Methyl methacrylate-modified polystyrene microspheres: an effective strategy to enhance the fluorescence of Eu-complexes.

The in vitro detection applications of europium complex-doped microspheres mainly rely on strong fluorescence intensity and a well-defined morphology. In this work, using methyl methacrylate-modified polystyrene microspheres has been proven an effective strategy to enhance the fluorescence and morphology of Eu-complexes. The experimental results showed that the modification resulted in the formation of a porous structure within the polystyrene microspheres, enhancing the doping uniformity and facilitating a more significant accumulation of fluorescent molecules. Furthermore, because of their encapsulation ability, microspheres efficiently confine the fluorescent molecules within them. In addition, the nano-scale porous structure endowed the microspheres with enhanced properties without compromising solvent swelling capability, thereby significantly boosting the fluorescence performance of porous PSMMA. In lateral flow immunoassays (LFIAs), PSMMA-Eu microspheres were effectively utilized to detect fentanyl with exceptional sensitivity by capitalizing on these benefits, capable of detecting concentrations as low as 0.10 ng mL-1. This technology has significant potential for rapid point-of-care screening and clinical applications.

Rapid determination of serum amyloid A using an upconversion luminescent lateral flow immunochromatographic strip.

The early diagnosis and real-time prognosis of cardiovascular diseases (CVDs) at the bedside are important. However, real-time detection of myocardial infarction involves the use of large-scale instrumentation and long test times. Herein, a simple, rapid and sensitive lateral flow immunochromatographic strip (LFIS) based on Yb/Er co-doped NaYF4 upconversion nanoparticles (UCNPs) was demonstrated for use in the detection of myocardial infarction. First, through heavy Yb/Er doping and an inert NaYF4 shell coating on the nanoparticles, the surface-related luminescence quenching effect of UCNPs was eliminated to enhance the upconversion luminescence. Second, through uniform coating of a SiO2 layer on the UCNPs, the biological affinity was improved to couple UCNPs and antibody proteins. Finally, through modification and activation with a specific antibody protein (serum amyloid A (SAA)), the UCNPs exhibited intense upconversion luminescence and high specificity when applied as a lateral flow immunochromatographic strip (LFIS). The developed UC-LFIS was highly sensitive (0.1 µg mL-1) and specific for detecting SAA in only 10 µL of serum. The UC-LFIS holds great potential for the early diagnosis and prognosis of CVDs.

Comparative transcriptome analysis of non-germinated and germinated spores of Enterocytozoon hepatopenaei (EHP) in vitro.

Enterocytozoon hepatopenaei (EHP), an obligate intracellular parasite classified as microsporidia, is an emerging pathogen with a significant impact on the global shrimp aquaculture industry. The understanding of how microsporidia germinate has been a key factor in exploring its infection process. However, the germination process of EHP was rarely reported. To gain insight into the germination process, we conducted a high-throughput sequencing analysis of purified EHP spores that had undergone in vitro germination treatment. This analysis revealed 137 differentially expressed genes, with 84 up-regulated and 53 down-regulated genes. While the functions of some of the genes remain unknown, this study provides important data on the transcriptomic changes before and after EHP germination, which can aid in further studies on the EHP infection mechanism.

Changes in the intestinal microbiota of Pacific white shrimp (Litopenaeus vannamei) with different severities of Enterocytozoon hepatopenaei infection.

The intestinal microbiota of the Pacific white shrimp Litopenaeus vannamei during Enterocytozoon hepatopenaei (EHP) infection was investigated by 16S rRNA gene-based analysis. The results showed that bacterial diversity in the intestine of L. vannamei was high, but it decreased with increasing severity of EHP infection. The relative abundances of the phyla Planctomycetes, Actinobacteria and Acidobacteria decreased significantly with a decrease in body size or EHP infection severity (P < 0.05). The most abundant genera were Pseudomonas, Methylobacterium, Bradyrhizobium, Bacteroides, Vibrio, Prevotella and so on. In addition, the relative abundances of some bacteria, such as Pseudomonas, Bradyrhizobium, Bacteroides and Vibrio, increased significantly with a decrease in body size or EHP infection severity (P < 0.05). These findings suggest that changes in the intestinal microbiota occur depending on the severity of EHP infection.

