Search Results (3,339)

The growth of MAPbBr₃ crystal-faced films is a critical challenge for advancing optoelectronic devices. This study presents a methodology for fabricating a (100) crystal-faced MAPbBr₃ film on a lattice-matched MgO/TiN composite substrate using a localized thermally driven inverse temperature crystallization technique. The metallic TiN buffer layer offers a 0.66% lattice mismatch to MAPbBr₃, minimizing interfacial strain. Furthermore, the orientation enhancement of the film induced by post-annealing was confirmed by X-ray diffraction, with the (200) peak FWHM decreasing from 0.042° to 0.028° and the intensity ratio of the (100) to (110) peaks increasing from 6.89 to 19.00. These structural improvements directly translate into enhanced optical performance. The annealed sample exhibited sharper Raman phonon modes at 49 cm⁻¹ and 151 cm⁻¹, a 1.8-fold photoluminescence intensity enhancement, and a 20.8% narrowing of the PL FWHM at 536 nm. Additionally, UV-Vis spectroscopy confirms the bandgap of MAPbBr₃, displaying a steeper absorption edge with a bandgap of 2.30 eV. These metrics provide compelling evidence of suppressed non-radiative recombination and improved optical homogeneity after annealing. By integrating TiN as an electron-transport and buffer layer to reduce strain and lattice mismatch, the MgO/TiN/MAPbBr₃ architecture offers a scalable, scientifically grounded pathway to improve MAPbBr₃’s optical performance. Full article

This study presents the design of a compact low-index-contrast structure capable of trapping electromagnetic waves within a highly confined region. The energy storage performance of the geometries was enhanced using a genetic algorithm that employed a binary (present/absent) assignment of insulating cylinders. Time-domain simulations performed with MEEP were experimentally validated using precisely positioned $\theta$-phase alumina rods, resulting in a 13 dB increase in receiver-antenna power within the microwave regime. The measurements showed a correlation exceeding 99% with the computational results over a dielectric constant range of 4.5 to 5.0. A quality factor of Q $=3.6\times {10}^3$ was measured at 5.08 GHz in the experiment. Subsequently, machine learning techniques were applied, further increasing the Q value to approximately ${10}^4$, even within such a small configuration. Furthermore, the proposed structure does not require a complete photonic bandgap; instead, relatively high-Q factors were achieved by suppressing radiation losses through a pattern of low-index dielectric rods. Full article

The escalating threat of antimicrobial resistance (AMR) and the environmental impact of industrial pollutants, particularly synthetic dyes, emphasize the pressing requirement for novel solutions. This study investigates the green synthesis of ZnO/Fe₂O₃ nanocomposites using Urtica dioica extract with the aim of achieving dual functionality as both antimicrobial agents and photocatalysts for pollutant degradation. The nanocomposites were synthesized with varying loads of Fe₂O₃ (5–50%) and characterized using X-ray diffraction (XRD) and diffuse reflectance spectroscopy (DRS). XRD analysis confirmed the presence of both the hexagonal wurtzite ZnO phase and the α-Fe₂O₃ hematite phase in all the composites, while DRS analysis revealed that the bandgap energy decreased progressively (from 1.89 to 1.72 eV) as the Fe₂O₃ content increased. The photocatalytic efficiency of the composites was evaluated by degrading methylene blue (MB), Congo Red (CR) and safranin O (SO) dyes under visible light. This demonstrated that the degradation performance depends on the composition, with the best activity being observed at 5% Fe₂O₃. Antioxidant activity was assessed using a DPPH• free radical scavenging assay. This showed that Urtica dioica extract exhibits superior radical scavenging capacity (maximum inhibition of 38%) compared to ZnO/Fe₂O₃ nanoparticles (maximum inhibition of 18%). The antibacterial efficacy against Pseudomonas aeruginosa was evaluated using direct confrontation and disk diffusion methods. This revealed that the activity was dose- and light-dependent, with enhanced performance under light exposure (10 mm inhibition zone) compared to dark conditions (1 mm). This study demonstrates the successful green synthesis of biphasic ZnO/Fe₂O₃ nanocomposites with promising photocatalytic and antimicrobial properties. While the results suggest possible synergistic interactions between the oxides, the underlying mechanisms, including potential charge transfer effects, require further investigation using advanced characterization techniques. Using Urtica dioica extract as a biogenic source provides a promising eco-friendly approach to synthesizing nanomaterials, with potential applications in wastewater treatment and the biomedical field. Full article

