Tunable structure of TiO2 deposited by DC magnetron sputtering to adsorb Cr (VI) and Fe (III) from water.

TiO2 thin films with mixtures of the anatase, rutile, and brookite phases were deposited on glass substrates via magnetron sputtering. Based on XRD and Raman results, the TiO2-0.47 and TiO2-3.47 films principally contained the brookite phase, while the TiO2-1.27 and TiO2-2.13 films were primarily anatase. The capacities of the TiO2 films to adsorb heavy metals were tested with Cr(VI) and Fe(III) solutions, and the maximum Cr(VI) and Fe(III) adsorption capacities were realized with the TiO2-0.47 film (334.5 mg/g) and TiO2-3.47 film (271.3 mg/g), respectively. SEM‒EDS results revealed the presence of Cr and Fe on the surfaces of the films, thus corroborating the ability of the TiO2 films to adsorb and remove heavy metals. They are strong candidates for use in wastewater treatment plants.

An enhanced photo(electro)catalytic CO2 reduction onto advanced BiOX (X = Cl, Br, I) semiconductors and the BiOI-PdCu composite.

The photoelectrocatalytic reduction of CO2 (CO2RR) onto bismuth oxyhalides (BiOX, X = Cl, Br, I) was studied through physicochemical and photoelectrochemical measurements. The successful synthesis of the BiOX compounds was carried out through a solvothermal methodology and confirmed by XRD measurements. The morphology was analyzed by SEM; meanwhile, area and pore size were determined through BET area measurements. BiOI and BiOCl present a lower particle size (3.15 and 2.71 µm, respectively); however, the sponge-like morphology presented by BiOI results in an increase in the BET area, which can enhance the catalytic activity of this semiconductor. In addition, DRS measurements allowed us to determine bandgap values of 1.9, 2.4, and 3.6 eV for BiOI, BiOBr, and BiOCl, respectively. Such results predict better visible light harvesting for BiOI. Photoelectrochemical measurements indicated that BiOX shows p-type semiconductor behavior, being the holes the majority charge carriers, making BiOI the most active material to carry out photoelectrocatalytic CO2RR. In the second stage, three different composites, BiOI-Pd, BiOI-Cu, and BiOI-PdCu, (BiOI-M; M = Pd, Cu, PdCu), were fabricated to study the influence of active metal nanoparticles (NP's) in the BiOI CO2RR activity. XRD measurements confirmed the interaction between BiOI and the metallic NP's, the three composites overpassed by 20% the BET area of pristine BiOI. Photoelectrochemical measurements indicate that all BiOI-metal composites are suitable materials to perform CO2 reduction in neutral media efficiently; however, the BiOI-PdCu composites surpassed the faradaic current of BiOI-Pd and BiOI-Cu at 0.85 V vs. RHE (3.15, 2.06 and 2.15 mA cm-2, respectively). BiOI-PdCu presented photoactivity to carry out the CO2 reduction evolving formic acid and acetic acid as the main products under visible-light irradiation.

Solar-driven CO2 reduction using modified earth-abundant ilmenite catalysts.

Photocatalytic CO2 reduction is an alternative technology to the depletion of highly pollutant fossil fuels through the generation of renewable solar-based fuels. This technology requires that the photocatalysts be obtained directly from nature to scale up the process. Taking that into consideration, this work proposed the fabrication of sodium iron titanate (NaFeTiO4) photocatalysts from earth-abundant ilmenite mineral. The photocatalysts exhibited full spectrum light response, good electron transfer due to its unique tunnel structure that favored the formation of rod-like morphology. These properties promoted the solar-driven CO2 reduction to generate formic acid (HCOOH) with high selectivity (157 µmol g-1 h-1). It was found that higher synthesis temperatures promoted the formation of Fe3+ species, which decreased the efficiency for CO2 reduction. Also, the possibility of reduced the CO2 molecules in the air was studied with the NaFeTiO4 samples, which resulted in an efficiency of up to 93 µmol g-1 h-1 of HCOOH under visible light. The stability of the solar-driven CO2 reduction with the NaFeTiO4 photocatalysts was confirmed after seven days of continuous evaluation.

Enhanced Photocatalytic Hydrogen Evolution from Water Splitting on Ta2O5/SrZrO3 Heterostructures Decorated with CuxO/RuO2 Cocatalysts.

Photocatalytic H2 generation by water splitting is a promising alternative for producing renewable fuels. This work synthesized a new type of Ta2O5/SrZrO3 heterostructure with Ru and Cu (RuO2/CuxO/Ta2O5/SrZrO3) using solid-state chemistry methods to achieve a high H2 production of 5164 µmol g-1 h-1 under simulated solar light, 39 times higher than that produced using SrZrO3. The heterostructure performance is compared with other Ta2O5/SrZrO3 heterostructure compositions loaded with RuO2, CuxO, or Pt. CuxO is used to showcase the usage of less costly cocatalysts to produce H2. The photocatalytic activity toward H2 by the RuO2/CuxO/Ta2O5/SrZrO3 heterostructure remains the highest, followed by RuO2/Ta2O5/SrZrO3 > CuxO/Ta2O5/SrZrO3 > Pt/Ta2O5/SrZrO3 > Ta2O5/SrZrO3 > SrZrO3. Band gap tunability and high optical absorbance in the visible region are more prominent for the heterostructures containing cocatalysts (RuO2 or CuxO) and are even higher for the binary catalyst (RuO2/CuxO). The presence of the binary catalyst is observed to impact the charge carrier transport in Ta2O5/SrZrO3, improving the solar to hydrogen conversion efficiency. The results represent a valuable contribution to the design of SrZrO3-based heterostructures for photocatalytic H2 production by solar water splitting.

