Search Results (361)

The optimization of BiVO₄-based structures significantly contributes to the development of a global system towards clean, renewable, and sustainable energies. Enhanced photocatalytic performance has been reported for numerous doped BiVO₄ materials. Bi³⁺-based compounds can be easily doped with rare earth (RE³⁺) ions due to their equal valence and similar ionic radius. This means that RE³⁺ ions could be regarded as active co-catalysts and dopants to enhance the photocatalytic activity of BiVO₄. In this study, a simple microwave-assisted approach was used for preparing nanostructured Bi_1−xEu_xVO₄ (x = 0, 0.03, 0.06, 0.09, and 0.12) samples. Microwave heating at 170 °C yields a bright yellow powder after 10 min of radiation. The materials are characterized through X-ray diffraction (XRD), transmission electron microscopy (TEM), ultraviolet–visible–near-infrared diffuse reflectance spectroscopy (UV-Vis-NIR DRS), photoluminescence spectroscopy (PL), and micro-Raman techniques. The effects of the different Eu³⁺ ion concentrations incorporated into the BiVO₄ matrix on the formation of the monoclinic scheelite (ms-) or tetragonal zircon-type (tz-) BiVO₄ structure, on the photoluminescent intensity, on the decay dynamics of europium emission, and on photocatalytic efficiency in the degradation of Rhodamine B (RhB) were studied in detail. Additionally, microwave chemistry proved to be beneficial in the synthesis of the tz-BiVO₄ nanostructure and Eu³⁺ ion doping, leading to an enhanced luminescent and photocatalytic performance. Full article

Packaging materials made from polypropylene (PP) can be used to protect cultural heritage objects from damage ensuring their long-life preservation. This research work concerns the assessment of recycled polypropylene hollow chamber sheets as potential packaging materials for archival collections and cultural heritage objects. It was carried out through a multidisciplinary diagnostic methodology combining mechanical methods, non-destructive imaging techniques in visible light (VIS), and ultraviolet-induced visible luminescence (UVL), as well as handheld digital microscopy, colorimetry, glossimetry, and SEM microanalysis. The results showed that the condition and mechanical performance of the specimens are affected by the ageing process. Full article

Selective gene delivery to defined cell populations remains one of the key challenges in lentiviral vector-based gene therapy. The vesicular stomatitis virus glycoprotein (VSV-G) confers high infectivity but lacks cell-type specificity because of the ubiquitous expression of its receptor, LDLR. To enable modular, receptor-specific targeting while retaining the production efficiency of VSV-G-pseudotyped vectors, we designed a bispecific adapter, 929-B6, comprising a VSV-G-binding nanobody and an ERBB2-binding DARPin 9.29. Anti-VSV-G nanobodies were isolated from an alpaca immune library and screened in cell-based pseudoreceptor assays to identify the optimal binder (VSVG-B6). The resulting adapter was evaluated with receptor-ablated (VSV-G_mut) and wild-type VSV-G-pseudotyped LVs across ERBB2-positive and -negative cell lines and in a mouse xenograft model. 929-B6 enabled efficient, receptor-specific transduction of ERBB2-expressing cells without increasing infection of ERBB2-negative controls. Pre-incubation of VSV-G_mut-pseudotyped LVs with 1–2 µg/mL 929-B6 increased transduction up to eight-fold in ERBB2⁺ cells, with similar but smaller effects for VSV-G and VSV-G_mut + 929R pseudotypes. Across breast cancer lines, transduction enhancement correlated with ERBB2 surface density, and co-culture experiments confirmed selective entry into ERBB2⁺ populations. In vivo imaging of ERBB2⁺ tumors revealed a visible tumor-localized luminescent signal following administration of 929-B6-treated vectors. The 929-B6 adapter provides a rapid, scalable means to retarget standard LV stocks toward chosen receptors without re-engineering the envelope or co-packaging pseudoreceptor plasmids. Its modularity suggests a generalizable platform for both gene therapy and oncolytic applications requiring flexible, receptor-defined tropism. Full article

