Search Results (472)

Inclusion bodies (IBs) in Escherichia coli are increasingly recognised as nanostructured materials with tunable morphology and functional potential. The N-terminal auxiliary activity family 10 (AA10) lytic polysaccharide monooxygenase (LPMO) domain from Caldibacillus cellulovorans (Ccel_p40) consistently forms IBs and, when fused to diverse proteins, generates functional IBs. Here, we examined whether this strong aggregation propensity is unique to Ccel_p40 or a broader feature of AA10 LPMOs. Four homologous domains from phylogenetically distinct microorganisms, Kallotenue papyrolyticum (Kpap_p40), Kibdelosporangium aridum (Kari_p40), Archangium lipolyticum (Alip_p40), and Phytohabitans suffuscus (Psuf_p40), were heterologously expressed in E. coli under identical cytosolic conditions. All homologues accumulated predominantly in the insoluble fraction, forming morphologically uniform IBs with sub-micron diameters (550–860 nm) and moderate polydispersity indices (0.45–0.54). SDS-PAGE densitometry indicated that most of each expressed protein partitioned into the insoluble fraction. Field-emission scanning electron microscopy revealed compact spherical aggregates, and Fourier-transform infrared spectroscopy showed β-sheet-enriched secondary structures characteristic of ordered IBs. These results indicate that the pronounced aggregation tendency previously observed for Ccel_p40 is conserved across the AA10 homologues examined. The findings support the view that the AA10 domain represents a promising scaffold for generating stable, recyclable protein nanoparticles and provides a comparative basis for future IB-based biotechnological designs. Full article

Two structurally tunable (propyl-3-ol)triphenyltin(IV) (Ph₃SnL₁) and (butyl-4-ol)triphenyltin(IV) (Ph₃SnL₂) compounds were investigated at the human serum transferrin (Tf) molecular interface to resolve how ligand architecture and protein metallation modulate organotin(IV) biocompound stability and lobe-selective binding. Steady-state fluorescence spectroscopy revealed efficient quenching of native Tf emission (λ_ex = 280 nm, 296–310 K, pH 7.4) without significant spectral displacement, indicating the predominant formation of non-fluorescent ground-state complexes. Calculated bimolecular quenching constants (K_q ~10¹² M⁻¹ s⁻¹) exceeded the diffusion-controlled aqueous limit, ruling out a collisional dynamic quenching mechanism and confirming static complexation as the principal origin of fluorescence suppression. Double-log binding analysis revealed moderate affinity (K_a ~10²–10³ M⁻¹) and an approximately single dominant binding event per protein (n ≈ 0.65–0.90). Temperature-dependent van’t Hoff evaluation yielded positive ΔH° and ΔS° values, supporting a spontaneous, entropy-favored association process largely governed by hydrophobic and dispersion-type contributions, consistent with lipophilic organotin(IV) scaffold accommodation. Iron (Fe³⁺) loading of Tf markedly enhanced ligand engagement, especially for Ph₃SnL₁, evidencing that metallation-induced lobe closure reshapes pocket accessibility and local polarity relevant for organotin(IV) binding presentation rather than simply strengthening empirical docking scores. Molecular docking localized the most stable Ph₃SnL₂ poses in the sterically confined, rigid C-lobe, while Ph₃SnL₁ preferentially penetrated the more adaptive N-lobe. ONIOM QM/MM refinement of docking poses confirmed strong interfacial stabilization (ΔE_int ≈ –38 to –62 kcal mol⁻¹) and clarified charge–packing interplay without invoking frontier orbital analysis. The results map multiscale structure–interaction relationships defining lobe preference and complex stability at the transferrin interface. Full article

Boro-antimonite glasses doped with Eu³⁺ and having the general composition (90-x) Sb₂O₃–xB₂O₃–10Li₂O-0.5Eu₂O₃ (x = 0 to 60 in 10 mol. % increment) were prepared using the melt quenching method. The influence of B₂O₃/Sb₂O₃ substitution on the spectroscopy and photoluminescence of Eu³⁺ ions was analyzed by studying the measured and calculated properties of these glasses. The relative value of a given property was shown to increase or decrease by up to 26% with the addition of up to 60 mol. % B₂O₃, while the number of Eu³⁺ ions per unit volume increased by approximately 32%. Strong emissions were obtained in association with the transitions of Eu³⁺ (⁵D₀→⁷F_j, j = 1–4). A weak, broad emission centered at 450 nm was also detected. This emission is clearly linked to the glass composition. It originates from a potential presence of Eu²⁺ ions. This enhances ⁵D₀ level emission via charge transfer. The radiative and experimental lifetimes of the ⁵D₀ level increase linearly with B₂O₃ content. This results in high quantum efficiency (η) ranging from 74 to nearly 84%. Tunable chromaticity, as defined by the CIE 1931 standard, was achieved, resulting in a warm orange-red color with high brightness. These new glasses have a variety of potential laser-related applications. Full article