Tapered Optical Fiber Detector for a Red Dye Concentration Measurement.

BACKGROUND: In this work, a detector based on optical fiber covered with Multi-Wall Carbon Nanotubes (MWCNTs) was used for sensing and removal of Alizarin from wastewaters. Alizarin is a strong anionic red dye that is part of the anthraquinone dye group. As a rule, this dye is used in the textile industry as a coloring agent. Experiments showed a good efficiency of wastewater treatment. This development could resolve the problem of water contamination with Alizarin red dye. METHODS: We used a single-mode fiber SMF-28e with a core diameter of 8.2 µm and a cladding diameter of 125 µm as a base for the tapered optical fiber detector. An MWCNTs array was synthesized on the tapered optical fiber detector surface by spray pyrolysis Chemical Vapor Deposition (CVD) method at 800oC for 20 min inside a tubular furnace, using ferrocene solution in toluene as a catalyst precursor. The formed structure was applied for Alizarin detection in water. RESULTS: According to the patent studies, the nanotubes completely covered the optical fiber surface and the array had a high density with minimal distance between nearby nanotubes. Carbon nanotubes were oriented along the radius of the optical fiber. The average diameter of carbon nanotubes was 24 nm. The optical absorbance levels increased as the Alizarin concentration increased from 50 mg/L to 1000 mg/L. MWCNTs on the optical fiber tapered section adsorbed the dye molecules from aqueous solution. Three intensive absorption bands with the wavelength of the 700, 714 and 730 nm appeared and their intensity increased as the Alizarin concentration increased. The accumulated Alizarin can be recovered by multiple immersing clean water. This property may make tapered optical fiber detector reusable and increase the economic expediency of the sensor application. CONCLUSION: The study showed higher Alizarin adsorption efficiency of the tapered optical fiber detector compared with relative detectors. This structure can be reusable for dye detection. Removal efficiency for Alizarin reached 98.6%, which makes the tapered optical fiber detector promising for wastewater treatment and dye elimination.

Flux synthesis of Ba2Li2/3Ti16/3O13 and its photocatalytic performance.

Barium-lithium titanate (Ba2Li2/3Ti16/3O13) was synthesized by using a flux method under some conditions with various chloride salts as the flux, thermal treatment temperatures, solute concentrations, and cooling rates. As a result, fine particles of this material with a rod-like morphology were obtained for the first time. It is suggested that this morphology with high crystallinity is responsible for the increase in the photocatalytic activity of this material without any co-catalyst for H2 and CO evolution from water and CO2. The observed photocatalytic performance is discussed taking into consideration the differences in physicochemical properties, obtained as a result of the synthesis using this method under the different conditions.

Photodegradation of indigo carmine and methylene blue dyes in aqueous solution by SiC-TiO2 catalysts prepared by sol-gel.

Indigo carmine and methylene blue dyes in aqueous solution were photodegraded using SiC-TiO(2) catalysts prepared by sol-gel method. After thermal treatment at 450°C, SiC-TiO(2) catalysts prepared in this work showed the presence of SiC and TiO(2) anatase phase. Those compounds showed specific surface area values around 22-25 m(2)g(-1), and energy band gap values close to 3.05 eV. In comparison with TiO(2) (P25), SiC-TiO(2) catalysts showed the highest activity for indigo carmine and methylene blue degradation, but this activity cannot be attributed to the properties above mentioned. Therefore, photocatalytic performance is due to the synergy effect between SiC and TiO(2) particles caused by the sol-gel method used to prepare the SiC-TiO(2) catalysts. TiO(2) nanoparticles are well dispersed onto SiC surface allowing the transfer of electronic charges between SiC and TiO(2) semiconductors, which avoid the fast recombination of the electron-hole pair during the photocatalytic process.

Methylene blue degradation by NaTaO3 sol-gel doped with Sm and La.

In this work, NaTaO(3) compounds doped with 1M% of La and Sm, were prepared by the sol-gel (SG) method and solid state (SS) reaction; and tested as photocatalysts on the degradation of methylene blue (MB) under UV light. The structural characterization by X-ray powder diffraction revealed that the crystallization of the NaTaO(3) phase prepared by the sol-gel method started at 600 degrees C, reaching maximum crystallization at 800 degrees C. It was determined that the presence of Sm and La retard the crystallization of the NaTaO(3) phase. On the other hand, the compounds synthesized in this work showed particle sizes in the nanometric scale, as it was observed by scanning electron microscopy (SEM). The specific surface area of the compounds synthesized by the sol-gel method, showed values 4 times higher than those obtained by the solid state reaction, favoring their functional and photocatalytic performance in the methylene blue degradation. In addition, the best photocatalytic performance was shown by the NaTaO(3) doped with Sm and heated at 600 degrees C, having a half-life time of 65 min.