Search Results (1,306)

The Sar-e-Sang lapis lazuli deposit has a mining history exceeding 5000 years, producing the world’s finest lapis lazuli. Recently, gem-quality forsterite has been discovered in the marble containing spinel, dolomite, and phlogopite at the periphery of the lapis lazuli ore body at the Pitawak mine, located east of the Sar-e-Sang deposit. The mineral assemblage indicates that the protolith of this marble is dolomite with aluminous and siliceous components. These forsterite crystals occur as colorless, transparent anhedral grains, exhibiting distinct red fluorescence under 365 nm ultraviolet light. To investigate the gemological and spectroscopic characteristics of the Pitawak mine forsterite, this study conducted and analyzed data from basic gemological analysis, electron probe microanalysis (EPMA), Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), ultraviolet–visible absorption spectroscopy (UV-VIS), Fourier-transform infrared spectroscopy (FTIR), laser Raman spectroscopy (RAMAN), and photoluminescence spectroscopy (PL) on four forsterite samples from the Pitawak mine. The analysis results reveal that the samples indicate a composition close to ideal forsterite with a crystal chemical formula of (Mg_2.00Fe_0.02)_Σ2.02Si_0.99O₄. The trace elements present include Fe, Mn, Ca, and minor amounts of Cr and Ni. The UV-VIS spectroscopy results show that the samples possess high transmittance across the visible light range with very weak absorption bands, contributing to the colorless and transparent appearance of Pitawak mine forsterite. This phenomenon is attributed to the extremely low content of chromophoric elements, which have a negligible effect on the forsterite’s color. PL spectroscopy indicates that the red fluorescence of the samples is caused by an emission peak near 642 nm. This emission peak arises from the spin-forbidden ⁴T₁ → ⁶A₁ transition of Mn²⁺ ions situated in octahedral sites within the forsterite structure. Full article

This study investigates phase formation in the Sr–Zn–Eu³⁺ orthophosphate system, focusing on double- and triple-phosphates. The isomorphisms and phase formation in Sr_3–1.5xEu_1+x(PO₄)₃, Sr_9–1.5xZn_1.5Eu_x(PO₄)₇, Sr_9.5–1.5xZnEu_x(PO₄)₇, Sr_3–xZn_xEu(PO₄)₃, and Sr_3–xZn_x(PO₄)₂ series were studied using powder X-ray diffraction and Rietveld refinement. A ternary phase diagram was constructed, identifying concentration limits for pure phases and multi-phase regions as well as areas of stabilization of strontiowhitlockite-, palmierite-, eulytite-, and strontiohurlbutite-type phases. The combinatorial complexity of Sr-based phosphates is discussed. The β-Sr₃(PO₄)₂ isostructural to whitlockite was found to exhibit the highest isomorphic capacity for Eu³⁺ cations, which is advantageous for its application as a red-emitting phosphor. Photoluminescence properties were studied, and analyzed based on structural data. Photoluminescence studies confirmed intense red-emission dominated by the ⁵D₀ → ⁷F₂ transition of Eu³⁺, with the β-Sr₃(PO₄)₂-based phosphor showing the highest emission intensity. Full article

Minimizing the spectrum overlaps of energy transfer (ET) is necessary but not sufficient for achieving high-sensitivity film thermosensing. Herein we have designed two blue emitters of DBA-BPAc and Z-DBABH exhibiting blue and bluish-green emissions, respectively, to hybridize with the red-emitting Ir(MDQ)₂(acac). Compared with Z-DBABH, DBA-BPAc shows a larger spectrum overlap of ET and a relatively smaller discrepancy in fluorescence thermal decay, while its emission spectrum displays a much smaller overlap with that of Ir(MDQ)₂(acac). The dual minimization of spectrum overlap of ET and emissions results in its superior ratiometric film thermosensing of the DBA-BPAc film in wide-range and high-temperature regions. The DBA-BPAc/Ir(MDQ)₂(acac) film exhibits a maximum relative sensitivity (S_r) of 3.36% °C⁻¹ at 166 °C, exceeding 0.43% °C⁻¹ in 50–265 °C. In comparison, the Z-DBABH/Ir(MDQ)₂(acac) system displays a reliable but relatively lower performance, with a maximum S_r of 1.92% °C⁻¹ (at 300 °C). The temperature resolution remains below 2.06 °C throughout the entire temperature range (20–300 °C), achieving a best value of 0.60 °C at 180 °C. Notably, both films display distinct naked-eye color transitions with temperature changes, enabling multi-level anti-counterfeiting applications. This work provides new insights for designing high-performance thermometers. Full article

