Search Results (184)

Despite significant progress in photoelectrochemical (PEC) water splitting, high fabrication costs and limited efficiency of photoanodes hinder practical applications. Bismuth vanadate (BiVO₄), with its low cost, non-toxicity, and suitable band structure, is a promising photoanode material but suffers from poor charge transport, sluggish surface kinetics, and photocorrosion. In this study, porous monoclinic BiVO₄ films are fabricated via a simplified successive ionic layer adsorption and reaction (SILAR) method, followed by borate treatment and PEC deposition of NiFeO_x. The resulting B/BiVO₄/NiFeO_x photoanode exhibits a significantly enhanced photocurrent density of 2.45 mA cm⁻² at 1.23 V vs. RHE—5.3 times higher than pristine BiVO₄. It also achieves an ABPE of 0.77% and a charge transfer efficiency of 79.5%. These results demonstrate that dual surface modification via borate and NiFeO_x is a cost-effective strategy to improve BiVO₄-based PEC water splitting performance. This work provides a promising pathway for the scalable development of efficient and economically viable photoanodes for solar hydrogen production. 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

This work describes the synthesis, crystal structure, and hydrophobicity tests of four bismuth(III)– and silver(I)–bromide complexes using the triammonium cations diethylenetriaminonium (H₃DETA³⁺) and N,N,N′,N″,N‴-pentamethyldiethylenetriammonium (H₃PMDTA³⁺). The prepared compounds are the 0D perovskites (H₃DETA)[BiBr₆] (1), (H₃DETA)₂[AgBr₄]Br₃ (2), and (H₃PMDTA)[BiBr₆] (3), as well as the 1D/2D mixed perovskite with minimum formula (H₃PMDTA)[Ag₃Br₆] (4), being the last three novel materials. Compounds 1 and 3 crystallize in the orthorhombic P2₁2₁2₁ space group and are discrete [BiBr₆]³⁻ units with the cation surrounding them. In both compounds, the bismuth(III) metal ion is found in a distorted octahedral coordination geometry. Compound 2 crystallizes in the monoclinic P2₁/c space group, and it is a mixed salt consisting of (H₃DETA)[AgBr₄] and (H₃DETA)Br₃, whereas the silver(I) complexes are also isolated. Finally, compound 4, which crystallizes in the orthorhombic space group Pbcn, is a combination of a 2D and 1D silver–bromide perovskite, with the cations filling the voids. The 2D structure has the minimal formula [Ag₄Br₇]³⁻, with the 1D coordination polymer [Ag₂Br₅]³⁻ being both built up by a combination of bromide ions acting as tetrahedra corner and edge-sharing bridging ligands. The silver(I) in 2 and 4 is found in a tetrahedral coordination geometry. All compounds were deposited on pristine FTO glass, resulting in an increase in the contact angle from 22° to 44°, 36°, 62°, and 54° for films of 1, 2, 3, and 4, respectively. Compounds 1 and 3 were also deposited onto Cs₂AgBiBr₆ film, and the contact angles were observed to be the same as when deposited directly onto the FTO cover glass. 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

In recent years, dielectric films with a high energy-storage capacity have attracted significant attention due to their wide applications in the fields of renewable energy, electronic devices, and power systems. Their fundamental principle relies on the polarization and depolarization processes of dielectric materials under external electric fields to store and release electrical energy, featuring a high power density and high charge–discharge efficiency. In this study, sodium bismuth titanate (NBT) micro-flakes synthesized via a molten salt method were treated with hydrogen peroxide and subsequently blended with a polyvinylidene fluoride (PVDF) matrix. An oriented tape-casting process was utilized to fabricate a dielectric thin film with enhanced energy storage capacity under a weakened electric field. Experimental results demonstrated that the introduction of modified NBT micro-flakes facilitated the interfacial interactions between the ceramic fillers and polymer matrix. Additionally, chemical interactions between surface hydroxyl groups and fluorine atoms within PVDF promoted the phase transition from the α to the β phase. Consequently, the energy storage density of PVDF-NBT composite increased from 2.8 J cm⁻³ to 6.1 J cm⁻³, representing a 110% enhancement. This design strategy provides novel insights for material innovation and interfacial engineering, showcasing promising potential for next-generation power systems. 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

A kind of magnetoplasmonic resonators is numerically designed with hexagonally arrayed Au/bismuth iron garnet (BIG) bilayer nanodiscks on Au thin film layers. Multi-physics coupling calculation on their magnetoplasmonic resonance features suggest that there exists a strong resonant coupling between the surface plasmon excited by the hexagonal grating and the waveguide modes induced by Au-BIG-Au, which can significantly enhance the transverse magneto-optical Kerr effect. Interestingly, a new type of circular oscillating can be induced in the optical-transparent BIG layers as the thickness of BIG layers is between 2 nm and 22 nm. This circular oscillating exhibits a distinct thickness-dependent feature, which can be attributed to the near field interference of the excited localized plasmon resonance between the two interfaces formed by the middle BIG nanodiscs in the top Au nanodisks and the bottom Au thin film layers according to the simulation. These unique magnetoplasmonic features endow this kind of magnetoplasmonic resonators with a greatly enhanced refractive index sensing property, with a calculated figure of merit (FOM) value of up to 7527 RIU⁻¹. Full article

