Synthesis Of Sb Research Articles

Reductive Segregation During the Synthesis of Sb−SnO2-Supported Iridium Electrocatalysts for the Oxygen Evolution Reaction

A metal-organic chemical deposition approach using an Ir(acac)3 precursor was employed to synthesise oxide−supported iridium-based electrocatalysts for the oxygen evolution reaction (OER) in acidic media. Inert and oxidising deposition conditions were explored in two temperature regimes, and the influence of these parameters on the physicochemical and electrochemical properties of catalysts consisting of IrOx supported on Sb–SnO2 (ATO) were studied. Surprisingly, it was found that increasing the deposition temperature up to 620 °C favoured the formation of reduced iridium phases even in the presence of an oxidising reaction environment. This was explained by a thermodynamic preference for reduced phases at high temperatures, as well as the presence of acetylacetonate ligand decomposition products serving as reducing agents. Similarly, the reductive segregation of Sb from the ATO support at high temperatures leads to the loss of conductivity of the support, and the formation of Ir–Sb–Sn alloyed nanoparticles. These processes resulted in a loss of OER performance for the materials prepared under high-temperature conditions. Our findings highlight the importance of carefully selecting the temperature range during the synthesis of oxidic support materials and electrocatalysts for the OER.

The heavy Carbene analogues SbH2 + and BiH2 +. Convergent quantum mechanical studies*

In 2021 Olaru, Mebs, and Beckmann reported the synthesis of remarkable cationic carbene analogues P R 2 + and As R 2 + . This work followed the same group's synthesis of Sb R 2 + and Bi R 2 + . To better understand these important systems, Sb H 2 + and Bi H 2 + have been studied with high level ab initio quantum mechanical methods. Geometries were optimised with the CCSDT(Q) method with the cc-pwCVTZ-PP basis set using small core pseudopotentials. Fundamental vibrational frequencies were computed to provide theoretical predictions for future synthetic studies. Relative energies with respect to P n + + H 2 ( Pn = Sb , Bi ) were determined at the CCSDT/CBS level of theory via the Focal Point Analysis method, and anharmonic zero-point vibrational energy and higher order contributions were also computed. For Sb H 2 + , we obtained R = 1.697 Å and θ = 90.8 ∘ with S b + + H 2 → Sb H 2 + reaction enthalpy of ΔH = − 18.71 kcal mol − 1 . For Bi H 2 + , the analogous results were R = 1.774 Å, θ = 89.7 ∘ , and ΔH = − 7.64 kcal mol − 1 for B i + + H 2 → Bi H 2 + .

Sb(V) Kaempferol and Quercetin Derivative Complexes: Synthesis, Characterization and Antileishmanial Activities.

Recent studies on Leishmaniasis treatment have confirmed the antiparasitic effects of flavonols and organic antimony pentavalent [(Sb(V)] complexes. This study aimed to identify new Sb(V) complexes by combining the benefits of antimonials and flavonols as well as by optimizing their properties. Kaempferol and quercetin peracetate were prepared using acetic anhydride in pyridine. By performing regioselective synthesis, 7-O-paramethylbenzyl as an electron-donating group and 7-O-paranitrobenzyl as an electron-withdrawing group were added to quercetin, and, then, the synthesis of Sb(V) kaempferol and quercetin derivative complexes were performed using SbCl5 solution in glacial acetic acid. The structures were confirmed by UV, ESI mass, IR, 1H-, and 13C-NMR spectral data, and the Stoichiometry of the ligand-metal complex by the mole ratio method. Computational molecular modeling was conducted using the Gaussian program. The structures were confirmed based on the results from UV, nuclear magnetic resonance (NMR), and electrospray ionization (ESI) mass analyses (3-12). Among the produced compounds, 11 and 12 as newly described, and other compounds as pre-defined compounds were identified. According to the results from biological test, kaempferol triacetate with more lipophilicity showed the highest anti-promastigote activity with an IC50 value of 14.93 ± 2.21 µM. As for anti-amastigote activity, despite the differences, all antimony complexes showed anti-amastigote effects in vitro with IC50 values of 0.52 to 14.50 µM. All flavonol Sb(V) complexes showed higher activity compared to meglumine antimonate in anti-amastigote effect. Inside the host macrophages, by breaking down the complex into antimony and quercetin or kaempferol analogs, the observed antiparasitic effects may have been related to both Sb(V)/Sb(III) conversion and flavonoid antileishmanial activities.