Remediated landfills require long-term monitoring due to ongoing processes such as settlement, water infiltration, leachate migration, and biogas emissions, which may lead to cover degradation and environmental risks. Traditional ground-based inspections are often time-consuming, costly, and limited in terms of spatial coverage. This study presents the application of Unmanned Aerial Vehicle (UAV)-based remote sensing methods for the structural assessment of a remediated landfill. A multi-sensor approach was employed, combining geometric data (Light Detection and Ranging (LiDAR) and photogrammetry), hydrological modeling (surface water accumulation and runoff), multispectral imaging, and thermal data. The results showed that subsidence-induced depressions modified surface drainage, leading to water accumulation, concentrated runoff, and vegetation stress. Multispectral imaging successfully identified zones of persistent instability, while UAV thermal imaging detected a distinct leachate-related anomaly that was not visible in red–green–blue (RGB) or multispectral data. By integrating geometric, hydrological, spectral, and thermal information, this paper demonstrates practical applications of remote sensing data in detecting cover degradation on remediated landfills. Compared to traditional methods, UAV-based monitoring is a low-cost and repeatable approach that can cover large areas with high spatial and temporal resolution. The proposed approach provides an effective tool for post-closure landfill management and can be applied to other engineered earth structures. Full article

Red mud is a highly alkaline solid waste with an annual emission of over 200 million tons, which requires large-scale utilization methods. Soil Cd remediation is a global concern, due to its high toxicity and strong mobility. Given red mud’s potential for soil Cd remediation, this study reviews its basic characteristics, the mechanisms of soil Cd immobilization by red mud, and the use of red mud-based passivators for agricultural soil Cd remediation. In general, red mud regulates soil pH, thus increasing the soil’s Cd adsorption capacity; provides abundant surface active sites for adsorption and complexation with soil Cd; introduces cations to immobilize Cd via ion exchange; and enriches Cd-resistant microbe species to reduce soil Cd toxicity. Furthermore, the potential environmental risks and suggestions on red mud application are discussed. Further research should focus on improving the remediation effectiveness of red mud on cadmium-contaminated agricultural soil, demonstrating its long-term efficacy and economic costs, and proposing practical technical models and standards for application. Full article

Mn⁴⁺-activated fluoride phosphors possess outstanding luminescent properties, making them highly suitable for applications in lighting and display technologies. However, the synthesis of such phosphors generally requires the use of large amounts of highly toxic aqueous HF, leading to serious environmental pollution. To eliminate the use of hazardous HF solution, a low-temperature molten salt method employing NH₄HF₂ was developed to synthesize the narrow-band red emitter Cs₂GeF₆: Mn⁴⁺ phosphor. Following the reaction, the product was washed with a dilute H₂O₂ solution to remove residual NH₄HF₂ and other impurities. The phase purity and morphology were analyzed by X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively, and the luminescence properties were examined via photoluminescence (PL) spectroscopy. The obtained phosphors exhibit bright red emission characteristics of Mn⁴⁺ under blue-violet excitation. Among them, Cs₂GeF₆: 0.08 Mn⁴⁺ shows the highest emission intensity, with an internal quantum efficiency (IQE) of 78%. A white light-emitting diode (WLED) fabricated by combining this phosphor with a blue chip and commercial Y₃Al₅O₁₂: Ce³⁺ (YAG) phosphor achieved a high luminous efficacy (LE) of ~146 lm/W, a correlated color temperature (CCT) of ~4396 K, and a color rendering index (Ra) of ~83, alongside excellent operational color stability. Full article