Visible-NIR Photodetectors Based on Low-Dimensional GeSe Micro-Crystals: Designed Morphology and Improved Photoresponsivity.

GeSe micro-sheets and micro-belts have been synthesized by a facile one-pot wet chemical method in 1-octadecene solvent and oleic acid solvent, respectively. The adsorption of more oleic acid molecules on the (002) plane promoted growth along [010] direction of the GeSe micro-belts and limited carrier transport in this direction, resulting in higher carrier concentration and mobility of the GeSe micro-belts. The performance of the photodetectors based on the single GeSe micro-sheet and the single GeSe micro-belt was investigated under illumination at 532 nm, 980 nm and 1319 nm. Both, photodetectors based on a single GeSe micro-sheet and a single GeSe micro-belt, exhibit a high photoresponse, short response/recovery times, and long-term durability. Moreover, the photodetector based on a single GeSe micro-belt displays a broadband response with a high responsivity (5562 A/W at 532 nm, 1546 A/W at 980 nm) and detectivity (3.01×1012 Jones at 532 nm, 8.38×1011 Jones at 980 nm). These excellent characteristics render single GeSe micro-belts very interesting for use as highly efficient photodetectors, especially in the NIR region.

Temperature dependent molecular fluorescence of [Agm]n+ quantum clusters stabilized by phosphate glass networks.

Molecule like silver quantum clusters ([Agm]n+ QCs) exhibit an ultrasmall size confinement resulting in efficient broadband fluorescence. However, free [Agm]n+ QCs are also chemically active, so their stabilization is required for practical applications. We report in this work a phosphate oxyfluoride glass network enabled stabilization strategy of [Agm]n+ QCs. A series of silver-doped P2O5-ZnF2-xAg glasses were prepared by a conventional melt-and-quench method. The NMR and XPS results reveal that two types of [P(O,F)4] tetrahedrons (Q1, Q2) form chain structures and Zn(iv) connects [P(O,F)4] chains into a 3-dimension network in the glasses. The frameworks with limited void spaces were designed to restrict the polymerization degree, m, of [Agm]n+ QCs; the negatively charged tetrahedrons were designed to restrict the charge, n, of [Agm]n+ QCs. Through optical and mass spectroscopy studies, silver quantum clusters, [Ag2]2+ and [Ag4]2+, were identified to be charge compensated by [ZnO4] tetrahedrons and surrounded with [P(O,F)4] complex anions. The fluorescence thus gives high quantum efficiencies of 55.2% and 83.4%, for P2O5-ZnF2-xAg glass stabilized [Ag2]2+ and [Ag4]2+ QCs, respectively. This further reveals that the peak fixed fluorescence of [Ag2]2+ and [Ag4]2+ can be described by molecular fluorescence mechanisms. These are parity-allowed singlet-singlet transitions (S1 → S0), parity-forbidden triplet-singlet transitions (T1 → S0) and intersystem crossings between singlets (S1) and triplets (T1). The phonon coupled intersystem crossing between singlets (S1) and triplets (T1) determines the phosphate stabilized [Ag4]2+ QCs to exhibit a series of temperature dependent fluorescence behaviors. These include fluorescence intensity (at 50-200 K), intensity ratio (FIR) (at 50-200 K), peak shift (at 100-300 K) and lifetime (at 300-450 K) with maximum sensitivities of 1.27% K-1, 0.94% K-1, 0.29% K-1 and 0.41% K-1, respectively. Therefore, phosphate stabilized [Ag4]2+ QCs can be applied as temperature sensing probes, especially at low temperatures (10-300 K) and for color-based visualized temperature sensors.

