Search Results (328)

Bismuth (Bi)-doped indium oxide (In₂O₃) has emerged as a promising thermoelectric material due to its tunable electrical and thermal properties. This study investigates the effects of Bi-doping on the thermoelectric performance of In₂O₃, focusing on its electrical conductivity, band structure, carrier concentration, mobility, Seebeck coefficient, power factor, thermal conductivity, and overall thermoelectric figure of merit (ZT). The incorporation of Bi into the In₂O₃ lattice significantly enhances the material’s electrical conductivity, attributed to the increased carrier concentration resulting from Bi acting as an effective dopant. However, this doping also leads to a broadening of the bandgap, which influences the electronic transport properties. The Seebeck coefficient (absolute value) is observed to decrease with Bi-doping, a consequence of the elevated carrier concentration. Despite this reduction, the overall power factor improves due to the substantial increase in electrical conductivity. Furthermore, Bi-doping effectively reduces both the total thermal conductivity and the lattice thermal conductivity of In₂O₃. This reduction is primarily due to enhanced phonon scattering caused by the introduction of Bi atoms, which disrupt the lattice periodicity and introduce point defects. The combined improvement in electrical conductivity and reduction in thermal conductivity results in a significant enhancement of the thermoelectric figure of merit (ZT) with highest ZT value increased from 0.055 to 0.402 at 973 K. The optimized Bi-doped In₂O₃ samples demonstrate a ZT value that surpasses that of undoped In₂O₃, highlighting the potential of Bi-doping for advancing thermoelectric applications. This work provides a comprehensive understanding of the underlying mechanisms governing the thermoelectric properties of Bi-doped In₂O₃ and offers valuable insights into the design of high-performance thermoelectric materials for energy conversion technologies. Full article

This work analyzes the radiation shielding effectiveness of biocompatible hydrogel pads containing carbohydrate-based polymer matrices (Alginate, Chitosan, and Cellulose) integrated with the high atomic number (Z) fillers Bismuth Oxide (Bi₂O₃) and Zinc Oxide (ZnO). The Monte Carlo-based toolkit, Geant4, was used to simulate the deposition of the dose throughout a multilayer phantom that mimics the skin (Epidermis, Dermis, Subcutaneous, and Muscle) with a pad on top irradiated with photon and electron beams from 50 keV to 1000 keV. The results indicated that Bi₂O₃ succeeded in causing greater absorption of photons at doses, particularly in deep-layer tissues, from the increase in the filler content as well as the pad thickness. The Cellulose–Bi₂O₃ composites (10 mm thick) not only showed the best deep-shielding property among all investigated combinations but also the Alginate-based pads generally performed better with regard to the surface dose attenuation. The results demonstrate the promising potential of high-Z-doped hydrogels in serving as flexible, light, and biocompatible shielding materials for superficial radiotherapy. Full article

A key issue with lead-cooled fast reactors is the corrosion vulnerability of fuel cladding and core components, which will endanger the structural materials’ integrity and the operational safety of the reactor system. The FeCrAlTi-ODS (Oxide Dispersion Strengthened) alloy coatings are prepared by the Magnetron Sputtering technique under different bias voltages to shield structural elements in lead-cooled fast reactors from corrosion caused by lead-bismuth eutectic (LBE). A comprehensive study examines their mechanical attributes and resistance to LBE-induced corrosion. Compared to the bare substrate of austenitic 316L steel, the FeCrAlTi-ODS alloy coatings exhibit significantly improved binding force and hardness. The hardness (H) reaches 11.52 GPa (twice that of the bare substrate), and the elastic modulus (E) reaches 172.89 GPa. After the corrosion of bare substrate 316L steel by LBE, the oxygen element penetrated was obvious, and the Nickel element underwent selective migration. The FeCrAlTi-ODS alloy coatings show promising LBE corrosion resistance, and the FeCrAlTi-ODS alloy coating prepared under different bias can effectively protect the substrate material, which is attributed to the formation of protective FeCr₂O₄ film on the surface. The compact oxide film significantly prevents the further infiltration of the oxygen element and the migration of metal elements. Full article