Lead-free double perovskites possess the capabilities of wide bandgap control, excellent photoelectric performance, and environmental friendliness. They are an ideal alternative system for addressing the heavy metal toxicity of lead-based perovskites and promoting their large-scale application. Precise control of their bandgap is key to the green transformation of optoelectronic devices. Bandgap, as a key parameter determining the photoelectric properties of materials, has limitations in traditional experimental determination and DFT calculation methods, such as being time consuming, labour intensive, costly, and difficult to achieve high-throughput screening. Deep learning provides an efficient solution to this problem, but current research has issues such as a single-model architecture and poor interpretability, which cannot effectively support bandgap regulation. This study utilised 2367 valid datasets of lead-free double perovskites sourced from the Materials Project database and relevant literature. Following preprocessing steps, including MinMaxScaler normalisation and Pearson correlation coefficient screening, the dataset was divided into a ratio of 7:1:2. The bandgap prediction capabilities of four models—MLP, deep ensemble learning, PINN, and Transformer—were systematically compared, with feature importance analysed using the SHAP method. The results show that the MLP model performs the best in medium-scale, structured feature prediction. The R² value of the test set is 0.9311, while the MAE, MSE, and RMSE are 0.1915 eV, 0.0975 eV², and 0.3122 eV, respectively. A total of 98% of the test samples have a prediction error of ≤0.4 eV, highlighting the stability of low bandgap systems. The Transformer is more suitable for large-scale, sequential feature prediction, while the MLP has limited generalisation ability for medium-to-high bandgap systems containing elements such as Si and Mg. The SHAP analysis revealed that the five electronic structure descriptors, such as B_HOMO+ and A_LUMO+, are the key influencing factors of the bandgap. The research results are helpful for the high-precision prediction and mechanism explanation of the bandgap of lead-free double perovskites, providing theoretical support for rational material design, performance optimisation, and bandgap-oriented regulation. They also point out the direction for subsequent model improvement. Full article

Wide bandgap (WBG) semiconductors such as gallium nitride (GaN) and silicon carbide (SiC) have revolutionized modern power electronics by enabling devices that operate at higher voltages, temperatures, and switching frequencies than their silicon counterparts. This paper reviews the material properties, device architectures, fabrication techniques, and thermal management strategies that underpin the performance of GaN and SiC technologies. We highlight key trade-offs between GaN and SiC in terms of voltage blocking capability, switching efficiency, and thermal robustness and discussed their application in electric vehicles, renewable energy systems, and power converters. Market adoption trends and manufacturing challenges are also analyzed, with attention to cost-performance dynamics and packaging innovations. Finally, we address the critical role of thermal boundary resistance and emerging reliability solutions, providing a perspective on the future trajectory of WBG device research and commercialization. Full article

CsPbBr₃ perovskite quantum dots (QDs) have attracted significant attention for optoelectronic applications owing to their outstanding optical properties, yet achieving controlled synthesis with high stability under mild conditions remains a challenge. The room-temperature synthesis of CsPbBr₃ perovskite quantum dots using a coprecipitation method is systematically investigated in this work, with an emphasis on how the structural and optical properties of the QDs are influenced by the Br/Pb ratio and OA/OAm ratio. The findings show that controlling the Br/Pb and OA/OAm ratios can effectively influence the size, crystalline phase, and surface passivation properties of CsPbBr₃ quantum dots. The photoluminescence peak shifts blue and the bandgap widens when the Br/Pb ratio rises due to a decrease in quantum dot size. This is mainly explained by more effective surface covering by Br⁻ ions and increased quantum confinement effects. The resultant quantum dots demonstrate ideal optical performance at a Br/Pb ratio of 75 and an OA/OAm ratio of 1.5, with dense ligand coverage, superior defect passivation, and markedly improved stability under UV irradiation and in aqueous environments. Variations in the Br/Pb and OA/OAm ratios affect the binding configuration and coverage of ligands on the quantum dot surface, thereby influencing the relationship between non-radiative recombination and the quantum confinement effect. The LED fabricated with the as-synthesized high-performance quantum dots demonstrates a wide color gamut, covering 129.45% of the NTSC standard, indicating strong potential for display applications. Full article