Phase separation strategy to facilely form fluorescent [Ag2]2+/[Agm]n+ quantum clusters in boro-alumino-silicate multiphase glasses.

By adjusting the content of ZnF2-SrF2/ZnO-SrO, a series of SiO2-Al2O3-B2O3-Na2O-ZnO/ZnF2-SrO/SrF2-Ag multiphase glasses was designed and prepared via a melt-quenching method. Under a phase separation strategy, negatively charged tetrahedrons ([BO4]-, [ZnO4]2-, and [AlO4]-) can be generated to stabilize different silver species (Ag+ ions; [Ag2]2+ pairs; [Agm]n+ quantum clusters ([Agm]n+ QCs)) in B2O3-rich and ZnO-Al2O3 rich sub-phases. The B2O3-rich sub-phase has a high solubility for Ag+ ions and [Agm]n+ QCs. The fluoride-rich phase shows a good ability to extract Na+ from the B2O3-rich sub-phase, significantly affects the solubility of Ag+ in the B2O3-rich sub-phase, and eventually determines the aggregation from Ag+ ions and Ag0 atom to [Agm]n+ QCs. The ZnO-Al2O3-rich or ZnO-SiO2-rich (i.e. SiO2-rich in GZnOSrO) phase has a relatively high solubility for [Ag2]2+ pairs. The Ag+/[Ag2]2+/[Agm]n+ QC fluorescent centers were identified by spectroscopic analysis, where the fluorescence bands are located in the ultraviolet, green-white and orange spectral regions, respectively. The fluorescent quantum yield (QY) of the [Agm]n+ QCs can be improved to 55.7%, and the combination of these three luminescent centers can achieve white light emission.

Facile Synthesis of γ-In2 Se3 Nanoflowers toward High Performance Self-Powered Broadband γ-In2 Se3 /Si Heterojunction Photodiode.

An effective colloidal process involving the hot-injection method is developed to synthesize uniform nanoflowers consisting of 2D γ-In2 Se3 nanosheets. By exploiting the narrow direct bandgap and high absorption coefficient in the visible light range of In2 Se3 , a high-quality γ-In2 Se3 /Si heterojunction photodiode is fabricated. This photodiode shows a high photoresponse under light illumination, short response/recovery times, and long-term durability. In addition, the γ-In2 Se3 /Si heterojunction photodiode is self-powered and displays a broadband spectral response ranging from UV to IR with a high responsivity and detectivity. These excellent performances make the γ-In2 Se3 /Si heterojunction very interesting as highly efficient photodetectors.

Stabilization of ultra-small [Ag2]2+ and [Agm]n+ nano-clusters through negatively charged tetrahedrons in oxyfluoride glass networks: To largely enhance the luminescence quantum yields.

Herein, three different silver species were stably formed in SiO2-Al2O3-B2O3-Na2O-ZnF2-CaF2 glasses and were identified by their characteristic luminescence bands: violet blue luminescence (Ag+: 4d95s1 → 4d10), green white molecular fluorescence (molecule-like [Agm]n+, named ML-Ag) and orange molecular fluorescence ([Ag2]2+ pairs). Due to the relatively low aggregation degrees of [Agm]n+ and [Ag2]2+, non-radiative transitions were highly suppressed, and the PL quantum yields (QYs) of ML-Ag and [Ag2]2+ pairs reached 73.7% and 89.7%, respectively. The substitution of 0.5B2O3-0.5Na2O with SiO2 promoted the partial reduction of Ag+ to Ag0 and the subsequent aggregation of Ag+ and Ag0 to form [Agm]n+ (ML-Ag). The absence of Na2O also resulted in an increasing amount of Ag+-Ag+ pairs with closing interionic distance to form [Ag2]2+ in glass. According to the X-ray photoelectron spectra (XPS) and magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectra, a solubility strategy and a charge compensation model were proposed to describe the transformations between different silver species. The formation of ML-Ag was further controlled via the solubility of Ag+ in glass, whereas [Ag2]2+ centers could be effectively produced by lowering the total amount of other competitive charge compensators, such as Na+, or by introducing negatively charged [BO4]-, [AlO4]-, and [ZnO4]2- tetrahedrons into the glass matrix.

