Strong texture tuning along different crystalline directions in glass-supported CeO2 thin films by ultrasonic spray pyrolysis.

The strong facet-dependent performance of glass-supported CeO2 thin films in different applications (catalysis, smart windows, etc.) has been the target of diverse fundamental and technological approaches. However, the design of accurate, cost-effective and scalable methods with the potential for large-area coverage that produce highly textured glass-supported CeO2 thin films remains a technological challenge. In the present work, it is demonstrated that under proper tuning conditions, the ultrasonic spray pyrolysis technique enables one to obtain glass-supported polycrystalline CeO2 films with noticeable texture along both the (100) and (111) directions, as well as with randomly oriented crystallites (no texture). The influence of flow rates, solution molarity, and substrate temperature on the texture and morphological characteristics, as well as optical absorption and Raman response of the deposited films, is evaluated. The obtained results are discussed on the basis of the combined dependence of the CeO2-exposed surfaces on the thermodynamic stability of the corresponding facets and the reaction kinetics, which modulate the crystallite growth direction.

Bismuth Oxide Nanoparticles Partially Substituted with EuIII, MnIV, and SiIV: Structural, Spectroscopic, and Optical Findings.

Interest in nanostructured partially substituted bismuth oxides has been increasing over the last years. Research on new synthesis methods, properties, and possible uses for these oxides is needed. The objective of this paper is to synthesize ß-Bi2O3, ß-Bi2O3:Eu3+, ß-Bi2O3:Mn4+, Bi12Bi0.8O19.2, Bi12Bi0.8O19.2/Li+, Bi12MnO20, and Bi12SiO20 nanoparticles and to investigate their structural, spectroscopic, and optical changes. Some of the causes that generated their properties are also discussed. These materials are important because the doping or partial substitution of bismuth oxide with these cations (Eu3+, Mn4+, and Si4+) modifies some properties such as optical absorption, reactivity toward CO2, among others. X-ray diffraction (in powders), high-resolution transmission electron microscopy, Fourier transform infrared (FTIR), resonance Raman scattering, diffuse reflectance, and solid-state magic-angle-spinning 29Si NMR were used for the characterization of the synthesized materials. We found that partial substitution of yellow Bi12Bi0.8O19.2 with Mn4+ and Si4+ changed the color to green and whitish, respectively. New bands in the Raman scattering and FTIR spectra of these oxides are deeply discussed. Raman scattering spectroscopy was a valuable and reliable technique to detect the Eu3+ and Mn4+ cations as dopants in the bismuth oxides. The 29Si chemical shift (δ) in Bi12SiO20 was -78.16 ppm, whereas in SiO2, it was around -110 ppm. This considerable shift in Bi12SiO20 occurred because of an increased shielding of the Si nucleus in the Si(O)4 tetrahedron. This shielding was provided by the low-electronegativity and highly polarizable Bi cations. The isovalent doping of ß-Bi2O3 nanoparticles with Eu3+ enhanced their thermal stability over 400 °C. Variation in the optical absorption and reactivity toward the acidic CO2 molecule of the partially substituted bismuth oxides was explained on the basis of the optical basicity and ionic-covalent parameter concepts. Some possible uses for the synthesized oxides are suggested.

Easy synthesis of high-purity BiFeO3 nanoparticles: new insights derived from the structural, optical, and magnetic characterization.

Synthesis of high-purity BiFeO3 is very important for practical applications. This task has been very challenging for the scientific community because nonstoichiometric Bi(x)Fe(y)O(z) species typically appear as byproducts in most of the synthesis routes. In the present work, we outline the synthesis of BiFeO3 nanostructures by a combustion reaction, employing tartaric acid or glycine as promoter. When glycine is used, a porous BiFeO3 network composed of tightly assembled and sintered nanocrystallites is obtained. The origin of high purity BiFeO3 nanomaterial as well as the formation of other byproducts is explained on the basis of metal-ligand interactions. Structural, morphological, and optical analysis of the intermediate that preceded the formation of porous BiFeO3 structures was accomplished. The thorough characterization of BiFeO3 nanoparticles (NPs) included powder X-ray diffraction (XRD); scanning electron microscopy (SEM) and high resolution transmission electron microscopy (HRTEM); thermogravimetric analysis (TGA); UV-vis electronic absorption (diffuse reflectance mode), Raman scattering, Mössbauer, and electron paramagnetic resonance (EPR) spectroscopies; and vibrating sample magnetometry (VSM). The byproducts like ß-Bi2O3 and 5 nm Bi2Fe4O9 NPs were obtained when tartaric acid was the promoter. However, no such byproducts were formed using glycine in the synthesis process. The average sizes of the crystallites for BiFeO3 were 26 and 23 nm, for tartaric acid and glycine promoters, respectively. Two band gap energies, 2.27 and 1.66 eV, were found for BiFeO3 synthesized with tartaric acid, obtained from Tauc's plots. A remarkable selective enhancement in the intensity of the BiFeO3 A1 mode, as a consequence of the resonance Raman effect, was observed and discussed for the first time in this work. For glycine-promoted BiFeO3 nanostructures, the measured magnetization (M) value at 20,000 Oe (0.64 emu g(-1)) was ∼5 times lower than that obtained using tartaric acid. The difference between the M values has been associated with the different morphologies of the BiFeO3 nanostructures.

Bismuth oxide aqueous colloidal nanoparticles inhibit Candida albicans growth and biofilm formation.

Multiresistance among microorganisms to common antimicrobials has become one of the most significant concerns in modern medicine. Nanomaterials are a new alternative to successfully treat the multiresistant microorganisms. Nanostructured materials are used in many fields, including biological sciences and medicine. Recently, it was demonstrated that the bactericidal activity of zero-valent bismuth colloidal nanoparticles inhibited the growth of Streptococcus mutans; however the antimycotic potential of bismuth nanostructured derivatives has not yet been studied. The main objective of this investigation was to analyze the fungicidal activity of bismuth oxide nanoparticles against Candida albicans, and their antibiofilm capabilities. Our results showed that aqueous colloidal bismuth oxide nanoparticles displayed antimicrobial activity against C. albicans growth (reducing colony size by 85%) and a complete inhibition of biofilm formation. These results are better than those obtained with chlorhexidine, nystatin, and terbinafine, the most effective oral antiseptic and commercial antifungal agents. In this work, we also compared the antimycotic activities of bulk bismuth oxide and bismuth nitrate, the precursor metallic salt. These results suggest that bismuth oxide colloidal nanoparticles could be a very interesting candidate as a fungicidal agent to be incorporated into an oral antiseptic. Additionally, we determined the minimum inhibitory concentration for the synthesized aqueous colloidal Bi2O3 nanoparticles.