Hafnium oxide (HfO₂) is predominantly used as a high-index material in multi-layer dielectric coatings for high-peak- and high-average-power lasers, but laser damage often initiates within the HfO₂ layers despite their wide bandgap. Oxygen deficiency during deposition can introduce vacancy-related sub-bandgap states and absorptive defects, lowering damage resistance. This study investigates how oxygen flow during HfO₂ deposition with ion beam sputtering (IBS) affects its stoichiometry, defect formation, and nanosecond laser-induced damage threshold (LIDT) and whether single-layer trends predict multilayer performance. Single layers were deposited at varying oxygen flows, characterized for optical and structural properties, and tested for the LIDT at 1064 nm and 355 nm. Increasing oxygen flow drove the layer toward near-stoichiometric HfO₂, reduced the refractive index, and altered the density of surface pinhole-like features. The single-layer LIDT at 355 nm increased with oxygen, whereas the 1064 nm LIDT was comparatively less sensitive to oxygen flow, consistent with the wavelength-dependent roles of absorptive precursors and microstructural defects. In contrast, a HfO₂-based high-reflector (HR) showed a higher LIDT at lower oxygen flow, indicating that the family of damage precursors changes between single layers and multilayers; in stacks, structural properties such as stress, gas entrapment and thermal dissipation may outweigh the isolated absorptive defects found in single layers. These results demonstrate that the optimal oxygen flow condition depends on both LIDT wavelength and film architecture. We identified, for single layers, a 15–35 sccm window for maximizing the 1064 nm LIDT and a high-flow optimum (45 sccm) for the 355 nm LIDT and, for 355 nm HR stacks, a distinct lower-flow regime (~10 sccm). Full article

Three cerium-based metal–organic frameworks (MOFs), Ce-BDC, Ce-BDC-NH₂, and Ce-BTC, were used as catalysts for the hydroxylation of several organic compounds, including those not relevant to environmental or biological systems. Structural characteristics were validated by FT-IR spectroscopy, while SEM imaging demonstrated rod-like morphologies of 100–200 nm in width for Ce-BDC-NH₂ and 50–100 nm for Ce-BTC. The optical properties, ascertained using diffuse reflectance spectra and Tauc analysis, revealed bandgaps of 3.0 eV, 2.9 eV, and 3.6 eV for Ce-BDC, Ce-BDC-NH₂, and Ce-BTC, respectively. Catalytic investigations revealed that Ce-MOFs effectively convert phenol into 1,4-dihydroxybenzene with an efficiency of 86–99%, as confirmed by UV–Vis spectroscopy and HPLC analysis using an authentic hydroquinone (1,4-dihydroxybenzene) standard. The Ce-MOFs efficiently oxidize the dyes methylene blue (MB) and Congo red (CR) and also promote the hydroxylation of L-tyrosine, indicating their relevance to biologically significant substrates. The high catalytic performance of Ce-MOF highlights the potential of Ce-based materials for environmental remediation, chemical transformation, and sustainable wastewater treatment. Full article

The 100 GHz-class ultrafast photonic integrated circuit (PIC) positions itself as a promising technology in the post-Moore era, when the bandwidth limit of metallic interconnections constrains current electronic integrated circuits. Nevertheless, the lack of an effective on-chip, CMOS-compatible laser source challenges the ongoing development of PIC. Germanium straintronics facilitate bandgap transformation from indirect to direct, thereby enabling effective band-to-band radiative recombination. Some parameters, such as nanowire diameters or crystalline orientation and strain direction, have a profound effect on the bandgap transformation of Ge nanowires. In this review, we will discuss changes in the fundamental physical properties of Ge nanowires under strain, including mechanical, electronic, optical, and thermal properties. Subsequently, we summarize common methods for strain engineering, as well as novel approaches that have emerged in recent years. Some notable application cases reported in the last few decades will be discussed in detail. This review may fill knowledge gaps and provide a solid background for forthcoming investigations of on-chip strained Ge lasers. Full article