KY₃F₁₀:Yb³⁺, Tm³⁺ upconversion microparticles (UCMPs) with varying Mn²⁺ doping concentrations were synthesized via a hydrothermal method. Under 980 nm laser excitation, the sample with 3 mol% Mn²⁺ doping demonstrated markedly enhanced luminescence performance, exhibiting a significant intensity increase compared to undoped samples. The as-synthesized UCMPs were successfully incorporated into an anti-counterfeiting ink. Target information was encrypted using a hash function to generate a QR code, which was then screen-printed onto substrate materials. Under 980 nm laser irradiation, the printed QR code exhibited visible blue fluorescence with high stability, confirming its anti-counterfeiting capability. Furthermore, an image recognition system for anti-counterfeiting, based on a hybrid Convolutional Neural Network-Bidirectional Long Short-Term Memory (CNN-BiLSTM) architecture, was developed on the Matlab platform. The system achieved 100% recognition accuracy for the luminescent QR code patterns, providing valuable insights for the development of deep learning-based image anti-counterfeiting technologies. Full article

Photoactivatable nitric oxide donors (photoNORMs) are promising agents for controlled NO release and real-time optical tracking in biomedical theranostics. Here, we report a comprehensive density functional theory (DFT) and time-dependent DFT (TDDFT) study on a series of hybrid ruthenium–gold nanocluster systems of the general formula [(L)Ru(NO)(SH)@Au₂₀], where L = salen, bpb, porphyrin, or phthalocyanine. Structural and bonding analyses reveal that the Ru–NO bond maintains a formal {RuNO}⁶ configuration with pronounced Ru → π*(NO) backbonding, leading to partial reduction of the NO ligand and an elongated N–O bond. Natural Bond Orbital (NBO), Natural Energy Decomposition Analysis (NEDA), and Extended Transition State–Natural Orbitals for Chemical Valence (ETS–NOCV) analyses confirm that Ru–NO bonding is dominated by charge-transfer and polarization components, while Ru–S and Au–S linkages exhibit a delocalized, donor–acceptor character coupling the molecular chromophore with the metallic cluster. TDDFT results reproduce visible–near-infrared (NIR) absorption features arising from mixed metal-to-ligand and cluster-mediated charge-transfer transitions. The calculated zero–zero transition and reorganization energies predict NIR-II emission (1.8–3.8 μm), a region of high biomedical transparency, making these systems ideal candidates for luminescence-based NO sensing and therapy. This study establishes fundamental design principles for next-generation Ru-based photoNORMs integrated with plasmonic gold nanoclusters, highlighting their potential as multifunctional, optically trackable theranostic platforms. Full article

Until 2021, experimental data on polysulfide groups in feldspathoids were limited to the properties of the S₃^•− chromophore center and the S₂^•− luminescence center in sodalite-group minerals. Interpretation of some spectroscopic data on other S-bearing groups in feldspathoids remained ambiguous because of significant differences between calculated data for isolated polysulfide species and experimental data for polysulfide groups in liquid sulfur, solutions, and matrix-isolated species published in different literature sources. For this reason, configurations of stable and metastable structures and parameters of the absorption spectra in the ultraviolet, visible, and near-infrared (UV-Vis-NIR) region and in the ESR and Raman spectra of various structure modifications of polysulfide S_n²⁻ anions, S_n^•− radical anions, and S_n neutral molecules (n = 2–6) as well as HS⁻ in the sodalite cage of sapozhnikovite have been calculated in frames of the density functional theory using the VASP and ORCA software packages. Taking into account the obtained results of theoretical calculations, spectroscopic properties of extra-framework polysulfide groups in natural tectosilicates belonging to the cancrinite and sodalite groups are discussed. The obtained results made it possible to confirm and partially clarify the interpretation of the experimental spectroscopic data for S-containing feldspathoids obtained by the authors of this work over the past five years. Full article

The synthesis and characterization of two new complexes, namely Pt(1,3-bis(4-(4-hexyl-2-thienyl)-pyridin-2-yl)-5-mesitylbenzene)Cl and Pt(1,3-bis(4-(4-hexyl-2-thienyl)-pyridin-2-yl)-5-(2-thienyl)benzene)Cl, are reported. Both exhibit luminescence quantum yields approaching unity (Φlum = 0.96–0.99) in the green region of the visible spectrum (534–554 nm) in diluted degassed dichloromethane solution. Similarly to other N^C^N platinum(II) complexes, a broad emission band grows in the deep red region (738–752 nm) upon increasing the concentration, due to the creation of bi-molecular emissive excited states. Interestingly, it appears that the introduction of a 2-thienyl group on the pyridine rings is a route to maintain excellent quantum yields even in concentrated solution. In order to have an insight into the electronic properties of the novel compounds, density functional theory (DFT) and time-dependent (TD)DFT approaches were employed to calculate the molecular geometry, the ground state, the electronic structure and the excited electronic states of the complexes, both as a monomers and dimers in solution. Full article