Next-generation therapeutic devices will rely on an intelligent integrated system that consolidates multiple functions into a single platform. These individual chemical components exhibit diverse physicochemical properties, demonstrating multifunctional characteristics. In this review, we focus on how the distinctive properties of upconversion nanoparticles (UCNPs), achieved via refined preparation methods, unlock novel functionalities in biomedical applications. Specifically, features such as near-infrared excitation, deep-tissue penetration, low autofluorescence, and tunable multicolor emission endow UCNPs with substantial potential in fields including deep-tissue imaging, targeted drug delivery, and photodynamic therapy. This article systematically reviews recent advances in the design and functionalization of UCNPs, elucidating their role in facilitating the development of integrated diagnostic and therapeutic platforms and fostering the establishment of intelligent responsive treatment systems. Finally, we address current technical challenges—including uniformity in large-scale production, long-term biosafety, and in vivo metabolic mechanisms—and provide insights into future interdisciplinary integration, clinical translation pathways, and their potential role in personalized medicine. Full article

We propose a strain-optimized design strategy for lattice-matched InAs_1−xSb_x/Al_1−yIn_ySb Type-I quantum wells (QWs) that emit across the near-to mid-infrared spectrum (2–5 µm). By combining elastic strain energy minimization with band offset calculations, we identify Type-I alignment for Sb contents (x ≤ 0.40) and In contents (0.10 < y ≤ 1). At the same time, Type-II dominates at higher Sb compositions (x ≥ 0.50). Using the transfer matrix method under the effective mass approximation, we demonstrate precise emission tuning via QW thickness (L_W) and compositional control, achieving a wavelength coverage of 2–5 µm with <5% strain-induced energy deviation. Our results provide a roadmap for high-efficiency infrared optoelectronic devices, addressing applications in sensing and communications technologies. Full article

Organic optoelectronic devices receive appreciable attention due to their low cost, ecology, mechanical flexibility, band-gap engineering, brightness, and solution process ability over a broad area. In this study, we designed and studied organic light-emitting diodes (OLEDs) consisting of an assembly of natural dyes, extracted from noble fir leaves (evergreen) and blue hydrangea flowers mixed with poly-methyl methacrylate (PMMA) as light emitters. We experimentally demonstrate the effective conversion of blue light emitted by an inorganic laser/photodiode into longer-wavelength red and green tunable photoluminescence due to the excitation of natural dye–PMMA nanostructures. UV-visible absorption and photoluminescence spectroscopy, ellipsometry, and Fourier transform infrared methods, together with optical microscopy, were performed for confirming and characterizing the properties of light-emitting diodes based on natural dyes. We highlighted the optical and physical properties of two different natural dyes and demonstrated how such characteristics can be exploited to make efficient LED devices. A strong pure red emission with a narrow full-width at half maximum (FWHM) of 23 nm in the noble fir dye–PMMA layer and a green emission with a FWHM of 45 nm in blue hydrangea dye–PMMA layer were observed. It was revealed that adding monolayer MoS₂ to the nanostructures can significantly enhance the photoluminescence of the natural dye due to a strong correlation between the emission bands of the inorganic–organic emitters and back mirror reflection of the excitation blue light from the monolayer. Based on the investigation of two natural dyes, we demonstrated viable pathways for scalable manufacturing of efficient hybrid OLEDs consisting of assembly of natural-dye polymers through low-cost, purely ecological, and convenient processes. Full article

Zn_1−xFe_xO nanocomposites (NCs) with varying Fe concentrations (x = 0, 0.1, 0.2, 0.3, and 0.4) were effectively prepared using the hydrothermal approach, and their morphology, structural, optical, and magnetic properties were systematically analyzed. XRD analysis confirmed Fe doping reduced crystallinity and crystallite size. TEM images of Zn_1−xFe_xO NCs exhibited smaller and more agglomerated nanostructures compared to the pure ZnO NPs. Raman and XPS analyses indicated increased lattice disorder, oxygen vacancies, and the coexistence of Fe²⁺/Fe³⁺ species. UV–Vis spectra showed enhanced visible light absorption and a tunable band gap, while PL results reflected defect-induced emission shifts and quenching, associated with zinc vacancies, interstitials, and oxygen-related defects. Magnetic measurements revealed a transition from diamagnetism to ferromagnetic-like behavior at room temperature for Fe content x ≥ 0.2, with magnetization strongly dependent on doping level. These results highlight Zn_1−xFe_xO for advanced optoelectronic and spintronic applications. Full article