Zinc titanate (ZnTiO₃) is a chemically stable and non-toxic oxide perovskite whose photovoltaic potential remains largely unexplored due to its wide indirect bandgap. This study evaluates whether oxygen-vacancy (F-center) engineering can tailor its electronic structure and improve its suitability as a photovoltaic absorber. Density Functional Theory (DFT) calculations using VASP (PAW − GGA/PBE + U) were performed to evaluate structural stability, electronic properties, and electron affinity, while optical absorption was modeled through a combined Tauc–Gaussian approach. Device performance was assessed via SCAPS-1D simulations in an FTO/ZnO/ZnTiO₃/Spiro-OMeTAD architecture. Oxygen vacancies induce bandgap narrowing from ~2.96 eV to ~1.47 eV and generate Ti-3d-dominated donor-like and deep intragap states. The calculated electron affinity is ~3.77 eV. Simulated single-layer devices reach Voc ≈ 1.11 V, Jsc ≈ 8.27 mA·cm⁻², FF ≈ 83%, and a maximum efficiency of ~7.65%, primarily limited by moderate absorption strength and defect-assisted recombination. Multilayer configurations indicate that geometric optimization can significantly enhance projected efficiency, approaching 19.25% under idealized conditions. Although vacancy engineering extends visible-light absorption, the intrinsic indirect band-gap character constrains the ultimate photovoltaic performance of ZnTiO₃. Full article

A synergistic and magnetically recoverable NiFe₂O₄–MWCNT–CA nanocomposite was developed for efficient UV-driven photodegradation of hazardous organic pollutants. Biogenic NiFe₂O₄ nanoparticles synthesized using Costus speciosus extract exhibited a crystallite size of 32.5 nm, which increased to 83.6 nm upon incorporation into the MWCNT–cellulose acetate matrix. XRD confirmed the preservation of the cubic spinel structure, while VSM analysis showed maintained ferrimagnetic behavior with a saturation magnetization of 9.64 emu/g, enabling rapid magnetic separation. Although BET analysis revealed a reduction in surface area from 112.46 to 30.99 m²/g due to hybridization, the conductive MWCNT network significantly enhanced charge separation and interfacial electron transport. The composite displayed a widened optical bandgap of 5.3 eV, necessitating UV excitation for photocatalytic activity. Under UV irradiation, it achieved rapid degradation of methylene blue (97%) and Congo red (91%) at 20 mg/L, with corresponding rate constants of 0.119 and 0.076 min⁻¹. Scavenger experiments confirmed hydroxyl radicals (•OH) as the dominant reactive species, followed by photogenerated holes (h⁺). These results demonstrate a robust and synergistically engineered photocatalyst with high efficiency in removing organic pollutants under UV illumination. Full article

Perovskite oxide photoanodes are attractive for alkaline water oxidation but are commonly limited by interfacial recombination and sluggish charge transfer. Here we enhance anisotropic SrTiO₃ (STO) photoelectrodes via Al doping by simple yet effective one-step hydrothermal method and identify an optimal composition at 4% Al. In 0.1 M NaOH (pH 13) under simulated AM 1.5G illumination, 4% Al:STO exhibits 2 times enhancement in photocurrent density and 80% increase in electrochemically active surface area compared with the pristine SrTiO₃, as evidenced by the reduced charge-transfer resistance and enlarged light–dark photocurrent gap. together with a markedly reduced interfacial impedance, indicating accelerated charge extraction and transfer. Band-structure analysis shows a positive shift in flat-band potential and slight band-gap narrowing after Al doping, providing more favorable carrier energetics. Steady-state and time-resolved photoluminescence further demonstrate strong PL quenching and a prolonged carrier lifetime for 4% Al:STO. ECSA analysis suggests increased electrochemically accessible surface sites at the optimal doping level. Overall, moderate Al doping synergistically tunes defects, band energetics, and interfacial kinetics to improve STO photoanodes for solar water splitting. Full article

