and ethylene-propylene copolymer were the dominant types of microplastic. Most microplastics were irregularly shaped and white in color with sizes ranging from 238.55 ± 50.74 to 450.69 ± 174.9 μm. An emission estimation revealed that products FS-01 and FW-03 contain 3.36 ± 0.20 g and 0.2 ± 0.05 g of isolatable microplastics per product. While the present study provides scientific evidence for the availability of microplastics in products in Sri Lankan markets, it also provides a great opportunity to develop relevant policies and regulations to control them.

Enhanced thermal stability and luminous properties of Dy3+/Tm3+/Eu3+ doped glass ceramics containing Sr4Bi(PO4)3O crystalline phases based on back energy transfer

White light emitting and optical temperature sensing materials with high thermal stability have broad market development prospects. The use of substrates with excellent thermal stability is a common idea to improve thermal stability, while the modulation of dopants to enhance thermal stability has been less studied. Therefore, in this work, Tm3+/Dy3+/Eu3+ doped transparent glass ceramics containing Sr4Bi(PO4)3O crystalline-phase were prepared by melt-crystallization method to achieve warm white light emission and optical temperature sensing with good thermal stability. Since the Tm3+-Dy3+ doped samples can only achieve cold white light emission, warm white light emission is obtained by adding Eu3+, which can emit red light. The application scenario of the material is expanded. The luminous intensities of Tm3+, Dy3+, and Eu3+ were 109.4 %, 89.1 %, and 70.7 % of those at room temperature, at 473 K. The increase in the emission intensity of Tm3+ was explained by the presence of back energy transfer (BET) from Dy3+ and Eu3+ to Tm3+. The chromaticity shift (Δε) of the samples was 2.43 × 10−4 and the luminescent colour was stable. The absolute sensitivity of the material can reach 0.69 K−1 at 473 K, and the relative sensitivity of the material can reach 1.60 % K−1 at 293 K. This work provides new ideas for the study of improving the thermal stability of materials.

Strategy of Charge Compensation for High-Performance Ni2+-Activated MgAl2O4 Spinel Near-Infrared Phosphor Synthesis via the Sol-Gel Combustion Method.

Near-infrared (NIR) phosphor conversion light-emitting diodes (pc-LEDs) have great application potential as NIR light sources in many fields such as food analysis, night vision illumination, and bioimaging for noninvasive medical diagnosis. In general, phosphors synthesized by a high-temperature solid-phase method have large particle sizes and have to be processed to fine powders by a grinding process, which may introduce surface defects and lower the luminous efficiency. Here, we report a sol-gel sintering method with ammonium nitrate and citric acid as the sacrificing agents to synthesize high purity, nanosized (less than 50 nm) Zr4+/Ni2+ codoped MgAl2O4 spinel NIR phosphors, in which MgAl2O4 spinel is the matrix, Ni2+ is the luminous center, and Zr4+ acts as the charge compensator. We systematically characterized the crystal structures and NIR luminescence properties of the Ni2+-doped MgAl2O4 and the Zr4+/Ni2+ codoped MgAl2O4. Under 390 nm light excitation, the emission spectrum of the Ni2+-doped MgAl2O4 phosphor covers 900-1600 nm, the half-peak width is 251 nm, and the peak position is located at 1230 nm. We demonstrated that by incorporating small amounts of Zr4+ as the charge compensator, the NIR emission intensity of the Zr4+/Ni2+ codoped MgAl2O4 nanosized phosphor was doubled over that of the Ni2+-doped MgAl2O4 phosphor. The optimal content of the charge compensator was 2 mol %. More importantly, the inclusion of Zr4+ led to a NIR phosphor with improved thermal stability in luminous properties, and the luminous intensity measured at 100 °C was 33.83% of that measured at room temperature (20 °C). This study demonstrates that NIR phosphor nanomaterials with high-purity and enhanced optical properties can be designed and synthesized through the charge compensation strategy by a sol-gel sintering method.

Strong cathode electroluminescence biosensor based on CeO2 functionalized PCN-222@Ag NPs for sensitive detection of p-Tau-181 protein

Electrochemiluminescence (ECL) biosensors provide a convenient and high sensitivity method for early disease diagnosis. However, creating luminophore arrays relying on powerful ECL signals remains a daunting task. Porphyrin-centered metal organic frameworks (MOFs) exhibit remarkable potential in ECL sensing applications. In this paper, based on a simple one-pot synthesis method, PCN-222@Ag NPs doped with CeO2 was synthesized to enhance the ECL performance. Due to the strong catalytic ability of CeO2, the ECL signal strength of the new material PCN-222@CeO2@Ag NPs is much higher than that of the PCN-222@Ag NPs and PCN-222. The luminous properties of PCN-222@CeO2@Ag NPs become more intense and stable due to the excellent electronic conductivity of Ag NPs. Based on the fact that CuS@PDA composite can quench the ECL signal of PCN-222@CeO2@Ag NPs, we constructed a novel sandwich ECL immune sensor for the detection of phosphorylated Tau 181 (p-Tau-181) protein. The ECL sensor has a great linear relationship with p-Tau-181 protein concentration, ranging from 1 pg/mL to 100 ng/mL. The detection limit is as low as 0.147 pg/mL. This work provides new ideas for developing sensitive ECL sensors for the p-Tau-181 protein, the marker of Alzheimer's disease.

Lattice occupation and luminous properties of the K3YSi2O7:Tm3+,Dy3+ phosphor for NUV-excited white LEDs

Lattice occupation and luminous properties of the K3YSi2O7:Tm3+,Dy3+ phosphor for NUV-excited white LEDs

Shape‐Editable Transparent Wood Based on In‐Situ Polymerization of Epoxy Vitrimers Embedded with Luminescent BODIPY Molecules for Smart Decoration Materials

AbstractTransparent wood (TW) combining unique anisotropic structure has broad application prospects in the field of advanced building furniture materials. Many efforts have been made to add quantum dots or nanoparticles to TW to endow it with additional functionality, such as luminescent, electrochromic, and thermochromic TW. However, luminous TW with shape‐editable functionality and its new applications have yet to be explored. Benefiting from the excellent luminescence performance in a diluted solution state, BODIPY (4,4‐difluoro‐4‐bora‐3a,4a‐diazas‐indacene) dyes have been widely used for bio‐sensing and bioimaging. In addition, vitrimers exhibit excellent stimuli‐responsive, shape‐memory, and reprocessing properties thanks to exchangeable dynamic covalent crosslinking networks, which are suitable for fabricating smart TW. Herein, combing these advantages, a dual‐functional transparent wood composite (P‐SEFTW) with photoluminescent and shape editable function was developed by introducing BODIPY dyes and vitrimers into the delignified wood (DW) templates. P‐SEFTW displays good UV luminescence, unique light guiding and directional scattering effects. Meanwhile, it shows excellent shape‐recovery, shape‐programming, shape‐erasing, and re‐programming capability under thermal‐stimulus. These characteristics enable TW to exhibit great prospect as an advanced smart and functional building material.