The palette of the fluorogen-activating protein FAST expanded into the far-red region by the development of a novel fluorogen, HBTR-3,5-DOM. This was achieved through a C=O to C=S substitution in the classic hydroxybenzylidene-rhodanine core, which induced a bathochromic shift of over 100 nm. The complexes of HBTR-3,5-DOM with FAST variants pFAST and F62L are characterized by absorption and emission maxima at 640–650 nm and ~670 nm, respectively, and are found to exhibit distinct fluorescence lifetimes. The fluorogen is successfully applied in genetically encoded live-cell imaging together with these FAST variants for various subcellular structures. Furthermore, its potential for multiplexed imaging is demonstrated by the simultaneous discrimination of two targeted proteins using fluorescence lifetime imaging microscopy (FLIM). Full article

Perovskite light-emitting diodes (PeLEDs) have garnered significant interest owing to their exceptional color purity, broadly tunable emission spectra, and cost-effective solution processability. However, blue PeLEDs continue to underperform in efficiency and operational stability compared to their red and green counterparts, primarily due to defect-induced non-radiative recombination losses and inefficient exciton management. Herein, we demonstrate a synergistic approach that integrates multi-cation compositional engineering with triplet exciton management by incorporating a high-triplet-energy material, mCBP (3,3-Di(9H-carbazol-9-yl)biphenyl), during film fabrication. Temperature-dependent photoluminescence reveals that mCBP incorporation significantly enhances the exciton binding energy from 49.36 meV to 68.84 meV and reduces phonon coupling strength, indicating improved exciton stability and suppressed non-radiative channels. The corresponding PeLEDs achieve a peak external quantum efficiency of 10.2% and a maximum luminance exceeding 12,000 cd/m², demonstrating the effectiveness of this solution-based triplet management strategy. This work highlights the critical role of scalable, solution-processed triplet exciton management strategies in advancing blue PeLED performance, offering a practical pathway toward high-performance perovskite-based display and lighting technologies. Full article

Tandem white organic light-emitting diodes (OLEDs), formed by stacking red, green, and blue organic electroluminescent units, offer a promising route toward high-resolution microdisplays. However, their performance is constrained by the intrinsically short lifetime of blue OLED sub-units. Replacing the unstable blue OLED with a long-lived GaN-based LED could address this limitation, but practical hybridization remains difficult because of incompatible fabrication routes and significant current imbalance between the inorganic and organic units. Here, we demonstrate the first hybrid GaN–OLED tandem white LEDs enabled by an interface-engineered charge-generation unit (CGU). By introducing an ITO/HAT-CN/LiNH₂-doped Bphen CGU, we simultaneously enhance the work function, strengthen the built-in electric field, and smooth the interfacial morphology. These synergistic effects promote efficient charge generation, yielding near-ideal voltage summation and well-balanced electron–hole injection. As a result, the hybrid tandem device shows a nearly twofold increase in current efficiency (from 28.1 to 58.6 cd A^–1) and significantly reduced spectral shift under varying current densities. We further demonstrate the generality of this approach by integrating the GaN emission with yellow OLEDs to produce stable blue–yellow hybrid white emission. This work establishes an applicable strategy for integrating GaN-LEDs and OLEDs, opening a pathway toward efficient, stable, and compact white light engines for next-generation microdisplay technologies. Full article