A novel catalyst, Tm₂FeSbO₇, was synthesized by employing the solid-phase high-temperature sintering method, and, for the first time, it was utilized to create a Z-type heterojunction with BiYO₃. A direct Z-scheme Tm₂FeSbO₇/BiYO₃ heterojunction photocatalyst (TBHP) was successfully produced by employing the ball-milling technique. X-ray diffraction analysis results indicated that Tm₂FeSbO₇ crystallized in a cubic pyrochlorestructure which owned the Fd-3m space group, with a unit cell parameter of 10.1769 Å, whereas BiYO₃ displayed a fluorite structure in the Fm-3m space group, with a unit cell parameter of 5.4222 Å. The Mossbauer spectrum of Tm₂FeSbO₇ showed that Fe³⁺ ions might locate at octahedral sites. The measured bandgap widths for the TBHP, Tm₂FeSbO_7, and BiYO₃ were 2.14 eV, 2.21 eV, and 2.30 eV, respectively. Multiple experimental results demonstrated that the TBHP exhibited a higher valence band ionization potential, a narrower band gap width, and a higher removal efficiency of the sulfamethoxazole (SMX) compared with the Dy₂TmSbO₇/BiHoO₃ heterojunction photocatalyst. Under visible-light irradiation (VISLI) of 115 min, the TBHP showcased exceptional photocatalytic elimination performance; therefore, the elimination rate of the SMX and the total organic carbon (TOC) mineralization rate reached 99.51% and 98.10%, respectively. In contrast to single-component Tm₂FeSbO₇, BiYO_3, or conventional nitrogen-doped titanium dioxide (N-TiO₂) catalyst, the TBHP exhibited removal efficiency enhancement for degrading the SMX by 1.17 times, 1.31 times, or 4.06 times. Simultaneously, the matching mineralization rate for removing the TOC density by employing the TBHP was 1.20 times, 1.34 times, or 4.73 times higher than that by employing Tm₂FeSbO₇, BiYO₃, or conventional N-TiO₂. Above experimental results indicated that the mineralization efficiency for removing TOC density by employing the TBHP was higher than that by employing Tm₂FeSbO₇, BiYO₃, or N-TiO₂. Radicals trapping experiments and the electron paramagnetic resonance spectroscopy results revealed that hydroxyl radicals, superoxide anions, and photoinduced holes were the primary active species during the catalytic elimination course of the SMX by employing the TBHP under VISLI. The results demonstrated that the direct Z-scheme TBHP, which was developed in this study, exhibited the maximal removal efficiency for degrading the SMX in contrast to Tm₂FeSbO₇, BiYO₃, or N-TiO₂. Additionally, the possible elimination routes and elimination mechanisms of the SMX were proposed. Therefore, an important scientific foundation for developing high-performance heterojunction catalysts was established. Full article

Contamination of water bodies caused by increasing human and industrial activities poses a serious threat to human health and environmental sustainability, highlighting the need for green and efficient remediation strategies. In this study, a facile hydrothermal synthesis followed by controlled calcination was developed to fabricate phase-pure α- and β-Bi₂O₃ with a unique coral-like hierarchical morphology as visible-light-active photocatalysts. Phase selectivity was achieved by tuning the calcination temperature, yielding pure β-Bi₂O₃ while preserving the hierarchical structure. Optical characterization revealed a narrower bandgap for β-Bi₂O₃ (2.24 eV) compared to α-Bi₂O₃ (2.75 eV), favoring visible-light absorption. Photocatalytic performance was evaluated using Rhodamine B as a model pollutant, where β-Bi₂O₃ achieved complete degradation within 240 min, significantly outperforming α-Bi₂O₃. The degradation followed pseudo-first-order kinetics, and the catalyst exhibited excellent robustness and reusability. To further demonstrate applicability toward persistent contaminants, Methyl Orange (MO) and the antibiotic ciprofloxacin (CIP) were employed as additional model pollutants. The coral-like β-Bi₂O₃ showed high visible-light activity toward MO, including complete removal under acidic conditions. Moreover, efficient degradation of CIP was achieved at neutral pH, with 90% removal within 150 min and complete degradation after 240 min. Overall, these results highlight coral-like β-Bi₂O₃ as an efficient standalone photocatalyst for visible-light-driven degradation of dye and pharmaceutical pollutants. Full article

Silicon carbide (SiC) is the leading wide bandgap semiconductor for high-power and high-temperature electronics, but the high defect density still limits device performance. This study investigates how inclusions, Basal Plane Dislocations (BPDs), and Threading Screw Dislocations (TSDs) in 4H-SiC substrates affect epitaxial defect formation. Twenty 200 mm SiC wafers were analyzed after epitaxial growth in two industrial Chemical Vapor Deposition (CVD) reactors, one using Trichlorosilane/Ethylene (Reactor A) and the other Silane/Propane (Reactor B). Defects were characterized using Candela (KLA), Altair (KLA), XRTmicron LAB (Rigaku), SICA (Lasertec), and Crossbeam (ZEISS) dual-beam SEM system. Statistical correlation showed that the conversion rate of embedded particles decreases with particle depth and increases with particle size. Reactor A exhibited lower propagation rates, indicating better suppression of substrate-related defects. SEM/FIB-EDX analyses suggested that carbon inclusions generate pits while metallic inclusions induce triangular defects. Dislocation analysis confirmed a strong correlation between TSDs and BPDs with carrots and triangular defects. BPD conversion rates were estimated at about 98.3% (Reactor A) and 99.8% (Reactor B). These results emphasize the importance of substrate quality and buffer layer optimization to minimize defect propagation. Full article