Water pollution caused by increasing industrial and human activity remains a serious environmental challenge, especially due to the persistence of organic contaminants in aquatic systems. Photocatalysis offers a promising and eco-friendly solution, but in the case of bismuth oxide (Bi₂O₃) there is still a limited understanding of how structural and morphological features influence photocatalytic performance. In this work, a straightforward hydrothermal synthesis method followed by controlled calcination was developed to produce phase-pure α- and β-Bi₂O₃ with tunable morphologies. By varying the hydrothermal temperature and reaction time, distinct structures were successfully obtained, including flower-like, broccoli-like, and fused morphologies. XRD analyses showed that the final crystal phase depends solely on the calcination temperature, with β-Bi₂O₃ forming at 350 °C and α-Bi₂O₃ at 500 °C. SEM and BET analyses confirmed that morphology and surface area are strongly influenced by the hydrothermal conditions, with the flower-like β-Bi₂O₃ exhibiting the highest surface area. UV–Vis spectroscopy revealed that β-Bi₂O₃ also has a lower bandgap than its α counterpart, making it more responsive to visible light. Photocatalytic tests using Rhodamine B showed that the flower-like β-Bi₂O₃ achieved the highest degradation efficiency (81% in 4 h). Kinetic analysis followed pseudo-first-order behavior, and radical scavenging experiments identified hydroxyl radicals, superoxide radicals, and holes as key active species. The catalyst also demonstrated excellent stability and reusability. Additionally, Methyl Orange (MO), a more stable and persistent azo dye, was selected as a second model pollutant. The flower-like β-Bi₂O₃ catalyst achieved 73% degradation of MO at pH = 7 and complete removal under acidic conditions (pH = 2) in less than 3 h. These findings underscore the importance of both phase and morphology in designing high-performance Bi₂O₃ photocatalysts for environmental remediation. Full article

Piezocatalytic therapy (PCT) is a promising strategy for combating implant-associated infections due to its high tissue penetration depth and non-invasive nature. However, its catalytic efficiency remains limited by inefficient electron–hole separation. In this work, an ultrasound-responsive heterojunction (BiOI/Ti₃C₂) was fabricated through in situ growth of bismuth iodide oxide on titanium carbide nanosheets. Subsequently, we integrated BiOI/Ti₃C₂ into poly(e-caprolactone) (PCL) scaffolds using selective laser sintering. The synergistic effect between BiOI and Ti₃C₂ significantly facilitated the redistribution of piezo-induced charges under ultrasound irradiation, effectively suppressing electron–hole recombination. Furthermore, abundant oxygen vacancies in BiOI/Ti₃C₂ provide more active sites for piezocatalytic reactions. Therefore, it enables ultrahigh reactive oxygen species (ROS) yields under ultrasound irradiation, achieving eradication rates of 98.87% for Escherichia coli (E. coli) and 98.51% for Staphylococcus aureus (S. aureus) within 10 minutes while maintaining cytocompatibility for potential tissue integration. This study provides a novel strategy for the utilization of ultrasound-responsive heterojunctions in efficient PCT therapy and bone regeneration. Full article

A strong interaction between Bi³⁺ and ZnO was used to successfully sensitize ZnO nanorods with quantum dots (QDs) of Bi₂O₃ through three different strategies. Although the Bi₂O₃ QDs had similar particle size distributions, their photocatalytic performance varied significantly, prompting the investigation of factors beyond particle size. The study revealed that the photochemical method selectively deposited Bi₂O₃ QDs onto electron-rich ZnO sites, providing a favorable pathway for efficient electron–hole separation and transfer. Consequently, abundant h⁺ and ·OH radicals were generated, which effectively degraded Rhodamine B (RhB). As demonstrated in the RhB degradation experiments, the Bi₂O₃/ZnO nanorod catalyst achieved an 89.3% degradation rate within 120 min, significantly outperforming catalysts with other morphologies. The photoluminescence (PL) and time-resolved photoluminescence (TRPL) results indicated that the Bi₂O₃/ZnO heterostructure constructed an effective interface to facilitate the spatial separation of photogenerated charge carriers, which effectively prolonged their lifetime. The electron paramagnetic resonance (EPR) results confirmed that the ·OH radicals played a key role in the degradation process. Full article