As global food demand grows, the limited availability of natural resources exacerbates environmental and food security challenges. Household food waste is a major yet underexplored issue, contributing to inefficiencies, economic losses, and environmental harm. This study applies the Environmental-Economic Footprint (EN-EC) index to assess household food waste in Ireland. By integrating environmental and economic data, this index facilitates a comprehensive dual-perspective evaluation of food waste impacts. Data were collected from 1000 Irish households, analyzing waste patterns across 12 food categories. Environmental impacts were quantified using global warming potential (GWP) and water footprint (WF), while economic costs were based on waste generation and disposal. The EN-EC index synthesizes these parameters to facilitate informed decision-making. On average, Irish households reported approximately 966 g (0.97 kg) of edible food waste per week, equivalent to around 50 kg annually per household. This amount results in substantial associated impacts, including greenhouse gas emissions and water consumption, quantified through literature-based footprint coefficients. Red meat, particularly beef, contributes disproportionately to environmental and economic burdens despite its relatively lower waste volume. A 50% reduction in meat waste could cut CO₂ emissions by 2.5 kg, water use by 563.50 L, and costs by €3623.48. These insights equip policymakers with targeted strategies to mitigate food waste, aligning with global sustainability goals. Full article

Chemical defenses help insects resist pathogen infection. The volatile compositions, emission patterns, and external immune functions of the red palm weevil (RPW), a major invasive pest now established in numerous countries including the Mediterranean Basin, North Africa, Middle East, and parts of Latin America and the Caribbean, are largely unknown. In this study, we examined RPW larval volatiles, analyzing their emission patterns across developmental stages and under pathogen stress from feeding Metarhizium anisopliae. RPW larvae shared a number of volatile components across stages, but the emission dynamics were significantly different. These volatile chemicals were primarily alcohols, phenols and aromatic hydrocarbons, and styrene was the predominant volatile. Furthermore, pathogen stress induced distinct volatile profiles: phenylacetaldehyde unidirectionally decreased, whereas n-nonanol, 4-ethylguaiacol, 2-phenylethanol, hexanal, and benzophenone levels increased. Antimicrobial analysis showed that these upregulated compounds broadly inhibited fungal and bacterial growth. Therefore, our results illustrated the immune defense role of RPW larval volatiles and their potential bioactive compounds, including n-nonanol, 4-ethylguaiacol, 2-phenylethanol, hexanal, and benzophenone. Full article

Calcium phosphates are one of the main materials used in biomedicine for bone regeneration purposes. To improve the properties of biocompatible β-Ca₃(PO₄)₂, doping by bioactive, antibacterial is actively used, as well as luminescent ions. Co-doped phosphates Ca_8−xSr_xZnEu(PO₄)₇ with a β-Ca₃(PO₄)₂ (β-TCP)-type structure were synthesized through solid-state synthesis. The β-TCP-type structure was confirmed using X-ray powder diffraction and FTIR spectroscopy. Photoluminescence data, including excitation and emission spectra, decay curves, lifetime values and quantum yields, were collected for all samples. Ca_8−xSr_xZnEu(PO₄)₇ phosphates exhibit strong red-emission due to 4f-4f transitions of Eu³⁺ ions in disordered oxygen surrounding, with quantum yields reaching 54%. The phosphates demonstrated biocompatibility through MTT assay, with successful differentiation of aMSCs into the osteogenic lineage. Antibacterial activity was tested against four bacteria (E. coli, S. aureus, P. aeruginosa, and E. faecalis) and a fungus (C. albicans). It was found that the samples demonstrated antibacterial properties. The growth of E. coli and E. faecalis is significant inhibited by Ca_8−xSr_xZnEu(PO₄)₇ samples with 0 ≤ x ≤ 6.0. Analysis of mixed salt solubility using Eu³⁺ ions as a fluorescent probe showed that increasing Sr²⁺ concentration in Ca_8−xSr_xZnEu(PO₄)₇ delays both β-TCP phase resorption and HAP phase precipitation. These results demonstrate the potential of Ca_8−xSr_xZnEu(PO₄)₇ phosphates for bioimaging and bone healing control. Full article

