Nanomaterials

This study demonstrates the fabrication of high-performance p-Cu₂O/n-β-Ga₂O₃ heterojunction barrier Schottky (JBS) diodes using copper as a low-work-function anode metal. By optimizing the Cu₂O spacing to 4 μm, the device achieves a turn-on voltage of 0.78 V, a breakdown voltage of 1700 V, and a specific on-resistance of 5.91 mΩ·cm², yielding a power figure of merit of 0.49 GW/cm². The JBS diode also exhibits stable electrical characteristics across the temperature range of 300–425 K. Under a 200 V reverse stress for 5000 s, the JBS diode shows only a 4.16% degradation in turn-on voltage and a 1.15-fold increase in dynamic specific on-resistance variation, highlighting its excellent resistance to stress-induced degradation. These results indicate that Cu₂O/Ga₂O₃ JBS diodes are promising candidates for next-generation high-efficiency and high-voltage power electronic applications.

This study presents the synthesis and comprehensive characterization of tin dioxide nanoparticles (SnO₂NPs). SnO₂NPs were obtained using a conventional wet-chemistry route and an environmentally friendly green-chemistry approach employing plant extracts from rooibos leaves (Aspalathus linearis), pomegranate seeds (Punica granatum), and kiwifruit peels (family Actinidiaceae). The thermal stability and decomposition profiles were analyzed by thermogravimetric analysis (TGA), while their structural and physicochemical properties were investigated using X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), ultraviolet–visible (UV–Vis) spectroscopy, dynamic light scattering (DLS), Raman spectroscopy, and attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectroscopy. Transmission electron microscopy (TEM) confirmed the nanoscale morphology and uniformity of the obtained particles. The photocatalytic activity of SnO₂NPs was evaluated via the degradation of methyl orange (MeO) under UV irradiation, revealing that nanoparticles synthesized using rooibos extract exhibited the highest efficiency (68% degradation within 180 min). Furthermore, surface-enhanced Raman scattering (SERS) spectroscopy was employed to study the adsorption behavior of L-phenylalanine (L-Phe) on the SnO₂NP surface. To the best of our knowledge, this is the first report demonstrating the use of pure SnO₂ nanoparticles as SERS substrates for biologically active, low-symmetry molecules. The calculated enhancement factor (EF) reached up to two orders of magnitude (10²), comparable to other transition metal-based nanostructures. These findings highlight the potential of SnO₂NPs as multifunctional materials for biomedical and sensing applications, bridging nanotechnology and regenerative medicine.

Doping lead-free halide perovskite nanocrystals with trivalent lanthanide ions has emerged as a promising strategy for engineering their optical properties in various photonic applications. Here, we report the design and synthesis of a series of lead-free double halide perovskite (Cs₂Na(In/Y/Gd)Cl₆) nanocrystals co-doped with a pair of different lanthanides (e.g., Tb³⁺, Dy³⁺, and Eu³⁺) as emission centers, and ns² ions (Sb³⁺ or Bi³⁺) as sensitizers. The tunability of the delayed photoluminescence spectral density was achieved through the selective excitation of lanthanide dopants either via ligand-to-metal charge transfer (e.g., Eu³⁺) or via ns² ion s-p transitions (e.g., Dy³⁺ or Tb³⁺). The intensities of the narrow lanthanide f-f emission bands can, therefore, be tuned by modulating the excitation wavelength and/or dopant ratio, allowing for the accurate engineering of the emission color coordinates and spectral density. We also demonstrated time-resolved tuning of the photoluminescence spectral density for the investigated nanocrystal host lattices co-doped with transition-metal (Mn²⁺) and lanthanide ions, owing to a large difference between the decay dynamics for Mn²⁺ d-d and lanthanide f-f transitions. The rational co-doping of double halide perovskite nanocrystals reported in this work provides a new strategy for generating pre-designed multilevel luminescent signatures for protection against counterfeiting.