The efficient synthetic routes and evaluates cytotoxic profiles of denitroaristolochic acids II–V (DAA-II–V) were demonstrated in this study. Based on retrosynthetic analysis, a modular synthetic strategy was developed through Suzuki–Miyaura coupling, Wittig reaction, and bismuth triflate-catalyzed intramolecular Friedel–Crafts cyclization to efficiently construct the phenanthrene core. Process optimization significantly improved yields: aryl bromide intermediate A reached 50.8% yield via bromination refinement, while arylboronic ester intermediate B overcame selectivity limitations. Combining Darzens condensation with Wittig reaction enhanced throughput, achieving 88.4% yield in the key cyclization. Structures were confirmed by NMR and mass spectra. CCK-8 cytotoxicity assays in human renal proximal tubular epithelial cells revealed distinct toxicological profiles: DAA-III and DAA-IV exhibited IC₅₀ values of 371 μM and 515 μM, respectively, significantly higher than the nitro-containing prototype AA-I (270 μM), indicating that the absence of nitro group attenuates but does not eliminate toxicity, potentially via altered metabolic activation. DAA-II and DAA-V showed no detectable cytotoxicity within assay limits, suggesting reduced toxicological impact. Structure–activity analysis exhibited that the nitro group is not essential for cytotoxicity, with methoxy substituents exerting limited influence on potency. This challenges the conventional DNA adduct-dependent toxicity paradigm, implying alternative mechanisms like oxidative stress or mitochondrial dysfunction may mediate damage in denitro derivatives. These systematic findings provide new perspectives for AA analog research and a foundation for the rational use and safety assessment of Aristolochiaceae plants. Full article

Water pollution is a global problem that severely impacts human and environmental health, water recycling, and the economy. In Mexico, due to water scarcity, potable water contains significant amounts of heavy metals (i.e., arsenic (As)); thus, there is a need for efficient and sustainable water treatment strategies. Bismuth oxyhalides, BiOX (X = Cl, Br, I), exhibit three-dimensional (3D) porous structures suitable for efficient adsorption activity. In addition, bismuth is an abundant and biocompatible element appropriate for fabricating sustainable environmental remediation technologies, such as adsorptive BiOX nanomaterials (NMs). In this study, we examine the adsorption capacity of BiOX (X = Cl, I), BiOX-GO (GO: graphene oxide) and GO NMs to remove methylene blue (MB), methyl orange (MO) and arsenite (AsO₃³⁻) from aqueous solution. BiOCl-GO 10%, BiOI, BiOI-GO 1%, BiOI-GO 10% and GO have an enhanced adsorption capacity, removing MB (20 ppm) within one hour using a low dose of NMs (1 mg/mL). In addition, BiOX-GO NMs can be easily separated from the solution and regenerated upon visible light activation due to the photocatalytic activity of the materials. The efficiency of the NMs under study for MO removal decreases, with the GO material having the highest efficiency (96%), followed by BiOX-GO 10% (78%). BiOCl-GO 1% removes arsenic from aqueous solution at low doses and short treatment times; 5 mg As/g adsorbent takes five hours; however, at longer adsorption times (24 h), BiOI-GO 1% excels in its arsenic removal capacity. Perlite-supported BiOCl NMs exhibit a weak capacity for water treatment due to the poor mechanical strength of perlite and the amount of surface-exposed BiOCl material. For the photocatalytic removal of arsenic (oxidation–adsorption), BiOI-GO 1% excels in arsenic removal with efficiencies > 70%. Full article