Against the backdrop of China’s dual-carbon goals, traditional road transportation has relatively high carbon emissions and is in urgent need of a low-carbon transition. The intermittency of photovoltaic (PV) power generation and the stochastic nature of electric vehicle (EV) charging demand introduce significant uncertainty for PV-energy storage-charging systems in highway service areas. Existing approaches often struggle to balance economic efficiency and reliability. This study develops a min-max-min robust optimization model for a full-route PV-energy storage-charging system. A box uncertainty set is used to characterize uncertainties in PV output and EV load, and a tunable uncertainty parameter is introduced to regulate risk. The model is solved using a column-and-constraint generation (C&CG) algorithm that decomposes the problem into a master problem and a subproblem. Strong duality, combined with a big-M formulation, enables an alternating iterative solution between the master problem and the subproblem. Simulation results demonstrate that the proposed algorithm attains the optimal solution and, relative to deterministic optimization, achieves a desirable trade-off between economic performance and robustness. Full article

Agricultural biomass has potential as a renewable and versatile carbon feedstock for developing eco-friendly and biodegradable polymers capable of replacing conventional petrochemical plastics. To address the growing environmental concerns associated with plastic waste and carbon emissions, lignocellulosic residues, edible crop by-products, and algal biomass were utilized as sustainable raw materials. These biomasses provided carbohydrate-, lipid-, and lignin-rich fractions that were deconstructed through optimised physical, chemical, and enzymatic pretreatments to yield fermentable intermediates, such as reducing sugars, organic acids, and fatty acids. The intermediates were subsequently converted through tailored microbial fermentation processes into biopolymer precursors, primarily polyhydroxyalkanoates (PHAs) and lactate-based monomers. The resulting monomers underwent polymerization via polycondensation and ring-opening reactions to produce high-performance biodegradable plastics with tunable structural and mechanical properties. Additionally, the direct extraction and modification of naturally occurring polymers, such as starch, cellulose, and lignin, were explored to develop blended and functionalized bioplastic formulations. Comparative evaluation revealed that these biomass-derived polymers possess favourable physical strength, thermal stability, and biodegradability under composting conditions. Life-cycle evaluation further indicated a significant reduction in greenhouse gas emissions and improved carbon recycling compared to fossil-derived counterparts. The study demonstrates that integrating agricultural residues into bioplastic production not only enhances waste valorization and rural bioeconomy but also supports sustainable material innovation for packaging, farming, and consumer goods industries. These findings position agriculture-based biodegradable polymers as a critical component of circular bioeconomy strategies, contributing to reduced plastic pollution and improved environmental sustainability. Full article

This review summarizes recent advances (2023–2025) in coumarin-based fluorescent probes, highlighting their structural modularity, tunable VIS–NIR photophysics, and broad applicability in detecting metal ions, biothiols, ROS/RNS, organelle-specific microenvironments, and amyloid-β aggregates. Particular emphasis is placed on multifunctional and organelle-targeted probes, as well as emerging NIR-emissive and theranostic systems enabling deep-tissue imaging and modulation of pathological processes. The perspectives section outlines current limitations and future directions toward clinically relevant coumarin-based imaging tools. A though the review focuses on literature published from 2023 onward, several earlier studies are cited selectively to clarify fluorescence mechanisms, illustrate reaction pathways, or provide essential photophysical benchmarks necessary for contextual understanding. Full article