A composite (N-rGO@ppy) of N-doped reduced graphene oxide (N-rGO) coated with polypyrrole (ppy) particles was successfully synthesized. The incorporation of N-rGO significantly mitigates the aggregation of ppy synthesized in situ, and the doped N atoms improve the conductivity of graphene oxide (GO), thereby enhancing N-rGO@ppy’s redox properties. Firstly, a glassy carbon electrode (GCE) modified with N-rGO@ppy (N-rGO@ppy/GCE) was used in combination with a bismuth film and square-wave anodic stripping voltammetry (SWASV) for the simultaneous trace analysis of Pb²⁺ and Cd²⁺. N-rGO@ppy/GCE exhibited distinct stripping peaks for Pb²⁺ and Cd²⁺, with a linear range of 1 to 500 μg L⁻¹. The limits of detection (LODs) were found to be 0.080 μg L⁻¹ for Pb²⁺ and 0.029 μg L⁻¹ for Cd²⁺, both of which are significantly below the standards set by the World Health Organization (WHO). Subsequently, the same electrochemical sensing strategy was adapted to a more portable screen-printed electrode (SPE) to accommodate the demand for in situ detection. The performance of N-rGO@ppy/SPE for analyzing Pb²⁺ and Cd²⁺ in actual samples, such as drinking water, milk, and honey, showed results consistent with those obtained from conventional graphite furnace atomic absorption spectrometry (GFAAS). Full article

Bismuth telluride (Bi₂Te₃) has attracted significant attention due to its broadband ultrafast optical response and strong nonlinearity at high laser fluence in the field of optoelectronic materials. The objective of this work is to study the effect of Al doping on the structure, linear optical properties, and nonlinear optical absorption behavior of Bi₂Te₃ thin films. The amorphous Al-doped Bi₂Te₃ thin films with varying Al doping concentrations were prepared using magnetron co-sputtering. The structure and linear optical properties were characterized using X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, spectroscopic ellipsometry, and UV/Vis/NIR spectrophotometry. The third-order nonlinear optical absorption properties of Al: Bi₂Te₃ thin films were investigated using the open-aperture Z-scan system with a 100 fs laser pulse width at a wavelength of 800 nm and a repetition rate of 1 kHz. The results indicate that Al dopant reduces both the refractive index and extinction coefficient and induces a redshift in the optical bandgap. The optical properties of the films can be effectively modulated by varying the Al doping concentration. Compared with undoped Bi₂Te₃ thin films, Al-doped Bi₂Te₃ thin films exhibit larger nonlinear optical absorption coefficients and higher damage thresholds and maintaining high transmittance. These findings provide experimental evidence and a reliable approach for the further optimization and design of ultrafast nonlinear optical devices. Full article

This paper shows the fabrication of a new environmentally friendly sensor, an activated glassy carbon electrode with an in situ deposited bismuth film (aGCE/BiF), to determine Cd(II) and Pb(II) at the nanotrace level. The electrochemical activation of the GCE surface was achieved in a solution of 0.1 M phosphate-buffered saline (PBS) of pH = 7 by performing five cyclic voltammetric scans in the range of −1.5–2.5 V at ν of 100 mV/s. The newly developed electrode provides several advantages, such as an increased electron active surface (compared to the glassy carbon electrode) and improved electron transfer kinetics. As a result, the new voltammetric procedure (square-wave anodic stripping voltammetry, SWASV) was established and optimized. With the SWASV method, the following calibration curves and low detection limits (LODs) were obtained for Cd(II) and Pb(II), respectively: 5–100 nM, 0.62 nM, 2–200 nM, and 0.18 nM. The newly prepared method was used to determine the amounts of Pb(II) and Cd(II) in the certified reference material, and the results agreed with the certified values. Moreover, the procedure was successfully applied to determine the Cd(II) and Pb(II) in river samples. The official and standard addition methods validated the measurement results. Full article

Bismuth-based perovskite derivatives, (CH₃NH₃)₃Bi₂I₉ (MBI), are promising non-toxic light-absorbing materials widely used in various photoelectric devices because of their excellent stability. However, MBI-based perovskite solar cells (PSCs) are limited by poor film quality, and the performance of such a device is far behind that of lead-based PSCs. In this work, the crystal structure and morphological properties of MBI films were compared across different preparation methods. The two-step vapor-assisted method can prepare continuous dense MBI films because MBI crystal nucleation is induced by the BiI₃ seed layer. The MBI film grown by this method is better for the production of excellent PSCs compared to the film prepared by the solution method. The best photovoltaic device based on the MBI film could obtain a power conversion efficiency of 1.13%. An MBI device is stored in the glove box for 60 days, and the device’s performance is maintained at 99%. These results indicate that the vapor-assisted deposition of MBI films can be an effective method to improve the performance of bismuth-based planar PSCs. Full article