Crystalline Hollow Microrods for Site-Selective Enhancement of Nonlinear Photoluminescence.

A class of one-dimensional hollow microstructure is described, which was formed by a kinetically controlled crystal growth process. A hexagonal-phase NaYbF4 microrod comprising isolated holes along the longitudinal axis was synthesized by a one-pot hydrothermal method with the assistance of citrate ligands. The structural void feature modulates light intensity across the microrods as a result of interference arising from light scattering and reflection by the inner walls. A single crystal comprising a structural void was doped with upconverting lanthanide ions. Upon near-infrared excitation of the doped crystal spatially resolvable optical codes were produced.

Shielding Upconversion by Surface Coating: A Study of the Emission Enhancement Factor.

Surface coating is a commonly used strategy to enhance upconversion emissions by shielding the luminescent core from surface quenching. In this work, we provide insights into the effect of surface coating on upconversion by investigating NaYF4 :Yb/Er nanoparticles and the corresponding NaYF4 :Yb/Er@NaYF4 core-shell nanoparticles, as a function of dopant concentration of Yb(3+) and excitation power. We observe declining emission enhancement factors with decreasing Yb(3+) concentration and increasing excitation power. Our mechanistic investigations suggest that the phenomenon originates from stepwise excitation in the upconversion process, as well as energy hopping among the Yb(3+) dopants. This increased understanding of the effect of surface coating on upconversion should be important towards the rational design of lanthanide-doped core-shell nanoparticles for various applications.

Establishing the Structural Integrity of Core-Shell Nanoparticles against Elemental Migration using Luminescent Lanthanide Probes.

Core-shell structured nanoparticles are increasingly used to host luminescent lanthanide ions but the structural integrity of these nanoparticles still lacks sufficient understanding. Herein, we present a new approach to detect the diffusion of dopant ions in core-shell nanostructures using luminescent lanthanide probes whose emission profile and luminescence lifetime are sensitive to the chemical environment. We show that dopant ions in solution-synthesized core-shell nanoparticles are firmly confined in the designed locations. However, annealing at certain temperatures (greater than circa 350 °C) promotes diffusion of the dopant ions and leads to degradation of the integrity of the nanoparticles. These insights into core-shell nanostructures should enhance our ability to understand and use lanthanide-doped luminescent nanoparticles.

Unlocking high photosensitivity direct laser writing and observing atomic clustering in glass.

The direct laser writing (DLW) of photoluminescent metal clusters is inspiring intensive research in functional glasses. However, understanding the influence of the host structure on cluster formation and visualizing DLW-induced clusters at the atomic scale remains challenging. In this work, we develop a highly photosensitive fluorophosphate glass through fluorine incorporation. The addition of fluorine establishes a conducive environment for Ag+ ions before DLW and enhances the availability of reducing agents and diffusion pathways during DLW. These advantages facilitate the formation of Ag clusters under low-energy single-pulsed DLW. Increasing laser energy results in a combination of Ag clusters and glasses defect, forming a dot + ring photoluminescent pattern. Atom probe tomography (APT), a technique capable of mapping the elemental spatial distribution and identifying clustering, is employed to gain more information on laser-induced clusters. Comparison of APT results between samples without and with DLW reveals the formation of Ag clusters after laser writing. The design concept and characterization enrich the understanding of Ag cluster behavior in glasses. This knowledge opens the possibility of rational design of clusters confined in glasses and inspires their synthesis for various applications.

Yb(3+)-doped GeS(2)-Ga2S(3)-CsCl glass with broad and adjustable absorption/excitation band for near-infrared luminescence.