Complex antimony pyrochlores Bi_2.7M_0.46Ni_0.70Sb₂O_10+Δ (M = Zn, Mg) were synthesized from oxide precursors, using the solid-state reaction method. For each composition variant, the pyrochlore phase formation process was studied during solid-state synthesis in the range of 500–1050 °C. The influence of zinc and magnesium on the phase formation process was established. The interaction of oxide precursors occurs at a temperature of 600 °C and higher, resulting in the formation of bismuth stibate (Bi₃SbO₇) as a binary impurity phase. Oxide precursors, including bismuth(III) and antimony(III,V) oxides, are fixed in the samples up to 750 °C, at which point the intermediate cubic phase Bi₃M_2/3Sb_7/3O₁₁ (sp. gr. Pn-3, M = Zn, Ni) is formed in the zinc system. Interacting with transition element oxides, it is transformed into pyrochlore. An intermediate phase with the Bi_4.66Ca_1.09VO_10.5 structure (sp. gr. Pnnm) was found in the magnesium system. The unit cell parameter of pyrochlore for two samples has a minimum value at 800 °C, which is associated with the onset of high-temperature synthesis of pyrochlore. The synthesis of phase-pure pyrochlores is confirmed by high-resolution Raman spectroscopy. The data interpretation showed that the cations in Ni/Zn pyrochlore are more likely to be incorporated into bismuth positions than in Ni/Mg pyrochlore. The nickel–magnesium pyrochlore is characterized by a low-porosity microstructure, with grain sizes of up to 3 μm, according to SEM data. Zinc oxide has a sintering effect on ceramics. Therefore, the grain size in ceramics is large and varies from 2 to 7 μm. Full article

Heterojunctions are commonly used in optoelectronic devices to improve device performance. However, interface defects and lattice mismatch often hinder carrier transport and reduce efficiency, emphasizing the need for further exploration of diverse heterojunction structures. In this study, a heterojunction device constructed from Bi₂O₃ and Ga₂O₃ is demonstrated. The microstructures and photoelectrical properties of Bi₂O₃ and Ga₂O₃ thin films were investigated. Bi₂O₃ and Ga₂O₃ thin films show a bandgap of 3.19 and 5.10 eV. The Bi₂O₃/Ga₂O₃ heterojunction-based device demonstrates rectification characteristics, with a rectification ratio of 2.72 × 10³ at ±4.5 V and an ON/OFF ratio of 1.07 × 10⁵ (4.5/−3.9 V). Additionally, we fabricated a sandwich-structured photodetector based on the Bi₂O₃/Ga₂O₃ heterojunction and investigated its ultraviolet photoresponse performance. The photodetector exhibits low dark current (0.34 pA @ −3.9 V) and fast response rise/fall time (<40/920 ms). This work offers important perspectives on the advancement of large-area, low-cost, and high-speed Bi₂O₃ film-based heterojunction photodetectors. Full article

Thin, dense and nanocrystal bismuth oxide films were prepared by the in situ plasma-assisted reactive evaporation (ARE) method using lead doping. Thin films were deposited at room temperature and at 500 °C temperature on glass and silicon substrates. X-ray diffraction, SEM, EDS, and optical measurements were applied to characterize these bismuth oxide films. The results showed that it is possible to synthesize the δ-Bi₂O₃ phase thin films at a temperature lower than 729 °C using an plasma-assisted reactive evaporation (ARE) method and stabilize it (to room temperature) using the additives of lead oxide. The influence of lead oxide concentration on phase formation was investigated. The optimal amount of lead oxide dopant was determined. An excess of lead oxide concentration forms PbO and δ-Bi₂O₃ mixture phases and nanorods appear in films. The synthesized δ-Bi₂O₃ phase was metastable; it transformed into the β-Bi₂O₃ phase after thermal impact during impedance measurements. The cross section of thin film sample shows the dense and monolithic structure. Optical measurements show that the optical band gap increases with increasing lead concentration. It was found that the highest total ionic conductivity of (Bi_1−xPb_0.26)₂O₃ is 0.165 S/cm at 1073 K temperature and activation energy is ΔE_tot = 0.5 eV. Full article

Thin films of bismuth(III) sulfide (Bi₂S₃) on fluorine doped tin oxide (FTO) coated glass slides were successfully formed by the chemical bath deposition (CBD) method. In this work, a new sulfur precursor L-cysteine was used instead of the typical sulfur precursors, such as urea, thiosulfate, or thioacetamide, used for the formation of the Bi₂S₃ films by the CBD method. The synthesized Bi₂S₃ thin film on the FTO substrate was subjected to characterization techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and UV–Visible spectroscopy analysis. An X-ray diffraction analysis showed that, initially, Bi₂S₃ films of an amorphous structure with elemental sulfur impurities were formed on the FTO surface. During the annealing of the samples, amorphous Bi₂S₃ was transformed into its crystalline phase with an average crystallite size of about 22.06 nm. The EDS studies confirmed that some of the sulfur that was not part of the Bi₂S₃ was removed from the films during annealing. The influence of the morphology of Bi₂S₃ films on their optical properties was confirmed by studies in the UV-visible range. Full article