A novel low-carbon 9Cr-ODS steel was exposed to corrosion in lead–bismuth eutectic saturated with oxygen at 500 °C for 1000 h, leading to the formation of three distinct layers of oxide film. From the outermost to the innermost layer, these included a Fe₃O₄ layer infiltrated with Pb, a FeCr₂O₄ layer, and an inner oxide zone. The inner oxide zone was primarily composed of an unoxidized matrix and Cr₂O₃. The formation of the inner oxide zone was primarily attributed to the preferential oxidation of Cr following the infiltration of insufficient O content. Two distinct morphologies of the inner oxide zone were identified: one is porous, while the other is non-porous. The porous morphology is characterized by low Fe content and Pb infiltration. The loss of Fe is the main factor contributing to the development of the porous inner oxide zone and the infiltration of Pb, while the short-range diffusion of Cr promotes the growth of Cr₂O₃, resulting in a needle-like morphology. Full article

This article reports on the long-term use, solid bismuth microelectrode arrays for the first time. The presented working microelectrode is characterized by particular advantages compared to bismuth film electrodes and solid single bismuth microelectrodes; these advantages include environmentally friendly properties and the amplification of recorded currents, which are subsequently more resistant to interference. The proposed solid bismuth microelectrode array was applied to develop an adsorptive stripping voltammetric procedure for Sunset Yellow determination. The main experimental parameters were optimized. The calibration graph was linear from 5 × 10⁻⁹ to 1 × 10⁻⁷ mol L⁻¹ (time of accumulation, 60 s). The detection limit was equal to 1.7 × 10⁻⁹ mol L⁻¹. The relative standard deviation for a concentration of Sunset Yellow of 2 × 10⁻⁸ mol L⁻¹ was 4.1% (n = 7). Potential interference effects were examined. The presented analytical procedure was applied for the determination of Sunset Yellow in isotonic beverages and the results were confirmed by HPLC as a comparative method. The correctness of the presented procedure was also confirmed by satisfactory recovery values obtained during the analysis of spiked environmental water samples. Full article

Transparent X-ray shielding polymer films were developed by bulk photo copolymerization of in situ prepared bismuth carboxylate prepolymers with polymerizable exomethylene moieties and N,N-dimethylacrylamide (DMAA). The bismuth-containing prepolymers were prepared via the polycondensation of BiPh₃, 2-octenylsuccinic acid (OSA), and itaconic acid (IA) bearing an exomethylene group for polymerization. OSA was a chain extender by intermolecular condensation and a stopper by intramolecular cyclization to inhibit cross-linkage. The resulting photocured films exhibit high visible-light transparency and high n_D, reaching 1.57. The X-ray shielding ability increased with the bismuth content and reached an aluminum equivalent of 0.80. Full article

The monitoring of heavy metals in aquatic ecosystems is of critical importance due to the toxic effects that these elements can have on wildlife and the potential risks that they pose to human health. Rivers situated in close proximity to agricultural regions are particularly susceptible to contamination from a combination of natural and anthropogenic sources. The study of bioaccumulation is of great importance for the early detection of environmental stressors. The combination of electrochemical techniques, such as square-wave anodic stripping voltammetry (SWASV), with automated flow-batch systems represents an efficient and cost-effective approach for the detection of trace metals in environmental samples. This study examines the bioaccumulation of cadmium and lead in Cyprinus carpio, a bioindicator of contamination in the Colorado River, Argentina. The fish were exposed to sublethal metal concentrations for 24, 48, and 96 h. Metal quantification was conducted using a novel automatic flow-batch system with SWASV and a bismuth film electrode. To the best of our knowledge, this constitutes the first application of this methodology on aquatic bioindicators for the assessment of metal accumulation in a natural environment. The technique demonstrated enhanced sensitivity and selectivity for the detection of trace metals. The bioaccumulation results demonstrated an increase in cadmium and lead concentrations in fish liver tissue after 96 h, reaching 10.5 µg g⁻¹ and 11.9 µg g⁻¹, respectively. Validation with inductively coupled plasma–atomic emission spectrometry (ICP-AES) demonstrated a satisfactory correlation, confirming the reliability of the method. This novel electrochemical approach offers enhanced accuracy and efficiency, making it a promising tool for environmental monitoring. The results indicate that Colorado River water is within safe levels for aquatic life regarding these metals. However, continuous monitoring is recommended to detect changes in contamination levels and protect ecosystem health, especially during water crises and under climate change. Full article