The luminescent property of Yb(3+) ions in GeS(2)-Ga(2)S(3)-CsCl glasses with different CsCl contents has been studied. All the samples demonstrate a broad excitation band in the UV or/and visible range, depending on the composition, which is attributed to the charge transfer of the Yb(3+)-S(2-)/Cl(-) couple. The width of the excitation/absorption band can be as large as 150 nm. Moreover, with the increase of CsCl content, the peak position of the band can be continuously adjusted from 458 to 380 nm, due to the increase of the local average electronegativity around Yb(3+) ions. The broad and adjustable excitation band makes the Yb(3+)doped GeS(2)-Ga(2)S(3)-CsCl glass interesting for modifying the solar spectrum by absorbing strongly in the UV/blue region for emission around 1 µm. This kind of material is the key to adapting the solar spectrum to the response of silicon photovoltaic solar cells.

Reversible Growth of Halide Perovskites via Lead Oxide Hydroxide Nitrates Anchored Zeolitic Imidazolate Frameworks for Information Encryption and Decryption.

The low formation energies of metal halide perovskites endow them with potential luminescent materials for applications in information encryption and decryption. However, reversible encryption and decryption are greatly hindered by the difficulty in robustly integrating perovskite ingredients into carrier materials. Here, we report an effective strategy to realize information encryption and decryption by reversible synthesis of halide perovskites, on the lead oxide hydroxide nitrates (Pb13O8(OH)6(NO3)4) anchored zeolitic imidazolate framework composites. Benefiting from the superior stability of ZIF-8 in combination with the strong bond between Pb and N evidenced by X-ray absorption spectroscopy and X-ray photoelectron spectroscopy, the as-prepared Pb13O8(OH)6(NO3)4-ZIF-8 nanocomposites (Pb-ZIF-8) can withstand common polar solvent attack. Taking advantage of blade-coating and laser etching, the Pb-ZIF-8 confidential films can be readily encrypted and subsequently decrypted through reaction with halide ammonium salt. Consequently, multiple cycles of encryption and decryption are realized by quenching and recovery of the luminescent MAPbBr3-ZIF-8 films with polar solvents vapor and MABr reaction, respectively. These results provide a viable approach to integrate the state-of-the-art materials perovskites and ZIF for applications in information encryption and decryption films with large scale (up to 6 × 6 cm2), flexibility, and high resolution (approximate 5 µm line width).

Bright Transparent Scintillators with High Fraction BaCl2 : Eu2+ Nanocrystals Precipitation: An Ionic-Covalent Hybrid Network Strategy toward Superior X-Ray Imaging Glass-Ceramics.

Metal halide crystals are bright but hygroscopic scintillator materials that are widely used in X-ray imaging and detectors. Precipitating them in situ in glass to form glass ceramics (GCs) scintillator offers an efficient avenue for large-scale preparation, high spatial resolution, and excellent stability. However, precipitating a high fraction of metal halide nanocrystals in glass to maintain high light yield remains a challenge. Herein, an ionic-covalent hybrid network strategy for constructing GCs scintillator with high crystallinity (up to ≈37%) of BaCl2 : Eu2+ nanocrystals is presented. Experimental data and simulations of glass structure reveal that the Ba2+ -Cl- clustering promotes the high crystallization of BaCl2 nanocrystals. The ultralow phonon energy (≈200 cm-1 ) of BaCl2 nanocrystals and good Eu reduction effect enable high photoluminescence inter quantum efficiency (≈80.41%) in GC. GCs with varied crystallinity of BaCl2 : Eu2+ nanocrystals demonstrate efficient radioluminescence and tunable scintillator performance. They either outperform Bi4 Ge3 O14 single crystal by over 132% steady-state light yield or provide impressive X-ray imaging resolutions of 20 lp mm-1 . These findings provide a new design strategy for developing bright transparent GCs scintillators with a high fraction of metal halide nanocrystals for X-ray high-resolution imaging applications.