This study employs simulation tools to design and evaluate lightweight, lead-free polymer composites incorporating polytetrafluoroethylene (PTFE), polyethylene (PE), and polyetherimide (PEI) for gamma radiation shielding in nuclear medicine. Targeting clinically relevant photon energies from Tc-99m (140 keV), I-131 (364 keV), and Cs-137 (662 keV), composites’ structural and shielding performance with Bi₂O₃ and WO₃ was assessed using XCOM and Phy-X/PSD. PEI emerged as the most suitable polymer for load-bearing and thermally exposed applications, offering superior mechanical stability and dimensional integrity. Bi₂O₃-WO₃ fillers for Tc-99m achieved a ~7000-fold increase in MAC, I-131 ~2063-fold, and Cs-137 ~1370-fold compared to PbO₂. The PEI-75Bi₂O₃-25WO₃ achieved a ~21-fold reduction in half-value layer (HVL) compared to lead for Tc-99m. For higher-energy isotopes of I-131 and Cs-137, HVL reductions of ~0.44-fold and ~0.08-fold, respectively, were achieved. The results demonstrate that high-Z dual filler polymer composites have an equal or enhanced attenuation properties to lead-based shielding, whilst also enhancing the polymer composites’ mechanical and thermal characteristics. As the use of ionizing radiation increases, so does the potential risks; high-Z dual filler polymer composites provide a sustainable, lightweight, non-toxic alternative to conventional lead shielding. Full article

Bismuth oxide (β-Bi₂O₃) is a promising visible-light-driven photocatalyst due to its narrow direct bandgap, but its practical application is hindered by rapid electron–hole recombination and limited surface active sites. This study demonstrates a sol-gel synthesis approach to tailor β-Bi₂O₃ nanoparticles through magnesium (Mg) doping, achieving remarkable enhancements in the photocatalytic degradation of organic pollutants and hydrogen evolution. The structural analysis through XRD, SEM, and EDX confirmed Mg-doping concentrations of 0.025 to 0.1 M led to crystallite size reduction from 79 nm to 13 nm, while the UV–Vis bandgap measurement showed it decreased from 3.8 eV to 3.08–3.3 eV. The photodegradation efficiency increased through Mg doping at a 0.1 M concentration, with the highest rate constant value of 0.0217 min⁻¹. The doping process led to VB potential reduction between 3.37 V (pristine) and 2.78–2.91 V across the doped samples when referenced to SCE. The photocatalytic performance of Mg_0.075Bi_1.925O₃ improved with its 3.2 V VB potential because the photoelectric band arrangement enhanced both light absorption and charge separation. The combination of modifications through Mg doping yielded an enhanced photocatalytic performance, which proves that magnesium doping is a pivotal approach to modifying β-Bi₂O₃ suitable for environmentally and energy-related applications. Full article

A new voltammetric sensor (BDDE/Nafion@Fe₃O₄/BiF) was fabricated by applying a nanocomposite drop of Fe₃O₄ magnetic nanoparticles in Nafion onto the polished boron-doped diamond electrode (BDDE) surface. Then, after drying (5 min at room temperature), the electrode was electrochemically modified with bismuth film (BiF) during in situ analysis. The Nafion@Fe₃O₄/BiF modification of the BDDE contributes to the acquisition of the highest differential-pulse adsorptive stripping voltammetric (DPAdSV) signals of caffeine (CAF) due to the improvement of electron transfer and the increase in the number of active sites on which CAF can be adsorbed. The DPAdSV signals exhibited a linearly varied oxidation peak with the CAF concentration range between 0.5 and 10,000 nM, leading to the 0.043 and 0.14 nM detection and quantification limits, respectively. The practical applicability of the DPAdSV procedure using the BDDE/Nafion@Fe₃O₄/BiF was positively confirmed with commercially available energy drinks. Full article