Monodisperse mesoporous hollow silica microcapsules present unique opportunities for advanced optical characterization due to their tunable nanostructure, high porosity and easy functionalization. A critical and challenging parameter in the optimization of these applications is the accurate determination of the effective refractive index, which governs light propagation and confinement within the nanostructured matrix of such mesoporous materials. In this study, individual mesoporous hollow silica microcapsules doped with Rhodamine B dye were analysed optically by exploiting whispering gallery mode (WGM) resonances, enabling non-destructive, single-particle refractometry with nanostructural sensitivity. Fourier Transform analysis of the fluorescence emission spectra revealed sharply defined, periodically spaced WGM peaks. For microcapsules with an 88 $\mu$m diameter, the measured intermodal spacing ($\Delta \lambda = 1.296$ nm) yielded an effective refractive index of 1.164. The measured value of the effective refractive index was cross-validated using Lorenz–Lorentz and Bruggeman effective medium models, both predicting porosity values (~63%) that closely match independent Brunauer–Emmett–Teller (BET) nitrogen adsorption measurements. The excellent agreement between optical and adsorption-based porosity demonstrates that WGM spectroscopy combined with Fourier analysis is a powerful, label-free, and non-invasive technique for correlating nanoscale porosity with macroscopic optical properties. This approach is widely applicable to single-particle analyses of nanostructured dielectric materials and opens new possibilities for in situ optical metrology in the development of advanced photonic, catalytic, and biomedical platforms. Full article

Magneto-photoluminescent hybrid materials (MPHMs) were prepared by incorporating cobalt ferrite nanoparticles (CFNs) into the fluorescent polymer poly(terephthalaldehyde-undecan-2-one) (PT2U). The CFNs, with a mean size of 3.95 nm, formed aggregates within the PT2U matrix (650–1042 nm) due to surface and interfacial interactions, modulating aggregate morphology and interparticle coupling. Magnetization studies revealed non-monotonic variations in saturation magnetization (30.3–16.2 emu/g), mean blocking temperature (39.3–43.1 K) and effective magnetic anisotropy energy density (2.14 × 10⁶–1.31 × 10⁶ erg/cm³) with increasing CFN content, consistent with the presence of canted surface spins and enhanced magnetizing interparticle interactions. Photoluminescence exhibited progressive quenching, dominated by collisional mechanisms at low CFN content and by interfacial CFN–PT2U interactions at higher loadings. Under a magnetic field (800 Oe), additional quenching occurred, attributed to magnetically induced polymer-chain rearrangements that disrupted the molecular stacking required for efficient aggregation-induced emission. These results demonstrate tunable magneto-photoluminescent coupling in MPHMs governed by surface and interfacial phenomena, providing insights for the design of functional and responsive hybrid materials. 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

Co-reactants are essential in co-reactant-based electrochemiluminescence (ECL) systems because they generate reactive intermediates that can oxidize or reduce ECL luminophores, thereby driving ECL emission. In the context of ECL, gold nanoclusters (Au NCs) have emerged as innovative luminophores, owing to their tunable electronic structures and excellent biocompatibility. However, their efficiency in ECL applications is often compromised by challenges such as limited excited-state generation and non-radiative losses. To tackle these practical challenges, advanced co-reactant engineering strategies have been developed to improve the performance of Au NCs in ECL systems. This review begins with a brief overview of the mechanisms of ECL. Subsequently, a systematic overview of various co-reactant engineering strategies is presented, including: (1) using innovative co-reactants to replace traditional ones due to their lower toxicity and better biocompatibility; (2) applying co-reaction accelerators to reduce the onset potential and improve the production of reactive intermediates from co-reactants; (3) combining co-reactants with luminophores or creating integrated nanostructure assemblies of co-reactants, co-reaction accelerators, and luminophores to achieve shorter electron transfer paths and reduced energy loss for stable high-intensity ECL emission; (4) utilizing host-guest strategies that encapsulate co-reactants within cavities to stabilize radical intermediates and minimize environmental quenching. This review provides a comprehensive overview of recent developments in co-reactant engineering for Au NCs-based ECL systems, thereby encouraging further exploration and understanding of these systems and expanding their potential applications. Full article

Two types of devices capable of switchable infrared spectral control are demonstrated by utilizing the phase-change characteristics of In₃SbTe₂ (Indium–Antimony–Tellurium, IST), which transitions from a low-loss dielectric amorphous phase to a high-loss metallic crystalline state. Through comprehensive structural design, theoretical calculation, simulation analysis, experimental measurement, and application demonstration, we realize distinct switching effects and functions of these two devices. In the first design, IST mono-layer thin films integrated with infrared-transparent substrates (KBr and ZnSe) enable switching between amorphous high transmittance and crystalline high reflectance states over the 2.5–15 μm range, suitable for infrared optical switches and stealth applications. In the second design, introducing a Si metasurface disk array atop the IST mono-layer thin film enables switching between broadband infrared transparency and narrowband high emissivity. This configuration allows independent spectral control of the infrared spectra within the non-atmospheric (5–8 μm) and atmospheric (8–14 μm) windows, providing a versatile platform for tunable thermal radiation management and adaptive infrared camouflage. Full article