Near-infrared emission of Yb3+ through energy transfer from ZnO to Yb3+ in glass ceramic containing ZnO nanocrystals.

Yb(3+)-doped glass and glass ceramic containing ZnO nanocrystals were prepared by the melting-quenching method and subsequent heat treatment. Intense near-IR emission around 1000 nm that originated from the transition of Yb(3+):(2)F(5/2)→(2)F(7/2) was generated as a result of energy transfer from oxygen interstitials in ZnO nanocrystals to Yb(3+) with energy transfer efficiency of about 10%. The quantum yield for the near-IR emission of Yb(3+) under the excitation of 390 nm was about 16.7%. These materials have potential application in achieving high-efficiency Si solar cells via spectrum modification.

Structure, Morphology, and Photoelectric Performances of Te-Sb2Se3 Thin Film Prepared via Magnetron Sputtering.

Antimony selenide (Sb2Se3) has been widely investigated as a promising absorber material for photovoltaic devices. However, low open-circuit voltage (Voc) limits the power conversion efficiency (PCE) of Sb2Se3-based cells, largely due to the low-charge carrier density. Herein, high-quality n-type (Tellurium) Te-doped Sb2Se3 thin films were successfully prepared using a homemade target via magnetron sputtering. The Te atoms were expected to be inserted in the spacing of (Sb4Se6)n ribbons based on increased lattice parameters in this study. Moreover, the thin film was found to possess a narrow and direct band gap of approximately 1.27 eV, appropriate for harvesting the solar energy. It was found that the photoelectric performance is related to not only the quality of films but also the preferred growth orientation. The Te-Sb2Se3 film annealed at 325 °C showed a maximum photocurrent density of 1.91 mA/cm2 with a light intensity of 10.5 mW/cm2 at a bias of 1.4 V. The fast response and recovery speed confirms the great potential of these films as excellent photodetectors.

Femtosecond laser writing of Er3+-doped CaF2 crystalline patterns in glass.

We report on the use of 800 nm, 250 kHz femtosecond laser pulses to precipitate Er(3+)-doped CaF(2) crystals inside oxyfluoride glass, which was confirmed with x-ray diffraction analysis. Confocal upconversion luminescence spectra show that the precipitated crystals have greatly enhanced upconversion luminescence intensity in comparison with unmodified glass. We demonstrate the possibility of three-dimensional optical data storage in the glass by the use of the confocal upconversion luminescence imaging.

Structural Origins of RF3/NaRF4 Nanocrystal Precipitation from Phase-Separated SiO2-Al2O3-RF3-NaF Glasses: A Molecular Dynamics Simulation Study.

Oxyfluoride glass-ceramics with RF3 or NaRF4 (R3+: rare earth elements) nanocrystals are considered as favorable hosts for luminescence applications. In this work, we utilized large-scale molecular dynamics (MD) simulations with effective partial charge potentials to study a series of oxyfluoride glasses that are of interest to the precipitation of RF3 or NaRF4 nanocrystals as previous experiment results suggested. The results show that phase separation exists in all glass compositions with fluoride-rich regions made up of R3+, Na+, and F- and oxide-rich regions consisting of aluminosilicate networks. These fluoride-enriched regions can serve as the precursor for RF3, cubic and hexagonal NaRF4, and NaF crystal precipitation. The results also confirm that the concentration of Na+ in the fluoride phase plays a key role in determining the crystal phases (RF3, NaRF4, or NaF) and crystal structure (cubic vs hexagonal NaRF4) to be precipitated. Consequently, this study shows that MD simulations with effective potentials can fill the gap in the structural understanding of oxyfluoride glass and provide insights into atomic scale information of the phase separation behavior that is useful in predicting the potential crystal types in oxyfluoride glass. When coupled with experimental validations, these simulations can expedite the exploration of novel luminescent oxyfluoride glass ceramics.