We report the synthesis and characterization of the two enantiomeric forms of a thienyl-substituted diketopyrrolopyrrole (DPP) derivative bearing chiral alkyl chains. Thin films were prepared either by spin-coating and drop-casting and analyzed by UV–Visible absorption, electronic circular dichroism (ECD), and circularly polarized (CP) luminescence (CPL). ECD spectra confirmed the opposite chirality of the (R) and (S) isomers, while CPL measurements of the S enantiomer demonstrated solid-state chiroptical activity. Preliminary device tests showed promising optoelectronic behavior, highlighting these chiral DPP materials as potential candidates for CP organic light-emitting diodes (CP-OLEDs) applications, combining strong chiroptical response with good film quality. Full article

In this work, systematic first-principles calculations were performed to investigate the multiband emissions of Bi-doped Y₃Ga(Al)₅O₁₂ phosphors. The predicted emissions of Bi³⁺ show that the violet narrow-band emission can be attributed to the ³P₁–¹S₀ transition of Bi³⁺ at Y sites, and both the metal-to-metal charge transfer (MMCT) of Bi³⁺ at Ga (Al) sites and the luminescence of Bi³⁺ dimers can generate visible emissions. Detailed formation energy calculations subsequently rule out the possibility that the visible emission originates from the MMCT of Bi³⁺ at Ga (Al), as the concentration of Bi_Y is much greater than that of B_Ga (or Bi_Al). To better understand the relationship between the nephelauxetic effect and the coordination environment, the vacuum-referred binding energy (VRBE) model was utilized to determine the energy levels of bismuth ions relative to the vacuum level in different systems and at different sites. The results provide insight into the relationship between the coordination environment and the emission properties of Bi³⁺ and are helpful for analyzing and optimizing the luminescent properties of bismuth-doped garnet-like materials. Full article

This study explores the development of luminescent wearables using machine embroidery with phosphorescent threads to enhance the visibility and safety of children in low-light environments, addressing the need for improved child protection in urban settings. Five embroidery designs incorporating sports, animal, celestial, and typographic motifs were created using Digitizer MBV 2.0 software and produced on a Janome MB4 embroidery machine with phosphorescent threads on black woven fabric for optimal contrast. The luminous performance was evaluated through photographic documentation and lux meter measurements in a controlled light-tight chamber, assessing light emission intensity and decay over time after UV activation. Results demonstrate that designs with higher stitch counts and densities exhibit stronger initial illuminance and longer persistence, with exponential decay curves highlighting rapid initial intensity loss. Variations in design size and stitch density showed linear correlations with illuminance. The study demonstrates the feasibility of luminescent embroidery as a scalable and child-friendly approach to enhancing low-light visibility and safety, combining functionality with aesthetic appeal. Full article

Metal–organic compounds, and especially those containing well-known antioxidant natural flavonoids (Chrysin, Chr) and metal ions (Ti(IV)), attract keen interest for their potential biological activity nutritionally and pharmacologically. To that end, chemical reactivity profiling in binary/ternary systems was investigated synthetically, revealing unique structural correlations between mononuclear (Ti(IV)-Chr) and tetranuclear assemblies (Ti(IV)-Chr-phen). Chemical profiling involved physicochemical characterization through elemental analysis, FT-IR, UV–Visible, 1D-2D NMR, ESI-MS spectrometry, solid-state luminescence, and X-ray crystallography, with theoretical work on intra(inter)molecular interactions of 3D assemblies pursued through Hirshfeld analysis and BVS calculations. An in-depth study of their chemical reactivity shed light onto specific structural properties in the solid-state and in solution, while concurrently exemplifying quenching behavior due to their distinct flavonoid pattern. In the framework of biological activity, the materials were investigated for their antibacterial properties toward Gram(−)-E. coli and Gram(+)-S. aureus, exhibiting an enhanced effect compared to the free ligand and metal ion. Further investigation of BSA denaturation revealed strong anti-inflammatory properties compared to Chr and Diclofenac, an anti-inflammatory agent. Finally, in vitro studies using physiological and cancer cell lines, including breast (MCF10A, MCF7) and lung tissues (MRC-5, A549), formulated a structure–tissue relation reactivity profile, thus justifying their potential as future metallodrugs. Full article