Au–ZnO heterogeneous nanoparticles (NPs) were successfully synthesized, and the intrinsic correlation between their spectral evolution and interfacial growth mechanism was systematically elucidated. With increasing Au content, the SPR absorption peak of Au exhibits a pronounced red shift, while the defect-related emission of ZnO is suppressed and the band-edge emission becomes broadened. These spectral variations are closely coupled with the interfacial growth process. Interfacial electron transfer and the formation of a Schottky barrier induce charge redistribution within ZnO and reduce oxygen vacancies, enabling ZnO to preferentially nucleate on the Au surface and subsequently evolve into a pyramidal structure. The resulting morphological transformation further enhances electron depletion and plasmonic coupling, lowering the effective plasmonic energy of Au and deepening the SPR red shift. Quantitative analysis based on Mie theory shows that approximately 12% of the free electrons in Au participate in interfacial transfer, confirming the cooperative role of strong electronic coupling in governing both growth dynamics and optical responses. This study provides deeper insight into the photophysical mechanisms of Au–ZnO heteronanocrystals and offers guidance for designing noble metal–semiconductor composites with tunable optoelectronic properties. Full article

The aim of this study was to assess the energy potential of woody grapevine (Vitis vinifera L.) shoots depending on the cultivation system, cultivar, and fruit colour. Field studies were conducted in 2024 at the Mendel University Vineyard in Lednice (Czech Republic) on Chardonnay, Merlot, Riesling, and Zweigelt cultivars, cultivated using the Guyot and Cordon systems. The cultivar analysis covered both the amount of biomass produced during pruning and its energy and emission properties. Laboratory tests of the energy potential of the biomass obtained were carried out at the University of Life Sciences in Lublin. The results showed that the varietal factor significantly influenced the biomass parameters—Chardonnay was characterised by the highest total plant weight (773.57 g), while Zweigelt (8.60 pcs.) had the highest number of shoots with the lowest unit weight (74.82 g). The Cordon system generated significantly higher biomass yields and more favourable combustion properties compared to Guyot. Differences in fruit colour indicate that, among the studied cultivars, white-berried varieties produce heavier shoots, whereas red varieties produce a greater number of shoots. The analysis of gas emissions showed a significant influence of the cultivar and training system, with the highest CO, CO₂, and NOx emissions recorded for the Zweigelt cultivar. The results emphasise that an integrated approach, taking into account both genotypic factors, training systems and phenotypic characteristics of the vines, is crucial for optimising the use of wine biomass as an energy source in the context of a circular economy. Full article

The osmium(II) polypyridyl complex [Os(tpy)(pydppn)]²⁺ (tpy = 2,2′:6′,2″-terpyridine; pydppn = 3-(pyrid-2′-yl)-4,5,9,16-tetraaza-dibenzo[a,c]naphthacene) was synthesized and characterized to evaluate the effect of an extended planar π-system on photophysical properties and DNA interactions. This complex represents the π-expanded analog of the previously studied [Os(tpy)(pydppz)]²⁺ system. Electrochemical studies revealed a reversible Os(II)/Os(III) oxidation at +0.99 V vs. SCE and five ligand-centered reductions, generally less negative than those of the smaller pydppz analog, consistent with enhanced electron-accepting ability. In acetonitrile, the complex exhibits UV absorption bands at 328 and 473 nm and near-infrared emission at 840 nm, assigned to a long-lived ³MLCT state (τ = 110 ns, Φ = 0.02). Upon titration with calf-thymus DNA, [Os(tpy)(pydppn)]²⁺ shows a pronounced light-switch effect, hypochromism, red-shifted MLCT bands, induced circular dichroism, and an increase in DNA melting temperature (ΔT_m = 8.9 ± 0.5 °C), consistent with intercalative binding. Viscometric titrations further support intercalation, with a binding constant K_B ≈ 1.2 × 10⁶ M⁻¹. Transient absorption spectroscopy indicates that DNA binding prolongs the excited-state lifetime and modifies vibrational relaxation pathways. These results highlight how π-system extension in Os(II) complexes modulates photophysical behavior and DNA affinity, offering insights for the rational design of NIR-emitting, DNA-targeted luminescent probes and potential phototherapeutic agents. Full article