Synthesis of Sb(V) Complexes with Pyridyl Cations and Application for Lead-free Perovskite Solar Cells

Lead halide perovskite has emerged as a promising photovoltaic material due to its excellent power conversion efficiency (PCE). However, the toxicity problem of lead-based perovskite hampers the commercialization of perovskite solar cells. Here, we develop several Sb(V) complexes with pyridyl cations and serve as absorber layer for lead-free perovskite solar cells. The designed complexes were based on 4-tert-butylpyridine (tBP) and N-ethylpyridinium (N-EtPy) cations with bandgaps of 2.01 eV and 1.95 eV, which showed their potential for solar cells and optoelectronic applications. We also found a chemical rule for stable Sb complexes in terms of the bond connectivity of pnictogen-antimony. Initial studies produce a solar cell with a PCE of 0.9% and offer inspiration for further exploration of environment-friendly perovskite families.

Effect of Sodium Tartrate on Controllable Synthesis of Sb2Se3 Nanorods and Its Catalytic Hydrogenation Performance for 4-Nitrophenol

Effect of Sodium Tartrate on Controllable Synthesis of Sb₂Se₃ Nanorods and Its Catalytic Hydrogenation Performance for 4-Nitrophenol

Synthesis and conductive performance of antimony-doped tin oxide-coated TiO2 by the co-precipitation method

The synthesis of Sb–SnO2/TiO2 (SST) composites by assembling antimony-doped tin oxide (Sb–SnO2) nanoparticles on the surface of titanium dioxide (TiO2) is systematically investigated. X-ray diffraction data show that the SST composite materials with good crystallinity can be indexed as anatase TiO2 phase and cassiterite SnO2 phase. The scanning electron microscopy and transmission electron microscopy indicate that Sb–SnO2 particles with average diameter of 25 nm have been successfully coated on the surface of TiO2. In addition, the Ti–O–Sn band can be detected on the surface of TiO2 through Fourier translation infrared spectroscopy. The influences of pH, Sn/Ti mole ratio, hydrolysis temperature and calcination temperature on the electrical resistivity of the SST powders are studied. Under the optimum experimental conditions, the electrical resistivity of the composite conductive powders is 2.546 × 103 Ω cm. Therefore, the SST composite conductive powders are useful as conductive fillers for the application in antistatic materials.

Solvothermal synthesis and analysis of Bi1−xSbx nanoparticles

Abstract Bismuth–antimony alloy nanoparticles have been synthesized by a facile solvothermal method using N,N-dimethylformamide and ethylene glycol as solvent/reducing agent; BiCl 3 , SbCl 3 and Bi(NO 3 ) 3 as precursors; and citric acid as a surface modifier/stabilizing agent. The particle size and size distribution of Bi nanoparticles were analyzed as a function of the synthesis conditions: molar ratio of precursor to surfactant, precursor concentration and reducing agent. Synthesis of Sb and Bi 0.88 Sb 0.12 under similar conditions was also investigated. The phase purity of nanoparticles was confirmed from X-ray diffraction and thermogravimetry and the nanoparticle morphology was investigated by transmission electron microscopy. A case study of Bi nanoparticles with detailed analysis of the particle morphology and size distribution of the nanoparticles is reported.

Synthesis of Sb<SUB>2</SUB>E<SUB>3</SUB> (E = S, Se) Nanorods with a Flat Cross Section by a Rapid Hot Injection Method

We report herein a simple colloidal synthesis route, i.e., rapid injection of E (E = S, Se) source into a hot solvent (1-octadecence, ODE) containing antimony precursor (antimony stearate), to grow Sb2E3 nanorods. The as-prepared nanorods were extensively characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), and high-resolution transmission electron microscopy (HRTEM). The mechanism for growth of Sb2E3 nanorods was also clarified from the view of crystal structure-directed growth. We believe that the method present here is a more straightforward and cost-effective route to prepare Sb2E3 nanocrystals with high quality.

One-step synthesis of Sb2O3 broom-like belts with controllable morphology

A direct and simple surfactant- and template-free route has been developed for the controlled synthesis of Sb2O3 belt-like microstructures. By adjusting the reactant ratio between SbCl3 and urea under solvothermal reaction conditions, broom-like belts and rods of Sb2O3 have been successfully prepared. X-ray powder diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HR-TEM), and X-ray photoelectron spectroscopy (XPS) has been used to characterize the phases and morphologies of the as-prepared products. A possible formation mechanism is also discussed.Key words: antimony trioxide, solvothermal synthesis, broom-like belts.

Possible tellurites of antimony obtained by the precipitation reactions

The only work concerning the synthesis of Sb 2(TeO 3) 3·5H 2O by mixing aqueous solutions of equimolar quantities of SbCl 3 and Na 2TeO 3 is that of Boncheva-Mladenova and Schopova [1]. In order to prevent SbCl 3 from being hydrolyzed, the latter was dissolved in 4 N HCl. In that work, however, there are no data concerning the possibilities of the precipitation reactions to form tellurites of different composition.