Three fluorophenyl-substituted cyclometalated Ir(III) complexes (Ir1–Ir3) have been synthesized by changing the position of the fluorine atom. All complexes exhibit distinct aggregation-induced phosphorescence emission (AIPE) characteristics in CH₃CN/H₂O and demonstrate satisfactory detection performance for 2,4,6-trinitrophenols (TNPs) with limits of detection of 124 nM, 101 nM, and 127 nM, respectively. In addition, Ir1–Ir3 possess excellent selectivity and anti-interference capability for TNP detection, showing outstanding performance even in different common water samples. The ultraviolet–visible absorption spectra and luminescence lifetimes of the complexes show that their quenching processes include both a static process and dynamic process, and the detection mechanism may be assigned to a combination of photo-induced electron transfer and an inner-filter effect. Full article

Dye-sensitized solar cells (DSSCs) are promising alternatives for power generation due to their environmental friendliness, cost effectiveness, and strong performance under diffused light. Conversely, their low spectral response in the ultraviolet (UV) region significantly obliterates their overall performance. The so-called luminescent down-shifting (LDS) presents a practical solution by converting high-energy UV photons into visible light that can be efficiently absorbed by sensitizer dyes. Herein, a conventional solid-state technique was applied for the synthesis of an LDS, europium (II)-doped barium orthosilicate (BaSiO₃:Eu²⁺) material. The material exhibited strong UV absorption, with prominent peaks near 400 nm and within the 200–300 nm range, despite a weaker response in the visible region. The estimated optical bandgap was 3.47 eV, making it well-suited for UV absorbers. Analysis of the energy transfer mechanism from the LDS material to the N719 dye sensitizer depicted a strong spectral overlap of $2\times {10}^{10}{\mathrm{M}}^{-1}{\mathrm{c}\mathrm{m}}^{-1}{\mathrm{n}\mathrm{m}}^4$, suggesting efficient energy transfer from the donor to the acceptor. The estimated Förster distance was approximately $6.83\mathrm{n}\mathrm{m}$, which matches the absorption profile of the dye-sensitizer. Our findings demonstrate the potential of BaSiO₃:Eu²⁺ as an effective LDS material for enhancing UV light absorption and improving DSSC performance through increased spectral utilization and reduced UV-induced degradation. Full article

Given the exceptional capabilities of femtosecond laser processing in achieving high-precision ablation for air-film cooling hole fabrication on turbine blades, it is imperative to develop an advanced monitoring methodology that enables real-time feedback control to automatically terminate the laser upon complete penetration detection, thereby effectively preventing backside damage. To tackle this issue, a spectrum-domain coherent imaging technique has been developed. This innovative approach adapts the fundamental principle of fiber-based Michelson interferometry by integrating the air-film hole into a sample arm configuration. A broadband super-luminescent diode with a 830 nm central wavelength and a 26 nm spectral bandwidth serves as the coherence-optimized illumination source. An optimal normalized reflectivity of 0.2 is established to maintain stable interference fringe visibility throughout the drilling process. The system achieves a depth resolution of 11.7 μm through Fourier transform analysis of dynamic interference patterns. With customized optical path design specifically engineered for through-hole-drilling applications, the technique demonstrates exceptional sensitivity, maintaining detection capability even under ultralow reflectivity conditions (0.001%) at the hole bottom. Plasma generation during laser processing is investigated, with plasma density measurements providing optical thickness data for real-time compensation of depth measurement deviations. The demonstrated system represents an advancement in non-destructive in-process monitoring for high-precision laser machining applications. Full article

Mineral fluorescence under different portions of the visible and invisible light spectrum has a long history of scientific study. In our study of marine sediments from the Georgia Bight, we have utilized the blue portion of the light spectrum in the 445 nanometer (nm) range. The use of fluorescence has proven very useful in microscopic analyses of carbonate minerals. While the sediment prism of the inner-to-mid continental shelf in the southeastern Atlantic is predominantly siliceous, the dissolution and deterioration of marine shell contribute a significant amount to the fabric of any sediment sample. Together with carbonate minerals such as dolomite, eroded from basement rock and redeposited on the shelf, a potentially robust fluorescent response was expected and observed in samples. In marine sediments, blue light illumination has produced an easily observed fluorescent response in both underwater and in laboratory settings. This fluorescence can be attributed to carbonate minerals—calcite/aragonite. Feldspars are major accessory minerals in the sediment prism of the Georgia Bight, and much of the observed fluorescence in our samples can be attributed to their presence. To identify specific minerals responsible for any observed fluorescence, X-ray diffraction and energy dispersive spectroscopy were utilized. This combined methodology of luminescent excitation, X-ray diffractometry and spectroscopy has produced the results reported herein. Full article